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Brief Summary

GUIDELINE TITLE

ACC/AHA 2007 guidelines on perioperative cardiovascular evaluation and care for noncardiac surgery.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: American College of Cardiology Foundation (ACCF), American Heart Association (AHA). ACC/AHA guideline update on perioperative cardiovascular evaluation for noncardiac surgery. A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines (Committee to Update the 1996 Guidelines). Bethesda (MD): American College of Cardiology Foundation; 2002. 58 p. [390 references]

Fleisher LA, Beckman JA, Freeman WK, Brown KA, Froeclich JB, Calkins H, Kasper EK, Chaikof E, Kersten JR, Fleischmann KE, Riegel B. ACC/AHA 2006 guideline update on perioperative cardiovascular evaluation on noncardiac surgery: focused update on perioperative beta-blocker therapy. A report of the American College of Cardiology/American Heart Association Task Force on Practice [trunc]. J Am Coll Cardiol 2006;47:1-12. [25 references]

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s)/intervention(s) for which important revised regulatory and/or warning information has been released.

  • August 16, 2007, Coumadin (Warfarin): Updates to the labeling for Coumadin to include pharmacogenomics information to explain that people's genetic makeup may influence how they respond to the drug.
  • June 8, 2007, Troponin-I Immunoassay: Class I Recall of all lots of the Architect Stat Troponin-I Immunoassay. The assay may report falsely elevated or falsely decreased results at and near a low level, which may impact patient treatment.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The American College of Cardiology/American Heart Association (ACC/AHA) classification of the recommendations for patient evaluation and treatment (classes I-III) and the levels of evidence (A-C) are defined at the end of the Major Recommendations field.

General Approach to the Patient

Table: Active Cardiac Conditions for Which the Patient Should Undergo Evaluation and Treatment Before Noncardiac Surgery (Class I, Level of Evidence: B)
Condition Examples
Unstable coronary syndromes Unstable or severe angina* (Canadian Cardiovascular Society [CCS] class III or IV)**
Recent myocardial infarction (MI)***
Decompensated heart failure (HF) (New York Heart Association [NYHA] functional class IV; worsening or new-onset HF)  
Significant arrhythmias High-grade atrioventricular block

Mobitz II atrioventricular block

Third-degree atrioventricular heart block

Symptomatic ventricular arrhythmias

Supraventricular arrhythmias (including atrial fibrillation) with uncontrolled ventricular rate (heart rate [HR] greater than 100 beats per minute at rest)

Symptomatic bradycardia

Newly recognized ventricular tachycardia
Severe valvular disease Severe aortic stenosis (mean pressure gradient greater than 40 mm Hg, aortic valve area less than 1.0 cm2, or symptomatic)

Symptomatic mitral stenosis (progressive dyspnea on exertion, exertional presyncope, or HF)

*According to Campeau (Campeau L. Letter: grading of angina pectoris. Circulation 1976;54:522-3).

**May include "stable" angina in patients who are unusually sedentary.

***The American College of Cardiology National Database Library defines recent MI as more than 7 days but less than or equal to 1 month (within 30 days).

Supplemental Preoperative Evaluation

Assessment of Left Ventricular (LV) Function

Recommendations for Preoperative Noninvasive Evaluation of Left Ventricular Function

Class IIa

  1. It is reasonable for patients with dyspnea of unknown origin to undergo preoperative evaluation of left ventricular (LV) function. (Level of Evidence: C)
  2. It is reasonable for patients with current or prior heart failure with worsening dyspnea or other change in clinical status to undergo preoperative evaluation of LV function if not performed within 12 months. (Level of Evidence: C)

Class IIb

  1. Reassessment of LV function in clinically stable patients with previously documented cardiomyopathy is not well established. (Level of Evidence: C)

Class III

  1. Routine perioperative evaluation of LV function in patients is not recommended. (Level of Evidence: B)

Assessment of Risk for Coronary Artery Disease (CAD) and Assessment of Functional Capacity

Recommendations for Preoperative Resting 12-Lead Electrocardiogram (ECG)

Class I

  1. Preoperative resting 12-lead ECG is recommended for patients with at least 1 clinical risk factor* who are undergoing vascular surgical procedures. (Level of Evidence: B)

    *Clinical risk factors include history of ischemic heart disease, history of compensated or prior heart failure, history of cerebrovascular disease, diabetes mellitus, and renal insufficiency.

