Files > SURGERY

name
SURGERY
number
130
location
^SRF(
description
Each entry in the SURGERY file contains information regarding a surgery case made up of an operative procedure, or multiple operative procedures for a patient. The file includes the information necessary for creating the Nurses' Intraoperative Report, Operation Report, and Anesthesia Report
Fields
#NameLocationTypeDetailsIndexDescription
.01patient(+)0;1POINTER2BThis is the name of the patient.
.011hospital admission status0;12SET OF CODESI:INPATIENT
O:OUTPATIENT
1:SAME DAY
2:ADMISSION
3:HOSPITALIZED
Definition Revised (2014): This field indicates the patient's hospital admission status on the date of surgery. Enter "1" or "S" if the operation was same day (the patient was not admitted); "2" or "A" if the patient was admitted on the date of surgery; or "3" or "H" if the patient was already hospitalized on the day prior to the date of surgery.
.015visit0;15POINTER9000010AVThis is the visit associated with this case.
.0155classification entered (y/n)0;20BOOLEAN1:YES
0:NO
This field indicates whether or not classification items have been addressed. This field is used by the software to decide whether to allow the user a choice to update classification information. If the field is NO or null, it will not permit a choice if the site parameter to enter classification information is turned on.
.016service connected0;16BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a service connected problem. This information may be passed to the VISIT file (#9000010) for use by PCE.
.017agent orange exposure0;17BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to Agent Orange Exposure. This information may be passed to the VISIT file (#9000010) for use by PCE.
.018ionizing radiation exposure0;18BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to Ionizing Radiation Exposure. This information may be passed to the VISIT file (#9000010) for use by PCE.
.019southwest asia conditions0;19BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem related to service in SW Asia. This information may be passed to the VISIT file (#9000010) for use by PCE.
.02op room procedure performed0;2POINTER131.7This is the name of the operating room where the principal operation is performed for this patient. It can be selected by entering the name or abbreviation of the operating room.
.021associated clinic0;21POINTER44This is the clinic associated with this surgical case or non-OR procedure. The entry made in this field will be used as the location of the encounter for PCE.
.022military sexual trauma0;22BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to Military Sexual Trauma. This information may be passed to the VISIT file (#9000010) for use by PCE.
.023head and/or neck cancer0;23BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to Head and/or Neck Cancer. This information may be passed to the VISIT file (#9000010) for use by PCE.
.024combat vet0;24BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to Combat. This information may be passed to the VISIT file (#9000010) for use by PCE.
.026proj 112/shad0;25BOOLEAN1:YES
0:NO
This field will be used to indicate if this surgery or non-OR procedure is treating a VA patient for a problem that is related to PROJ 112/SHAD. This information may be passed to the VISIT file (#9000010) for use by PCE.
.03major/minor0;3SET OF CODESJ:MAJOR
N:MINOR
Definition Revised (2004): Major - Any operation performed under general, spinal, or epidural anesthesia plus all inguinal herniorrhaphies, carotid endarterectomies, parathyroidectomies, thyroidectomies, breast lumpectomies, or endovascular AAA repairs regardless of anesthesia administered. Minor - All operations not designated as Major.
.035case schedule type0;10SET OF CODESEM:EMERGENCY
EL:ELECTIVE
A:ADD ON (NON-EMERGENT)
S:STANDBY
U:URGENT
This is the code describing how this case was scheduled. It is important that this field is entered. The Scheduler may use this field when updating the schedule due to cancellations or insertions. Non-Cardiac Definition of Emergency Case (2004): An emergency case is usually performed as soon as possible and no later than 12 hours after the patient has been admitted to the hospital or after the onset of related preoperative symptomatology. Answer EMERGENCY if the surgeon and anesthesiologist report the case as emergent
.037case schedule order0;11FREE TEXTThis is the sequence in which the surgeon expects to do the case if he or she has more than one case scheduled for this day. This field is optional, but is very useful to the person scheduling cases if the surgeon has more than one case.
.04surgery specialty(+)0;4POINTER137.45Definition Revised (2007): This is the surgical specialty credited for doing this operative procedure. Many reports, including the Annual Report of Surgical Procedures, are sorted by the surgical specialty. This field should be entered prior to completion of this case. (If you enter '?' in the surgical package, it will display the entire local surgical specialty list and a copy of the national list can be found in the Operations Manual.)
.05req clean or contaminated0;5SET OF CODESC:CLEAN
D:CONTAMINATED
This is the description of the wound class for the case. The code entered is used when scheduling the operating room for this procedure.
.07preop skin integ0;7POINTER135.2This is the preoperative assessment of the patient's skin integrity upon arrival to the operating room. The information entered will appear on the Nurse Intraoperative Report.
.08preop skin color0;8SET OF CODESA:ASHEN
LBR:LIGHT BROWN
DBR:DARK BROWN
PI:PINK
PA:PALE
F:FLUSHED
M:MOTTLED
C:CYANOTIC
I:ICTERIC
This is the code corresponding to the preoperative assessment of the patient's skin color upon arrival to the operating room. If entered, this information will appear on the Nurse Intraoperative Report.
.09date of operation(+)0;9DATE-TIMEThis is the date that the case was performed. The date of operation must be entered for all cases.
.11trans to or by.1;1POINTER131.01This is the method or device used to deliver the patient to the operating room. This field is optional, but may be useful for documentation of the case.
.111or circ support19;0MULTIPLE130.28This is information about the nurses with circulating role responsibilities.
.112or scrub support23;0MULTIPLE130.36This is information about the person with scrub role responsibilities.
.12hair removal by.1;2POINTER200This is the person responsible for removing the patient's hair in preparation for the operative procedure (if necessary).
.13restr & position aids20;0MULTIPLE130.31This is information related to restraints and positioning aids used during this operative procedure.
.14primary surgeon(+).1;4POINTER200This is the name of the person performing the major portion of the principal operative procedure. This field is required as part of the Operation Report. This field may be restricted by locally determined keys so that only people with the appropriate keys can be entered.
.15first asst.1;5POINTER200This is the name of the person assisting the surgeon during the operative procedure. The information entered here appears on the Operation Report and Nurse Intraoperative Report.
.16second asst.1;6POINTER200This is the name of the second person assisting the surgeon during the operative procedure. If entered, this information appears on the Operation Report and Nurse Intraoperative Report.
.164attending surgeon.1;13POINTER200This is the name of the attending staff surgeon responsible for this case. This information appears on the Operation Report, Nurse Intraoperative Report, and Attending Surgeon Report.
.165*attending code - not used.1;16SET OF CODES0:LEVEL 0. ATTENDING DOING THE OPERATION
1:LEVEL 1. ATTENDING IN O.R. ASSISTING THE RESIDENT
2:LEVEL 2. ATTENDING IN O.R., NOT SCRUBBED
3:LEVEL 3. ATTENDING NOT PRESENT IN O.R. SUITE, IMMEDIATELY AVAILABLE
NOTE: This field is replaced by the new ATTENDING CODE field (#.166). This is the code corresponding to the highest level of supervision provided by the attending staff surgeon for this case. This information appears in the Operation Report, Nurse Intraoperative Report, and Attending Surgeon Report. 0 The staff practitioner performs the case but may be assisted by a resident. 1 The supervising practitioner is physically present in the operative or procedural suite and directly involved in the procedure. The resident performs major portions of the procedure. 2 The supervising practitioner is physically present in the operative or procedural suite and immediately available for consultation. The supervising practitioner may observe and provide direction. The resident performs the procedure 3 The supervising practitioner is not physically present in the operative or procedural suite, but is in the facility or on the VA campus. The supervising practitioner is immediately available for resident supervision or consultation as needed. Local policy, as approved by the VISN Academic Affiliations Officer, should define the standard for "availability" of the supervising practitioner. NOTE: The service chief and chief of staff are responsible for periodically reviewing cases done under Level 3 supervision.
.166attending/res sup code.1;10POINTER132.9This is the code corresponding to the highest level of resident supervision provided by the attending staff surgeon for this case.
.167perfusionist.1;19POINTER200This is the name of the person operating the cardio-pulmonary or organ perfusion apparatus. Although not required, this information may be valuable in documenting the case. If entered, it will appear on the Nurse Intraoperative Report.
.168asst perfusionist.1;20POINTER200This is the name of the person assisting the perfusionist. If applicable, this information may be valuable in documentation of this case.
.175skin prep agents.1;7POINTER135.1This is the type of agent used to wash and prepare the operative site. If entered, this information appears on the Nurse Intraoperative Report and is useful in documenting the case.
.18skin prepped by (1).1;8POINTER200This is the name of the person responsible for applying the agent used to wash and prepare the operative site. If entered, this information will appear on the Nurse Intraoperative Report.
.19preop mood.1;9POINTER135.3This is the preoperative assessment of the patient's emotional status upon arrival to the operating room. It may be useful in the documentation of the case. If entered, this information will appear on the Nurse Intraoperative Report.
.195preop converse.1;14SET OF CODESTC:TALKS CONSTANTLY
IC:INITIATES CONVERSATION
RQ:RESPONDS TO QUESTIONS
NA:NOT ANSWER QUESTIONS
A:APHASIC
D:DYSPHASIC
This is the preoperative assessment of the patient's demonstrated verbal responses upon arrival to the operating room. Although optional, this field may be valuable in documenting this case.
.196preop conscious.1;15POINTER135.4This is the preoperative assessment of the patient's level of consciousness upon arrival to the operating room. Although optional, this information may be useful in documenting the case.
.202nurse present time.2;7DATE-TIMEThis is the date and time that the nurse was present in the operating room. Times entered without a date will be converted to the date of operation at that time.
.203time pat in hold area.2;15DATE-TIMEThis is the date and time that the patient arrived in the holding area. Times entered without a date will be converted to the date of operation at that time.
.204anes avail time.2;8DATE-TIMEThis is the date and time that the anesthetist is available to service the patient. Although optional, this information is useful for evaluating operation delays.
.205time pat in or.2;10DATE-TIMEThis is the date and time that the patient was transported into the operation room. Times entered without a date will be converted to the date of operation at that time. Definition Revised (2004): Patient in Room (PIR): Time when patient enters the OR/PR.
.206surg present time.2;9DATE-TIMEThis is the date and time that the surgeon is available to begin the operative procedure. Although not mandatory, this information is useful for evaluating hospital delays.
.21anes care start time.2;1DATE-TIMEThis is the date and time that the anesthesia care began. It is required as part of the anesthesia report. The definition of what constitutes the time anesthesia care begins may vary depending on local anesthesia policy. Non-Cardiac Definition Revised(2004): Anesthesia Start (AS): Time when a member of the anesthesia team begins preparing the patient for an anesthetic.
.213anes care time block50;0MULTIPLE130.213This is the date and time for which anesthesia care is provided.
.214anes care billable time flag.2;17BOOLEAN1:YES
0:NO
This field is a flag that indicates all anesthesia care time has been entered for a case. It is used in calculating the total anesthesia billable time. "Yes" indicates all time has been entered. "No" indicates time entry is not complete.
.215induction complete.2;11DATE-TIMEThis is the date and time that the anesthetist declares the patient ready for the start of the operative procedure. Although optional, this information may be useful in management studies.
.218anes care billable timeCOMPUTEDThis is the total anesthesia care billable time in minutes. It is calculated from all time intervals entered in the multiple anesthesia start and end time fields..
.22time operation began.2;2DATE-TIMEThis is the date and time that the operation began. The definition of this time is usually 'knife fall', but may vary according to local surgery service protocol. Non-Cardiac Definition Revised(2004): Procedure/Surgery Start Time (PST): Time the procedure is begun (e.g., incision for a surgical procedure).
.23time operation ends.2;3DATE-TIMEDefinition Revised (2004): Procedure/Surgery Finish (PF): Time when all instrument and sponge counts are completed and verified as correct; all postoperative radiological studies to be done in the OR/PR are completed; all dressings and drains are secured; and the physician/surgeons have completed all procedure-related activities on the patient. Should the patient expire in the operating room, indicate the time the patient was pronounced dead.
.232time pat out or.2;12DATE-TIMEThis is the date and time that the patient is taken from the operating room. Times entered without a date will be converted to the date of operation at that time. This information is very significant for operating room management studies. Definition Revised (2011): Indicate the time the patient was transported out of the operating room. If the patient dies prior to leaving the OR, then indicate the time of death for this data element.
.234or clean start time.2;13DATE-TIMEThis is the date and time when the 'end of case' or terminal cleaning began. Times entered without a date will be converted to the date of operation at that time.
.236or clean end time.2;14DATE-TIMEThis is the date and time when the 'end of case' or terminal cleaning ended. Times entered without a date will be converted to the date of operation at that time.
.24anes care end time.2;4DATE-TIMEThis is the date and time that anesthesia care ends. Its definition may vary according to local anesthesia policy. Acceptable time formats include 7:45, 745, T@7:45 and JAN 1@7:45. Times entered without a date will be converted to the date of the operation at that time. Non-Cardiac Definition Revised (2004): Anesthesia Finish (AF): Time at which anesthesiologist turns over care of the patient to a post anesthesia care team (either PACU or ICU).
.25blood loss (ml).2;5NUMERICThis is the number of milliliters (0-100000) of blood estimated to be lost during the operative procedure (EBL). This information appears on the Nurse Intraoperative report, if entered.
.255total urine output (ml).2;16NUMERICThis is the total number of milliliters (0-100000) of urine output during the operative procedure. If entered, this information appears on the Nurse Intraoperative Report.
.27replacement fluid type4;0MULTIPLE130.04This is information related to the replacement fluid given intravascularly during the operative procedure.
.28general comments5;0WORD-PROCESSINGThese are general comments about the operative procedure. Any information not provided for elsewhere can be entered here.
.29nursing care comments7;0WORD-PROCESSINGThese are comments on this case required for documentation on the Nurse Intraoperative Report.
.293monitors27;0MULTIPLE130.41This is information related to invasive or non-invasive monitors used during this case.
.31princ anesthetist.3;1POINTER200This is the name of the principal anesthesiologist or CRNA (or surgeon, if local anesthesia). This information is extremely important for the Anesthesia Report.
.32relief anesthetist.3;2POINTER200This is the name of the anesthetist relieving the principal anesthetist, if applicable. If entered, this information appears on the Anesthesia Report.
.33asst anesthetist.3;3POINTER200This is the name of the person assisting the principal anesthetist. If entered, this information appears on the Anesthesia Report.
.34anesthesiologist supvr.3;4POINTER200This is the name of anesthesia supervisor. He or she may be the same person entered in the 'PRINC ANESTHETIST' or 'ASST ANESTHETIST' fields. This information is required if the principal anesthetist is in a training status, or CRNA.
.345anes supervise code.3;6POINTER132.95This is the code corresponding to the highest level of supervision of the anesthesiology staff supervisor. This information appears on the Anesthesia Report.
.3511anes personally performed.2;19BOOLEAN0:NO
1:YES
Answer yes only if the anesthesiologist personally performed the entire anesthesia procedure.
.3512num of concurrent anes cases.2;20NUMERICIncluding this case, enter the number of cases that the anesthesiologist supervised where the time of the anesthesia care overlapped with this care. This field is required to support billing for the care and is critical for accurate coding of the primary anesthesia procedure. Enter a zero if the anesthesiologist personally performed the care. Enter 1 if the principal anesthetist was not an anesthesiologist and was medically directed by an anesthesiologist.
.3513anes concurrent cases55;0MULTIPLE130.3513This field is for information only and is not required. It will assist in correcting potential errors if a start or end time is edited since other cases could be affected by the edit.
.3514anes medically directed.2;22BOOLEAN0:NO
1:YES
If the principal anesthetist was other than an anesthesiologist, answer yes if an anesthesiologist supervised the care. Answering no indicates that the anesthetist was unsupervised.
.3515anes physician available.2;23BOOLEAN0:NO
1:YES
If the anesthetist was a resident, answer yes if the teaching physician was present during all key portions of the procedure and immediately available during the entire procedure.
.36min intraop temperature (c).3;7NUMERICThis is the lowest temperature of the patient during the operative procedure. If entered, this information will appear on the Nurse Intraoperative Report.
.37anesthesia technique6;0MULTIPLE130.06This is information about the anesthesia technique used during this case.
.375medications22;0MULTIPLE130.33This is information about medication for this case.
.39irrigation26;0MULTIPLE130.08This is information related to the irrigation solution.
.42other procedures13;0MULTIPLE130.16This is information related to procedures performed in addition to the principal procedure.
.43planned postop care.4;3POINTER131.6This is the code corresponding to the location of care after the patient leaves the operating room and/or the post-anesthesia care unit.
.44or set-up time.4;4NUMERICThis is the number of minutes (0-999) necessary to prepare the operating room for the admission of the patient for the surgical procedure.
.46op disposition.4;6POINTER131.6This is the destination of the patient upon transfer from OR staff care.
.47prosthesis installed1;0MULTIPLE130.01This is information related to the prosthesis used for this operative procedure.
.48time tourniquet applied2;0MULTIPLE130.02This is information related to the application of a tourniquet.
.52final counts verify correct.5;1SET OF CODESY:CORRECT
N:INCORRECT
U:UNKNOWN
This is the code corresponding to the status of the final count at the end of the surgical procedure.
.522verifier.5;12POINTER200This is the person responsible for verifying that the final sponge, sharps, and instrument counts are correct at the end of this operative procedure.
.523*inst cnt correct.5;10SET OF CODESY:CORRECT
N:INCORRECT
U:UNKNOWN
Enter the code corresponding to the status of the final instrument count at the end of the surgical procedure. This field is marked for deletion.
.525inst cnt verf by.5;11POINTER200This is the name of the person accountable for verification of the final instrument count.
.54*surgery position.5;3POINTER132This field has been asterisked for deletion 18 months from the release of version 3.0 of the DHCP Surgery package. A multiple field titled SURGERY POSITION will be used in it's place.
.55electroground position.5;4POINTER138This is the code corresponding to the area of placement of the dispersive electrode pad.
.56foley catheter size.5;5NUMERICThis is the size of the Foley catheter.
.57foley catheter inserted by.5;6POINTER200This is the name of the person accountable for insertion of the Foley catheter. Although this information is optional, it may be useful in documentation of this case.
.61preop temperature.6;1NUMERICThis is the most recent ward-recorded temperature of the patient prior to transport to the operating room.
.615preop weight (kg).6;10NUMERICThis is the most recent ward-recorded weight of the patient prior to transport to the operating room.
.62preoperative heart rate.6;2NUMERICThis is the most recent ward-recorded heart rate of the patient prior to transport to the operating room.
.63preop blood pressure.6;3FREE TEXTThis is the most recent ward recorded blood pressure of the patient prior to transport to the operating room. Although optional, this information may be useful for documentation of this case.
.64preop respiratory rate.6;4NUMERICthis is the most recent ward-recorded respiratory rate of the patient prior to transport to the operating room.
.65final anesthesia temp (c).6;5NUMERICThis is the temperature, in degrees centigrade, at the time of the end of anesthesia care.
.66postop pulse.6;6NUMERICThis is the pulse rate of the patient upon admission to the care area immediately after the surgical procedure.
.67postop bp.6;7FREE TEXTThis is the patient's blood pressure upon admission to the care area immediately after the surgical procedure. Although this information is optional, it may be useful in documentation of this case.
.68postop resp.6;8NUMERICThis is the respiratory rate of the patient upon admission to the care area immediately after the surgical procedure.
.69time-out document completed by.6;9POINTER200VASQIP Definition (2014): This is the name of the person verifying the patient's identification band, Social Security Number, surgical site/procedure, and the entry of a valid operative consent on the patient's record.
.72other preop diagnosis14;0MULTIPLE130.17This is information related to any diagnosis in addition to the principal preoperative diagnosis.
.74other postop diags15;0MULTIPLE130.18This is information related to any postoperative diagnosis in addition to the principal postoperative diagnosis.
.75electrocautery unit.7;5FREE TEXTThis is information identifying the electrosurgical unit utilized during the operative procedure. The information may include, but is not limited to, unit number, ground pad lot number and/or expiration date, coag setting, cut setting, blend-BI:Setting and Bipolar BP:Setting. Examples: Electrocautery Unit: #7 HP206 COAG:50 CUT:50 BI:1 Electrocautery Unit: DAISY:18% or DAISY BP:18% Electrocautery Unit: VL#2 EXP 3/20/91 COAG:30 CUT:20 BI:2 #2 BP:20 (VL-VALLEYLAB)
.757thermal unit21;0MULTIPLE130.32This is information related to the temperature controlling device.
.76postop skin integ.7;6POINTER135.2This is the code corresponding to the assessment of the patient's skin integrity after the operative procedure. If entered, this information will appear on the Nurse Intraoperative Report.
.77postop skin color.7;7SET OF CODESA:ASHEN
LBR:LIGHT BROWN
DBR:DEEP BROWN
PI:PINK
PA:PALE
F:FLUSHED
C:CYANOTIC
I:ICTERIC
This is the code corresponding to the patient's skin color after the operative procedure. If entered, this information will appear on the Nurse Intraoperative Report.
.79pacu disposition.7;9POINTER131.6This is the code corresponding to the destination of the patient immediately after release from the post-anesthesia care unit.
.81postop mood.8;1POINTER135.3This is the code corresponding to the assessment of the patient's mood following the operative procedure. If entered, this information will appear on the Nurse Intraoperative Report.
.82postop convers.8;2SET OF CODESTC:TALKS CONSTANTLY
IC:INITIATES CONVERSATION
RQ:RESPONDS TO QUESTIONS
NA:NOT ANSWER QUESTIONS
A:APHASIC
D:DYSPHASIC
This is the code corresponding to the assessment of the patient's demonstrated verbal responses at the completion of the surgical procedure.
.821postop conscious.8;10POINTER135.4This is the code corresponding to the assessment of the patient's level of consciousness following the operative procedure. If entered, this information will appear on the Nurse Intraoperative Report.
.84end pulse.8;4NUMERICThis is the patient's pulse rate at the end of the operative procedure.
.85end bp.8;5FREE TEXTThis is the patient's systolic/diastolic blood pressure at the end of the operative procedure. Although optional, this information may be useful in documentation of this case.
.86end resp.8;6NUMERICThis is the patient's rate of respiration at the end of the operative procedure. This information may be useful in documentation of this case.
.875packing.8;11SET OF CODESV:VASOLINE
I:IODOFORM
P:PLAIN
B:BETADINE
D:DENTALPACKS
O:OTHER
N:NONE
This is the code corresponding to the type of packing placed during the procedure that will remain in place when the patient is discharged from the operating room.
.971patient education/assessment.97;1SET OF CODESY:YES
N:NO
I:INAPPLICABLE
U:UNKNOWN
This indicates whether preoperative patient education and assessment, with documentation of a care plan, were completed during the perioperative care of the patient.
.972consent sig&wit.97;2SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether there is a properly signed and witnessed operative consent present in the patient's medical record.
.973bath & shampoo.97;3SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates if the patient's preoperatively prescribed bath and shampoo were completed.
.974rec&xray ready.97;4SET OF CODESY:YES
N:NO
I:INCOMPLETE
This indicates whether the patient's x-rays and records are complete.
.975enema(s) if ord.97;5SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the administration of preoperative enema(s) were completed, if ordered.
.976npo as ord/clin mid.97;6SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether NPO orders were completed prior to the operative procedure as ordered by the surgeon.
.977*clerk chn days before.97;7NUMERICThis field is not being used and is marked for deletion.
.981*verfify id tag ssn.98;1SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the identification bracelet and social security number verification was completed, legal and correct. This field has been marked for deletion.
.9811care plan in chart.98;10SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the nursing care plan is present on the patient's medical record prior to transport of the patient into the operating room.
.9812address plate.98;11SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates if the patient's address plate is present on the patient's medical record prior to transport to the operating room.
.9813patient voided.98;12SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient voided prior to being transported to the operating room.
.9814preop med&rail up.98;13SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether preoperative medication was administered and the side rails of the bed were placed in the 'up' position.
.9815*clerk chn date procedure.98;14NUMERICThis field has been marked for deletion. It should not be used.
.982prosthesis rem.98;2SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether prosthetics (dentures, jewelry, hair pieces) have been removed prior to transport to the operating room.
.983cig, match & val rem.98;3SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient's tobacco products, matches and valuables have been removed from his or her possession prior to being transported to the operating room.
.984valuables secured.98;4SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient's valuables have been secured according to hospital policy.
.985oral hygiene.98;5SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient's oral hygiene was completed prior to being transported to the operating room.
.986freshly shaved.98;6SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient's facial hair was freshly shaved prior to being transported to the operating room.
.987clean dressing.98;7SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates if all appropriate wounds have had clean dressings applied prior to transport to the operating room.
