Remote Ischemic Preconditioning and Outcomes of Cardiac Surgery

被引:560
作者
Hausenloy, D. J. [1 ,2 ,11 ,12 ]
Candilio, L. [1 ]
Evans, R. [3 ]
Ariti, C. [4 ]
Jenkins, D. P. [10 ]
Kolvekar, S. [5 ]
Knight, R. [3 ]
Kunst, G. [6 ,7 ]
Laing, C. [8 ]
Nicholas, J. [3 ]
Pepper, J. [9 ]
Robertson, S. [3 ]
Xenou, M. [1 ]
Clayton, T. [3 ]
Yellon, D. M. [1 ,2 ]
机构
[1] UCL, Hatter Cardiovasc Inst, London WC1E 6HX, England
[2] Univ Coll London Hosp, Biomed Res Ctr, Natl Inst Hlth Res, London, England
[3] London Sch Hyg & Trop Med, Clin Trials Unit, London, England
[4] Nuffield Trust, London, England
[5] Univ Coll London Hosp, Heart Hosp, London, England
[6] Kings Coll London, London WC2R 2LS, England
[7] Kings Coll Hosp London, London, England
[8] Royal Free Hosp, London, England
[9] Royal Brompton & Harefield NHS Trust, Natl Inst Hlth Res, Cardiovasc Biomed Res Unit, London, England
[10] Papworth Hosp, Cambridge CB3 8RE, England
[11] Natl Heart Ctr Singapore, Natl Heart Res Inst, Singapore, Singapore
[12] Duke Natl Univ Singapore, Cardiovasc & Metab Disorders Program, Singapore, Singapore
基金
英国医学研究理事会;
关键词
BYPASS GRAFT-SURGERY; PERCUTANEOUS CORONARY INTERVENTION; CONTROLLED CLINICAL-TRIAL; ARTERY-DISEASE; METAANALYSIS; INJURY; CARDIOPROTECTION; MYOCARDIUM; ISOFLURANE; IMPROVE;
D O I
10.1056/NEJMoa1413534
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Whether remote ischemic preconditioning (transient ischemia and reperfusion of the arm) can improve clinical outcomes in patients undergoing coronary-artery bypass graft (CABG) surgery is not known. We investigated this question in a randomized trial. METHODS We conducted a multicenter, sham-controlled trial involving adults at increased surgical risk who were undergoing on-pump CABG (with or without valve surgery) with blood cardioplegia. After anesthesia induction and before surgical incision, patients were randomly assigned to remote ischemic preconditioning (four 5-minute inflations and deflations of a standard blood-pressure cuff on the upper arm) or sham conditioning (control group). Anesthetic management and perioperative care were not standardized. The combined primary end point was death from cardiovascular causes, nonfatal myocardial infarction, coronary revascularization, or stroke, assessed 12 months after randomization. RESULTS We enrolled a total of 1612 patients (811 in the control group and 801 in the ischemic-preconditioning group) at 30 cardiac surgery centers in the United Kingdom. There was no significant difference in the cumulative incidence of the primary end point at 12 months between the patients in the remote ischemic preconditioning group and those in the control group (212 patients [26.5%] and 225 patients [27.7%], respectively; hazard ratio with ischemic preconditioning, 0.95; 95% confidence interval, 0.79 to 1.15; P = 0.58). Furthermore, there were no significant between-group differences in either adverse events or the secondary end points of perioperative myocardial injury (assessed on the basis of the area under the curve for the high-sensitivity assay of serum troponin T at 72 hours), inotrope score (calculated from the maximum dose of the individual inotropic agents administered in the first 3 days after surgery), acute kidney injury, duration of stay in the intensive care unit and hospital, distance on the 6-minute walk test, and quality of life. CONCLUSIONS Remote ischemic preconditioning did not improve clinical outcomes in patients undergoing elective on-pump CABG with or without valve surgery.
引用
收藏
页码:1408 / 1417
页数:10
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