  2. Preoperative resting 12-lead ECG is recommended for patients with known coronary heart disease, peripheral arterial disease, or cerebrovascular disease who are undergoing intermediate-risk surgical procedures. (Level of Evidence: C)

Class IIa

  1. Preoperative resting 12-lead ECG is reasonable in persons with no clinical risk factors who are undergoing vascular surgical procedures. (Level of Evidence: B)

Class IIb

  1. Preoperative resting 12-lead ECG may be reasonable in patients with at least 1 clinical risk factor who are undergoing intermediate-risk operative procedures. (Level of Evidence: B)

Class III

  1. Preoperative and postoperative resting 12-lead ECGs are not indicated in asymptomatic persons undergoing low-risk surgical procedures. (Level of Evidence: B)

Recommendations for Noninvasive Stress Testing Before Noncardiac Surgery

Class I

  1. Patients with active cardiac conditions (see the Table above) in whom noncardiac surgery is planned should be evaluated and treated per American College of Cardiology/American Heart Association (ACC/AHA) guidelines (see the original guideline document for the list of guidelines) before noncardiac surgery. (Level of Evidence: B)

Class IIa

  1. Noninvasive stress testing of patients with 3 or more clinical risk factors and poor functional capacity (less than 4 metabolic equivalents [METs]) who require vascular surgery (i.e., aortic and other major vascular and peripheral vascular surgery) is reasonable if it will change management. (Level of Evidence: B)

Class IIb

  1. Noninvasive stress testing may be considered for patients with at least 1 to 2 clinical risk factors and poor functional capacity (less than 4 METs) who require intermediate-risk noncardiac surgery if it will change management. (Level of Evidence: B)
  2. Noninvasive stress testing may be considered for patients with at least 1 to 2 clinical risk factors and good functional capacity (greater than or equal to 4 METs) who are undergoing vascular surgery. (Level of Evidence: B)

Class III

  1. Noninvasive testing is not useful for patients with no clinical risk factors undergoing intermediate-risk noncardiac surgery. (Level of Evidence: C)
  2. Noninvasive testing is not useful for patients undergoing low-risk noncardiac surgery. (Level of Evidence: C)

Perioperative Therapy

Preoperative Coronary Revascularization With Coronary Artery Bypass Grafting (CABG) or Percutaneous Coronary Intervention

(All of the Class I indications below are consistent with the ACC/AHA 2004 Guideline Update for Coronary Artery Bypass Graft Surgery.)

Class I

  1. Coronary revascularization before noncardiac surgery is useful in patients with stable angina who have significant left main coronary artery stenosis. (Level of Evidence: A)
  2. Coronary revascularization before noncardiac surgery is useful in patients with stable angina who have 3-vessel disease. (Survival benefit is greater when left ventricular ejection fraction is less than 0.50.) (Level of Evidence: A
  3. Coronary revascularization before noncardiac surgery is useful in patients with stable angina who have 2-vessel disease with significant proximal left anterior descending stenosis and either ejection fraction less than 0.50 or demonstrable ischemia on noninvasive testing. (Level of Evidence: A)
  4. Coronary revascularization before noncardiac surgery is recommended for patients with high-risk unstable angina or non–ST-segment elevation myocardial infarction (MI).* (Level of Evidence: A)

    *High-risk unstable angina/non–ST-elevation MI patients were identified as those with age greater than 75 years, accelerating tempo of ischemic symptoms in the preceding 48 hours, ongoing rest pain greater than 20 minutes in duration, pulmonary edema, angina with S3 gallop or rales, new or worsening mitral regurgitation murmur, hypotension, bradycardia, tachycardia, dynamic ST-segment change greater than or equal to 1 mm, new or presumed new bundle-branch block on ECG, or elevated cardiac biomarkers, such as troponin.

