The role of remote ischemic preconditioning in organ protection after cardiac surgery: a meta-analysis

被引:21
|
作者
Yasin, Nur A. B. Haji Mohd [1 ]
Herbison, Peter [2 ]
Saxena, Pankaj [1 ,3 ,4 ,5 ]
Praporski, Slavica [5 ]
Konstantinov, Igor E. [5 ]
机构
[1] Univ Edinburgh, Coll Med & Vet Med, Edinburgh, Midlothian, Scotland
[2] Univ Otago, Dept Prevent & Social Med, Dunedin, New Zealand
[3] Univ Western Australia, Sch Surg, Perth, WA 6009, Australia
[4] Mayo Clin, Div Cardiovasc Surg, Rochester, MN USA
[5] Univ Melbourne, Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
关键词
Cardiac surgery; Coronary artery bypass surgery; Cardiopulmonary bypass; Renal failure; Congenital heart disease; BYPASS GRAFT-SURGERY; ACUTE KIDNEY INJURY; ACUTE-RENAL-FAILURE; CREATINE-KINASE MB; TROPONIN-I; MYOCARDIAL INJURY; CARDIOPULMONARY BYPASS; REPERFUSION INJURY; HEART-DISEASE; MORTALITY;
D O I
10.1016/j.jss.2013.09.006
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Remote ischemic preconditioning (RIPC) appears to protect distant organs from ischemia-reperfusion injury. We undertook meta-analysis of clinical studies to evaluate the effects of RIPC on organ protection and clinical outcomes in patients undergoing cardiac surgery. Methods: A review of evidence for cardiac, renal, and pulmonary protection after RIPC was performed. We also did meta-regressions on RIPC variables, such as duration of ischemia, cuff pressure, and timing of application of preconditioning. Secondary outcomes included length of hospital and intensive care unit stay, duration of mechanical ventilation, and mortality at 30 days. Results: Randomized control trials (n = 25) were included in the study for quantitative analysis of cardiac (n = 16), renal (n = 6), and pulmonary (n = 3) protection. RIPC provided statistically significant cardiac protection (standardized mean difference [SMD], -0.77; 95% confidence interval [CI], -1.15, -0.39; Z = 3.98; P < 0.0001) and on subgroup analysis, the protective effect remained consistent for all types of cardiac surgical procedures. However, there was no evidence of renal protection (SMD, 0.74; 95% CI, 0.53, 1.02; Z = 1.81; P = 0.07) or pulmonary protection (SMD, 0.03; 95% CI, 0.56, 0.50; Z = 0.12; P = 0.91). There was no statistical difference in the short-term clinical outcomes between the RIPC and control groups. Conclusions: RIPC provides cardiac protection, but there is no evidence of renal or pulmonary protection in patients undergoing cardiac surgery using cardiopulmonary bypass. Larger multicenter trials are required to define the role of RIPC in surgical practice. Crown Copyright (C) 2014 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:207 / 216
页数:10
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