Welcome to NQMC. Skip directly to: Search Box, Navigation, Content.


Complete Summary


TITLE

Surgical care improvement project: percent of surgery patients on beta-blocker therapy prior to admission who received a beta-blocker during the perioperative period.

SOURCE(S)

  • Specifications manual for national hospital quality measures, version 2.3b. Centers for Medicare & Medicaid Services (CMS), The Joint Commission; 2007 Oct. various p.

Measure Domain

PRIMARY MEASURE DOMAIN

SECONDARY MEASURE DOMAIN

Does not apply to this measure

Brief Abstract

DESCRIPTION

This measure is used to assess the percent of surgery patients on beta-blocker therapy prior to admission who received a beta-blocker during the perioperative period*.

*The perioperative period for the Surgical Care Improvement Project (SCIP) cardiac measures is defined as 24 hours prior to surgical incision through discharge from post-anesthesia care/recovery area.

RATIONALE

In patients at risk of cardiovascular complications in a variety of medical conditions, beta-blockers have been shown to reduce that risk. Studies show that patients with a history of myocardial infarction who have had beta-blocker therapy initiated and continued, have a 20 to 30 percent reduction in subsequent coronary events, cardiovascular mortality, and all-cause mortality (Yusuf, Prog Cardiovasc Dis, 1985). In a meta-analysis by McGory et al. (Surgery, 2005), long-term cardiac mortality and myocardial ischemia were reduced significantly by perioperative beta blockade. Patients maintained on beta-blockers, without complications that might warrant discontinuation, are good candidates for continuation of beta-blockers through the perioperative period.

PRIMARY CLINICAL COMPONENT

Cardiovascular complications; prevention; beta blocker therapy

DENOMINATOR DESCRIPTION

All surgery patients on beta-blocker therapy prior to admission (see the related "Denominator Inclusions/Exclusions" field in the Complete Summary)

NUMERATOR DESCRIPTION

Surgery patients on beta-blocker therapy prior to admission who receive a beta-blocker during the perioperative period*

*The perioperative period for the Surgical Care Improvement Project (SCIP) cardiac measures is defined as 24 hours prior to surgical incision through discharge from post-anesthesia care/recovery area.

Evidence Supporting the Measure

EVIDENCE SUPPORTING THE CRITERION OF QUALITY

  • A clinical practice guideline or other peer-reviewed synthesis of the clinical evidence
  • A systematic review of the clinical literature
  • One or more research studies published in a National Library of Medicine (NLM) indexed, peer-reviewed journal

Evidence Supporting Need for the Measure

NEED FOR THE MEASURE

Use of this measure to improve performance

EVIDENCE SUPPORTING NEED FOR THE MEASURE

State of Use of the Measure

STATE OF USE

Current routine use

CURRENT USE

Accreditation
Collaborative inter-organizational quality improvement
External oversight/Medicaid
External oversight/Medicare
Internal quality improvement

Application of Measure in its Current Use

CARE SETTING

Hospitals

PROFESSIONALS RESPONSIBLE FOR HEALTH CARE

Measure is not provider specific

LOWEST LEVEL OF HEALTH CARE DELIVERY ADDRESSED

Single Health Care Delivery Organizations

TARGET POPULATION AGE

Age greater than or equal to 18 years

TARGET POPULATION GENDER

Either male or female

STRATIFICATION BY VULNERABLE POPULATIONS

Unspecified

Characteristics of the Primary Clinical Component

INCIDENCE/PREVALENCE

Unspecified

ASSOCIATION WITH VULNERABLE POPULATIONS

Unspecified

BURDEN OF ILLNESS

Unspecified

UTILIZATION

Unspecified

COSTS

Unspecified

Institute of Medicine National Healthcare Quality Report Categories

IOM CARE NEED

Staying Healthy

IOM DOMAIN

Effectiveness
Timeliness

Data Collection for the Measure

CASE FINDING

Users of care only

DESCRIPTION OF CASE FINDING

All surgery patients, age 18 years and older, on beta-blocker therapy prior to admission (see the "Denominator Inclusions/Exclusions" field)

DENOMINATOR SAMPLING FRAME

Patients associated with provider

DENOMINATOR INCLUSIONS/EXCLUSIONS

Inclusions
Discharges with an International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) Principal Procedure Code of selected surgeries as defined in Appendix A, Table 5.10, of the original measure documentation and who were on beta-blocker therapy prior to admission

Exclusions

  • Patients who are less than 18 years of age
  • Patients who did not receive beta-blockers due to contraindications as documented in the medical record
  • Patients whose ICD-9-CM principal procedure occurred prior to the date of admission
  • Patients whose ICD-9-CM principal procedure was performed entirely by laparoscope
  • Patients who expired during the perioperative period
  • Pregnant patients taking a beta-blocker prior to admission
  • Patients involved in clinical trials