  5. Coronary revascularization before noncardiac surgery is recommended in patients with acute ST-elevation MI. (Level of Evidence: A)

Class IIa

  1. In patients in whom coronary revascularization with percutaneous coronary intervention (PCI) is appropriate for mitigation of cardiac symptoms and who need elective noncardiac surgery in the subsequent 12 months, a strategy of balloon angioplasty or bare-metal stent placement followed by 4 to 6 weeks of dual-antiplatelet therapy is probably indicated. (Level of Evidence: B)
  2. In patients who have received drug-eluting coronary stents and who must undergo urgent surgical procedures that mandate the discontinuation of thienopyridine therapy, it is reasonable to continue aspirin if at all possible and restart the thienopyridine as soon as possible. (Level of Evidence: C)

Class IIb

  1. The usefulness of preoperative coronary revascularization is not well established in high-risk ischemic patients (e.g., abnormal dobutamine stress echocardiogram with at least 5 segments of wall-motion abnormalities). (Level of Evidence: C)
  2. The usefulness of preoperative coronary revascularization is not well established for low-risk ischemic patients with an abnormal dobutamine stress echocardiogram (segments 1 to 4). (Level of Evidence: B)

Class III

  1. It is not recommended that routine prophylactic coronary revascularization be performed in patients with stable CAD before noncardiac surgery. (Level of Evidence: B)
  2. Elective noncardiac surgery is not recommended within 4 to 6 weeks of bare-metal coronary stent implantation or within 12 months of drug-eluting coronary stent implantation in patients in whom thienopyridine therapy or aspirin and thienopyridine therapy will need to be discontinued perioperatively. (Level of Evidence: B)
  3. Elective noncardiac surgery is not recommended within 4 weeks of coronary revascularization with balloon angioplasty. (Level of Evidence: B)

Perioperative Medical Therapy

Recommendations for Beta-Blocker Medical Therapy

Care should be taken in applying recommendations on beta-blocker therapy to patients with decompensated heart failure, nonischemic cardiomyopathy, or severe valvular heart disease in the absence of coronary heart disease.

Class I

  1. Beta blockers should be continued in patients undergoing surgery who are receiving beta blockers to treat angina, symptomatic arrhythmias, hypertension, or other ACC/AHA Class I guideline indications. (Level of Evidence: C)
  2. Beta blockers should be given to patients undergoing vascular surgery who are at high cardiac risk owing to the finding of ischemia on preoperative testing. (Level of Evidence: B)

Class IIa

  1. Beta blockers are probably recommended for patients undergoing vascular surgery in whom preoperative assessment identifies coronary heart disease (CHD). (Level of Evidence: B)
  2. Beta blockers are probably recommended for patients in whom preoperative assessment for vascular surgery identifies high cardiac risk, as defined by the presence of more than 1 clinical risk factor (defined under "Recommendations for Preoperative Resting 12-Lead ECG," above). (Level of Evidence: B)
  3. Beta blockers are probably recommended for patients in whom preoperative assessment identifies CHD or high cardiac risk, as defined by the presence of more than 1 clinical risk factor (defined under "Recommendations for Preoperative Resting 12-Lead ECG," above), who are undergoing intermediate-risk or vascular surgery. (Level of Evidence: B)

Class IIb

  1. The usefulness of beta blockers is uncertain for patients who are undergoing either intermediate-risk procedures or vascular surgery, in whom preoperative assessment identifies a single clinical risk factor (defined under "Recommendations for Preoperative Resting 12-Lead ECG," above). (Level of Evidence: C)
  2. The usefulness of beta blockers is uncertain in patients undergoing vascular surgery with no clinical risk factors who are not currently taking beta blockers. (Level of Evidence: B)

Class III

  1. Beta blockers should not be given to patients undergoing surgery who have absolute contraindications to beta blockade. (Level of Evidence: C)

Table: Recommendations for Perioperative Beta-Blocker Therapy Based on Published Randomized Clinical Trials