.988clean hosp cloth.98;8SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has clean hospital clothing prior to being transported to the operating room.
.989levin tube/cath.98;9SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether a Levin tube/catheter is present prior to transport to the operating room.
.991u/a in 48 hrs.99;1SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has had a urinalysis within 48 hours prior to being transported to the operating room.
.9911*clerk chn rec for maj surg.99;10NUMERICThis field has been marked for deletion. It should not be used.
.992cbc in 48 hrs.99;2SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has had a CBC within 48 hours prior to being transported to the operating room.
.993blood type&xmatch.99;3SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has had blood typing and crossmatching done.
.994*bleeding & ptt time in 48 hrs.99;4SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has had bleed and PTT time within 48 hours prior to being transported to the operating room. This field has been marked for deletion in the next version of the Surgery package.
.995*bun in 7 days.99;5SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This indicates whether the patient has had a BUN within 7 days prior to being transported to the operating room. This field has been marked for deletion in the next version of the Surgery package.
.996*blood sugar in 7 days.99;6SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This field determines whether the patient has had a blood sugar test within the last 7 days. This field has been marked for deletion in the next release of the Surgery software.
.997*serology report.99;7SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This field has been marked for deletion. It should not be used.
.998chest xray in 7 days.99;8SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This field determines whether the patient has had a chest x-ray within the last seven days.
.999ekg in 24 hrs.99;9SET OF CODESY:YES
N:NO
I:INAPPLICABLE
This field determines whether the patient has had an EKG within the last 24 hours.
1.01req anesthesia technique1.0;1SET OF CODESL:LOCAL
S:SPINAL
B:BLOCK
G:GENERAL
C:CHOICE
MAC:MONITORED ANESTHESIA CARE
E:EPIDURAL
This is the surgeon's choice of anesthesia for the proposed operative procedure. This information will appear on the Schedule of Operations.
1.02req froz sect1.0;2BOOLEANY:YES
N:NO
This indicates whether laboratory support is needed to perform frozen section diagnostic tests during the operative procedure.
1.03req preop x-ray1.0;3FREE TEXTThese are the types of preop x-ray films and reports required for delivery to the operating room prior to the surgical procedure.
1.035intraoperative x-rays1.0;5SET OF CODESY:YES
N:NO
C:C-ARM
This indicates if radiology personnel is needed in the operating room for intraoperative radiologic procedures.
1.04req photo1.0;4BOOLEANY:YES
N:NO
This indicates whether Medical Media personnel need to be present in the operating room to obtain photographs during the operative procedure.
1.05req blood kind11;0MULTIPLE130.14This is information related to the blood product required during this operative procedure.
1.052req blood avail1.0;9BOOLEANY:YES
N:NO
This indicates whether the requested blood components are available.
1.09wound classification1.0;8SET OF CODESC:CLEAN
CC:CLEAN/CONTAMINATED
D:CONTAMINATED
I:DIRTY/INFECTED
Definition Revised (2007): Indicate whether the wound has been classified by the primary surgeon as: >> Class 1 - Clean (C): Respiratory, alimentary, genital, or uninfected urinary tracts are not entered. Uninfected surgical wounds. No inflammation is encountered. Closed primarily and, if necessary, drained with closed drainage. Surgical incisional wounds that occur with nonpenetrating (eg blunt) trauma should be included in this category if they meet the criteria. [No hollow organ (e.g. bladder, stomach, vagina, lung, etc.) is entered; no breaks in aseptic technique.] Examples: - Exploratory laparotomy - Mastectomy or breast reduction - Neck dissection - Nonpenetrating blunt trauma - Thyroidectomy - Total hip replacement - Vascular operations (e.g. AAA, AV fistula, CEA, aortoiliac bypass) - Hernia repair - CABG, AVR - Craniotomy, majority neurosurgery - Pleura biopsy - Sternotomy - Abdominoplasty - Bone anchored hearing aids (BAHA) - Penile prosthesis placement - Dupuytren's release, finger - Liposuction - Carpal tunnel release - Hydrocele repair >> Class 2 - Clean/Contaminated (CC): Respiratory, alimentary, genital, or urinary tracts are entered under controlled conditions and without unusual contamination. Specifically, procedures involving the biliary tract, appendix, vagina, and oropharynx are included in this category, provided no evidence of infection or major breaks in technique are encountered. (Hollow organ entered but controlled; no inflammation; primary wound closure; minor break in aseptic technique; mechanical drain used.) Examples: - Bronchoscopy - Routine appendectomy - Cholecystectomy (e.g., any approach) - Laryngectomy - Small bowel resection - Oropharynx entered - GYN procedures - Vagina entered - Whipple pancreaticoduodenectomy - Pulmonary resection - Transurethral resection of prostate - Head & Neck cancer operations (e.g., oropharynx) - Sigmoid colectomy - Minor break in technique - Gastrointestinal or respiratory tract entered without significant spillage - Genitourinary tract entered in absence of infected urine >> Class 3 - Contaminated (D): Open fresh, accidental (e.g. traumatic) wounds. Procedures that have major breaks in sterile technique (eg, open cardiac massage) or gross spillage from the gastrointestinal tract and incisions in which acute, nonpurulent inflammation is encountered are included in this category. Examples: - Appendectomy for gangrenous appendicitis - Bile spillage during cholecystectomy - Diverticulitis - Laparotomy for penetrating injury with intestinal spillage - Entrance of genitourinary or biliary tracts in presence of infected urine or bile - Necrotic tissue without evidence of purulent drainage (e.g. dry gangrene) >> Class 4 - Dirty/Infected (I): Old traumatic wounds that have retained devitalized tissue and those that involve existing clinical infection or perforated viscera. This definition suggests that the organisms causing postoperative infection were present in the surgical field before the procedure. (Untreated, uncontrolled spillage from an internal organ; pus in operative wound; open suppurative wound; severe inflammation.) Examples: - Excision and drainage of abscess - Myringotomy for otitismedia - Perforated bowel - Peritonitis (abdominal exploration for acute bacterial peritonitis) - Acute bacterial inflammation, without pus - Transection of 'clean' tissue for the purpose of surgical access to a collection of pus - Traumatic wound with foreign bodies, fecal contamination, or delayed treatment, or all of these; or from dirty source
1.098date/time or request made1.0;11DATE-TIMEThis is the date and time that the operation request was made. This information is automatically entered at the time of request. If the request date is changed, this field will be updated to reflect the new date/time requested.
1.099surg sched person1.0;10POINTER200This is the name of the person requesting or scheduling this operative procedure.
1.11pac(u) admit score1.1;1NUMERICThis is the objective evaluation numerical score of the patient upon admission to the post anesthesia care unit.
1.12pac(u) disch score1.1;2NUMERICThis is the objective evaluation numeric score of the patient at discharge from the post anesthesia care unit.
1.13asa class1.1;3POINTER132.8VASQIP Definition (2010): Record the American Society of Anesthesiology (ASA) Physical Status Classification of the patient's present physical condition on a scale from 1-6 as it appears on the anesthesia record. Most likely there will be a 2nd assessment of the ASA class prior to anesthesia induction. If this is available, report this most recent assessment. The definitions are: ASA 1 - A normal healthy patient ASA 2 - A patient with mild systemic disease ASA 3 - A patient with severe systemic disease ASA 4 - A patient with severe systemic disease that is a constant threat to life ASA 5 - A moribund patient who is not expected to survive without the operation ASA 6 - A declared brain-dead patient whose organs are being removed for donor purposes ASA 6 cases should be excluded. Classification numbers followed by an 'E' indicate an emergency. Select N for NONE ASSIGNED if no ASA Class is assigned for this patient.
1.14intraoperative occurrences10;0MULTIPLE130.13This is information related to any intraoperative occurrences. If there are no occurrences, leave this field blank. 'NONE' is not an acceptable answer.
1.145returned to surgery29;0MULTIPLE130.43This is information related to the patient's return to surgery within 30 days of a prior operative procedure.
1.15surgeon's dictation12;0WORD-PROCESSINGThis is the Surgeon's dictated operation note.
1.16postop occurrence16;0MULTIPLE130.22This is information related to postoperative occurrences.
1.17admit pac(u) time1.1;7DATE-TIMEThis is the date/time that the patient was admitted to the post anesthesia care unit (recovery room). Times entered without a date will be converted to the date of operation at that time.
1.18pac(u) disch time1.1;8DATE-TIMEThis is the date/time that the patient is discharged from the post anesthesia care unit (recovery room). Times entered without a date will be converted to the date of operation at that time. Non-Cardiac Definition Revised (2004): Discharge from Post-Anesthesia Care Unit (DPACU): Time patient is transported out of PACU.
1.19postop anes note date1.1;9DATE-TIMEThis is the date and time that the postoperative note is written in the patient's chart. Times entered without a date will be converted to the date of operation at that time.
1.2postop anes note48;0WORD-PROCESSINGThis is the postoperative anesthesia note for this patient.
1.21operation timeCOMPUTEDThis is the number of minutes between the operation start and end times.
1.22anesth induct timeCOMPUTEDThis is the total number of minutes between the anesthesia care start and induction complete times.
1.23anes care timeCOMPUTEDThis is the number of minutes between the anesthesia care start time and anesthesia care end time.
1.24patient in or timeCOMPUTEDThis is the number of minutes the patient was in the operating room.
1.25or clean up timeCOMPUTEDThis is the number of minutes between the OR clean up start time and OR clean up end time.
1.26pac(u) timeCOMPUTEDThis is the number of minutes the patient spent in the PAC(U).
4skin prepped by (2).1;12POINTER200This is the name of a second person performing skin preparation, if applicable. When entered, this information appears on the Nurse Intraoperative Report.
5skin prepped by (3).1;17POINTER200This is the name of the third person performing the preoperative skin preparation. If entered, this information will appear on the Nurse Intraoperative Report.
6electroground position (2).5;13POINTER138This is the code corresponding to the placement of the second dispersive electrode pad.
7dressing condition31;1SET OF CODESD:DRY
S:SEROSANGUINOUS
SA:SANGUINOUS
N:NO DRESSING
This is the status of the drainage on the dressing. Although optional, this information may be useful in documentation of this case.
8second skin prep agent31;2POINTER135.1This is the name of the SECOND antimicrobial agent used to wash and prepare the operative site. Although optional, this information may be useful in documentation of the case.
9time nurse out of or31;3DATE-TIMEThis is the date and time that the circulating nurse completed duties for the operative procedure and left the operating room.
10scheduled start time31;4DATE-TIMEThis is the date and time that this operative procedure is scheduled to begin.
11scheduled end time31;5DATE-TIMEThis is the date and time that this operative procedure is scheduled to end.
12in or to anes startCOMPUTEDThis is the number of minutes between the time anesthesia care began and time that the patient left the operating room.
13anes start to op startCOMPUTEDThis is the number of minutes between the time that anesthesia care started and time that the operation began.
14in or to op start timeCOMPUTEDThis is the time between the time the patient enters the operating room to the operation start time.
15date/time of dictation31;6DATE-TIMEThis is the date and time that dictation of the operative summary was completed.
17cancel date30;1DATE-TIMEThis is the date and time that the operative procedure was canceled.
17.5cancellation timeframe30;5SET OF CODES1:SURGERY CANCELLED <48 HRS BEFORE SCHEDULED SURGERY
2:SURGERY CANCELLED >48 HRS BEFORE SCHEDULED SURGERY
VASQIP Definition (2014): This indicates when the surgery was cancelled; either less than 48 hours prior to the scheduled surgery time or more than 48 hours prior to the scheduled surgery time.
18primary cancel reason31;8POINTER135VASQIP Definition (2014): This is the reason that this surgical case was cancelled. List of valid reasons: 1) Patient Related Issue (e.g., patient did not follow pre-surgery instructions, patient chooses to cancel for any reason) 2) Environmental Issue (OR availability impacted by e.g., air handling, electrical outage, emergency construction, flood, tornado, blizzard, hurricane causing OR hospital closure. If due to staff availability, use #3) 3) Staff Issue (e.g., unavailable surgeon, anesthesia or nursing staff; no documented consent, provider cancels due to change in patient treatment plan) 4) Patient Health Status (Provider cancels due to change in patient health status) 5) More clinically urgent/emergent case superseded this scheduled case 6) Scheduling Issues Not Created By An Emergency Case (previous case overtime, case delayed, double booked, general time constraints, administrative scheduling error) 7) Unavailable Bed 8) Unavailable Equipment [excluding RME] (e.g., vendor, c-arm, implant, malfunctioning equipment) 9) Unavailable Reusable Medical Equipment (RME) (includes defective packaging, damaged instruments or failure of Sterile Processing Services [SPS] to provide reprocessed equipment in a timely manner) 10) Patient scheduled into an earlier date for surgery.
19cancellation comments30;4FREE TEXTThis is the cancellation comments field. If "OTHER" is selected for the CANCEL REASON field (#18), the user will be prompted to enter a comment in this field.
20diagnostic/therapeutic (y/n)31;9BOOLEANY:YES
N:NO
This indicates if the anesthesia technique is an anesthesia diagnostic/ therapeutic procedure.
21wait time start31;11DATE-TIMEThis is start of the patient's "wait" for Surgery. Typically, this is the date that the patient was notified that Surgery is needed.
22tubes and drains3;1FREE TEXTThis is the type and placement of tubes and drains during the operative process.
23referring physician18;0MULTIPLE130.03This is information related to the referring physician.
24lock caseLOCK;1SET OF CODES1:LOCKED
0:UNLOCKED
This indicates whether this case has been completed and locked. Locked cases can only be edited if unlocked by the Chief of Surgery or his or her designee.
25discharged via.7;4POINTER131.01This is the code corresponding to the mode of transport used to move the patient from the care area.
26principal procedure(+)OP;1FREE TEXTThis is the name of the principal procedure for this case. All cases must have a principal procedure. The principal procedure must be 3 to 135 characters in length. The procedure name must not contain a semicolon (;), an at-sign (@), an up- arrow (^) or control characters. If the procedure name is longer than 30 characters, it must contain at least one space in every 31 characters of length. If a comma is being used to separate information, a space should follow the comma. Non-Cardiac Definition Revised (2004): The most complex of all the procedures by the primary operating team during this trip to the operating room. Your answer must be at least 3 characters in length. Do not enter an additional procedure if it is covered by a single CPT code. (Note that a single CPT code can cover more than one procedure, e.g., cholecystectomy and common bile duct exploration have a single CPT code). Additional procedures requiring separate CPT codes and/or concurrent procedures will be entered separately below. An exploratory laparotomy should be entered as the principal operative procedure only when no other procedure eligible for assessment has been performed in that particular surgical case.
27planned prin procedure code OP;2POINTER81This is the Current Procedural Terminology (CPT) code corresponding with the planned principal procedure. A CPT modifier on the CPT code may be included by appending the modifier to the CPT code separated by a hyphen in the format "XXXXX-YY" where "XXXXX" is the five character CPT code and "YY" is the two character CPT modifier.
27.5prin assoc diagnosisPADX;0MULTIPLE130.275This Surgery sub-file is used to store the Procedure/Diagnosis association data.
28prin. procedure cpt modifierOPMOD;0MULTIPLE130.028
29*procedure completedOP;4BOOLEANY:YES
N:NO
This indicates whether the principal operative procedure was completed. This field has been marked for deletion.
30other scrubbed assistants28;0MULTIPLE130.23This is information about other persons in the operating room in addition to those already listed as scrubbed.
31other persons in or32;0MULTIPLE130.24This is information related to other persons, not scrubbed or otherwise identified, present in the operating room.
32principal pre-op diagnosis33;1FREE TEXTThis is the preoperative diagnosis for which the surgical procedure is being performed.
32.5prin pre-op icd diagnosis code34;3POINTER80This is the principal Pre-OP ICD diagnosis code. It should be entered for all cases.
33principal diagnosis33;2FREE TEXTThis is the principal diagnosis for which the non-OR procedure is being performed.
34principal post-op diag34;1FREE TEXTThis is the principal postoperative diagnosis.
35concurrent caseCON;1POINTER130Definition Revised (2004): An additional operative procedure performed by a different surgical team (i.e., a different specialty/service) under the same anesthetic which has a CPT code different from that of the Principal Operative Procedure (e.g., fixation of a femur fracture in a patient undergoing a laparotomy for trauma). This field should be verified and, if need be, edited postoperatively by the Nurse Reviewer in accordance with the official operating room log.
36requestedREQ;1NUMERICThis indicates whether this case was requested.
37estimated case length.4;1FREE TEXTThis is the amount of time estimated to perform this operative procedure. Your answer should be in the format of "HOURS:MINUTES". For example, if the procedure will last 2 and 1/2 hours, your answer would be 2:30.
38request blood availability0;6BOOLEANY:YES
N:NO
This determines whether blood will be requested for this surgical procedure. Enter 'YES' if blood will be requested. Otherwise, enter 'NO'.
39date of transcription31;7DATE-TIMEThis is the date and time that transcription of the operative summary was completed.
40crossmatch, screen, autologous0;13SET OF CODEST:TYPE & CROSSMATCH
S:SCREEN
A:AUTOLOGOUS
This determines whether the requested blood will be typed and crossmatched, screened, or autologous.
41dressing35;1FREE TEXTThese are the dressing(s) used for this case. Although optional, this information may be useful in documentation of this case.
42delay cause17;0MULTIPLE130.042This is information related to the reason why this case did not begin at its scheduled start time.
43case verificationVER;1BOOLEANY:YES
N:NO
This indicates whether the principal operative procedure, CPT code, perioperative occurrences and diagnosis were verified by the surgeon.
44sponge final count correct25;1SET OF CODESY:YES
N:NO, SEE NURSING CARE COMMENTS
N/A:NOT APPLICABLE
NA:NOT APPLICABLE
This indicates whether the sponge final count was correct. If entered, this information will appear on the Nurse Intraoperative Report.
45sharps final count correct25;2SET OF CODESY:YES
N:NO, SEE NURSING CARE COMMENTS
N/A:NOT APPLICABLE
NA:NOT APPLICABLE
This indicates whether the sharps final count was correct. If entered, this information will appear on the Nurse Intraoperative Report. The type of information entered in this field is determined by local hospital policy.
46instrument final count correct25;3SET OF CODESY:YES
N:NO, SEE NURSING CARE COMMENTS
N/A:NOT APPLICABLE
NA:NOT APPLICABLE
This indicates whether the instrument final count was correct for this case. This information appears on the Nurse Intraoperative Report. The type of information entered in this field is determined by local hospital policy.
47sponge, sharps, & inst counter25;4POINTER200This is the name of the person doing the final count of sponges, sharps and instruments. If entered, this information appears on the Nurse Intraoperative Report.
48count verifier25;5POINTER200This is the name of the person responsible for verifying the final sponge, sharps and instrument counts.
49specimens9;0WORD-PROCESSINGThese are the names of specimens sent to the lab for analysis.
50division8;1POINTER4This is the name of the institution credited for performing this operative procedure.
51preop attending concurrence24;1BOOLEANY:YES
N:NO
This field serves as a flag that the attending has concurred with the preoperative workup.
52postop attending concurrence24;2BOOLEANY:YES
N:NO
This field serves as a flag that the attending concurs with the postoperative workup.
53non-operative occurrences36;0MULTIPLE130.053These are occurrences that are not related to a surgical procedure. If there are not any non-operative occurrences, leave this field blank. Do not enter 'NO' or 'NONE'.
54occurrence/no procedure37;1BOOLEAN1:YES
0:NO
This indicates that this case was a occurrence, not related to a surgical procedure.
55indications for operations40;0WORD-PROCESSINGThis is a brief statement of the indications for this operative procedure. The information you enter here prints automatically as the first part of the operative summary.
56pre-admission testing35;2BOOLEANY:YES
N:NO
This indicates whether pre-admission testing was complete. It will be reflected on the Schedule of Operations for outpatients.
57esu coag range.7;1FREE TEXTThis is the power setting range on the Electrosurgical Unit during coagulation. This information is optional, but may be useful in documenting the case.
58esu cutting range.7;2FREE TEXTThis is the power setting range on the Electrosurgical Unit during cutting. This information is optional, but may be useful in documenting the case.
59operative findings38;0WORD-PROCESSINGThis field contains a brief description of the operative findings which appears on the Tissue Examination Report.
60brief clin history39;0WORD-PROCESSINGThis field contains a brief clinical history for this patient. It will appear on the Tissue Examination Report.
61diagnostic results confirm by.6;11POINTER200This is the name of the person responsible for verifying that the essential diagnostic procedure requirements, as per medical center policy, are available.
62gastric output.2;6NUMERICThis is the gastric output during the operative procedure. It is recorded in cc's, and appears on the Nurse Intraoperative Report.
63iv started by.3;5POINTER200This is the name of the person that started the IV for this operative procedure.
64cultures41;0WORD-PROCESSINGThese are the names of cultures sent to the laboratory for examination.
65surgery position42;0MULTIPLE130.065This is the position in which the patient is placed for this operative procedure. This information will appear on the Nurse Intraoperative Report.
66planned prin diagnosis code34;2POINTER80This is the planned principal postoperative ICD diagnosis code assigned by the clinician.
67cancellation avoidable30;2BOOLEANY:YES
N:NO
This field contains a set of codes used to flag a cancellation as being avoidable or unavoidable. It is used when determining the percentage of avoidable cancellations.
68scheduled procedureSP;1FREE TEXTThis field contains the scheduled (or original) principal procedure for this case. It will be compared to the actual procedure completed.
69coding verifierVER;2POINTER200This is the person who last updated procedure and/or diagnosis descriptions and/or codes for this case using the Update/Verify Procedure/Diagnosis Codes [SRCODING EDIT] option. This field is updated automatically by the option when information is changed.
70cancelled by30;3POINTER200This is the name of the person who cancelled this surgical case. This information is automatically entered when a case is cancelled.
71time out verifiedVER;3SET OF CODESY:YES
N:NO (see TIME OUT VERIFIED COMMENTS)
This field refers to the completion of a "Time Out" verification process prior to the start of the procedure. A designated member of the OR team states the name of the patient, the procedure to be performed, the location of the site (including laterality if applicable), and the specifications of the implant to be used (if applicable). At a minimum, this process must include the surgeon the circulating nurse, and the anesthesia provider. This practice is further defined by local hospital policy. If entered "NO", a justification should be documented in the Time Out Verified Comments.
72preoperative imaging confirmedVER;4SET OF CODESY:YES
I:IMAGING NOT REQUIRED FOR THIS PROCEDURE
N:NO - IMAGING REQUIRED BUT NOT VIEWED (see IMAGING CONFIRMED COMMENTS)
This field refers to the completion of the verification process for the presence of relevant imaging data to confirm the operative site for the correct patient are available, properly labeled and properly presented, and verified by two members of the operating team prior to the start of the procedure. This practice is further defined by local hospital policy. If entered "NO", a justification should be documented in the Imaging Confirmed Comments.
73marked site confirmedVER;5SET OF CODESY:YES
M:MARKING NOT REQUIRED FOR THIS PROCEDURE
N:NO - MARKING REQUIRED BUT NOT DONE (see MARKED SITE COMMENTS)
The site can and must be marked in almost all cases. Mucous membranes and other sites not on the skin cannot be marked using standard methods and do not need to be. See applicable VHA Handbooks and Directives for further information and guidance. If entered "NO", a justification should be documented in the Marked Site Comments.
74time-out completed.6;12DATE-TIMEVASQIP Definition (2014): This indicates the actual time when the entire Time-Out process was completed by the OR team. It will be documented using Military Time format.
75tov timestampVERD;3DATE-TIMEThis field is updated whenever the TIME OUT VERIFIED field (#71) is entered or changed.
76imag timestampVERD;4DATE-TIMEThis field is updated whenever the PREOPERATIVE IMAGING CONFIRMED field (#72) is entered or changed.
77site mark timestampVERD;5DATE-TIMEThis field is updated whenever the MARKED SITE CONFIRMED field (#73) is entered or changed.
78previously scheduled caseSP;2POINTER130This field identifies the previously scheduled case that was cancelled and replaced by this case.
79rescheduled caseSP;3POINTER130This field identifies the new surgery case that will be scheduled later to replace this cancelled case.
80spd comments80;0WORD-PROCESSINGThis word-processing field contains any information for SPD that cannot be entered elsewhere. These comments will be sent to SPD via the Surgery/CoreFLS interface.
81dynamed notified31;10BOOLEAN1:YES
0:NO
YES indicates at least one notification has been sent to DynaMed by way of the CoreFLS interface. A null value or zero indicates no notification has been sent. The first notification sent to DynaMed will be a NEW APPOINTMENT notification. Subsequent notifications will be for edit, cancel or delete notifications, as appropriate.
