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Original Articles |
From the Division of Cardiology (S.G., G.P., E.O.M.), and Division of Cardiothoracic Surgery (H.B.W.), Minneapolis VA Medical Center and the University of Minnesota, Minneapolis, Minn.; the Cooperative Studies Program Coordinating Center (T.E.M., D.J.R.) and the Division of Peripheral Vascular Surgery (F.L.), VA Hospital, Hines, Ill.; Division of Cardiology Southern Arizona VA Healthcare System and the University of Arizona Sarver Heart Center (S.G.), Tucson, Ariz.; and Division of Cardiology, VA Medical Center (G.C.L.), Portland, Ore.
Correspondence to Edward O. McFalls, MD, PhD, Division of Cardiology (111C), VA Medical Center, 1 Veterans Drive, Minneapolis, MN 55417. E-mail mcfal00l{at}umn.edu
Received September 2, 2008; accepted December 9, 2008.
| Abstract |
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Methods and Results— The Coronary Artery Revascularization Prophylaxis Trial was a randomized, controlled trial that tested the long-term benefit of a preoperative coronary artery revascularization before elective vascular surgery. Using preoperative baseline characteristics to determine the RCRI, we tested the benefit of preoperative revascularization on death and nonfatal myocardial infarction in patients with multiple risks. Among 462 patients undergoing vascular surgery, there were 72 complications (15.6%) within 30 days postsurgery, including 15 deaths (3.2%) and 57 nonfatal myocardial infarctions (12.3%). The postoperative risk of death and nonfatal myocardial infarction after surgery increased according to the RCRI (odds ratio, 1.73; 95% CI, 1.26 to 2.38; P<0.001), with a rate of 1.6% in patients with no risk that increased to 23.4% in patients with
3 risks. Preoperative revascularization had no influence on the incidence of complications in any risk subset (odds ratio, 0.86; 95% CI, 0.50 to 1.49; P=0.60). Among those individuals with
2 risks who also demonstrated ischemia on a preoperative stress-imaging test (N=146), the incidence of events was 23% in patients with and without preoperative revascularization (P=0.95).
Conclusions— The risk of death and nonfatal myocardial infarction is accurately predicted by the RCRI in patients undergoing vascular surgery but is not reduced in any high-risk subset of the RCRI with preoperative coronary artery revascularization.
Key Words: peripheral arterial disease revascularization outcomes
| Introduction |
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Editorial see p 61
Clinical Perspective see p 73
| SUMMARY |
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| Methods |
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The study design has been previously described.7,8 In brief, patients undergoing vascular surgery were screened at 18 Veterans Affairs Medical Centers (March 1999 through February 2003) during the enrollment period for the randomization process. Patients were considered eligible for the study if they were scheduled for a vascular operation for either an expanding abdominal aortic aneurysm or arterial occlusive disease of the lower extremities. Inclusion criteria for cardiac risks were the presence of multiple accepted cardiac risks or, with indeterminate number of risks, an abnormal preoperative stress-imaging test.8,9 Patients were excluded from consideration of randomization if they required an urgent vascular operation or had a severe comorbidity. A baseline screening form was completed after randomization and included all clinical variables and baseline laboratory results. By study design, all randomized patients had undergone preoperative coronary angiography and had significant coronary artery disease (CAD) that was amenable to revascularization. The decision for preoperative coronary artery revascularization was randomly assigned. The revascularization strategy, either with coronary artery bypass grafting versus percutaneous coronary intervention, was left at the discretion of the local site. The trial was completed before use of drug-eluting stents. The RCRI was enumerated in each patient and included the following variables: a history of CAD (angina, prior MI, pathological q waves, or treated ventricular arrhythmias), history of cerebrovascular disease (prior stroke or transient ischemic attack), history of congestive heart failure, insulin-dependent diabetes mellitus, serum creatinine >2.0 mg/dL, and an abdominal operation.1 Only those vascular operations involving an intra-abdominal approach were considered high risk in the present cohort.