Surgery No Clinical Risk Factors 1 or More Clinical Risk Factors CHD or High Cardiac Risk Patients Currently Taking Beta Blockers
Vascular Class IIb, Level of Evidence: B Class IIa, Level of Evidence: B Patients found to have myocardial ischemia on preoperative testing: Class I, Level of Evidence: B*

Patients without ischemia or no previous test: Class IIa, Level of Evidence: B
Class I, Level of Evidence: B
Intermediate risk ... Class IIb, Level of Evidence: C Class IIa, Level of Evidence: B Class I, Level of Evidence: C
Low risk Class I, Level of Evidence: C

See Table 4 of the original guideline document for definition of procedures. Ellipses (…) indicate that data were insufficient to determine a class of recommendation or level of evidence. See text for further discussion. CHD indicates coronary heart disease.

*Applies to patients found to have coronary ischemia on preoperative testing

Recommendations for Statin Therapy

Class I

  1. For patients currently taking statins and scheduled for noncardiac surgery, statins should be continued. (Level of Evidence: B)

Class IIa

  1. For patients undergoing vascular surgery with or without clinical risk factors, statin use is reasonable. (Level of Evidence: B)

Class IIb

  1. For patients with at least 1 clinical risk factor who are undergoing intermediate-risk procedures, statins may be considered. (Level of Evidence: C)

Recommendations for Alpha-2 Agonists

Class IIb

  1. Alpha-2 agonists for perioperative control of hypertension may be considered for patients with known CAD or at least 1 clinical risk factor who are undergoing surgery. (Level of Evidence: B)

Class III

  1. Alpha-2 agonists should not be given to patients undergoing surgery who have contraindications to this medication. (Level of Evidence: C)

Preoperative Intensive Care Monitoring

Class IIb

  1. Preoperative intensive care monitoring with a pulmonary artery catheter for optimization of hemodynamic status might be considered; however, it is rarely required and should be restricted to a very small number of highly selected patients whose presentation is unstable and who have multiple comorbid conditions. (Level of Evidence: B)

Anesthetic Considerations and Intraoperative Management

Choice of Anesthetic Technique and Agent

Recommendations for Use of Volatile Anesthetic Agents

Class IIa

  1. It can be beneficial to use volatile anesthetic agents during noncardiac surgery for the maintenance of general anesthesia in hemodynamically stable patients at risk for myocardial ischemia. (Level of Evidence: B)

Prophylactic Intraoperative Nitroglycerin

Class IIb

  1. The usefulness of intraoperative nitroglycerin as a prophylactic agent to prevent myocardial ischemia and cardiac morbidity is unclear for high-risk patients undergoing noncardiac surgery, particularly those who have required nitrate therapy to control angina. The recommendation for prophylactic use of nitroglycerin must take into account the anesthetic plan and patient hemodynamics and must recognize that vasodilation and hypovolemia can readily occur during anesthesia and surgery. (Level of Evidence: C)

Use of Transesophageal Echocardiography

Class IIa

  1. The emergency use of intraoperative or perioperative transesophageal echocardiography is reasonable to determine the cause of an acute, persistent, and life-threatening hemodynamic abnormality. (Level of Evidence: C)

Maintenance of Body Temperature

Class I

  1. Maintenance of body temperature in a normothermic range is recommended for most procedures other than during periods in which mild hypothermia is intended to provide organ protection (e.g., during high aortic cross-clamping). (Level of Evidence: B)

Perioperative Control of Blood Glucose Concentration

Class IIa

  1. It is reasonable that blood glucose concentration be controlled* during the perioperative period in patients with diabetes mellitus or acute hyperglycemia who are at high risk for myocardial ischemia or who are undergoing vascular and major noncardiac surgical procedures with planned intensive care unit admission. (Level of Evidence: B)

    *Blood glucose levels less than 150 milligrams/deciliter (mg/dL) appear to be beneficial.

