Cardiac testing for noncardiac surgery: past, present, and future

Cardiac testing for noncardiac surgery: past, present, and future

Editorial Cardiac Testing for Noncardiac Surgery: Past, Present, and Future John E. Tetzlaff, MD,* Ibrahim Farid, MD† Division of Anesthesiology and C...

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Editorial Cardiac Testing for Noncardiac Surgery: Past, Present, and Future John E. Tetzlaff, MD,* Ibrahim Farid, MD† Division of Anesthesiology and Critical Care Medicine, The Cleveland Clinic Foundation, Cleveland, OH

*Director, Center for Anesthesiology Education †Fellow Address correspondence to Dr. Tetzlaff at the Division of Anesthesiology and Critical Care Medicine, E-30, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA. E-mail: [email protected] Received for publication April 11, 2002; revised manuscript accepted for publication May 7, 2002.

The evaluation of risk is a fundamental part of the role of the anesthesiologist in the perioperative period. For elective surgery, this evaluation begins with identification of correctable elements of co-morbidity and appropriate intervention to reduce risk and/or improve outcome. Optimum anesthetic care requires a balance between sensitive detection of risk and cost-effective utilization of expensive resources. The preparation of the patient with known cardiovascular disease for noncardiac surgery is an excellent example of this dilemma. Formal risk-stratification has been a regular part of the daily practice of anesthesiology since the 1960s, with the assignment of an American Society of Anesthesiologists (ASA) physical status classification as a part of every anesthetic administered. Sponsored by the ASA and published by Dripps et al.,1 ASA physical status assignment was designed to predict risk. Subsequent large-scale reviews have shown ASA physical status classifications to correlate with the incidence of major morbidity and mortality,2,3 although not in a manner that lends itself to predicting specific cardiac risk, or guiding cardiac testing for elective surgery. The desire to identify a means to predict perioperative cardiac risk has been driven by the observation that adverse cardiac events correlate with certain kinds of surgery, including carotid artery surgery,4 aortic aneurysm repair,5 and peripheral revascularization procedures.6 Recognizing that vascular surgery was highly associated with adverse cardiac events, Hertzer et al.7 advocated routine cardiac catheterization before vascular surgery, and achieved a very low mortality after major aortic surgery. Subsequent review of this approach revealed normal coronaries in only 8% of more than 1,000 patients scheduled for peripheral vascular surgery, with a significant incidence (14%) with severe correctable coronary artery disease that was not suspected by the clinical history.8 Coronary angiography led to coronary artery bypass graft procedures in 130 patients in this series who subsequently underwent aortic surgery, with less than 1% mortality. Screening with routine cardiac catheterization did not expand from these studies into a general risk prediction strategy due to the cost and morbidity associated with the procedures. Other approaches have included routine screening with exercise stress testing,9 dipyridamole-thallium imaging,6 and dobutamine stress echocardiography.10 Although some data are supportive,11 routine screening ultimately proves less than ideal for preoperative preparation for large populations of patients due to risk, cost, and logistics.12 In an attempt to combine patient factors with surgical issues, Goldman et al.13