82time out verified comments82;0WORD-PROCESSINGThis word-processing field contains comments related to the TIME OUT VERIFIED field. The information entered in this field clarifies entry that is entered as "NO".
83imaging confirmed comments83;0WORD-PROCESSINGThis word-processing field contains comments related to the PREOPERATIVE IMAGING CONFIRMED field. The information entered in this field clarifies entry that is entered as "NO".
84marked site comments84;0WORD-PROCESSINGThis word-processing field contains comments related to the MARKED SITE CONFIRMED field. The information entered in this field clarifies entry that is entered as "NO".
85checklist comment51;0WORD-PROCESSINGThis field is a comment that is required if any of the listed below fields for the Time Out Verified Utilizing Checklist had a response of "No". - CONFIRM PATIENT IDENTITY (#600) - PROCEDURE TO BE PERFORMED (#601) - VALID CONSENT FORM (#603) - CONFIRM PATIENT POSITION (#604) - CORRECT MEDICAL IMPLANTS (#607) - ANTIBIOTIC PROPHYLAXIS (#608) - APPROPRIATE DVT PROPHYLAXIS (#609) - BLOOD AVAILABILITY (#610) - AVAILABILITY OF SPECIAL EQUIP (#611) - SITE OF PROCEDURE (#602) - MARKED SITE CONFIRMED (#605) - REOPERATIVE IMAGES CONFIRMED (#606)
100order number0;14POINTER100This is the pointer to the ORDER file (100). It will be created when a case is requested.
101staff/resident.1;3SET OF CODESR:RESIDENT
S:STAFF
This determines whether the surgeon was a resident or staff. It will be used for categorizing procedures in the Annual Report of Surgical Procedures.
102reason for no assessmentRA;7SET OF CODES0:NON-SURGEON CASE
1:ANESTHESIA TYPE
2:EXCEEDS MAX ASSMNTS
3:EXCEEDS MAX TURPS
4:STUDY CRITERIA
5:PREVIOUS CASE
6:10% RULE
7:PRIOR INDEX PROC
8:CONCURRENT CASE
9:EXCEEDS MAX HERNIAS
VASQIP Definition (2014): This is the reason why no assessment was entered for this particular surgical case. It should be entered if any major procedure was excluded from the risk assessment module. 0 - Non-surgeon performed the procedure 2 - Number of surgical cases entered into the Surgical Risk Study exceeded 36 over an 8 day time frame 3 - Number of TURPs or TURBTs exceeded 5 cases over an 8 day time frame 4 - Study exclusion criteria prohibits patient entry 6 - Surgical Quality Nurse exclusion of up to 10% of assessments within the fiscal year 8 - Case was a concurrent case, secondary to an assessed primary case 9 - Number of hernias exceeded 5 cases over an 8 day time frame
103anesthetist category.3;8SET OF CODESA:ANESTHESIOLOGIST
N:NURSE ANESTHETIST
O:OTHER
This field holds the category of the principal anesthetist which is used on the Anesthesia AMIS report to enumerate the number of anesthetics administered by each category.
118non-or procedureNON;1BOOLEANY:YES
This field is a flag signifying this case is a non-OR surgical procedure.
119non-or locationNON;2POINTER44This is the location (file 44) where this non-OR procedure was performed.
120date of procedure(+)NON;3DATE-TIMEThis is the date that the non-OR procedure was performed. The date of procedure must be entered for all non-OR cases.
121time procedure beganNON;4DATE-TIMEThis is the date and time that the non-OR procedure began.
122time procedure endedNON;5DATE-TIMEThis is the date and time that all the procedures for this non-OR case are complete.
123provider(+)NON;6POINTER200This is the person who performs the major portion of the principal non-OR procedure. This field is required for several reports.
124attend providerNON;7POINTER200This is the name of the attending staff provider responsible for this case. This information appears on several reports.
125medical specialty(+)NON;8POINTER723 This is the medical specialty credited for doing this non-OR procedure. Many reports are sorted by the medical specialty. This field should be entered prior to completion of this non-OR procedure.
126procedure occurrence43;0MULTIPLE130.0126This is a occurrence that is related to a non-O.R. procedure. If there are not any non-O.R. procedure occurrences, this field should be left blank. Do not enter 'NO' or 'NONE'.
127sequential compression device.7;3BOOLEANY:YES
N:NO
This determines whether a sequential compression device was used.
128laser type.7;8FREE TEXTThis determines whether a laser was used during this procedure. If applicable, enter the type of laser used during this surgical procedure.
129laser unit44;0MULTIPLE130.0129These are the laser units, if any, used during this procedure.
130cell saver45;0MULTIPLE130.013These are the cell savers, if any, used during this procedure.
131device(s)46;1FREE TEXTThis field documents devices used in this procedure that are not documented elsewhere.
200operations this admission200;51NUMERICThis is the total number of surgical procedures, prior to the index or principal operation, which required the patient to be taken to the operating room for any type of surgical intervention during this hospital admission. Include all procedures whether or not they are part of the inclusion/exclusion criteria.
201redo procedure200;53SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the principal operative procedure was a reoperation in the same anatomic location for the same purpose as the first operation regardless of the length of time from the original surgical date.
202*current smoker200;3SET OF CODESY:YES
N:NO
NS:NO STUDY
This field has been flagged as obsolete for VASQIP. It should no longer be used. Non-Cardiac Definition Revised (2006): If the patient has smoked cigarettes in the year prior to admission for surgery enter YES. Do not include patients who smoke cigars or pipes or use chewing tobacco.
202.1pack/years208;9FREE TEXTDefinition Revised (2004): If the patient has ever been a smoker, enter the total number of pack/years of smoking for this patient. Pack-years are defined as the number of packs of cigarettes smoked per day times the number of years the patient has smoked. If the patient has never been a smoker, enter "0". If pack-years are >200, just enter 200. If smoking history cannot be determined, enter "NS". The possible range for number of pack-years is 0 to 200. If the chart documents differing values for pack year cigarette history, or ranges for either packs/day or number of years patient has smoked, select the highest value documented, unless you are confident in a particular documenter's assessment (e.g., preoperative anesthesia evaluation often includes a more accurate assessment of this value because of the impact it may have on the patient's response to anesthesia).
203history of copd200;11BOOLEANY:YES
N:NO
VASQIP Definition (2011): Chronic obstructive pulmonary disease (such as emphysema and/or chronic bronchitis) resulting in any one or more of the following: - Functional disability from COPD (e.g., dyspnea, inability to perform ADLs) - Hospitalization in the past for treatment of COPD - Requires chronic bronchodilator therapy with oral or inhaled agents (see list of bronchodilators below) - An FEV1 of <75% of predicted on pulmonary function testing Do not include patients whose only pulmonary disease is acute asthma, an acute and chronic inflammatory disease of the airways resulting in bronchospasm. Do not include patients with diffuse interstitial fibrosis or sarcoidosis. (This list may not be all-inclusive. Please check your hospital formulary)
204ventilator dependent200;10SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): A preoperative patient requiring ventilator-assisted respirations at any time during the 48 hours preceding surgery. This does not include the treatment of sleep apnea with CPAP.
205prior mi206;14SET OF CODES0:NO
1:YES, < OR EQUAL TO 7 DAYS PRIO TO SURG
2:YES, BETWEEN 7 DAYS AND 6 MONTHS PRIOR TO SURG
3:UNKNOWN
Definition Revised (2014): Indicate if the patient has a history of myocardial infarction within 6 months prior to surgery as diagnosed in his or her medical records. Select the one appropriate response: 0. No 1. Yes, less than or equal to 7 days prior to surgery 2. Yes, between 7 days and 6 months prior to surgery 3. Unknown
206vascular (y/n)200;40SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has any vascular problems.
207congestive heart failure206;19SET OF CODESN:NONE
I:CARDIAC DISEASE, NO SYMPTOMS
II:SLIGHT LIMITATION
III:MARKED LIMITATION
IV:SYMPTOMS AT REST
U:UNKNOWN
Definition Revised (2014): Indicate whether the patient has congestive heart failure if the patient chart or patient self-report indicates a history of congestive heart failure within the 30 days before surgery. The New York Heart Association functional classification is used as a subjective assessment of the severity of congestive heart failure. Indicate the one most appropriate response: None - no congestive heart failure. Class I - cardiac disease, no symptoms of abnormal fatigue, dyspnea, or angina. Class II - slight limitation of physical activity by fatigue, dyspnea, or angina. The patient gets unusual fatigue, dyspnea, and/or angina only upon performing more strenuous activities, such as climbing two or more flights of stairs without stopping. Class III - marked limitation of physical activity by fatigue, dyspnea, or angina. The patient gets unusual fatigue, dyspnea, and/or angina upon performing ordinary activities, such as walking several blocks or climbing a flight of stairs. Class IV - symptoms at rest and/or inability to carry out any physical activity without symptoms of fatigue, dyspnea or angina. The patient has symptoms of unusual fatigue, dyspnea, and/or angina at rest or when performing minimal activity, such as walking across the room. Unknown - Unknown
208*hypertension requiring meds200;36SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): The patient has a persistent elevation of systolic blood pressure >140 mm Hg or a diastolic blood pressure >90 mm Hg or requires an antihypertensive treatment (e.g., diuretics, beta blockers, ACE inhibitors, calcium channel blockers) at the time the patient is being considered as a candidate for surgery which should be no longer than 30 days prior to surgery. Hypertension must be documented in the patient's chart.
209cardiomegaly206;6BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the patient has generalized cardiac enlargement of any or all of the cardiac chambers by standard or portable chest x-ray within 30 days preceding surgery.
210central nervous system (y/n)200;18SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of illness related to the central nervous system (CNS).
211currently on dialysis200;39SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2006): Acute or chronic renal failure requiring periodic peritoneal dialysis, hemodialysis, hemofiltration, hemodiafiltration, or ultrafiltration within 2 weeks prior to surgery.
212ascites200;15SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2010): Ascites within 30 days prior to surgery: The presence of fluid in the peritoneal cavity noted on physical examination, abdominal ultrasound, or abdominal CT/MRI within 30 days prior to the operation. Documentation should state a history of or active liver disease (e.g. jaundice, encephalopathy, hepatomegaly, portal hypertension, liver failure, or spider telangiectasia).
213esophageal varices200;16SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Esophageal varices are engorged collateral veins in the esophagus that bypass a scarred liver to carry portal blood to the superior vena cava. A sustained increase in portal pressure results in esophageal varices that are most frequently demonstrated by direct visualization at esophagoscopy. Esophageal varices must be present preoperatively and must be documented on a recent EGD or CT scan performed within 6 months prior to the surgical procedure.
214pgy of primary surgeon200;52NUMERICDefinition Revised (2004): Enter the number of surgical residency postgraduate years of the primary surgeon (1-12). Enter 0 if the primary surgeon is a staff/attending surgeon and not a surgical resident or fellow. PGYs greater than 12 should be reported as '12'.
215weight loss > 10%200;48SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): A >10% decrease in body weight in the six month interval immediately preceding surgery as manifested by serial weights in the chart, as reported by the patient, or as evidenced by change in clothing size or severe cachexia. Exclude patients who have intentionally lost weight as part of a weight reduction program.
216bleeding disorders200;49SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2014): Bleeding (coagulation) disorder is a condition that places the patient at risk for excessive bleeding due to a deficiency of blood clotting elements (e.g., vitamin K deficiency, hemophilia, von Willebrand disease). Answer YES if the patient has a documented bleeding (coagulation) disorder that is either chronic or acute.
217transfusion > 4 rbc units200;50SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Preoperative loss of blood necessitating a minimum of 5 units of whole blood/packed red cells transfused during the 72 hours prior to surgery including any blood transfused in the emergency room.
218open wound200;46SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Evidence of an open wound that communicates to the air by direct exposure, with or without cellulitis or purulent exudate. This does not include osteomyelitis or localized abscesses. The wound must communicate to the air by direct exposure. Report mandible fractures under this preoperative variable.
218.1preoperative sepsis206;8SET OF CODESY:YES
N:NONE
1:SIRS
2:SEPSIS
3:SEPTIC SHOCK
NS:NO STUDY
Definition Revised (2014): 2. Sepsis is the systematic response to infection. Answer YES if both of the following criteria are met: a) Clinical documentation of infection (such as wound with purulent drainage, ruptured bowel with free air, etc.); or a positive culture from any site thought to be causative; or specialized laboratory evidence of causative infection (such as viral DNA in blood). AND b) The presence of two or more of the following systemic responses: - Temperature > 38 degrees C or < 36 degrees C - HR > 90 beats/minute - RR > 20 breaths /minute or PaCO2 < 32 mmHg - WBC > 12,000 cell/mm3, < 4,000cells/mm3, or > 10% immature neutrophils ("bands") 3. Severe Sepsis/Septic Shock: Sepsis is considered severe when it is associated with organ and/or circulatory dysfunction. Terminology such as Severe Sepsis/Septic Shock/Refractory Septic Shock and Multiple Organ Dysfunction Syndrome (MODS) all fall into this category. Answer YES if the definition of SEPSIS is present AND there is documented organ and/or circulatory dysfunction defined by one or more of the following: - Areas of acutely mottled skin not related to peripheral vascular disease - Capillary refilling requires three seconds or longer not related to peripheral vascular disease - Urine output <0.5 mL/kg for at least one hour, or renal replacement therapy - Lactate >2 mmol/L - Abrupt change in mental status - Abnormal EEG findings - Platelet count < 100,000 platelets/mL - Disseminated intravascular coagulation (DIC) - Acute lung injury or acute respiratory distress syndrome (ARDS) - New cardiac dysfunction as defined by ECHO or direct measurement of the cardiac index - An arterial systolic blood pressure (SBP) of <=90 mm Hg or a mean arterial pressure (MAP) <=70 mm Hg for at least 1 hour despite adequate fluid resuscitation, adequate intravascular volume status, or the need for vasopressors to maintain SBP >= 90 mm Hg or MAP >=70 mm Hg.
219preoperative hemoglobin201;20FREE TEXTDefinition Revised (2004): Indicate the patient's hemoglobin result (g/dl) preoperatively evaluated closest to surgery but not greater than 30 days before surgery. Entering "NS" for "No Study/Unknown" is not allowed.
220*previous pci200;32SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): The patient has undergone or has had an attempt at percutaneous coronary intervention at any time. This includes either balloon dilatation or stent placement. This does not include valvuloplasty procedures.
221preoperative cpk201;6NUMERICThis is the result of the preoperative creatinine phosphokinase (CPK) test.
222preoperative mb band201;7NUMERICThis is the value of the preoperative methyline blue (MB) band. Your answer must be between 0 and 50.
223preoperative serum creatinine201;4FREE TEXTDefinition Revised (2011): This is the serum creatinine result (mg/dl) most closely preceding surgery - not to exceed 30 days for Cardiac surgery. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is allowed for non-cardiac case assessments.
224preoperative bun201;5FREE TEXTThis is the result of the preoperative Blood Urea Nitrogen (BUN) test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
225preoperative serum albumin201;8FREE TEXTDefinition Revised (2011): This is the serum albumin result (g/dl) most closely preceding surgery - not to exceed 30 days for Cardiac surgery. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is allowed for non-cardiac case assessments.
226preoperative sgpt201;10NUMERICThis is the result of the preoperative serum glutamic pyruvic transaminase (SGPT) test.
227preoperative sgot201;11FREE TEXTThis is the result of the preoperative serum glutamic oxaloacetic (SGOT) test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
228preoperative total bilirubin201;9FREE TEXTThis is the result of the preoperative total bilirubin test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
229preoperative alk phosphatase201;12FREE TEXTThis is the result of the preoperative alkaline phosphatase test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
230preoperative wbc201;13FREE TEXTThis is the result of the preoperative white blood count (WBC). Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
231preoperative platelet count201;15FREE TEXTThis is the result of the preoperative platelet count. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
232preoperative pt201;17FREE TEXTThis is the result of the preoperative prothombin time (PT). Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
233preoperative ptt201;16FREE TEXTThis is the result of the preoperative partial thromboplastin time (PTT). Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
234preoperative hematocrit201;14FREE TEXTThis is the result of the preoperative hematocrit test. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
235assessment statusRA;1SET OF CODESI:INCOMPLETE
C:COMPLETE
T:TRANSMITTED
N:NO ASSESSMENT
This is the current status of the surgery risk assessment. When creating a new assessment, the status will automatically be entered as 'INCOMPLETE'. Upon completion of the assessment, this field will be updated to 'COMPLETED'. After the assessment is transmitted, this field will be automatically updated to 'TRANSMITTED'.
236height206;1FREE TEXTVASQIP Definition (2010): Height: Report the patient's most recent height before surgery documented in the medical record in either inches (25 to 86 in) or centimeters (63 to 218 cm). If you are entering the patient's height in centimeters, enter 'C' after the number of centimeters. Your answer should be in one of the following two formats. 68 (representing inches) 173C (representing centimeters) The software pulls the most recent height measurement, regardless of when it was taken. The date of the measurement returned by the capture process is displayed on the data input screen.
236.1height measurement date200.1;7DATE-TIMEThis is the date of the patient's height measurement. This date is taken from the VITALS software.
237weight206;2FREE TEXTVASQIP Definition (2010): Weight: Report the patient's most recent weight before surgery documented in the medical record in either pounds (50 to 999 lbs) or kilograms (23 to 453 kg). If you are entering the patient's weight in kilograms, enter 'K' after the number of kilograms. The software pulls the latest value up to 30 days prior to surgery. If no value is found in the Vitals software, the nurse reviewer must enter the value manually. Your answer should be in one of the following formats. 178 (weight in pounds) 80K (weight in Kilograms)
237.1preoperative sleep apnea200.1;8SET OF CODES1:NONE - LEVEL 1
2:SUSPICION OF SLEEP APNEA - LEVEL 2
3:SLEEP APNEA CONFIRMED - LEVEL 3
VASQIP Definition (2014): Sleep Apnea is a disorder of respiration whereby the individual has hypoxic and/or apneic periods during sleep due to prolapse or flaccidity of oropharyngeal structures, which improves with positive airway pressure (i.e., CPAP or BIPAP). Select one of the following categories that best indicates the patient's level of sleep apnea. Level 1 = None: No diagnosis or suspicion of Sleep Apnea Level 2 = Suspicion of Sleep Apnea: No sleep study has been done, however the patient has TWO or MORE of the following risk factors for Sleep Apnea: a) Obesity (BMI > 35) b) Thick neck (men > 17 inches, women > 16 inches) c) Snoring, loud or frequent d) Observed apneas (partner/roommate reported observing obstruction episodes during sleep) e) Frequent arousals from sleep or choking during sleep f) Daytime somnolence g) Patient reports diagnosis of sleep apnea even if sleep study results are not in the medical record Level 3 = Sleep Apnea: Sleep apnea confirmed by Sleep Study OR patient currently uses CPAP/BIPAP at home. Answer Options: - None - Suspicion of Sleep Apnea - Sleep Apnea Confirmed
238dnr status200;7SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): If the patient has had a Do-Not-Resuscitate (DNR) order written in the physician's order sheet of the patient's chart and it has been signed or co-signed by an attending physician [this is the only condition under which a DNR order is official in the VA in the 30 days prior to this surgery], enter "YES". If the DNR order as defined above was rescinded immediately prior to surgery in order to operate on the patient, enter "YES". Answer "NO" if DNR discussions are documented in the progress note, but no official DNR order has been written in the physician order sheet or if the attending physician has not signed the official order.
239preoperative hemoglobin, date202;20DATE-TIMEThis is the date that the preoperative hemoglobin test was performed.
240functional health status200;8SET OF CODES1:INDEPENDENT
2:PARTIALLY DEPENDENT
3:TOTALLY DEPENDENT
4:UNKNOWN
VASQIP Definition (2011): This is a question that focuses on the patient's abilities to perform activities of daily living (ADLs) in the 30 days prior to surgery. Activities of daily living are defined as 'the activities usually performed in the course of a normal day in a person's life'. ADLs include: bathing, feeding, dressing, toileting, and mobility. Report the corresponding level of self-care for activities of daily living demonstrated by this patient at the time the patient is being considered as a candidate for surgery (which should be no longer than 30 days prior to surgery). If the patient's status changes prior to surgery, that change should be reflected in your assessment. For this time point, report the level of functional health status as defined by the following criteria. (1) Independent: The patient does not require assistance from another person for any activities of daily living. This includes a person who is able to function independently with prosthetics, equipment, or devices. (2) Partially dependent: The patient requires some assistance from another person for activities of daily living. This includes a person who utilizes prosthetics, equipment, or devices but still requires some assistance from another person for ADLs. (3) Totally dependent: The patient requires total assistance for all activities of daily living. (4) Unknown: If unable to ascertain the functional status. All patients with psychiatric illnesses should be evaluated for their ability to function with or without assistance with ADLs just as the non-psychiatric patient. For instance, if a patient with schizophrenia is able to care for him/herself without the assistance of nursing care, he/she is considered independent.
241pulmonary (y/n)200;9SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of pulmonary illnesses.
242cardiac (y/n)200;30SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of cardiac illnesses.
243renal (y/n)200;37SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of renal illnesses.
244hepatobiliary (y/n)200;13SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of hepatobiliary illnesses.
245nutritional/immune/other200;44SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of illness related to nutrition, immune deficiencies or other general deficiencies.
246etoh > 2 drinks/day200;4SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): The patient admits to drinking >2 ounces of hard liquor or more than two 12 oz. cans of beer or more than two 6 oz. glasses of wine per day in the two weeks prior to admission. If the patient is a "binge drinker" divide out the numbers of drinks during the binge by seven days, and then apply the definition.
247length of post-op stay205;1FREE TEXTDefinition Revised (2004): The software will automatically calculate the total number of days that the patient stayed in the acute care services of the medical center. The number of days should include the day after surgery and the date of discharge or transfer to intermediate or chronic care facilities. Enter NA if LENGTH OF POST-OP STAY is not applicable.
248superficial incisional ssi205;6SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Superficial incisional SSI is an infection that occurs within 30 days after the operation and infection involves only skin or subcutaneous tissue of the incision and at least one of the following: - Purulent drainage, with or without laboratory confirmation, from the superficial incision. - Organisms isolated from an aseptically obtained culture of fluid or tissue from the superficial incision. - At least one of the following signs or symptoms of infection: pain or tenderness, localized swelling, redness, or heat and superficial incision is deliberately opened by the surgeon, unless incision is culture-negative. - Diagnosis of superficial incisional SSI by the surgeon or attending physician. Do not report the following conditions as SSI: - Stitch abscess (minimal inflammation and discharge confined to the points of suture penetration). - Infected burn wound. - Incisional SSI that extends into the fascial and muscle layers (see deep incisional SSI).
249deep incisional ssi205;7SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Deep Incision SSI is an infection that occurs within 30 days after the operation and the infection appears to be related to the operation and infection involved deep soft tissues (e.g., fascial and muscle layers) of the incision and at least one of the following: - Purulent drainage from the deep incision but not from the organ/space component of the surgical site. - A deep incision spontaneously dehisces or is deliberately opened by a surgeon when the patient has at least one of the following signs or symptoms: fever (>38 C), localized pain, or tenderness, unless site is culture-negative. - An abscess or other evidence of infection involving the deep incision is found on direct examination, during reoperation, or by histopathologic or radiologic examination. - Diagnosis of a deep incision SSI by a surgeon or attending physician. Note: - Report infection that involves both superficial and deep incision sites as deep incisional SSI. - Report an organ/space SSI that drains through the incision as a deep incisional SSI.