Class IIb

  1. The usefulness of strict control of blood glucose concentration* during the perioperative period is uncertain in patients with diabetes mellitus or acute hyperglycemia who are undergoing noncardiac surgical procedures without planned intensive care unit admission. (Level of Evidence: C)

Perioperative Surveillance

Intraoperative and Postoperative Use of Pulmonary Artery Catheters (PACs)

Recommendations for Perioperative Use of PACs

Class IIb

  1. Use of a PAC may be reasonable in patients at risk for major hemodynamic disturbances that are easily detected by a PAC; however, the decision must be based on 3 parameters: patient disease, surgical procedure (i.e., intraoperative and postoperative fluid shifts), and practice setting (experience in PAC use and interpretation of results), because incorrect interpretation of the data from a PAC may cause harm. (Level of Evidence: B)

Class III

  1. Routine use of a PAC perioperatively, especially in patients at low risk of developing hemodynamic disturbances, is not recommended. (Level of Evidence: A)

Intraoperative and Postoperative Use of ST-Segment Monitoring

Class IIa

  1. Intraoperative and postoperative ST-segment monitoring can be useful to monitor patients with known CAD or those undergoing vascular surgery, with computerized ST-segment analysis, when available, used to detect myocardial ischemia during the perioperative period. (Level of Evidence: B)

Class IIb

  1. Intraoperative and postoperative ST-segment monitoring may be considered in patients with single or multiple risk factors for CAD who are undergoing noncardiac surgery. (Level of Evidence: B)

Surveillance for Perioperative MI

Class I

  1. Postoperative troponin measurement is recommended in patients with ECG changes or chest pain typical of acute coronary syndrome. (Level of Evidence: C)

Class IIb

  1. The use of postoperative troponin measurement is not well established in patients who are clinically stable and have undergone vascular and intermediate-risk surgery. (Level of Evidence: C)

Class III

  1. Postoperative troponin measurement is not recommended in asymptomatic stable patients who have undergone low-risk surgery. (Level of Evidence: C)

Definitions:

Applying Classification of Recommendations and Level of Evidence

  SIZE OF TREATMENT EFFECT
CLASS I

Benefit >>> Risk

Procedure/Treatment SHOULD be performed/ administered
CLASS IIa

Benefit >> Risk
Additional studies with focused objectives needed


IT IS REASONABLE to perform procedure/ administer treatment
CLASS IIb

Benefit > Risk
Additional studies with broad objectives needed; additional registry data would be helpful


Procedure/Treatment MAY BE CONSIDERED
CLASS III

Risk > Benefit
No additional studies needed


Procedure/Treatment should NOT be performed/ administered SINCE IT IS NOT HELPFUL AND MAY BE HARMFUL
Estimate of Certainty (Precision) of Treatment Effect LEVEL A

Multiple (3–5) population risk strata evaluated*

General consistency of direction and magnitude of effect
  • Recommendation that procedure or treatment is useful/effective
  • Sufficient evidence from multiple randomized trials or meta-analyses
  • Recommendation in favor of treatment of procedure being useful/effective
  • Some conflicting evidence from multiple randomized trials or meta-analyses
  • Recommendation's usefulness/efficacy less well established
  • Greater conflicting evidence from multiple randomized trials or meta-analyses
  • Recommendation that procedure or treatment is not useful/effective and may be harmful
  • Sufficient evidence from multiple randomized trials or meta-analyses
LEVEL B

Limited (2–3) population risk strata evaluated*
  • Recommendation that procedure or treatment is useful/effective
  • Limited evidence from single randomized trial or nonrandomized studies
  • Recommendation in favor of treatment of procedure being useful/effective
  • Some conflicting evidence from single randomized trial or nonrandomized studies
  • Recommendation's usefulness/efficacy less well established
  • Greater conflicting evidence from single randomized trial or nonrandomized studies
  • Recommendation that procedure or treatment is not useful/effective and may be harmful
  • Limited evidence from single randomized trial or nonrandomized studies
LEVEL C

Very limited (1–2) population risk strata evaluated*
  • Recommendation that procedure or treatment is useful/effective
  • Only expert opinion, case studies, or standard-of-care
  • Recommendation in favor of treatment of procedure being useful/effective
  • Only diverging expert opinion, case studies, or standard-of-care
  • Recommendation's usefulness/efficacy less well established
  • Only diverging expert opinion, case studies, or standard-of-care
  • Recommendation that procedure or treatment is not useful/effective and may be harmful
  • Only expert opinion, case studies, or standard-of-care