Of 510 patients who were randomized into the CARP Trial, 462 underwent their intended vascular operation and comprise the present cohort. Of the 258 patients assigned to revascularization, 225 (87%) underwent the planned vascular operation, as did 237 of the 252 patients (94%) assigned to no preoperative revascularization. Of the 33 patients assigned to revascularization who did not undergo vascular surgery, 18 declined the surgery, 10 died after uncomplicated coronary artery bypass grafting or percutaneous coronary intervention, and 5 developed a severe coexisting condition. Of the 15 patients assigned to no revascularization who did not undergo vascular surgery, 9 declined, 1 died after urgent coronary artery bypass grafting, and 6 developed a severe comorbid condition. The study end point was the composite of death and nonfatal MI within 30 days of vascular surgery. After surgery, blood for cardiac enzymes was collected and an ECG was performed each day for 4 days in all patients and assessed at local sites for the presence of a perioperative MI. A perioperative MI after vascular surgery was defined by an elevation of the locally measured cardiac enzymes above the normal reference value in association with a clinical correlate of myocardial ischemia.10 The specific cardiac biomarker was troponin I or T in 431 (93%) and creatine kinase (CK) MB-fraction mass in 31 (7%) patients. By study design, an end-point committee, independent of the CARP investigators, reviewed all source documents and confirmed the presence of all end points, including a perioperative MI.11 As part of this analysis, patients were grouped according to their RCRI without knowledge of their outcomes, and intergroup differences in complications were determined by logistic regression analyses and backward elimination. Odds ratio (OR) estimates and 95% CIs were obtained for risk variables in the model, including the impact of coronary artery revascularization and perioperative therapy on reduction of death and nonfatal MI in each group. Data are expressed as means and SDs and intergroup differences are considered significant at the P<0.05 level. The authors had full access to and take full responsibility for the integrity of the data. All authors have read and agree to the manuscript as written.
| Results |
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In the present cohort, the specific risks defined by the RCRI included abdominal surgery (N=274; 59%), history of ischemic heart disease (N=188; 41%), prior congestive heart failure (N=45; 10%), known cerebrovascular disease (N=93; 20%), insulin-dependent diabetes mellitus (N=90; 20%), and baseline creatinine >2.0 mg/dL (N=17; 4%). Of 462 patients undergoing their intended vascular operation, 231 (50%) had 2 or more cardiac risks and they had a higher prevalence of multivessel CAD, left ventricular dysfunction, diabetes mellitus, and renal failure (Table 1).
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3 risks (Figure). By logistic regression analysis, the RCRI was an independent predictor of the composite of death and nonfatal MI at 30 days (OR, 1.73; 95% CI, 1.26 to 2.38; P<0.001). Perioperative use of antiplatelet agents and β-blockers within 24 hours of vascular surgery was similar in all risk subsets.
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| Discussion |
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Clinical variables that comprise the RCRI include a history of ischemic heart disease, congestive heart failure, cerebrovascular disease, insulin-treated diabetes, creatinine >2.0 mg/dL, and need for a high-risk operation. In the derivation and validation of the index, complication rates in patients with 0, 1, 2, or
3 RCRI variables were 0.4%, 1%, 7%, and 11%.1 Application of this risk index may be an important means of selecting patients at intermediate risk who may benefit from additional preoperative testing, such as noninvasive stress-imaging tests.3,4 It also has utility in risk stratifying those patients who might benefit from perioperative β-blocker therapy.2 In the present cohort from the CARP Trial, the composite of death and nonfatal MI after vascular surgery was highly dependent on the RCRI obtained from baseline characteristics, as noted by the incremental complication rate from 1.6%, 13.0%, 20.4%, and 23.4% in patients with 0, 1, 2, or
3 RCRI variables. This demonstrates that the risk index is generalizeable to even those patients who have documented CAD who undergo vascular surgery, which is considered high risk.
According to the current ACC/AHA Guidelines on preoperative management, noncardiac surgical procedures with anticipated event rates
5% are considered to be high-risk operations.6 Current guidelines incorporate the RCRI into the stepwise approach to management of these patients with poor or unknown functional class (step 5). Under the assumption that the perioperative event rate is <5%, as might be assumed when the RCRI is
2, the recommendations are to proceed with noncardiac surgery without additional testing but with the option of administering tight heart-rate control.6 On the basis of the findings of our analysis of the CARP Trial, in which all patients had significant CAD and all underwent vascular surgery, a RCRI cutoff of
1 may be more appropriate to identify high-risk vascular patients (event rate >10%) who may benefit from intensive pharmacological therapy before their planned operation.
