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Antioxidant treatment to reduce mortality and serious adverse events in adult surgical patients: A systematic review with meta‐analysis and trial sequential analysis

医学 安慰剂 荟萃分析 相对风险 随机对照试验 围手术期 临床试验 不利影响 子群分析 科克伦图书馆 出版偏见 内科学 外科 置信区间 病理 替代医学
作者
Sofie S. Pedersen,Maria Louise Fabritius,Emilie Katrine Kongebro,Christian S. Meyhoff
出处
期刊:Acta Anaesthesiologica Scandinavica [Wiley]
卷期号:65 (4): 438-450 被引量:7
标识
DOI:10.1111/aas.13752
摘要

Abstract Background Hyperoxia during anesthesia can increase cellular oxidative stress, and perioperative antioxidant treatment may reduce the resulting damage. The aim of this review was to evaluate risks and benefits of antioxidant treatment in surgical patients. We hypothesized that antioxidant treatment reduced mortality compared to placebo/no intervention. Methods This systematic review with meta‐analyses and trial sequential analysis (TSA) was conducted using Cochrane standards and GRADE methodology. Randomized clinical trials comparing perioperative antioxidant treatment vs. placebo/no intervention in adults were included. Primary outcome was mortality at longest follow‐up. Results Ninety‐seven trials with 8156 patients were included. The most common interventions were N‐Acetylcysteine (36 trials) and vitamin C (29 trials). Trials were primarily performed during cardiac surgery (53 trials). Fifty‐six trials with 4890 patients reported information on mortality (243 events). The meta‐analysis of mortality at longest follow‐up showed a reduced mortality in antioxidant treated patients (RR 0.74, 95% CI 0.59; 0.94, I 2 0%), however, TSA‐adjusted CI was broadened (0.55‐1.02) and only 31% of the required information size was reached. Furthermore, in the subgroup of three trials with overall low risk of bias the RR for mortality was 1.18 (95% CI 0.39, 3.63). Based on GRADE, our findings are of low quality of evidence due to high risk of bias, imprecision, and indirectness. Conclusion We found a 26% relative risk reduction of mortality in surgical patients treated with antioxidants but the quality of evidence supporting our findings is low and influenced by clinical heterogeneity and high risk of systematic‐ and random errors.

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