*Data available from clinical trials or registries about the usefulness/efficacy in different subpopulations, such as gender, age, history of diabetes, history of prior myocardial infarction, history of heart failure, and prior aspirin use. A recommendation with Level of Evidence B or C does not imply that the recommendation is weak. Many important clinical questions addressed in the guidelines do not lend themselves to clinical trials. Even though randomized trials are not available, there may be a very clear clinical consensus that a particular test or therapy is useful or effective.

NOTE: In 2003, the American College of Cardiology/American Heart Association (ACC/AHA) Task Force on Practice Guidelines developed a list of suggested phrases to use when writing recommendations. All guideline recommendations have been written in full sentences that express a complete thought, such that a recommendation, even if separated and presented apart from the rest of the document (including headings above sets of recommendations), would still convey the full intent of the recommendation. It is hoped that this will increase readers' comprehension of the guidelines and will allow queries at the individual recommendation level. (See Table 1 in the original guideline document for a list of suggested phrases for writing recommendations.)

CLINICAL ALGORITHM(S)

The original guideline document contains clinical algorithms for:

  • Cardiac evaluation and care for noncardiac surgery based on active clinical conditions, known cardiovascular disease, or cardiac risk factors for patients 50 years of age or greater
  • Proposed approach to the management of patients with previous percutaneous coronary intervention (PCI) who require noncardiac surgery, based on expert opinion
  • Treatment for patients requiring PCI who need subsequent surgery

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

1996 Mar 15 (revised 2007 Oct)

GUIDELINE DEVELOPER(S)

American College of Cardiology Foundation - Medical Specialty Society
American Heart Association - Professional Association

SOURCE(S) OF FUNDING

The American College of Cardiology Foundation and the American Heart Association. No outside funding accepted.

GUIDELINE COMMITTEE

American College of Cardiology/American Heart Association Task Force on Practice Guidelines

Writing Committee to Revise the 2002 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Committee Members: Lee A. Fleisher, MD, FACC, FAHA, Chair; Joshua A. Beckman, MD, FACC; Kenneth A. Brown, MD, FACC, FAHA; Hugh Calkins, MD, FACC, FAHA; Elliott Chaikof, MD; Kirsten E. Fleischmann, MD, MPH, FACC; William K. Freeman, MD, FACC; James B. Froehlich, MD, MPH, FACC; Edward K. Kasper, MD, FACC; Judy R. Kersten, MD, FACC; Barbara Riegel, DNSc, RN, FAHA; John F. Robb, MD, FACC

Task Force Members: Sidney C. Smith, JR., MD, FACC, FAHA, Chair; Alice K. Jacobs, MD, FACC, FAHA, Vice-Chair; Cynthia D. Adams, MSN, PhD, FAHA; Jeffrey L. Anderson, MD, FACC, FAHA; Elliott M. Antman, MD, FACC, FAHA; Christopher E. Buller, MD, FACC; Mark A. Creager, MD, FACC, FAHA; Steven M. Ettinger, MD, FACC; David P. Faxon, MD, FACC, FAHA; Valentin Fuster, MD, PhD, FACC, FAHA, FESC; Jonathan L. Halperin, MD, FACC, FAHA; Loren F. Hiratzka, MD, FACC, FAHA; Sharon A. Hunt, MD, FACC, FAHA; Bruce W. Lytle, MD, FACC, FAHA; Rick Nishimura, MD, FACC, FAHA; Joseph P. Ornato, MD, FACC, FAHA; Richard L. Page, MD, FACC, FAHA; Barbara Riegel, DNSc, RN, FAHA*; Lynn G. Tarkington, RN; Clyde W. Yancy, MD, FACC