250systemic sepsis205;35SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Sepsis is a vast clinical entity that takes a variety of forms. The spectrum of disorders spans from relatively mild physiologic abnormalities to septic shock. Please report the most significant level using the criteria below: 1. Sepsis: Sepsis is the systemic response to infection. Report this variable if the patient has clinical signs and symptoms of SIRS. SIRS is a widespread inflammatory response to a variety of severe clinical insults. This syndrome is clinically recognized by the presence of two or more of the following: - Temp >38 degrees C or <36 degrees C - HR >90 bpm - RR >20 breaths/min or PaCO2 <32 mmHg(<4.3 kPa) - WBC >12,000 cell/mm3, <4000 cells/mm3, or >10% immature (band) forms - Anion gap acidosis: this is defined by either: [Na + K] - [Cl + HCO3 (or serum CO2)]. If this number is greater than 16, then an anion gap acidosis is present. or Na - [Cl + HCO3 (or serum CO2)]. If this number is greater than 12, then an anion gap acidosis is present. and one of the following: - positive blood culture - clinical documentation of purulence or positive culture from any site thought to be causative 2. Severe Sepsis/Septic Shock: Sepsis is considered severe when it is associated with organ and/or circulatory dysfunction. Report this variable if the patient has the clinical signs and symptoms of SIRS or sepsis AND documented organ and/or circulatory dysfunction. Examples of organ dysfunction include: oliguria, acute alteration in mental status, acute respiratory distress. Examples of circulatory dysfunction include: hypotension, requirement of inotropic or vasopressor agents. * For the patient that had sepsis preoperatively, worsening of any of the above signs postoperatively would be reported as a postoperative sepsis. Examples: A patient comes into the emergency room with signs of sepsis - WBC 31, Temperature 104. CT shows an abdominal abscess. He is given antibiotics and is then taken emergently to the OR to drain the abscess. He receives antibiotics intraoperatively. Postoperatively his WBC and Temperature are trending down. POD#1 WBC 24, Temp 102 POD#2 WBC 14, Temp 100 POD#3 WBC 10, Temp 99 This patient does not have postoperative sepsis as his WBC and Temperature are improving each postoperative day. Patient comes into the ER with s/s of sepsis - WBC 31, Temp 104. CT shows an abdominal abscess. He is given antibiotics and is taken emergently to the OR to drain the abscess. He receives antibiotics intraoperatively. Postoperatively his WBC and Temp are as follows: POD#1 WBC 28, Temp 103 POD#2 WBC 24, Temp 102.6 POD#3 WBC 22, Temp 102 POD#4 WBC 21, Temp 101.6 POD#5 WBC 30, Temp 104 This patient does have postoperative sepsis because on postoperative day #5, his WBC and Temperature increase. The patient is having worsening of the defined signs of sepsis.
251pneumonia205;10SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Inflammation of the lungs caused primarily by bacteria, viruses, and/or chemical irritants, usually manifested by chills, fever, pain in the chest, cough, purulent, bloody sputum. Enter YES if the patient has pneumonia meeting the definition of pneumonia below AND pneumonia not present preoperatively. Pneumonia must meet one of the following TWO criteria: Criterion 1. Rales or dullness to percussion on physical examination of chest AND any of the following: a. New onset of purulent sputum or change in character of sputum b. Organism isolate from blood culture c. Isolation of pathogen from specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy OR Criterion 2. Chest radiographic examination shows new or progressive infiltrate, consolidation, cavitation, or pleural effusion AND any of the following: a. New onset of purulent sputum or change in character of sputum b. Organism isolated from blood culture c. Isolation of pathogen from specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy d. Isolation of virus or detection of viral antigen in respiratory secretions e. Diagnostic single antibody titer (IgM) or fourfold increase in paired serum samples (IgG) for pathogen f. Histopathologic evidence of pneumonia *If pneumonia was present preoperatively and resolved postoperatively and a new pneumonia is identified within 30 days after surgery, the following criteria must be met in order to report as a postoperative pneumonia occurrence: - Patient must have completed the antibiotic course for the previous pneumonia. - Patient must have evidence of a clear chest x-ray after the previous pneumonia and prior to the new pneumonia. - There must be evidence of a new isolate of micro-organism on culture.
252pulmonary embolism205;12SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Lodging of a blood clot in a pulmonary artery with subsequent obstruction of blood supply to the lung parenchyma. The blood clots usually originate from the deep leg veins or the pelvic venous system. Enter "YES" if the patient has a V-Q scan interpreted as high probability of pulmonary embolism or a positive pulmonary arteriogram or positive CT angiogram or positive Spiral CT exam. Treatment usually consists of: - Initiation of anticoagulation therapy - Placement of mechanical interruption (e.g. Greenfield Filter), for patients in whom anticoagulation is contraindicated or already instituted.
253other respiratory occurrence205;14POINTER80Definition Revised (2004): Enter any other respiratory occurrences that you feel to be significant and that are not covered by the predefined respiratory occurrence categories. Enter the ICD-CM code for this entry.
254acute renal failure205;17SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2011): Indicate if the patient developed new renal failure requiring renal replacement therapy or experienced an exacerbation of preoperative renal failure requiring initiation of renal replacement therapy (not on renal replacement therapy preoperatively) within 30 days postoperatively. Renal replacement therapy is defined as venous to venous hemodialysis [CVVHD], continuous venous to arterial hemodialysis [CVAHD], peritoneal dialysis, hemofiltration, hemodiafiltration or ultrafiltration. TIP: If the patient refuses dialysis, report as an occurrence because he/she did require dialysis.
255urinary tract infection205;18SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Postoperative symptomatic urinary tract infection must meet one of the following TWO criteria: 1. One of the following: fever (>38 degrees C), urgency, frequency, dysuria, or suprapubic tenderness AND a urine culture of >100,000 colonies/ml urine with no more than two species of organisms OR 2. Two of the following: fever (>38 degrees C), urgency, frequency, dysuria, or suprapubic tenderness AND any of the following: - Dipstick test positive for leukocyte esterase and/or nitrate - Pyuria (>10 WBCs/cc or >3 WBC/hpf of unspun urine) - Organisms seen on Gram stain of unspun urine - Two urine cultures with repeated isolation of the same uropathogen with >100 colonies/ml urine in non-voided specimen - Urine culture with <100,000 colonies/ml urine of single uropathogen in patient being treated with appropriate antimicrobial therapy - Physician's diagnosis - Physician institutes appropriate antimicrobial therapy
256stroke/cva205;21SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definitions (2011): Indicate if the patient developed a new neurologic deficit with onset immediately post-operatively or occurring within the 30 days after surgery. Neurologic deficits are defined as an embolic, thrombotic, or hemorrhagic vascular accident or stroke with motor, sensory, or cognitive dysfunction (e.g., hemiplegia, hemiparesis, aphasia, sensory deficit, impaired memory).
257postop bleeding/transfusions205;32SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Any transfusion (including autologous) of packed red blood cells or whole blood given from the time the patient leaves the operating room up to and including 72 hours postoperatively. Enter YES for five or more units of packed red blood cell units in the postoperative period including hanging blood from the OR that is finished outside of the OR. If the patient receives shed blood, autologous blood, cell saver blood or pleurovac postoperatively, this is counted if greater than four units. The blood may be given for any reason.
258myocardial infarction205;27SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2014): Indicate the presence of a peri-operative MI that occurs either intraoperatively or postoperatively within 30 days: The term acute MI should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any ONE of the following criteria meets the diagnosis for MI: 1. Detection of a rise and/or fall of cardiac biomarker values [preferably cardiac troponin (cTn)] with at least one value above the 99th percentile Upper Reference Limit (URL) AND at least one of the following: a. Symptoms suggestive of myocardial ischemia b. New or presumed new significant ST-segment-T wave (ST-T) changes c. New left bundle branch block (LBBB). d. Development of pathological Q waves in the ECG e. Imaging evidence of new loss of viable myocardium f. New regional wall motion abnormality g. Identification of an intracoronary thrombus by angiography or autopsy 2. Cardiac death with symptoms suggestive of myocardial ischemia and presumed new ischemic ECG changes or new LBBB, but death occurred before cardiac biomarkers were obtained, or before cardiac biomarker values would be increased. 3. Percutaneous coronary intervention (PCI) related MI is arbitrarily defined by elevation of cTn values (>5x 99th percentile URL) in patients with normal baseline values (<99th percentile URL) or a rise of cTn values >20% if the baseline values are elevated and are stable or falling, AND at least one of the following: a. Symptoms suggestive of myocardial ischemia b. Presumed new ischemic ECG changes c. Angiographic findings consistent with a procedural complication d. Imaging evidence of new loss of viable myocardium e. New regional wall motion abnormality 4. Stent thrombosis associated with MI when detected by coronary angiography or autopsy in the setting of myocardial ischemia and with a rise and/or fall of cardiac biomarker values with at least one value above the 99th percentile URL. 5. Coronary artery bypass grafting (CABG) related MI is arbitrarily defined by elevation of cardiac biomarker values (>10x 99th percentile URL) in patients with normal baseline cTn values (<99th percentile URL), AND at least one of the following a. Development of pathological Q waves in the ECG b. New LBBB c. Angiographic documented new graft or new native coronary artery occlusion d. Imaging evidence of new loss of viable myocardium e. New regional wall motion abnormality
259pulmonary edema205;28SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has developed postoperative distress requiring treatment and diagnosis of CHF or pulmonary edema or Adult Respiratory Distress Syndrome.
260date transmittedRA;4DATE-TIMEThis is the date (or date/time) that this surgery risk assessment was transmitted.
260.1date of last transmissionRA;8DATE-TIMEThis is the date of the retransmission if this risk assessment has been retransmitted to the national database. An assessment can be updated and retransmitted within 14 days of the original transmission date. If there was no retransmission of this assessment, this is the date of the original transmission.
261graft/prosthesis/flap failure205;33SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Mechanical failure of an extracardiac graft/or prosthesis including myocutaneous flaps and skin grafts requiring return to the operating room, interventional radiology, or a balloon angioplasty.
262return to or within 30 days205;4SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Returns to the operating room include all surgical procedures that required the patient to be taken to the surgical operating room for intervention of any kind will automatically be entered by the software.
263dvt/thrombophlebitis205;34SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2014): The identification of a new blood clot or thrombus within the deep venous system of an extremity, which may be coupled with inflammation. This does not include intra-parenchymal clots of solid organs or free intra-peritoneal clots. This diagnosis is confirmed by a duplex, venogram, CT scan or other imaging modality. The patient must be treated with or have documented recommendation for: therapeutic anti-coagulation therapy OR placement of a vena cava filter OR clipping of the vena cava.
264*cerebral vascular disease206;17BOOLEANY:YES
N:NO
This field has been flagged as obsolete for VASQIP. It should no longer be used. This determines whether the patient has disease of the arteries to the head manifested by previous stroke (cerebral vascular accident), and/or transient ischemic attack (TIA), and/or prior surgical repair (e.g. carotid endarterectomy), and/or greater than or equal to 50% obstruction of luminal diameter documented by contrast angiography or duplex ultrasound examination.
265peripheral arterial disease206;16SET OF CODESY:YES
N:NO
1:NO
2:YES-W/O ANGI,REVASC,or AMPUT
3:YES-W HX ANGI,REVASC,or AMPUT
4:UNKNOWN
VASQIP Definition (2014): Indicate if the patient has peripheral arterial disease (previously "peripheral vascular disease"), defined as disease of the arteries to legs below bifurcation of aorta manifested by at least one of the following: exertional claudication, ischemic rest pain, prior revascularization procedure(s) on vessels to legs, absent or diminished pulses in legs, or angiographic evidence of non-iatrogenic peripheral arterial obstruction greater than or equal to 50% of luminal diameter. Indicate the one appropriate response: 1. No 2. YES, WITHOUT ANGIOPLASTY, REVASCULARIZATION, OR AMPUTATION PROCEDURE 3. YES, WITH ANY HISTORY OF ANGIOPLASTY, OR REVASCULARIZATION, OR AMPUTATION PROCEDURE, REGARDLESS OF LATERALITY 4. UNKNOWN
266*previous cardiac surgery200;33SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2006): Any major cardiac surgical procedure (performed either as an 'off-pump' repair or utilizing cardiopulmonary bypass). This includes coronary artery bypass graft surgery, valve replacement or repair, repair of atrial or ventricular septal defects, great thoracic vessel repair, cardiac transplant, left ventricular aneurysmectomy, insertion of left ventricular assist devices, etc. Do not include pacemaker insertions or automatic implantable cardioverter-defibrillator (AICD) insertions.
267angina severity206;18SET OF CODESN:NONE
I:CLASS I
II:CLASS II
III:CLASS III
IV:CLASS IV
U:UNKNOWN
VASQIP Definition (2014): Indicate whether the patient has angina, defined as pain or discomfort between the diaphragm and mandible resulting from myocardial ischemia, usually precipitated by exertion or emotion and relieved by rest or nitroglycerin. The Canadian Cardiovascular Society (CCS) classification is used to record severity of angina. Indicate the one appropriate response, according to the most severe angina in the 30 days prior to surgery: None - No angina Class I - Ordinary physical activity, such as walking or climbing stairs does not cause angina. Angina may occur with strenuous or rapid or prolonged exertion at work or recreation. Class II - There is slight limitation of ordinary activity. Angina may occur with walking or climbing stairs rapidly, walking uphill, walking or stair climbing after meals or in the cold, in the wind, or under emotional stress, or walking more than two blocks on the level, or climbing more than one flight of stairs under normal conditions at a normal pace. Class III - There is marked limitation of ordinary physical activity. Angina may occur after walking one or two blocks on the level or climbing one flight of stairs under normal conditions at a normal pace. Class IV - There is inability to carry on any physical activity without discomfort. Angina may be present at rest. Unknown - Unknown
268hepatomegaly200;14SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has the presence of hepatomegaly. Hepatomegaly is defined as enlargement of the liver indicated usually by palpation of the lower border of the liver below the right costal margin or a liver span greater than 10 cm. Hepatomegaly may be noted in acute hepatitis, fatty infiltration, passive congestion, and early biliary obstruction. It is usually noted by the physician under the abdominal portion of the H&P.
269pregnancy200.1;3SET OF CODESNO:NO
NA:NOT APPLICABLE
Y:YES
Definition Revised (2007): Pregnancy is the process by which a woman carries a developing fetus in her uterus, beginning at conception and ending in birth, miscarriage or abortion. Answer Yes if there is documentation in the patient's medical record that the patient is currently pregnant.
270preoperative serum sodium201;1FREE TEXTThis is the result of the preoperative serum sodium test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
271preoperative potassium201;2NUMERICThis is the result of the preoperative potassium test.
272date assessment completedRA;5DATE-TIMEThis is the date that the Assessment was completed. This field will be updated if the assessment was transmitted in error.
272.1assessment completed byRA;9POINTER200This is the name of the person who completed this surgery risk assessment.
273preoperative glucose201;3NUMERICThis is the result of the preoperative glucose test.
274highest serum sodium203;1FREE TEXTThis is the highest result of a postoperative serum sodium test for the selected patient. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
275highest potassium203;3FREE TEXTThis is the highest result of a potassium test for the selected patient. Data input must be 1 to 3 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
276highest glucose203;5NUMERICThis is the highest result of a postoperative glucose test for the patient selected.
277highest serum creatinine203;6FREE TEXTThis is the highest postoperative serum creatinine result for the selected patient. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
278highest cpk203;7FREE TEXTThis is the highest result of a postoperative CPK test for the patient selected. Data input must be 1 to 6 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
279highest cpk-mb203;8FREE TEXTThis is the highest result of a postoperative CP-MB Band for this patient. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
280highest total bilirubin203;9FREE TEXTThis is the highest postoperative total bilirubin result recorded for this patient. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
281highest wbc203;10FREE TEXTThis is the highest postoperative WBC for the patient selected. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
282lowest serum albumin203;11NUMERICThis is the lowest postoperative serum albumin result for the patient selected.
283lowest hematocrit203;12FREE TEXTThis is the lowest postoperative hematocrit result recorded for this patient. Data input must be 1 to 4 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
284assessment typeRA;2SET OF CODESC:CARDIAC
N:NON-CARDIAC
This determines whether this surgical risk assessment is a cardiac or non-cardiac procedure.
285on ventilator >48 hours205;13SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2011): Total duration of ventilator-assisted respirations during postoperative hospitalization was >48 hours. This can occur at any time during the 30-day period postoperatively. This time assessment is CUMULATIVE, not necessarily consecutive. Ventilator-assisted respirations can be via endotracheal tube, nasotracheal tube, or tracheostomy tube.
286other urinary tract occurrence205;19POINTER80Definition Revised (2004): Enter any other urinary occurrences which you feel to be significant and that are not covered by the predefined urinary tract occurrence categories. Enter the ICD-CM code for this entry.
287peripheral nerve injury205;23SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Peripheral nerve damage may result from damage to the nerve fibers, cell body, or myelin sheath during surgery. Peripheral nerve injuries which result in motor deficits only to the cervical plexus, brachial plexus, ulnar plexus, lumbar-sacral plexus (sciatic nerve), peroneal nerve, and/or the femoral nerve should be included.
288preoperative cpk, date202;6DATE-TIMEThis is the date that the preoperative CPK was performed.
289preoperative mb band, date202;7DATE-TIMEThis is the date that the preoperative MB Band was performed.
290preop serum creatinine, date202;4DATE-TIMEThis is the date that the preoperative Serum Creatinine test was performed.
291preoperative bun, date202;5DATE-TIMEThis is the date that the preoperative BUN was performed.
292preop serum albumin, date202;8DATE-TIMEThis is the date that the preoperative Serum Albumin test was performed.
293sgpt, date performed202;10DATE-TIMEThis is the date that the preoperative SGPT was performed.
294sgot, date performed202;11DATE-TIMEThis is the date that the preoperative SGOT was performed.
295preop total bilirubin, date202;9DATE-TIMEThis is the date that the preoperative total bilirubin was performed.
296preop alk phosphatase, date202;12DATE-TIMEThis is the date that the preoperative alkaline phosphatase test was performed.
297preoperative wbc, date202;13DATE-TIMEThis is the date that the preoperative WBC test was performed.
298preop platelet count, date202;15DATE-TIMEThis is the date that the preoperative platelet count was performed.
299preoperative pt, date202;17DATE-TIMEThis is the date that the preoperative PT test was performed.
300preoperative ptt, date202;16DATE-TIMEThis is the date that the preoperative PTT test was performed.
301preop hematocrit, date202;14DATE-TIMEThis is the date that the preoperative hematocrit was performed.
302preoperative glucose, date202;3DATE-TIMEThis is the date that the preoperative glucose test was performed.
303preop potassium, date202;2DATE-TIMEThis is the date that the preoperative potassium test was performed.
304preop serum sodium, date202;1DATE-TIMEThis is the date that the preoperative serum sodium test was performed.
305high serum sodium, date204;1DATE-TIMEThis is the date that the highest Serum Sodium result was recorded.
306high potassium, date204;3DATE-TIMEThis is the date that the highest Potassium result was recorded.
307high glucose, date204;5DATE-TIMEThis is the date that the highest Glucose result was recorded.
308high serum creatinine, date204;6DATE-TIMEThis is the date that the highest Serum Creatinine result was recorded.
309high cpk, date204;7DATE-TIMEThis is the date that the highest CPK result was recorded.
310high cpk-mb, date204;8DATE-TIMEThis is the date that the highest CPK-MB Band result was recorded.
311high total bilirubin, date204;9DATE-TIMEThis is the date that the highest Total Bilirubin was recorded.
312highest wbc, date204;10DATE-TIMEThis is the date that the highest WBC was recorded.
313low serum albumin, date204;11DATE-TIMEThis is the date that the lowest Serum Albumin result was recorded.
314low hematocrit, date204;12DATE-TIMEThis is the date that the lowest Hematocrit result was recorded.
315preoperative pt control201;19NUMERICThis is the result of the preoperative PT control. Your answer must be between 9 and 15.
316preoperative ptt control201;18NUMERICThis is the preoperative PTT control result. Your answer must be between 15 and 40.
318respiratory occurrences205;9SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient had postoperative respiratory occurrences. A respiratory occurrence is defined as an impairment to the lungs to perform their ventilatory function. This may be due to impairment of gas exchange in the lung or obstruction of the free flow of air to the lung.
319urinary tract occurrences205;15SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has had postoperative urinary tract occurrences. Urinary tract occurrences are defined as difficulties related to the organs and ducts participating in the secretion and elimination of urine.
320cns occurrences205;20SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has had any postoperative central nervous system (CNS) occurrences. These occurrences are defined as difficulties related to the brain and spinal cord, with their nerves and end-organs that control voluntary acts.
321cardiac occurrences205;25SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has had any postoperative cardiac occurrences. Cardiac occurrences are defined as difficulties encountered involving the cardiac system.
322other occurrences205;30SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has had postoperative occurrences, such as Graft/Prosthesis Failure or Unplanned Return to OR, not included in any of the other categories.
323create risk assessmentRA;6BOOLEANY:YES
N:NO
This determines whether a risk assessment will be created for this surgical case. If answered 'NO', the information will automatically be completed so that the information will be transmitted without any additional intervention.
324drug addiction200;5SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether this patient has a history of recreational or narcotic substance abuse. There is no time limit on this data element.
325dyspnea200;6SET OF CODES1:NO
2:MODERATE EXERTION
3:AT REST
NS:NO STUDY
Definition Revised (2007): The patient describes difficult, painful, or labored breathing. Dyspnea may be symptomatic of numerous disorders that interfere with adequate ventilation or perfusion of the blood with oxygen. The dyspneic patient is subjectively aware of difficulty with breathing. Select one of the following categories that best indicates the patient's subjective experience coupled with your objective assessment: (1) No dyspnea (2) Dyspnea upon moderate exertion (e.g., is unable to climb one flight of stairs without shortness of breath) (3) Dyspnea at rest (e.g., cannot complete a sentence without needing to take a breath) The time frame is at the time the patient is being considered as a candidate for surgery (which should be no longer than 30 days prior to surgery). If the patient's dyspnea status worsens prior to surgery, report the most severe.
326current pneumonia200;12SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Report patients with evidence of pneumonia at the time the patient is brought to the OR. Patients with pneumonia must meet ONE of the following two criteria: Criterion 1. Rales or dullness to percussion on physical examination of chest AND any of the following: a. New onset of purulent sputum or change in character of sputum b. Organism isolate from blood culture c. Isolation of pathogen from specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy OR Criterion 2. Chest radiographic examination shows new or progressive infiltrate, consolidation, cavitation, or pleural effusion AND any of the following: a. New onset of purulent sputum or change in character of sputum b. Organism isolated from blood culture c. Isolation of pathogen from specimen obtained by transtracheal aspirate, bronchial brushing, or biopsy d. Isolation of virus or detection of viral antigen in respiratory secretions e. Diagnostic single antibody titer (IgM) or fourfold increase in paired serum samples (IgG) for pathogen f. Histopathologic evidence of pneumonia
327active hepatitis200;17SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has active hepatitis. Active Hepatitis is defined as an active inflammation of the liver evidenced by elevated liver enzymes. The most common causes are viral hepatitis documented by positive serologies (A,B, or C) and recent excessive alcohol intake, or drug induced hepatitis.
328renal failure200;38SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): The clinical condition associated with rapid, steadily increasing azotemia (increase in BUN), and a rising creatinine of above 3 mg/dl. Acute renal failure should be noted within 24 hours prior to surgery.
329*revascularization/amputation200;41SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Any type of angioplasty or revascularization procedure for atherosclerotic peripheral vascular disease (PVD) (e.g., aorto-femoral, femoral-femoral, femoral-popliteal) or a patient who has had any type of amputation procedure for PVD (e.g., toe amputations, transmetatarsal amputations, below the knee or above the knee amputations). Patients who have had amputation for trauma or a resection of abdominal aortic aneurysms should not be included.
330rest pain/gangrene (y/n)200;42SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Rest pain is a more severe form of ischemic pain due to occlusive disease, which occurs at rest and is manifested as a severe, unrelenting pain aggravated by elevation and often preventing sleep. Gangrene is a marked skin discoloration and disruption indicative of death and decay of tissues in the extremities due to severe and prolonged ischemia. Include patients with ischemic ulceration and/or tissue loss related to peripheral vascular disease. Do not include Fournier's gangrene. Report only if within the 30 days preoperatively.
331absent peripheral pulses200;43SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has been diagnosed on the physical examination to have absent femoral, popliteal, or pedal pulses. If he or she has had a previous amputation, record pulses as present or absent in the remaining limb.
332impaired sensorium200;19SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient is acutely confused and/or delirious and responds to verbal and/or mild tactile stimulation. Patients should be noted to have developed an impaired sensorium if they have mental status changes, and/or delirium in the context of the current illness. Patients with chronic or long-standing mental status changes secondary to chronic mental illness (e.g., schizophrenia) or chronic dementing illnesses (e.g., multi-infarct dementia, senile dementia of the Alzheimer's type) should not be included. This assessment of the patient's mental status should be within 48 hours prior to the surgical procedure. If the patient develops impaired sensorium, then progresses to a coma, and remains in a coma entering surgery, report just coma. Example: A patient is admitted to the orthopedics service after a fall with a fractured hip. The patient is also noted to be dehydrated and febrile. He is disoriented to place and time and seems confused. His family reports that he has been oriented and alert prior to the fall. This patient has an impaired sensorium on the basis of his confusion and disorientation. Example: A patient is admitted to the general surgical service with biliary sepsis and high spiking fevers. While febrile, the patient is noted by the clinician to be disoriented and confused. This patient has an impaired sensorium. Example: A long-term resident of a VA nursing home with chronic schizophrenia is admitted for an elective hernia repair. He is noted to have long-standing mental status changes and is chronically disoriented to place, time, and person. Although this patient has disorientation, his mental status changes are long-standing, chronic, and unchanged and would not qualify for "impaired sensorium." Note: These examples would apply only if noted within 48 hours prior to surgery
333coma200;21SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient is unconscious, postures to painful stimuli, or is unresponsive to all stimuli entering surgery. This does not include drug-induced coma.