The principal new finding of our study is that none of the high-risk subsets defined by the RCRI demonstrated a benefit of coronary artery revascularization, including those individuals with multiple risks who had evidence of ischemia on preoperative stress imaging. These data support the findings of the main randomized trial that preoperative coronary artery revascularization does not improve long-term survival after vascular surgery.7 It also supports the findings from the DECREASE-V pilot study, in which a strategy of preoperative revascularization does not reduce the composite of death and nonfatal MI, even among patients with high-risk stress- imaging test results.12
Limitations
Certain limitations of the present analysis should be noted. It is possible that we have been overly conservative in estimating the RCRI, because only those patients with documented CAD defined by a history of cardiac events were given a risk score. In addition, although vascular surgery is considered a risk, we considered only those individuals who underwent an abdominal aortic operation as the highest risk. By excluding study patients that did not undergo their planned vascular operation, we might have underestimated the early mortality hazard associated with coronary revascularization, which was higher for patients assigned to a strategy of prophylactic revascularization. Patients included in this post hoc analysis were part of a randomized clinical trial and, therefore, were selected on the basis of predetermined inclusion and exclusion criteria.7,8 Because CARP was conducted at Veterans Affairs hospitals, the study cohort was predominantly male.
| Conclusions |
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| Acknowledgments |
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This work was supported by the Cooperative Studies Program of the Department of Veterans Affairs Office of Research and Development.
Disclosures
Dr Garcia is a recipient of the Society for Cardiac Angiography and Interventions/Cordis Fellowship Program Award. Dr Littooy has served as an expert witness in malpractice lawsuits involving vascular surgery cases. Dr Larsen has received research grants as part of the ACUITY and AIM HIGH trials. The remaining authors report no conflicts.
| References |
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7. McFalls E, Ward H, Moritz T, Goldman S, Krupski W, Littooy F, Pierpont G, Santilli S, Rapp J, Hattler B, Shunk K, Jaenicke C, Thottapurathu L, Ellis N, Reda D, Henderson W. Coronary artery revascularization before elective major vascular surgery. N Engl J Med. 2004; 351: 2795–2804.
8. McFalls E, Ward H, Krupski W, Goldman S, Littooy F, Eagle K, Nyman J, Moritz T, McNabb S, Henderson W. Prophylactic coronary artery revascularization for elective vascular surgery: study design. Control Clin Trials. 1999; 20: 297–308.[CrossRef][Medline]
9. Eagle K, Coley C, Newell J, Brewster D, Darling C, Strauss W, Guiney T, Boucher C. Combining clinical and thallium data optimizes preoperative assessment of cardiac risk before major vascular surgery. Ann Intern Med. 1989; 110: 859–866.
10. Thygesen K, Alpert J, White H. Universal definition of myocardial infarction. Circulation. 2007; 116: 2634–2653.
11. McFalls EO, Ward HB, Moritz TE, Apple FE, Goldman S, Pierpont G, Larsen GC, Hattler B, Shunk K, Littooy F, Santilli S, Thottapurathu L, Krupski W, Reda DJ, Henderson WG. Predictors and outcomes of a perioperative myocardial infarction following elective vascular surgery in patients with documented coronary artery disease: results of the CARP trial. Eur Heart J. 2008; 29: 394–401.
12. Poldermans D, Schouten O, Vidakovic R, Bax J, Thomson I, Hoeks S, Feringa H, Dunkelgrun M, de Jaegere P, Maat A, van Sambeek M, Kertai M, Boersma E; DECREASE Study Group. A clinical randomized trial to evaluate the safety of a noninvasive approach in high-risk patients undergoing major vascular surgery: the DECREASE-V Pilot Study. J Am Coll Cardiol. 2007; 49: 1763–1769.
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It is unclear whether preoperative coronary revascularization reduces postoperative cardiac complications in high-risk patients undergoing vascular surgery as defined by the Revised Cardiac Risk Index (RCRI). Using preoperative baseline characteristics to determine the RCRI, we validated the RCRI in patients undergoing vascular surgery and evaluated the benefit of preoperative revascularization on death and nonfatal myocardial infarction among patients with varying risk. The postoperative risk of death and nonfatal myocardial infarction after surgery increased according to the RCRI (odds ratio, 1.73; 95% CI, 1.26 to 2.38; P<0.001), with a rate of 1.6% in patients with no risk that increased to 23.4% in patients with
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