*Former Task Force member during this writing effort

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

The American College of Cardiology/American Heart Association (ACC/AHA) Task Force on Practice Guidelines makes every effort to avoid any actual, potential, or perceived conflict of interest that might arise as a result of an industry relationship or personal interest of the writing committee. Specifically, all members of the writing committee, as well as peer reviewers of the document, were asked to provide disclosure statements of all such relationships that might be perceived as real or potential conflicts of interest. Writing committee members were also strongly encouraged to declare a previous relationship with industry that may be perceived as relevant to guideline development. If a writing committee member developed a new relationship with industry during their tenure, they are required to notify guideline staff in writing. The continued participation of the writing committee member was reviewed. These statements were reviewed by the parent task force, reported orally to all members of the writing committee at each meeting, and updated and reviewed by the writing committee as changes occurred.

Table: ACC/AHA Writing Committee to Revise the 2002 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery: Author Relationships With Industry

Committee Member Consultant Research Grant Scientific Advisory Board Speakers' Bureau Other
Joshua A. Beckman Bristol-Myers Squibb None Sanofi-Aventis Bristol-Myers Squibb*; Merck; Eli Lilly; Sanofi-Aventis* None
Kenneth A. Brown GE Healthcare None None None None
Hugh Calkins None None None None None
Elliot Chaikof None None None None None
Kirsten E. Fleischmann None None None None Pfizer (QI/CME Initiatives)
Lee A. Fleisher None None None None None
William K. Freeman None None None None None
James B. Froehlich Pfizer None Sanofi-Aventis Sanofi-Aventis; Otsuka; Pfizer; Merck None
Edward K. Kasper Scios None None None None
Judy R. Kersten Abbott Laboratories Abbott Laboratories* None Abbott Laboratories* None
Barbara Riegel None None None None None
John F. Robb None None None None None

This table represents the actual or potential relationships with industry that were reported on May 11, 2007. This table was updated in conjunction with all meetings and conference calls of the writing committee. QI/CME indicates quality improvement/continuing medical education.
*Significant relationship (greater than $10,000)

See Appendix II in the original guideline document for peer reviewer relationships with industry.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: American College of Cardiology Foundation (ACCF), American Heart Association (AHA). ACC/AHA guideline update on perioperative cardiovascular evaluation for noncardiac surgery. A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines (Committee to Update the 1996 Guidelines). Bethesda (MD): American College of Cardiology Foundation; 2002. 58 p. [390 references]

Fleisher LA, Beckman JA, Freeman WK, Brown KA, Froeclich JB, Calkins H, Kasper EK, Chaikof E, Kersten JR, Fleischmann KE, Riegel B. ACC/AHA 2006 guideline update on perioperative cardiovascular evaluation on noncardiac surgery: focused update on perioperative beta-blocker therapy. A report of the American College of Cardiology/American Heart Association Task Force on Practice [trunc]. J Am Coll Cardiol 2006;47:1-12. [25 references]

GUIDELINE AVAILABILITY

Electronic copies: Available in Portable Document Format (PDF) from the American College of Cardiology (ACC) Web site; electronic copies are also available in PDF from the American Heart Association (AHA) Web site

Print copies: Available from the American College of Cardiology, Resource Center, 9111 Old Georgetown Rd, Bethesda, MD 20814-1699; (800) 253-4636 (US only).

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on June 30, 1998. The information was verified by the guideline developer on December 1, 1998. This summary was updated by ECRI on April 30, 2002. The updated information was verified by the guideline developer on August 7, 2002. This NGC summary was updated on May 12, 2006. The updated information was verified by the guideline developer on June 15, 2006. This summary was updated by ECRI on March 6, 2007 following the U.S. Food and Drug Administration (FDA) advisory on Coumadin (warfarin sodium). This summary was updated by ECRI Institute on July 12, 2007 following the U.S. Food and Drug Administration (FDA) advisory on Troponin-1 Immunoassay. This summary was updated by ECRI Institute on September 7, 2007 following the revised U.S. Food and Drug Administration (FDA) advisory on Coumadin (warfarin). This NGC summary was updated by ECRI Institute on November 20, 2007. The updated information was verified by the guideline developer on January 7, 2008.

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