334*history of tia's200;25SET OF CODESY:YES
N:NO
NS:NO STUDY
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2004): Transient ischemic attacks (TIAs) are focal neurologic deficits (e.g. numbness of an arm or amaurosis fugax) of sudden onset and brief duration (usually <30 minutes), which usually reflect dysfunction in a cerebral vascular distribution. These attacks may be recurrent and, at times, may precede a stroke.
335*cva/stroke with neuro deficit200;26SET OF CODESY:YES
N:NO
NS:NO STUDY
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2004): History of a cerebrovascular accident (embolic, thrombotic, or hemorrhagic) with persistent residual motor, sensory, or cognitive dysfunction. (e.g., hemiplegia, hemiparesis, aphasia, sensory deficit, impaired memory). If the neurological deficit is hemiplegia/hemiparesis, also enter YES to Hemiplegia/Hemiparesis in addition to CVA/Stroke.
336*cva/stroke - no neuro deficit200;27SET OF CODESY:YES
N:NO
NS:NO STUDY
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2004): History of a cerebrovascular accident (embolic, thrombotic, or hemorrhagic) with neurologic deficit(s) lasting at least 30 minutes, but no current residual neurologic dysfunction or deficit.
337neuro degenerative disease200;28SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has neuromuscular degenerative disease. It is defined as any of a number of congenital, hereditary, or acquired diseases resulting in chronic neurological deficits. Common examples of these diseases include muscular dystrophy, amyotrophic lateral sclerosis (ALS or 'Lou Gerhig's Disease'), multiple sclerosis, and poliomyelitis.
338disseminated cancer (y/n)200;45SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2010): Disseminated cancer: Patients who have cancer known to be present prior to the start of surgery that: (1) Has spread to one site or more sites in addition to the primary site AND (2) In whom the presence of multiple metastases indicates the cancer is widespread, fulminant, or near terminal. Other terms describing disseminated cancer include "diffuse," "widely metastatic," "widespread," or "carcinomatosis", or AJCC "Stage IV" cancer. Common sites of metastases include major organs (e.g., brain, lung, liver, meninges, abdomen, peritoneum, pleura, and bone). You may use the National Cancer Institute as a reference in determining whether a patient has AJCC Stage IV cancer, when the TNM information is the only information documented. Refer to the following website for assistance with translating TNM values with AJCC staging: http://www.cancer.gov/cancertopics/pdq/adulttreatment Examples: - A patient with a primary breast cancer with positive nodes in the axilla does NOT qualify for this definition. The tumor has spread to a site other than the primary site, but does not have widespread metastases. A patient with primary breast cancer with positive nodes in the axilla AND liver metastases does qualify, because the tumor has spread to the axilla and other major organs. - A patient with colon cancer and no positive nodes or distant metastases does NOT qualify. A patient with colon cancer and several local lymph nodes positive for tumor, but no other evidence of metastatic disease does NOT qualify. A patient with colon cancer with liver metastases and/or peritoneal seeding with tumor does qualify. - A patient with adenocarcinoma of the prostate confined to the capsule does NOT qualify. A patient with prostate cancer that extends through the capsule of the prostate only does NOT qualify. A patient with prostate cancer with bony metastases DOES qualify. Report Acute Lymphocytic Leukemia (ALL), Acute Myelogenous Leukemia (AML) and Stage IV Lymphoma under this variable. Do not report Chronic Lymphocytic Leukemia (CLL), Chronic Myelogenous Leukemia (CML), Multiple Myeloma or Lymphomas that are Stage I-III as disseminated cancer.
338.1chemotherapy in last 30 days206;3SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Enter "YES" if the patient had any chemotherapy treatment for cancer in the 30 days prior to surgery. Chemotherapy may include, but is not restricted to, oral and parenteral treatment with chemotherapeutic agents for malignancies such as colon, breast, lung, head and neck, and gastrointestinal solid tumors as well as lymphatic and hematopoietic malignancies such as lymphoma, leukemia, and multiple myeloma. Do not count if treatment consists solely of hormonal therapy. (See Operations Manual for list of chemotherapeutic agents.) Chemotherapy treatment must be for malignancy.
338.2radiotherapy in last 90 days206;4SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Enter "YES" if the patient had any radiotherapy treatment for cancer in the 90 days prior to surgery. If the patient had radiation seeds implanted, count if implantation is within 90 days prior to the operation.
339steroid use for chronic cond.200;47SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient has required the regular administration of oral or parenteral corticosteroid medications (e.g., Prednisone, Decadron) in the 30 days prior to admission for a chronic medical condition (e.g., COPD, asthma, rheumatologic disease, rheumatoid arthritis, inflammatory bowel disease). Do not include topical corticosteroids applied to the skin or corticosteroids administered by inhalation or rectally. Do not include patients who only receive short course steroids (duration 10 days or less) in the 30 days prior to surgery. (See list of corticosteroids in Operations Manual.)
340intraop rbc units transfused200;54FREE TEXTDefinition Revised (2014): Indicate the number of packed or whole red blood cells given during the operative procedure as it appears on the anesthesia record. The amount of blood reinfused from the cell saver should also be noted here. The algorithm for cell saver volume to RBC unit determination is: 0 units - 0-124 cc's 1 unit - 125 - 375 cc's 2 units - 376 - 625 cc's 3 units - 626 - 875 cc's
34130 day postop status205;2SET OF CODES1:DISCHARGED ALIVE
2:DIED IN HOSPITAL
3:REMAINS IN VAMC FACILITY
4:TRANSFERRED TO ANOTHER VAMC
5:READMITTED
NS:NO STUDY
This is the patient's status 30 days postoperatively. Please select one of the following categories. 1. Discharged alive to home, nursing home, rehabilitation, or psychiatric facility 2. Died in Hospital perioperatively or postoperatively 3. Still in your VAMC facility in the ICU, on a medical-surgical floor, or undergoing rehabilitation therapy. 4. Transferred to the ICU or acute care floor of another VAMC facility from your VAMC without going home 5. Patient was discharged home, but was readmitted to any hospital within 30 days postoperatively due to a postoperative complication as confirmed by the Chief Surgical Resident, Principle Investigator, or Chief of Surgery. If the patient was readmitted due to a postoperative complication, please enter the information in the outcome section of the assessment.
342date of death205;3FREE TEXTIf the patient has died, this is the date/time of death.
342.130 day death205;41BOOLEANY:YES
N:NO
This field indicates whether operative death has occurred within 30 days of surgery. This field auto populates based on an entry into the DATE OF DEATH field (#342). If Date of Death occurs within 30 days or less of the Date of Operation, then this field is automatically updated to "Yes" when the Date of Death is saved. If the Date of Death is greater than 30 days from the Date of Operation or "NA" is entered then this field is automatically updated to "No" when the Date of Death is saved.
343other cns occurrence205;24POINTER80Definition Revised (2004): Enter any other neurologic related occurrences, which you feel to be significant and that are not covered by the predefined CNS occurrence categories. Enter the ICD-CM code for this entry.
344other cardiac occurrence205;29POINTER80Definition Revised (2004): Enter any other cardiac related surgical occurrences which you feel to be significant and that are not covered by the predefined occurrence categories. Enter the ICD-CM code for this entry.
345ileus/bowel obstruction205;31SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has prolonged ileus or bowel obstruction. Ileus is obstruction of the intestines from a variety of causes including mechanical obstruction, peritonitis, adhesions, or post surgically as a result of functional dysmotility by the bowel. Bowel obstruction is any hindrance to the passage of the intestinal contents. Prolonged ileus or obstruction is defined as persisting longer than 5 days postoperatively.
346*diabetes200;2SET OF CODESN:NO
O:ORAL
I:INSULIN
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2004): Diabetes mellitus is a metabolic disorder of the pancreas whereby the individual requires daily dosages of exogenous parenteral insulin or an oral hypoglycemic agent to prevent a hyperglycemic/metabolic acidosis. Report the treatment regimen of the patient's chronic, long-term management. Do not include a patient if diabetes is controlled by diet alone. No: No diagnosis of diabetes or diabetes controlled by diet alone Oral: A diagnosis of diabetes requiring therapy with an oral hypoglycemic agent (see list of oral hypoglycemic agents in Operations Manual) Insulin: A diagnosis of diabetes requiring daily insulin therapy (see list of insulin therapy agents in Operations Manual)
347fev1206;5FREE TEXTThis is the forced expiratory volume in one second from the most recent pulmonary function test prior to surgery. Enter 'NS' if there has been no pulmonary function tests in the preceding year.
348pulmonary rales206;7BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the chart documents rales not clearing with cough (and not due to pneumonic process) heard within two weeks before surgery. Do not include rales that clear with coughing, as these are usually due to atelectasis and carry a much more benign connotation. Please note, crackles are another common approach to noting that rales are present.
349active endocarditis206;10BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the patient is being treated with antibiotics for active infection on or near a cardiac valve at the time of surgery or within 2 weeks prior to surgery. Endocarditis is defined as two or more blood cultures positive for the same organism, usually with evidence of a valvular vegetation or valve dysfunction by cardiac ultrasound. In the absence of positive blood cultures, there should be clear evidence of valve infection and/or destruction by ultrasound or direct observation at surgery with subsequent histologic confirmation.
350resting st depression206;11BOOLEANY:YES
N:NO
This determines whether the patient has a ST-segment depression greater than or equal to 1 mm in any lead on standard resting electrocardiogram (ECG), and/or ECG diagnosis of subendocardial ischemia, left ventricular strain, or left ventricular hypertrophy with repolarization abnormality.
351*pci206;13SET OF CODES1:NONE RECENT
2:12-72 HOURS PRIOR TO SURGERY
0:NONE
3:<12 hrs
12:12 - 72 hrs
72:>72 hrs - 7 days
7:>7 days
Definition Revised (2004): Indicate whether/when the patient had a percutaneous coronary intervention (PCI) prior to surgery. Previously, this data field was listed as a percutaneous transluminal coronary angiography (PTCA) [e.g., balloon angioplasty, directional coronary atherectomy (DCA), transluminal extraction catheter (TEC), stent, rotoblader, etc.] Indicate the one appropriate response, even if the procedure was not fully successful.
352num of prior heart surgeries206;15SET OF CODESY:YES
0:NONE
1:1
2:2
3:3
>:>3
Definition Revised (2006): Indicate the number of previous heart surgeries the patient has had upon current admission, by referencing the patient history. The prior heart surgery/ies would have occurred during a separate hospitalization (more than 30 days prior to current surgery). Both on and off-pump cardiac surgical procedures should be considered. Count all surgical procedures performed during separate hospital admissions (not the number of grafts, and not additional procedures performed during the same admission due to a postoperative occurrence). Indicate the one appropriate response: 0, 1, 2, 3, >3.
353current diuretic use206;20BOOLEANY:YES
N:NO
This determines whether the patient has used any diuretic preparation within the two weeks prior to surgery.
354current digoxin use206;21BOOLEANY:YES
N:NO
This determines whether the patient has used a digitalis preparation (digoxin, Lanoxin, digitoxin, ect.) within the two weeks prior to surgery.
355iv ntg within 48 hours206;22BOOLEANY:YES
N:NO
This determines whether the patient was administered nitroglycerin intravenously within 48 hours prior to surgery.
356preoperative use of iabp206;23BOOLEANY:YES
N:NO
This determines whether there was any use of an intra-aortic balloon pump (IABP) within the two weeks prior to surgery.
357lvedp206;24FREE TEXTDefinition Revised (2004): Indicate the patient's left ventricular end-diastolic pressure measured following the a-wave (if present) at the cardiac catheterization most recent prior to surgery. If LVEDP was not measured, entering "NS" for "No Study/Unknown" is also allowed.
358aortic systolic pressure206;25FREE TEXTDefinition Revised (2004): Indicate the patient's aortic systolic pressure measured prior to left ventricular angiography at the catheterization most recent prior to surgery. If aortic systolic pressure was not measured, entering "NS" for "No Study/Unknown" is also allowed.
359pa systolic pressure206;26FREE TEXTDefinition Revised (2004): For patients having a right heart catheterization, indicate the patient's pulmonary artery (PA) systolic pressure at the catheterization most recent prior to surgery. PA pressures obtained in the operating room prior to surgery are acceptable if they are obtained prior to anesthesia induction. If no right heart catheterization performed, entering "NS" for "No Study/Unknown" is also allowed.
360paw mean pressure206;27FREE TEXTDefinition Revised (2004): For patients having a right heart catheterization, indicate the patient's mean pulmonary artery wedge (PAW) [also called pulmonary capillary] pressure or left atrial pressure measured at the catheterization most recent prior to surgery. PAW pressures obtained in the operating room prior to surgery are acceptable if they are obtained prior to anesthesia induction. If no right heart or transseptal catheterization performed, entering "NS" for "No Study/Unknown" is also allowed.
361left main stenosis206;28FREE TEXTDefinition Revised (2004): Indicate the most severe percent diameter reduction of the left main coronary artery, including its most distal portion. If there is no obstruction of the left main coronary artery, indicate zero. Entering "NS" for "No Study/Unknown" is also allowed.
362coronaries with stenosis206;29NUMERICThis is the category corresponding to the number of major coronaries with stenosis greater than or equal to 50%. The categories are as follows. 0 - no stenosis in any coronary artery greater than or equal to 50% (exclude diagonals) 1 - one or more stenoses greater than or equal to 50% in the left anterior descending (does not include diagonals) or, circumflex (circumflex includes the marginal branches and ramus intermedius), or the right (right includes the posterior descending even if a branch of the circumflex) 2 - Stenoses greater than or equal to 50% in the left main coronary artery, or the left anterior descending (does not include diagonals) and the right (right includes the posterior descending even if a branch of the circumflex), or the left anterior descending (does not include diagonals) and circumflex (circumflex includes the marginals and ramus intermedius), or the circumflex (circumflex includes the marginals and ramus intermedius) and the right (right includes the posterior descending even if a branch of the circumflex) 3 - Stenoses greater than or equal to 50% in the left anterior descending (does not include diagonals) and the circumflex (circumflex includes the marginals and ramus intermedius) and right (right includes the posterior descending even if a branch of the circumflex) or left main and right (right includes the posterior descending even if a branch of the circumflex)
362.1lad stenosis206;33FREE TEXTDefinition Revised (2004): Indicate the most severe percent stenosis in the left anterior descending coronary artery. Synonyms for this artery include: LAD, AD, and anterior descending (but does not include the diagonals). If there is no obstruction of the LAD, indicate zero. Entering "NS" for "No Study/Unknown" is also allowed.
362.2right coronary stenosis206;34FREE TEXTDefinition Revised (2004): Indicate the most severe percent stenosis in the right coronary artery. Include the proximal third of the posterior descending coronary artery. The right coronary artery initially runs in the groove between the right ventricle and right atrium; it usually gives off branches to both the right and left ventricles and the right atrium. The branches to the right atrium (sinus node artery) and right ventricle (conus branch and acute marginal branches) are commonly ignored when describing coronary artery disease. However, the right coronary artery is the most common source for the posterior descending coronary artery and often gives-off branches to the posterior-lateral free wall of the left ventricle. These are often known as left ventricular extension branches and are considered branches of the circumflex for the coding of severity of coronary disease. If there is no obstruction of these coronary arteries, indicate zero. Entering "NS" for "No Study/Unknown" is also allowed.
362.3circumflex stenosis206;35FREE TEXTDefinition Revised (2004): Indicate the most severe percent stenosis in the circumflex coronary artery, including marginal branches and ramus intermedius considered to be of adequate size for bypass grafting. Both the anatomy and nomenclature for describing the circumflex coronary artery can be confusing -- in part, because of the marked variability from patient to patient. The true circumflex lies in the groove separating the left atrium from the left ventricle (A-V groove) for a variable distance following its origination from the left main coronary artery. Typically, it gives-off one or more branches that leave the A-V groove to supply the posterior-lateral free wall of the left ventricle. These are known as marginal branches. A few patients have a branch to the posterior-lateral free wall of the left ventricle arising exactly at the bifurcation of the left main coronary artery into the left anterior descending coronary artery and the circumflex coronary artery. Strictly speaking, this vessel is neither a diagonal branch of the left anterior descending coronary artery nor a marginal branch of the circumflex coronary artery. This is often called the "ramus intermedius" or "trifurcation branch". If there is no obstruction of these coronary arteries, indicate zero. Entering "NS" for "No Study/Unknown" is also allowed.
363lv contraction score206;30SET OF CODESI:> OR EQUAL 0.55 NORMAL
II:0.45-0.54 MILD DYSFUNC.
III:0.35-0.44 MOD. DYSFUNC.
IIIa:0.40-0.44 MOD. DYSFUNC. A
IIIb:0.35-0.39 MOD. DYSFUNC. B
IV:0.25-0.34 SEVERE DYSFUNC.
V:<0.25 VERY SEVERE DYSFUNC.
NS:NO STUDY
Definition Revised (2004): Indicate the left ventricular contraction grade, where the function is assessed from the preoperative contrast ventriculogram, radionuclide angiogram, or 2-D echocardiogram. If ejection fraction is available, indicate the corresponding grade; otherwise, indicate the grade that qualitatively reflects left ventricular function. Ejection fraction is defined as the proportion of blood that is ejected during each ventricular contraction compared with the total ventricular filling volume. Indicate the one most appropriate response: I - Ejection fraction >= 0.55 or narrative reports indicating normal left ventricular function. II - Ejection fraction range from 0.45 to 0.54 or narrative report indicating mild left ventricular dysfunction. IIIa - Ejection fraction range from 0.40 to 0.44 or narrative report indicating moderate left ventricular dysfunction. If "moderate" is the only rating available, select this category. IIIb - Ejection fraction range from 0.35 to 0.39 or narrative report indicating moderately severe left ventricular dysfunction. IV - Ejection fraction range from 0.25 to 0.34 or narrative report indicating severe left ventricular dysfunction. V - Ejection fraction < 0.25 or narrative report indicating very severe left ventricular dysfunction. NS - If unable to make an assessment of the patient's left ventricular contraction grade or no study was performed, entering "NS" for "No Study/Unknown" is also allowed.
364estimate of mortality206;31NUMERICDefinition Revised (2006): This is the physician's (cardiologist or cardiac surgeon) subjective estimate of operative mortality based on the assessment of the total clinical picture. (To avoid bias introduced by knowledge of outcome, this must be completed preoperatively. Do not calculate from the computer program provided to you.)
364.1estimate of mortality, date206;32FREE TEXTThis is the date and time that the estimate of mortality information was collected.
365*number with vein207;1NUMERICThis is the number of coronary artery bypass graft (CABG) anastomoses to native coronary arteries with vein regardless of whether other procedures were performed. Do not leave this information blank. If no coronary artery bypass grafts were performed, enter '0'.
366*number with ima207;2NUMERICThis is the number of coronary artery bypass graft (CABG) anastomoses to native coronary arteries with internal mammary arteries (IMA) regardless of whether other procedures were performed. Do not leave this field blank. If no coronary artery bypass grafts were performed, enter '0'.
367*aortic valve procedure207;3SET OF CODESY:YES
N:NONE
M:MECHANICAL
S:STENTED BIOPROSTHETIC
B:STENTLESS BIOPROSTHETIC
H:HOMOGRAFT
PR:PRIMARY REPAIR
PA:PRIMARY REPAIR & ANNULOPLASTY DEVICE
AN:ANNULOPLASTY DEVICE ALONE
AU:AUTOGRAFT (ROSS)
O:OTHER
VASQIP Definition (2010): Indicate if the patient had an aortic valve replacement (either the native or a prosthetic valve) or a repair (on the native valve to relieve stenosis and/or correct regurgitation -annuloplasty, commissurotomy, etc.); performed with or without additional procedure(s); either with or without placing the patient on cardiopulmonary bypass. (If a repair was attempted, but a replacement occurred, indicate the details of the replacement valve.) Indicate the one most appropriate procedure: * None * Mechanical Valve * Stented Bioprosthetic Valve * Stentless Bioprosthetic Valve * Homograft * Primary Valve Repair * Primary Valve Repair and Annuloplasty Device * Annuloplasty Device alone * Autograft Procedure (Ross Procedure) * Other
368*mitral valve procedure207;4SET OF CODESY:YES
N:NONE
M:MECHANICAL
S:STENTED BIOPROSTHETIC
B:STENTLESS BIOPROSTHETIC
H:HOMOGRAFT
PR:PRIMARY REPAIR
PA:PRIMARY REPAIR & ANNULOPLASTY DEVICE
AN:ANNULOPLASTY DEVICE ALONE
AU:AUTOGRAFT (ROSS)
O:OTHER
VASQIP Definition (2010): Indicate if the patient had a mitral valve replacement (either the native or a prosthetic valve) or a repair (on the native valve to relieve stenosis and/or correct regurgitation -annuloplasty, commissurotomy, etc.); performed with or without additional procedure(s); either with or without placing the patient on cardiopulmonary bypass. (If a repair was attempted, but a replacement occurred, indicate the details of the replacement valve.) Indicate the one most appropriate procedure: * None * Mechanical Valve * Stented Bioprosthetic Valve * Stentless Bioprosthetic Valve * Homograft * Primary Valve Repair * Primary Valve Repair and Annuloplasty Device * Annuloplasty Device alone * Autograft Procedure (Ross Procedure) * Other
369*tricuspid valve procedure207;5SET OF CODESY:YES
N:NONE
M:MECHANICAL
S:STENTED BIOPROSTHETIC
B:STENTLESS BIOPROSTHETIC
H:HOMOGRAFT
PR:PRIMARY REPAIR
PA:PRIMARY REPAIR & ANNULOPLASTY DEVICE
AN:ANNULOPLASTY DEVICE ALONE
AU:AUTOGRAFT (ROSS)
O:OTHER
VASQIP Definition (2010): Indicate if the patient had a tricuspid valve replacement (either the native or a prosthetic valve) or a repair (on the native valve to relieve stenosis and/or correct regurgitation -annuloplasty, commissurotomy, etc.); performed with or without additional procedure(s); either with or without placing the patient on cardiopulmonary bypass. (If a repair was attempted, but a replacement occurred, indicate the details of the replacement valve.) Indicate the one most appropriate procedure: * None * Mechanical Valve * Stented Bioprosthetic Valve * Stentless Bioprosthetic Valve * Homograft * Primary Valve Repair * Primary Valve Repair and Annuloplasty Device * Annuloplasty Device alone * Autograft Procedure (Ross Procedure) * Other
370valve repair207;6SET OF CODESY:YES
1:AORTIC
2:MITRAL
3:TRICUSPID
4:OTHER/COMBINATION
5:NONE
Definition Revised (2006): Indicate if the patient has had any reparative procedure to a native valve, either with or without placing the patient on cardiopulmonary bypass. Valve repair is defined as a procedure performed on the native valve to relieve stenosis and/or correct regurgitation (annuloplasty, commissurotomy, etc.); the native valve remains in place. Indicate the one appropriate response.
371*lv aneurysmectomy207;7BOOLEANY:YES
N:NO
This determines whether the patient had a resection or plication of a left ventricular aneurysm with or without additional procedures.
372*great vessel repair (y/n)207;8BOOLEANY:YES
N:NO
Definition Revised (2006): Indicate if patient had a thoracic great vessel open repair of the aorta (ascending, transverse, and/or descending) or other great vessels, with or without cardiopulmonary bypass, with or without aortic valve replacement, CABG, or other procedure but excluding an endovascular repair of the descending thoracic aorta.
373*cardiac transplant207;9BOOLEANY:YES
N:NO
Definition Revised (2006): Indicate if an orthotopic or heterotopic transplant was performed at this procedure either with or without placing the patient on cardiopulmonary bypass. (YES/NO) Heart-lung transplant should be listed under "Other cardiac procedures."
374electrophysiologic procedure207;10BOOLEANY:YES
N:NO
This determines whether any procedure was performed with cardiopulmonary bypass to correct an electrophysiologic disturbance, such as resection of bypass tract(s) for WPW or endocardial resection for ventricular tachycardia. (This does not include implantation of automatic internal cardiac defibrillator AICD)
375misc. cardiac procedures207;11BOOLEANY:YES
N:NO
This determines whether there were any miscellaneous cardiac procedures performed.
376*asd repair207;12BOOLEANY:YES
N:NO
This determines if there was a procedure performed to repair an atrial septal defect.
377*myxoma resection207;14BOOLEANY:YES
N:NO
This determines whether a resection of an atrial myxoma was performed.
