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


Brief Summary

GUIDELINE TITLE

Additional perioperative assessment. In: I guidelines for perioperative evaluation.

BIBLIOGRAPHIC SOURCE(S)

  • Committee on Perioperative Evaluation (CAPO), Brazilian Society of Cardiology. Additional perioperative assessment. In: I guidelines for perioperative evaluation. Arq Bras Cardiol 2007;89(6):e194-7. [20 references]

GUIDELINE STATUS

This is the current release of the guideline.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The definitions for levels of evidence (A-D) and classes of recommendation (I-III) are provided at the end of the "Major Recommendations" field.

Non-invasive Testing

Moderate-risk patients who will be submitted to vascular surgeries should always have a non-invasive test to detect myocardial ischemia (Class I, Level of evidence D).

Recommendations for Requesting Non-invasive Tests

Class I

  • Indicated for patients with intermediate clinical predictors and who will be submitted to vascular surgeries

Class IIa

  • Indicated when at least two of the three items below are present
    1. Presence of angina functional classes I or II, history of myocardial infarction or pathological Q wave, previous or compensated heart failure, diabetes mellitus or renal failure
    2. Low functional capacity: less than 4 maximum exercise tolerance units (METs)
    3. High-risk surgeries: peripheral vascular surgeries or aortic surgery, lengthy surgeries with considerable blood loss or shifts in body fluids

Class IIb

  • Indicated for patients who have not undergone functional testing in the previous two years and who have
    1. Coronary artery disease or
    2. At least two risk factors for coronary artery disease (CAD) (hypertension, smoking, dyslipidemia, diabetes mellitus, positive family history)

Class III

  • In patients who are not candidates for myocardial revascularization and whose non-cardiac surgical plan cannot be changed because of the results of a functional test.

Recommendations for Analyzing Resting Left Ventricular (LV) Function

Class I

  • Clinical suspicion of aortic stenosis; Level of Evidence B

Class IIa

  • Patients with congestive heart failure (CHF) without previous assessment of ventricular function; Level of Evidence D
  • Grade III obesity; Level of Evidence D
  • Preoperative assessment of liver transplant; Level of Evidence D

Class IIb

  • Detection of valvular heart disease; Level of Evidence B

Class III

  • Routinely for all patients; Level of Evidence D

Recommendations for Requesting a Perioperative Exercise Electrocardiogram

Class IIa

  • Indicated when the two factors below are present
    1. Presence of intermediate clinical predictors of risk: angina functional class I or II, history of myocardial infarction or pathological Q wave, previous or compensated heart failure, diabetes mellitus or renal failure
    2. High-risk surgery: aortic or peripheral vascular surgeries, lengthy surgeries with considerable blood loss or shifts in body fluids

Class IIb

  • Indicated for patients without a functional assessment in the previous two years and
    1. Known to have coronary artery disease
    2. With at least two risk factors for CAD (hypertension, smoking, dyslipidemia, diabetes mellitus, positive family history)

Class III

  • In patients who are not candidates for myocardial revascularization and whose non-cardiac surgical plan cannot be changed because of the results of a functional test
  • Routinely for all patients

Dobutamine Stress Echocardiography

Evidences indicate that low-risk patients will not benefit from non-invasive tests unless their functional capacity is low (<4METs) and they are candidates for high-risk surgeries (Level of Evidence B). On the other hand, patients with 3 or more minor clinical predictors should be considered intermediate-risk patients. (Level of Evidence D) All patients with intermediate risk for cardiac events and low functional capacity (<4METs) and those with good or excellent functional capacity (>4METs) who will be submitted to high-risk surgeries (Level of Evidence B) must undergo stress echocardiography. Consider doing a coronary cineangiography in patients with major clinical predictors for cardiovascular events. (Level of Evidence B).

