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高危非心脏手术患者全身麻醉中添加一氧化二氮的安全性(ENIGMA-II):一项随机、单盲试验。

The safety of addition of nitrous oxide to general anaesthesia in at-risk patients having major non-cardiac surgery (ENIGMA-II): a randomised, single-blind trial.

出版信息

Lancet. 2014 Oct 18;384(9952):1446-54. doi: 10.1016/S0140-6736(14)60893-X.

Abstract

BACKGROUND

Nitrous oxide is commonly used in general anaesthesia but concerns exist that it might increase perioperative cardiovascular risk. We aimed to gather evidence to establish whether nitrous oxide affects perioperative cardiovascular risk.

METHODS

We did an international, randomised, assessor-blinded trial in patients aged at least 45 years with known or suspected coronary artery disease having major non-cardiac surgery. Patients were randomly assigned via automated telephone service, stratified by site, to receive a general anaesthetic with or without nitrous oxide. Attending anaesthetists were aware of patients' group assignments, but patients and assessors were not. The primary outcome measure was a composite of death and cardiovascular complications (non-fatal myocardial infarction, stroke, pulmonary embolism, or cardiac arrest) within 30 days of surgery. Our modified intention-to-treat population included all patients randomly assigned to groups and undergoing induction of general anaesthesia for surgery. This trial is registered at ClinicalTrials.gov, number NCT00430989.

FINDINGS

Of 10,102 eligible patients, we enrolled 7112 patients between May 30, 2008, and Sept 28, 2013. 3543 were assigned to receive nitrous oxide and 3569 were assigned not to receive nitrous oxide. 3483 patients receiving nitrous oxide and 3509 not receiving nitrous oxide were assessed for the primary outcome. The primary outcome occurred in 283 (8%) patients receiving nitrous oxide and in 296 (8%) patients not receiving nitrous oxide (relative risk 0·96, 95% CI 0·83–1·12; p=0·64). Surgical site infection occurred in 321 (9%) patients assigned to nitrous oxide, and in 311 (9%) patients in the no-nitrous oxide group (p=0·61), and severe nausea and vomiting occurred in 506 patients (15%) assigned to nitrous oxide and 378 patients (11%) not assigned to nitrous oxide (p<0·0001).

INTERPRETATION

Our findings support the safety profile of nitrous oxide use in major non-cardiac surgery. Nitrous oxide did not increase the risk of death and cardiovascular complications or surgical-site infection, the emetogenic effect of nitrous oxide can be controlled with antiemetic prophylaxis, and a desired effect of reduced volatile agent use was shown.

FUNDING

Australian National Health and Medical Research Council; Australian and New Zealand College of Anaesthetists; Heart and Stroke Foundation of Quebec, Heart and Stroke Foundation of Ontario, Canada; General Research Fund of the Research Grant Council, Hong Kong Special Administrative Region, China.

摘要

背景

氧化亚氮通常用于全身麻醉,但人们担心它可能会增加围手术期心血管风险。我们旨在收集证据,以确定氧化亚氮是否会影响围手术期心血管风险。

方法

我们在年龄至少为 45 岁、患有已知或疑似冠状动脉疾病并接受非心脏大手术的患者中进行了一项国际性、随机、评估者设盲试验。患者通过自动电话服务按组分配,按部位分层,接受含有或不含有氧化亚氮的全身麻醉。主治麻醉师了解患者的分组情况,但患者和评估者不知情。主要终点是手术 30 天内死亡和心血管并发症(非致命性心肌梗死、中风、肺栓塞或心脏骤停)的综合指标。我们的修改意向治疗人群包括所有随机分配到组并接受全身麻醉诱导以进行手术的患者。该试验在 ClinicalTrials.gov 注册,编号为 NCT00430989。

结果

在 10102 名合格患者中,我们于 2008 年 5 月 30 日至 2013 年 9 月 28 日期间招募了 7112 名患者。3543 名患者被分配接受氧化亚氮,3569 名患者被分配不接受氧化亚氮。3483 名接受氧化亚氮的患者和 3509 名不接受氧化亚氮的患者被评估主要结局。接受氧化亚氮的 283 名(8%)患者和不接受氧化亚氮的 296 名(8%)患者发生了主要结局(相对风险 0.96,95%CI 0.83-1.12;p=0.64)。接受氧化亚氮的 321 名(9%)患者和不接受氧化亚氮的 311 名(9%)患者发生手术部位感染(p=0.61),接受氧化亚氮的 506 名(15%)患者和不接受氧化亚氮的 378 名(11%)患者发生严重恶心和呕吐(p<0.0001)。

解释

我们的研究结果支持氧化亚氮在非心脏大手术中的安全性。氧化亚氮并未增加死亡和心血管并发症或手术部位感染的风险,可以通过止吐预防来控制氧化亚氮的致吐作用,并且显示出减少挥发性麻醉剂使用的预期效果。

资金来源

澳大利亚国家卫生和医学研究委员会;澳大利亚和新西兰麻醉师学院;魁北克心脏和中风基金会,安大略省心脏和中风基金会,加拿大;中国香港特别行政区研究资助局的一般研究基金。

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