378*myectomy207;16BOOLEANY:YES
N:NO
Definition Revised (2011): Indicate if patient had resection of a portion of the interventricular septum, with or without placing the patient on cardiopulmonary bypass. (YES/NO)
379*other tumor resection207;18BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if patient had resection of any tumor other than atrial myxoma from the heart either with or without placing the patient on cardiopulmonary bypass.
380*vsd repair207;13BOOLEANY:YES
N:NO
This determines whether the patient had a procedure performed to repair a ventricular septal defect.
381*foreign body removal207;15BOOLEANY:YES
N:NO
This determines whether a procedure was performed to remove any foreign body (e.g. bullet or catheter fragment) from the heart with the aid of cardiopulmonary bypass.
382*pericardiectomy207;17BOOLEANY:YES
N:NO
This determines whether the patient had a resection of the parietal pericardium with the aid of cardiopulmonary bypass. (NOTE: most pericardiectomies are performed without cardiopulmonary bypass)
383other procedures (y/n)207;19BOOLEANY:YES
N:NO
This determines whether the patient had any other surgical procedure on the heart and/or great vessels (including AICD placement) requiring cardiopulmonary bypass.
383.1other cardiac procedures207.1;1FREE TEXTDefinition Revised (2004): This is the free text description of other procedures requiring cardiopulmonary bypass that were performed on this patient at the same time as the primary cardiac procedure.
384operative death208;1BOOLEANY:YES
N:NO
Definition Revised (2006): Indicate if the patient died within the 30 days after surgery in or out of the hospital regardless of cause; or within the index hospitalization regardless of cause; or patient died greater than 30 days as a direct result of a perioperative occurrence of the surgery (e.g., mediastinitis). ("Discharge" can be noted when the patient leaves the Acute Care arena.)
385*perioperative mi208;2BOOLEANY:YES
N:NO
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2011): Indicate the presence of a peri-operative MI as documented by the following criteria: 0-24 Hours Post-Op The CK-MB (or CK if MB not available) must be greater than or equal to 5-times the upper limit of normal, with or without new Q waves present in two or more contiguous ECG leads. No symptoms required. >24 Hours Post-Op Indicate the presence of a peri-operative MI (> 24 hours post-op) as documented by at least one of the following criteria: 1. Evolutionary ST- segment elevations 2. Development of new Q-waves in two or more contiguous ECG leads 3. New or presumably new LBBB pattern on the ECG 4. The CK-MB (or CK if MB not available) must be greater than or equal to 3 times the upper limit of normal. Because normal limits of certain blood tests may vary, please check with your lab for normal limits for CK-MB and total CK. Defining Reference Control Values (Upper Limit of Normal): Reference values must be determined in each laboratory by studies using specific assays with appropriate quality control, as reported in peer-reviewed journals. Acceptable imprecision (coefficient of variation) at the 99th percentile for each assay should be defined as < or = to 10%. Each individual laboratory should confirm the range of reference values in their specific setting. This element should not be coded as an adverse event for evolving MI's unless their enzymes peak, fall, and then have a second peak.
386endocarditis208;3BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the chart documents that active endocarditis was present within 30 days postoperatively. Endocarditis is defined as any postoperative intracardiac infection (usually on a valve) documented by two or more positive blood cultures with the same organism, and/or development of vegetations and valve destruction seen by echo or repeat surgery, and/or histologic evidence of infection at repeat surgery or autopsy. Patients with preoperative endocarditis who have the above evidence of persistent infection should be included.
387low cardiac output > 6 hours208;4BOOLEANY:YES
N:NO
This determines whether the patient has had a postoperative cardiac index of less than 2.0 L/min/M2 and/or peripheral manifestations (e.g. oliguria) of low cardiac output present for 6 or more hours following surgery requiring inotropic and/or intra-aortic balloon pump support.
388mediastinitis208;5BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the patient developed a bacterial infection involving the sternum or deep to the sternum requiring drainage and anti-microbial therapy diagnosed within 30 days after surgery.
389reoperation for bleeding208;6BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if there was any re-exploration of the thorax for suspected bleeding within 30 days of surgery.
390*stroke208;8BOOLEANY:YES
N:NO
This field has been flagged as obsolete for VASQIP. It should no longer be used. Cardiac Definition Revised (2004): Indicate if there was any new objective neurologic deficit lasting > 72 hours with onset immediately post-operatively or occurring within the 30 days after surgery.
391repeat cardiac surg procedure208;7BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate the CPB status if the patient underwent a repeat operation on the heart after the patient had left the operating room from the initial operation and within current hospitalization or within 30 days of the initial operation.
392other occurrences (icd)205;36POINTER80Definition Revised (2004): Enter any other surgical occurrences which you feel to be significant and that are not covered by the predefined occurrence categories. Enter the ICD-CM code for this entry.
393re-transmissionRA;3NUMERICThis determines whether the assessment will be re-transmitted. It will automatically be set to '1' when a transmitted assessment is updated to an INCOMPLETE status to edit and re-transmit.
394*history of mi200;31SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): The history of a non-Q wave or a Q wave infarct in the six months prior to surgery as diagnosed in the patient's medical record.
395*angina one month prior200;34SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Pain or discomfort between the diaphragm and the mandible resulting from myocardial ischemia. Typically angina is a dull, diffuse (fist-sized or larger) substernal chest discomfort precipitated by exertion or emotion and relieved by rest or nitroglycerine. Radiation to the arms and shoulders often occurs, and occasionally to the neck, jaw (mandible, not maxilla), or interscapular region. Documentation in the chart by the physician should state 'angina' or 'anginal equivalent'. For patients on anti-anginal medications, enter 'yes' only if the patient has had angina at any time within 30 days prior to surgery.
396*chf within one month200;35SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Congestive Heart Failure is the inability of the heart to pump a sufficient quantity of blood to meet the metabolic needs of the body or can do so only at increased ventricular filling pressure. Only newly diagnosed CHF within the previous 30 days or a diagnosis of chronic CHF with new signs or symptoms in the 30 days prior to surgery fulfills this definition. Common manifestations are: - Abnormal limitation in exercise tolerance due to dyspnea or fatigue - Orthopnea (dyspnea on lying supine) - Paroxysmal nocturnal dyspnea (PND-awakening from sleep with dyspnea) - Increased jugular venous pressure - Pulmonary rales on physical examination - Cardiomegaly - Pulmonary vascular engorgement Should be noted in the medical record as CHF, congestive heart failure, or pulmonary edema.
397severe head trauma (y/n)200;20SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has sustained open or closed trauma to the head from external force, violence, or accident with resulting impairment in neurological function as manifested by motor, sensory, or cognitive impairments.
398quadriplegia (y/n)200;22SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient has sustained acute or chronic neuromuscular injury resulting in total or partial paralysis or paresis (weakness) of all four extremities.
399paraplegia (y/n)200;23SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient has sustained acute or chronic neuromuscular injury resulting in total or partial paralysis or paresis (weakness) of the lower extremities.
400hemiplegia/hemiparesis (y/n)200;24SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient has sustained acute or chronic neuromuscular injury resulting in total or partial paralysis or paresis (weakness) of one side of the body. Enter YES if the patient has hemiplegia/hemiparesis (that has not recovered or been rehabilitated) upon arrival to the OR. Enter YES if there is hemiplegia or hemiparesis associated with a CVA/Stroke also.
401tumor involving cns (y/n)200;29SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2007): Space-occupying tumor of the brain and spinal cord, which may be benign (e.g., meningiomas, ependymoma, oligodendroglioma) or primary (e.g., astrocytoma, glioma, glioblastoma multiform) or secondary malignancies (e.g., metastatic lung, breast, malignant melanoma). Other tumors that may involve the CNS include lymphomas and sarcomas. Answer "YES" even if the tumor was not treated. A patient with metastatic cancer with boney mets to spine is a CNS tumor. Answer "NO" if tumor was removed.
402general (y/n)200;1BOOLEANY:YES
N:NO
This determines whether the patient has any general medical problems, such as diabetes, dyspnea, or alcohol related illnesses.
403wound occurrences205;5SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient had any postoperative wound occurrences.
404wound disruption205;8SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2014): Separation of the skin and musculofascial layers of a surgical wound (any surgical site whether primary or secondary, e.g. vein harvest incision), which may be partial or complete.
405low serum sodium203;2FREE TEXTThis is the lowest postoperative serum sodium result recorded within 30 days postoperatively. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
406low potassium203;4FREE TEXTThis is the lowest recorded postoperative potassium result. Data input must be 1 to 3 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
407low sodium, date204;2DATE-TIMEThis is the date that the lowest serum sodium test result was recorded.
408low potassium, date204;4DATE-TIMEThis is the date that the lowest potassium test result was recorded.
409renal insufficiency205;16SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): The reduced capacity of the kidney to perform its function as evidenced by a rise in creatinine of >2 mg/dl from preoperative value, but with no requirement for dialysis.
410coma > 24 hours postop205;22SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2011): Indicate if either postoperatively or within 30 days of surgery there was a significantly decreased level of consciousness (exclude transient disorientation or psychosis) for greater than or equal to 24 hours as evidenced by lack of response to deep, painful stimuli. Do not include drug-induced coma (e.g. Propofol drips, etc.)
411cardiac arrest req cpr205;26SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2011): Indicate if there was any cardiac arrest requiring external or open cardiopulmonary resuscitation (CPR) occurring in the operating room, ICU, ward, or out-of-hospital after the chest had been completely closed and within 30 days of surgery. Patients with AICDs that fire but the patient does not lose consciousness should be excluded. If patient had cardiac arrest requiring CPR, indicate whether the arrest occurred intraoperatively or postoperatively. Indicate the one appropriate response: - intraoperatively: occurring while patient was in the operating room - postoperatively: occurring after patient left the operating room.
412unplanned intubation (y/n)205;11SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Patient required placement of an endotracheal tube and mechanical or assisted ventilation because of the onset of respiratory or cardiac failure manifested by severe respiratory distress, hypoxia, hypercarbia, or respiratory acidosis. In patients who were intubated for their surgery, unplanned intubation occurs after they have been extubated after surgery. In patients who were not intubated during surgery, intubation at any time after their surgery is considered unplanned.
413transfer status208;11SET OF CODES1:NOT TRANSFERRED
2:NON-VAMC ACUTE CARE HOSPITAL
3:VAMC ACUTE CARE HOSPITAL
4:NON-VA NURSING/CHRONIC CARE/SCI/INTERMEDIATE CARE FACILITY
5:VA NURSING HOME/CHRONIC CARE/SCI/INTERMEDIATE CARE FACILITY
6:OTHER
Definition Revised (2004): Was the patient transferred directly from another healthcare facility and admitted to this hospital? Please select from the following choices. If the patient was admitted from home, select #1. If the patient was transferred from another facility, please select from choices #2-6. (1) Not transferred from a health care facility; admitted directly from home (2) Non-VAMC Acute Care Hospital (3) VAMC Acute Care Hospital (4) Non-VA Nursing Home/Chronic Care Facility/Spinal Cord Injury Unit/Intermediate Care Unit (5) VA Nursing Home/Chronic Care Facility/Spinal Cord Injury Unit/Intermediate Care Unit (6) Other (for example, Domiciliary) * If a patient arrives from another hospital's emergency department, report as #1. If you cannot determine what kind of facility, enter "OTHER".
414cardiac surgical priority208;12SET OF CODES1:ELECTIVE
2:URGENT
3:EMERGENT (ONGOING ISCHEMIA)
4:EMERGENT (HEMODYNAMIC COMPROMISE)
5:EMERGENT (ARREST WITH CPR)
If this is a cardiac procedure, this is the surgical priority reflecting the patient's cardiovascular condition at the time of transport to the operating room: 1. Elective - Patient placed on elective schedule with surgery usually performed > 72 hours following catheterization. 2. Urgent - Clinical condition mandates prompt surgery usually within 12 to 72 hours of catheterization (patients clinically stable on a circulatory support system should be included in this category). 3. Emergent (ongoing ischemia) - Clinical condition mandates immediate surgery usually on day of catheterization because of ischemia despite medical therapy, such as intravenous nitroglycerine. Ischemia should be manifested as chest pain and/or ST-segment depression. 4. Emergent (hemodynamic compromise) - Persistent hypotension (arterial systolic pressure < 80 mm Hg) and/or low cardiac output (cardiac index < 2.0 L/min/MxM) despite iontropic and/or mechanical circulatory support mandates immediate surgery within hours of the cardiac catheterization. 5. Emergent (arrest with CPR) - Patient is taken to the operating room in full cardiac arrest with the circulation supported by cardiopulmonary resuscitation (excludes patients being adequately perfused by a cardiopulmonary support system).
414.1surgical priority, date208;13DATE-TIMEThis is the date and time that the cardiac surgical priority information was collected.
415mitral regurgitation206;9SET OF CODES0:NONE
1:MILD
2:MODERATE
3:SEVERE
NS:NO STUDY
Definition Revised (2004): Indicate the severity of any mitral regurgitation documented for the patient. This question should be answered using either the left ventricular angiogram or the cardiac ultrasound examination. Adjectives used to describe the severity of the mitral regurgitation on the cardiac cath report should be converted to a four-point scale: 1+ = mild, 2 or 3+ = moderate, and 4+ = severe. Diagnosis by angiogram: ======================= The following definitions should be used to assess the presence/severity of mitral regurgitation based on the interpretation of the contrast left ventricular angiogram: None/Trivial - There is no visible systolic regurgitation across the mitral valve. Trace or trivial notations of mitral regurgitation should be listed as none. Mild - Definite contrast can be seen in the left atrium following left ventricular injection, but the left atrium never fills to the same opacity as the left ventricle. Moderate - The left atrium fills to the same opacity as the left ventricle over two or more systoles. Severe - The left atrium fills to the same opacity as the left ventricle over a single systole. NS - If unable to make an assessment of the patient's left ventricular contraction grade or no study was performed, entering "NS" for "No Study/Unknown" is also allowed. Diagnosis by cardiac ultrasound: ================================ The following definitions are commonly used to assess the presence/severity of mitral regurgitation based on the interpretation of the cardiac ultrasound examination: None/Trivial - No regurgitant jet is seen on the Doppler study. Trace or trivial notations of mitral regurgitation should be listed as none. Mild - The area of the regurgitant jet is 0 - 4 cm2. Moderate - The area of the regurgitant jet is >4 - 8 cm2. Severe - The area of the regurgitant jet is greater than 8 cm2 or greater than one third of the total left atrial area. NS - If no study was performed, entering "NS" for "No Study/Unknown" is also allowed.
416*number with other conduit207;20NUMERICDefinition Revised (2004): This is the number of coronary artery bypass graft (CABG) anastomoses to native coronary arteries with other conduit(s) regardless of whether other procedures were performed. Do not leave this information blank. If no coronary artery bypass grafts with other conduits were performed, enter '0'.
417race208;10SET OF CODES1:HISPANIC, WHITE
2:HISPANIC, BLACK
3:AMERICAN INDIAN OR ALASKA NATIVE
4:BLACK, NOT OF HISPANIC ORIGIN
5:ASIAN OR PACIFIC ISLANDER
6:WHITE, NOT OF HISPANIC ORIGIN
7:UNKNOWN
This is the race of the patient. This is a standard set of codes and should not be edited.
418hospital admission date208;14FREE TEXTDefinition Revised (2011): The date and time of the hospital admission to this VAMC associated with this surgical case as found in the PIMS package. If the patient was admitted directly to surgery and then admitted to the hospital, use the date of surgery as the date of admission. Entering NA for "NOT APPLICABLE" is allowed for non-cardiac surgery patients.
419hospital discharge date208;15FREE TEXTDefinition Revised (2011): Indicate the date of the hospital discharge associated with this surgical case. Patients transferred to a referring facility should be indicated as discharged from current admission. Patients transferred to the psychiatric unit or any chronic care facility located at the VA facility (e.g., a nursing home) should be indicated as discharged from current admission at the date and time of the transfer to this different facility. (Do not indicate the date of data input, unless the patient was actually discharged on this same date.) Patients who remain as inpatients for reasons other than for post- open heart procedures should continue to be followed until discharged (including the rehabilitation service) even if the cardiothoracic team discharges the patient from their service or would discharge the patient home. If the patient remains in the hospital and/or has subsequent surgeries, indicate such in the CARDIAC RESOURCE DATA COMMENTS field (#431.)
420admission/transfer date208;16FREE TEXTDefinition Revised (2004): If the patient was not initially admitted to the surgical service, the date and time of transfer to surgical service for this surgical episode will be entered from the PIMS package. Enter 'NA' if this date is not applicable, e.g. outpatient not admitted or observed.
421discharge/transfer date208;17FREE TEXTDefinition Revised (2004): The date and time of the patient's discharge or transfer from the surgical or medical service to a chronic care setting. i.e., spinal cord injury unit, psychiatric facility or psychiatric unit, nursing home care unit or facility, or intermediate medicine. Acute care beds must be established locally with the assistance of your station IRM service.
430cardiac risk preop comments206.1;1FREE TEXTDefinition Revised (2006): Indicate in the comment field any preoperative patient risk factors (not previously entered above) that may contribute to this patient's risk of operative mortality. (The maximum length of this field is 130 characters.)
431cardiac resource data comments206.2;1FREE TEXTDefinition Revised (2014): Indicate additional comments related to this case prior to transmission to Denver by the SQN/Data Manager (limit 130 characters).
439batista procedure used (y/n)207;23BOOLEANY:YES
N:NO
Was the Batista procedure used, Yes or No?
440cardiac catheterization date207;21DATE-TIMERecord the appropriate date of the most recent cardiac catheterization prior to surgery. Enter NS if unknown or not applicable.
441minimally invasive proc (y/n)207;22BOOLEANY:YES
N:NO
Was a minimally invasive procedure technique used, Yes or No?
442employment status preoperative208;18SET OF CODES1:EMPLOYED FULL TIME
2:EMPLOYED PART TIME
3:NOT EMPLOYED
4:SELF EMPLOYED
5:RETIRED
6:ACTIVE MILITARY DUTY
9:UNKNOWN
Employment status preoperatively is to be defined in the broad sense of regularly performed work activity with remuneration.
443intraop disseminated cancer200.1;4SET OF CODESY:YES
N:NO
NS:NO STUDY
VASQIP Definition (2010): Intraoperative Disseminated Cancer: Patients who have cancer that was found during the operative procedure that: (1) Has spread to one site or more sites in addition to the primary site AND (2) In whom the presence of multiple metastases indicates the cancer is widespread, fulminant, or near terminal. Other terms describing disseminated cancer include "diffuse," "widely metastatic," "widespread," or "carcinomatosis" or AJCC "Stage IV" cancer. Common sites of metastases include major organs (e.g., brain, lung, liver, meninges, abdomen, peritoneum, pleura, and bone). You may use the National Cancer Institute as a reference in determining whether a patient has AJCC Stage IV cancer, when the TNM information is the only information documented. Refer to the following website for assistance with translating TNM values with AJCC staging: http://www.cancer.gov/cancertopics/pdq/adulttreatment Examples: - A patient with a primary breast cancer with positive nodes in the axilla does NOT qualify for this definition. The tumor has spread to a site other than the primary site, but does not have widespread metastases. A patient with primary breast cancer with positive nodes in the axilla AND liver metastases does qualify, because the tumor has spread to the axilla and other major organs. - A patient with colon cancer and no positive nodes or distant metastases does NOT qualify. A patient with colon cancer and several local lymph nodes positive for tumor, but no other evidence of metastatic disease does NOT qualify. A patient with colon cancer with liver metastases and/or peritoneal seeding with tumor does qualify. - A patient with adenocarcinoma of the prostate confined to the capsule does NOT qualify. A patient with prostate cancer that extends through the capsule of the prostate only does NOT qualify. A patient with prostate cancer with bony metastases DOES qualify. * Report Acute Lymphocytic Leukemia (ALL), Acute Myelogenous Leukemia (AML) and Stage IV Lymphoma under this variable. Do not report Chronic Lymphocytic Leukemia (CLL), Chronic Myelogenous Leukemia (CML), Multiple Myeloma or Lymphomas that are Stage I-III as disseminated cancer.
444preoperative anion gap203;15FREE TEXTThis is the result of the preoperative Anion Gap calculation. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
444.1preop anion gap, date204;15DATE-TIMEThis is the date the preoperative Anion Gap was recorded.
445highest anion gap203;16FREE TEXTThis is the result of the highest postoperative anion gap recorded. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
445.1high anion gap, date204;16DATE-TIMEThis is the date that the highest postoperative Anion Gap was recorded.
446intraoperative ascites200.1;6BOOLEANY:YES
N:NO
VASQIP Definition (2010): Intraoperative Ascites: The presence of fluid accumulation in the peritoneal cavity noted during the operative procedure. Documentation should state a history of or active liver disease (e.g. jaundice, encephalopathy, hepatomegaly, portal hypertension, liver failure, or spider telangiectasia).
447clostridium difficile colitis205;39SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2008): C. difficile-associated disease occurs when the normal intestinal flora is altered, allowing C. difficile to flourish in the intestinal tract and produce a toxin that causes a watery diarrhea. C. difficile diarrhea is confirmed by the presence of a toxin in a stool specimen. Answer yes only if you have a positive culture for C. difficile and/or a toxin assay and diagnosis of C. difficile documented in the chart.
448postop atrial fibrillation205;40BOOLEANY:YES
N:NO
VASQIP Definition (2010) Indicate whether the patient had a new onset of atrial fibrillation/flutter (AF) requiring treatment. Does not include recurrence of AF which had been present preoperatively.
450total ischemic time206;36NUMERICRecord in minutes the duration of time the ascending aorta is totally cross-clamped. Do not include the duration of partial aorta cross-clamp used for sewing the proximal anastomoses.
451total cpb time206;37NUMERICRecord in minutes the total cardiopulmonary bypass time. This includes the total duration of full and partial cardiopulmonary bypass from all episodes of cardiopulmonary bypass. This information can generally be found on the perfusionist record and/or the anesthesia record.
452observation admission date208.1;1FREE TEXTDefinition Revised (2004): An observation patient is one who presents with a medical condition with a significant degree of instability or disability, and who needs to be monitored, evaluated and assessed for either admission to inpatient status or assignment to care in another setting. An observation patient can occupy a special bed set aside for this purpose or may occupy a bed in any unit of a hospital, i.e., urgent care, medical unit. These types of patients should be evaluated against standard inpatient criteria. These beds are not designed to be a holding area for Emergency Rooms. The length-of-stay in observation beds will not exceed 23 hours. Following surgery, if the patient was admitted for observation, this is the date and time of admission for observation. If this information is not applicable, enter NA.
453observation discharge date208.1;2FREE TEXTDefinition Revised (2004): If the patient was admitted for observation following surgery, this is the date and time of discharge from observation. If this information in not applicable, enter NA.
454observation treating specialty208.1;3POINTER42.4Definition Revised (2004): If the patient was admitted for observation following surgery, this is the observation treating specialty to which the patient was admitted. If this information is not applicable, enter NA.
455highest serum troponin i203;13FREE TEXTThis is the result of the highest postoperative serum cardiac troponin I test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
455.1high serum troponin i, date204;13DATE-TIMEThis is the date that the highest postop serum troponin I was performed.
456highest serum troponin t203;14FREE TEXTThis is the result of the highest postoperative serum cardiac troponin T test. Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
456.1high serum troponin t, date204;14DATE-TIMEThis is the date that the highest postop serum troponin T was performed.
457hdl (cardiac)201;21FREE TEXTDefinition Revised (2006): Indicate the HDL result (mg/dl) preoperatively evaluated closest to surgery. Entering "NS" for "No Study" is allowed.
457.1hdl, date202;21FREE TEXTDefinition Revised (2006): Indicate the date that the preoperative HDL value was assessed. Enter "NS" for No Study if the HDL test was not performed.
458serum triglyceride (cardiac)201;22FREE TEXTDefinition Revised (2006): Indicate the Serum Triglyceride result (mg/dl) preoperatively evaluated closest to surgery. Entering "NS" for "No Study" is allowed.
458.1serum triglyceride, date (car)202;22FREE TEXTDefinition Revised (2006): Indicate the date that the preoperative Serum Triglyceride value was assessed. Enter "NS" for No Study if the Serum Triglyceride test was not performed.
459serum potassium (cardiac)201;23FREE TEXTDefinition Revised (2004): Indicate the serum potassium result (mg/L) preoperatively evaluated closest to surgery but not greater than 90 days before surgery. Entering "NS" for "No Study" is allowed.
459.1serum potassium, date(cardiac)202;23FREE TEXTDefinition Revised (2004): Indicate the date that the preoperative Serum Potassium value was assessed. Enter "NS" for No Study if the Serum Potassium test was not performed or was performed more than 90 days before surgery.