Recommendations for Stress Echocardiography/Stress Myocardial Perfusion Scintigraphy

Class I

  • Indicated for intermediate-risk patients who will be submitted to vascular surgeries

Class IIa

  • Indicated when at least two of the following factors are present
    1. Presence of intermediate clinical predictors of risk: angina functional class I or II, history of myocardial infarction or pathological Q wave, previous or compensated heart failure, diabetes mellitus or renal failure
    2. Low functional capacity: below 4 METs
    3. High-risk surgeries: peripheral vascular or aortic surgeries, lengthy surgeries with considerable blood loss or shifts of body fluids

Class IIb

  • Indicated for patients who have not been submitted to functional assessment in the previous two years and
    1. Known to have coronary artery disease
    2. With at least two risk factors for CAD (hypertension, smoking, dyslipidemia, diabetes mellitus, positive family history)

Class III

  • In patients who are not candidates for myocardial revascularization and whose non-cardiac surgical plan cannot be changed because of the results of a functional test
  • Routinely for all patients

Recommendations for Coronary Cineangiography

Class I

  • High-risk non-invasive test
  • Presence of major clinical predictors
  • High-risk acute coronary syndrome
  • Positive non-invasive test with proven ischemia and LV dysfunction

Class IIa

  • Low- or moderate-risk non-invasive test with preserved ventricular function

Class III

  • Patients who are not candidates for myocardial revascularization

Definitions:

Levels of Evidence

  1. Sufficient evidence from multiple randomized trials or meta-analyses
  2. Limited evidence from single randomized trial or non-randomized studies
  3. Evidence only from case reports and series
  4. Expert opinion or standard of care

Class of Recommendation

Class I: Conditions for which there is evidence for and/or general agreement that the procedure/therapy is useful and effective

Class II: Conditions for which there is conflicting evidence and/or a divergence of opinion about the usefulness/efficacy of performing the procedure/therapy

Class IIa: Weight of evidence/opinion is in favor of usefulness/efficacy

Class IIb: Usefulness/efficacy is less well established by evidence/opinion

Class III: Conditions for which there is evidence for and/or general agreement that the procedure/therapy is not useful/effective and in some cases may be harmful

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for most of the recommendations (see the "Major Recommendations" field).

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Committee on Perioperative Evaluation (CAPO), Brazilian Society of Cardiology. Additional perioperative assessment. In: I guidelines for perioperative evaluation. Arq Bras Cardiol 2007;89(6):e194-7. [20 references]

ADAPTATION

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

DATE RELEASED

2007

GUIDELINE DEVELOPER(S)

Brazilian Society of Cardiology

SOURCE(S) OF FUNDING

Brazilian Society of Cardiology

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Writing Committee Members: Danielle Menosi Gualandro; Claudio Pinho; Gilson Feitosa; Bruno Caramelli

Task Force Members: Alina Coutinho Rodrigues Feitosa; Beatriz Ayub; Bruno Caramelli; Carisi A. Polanczyk; Carolina L. Zilli Vieira; Claudio Pinho; Daniela Calderaro; Danielle Menosi Gualandro; Denise Iezzi; Dirk Schreen; Dimas T. Ikeoka; Elbio Antonio D'Amico; Elcio Pfeferman; Emerson Quintino de Lima; Emmanuel de Almeida Burdmann; Fábio Santana Machado; Filomena Regina Barbosa Gomes Galas; Gilson Soares Feitosa-Filho; Heno Ferreira Lopes; Henrique Pachón; João César Nunes Sbano; José Augusto Soares Barreto Filho; José L. Andrade; Roberto Henrique Heinisch; Luciana Moraes dos Santos; Luciana S. Fornari; Ludhmila Abrahão Hajjar; Luis Eduardo P. Rohde; Luiz Francisco Cardoso; Marcelo Luiz Campos Vieira; Maristela C. Monachini; Pai Ching Yu; Paula Ribeiro Villaça; Paulo Grandini; Renato S. Bagnatori; Roseny dos Reis Rodrigues; Sandra F. Menosi Gualandro; Walkiria Samuel Avila; Wilson Mathias Jr.

Support: Committee on Perioperative Evaluation (CAPO), Brazilian Society of Cardiology

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

None available

NGC STATUS

This NGC summary was completed by ECRI Institute on June 3, 2008. The information was verified by the guideline developer on July 2, 2008.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions. For reproduction of these guidelines, please contact Bruno Caramelli, Comissão de Avaliacão Perioperatória da Brasileira de Cardiologia – CAPO, Alameda Santos, 705 - 11° andar, São Paulo SP, Brazil CEP: 01419-001.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
DHHS Logo