Abstract

We evaluated whether volatile anesthetics can improve the postoperative outcomes of non-cardiac surgery in patients with preoperative myocardial injury defined by the cardiac troponin elevation. From January 2010 to June 2018, 1254 adult patients with preoperative myocardial injury underwent non-cardiac surgery under general anesthesia and were enrolled in this study. Patients were stratified into following two groups according to anesthetic agents; 115 (9.2%) patients whose anesthesia was induced and maintained with continuous infusion of propofol and remifentanil (TIVA group) and 1139 (90.8%) patients whose anesthesia was maintainted with volatile anesthetics (VOLATILE group). The primary outcome was 30-day mortality. To diminish the remifentanil effect, a further analysis was conducted after excluding the patients who received only volatile anesthetics without remifentanil infusion. In a propensity-score matched analysis, 30-day mortality was higher in the TIVA group than the VOLATILE group (17.0% vs. 9.1%; hazard ratio [HR] 2.60; 95% confidence interval [CI], 1.14–5.93; p = 0.02). In addition, the TIVA group showed higher 30-day mortality than the VOLATILE group, even after eliminating the effect of remifentanil infusion (15.8% vs. 8.3%; HR 4.62; 95% CI, 1.82–11.74; p = 0.001). In our study, the use of volatile anesthetics showed the significant survival improvement after non-cardiac surgery in patients with preoperative myocardial injury, which appears to be irrelevant to the remifentanil use. Further studies are needed to confirm this beneficial effect of volatile anesthetics.Clinical trial number and registry URL: KCT0004349 (www.cris.nih.go.kr)

Highlights

  • Cardioprotective effect of volatile anesthetics has been proven in numerous studies [1,2,3,4]

  • The aim of our study was to evaluate whether volatile anesthetics can improve 30-day mortality following non-cardiac surgery in patients with preoperative myocardial injury defined by the cardiac troponin elevation

  • According to the anesthetics used during anesthetic maintenance, the enrolled patients were grouped as follows: the TIVA group (n = 115), defined as the patients whose anesthesia was induced and maintained with continuous infusion of propofol and remifentanil without using a volatile anesthetic agent and the VOLATILE group (n = 1139), defined as the patients whose anesthesia was maintained with volatile anesthetics regardless of induction agents

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Summary

Introduction

Cardioprotective effect of volatile anesthetics has been proven in numerous studies [1,2,3,4]. The use of volatile anesthetics has been recommended to reduce postoperative mortality in patients undergoing major non-cardiac and cardiac surgeries [5,6,7]. A leading cause of postoperative mortality in non-cardiac surgery is myocardial injury [9], which was defined as the evidence of elevated cardiac troponin values with at least one value above the 99th percentile upper reference limit [9,10]. As well as postoperative myocardial injury, preoperative cardiac troponin elevation has been reported to be strongly associated with postoperative mortality in patients undergoing non-cardiac surgery [11,12,13]. Since volatile anesthetics can reduce myocardial infarct size and cardiac biomarkers [1], the use of volatile anesthetics might be effective to improve clinical outcomes after non-cardiac surgery, especially in patients with preoperative elevation of cardiac troponin

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