460serum bilirubin (cardiac)201;24FREE TEXTDefinition Revised (2004): Indicate the serum bilirubin result (mg/dl) preoperatively evaluated closest to surgery but not greater than 90 days before surgery. Entering "NS" for "No Study" is allowed.
460.1serum bilirubin, date (card)202;24FREE TEXTDefinition Revised (2004): Indicate the date that the preoperative Serum Bilirubin value was assessed. Enter "NS" for No Study if the Serum Bilirubin test was not performed or was performed more than 90 days before surgery.
461ldl (cardiac)201;25FREE TEXTDefinition Revised (2006): Indicate the LDL result (mg/dl) preoperatively evaluated closest to surgery. Entering "NS" for "No Study" is allowed.
461.1ldl, date (cardiac)202;25FREE TEXTDefinition Revised (2006): Indicate the date that the preoperative LDL value was assessed. Enter "NS" for No Study if the LDL test was not performed.
462total cholesterol (cardiac)201;26FREE TEXTDefinition Revised (2006): Indicate the Total Cholesterol result (mg/dl) preoperatively evaluated closest to surgery. Entering "NS" for "No Study" is allowed.
462.1total cholesterol, date202;26FREE TEXTDefinition Revised (2006): Indicate the date that the preoperative Total Cholesterol value was assessed. Enter "NS" for No Study if the Cholesterol test was not performed.
463*hypertension206;38BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if the patient has a documented history of hypertension with or without current treatment of antihypertensive medication(s). If a diuretic agent is prescribed to treat hypertension, indicate Yes for both the hypertension and the diuretic questions. (YES/NO).
464*number with radial artery207;24NUMERICThis is the number of coronary artery bypass graft (CABG) anastomoses to native coronary arteries with radial artery(ies) regardless of whether other procedures were performed. Do not leave blank, enter "zero" in the appropriate place if no coronary artery bypass grafts were performed with radial artery. Note that any CABG distal anastomoses performed without placing the patient on cardiopulmonary bypass are to be recorded.
465*number with other artery207;25NUMERICThis is the number of coronary artery bypass graft (CABG) anastomoses to native coronary arteries with other artery(ies) regardless of whether other procedures were performed. Do not leave blank, enter "zero" in the appropriate place if no coronary artery bypass grafts were performed with other artery(ies). Note that any CABG distal anastomoses performed without placing the patient on cardiopulmonary bypass are to be recorded.
466tracheostomy206;39BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if a procedure to cut into the trachea and insert a tube to overcome tracheal obstruction or to facilitate extended mechanical ventilation was performed within 30 days of surgery.
467new mechanical circulatory206;40BOOLEANY:YES
N:NO
Definition Revised (2014): Indicate if the patient left the operating room suite with or required post-op placement of a new IABP, ECMO, or VAD for circulatory support within 30 days post-operatively.
468incision type207;26SET OF CODESFS:FULL STERNOTOMY
FT:FULL THORACOTOMY
LP:LIMITED PARASTERNAL APPROACH
LS:LIMITED STERNOTOMY
LT:LIMITED THORACOTOMY
OL:OTHER LIMITED SURG APPROACH
NS:NO STUDY/UNKNOWN
This describes the incision used for cardiac access, according to the operative report. (Do not include incisions for port access.) Enter NS if incision type is unknown. - Limited Sternotomy: The incision cuts through a small portion (less than half of the length) of the sternum (the narrow, flat bone in the median line of the thorax in the front of the chest). - Full Sternotomy: The incision cuts through the entire length of the sternum (the narrow, flat bone in the median line of the thorax in the front of the chest). - Limited Thoracotomy: A small surgical incision through a portion of the chest wall, but not along the sternum. For example, an anterolateral thoracotomy approach may be used in LIMA to LAD grafting. - Full Thoracotomy: A larger surgical incision running across the chest wall, but not along the sternum. This may be a left submammary incision, which requires the resection of the fourth costal cartilage and /or deflation of the left lung. - Limited Parasternal Approach: The incision cuts beside a small portion (less than 0.5 of the length) of the sternum, on a line midway between the sternal margin and an imaginary line passing through the nipple. - Other Limited Surgical Approach: An incision or incision set used to visualize the operating field that is not listed above.
469convert from off pump to cpb207;27SET OF CODES1:NO (began off-pump/ stayed off-pump)
2:YES-PLANNED
3:YES-UNPLANNED
4:YES-UNKNOWN IF PLANNED
5:NA (began on-pump/ stayed on-pump)
NS:NO STUDY/UNKNOWN
Definition Revised (2004): Indicate whether patient was converted from off cardiopulmonary bypass assistance to on cardiopulmonary bypass during the cardiac surgical procedure. Indicate the one appropriate response: No - There was no conversion that occurred for the off-pump case performed (i.e., the off-pump case remained off-pump throughout the operation). NA - The procedure was NOT an off-pump case (i.e., procedure began on-pump and remained on- pump throughout the case). [The default will be set to N/A.] Yes, planned - The procedure was begun as an off-pump procedure but changed to on-pump for any length of time; the change was planned due to decision made prior to operation to perform some vessels off-pump and some on-pump in order to minimize total CPB time. Yes, unplanned - The procedure was begun as an off-pump procedure but changed to on-pump for any length of time; the change was unplanned and determined in the operating room due to inability to safely perform revascularization. NS/Unknown - If documentation is not sufficient to answer, entering "NS" for "No Study/Unknown" is also allowed.
470d/t patient extubated208;22FREE TEXTDefinition Revised (2008): Indicate the date that the endotracheal tube is pulled for the first time after surgery. If a tracheostomy is performed to replace an oral intubation tube, intubation is considered continuous so the patient has not been extubated as long as the patient continues to require ventilator support. If the patient dies while intubated, indicate the date of death for this data element. Indicate "extubated prior to leaving the OR" in the Resource Comment if patient is extubated prior to leaving the OR. RI - The patient remains intubated and on ventilator at 30 days after surgery.
471d/t patient disch from icu208;23FREE TEXTVASQIP Definition (2010): This is the first date and time of the discharge from the intensive care unit (ICU). ICU is usually a surgical unit (SICU), although it may also include a post-anesthesia recovery unit off the operating room. It may also be a general ICU in which medical patients are also managed (MICU, CCU). This will always be the unit into which the patient goes immediately after surgery and is stabilized, ventilated and ultimately extubated. Do not include lower acuity units where the patient goes subsequently (i.e. stepdown, transitional care, telemetry, etc.). Do not include subsequent readmissions to the ICU. RI - The patient remains in ICU at 30 days after surgery.
472*cardiac surg performed non-va206;41SET OF CODESY:YES
N:NO
NS:UNKNOWN
Definition Revised (2004): Indicate whether the patient's cardiac surgery was performed in a non-VA facility through a contracted arrangement, even if part of the post-surgical care is provided at the VA. A "contract" facility is one established to be an affiliate with the VA medical center, and it is most typically a University Hospital. In rare cases a "contract" facility may be a community hospital when there is no University affiliate for the VAMC. By contrast, a "fee-basis" patient surgery should not be indicated as a "contract" facility. Typically, a "fee-basis" establishment is an agreement by the VA Chief of Staff to out-source a patient to a community hospital. That hospital then bills the Chief of Staff for care rendered on the patient. VASQIP does not wish to capture the patient data on the "fee-basis" patients. If the patient is not entered into VISTA, send a paper form to Denver for hand-entry, unless your facility contracts-out a majority of its cases. Enter "NS" if funding for the procedure is not known. The default is to NO if a response is not entered.
473homeless209;1SET OF CODESY:YES
N:NO
NS:NO STUDY/UNKNOWN
Definition Revised (2004): If the patient indicates he/she does not have a fixed dwelling, indicate the person's status as homeless.
474preop circulatory device209;2SET OF CODESN:NONE
I:IABP
V:VAD (includes BIVAD)
A:ARTIFICIAL HEART
O:OTHER
VASQIP Definition (2010): Indicate whether there was any use of any device to assist ventricular function at the time the patient presents for surgery (or placed in the OR before anesthesia induction). Indicate the one appropriate response: None - No New Mechanical Circulatory Device was placed. IABP - An intra-aortic balloon pump was placed to assist ventricular function. VAD - A ventricular assist device (e.g., LVAD, BIVAD) was placed to assist ventricular function. Artificial Heart - An artificial heart was placed to assist ventricular function. Other - An other type of Mechanical Circulatory Device was placed.
475*diabetes (cardiac)209;3SET OF CODESN:NO
D:DIET
O:ORAL
I:INSULIN
This field has been flagged as obsolete for VASQIP. It should no longer be used. Definition Revised (2006): Indicate if the patient has diabetes treated with diet, oral, and/or insulin therapy. Diabetes is defined as a metabolic disorder of the pancreas whereby the individual requires daily dosages of exogenous parenteral insulin or an oral hypoglycemic agent to prevent a hyperglycemic/metabolic acidosis. If the patient is on both Oral and Insulin therapy, indicate Insulin therapy. Indicate the one most appropriate response. No - no diagnosis of diabetes. Diet - a diagnosis of diabetes that is controlled by diet alone in the two weeks preceding surgery (the only prescribed treatment has been diabetic relief). Oral - a diagnosis of diabetes requiring therapy with an oral hypoglycemic agent in the two weeks preceding surgery. Insulin - a diagnosis of diabetes requiring daily insulin therapy in the two weeks preceding surgery.
476procedure type209;4SET OF CODESC:CATH
I:IVUS
B:BOTH/COMBINATION
NS:NO STUDY/UNKNOWN
Definition Revised (2004): Indicate which test was used for the cardiac catheterization and/or angiographic data. Indicate the one most appropriate response: Cath - A diagnostic procedure in which a catheter is introduced into a large vein, usually of an arm or leg, and threaded through the circulatory system to the heart to determine blood pressure and the rate of flow in the vessels and chambers of the heart and the identification of abnormal anatomy. IVUS - Intravascular Ultrasound may be used either alone or in combination with results from the cardiac catheterization. If used alone, indicate IVUS as the only test from which procedure results are calculated. Both - If both IVUS and Cath are available and both tests were analyzed for the results, indicate Both/Combination. NS - If no cath study is available, entering NS for "No Study/Unknown" is also allowed.
477aortic stenosis209;5SET OF CODES0:NONE/TRIVIAL
1:MILD
2:MODERATE
3:SEVERE
NS:NO STUDY
Definition Revised (2007): Indicate the severity of any aortic stenosis documented. This question should be answered using either the left ventricular angiogram (hemodynamic cath data) or the cardiac ultrasound examination. Numbers may be converted to describe the severity of the aortic stenosis on the cardiac cath report to the adjectives describing the severity: 1+ = mild, 2 or 3+ = moderate, and 4+ = severe. Both transvalvular gradient and estimated valve orifice area are used to assess the severity of obstruction (stenosis) of a valve. The transvalvular pressure gradient is obtained by converting the velocity of blood flow across the valve measured by the Doppler principle to pressure drop using the Bernoulli equation. The pressure drop, which is dependent on flow, can be converted to estimated valve orifice area if flow is known. If the echo report uses an adjective to describe the severity of stenosis, indicate the corresponding adjective. Use the following to convert mean (not peak) transvalvular gradients, orifice areas, or both, to the descriptive categories. Indicate the one most appropriate response: None/Trivial - The mean pressure gradient is < 5 mm Hg, and/or orifice area is > 2.5 cm2, and/or the aortic valve leaflets or aortic flow velocity is stated to be normal (< 1.0 M/sec). Mild - The mean pressure gradient is 5 - 20 mm Hg and/or the orifice area is 1.7 - 2.5 cm2 Moderate - The mean pressure gradient is >20 - 50 mm Hg and/or the valve orifice area is 1.0 -1.6 cm2 Severe - The mean pressure gradient is > 50 mm Hg and/or the valve orifice area is < 1.0 cm2 NS - If no study was performed, entering "NS" for "No Study/Unknown" is also allowed.
478re-do lad stenosis209;6FREE TEXTDefinition Revised (2004): If a re-do, indicate the most severe percent stenosis in the graft to the left anterior descending coronary artery. Entering "NS" for "No Study/Unknown" is also allowed.
479re-do rt coronary stenosis209;7FREE TEXTDefinition Revised (2004): If a re-do, indicate the most severe percent stenosis in the graft to the right coronary artery or posterior descending coronary artery. Entering "NS" for "No Study/Unknown" is also allowed.
480re-do circumflex stenosis209;8FREE TEXTDefinition Revised (2004): If a re-do, indicate the most severe percent stenosis in the graft to the circumflex coronary artery, including marginal branches and ramus intermedius considered to be of adequate size for bypass grafting. Entering "NS" for "No Study/Unknown" is also allowed.
481*bridge to transplant/device209;9SET OF CODESY:YES
N:NONE
B:BRIDGE TO TRANSPLANT
D:DESTINATION THERAPY
Definition Revised (2006): Indicate if patient received a mechanical support device (excluding IABP) as a bridge to cardiac transplant during the same admission as the transplant procedure; or patient received the device as destination therapy (does not intend to have a cardiac transplant), either with or without placing the patient on cardiopulmonary bypass.
482*maze procedure209;10BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if patient had a Maze procedure either with or without placing the patient on cardiopulmonary bypass. A Maze procedure is a surgical intervention used to interrupt atrial conduction pathways often associated with atrial fibrillation or atrial flutter. It may be performed alone or in combination with other cardiac procedures. (YES/NO).
483*tmr209;11BOOLEANY:YES
N:NO
Definition Revised (2004): Indicate if patient received a transmyocardial laser procedure (TMR) to make "channels" or small holes directly into the heart muscle, either with or without placing the patient on cardiopulmonary bypass. The TMR may be done in combination with a CABG procedure or as a stand-alone procedure.
484*other cardiac procedures-list209.1;1FREE TEXTDefinition Revised (2006): Specify if any cardiac surgical procedure (not listed above) was performed alone or in conjunction with the index procedure, either with or without placing the patient on cardiopulmonary bypass.
485prior heart surgery206;42FREE TEXTDefinition Revised (2014): Indicate all applicable types of heart surgery performed, either on or off-pump. Indicate all appropriate responses: None - Patient has not had a previous cardiac surgery procedure CABG-only - Patient has had a previous coronary artery bypass graft (CABG-only) procedure Valve-only - Patient has had a previous valve-only procedure CABG/Valve - Patient has had a previous combination CABG/valve procedure Other - Patient has had a previous cardiac procedure(s) other than CABG and Valve surgery, such as repair of atrial or ventricular septal defects, great thoracic vessel repair, cardiac transplant, left ventricular aneurysmectomy, insertion of ventricular assist devices, total artificial hearts, Maze procedures, etc." (Do not include pacemaker insertions or automatic implantable cardioverter-defibrillator (AICD) insertions; do not include pericardectomy if done off pump). CABG/Other - Patient has had a previous cardiac surgery that included a CABG with a concurrent "Other" cardiac procedure. Unknown - Unknown
486gastrointestinal (y/n)200.1;1SET OF CODESY:YES
N:NO
NS:NO STUDY
This determines whether the patient has a history of gastrointestinal problems such as esophageal varices.
487preoperative inr201;27FREE TEXTThis is the result of the preoperative INR (International Normalized Ratio). Data input must be 1 to 5 numeric characters in length which may include a prefix of a less than or greater than sign "<" or ">". Entering "NS" for "No Study" is also allowed.
487.1preoperative inr, date202;27DATE-TIMEThis is the date that the preoperative INR was performed.
488organ/space ssi205;37SET OF CODESY:YES
N:NO
NS:NO STUDY
Definition Revised (2004): Organ/Space SSI is an infection that occurs within 30 days after the operation and the infection appears to be related to the operation and the infection involves any part of the anatomy (e.g., organs or spaces), other than the incision, which was opened or manipulated during an operation and at least one of the following: - Purulent drainage from a drain that is placed through a stab wound into the organ/space. - Organisms isolated from an aseptically obtained culture of fluid or tissue in the organ/space. - An abscess or other evidence of infection involving the organ/space that is found on direct examination, during reoperation, or by histopathologic or radiologic examination. - Diagnosis of an organ/space SSI by a surgeon or attending physician. Site-Specific Classifications of Organ/Space Surgical Site Infection -------------------------------------------------------------------- Arterial or venous infection Meningitis or ventriculitis Breast abscess or mastitis Myocarditis or pericarditis Disc space Oral cavity (mouth, tongue, or Ear, mastoid gums) Endocarditis Osteomyelitis Endometritis Other infections of the lower Eye, other than conjunctivitis respiratory tract (e.g. abscess Gastrointestinal tract or empyema) Intra-abdominal, not specified Other male or female reproductive elsewhere tract Intracranial, brain abscess or Sinusitis dura Spinal abscess without meningitis Joint or bursa Upper respiratory tract Mediastinitis Vaginal cuff
489other wound occurrence205;38POINTER80Definition Revised (2004): Enter any other wound occurrences that you feel to be significant and that are not covered by the predefined wound occurrence categories. Enter the ICD-CM code for this entry. (Example: Seromas, ICD-CM code: 998.13)
490*repeat ventilator w/in 30 day209;12BOOLEANY:YES
N:NO
Definition Revised (2008): Indicate if the patient was placed on ventilator support postoperatively within 30 days and this repeat ventilator support is related to the index operation (For example, the patient is on the ventilator intra-op and immediately post-op. Then patient is weaned and the ventilator is discontinued. Later, the patient gets into trouble and mechanical ventilation has to be reinstated.) However, if the patient returns to the OR within 30 days and gets extubated immediately after, it is not considered repeat ventilator support.
491other non-ct procedures209.2;1FREE TEXTDefinition Revised (2004): If any other procedure - other than cardiothoracic - performed requiring placing the patient on cardiopulmonary bypass, specify details into the comment field. If no other non-CT procedure requiring CPB was performed, indicate "NS" for "No Study/Unknown" in the text field.
492preop funct. health status200.1;2SET OF CODES1:INDEPENDENT
2:PARTIALLY DEPENDENT
3:TOTALLY DEPENDENT
4:UNKNOWN
Definition Revised (2008): This is a question that focuses on the patient's abilities to perform activities of daily living (ADLs) in the 30 days prior to surgery. Activities of daily living are defined as 'the activities usually performed in the course of a normal day in a person's life'. ADLs include: bathing, feeding, dressing, toileting, and mobility. Report the corresponding level of self-care for activities of daily living demonstrated by this patient at the time the patient is being considered as a candidate for surgery (which should be no longer than 30 days prior to surgery). If the patient's status changes prior to surgery, that change should be reflected in your assessment. For this time point, report the level of functional health status as defined by the following criteria. (1) Independent: The patient does not require assistance from another person for any activities of daily living. This includes a person who is able to function independently with prosthetics, equipment, or devices. (2) Partially dependent: The patient requires some assistance from another person for activities of daily living. This includes a person who utilizes prosthetics, equipment, or devices but still requires some assistance from another person for ADLs. (3) Totally dependent: The patient requires total assistance for all activities of daily living. (4) Unknown: If unable to ascertain the functional status for the time point of 'prior to the current illness' only, report as unknown. All patients with psychiatric illnesses should be evaluated for their ability to function with or without assistance with ADLs just as the non-psychiatric patient. For instance, if a patient with schizophrenia is able to care for him/herself without the assistance of nursing care, he/she is considered independent.
493*pulmonary valve procedure207;28SET OF CODESN:NONE
M:MECHANICAL
S:STENTED BIOPROSTHETIC
B:STENTLESS BIOPROSTHETIC
H:HOMOGRAFT
PR:PRIMARY REPAIR
PA:PRIMARY REPAIR & ANNULOPLASTY DEVICE
AN:ANNULOPLASTY DEVICE ALONE
AU:AUTOGRAFT (ROSS)
O:OTHER
VASQIP Definition (2010): Indicate if the patient had a pulmonary valve replacement (either the native or a prosthetic valve) or a repair (on the native valve to relieve stenosis and/or correct regurgitation -annuloplasty, commissurotomy, etc.); performed with or without additional procedure(s); either with or without placing the patient on cardiopulmonary bypass. (If a repair was attempted, but a replacement occurred, indicate the details of the replacement valve.) Indicate the one most appropriate procedure: * None * Mechanical Valve * Stented Bioprosthetic Valve * Stentless Bioprosthetic Valve * Homograft * Primary Valve Repair * Primary Valve Repair and Annuloplasty Device * Annuloplasty Device alone * Autograft Procedure (Ross Procedure) * Other
500pfss account referencePFSS;1POINTER375This is the PFSS Account Reference number by which Surgery will reference an external account number for purposes of attaching charges for 1st or 3rd party billing.
502*other cardiac procedures (y/n)209;13BOOLEANY:YES
N:NO
Definition Revised (2006): Indicate if any cardiac surgical procedure (not listed above) was performed alone or in conjunction with the index procedure, either with or without placing the patient on cardiopulmonary bypass (YES/NO).
504hemoglobin a1c201;28FREE TEXTDefinition Revised (2006)/(2007): Indicate the Hemoglobin A1c result (%) preoperatively evaluated closest to surgery. Entering "NS" for "No Study" is allowed.
504.1hemoglobin a1c, date202.1;1FREE TEXTDefinition Revised (2006)/(2007): Indicate the date that the preoperative Hemoglobin A1c value was assessed. Enter "NS" for No Study if the Hemoglobin A1c test was not performed.
505*endovascular repair207.1;2BOOLEANY:YES
N:NO
VASQIP Definition (2010): Indicate if the patient had an endovascular repair of the descending thoracic aorta, ascending aorta, and/or aortic arch (e.g., aneurysm, pseudoaneurysm, dissection, penetrating ulcer, intramural hematoma, or traumatic disruption) with or without involving coverage of left subclavian artery origin, initial endoprosthesis plus descending thoracic aortic extension(s), if required, to level of celiac artery origin, with or without cardiopulmonary bypass. To include in VASQIP, an attending cardiothoracic surgeon must have been present and involved in the procedure. It is typically done under general anesthesia and may be performed in the operating room or interventional radiology operating area.
506hair removal methodVER;6SET OF CODESC:CLIPPER
D:DEPILATORY
N:NO HAIR REMOVED
P:PATIENT REMOVED OWN HAIR
S:SHAVING
U:NOT DOCUMENTED
O:OTHER
This is the method used to remove hair prior to surgery. Shaving is not a preferred method for hair removal. If SHAVING is selected, a comment must be entered in the HAIR REMOVAL COMMENTS field explaining why SHAVING was used. If OTHER is selected, comments must be entered explaining the method used.
507bnp201;29FREE TEXTVASQIP Definition (2010): Indicate the BNP result (pg/mL) preoperatively evaluated closest to surgery but not greater than 180 days before surgery. Entering "NS" for "No Study" is allowed.
507.1bnp date202.1;2FREE TEXTVASQIP Definition (2010): Indicate the date that the preoperative BNP value was assessed. Enter "NS" for No Study if the BNP test was not performed.
508hair removal comments49;0WORD-PROCESSINGIf SHAVING is selected as the hair removal method, a comment must be entered explaining why SHAVING was used. If OTHER is selected as the hair removal method, comments must be entered explaining the method used.
509preop atrial fibrillation208;19BOOLEANY:YES
N:NO
VASQIP Definition (2010): This field indicates whether atrial fibrillation or flutter is present within two weeks of the procedure. Enter YES or NO. Note: NS is not allowed.
510*current smoker (cardiac)200.1;5SET OF CODES1:NEVER A SMOKER
2:WITHIN 2 WEEKS OF SURGERY
3:2 WEEKS TO 3 MONTHS PRIOR TO SURGERY
4:>3 MONTHS PRIOR TO SURGERY (REMOTE SMOKER)
This field has been flagged as obsolete for VASQIP. It should no longer be used. Cardiac Definition Revised (2006): Indicate the patient's smoking status from information from the patient, or the chart, that best describes the patient's use of tobacco in any form (pipe, cigar, cigarette, tobacco chew). If more than one representation is found, please record according to the most conservative (most recent) quit date: 1 = never a smoker 2 = smoking within two weeks prior to surgery 3 = smoking within 2 weeks to 3 months prior to surgery 4 = remote smoker (more than 3 months prior to surgery)
512*maze procedure209;14SET OF CODESN:NO MAZE PERFORMED
F:FULL MAZE
M:MINI MAZE
Definition Revised (2006): Indicate if patient had a Maze procedure either with or without placing the patient on cardiopulmonary bypass. A Maze procedure is a surgical intervention used to interrupt abnormal atrial conduction pathways that cause atrial fibrillation or atrial flutter. It may be performed alone or in combination with other cardiac procedures. (A Maze does not include an amputation/resection of the atrial appendage as an isolated procedure; an intraoperative electrophysiologic mapping procedure; nor any surgical or ablation procedure conducted on the ventricle for control of ventricular arrhythmias.) Indicate the one most appropriate response: No - No Maze performed Full Maze - The procedure is most often performed on-bypass through a median sternotomy. A combination of incisions and thermal (cryo) or radiofrequency ablations of the atrial wall pathways are done, typically including amputation/resection of the one or both atrial appendices. The procedure thus creates a "maze" of electrical propogation roots involving the entire atrial myocardium with only one side of entrance (the sinus node) and one side of exit (the AV node). Mini-Maze - A more limited and simpler procedure than the traditional full maze, the Mini-Maze is based on the finding that in most patients, ectopic foci located in the pulmonary veins are responsible for the initiation of atrial fib. Radiofrequency or a cryo-ablation probe is used either inside or outside of the pulmonary vein ostia to destroy the foci. It can be performed with or without resection of the atrial appendage and includes no incision or minimal incisions to the left atrium, rather than the extensive atrial surgical procedure conducted for the full Maze. The Mini can be performed on or off bypass through a median sternotomy or performed thorascopically to the outside of the pulmonary veins.