RELATIONSHIP OF DENOMINATOR TO NUMERATOR

All cases in the denominator are equally eligible to appear in the numerator

DENOMINATOR (INDEX) EVENT

Clinical Condition
Institutionalization
Therapeutic Intervention

DENOMINATOR TIME WINDOW

Time window precedes index event

NUMERATOR INCLUSIONS/EXCLUSIONS

Inclusions
Surgery patients on beta-blocker therapy prior to admission who receive a beta-blocker during the perioperative period*

*The perioperative period for the Surgical Care Improvement Project (SCIP) cardiac measures is defined as 24 hours prior to surgical incision through discharge from post-anesthesia care/recovery area.

Exclusions
None

MEASURE RESULTS UNDER CONTROL OF HEALTH CARE PROFESSIONALS, ORGANIZATIONS AND/OR POLICYMAKERS

The measure results are somewhat or substantially under the control of the health care professionals, organizations and/or policymakers to whom the measure applies.

NUMERATOR TIME WINDOW

Episode of care

DATA SOURCE

Administrative data
Medical record

LEVEL OF DETERMINATION OF QUALITY

Individual Case

PRE-EXISTING INSTRUMENT USED

Unspecified

Computation of the Measure

SCORING

Rate

INTERPRETATION OF SCORE

Better quality is associated with a higher score

ALLOWANCE FOR PATIENT FACTORS

Unspecified

STANDARD OF COMPARISON

External comparison at a point in time
External comparison of time trends
Internal time comparison

Evaluation of Measure Properties

EXTENT OF MEASURE TESTING

Unspecified

Identifying Information

ORIGINAL TITLE

SCIP-Card-2: surgery patients on beta-blocker therapy prior to admission who received a beta-blocker during the perioperative period.

MEASURE COLLECTION

MEASURE SET NAME

SUBMITTER

Centers for Medicare & Medicaid Services
Joint Commission, The

DEVELOPER

Centers for Medicare & Medicaid Services/The Joint Commission

FUNDING SOURCE(S)

All external funding for measure development has been received and used in full compliance with The Joint Commission's Corporate Sponsorship policies, which are available upon written request to The Joint Commission.

COMPOSITION OF THE GROUP THAT DEVELOPED THE MEASURE

The Joint Commission worked with the Centers for Medicare & Medicaid Services, who assembled and maintained the Technical Expert Panel, for development of the Surgical Improvement Project (SIP) measures, The SIP set subsequently transitioned to the Surgical Care Improvement Project (SCIP) effective July 1, 2006.

SCIP Partners include the Steering Committee of 10 national organizations who have pledged their commitment and full support for SCIP:

  • Agency for Healthcare Research and Quality
  • American College of Surgeons
  • American Hospital Association
  • American Society of Anesthesiologists
  • Association of Perioperative Registered Nurses
  • Centers for Disease Control and Prevention
  • Centers for Medicare & Medicaid Services
  • Institute for Healthcare Improvement
  • The Joint Commission
  • Veterans Health Administration

FINANCIAL DISCLOSURES/OTHER POTENTIAL CONFLICTS OF INTEREST

Expert panel members have made full disclosure of relevant financial and conflict of interest information in accordance with the Joint Commission's Conflict of Interest policies, copies of which are available upon written request to The Joint Commission.

ENDORSER

National Quality Forum

ADAPTATION

Measure was not adapted from another source.

RELEASE DATE

2006 Jun

REVISION DATE

2007 Oct

MEASURE STATUS

Please note: This measure has been updated. The National Quality Measures Clearinghouse is working to update this summary.

SOURCE(S)

  • Specifications manual for national hospital quality measures, version 2.3b. Centers for Medicare & Medicaid Services (CMS), The Joint Commission; 2007 Oct. various p.

MEASURE AVAILABILITY

COMPANION DOCUMENTS

The following are available:

NQMC STATUS

This NQMC summary was completed by ECRI on May 8, 2007. The information was verified by the measure developer on July 24, 2007. This NQMC summary was updated by ECRI Institute on October 26, 2007.

COPYRIGHT STATEMENT

The Specifications Manual for National Hospital Quality Measures [Version 2.3b, October, 2007] is the collaborative work of the Centers for Medicare & Medicaid Services and The Joint Commission. The Specifications Manual is periodically updated by the Centers for Medicare & Medicaid Services and The Joint Commission. Users of the Specifications Manual for National Hospital Quality Measures should periodically verify that the most up-to-date version is being utilized.

Disclaimer

NQMC DISCLAIMER