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created a scoring system designed to predict perioperative adverse cardiac events by assigning points based on risk factors. Factors found to correlate with cardiac events included recent myocardial infarction (MI), uncompensated congestive heart failure, and emergency surgery. This scoring system was shown subsequently to be capable of identifying the patients who were at highest risk, but it was not effective in stratifying those patients at lesser risk, and, finally, it was only minimally helpful in guiding preoperative assessment. Isolated observations also have some influence in risk assessment. Although any cardiac event is worthy of prevention, perioperative MI requires particular attention due to the high mortality, even compared with MI that occurs outside the hospital.14 The risk of subsequent surgery after successful coronary artery bypass grafting is greatly reduced,7,8,15 and may approach the risk found in patients without cardiac disease.16 Besides coronary artery disease, other cardiovascular diseases, such as uncontrolled hypertension,17 valvular heart disease,18 cardiomyopathy,19 and asymmetrical septal hypertrophy,20 correlate with increased risk of adverse perioperative cardiac events. Functional status and activity level of the patient correlate with cardiac risk. Those patients with good exercise capacity have low risk,21 whereas sedentary patients have significantly increased risk.22,23 Functional status is relatively easy to determine with the information collected by interviewing the patient and correlates well with maximum oxygen utilization24 and exercise capacity.25 The observation that perioperative myocardial ischemia (POMI) sometimes precipitates MI26 and increases perioperative cardiac risk has led to a variety of pharmacologic interventions designed to reduce POMI. Although nitroglycerin has a clear therapeutic role in the treatment of acute myocardial ischemia, administration before ischemia has not been shown to prevent POMI. Prophylactic use of calcium channel blockers does not decrease POMI27 and, indeed, may increase risk.28 In contrast, ␤-blockers have clearly demonstrated efficacy as protection for patients with cardiac disease who are undergoing noncardiac surgery. This finding has been shown in patients undergoing different surgical procedures,29 vascular patients,30 and orthopedic patients,31 and it may reduce events for up to 2 years after surgery.32 The wealth of new information led to the formation of an unprecedented consensus group, convened to create a uniform approach to presurgical preparation of patients with cardiac disease scheduled for noncardiac surgery. Unique elements of this group were the multidisciplinary structure (internists, cardiologists, surgeons, and anesthesiologists) and the agreement that crossed traditional specialty lines. The resulting guidelines, often referred to as American College of Cardiology/American Heart Association (ACC/AHA) guidelines because of the site of primary publication, have been widely adopted since publication in 1996.33 The guidelines take a step-wise approach to presurgical preparation that includes surgical factors, medical risk factors, and the functional status of the patient, and by the use of an algorithm, arriving at a 322

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uniform application. Surgical and medical risk factors are classified as low, intermediate, or high risk. Functional status is defined by oxygen utilization or metabolic-equivalents and the value specified for low, intermediate, or high activity levels. It specifically states that excellent functional status precludes further cardiac testing for the majority of surgical procedures. Uncontrolled hypertension, valvular heart disease (especially aortic stenosis), and cardiomyopathy are identified as factors that significantly increase risk and indicate functional studies. The role of prophylactic ␤-blockers is acknowledged, and the nonspecific role of anesthetic drugs and the benefit of excellent postoperative analgesia are emphasized. Although obvious, it is specifically stated that abnormal findings must be treated, although the options remain numerous. The choice of functional study is also unspecified. Although the result of widespread use of ACC/AHA guidelines has been a more uniform approach, there is also a perception of increased testing.12 Subsequent evaluation of the results of guidelines use has revealed a few observations. The medical risk assessment may be more sensitive to risk than the surgical issues, although the surgical risk may be more specific.34 The review of Lustik et al.35in this issue of the Journal of Clinical Anesthesia further challenges some of the elements of these guidelines, based on observed limitations of supporting evidence. Many of the studies did not use control groups, whereas others failed to use randomization, introducing investigator bias into the outcome. These authors correctly state that functional studies are designed to identify critical coronary stenosis, even though there is increasing evidence that many perioperative MIs result from coronary arteries with noncritical stenosis. Although interventional procedures and coronary artery bypass grafting reduce the risk of subsequent surgical procedures, many of the reports that identify reduced risk do not take into account the morbidity and mortality of the interventional procedures. Some procedures, such as angioplasty, may convert a stable state into an unstable one, if plaque activation causes unstable angina or if acute restenosis occurs. This is a dynamic issue, because the introduction of stenting has greatly reduced acute reocclusion, and the introduction of potent antiplatelet drugs (e.g., clopidogrel) have almost eliminated plaque activation. So it is once more obvious that a change will occur in our approach to preoperative optimization of patients with cardiac disease for noncardiac surgery. Lustik et al.35 have proposed an alternative to the ACC/AHA guidelines that they believe will reduce testing by focusing on functional status and beta-blockade. The consensus group has reconvened, and there likely will be revision of the ACC/ AHA guidelines this year. It is already clear that we will be increasing the use of beta-blockade,36 and for low and intermediate risk surgery, prophylactic beta-blockade may replace functional testing for some of our patients. Further information about functional status may also influence our choices in the future, as may the use of other classes of drugs, such as angiotensin-converting enzyme inhibitors, to reduce perioperative risk.

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