513surgery consult date209;15FREE TEXTIndicate the date that the patient was first consulted by Surgery for the operation as typically documented by a note by a member of Surgery Specialty that will perform the procedure (e.g., attending surgeon, fellow, nurse). For non-cardiac assessments, enter NA if this date is not applicable or cannot be determined. For Cardiothoracic (CT) Surgery, this date is usually on or just after the diagnostic catheterization date.
515primary cause for delay209;16SET OF CODESRL:RESOURCE LIMITATION
PH:PATIENT HEALTH
PP:PATIENT PREFERENCE
O:OTHER
NS:NO STUDY/UNKNOWN
N:NONE
Definition Revised (2008): This field contains the primary cause for delay. If a Cardiac patient's surgery is greater than 30 days from initial VA Cardiothoracic Surgery Consultation (as calculated between the CT CONSULT DATE to DATE OF SURGERY), user shall enter cause as defined in the field. If date is less than or equal to 30 days, system shall automatically default entry to None. - Resource Limitation: Due to staffing or other facility limitation, e.g., OR scheduling, physician availability, ICU bed capacity - Patient Health: Due to patient health issue, e.g., vascular consult, additional tests - Patient Preference: Due to a non-health related patient preference, e.g., vacation - Other - NS/Unknown: Unable to Locate Reason for Delay. Entering "NS" for "No Study/Unknown" is also allowed. - None
516surgery consult requested209;17FREE TEXTThis is the date that the patient's physician requests that Surgery Service consult with the patient. It is not the date that the consult took place. Enter NA if this date is not applicable or cannot be determined.
517tobacco use200.1;9SET OF CODES1:NEVER USED TOBACCO
2:NO USE IN LAST 12 MOS
3:CIGARETTES ONLY
4:OTHER (NO CIGARETTES)
5:CIGARETTES PLUS OTHER
VASQIP Definitions (2011): Indicate the patient's type of tobacco product used in the 12 months prior to surgery. Select one: 1 = Never used tobacco 2 = No tobacco use in the last 12 months 3 = Cigarettes only 4 = Pipe, cigar, snuff, or chewing tobacco only (no cigarettes) 5 = Cigarettes plus one or more of pipe, cigar, snuff, or chewing tobacco
518tobacco use timeframe200.1;10SET OF CODES1:WITHIN 2 WEEKS
2:2 WKS TO 3 MOS
3:3 TO 12 MONTHS
NA:NOT APPLICABLE
VASQIP Definitions (2011): If the patient used tobacco products in the 12 months prior to surgery, indicate the timeframe: 1 = within the 2 weeks prior to surgery 2 = between 2 weeks and 3 months prior to surgery 3 = between 3 months and 12 months prior to surgery
519diabetes mellitus chronic200.1;11SET OF CODES1:NO
2:DIET
3:ORAL
4:INSULIN
VASQIP Definitions (2011): Indicate the chronic, long-term treatment regimen for patients with a diagnosis of Diabetes Mellitus. Diabetes Mellitus is defined as a metabolic disorder of the pancreas whereby the individual requires diet modification, daily dosages of exogenous parenteral insulin or an oral hypoglycemic agent to prevent a hyperglycemic/metabolic acidosis. If the patient is on both Oral and Insulin therapy, indicate Insulin therapy. No - no diagnosis of diabetes Diet - a diagnosis of diabetes that is controlled by diet alone Oral - a diagnosis of diabetes requiring therapy with an oral hypoglycemic agent Insulin - a diagnosis of diabetes requiring daily insulin therapy
520diabetes mellitus preop mgmt200.1;12SET OF CODES1:NO
2:DIET
3:ORAL
4:INSULIN
VASQIP Definitions (2011): Indicate the treatment regimen for patients with a diagnosis of Diabetes Mellitus in the two weeks prior to surgery. Diabetes Mellitus is defined as a metabolic disorder of the pancreas whereby the individual requires diet modification, daily dosages of exogenous parenteral insulin or an oral hypoglycemic agent to prevent a hyperglycemic/metabolic acidosis. If the patient is on both Oral and Insulin therapy, indicate Insulin therapy. No - no diagnosis of diabetes Diet - a diagnosis of diabetes that is controlled by diet alone in the two weeks preceding surgery Oral - a diagnosis of diabetes requiring therapy with an oral hypoglycemic agent in the two weeks preceding surgery Insulin - a diagnosis of diabetes requiring daily insulin therapy in the two weeks preceding surgery
521cvd repair/obstruction200.1;13SET OF CODES0:NO CVD
1:YES - NO SURGICAL REPAIR
2:YES - PRIOR SURGICAL REPAIR
VASQIP Definitions (2011): Select one of the following if patient has indication of Cerebrovascular Disease (CVD): 0 = No CVD indication 1 = Yes, CVD indication by documented obstruction of carotid artery luminal diameter greater than or equal to 50% obstruction of the carotid artery documented by contrast angiography or duplex ultrasound examination which did not result in surgical repair. 2 = Yes, CVD indication resulting in prior carotid artery surgical repair (e.g., carotid endarterectomy or stenting).
522history of cvd200.1;14SET OF CODES0:NO CVD
1:HISTORY OF TIA'S
2:CVA/STROKE - NO NEURO DEFICIT
3:CVA/STROKE W/ NEURO DEFICIT
VASQIP Definitions (2011): Indicate if the patient has a history of cerebrovascular accident by selecting one of the following indications: (If multiple events, select the one with greatest severity.): 0 = No CVD 1= History of Transient Ischemic Attacks: Transient ischemic attacks (TIAs) are focal neurologic deficits (e.g. numbness of an arm or amaurosis fugax) of sudden onset and brief duration (usually <30 minutes), which usually reflect dysfunction in a cerebral vascular distribution. These attacks may be recurrent and, at times, may precede a stroke 2= CVA/Stroke with no neurological deficit: History of a cerebrovascular accident (embolic, thrombotic, or hemorrhagic) with neurologic deficit(s) lasting at least 30 minutes, but no current residual neurologic dysfunction or deficit 3= CVA/Stroke with neurological deficit: History of a cerebrovascular accident (embolic, thrombotic, or hemorrhagic) with persistent residual motor, sensory, or cognitive dysfunction. (e.g., hemiplegia, hemiparesis, aphasia, sensory deficit, impaired memory)
600confirm patient identityVER;7BOOLEANY:YES
N:NO
This field verifies the patient identity has been confirmed. Your answer should be "Yes" or "No". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
601procedure to be performedVER;8BOOLEANY:YES
N:NO
This field verifies the procedure to be performed has been confirmed. Your answer should be "Yes" or "No". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
602site of procedureVER;9BOOLEANY:YES
N:NO
This field verifies the site of procedure, including laterality, has been confirmed. Your answer should be "Yes" or "No". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
603confirm valid consentVER;10SET OF CODESY:YES
N:NO
1:YES, i-MED
2:YES, PAPER
3:YES, TELEPHONE
4:NO, EMERGENCY
5:NO, NOT EMERGENCY
VASQIP Definition (2014): This field verifies that a valid consent form has been confirmed. Your answer should be one of the following: 1-YES, i-MED 2-YES, PAPER 3-YES, TELEPHONE 4-NO, EMERGENCY 5-NO, NOT EMERGENCY If you answer 4 or 5, you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
604confirm patient positionVER;11BOOLEANY:YES
N:NO
This field verifies that the patient position has been confirmed. Your answer should be "Yes" or "No". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
605marked site confirmedVER;12BOOLEANY:YES
N:NO
The site must be marked in all cases. If the patient refuses marking, or if the site is inappropriate to marking, such as mucous membranes and other sites not on the skin that cannot be marked using standard methods, then wristbands must be used for marked site. See applicable VHA Handbooks and Directives for further information and guidance. If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
606preoperative images confirmedVER;13SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
This field refers to the completion of the verification process for the presence of relevant imaging data to confirm the operative site for the correct patient are available, properly labeled and properly presented, and verified by two members of the operating team prior to the start of the procedure. This practice is further defined by local hospital policy. If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
607correct medical implantsVER;14SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
This field verifies that the availability of correct medical implant(s) has been confirmed. Your answer should be "Yes", "No" or "NA". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
608antibiotic prophylaxisVER;15SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
NI:NOT INDICATED
VASQIP Definition (2014): This field verifies that the appropriate antibiotic prophylaxis has been confirmed. Your answer should be "Yes", "No" or "NI". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
609appropriate dvt prophylaxisVER;16SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
NI:NOT INDICATED
VASQIP Definition (2014): This field verifies that the appropriate deep vein thrombosis prophylaxis has been confirmed. Your answer should be "Yes", "No" or "NI". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
610blood availabilityVER;17SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
VASQIP Definition (2014): This field verifies that the blood availability has been confirmed. Your answer should be "Yes", "No" or "NA". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
611availability of special equipVER;18SET OF CODESY:YES
N:NO
NA:NOT APPLICABLE
This field verifies that the availability of special equipment has been confirmed. Your answer should be "Yes", "No" or "NA". If you answer "NO", you'll be asked to justify your answer in the CHECKLIST COMMENT (#85) field.
612original desired date.9;1DATE-TIMEThis field is the original desired date for surgery to occur, as agreed upon by the provider and patient. That agreed upon date is when the patient desires the surgery to occur and when the provider feels it is appropriate to schedule the surgery. If the DESIRED PROCEDURE DATE field (#616) is updated, the value of this field will not change.
613d/t of desired procedure date.9;2DATE-TIMEThis field is the Date/Time stamp for when the provider saves the ORIGINAL DESIRED DATE field (#612) for surgical case in the system.
614original scheduled date.9;3DATE-TIMEThis field is the original scheduled date for surgery to occur, as entered by the OR scheduler.
615d/t of scheduled date entry.9;4DATE-TIMEThis field is the Date/Time stamp for when the OR Scheduler saves the ORIGINAL SCHEDULED DATE field (#614) for the surgical case in the system.
616desired procedure date.9;5DATE-TIMEThis field is the desired date for surgery to occur, as agreed upon by the provider and patient. That agreed upon date is when the patient desires the surgery to occur and when the provider feels it is appropriate to schedule the surgery.
617scheduled date.9;6DATE-TIMEThis field is updated with the new date whenever the OR Scheduler modifies the SCHEDULED START TIME field (#10) for the surgical case.
618positive drug screening200;55SET OF CODESY:YES
N:NO
NA:NA
1:NOT DONE
2:NEGATIVE RESULT
3:POS NOT Rx
4:POS Rx
VASQIP Definition (2014): Indicate if any drug screening (e.g., blood or urine) was performed within 2 weeks prior to surgery. If patient is being prescribed a medication, such as methadone, respond with yes or no as indicated below. 1. Not Done - drug screening was not performed 2. Drug screening was performed and the result was negative 3. Drug screening was performed and the result was positive for substance not prescribed 4. Drug screening was performed and the result was positive for a prescribed substance
619immed use-contamination52;1NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to contamination of a specialty item (one of a kind) in the OR.
620immed use-sps/or mgt issue52;2NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to SPS processing and OR management issues (unsterile from SPS, hole in package, available in SPS but not sterilized, not processed in time, missing in set, or broken in set).
621immed use-emergency case52;3NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to an Emergency Case, such as instruments used on previous case.
622immed use-no better option52;4NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to items for which there may be no better option (batteries, radioactive implants (seeds)).
623immed use-loaner instrument52;5NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to loaner or short notice instrument excluding implants (instrument(s) not available with sufficient time to reprocess completely).
624immed use-decontamination52;6NUMERICIndicate the number of cycles of Immediate Use Steam Sterilization due to contamination of instruments already in use in OR for any reason not included in tracking.
630possible item retention25;6BOOLEANY:YES
N:NO
VASQIP Definition (2014): A retained surgical item includes instruments, sharps, sponges or any materials used by the surgical team performing the operative procedure. Sharps include surgical needles, aspirating needles, blunt needles, scalpel blades or any items with a sharp or pointed edge posing a risk for skin puncture by the surgical team. Sponges include cotton gauze sponges, laparotomy pads, surgical towels or any absorbent materials not intended to remain in the patient's body after the surgical procedure is completed.
633wound sweep25;7BOOLEANY:YES
N:NO
VASQIP Definition (2014): This indicates that a both a visual and manual methodical wound exploration is performed prior to closing the surgical wound to ensure that all surgical items are accounted for and extracted. This question must be answered if any of the final sponge, sharps or instrument counts are recorded as incorrect.
635wound sweep comments53;0WORD-PROCESSINGVASQIP Definition (2014): These are comments related to the reason(s) a wound sweep was or was not performed that may be useful in the documentation of this case and/or subsequent comments related to the wound sweep findings.
636intra-operative x-ray25;8BOOLEANY:YES
N:NO
VASQIP Definition (2014): This indicates that a radiograph of the entire surgical field to rule out a retained surgical item was performed and interpreted by a physician at the completion of the surgical procedure, prior to the patient's transfer from the Operating Room. This question must be answered if any of the final sponge, sharps or instrument counts are recorded as incorrect.
637intra-operative x-ray comments54;0WORD-PROCESSINGVASQIP Definition (2014): These are comments related to the reason(s) an intraoperative x-ray was or was not performed that may be useful in the documentation of this case and/or subsequent comments related to the radiograph findings.
638laterality of procedureOP;5SET OF CODES1:NA
2:LEFT
3:RIGHT
4:BILATERAL
This indicates that the side of the procedure is identified as either left, right or bilateral, when applicable to the procedure.
639report given to25;9POINTER200This indicates the name of the staff member who received the postoperative report from the OR staff member.
640pci200;56SET OF CODES1:NONE
2:<12 HRS OF SURG
3:>12 HRS - 7 DAYS
4:>7 DAYS
5:UNKNOWN
VASQIP Definition (2014): Indicate the time period of the patient's most recent percutaneous coronary artery intervention (PCI) prior to surgery. This does not include percutaneous valve interventions including valvuloplasty and valve replacement. Indicate the one appropriate response, even if the procedure was not fully successful: 1. None - The patient never had a previous PCI. 2. <12 hr of surg - The patient had a PCI less than 12 hours prior to surgery. 3. >12 hr - 7 days - The patient had a PCI between 12 hours and 7 days prior to surgery. 4. >7 days - The patient had a PCI more than 7 days prior to surgery. 5. Unknown
641hypertension200;57SET OF CODES1:NO
2:YES WITHOUT MED
3:YES WITH MED
4:UNKNOWN
VASQIP Definition (2014): Indicate if the patient has a documented history of hypertension within the 30 days prior to surgery. Select the one appropriate response: 1. No history of hypertension 2. Yes without medication therapy 3. Yes with medication therapy (antihypertensive therapy: diuretics, beta blockers, ACE inhibitors, calcium channel blockers, etc.) 4. Unknown
642bleeding risk due to med200;58SET OF CODES1:NO BLEEDING RISK MED
2:CHRONIC ASPIRIN NOT D'C
3:BLEEDING RISK MED D'C
4:BLEEDING RISK MED NOT D'C
VASQIP Definition (2014): Bleeding risk due to medication is present if a patient is on chronic anticoagulation, an antiplatelet agent, thrombin inhibitor or thrombolytic agent that was not discontinued prior to midnight the day of surgery . Select the one appropriate response: 1. The patient does not take medications that increase bleeding risk 2. The patient was only on chronic aspirin therapy which was not discontinued prior to midnight the day of surgery (>=81 mg/day) 3. The patient was on pre-operative medication(s) that increase bleeding risk, but discontinued prior to midnight the day of surgery 4. The patient was on pre-operative medication(s) that increase bleeding risk, and one or more were NOT discontinued prior to midnight the day of surgery
643angina timeframe200;59SET OF CODES1:NO ANGINA
2:W/N 14 DAY OF SURGERY
3:W/N 15-30 DAYS OF SURGERY
4:UNKNOWN
VASQIP Definition (2014): Indicate time period when the angina was most recently present: 1. No Angina 2. Within 14 days prior to surgery 3. Within 15-30 days prior to surgery 4. Unknown
644symptomatic uti205;42BOOLEANY:YES
N:NO
Definition Revised (2014): SYMPTOMATIC UTI - CULTURE plus SIGN/SYMPTOM within 1 calendar day of each other: a. UTI Signs/Symptoms: Urg/Freq/Dys Yes = Patient has urgency, frequency, or dysuria with no other recognized cause No = Patient does not complain of urgency, frequency or dysuria OR has a catheter in place b. UTI Signs/Symptoms: Fever Yes = Patient has a fever > 38C at the time of culture or onset of symptoms No = Patient does not have a fewer > 38C at the time of culture or onset of signs or symptoms c. UTI Signs/Symptoms: Tenderness Yes = Patient has suprapubic tenderness, costovertebral angle pain or tenderness with no other recognized cause No = Patient does not have suprapubic tenderness, costovertebral angle pain or tenderness d. UTI Culture: (must choose 1 or 2) 1. Patient has a positive urine culture that is > 10^5 colony- forming units (CFU)/ml with no more than 2 species of microorganisms 2. A positive urine culture of >=10^3 and <10^5 colony-forming units (CFU)/ml with no more than 2 species of microorganisms plus one of the following three items: a) positive dipstick for leukocyte esterase and/or nitrate; b) Pyuria (urine specimen with > 10 white blood cell [WBC]/mm3 of unspun urine or > 3 WBC high-power field of spun urine) or c) microorganisms seen of Gram's stain of unspun urine INDWELLING URETHRAL CATHETER > 2 CALENDAR DAYS At the time of the procedure or during the post-operative 30 day period, did the patient have an indwelling urethral catheter in for > 2 calendar days (with day 1 being the day of catheter insertion) 1) Yes, in place on the day of UTI Signs/Symptoms and UTI Culture obtained 2) Yes, removed the day of or the day before UTI Signs/Symptoms and UTI Culture obtained 3) No, urethral catheter in place < or = to 2 calendar days but had an indwelling urethral catheter in place at time of UTI Signs/ Symptoms and UTI Culture obtained 4) No, urethral catheter in place < or = 2 calendar days and indwelling urethral catheter was not in place at the time of UTI Signs/Symptoms and UTI Culture obtained 5) No, did not have an indwelling urethral catheter at the time of the procedure or during the post-operative 30 day period
645mechanical vent w/n 30 days205;43BOOLEANY:YES
N:NO
Definition Revised (2014): Indicate if ventilator support required within 30 days after initial post-operative extubation: If the patient was placed on ventilator support postoperatively for any reason within 30 days AND occurred during the same admission in-hospital. (For example, the patient is on the ventilator intra-op and immediately post-op. Then patient is weaned and the ventilator is discontinued. Later, the patient gets into trouble and mechanical ventilation has to be reinstated.) In patients who were not intubated during surgery, intubation at any time after their surgery is considered an occurrence.
901airway index.3;9SET OF CODES1:1. INDEX LESS THAN OR EQUAL TO 0
2:2. INDEX > 0 AND LESS THAN OR EQUAL TO 2
3:3. INDEX > 2 AND LESS THAN OR EQUAL TO 3
4:4. INDEX > 3 AND LESS THAN OR EQUAL TO 4
5:5. INDEX GREATER THAN 4
This field describes the degree of difficulty of airway management on a scale of 1 to 5, 1 being least difficult and 5 being most difficult. The value of this field is based on a computed performance index using the oral-pharyngeal (OP) class and the mandibular space (MS). Performance index = 2.5 x OP - MS length (converted to centimeters) Airway Index ------------ 1 - Performance Index less than 0 2 - Performance index greater than 0 and less than 2 3 - Performance index greater than 2 and less than 3 4 - Performance index greater than 3 and less than 4 5 - Performance index greater than 4
901.1mallampati scale.3;11SET OF CODES1:CLASS 1
2:CLASS 2
3:CLASS 3
4:CLASS 4
Definition Revised (2004): The Mallampati classification relates tongue size to pharyngeal size. This test is performed with the patient in sitting position, the head held in a neutral position, the mouth wide open, and the tongue protruding to the maximum. The subsequent classification is assigned based upon the pharyngeal structures that are visible: Class I - visualization of the soft palate, fauces, uvula, and anterior and posterior pillars. Class II - visualization of the soft palate, fauces, and uvula. Class III - visualization of the soft palate and the base of the uvula. Class IV - soft palate is not visible at all. The classification assigned by the clinician may vary if the patient is in the supine position (instead of sitting). If the patient phonates, this falsely improves the view. If the patient arches his or her tongue, the uvula is falsely obscured. A class I view suggests ease of intubation and correlates with a laryngoscopic view grade I 99 to 100% of the time. Class IV view suggests a poor laryngoscopic view, grade III or IV 100% of the time. Refer to the Operations Manual for a visual depiction of the Mallampati Classification.
901.2mandibular space.3;12NUMERICIn the sitting position with head extended, enter the distance between the inside of the mentum and the top of the thyroid cartilage in millimeters. The mandibular space (MS) and the oral-pharyngeal (OP) score are used in figuring a performance index which is translated to the patient's airway index. (Performance Index = 2.5 x OP - MS length in cm)
903death unrelated/related.4;7SET OF CODESU:UNRELATED
R:RELATED
This indicates if death was unrelated to this surgery.
904review of death comments47;0WORD-PROCESSINGThis word processing field contains comments about the review of death.
905ready to transmit?.4;2SET OF CODESR:READY
T:TRANSMITTED
This field is set to R (ready) by a MUMPS cross reference the TIME PAT OUT OR field. When this case is transmitted to the national database at the end of the quarter, this field will be updated to T (transmitted). This field serves as a flag that indicates the transmission status of this case.
1000tiu operative summaryTIU;1POINTER8925This is the operative summary for this case stored in TIU.
1001tiu nurse intraop reportTIU;2POINTER8925This is the Nurse Intraoperative Report for this case stored in TIU.
1002tiu procedure report (non-or)TIU;3POINTER8925This is the Procedure Report (Non-OR) for this non-OR procedure.
1003tiu anesthesia reportTIU;4POINTER8925This is the Anesthesia Report for this case.
1004dictated summary expectedTIU;5BOOLEAN1:YES
0:NO
This field indicates if the provider will dictate a summary of this procedure to be electronically signed. Enter YES if a dictated summary is expected. Enter NO or leave blank if no summary is expected.
1005cpt on nurse reportTIU;6BOOLEAN1:YES
0:NO
This field reflects the content of the CPT ON NURSE INTRAOP site parameter in SURGERY SITE PARAMETERS file (#133). This field will be set at the time the Nurse Intraoperative Report is signed and will be checked any time an automatic addendum is made to the report to determine whether the CPT codes should appear on the report.
1006icd on nurse reportTIU;7BOOLEAN1:YES
0:NO
This field reflects the content of the ICD ON NURSE INTRAOP site parameter in SURGERY SITE PARAMETERS file (#133). This field will be set at the time the Nurse Intraoperative Report is signed and will be checked any time an automatic addendum is made to the report to determine whether the ICD codes should appear on the report.
2005image2005;0MULTIPLE130.02005This sub-file contains pointers to images in the Imaging file (#2005) that are related to this case.

Referenced by 7 types

  1. OE/RR PATIENT EVENT (100.2) -- surgery
  2. SURGERY (130) -- concurrent case, previously scheduled case, rescheduled case
  3. SURGERY PROCEDURE/DIAGNOSIS CODES (136) -- surgery case
  4. SURGERY TRANSPLANT ASSESSMENTS (139.5) -- surgery case
  5. PFSS ACCOUNT (375) -- surgical case #
  6. INTERNAL DISTRIBUTION ORDER/ADJ. (445.3) -- scheduled operation
  7. TIU DOCUMENT (8925) -- requesting package reference