He K, Zhao H, Zhou H C
Jinan Central Hospital , China.
Jinan Seventh People's Hospital , China.
Ann R Coll Surg Engl. 2016 Jul;98(6):358-66. doi: 10.1308/rcsann.2016.0152. Epub 2016 May 3.
Introduction Shivering is one of the most frequent complications of operation during the postanaesthesia period. Ondansetron has been proved to be valid in preventing postanaesthesia shivering (PAS) in several studies. However, its efficiency and safety are still disputable. We therefore performed an updated meta-analysis of randomised controlled trials (RCTs) for evaluation and to clarify this issue. Methods A literature search using the PubMed, Embase™ and Cochrane Library databases was performed (from inception to January 2015). RCTs that evaluated the efficiency and safety of ondansetron in the prevention of PAS were included in the meta-analysis. The primary outcome measure was incidence of PAS, and secondary outcomes included subgroup analysis and the side effects of ondansetron. Results A total of 8 RCTs containing 905 subjects were identified as suitable for this review. Compared with placebo, ondansetron was associated with a significant reduction of PAS (relative risk [RR]: 0.33, 95% confidence interval [CI]: 0.19-0.58, p=0.0001) while no difference was detected between ondansetron and pethidine (RR: 0.89, 95% CI: 0.41-1.94, p=0.78). There was no significant difference between ondansetron and placebo or pethidine in terms of risk of bradycardia but ondansetron was associated with a lower risk of hypotension (RR: 0.26, 95% CI: 0.08-0.79, p=0.020) than placebo. There was no difference in hypotension when ondansetron was compared with pethidine. Conclusions Ondansetron can prevent PAS effectively and reduce the risk of hypotension.
寒战是麻醉后时期手术最常见的并发症之一。在多项研究中,昂丹司琼已被证明在预防麻醉后寒战(PAS)方面有效。然而,其有效性和安全性仍存在争议。因此,我们进行了一项更新的随机对照试验(RCT)的荟萃分析,以评估并阐明这个问题。
使用PubMed、Embase™和Cochrane图书馆数据库进行文献检索(从数据库建立至2015年1月)。评估昂丹司琼预防PAS有效性和安全性的RCT被纳入荟萃分析。主要结局指标是PAS的发生率,次要结局包括亚组分析和昂丹司琼的副作用。
共确定8项RCT(包含905名受试者)适合本综述。与安慰剂相比,昂丹司琼可显著降低PAS的发生率(相对危险度[RR]:0.33,95%置信区间[CI]:0.19 - 0.58,p = 0.0001),而昂丹司琼与哌替啶之间未检测到差异(RR:0.89,95% CI:0.41 - 1.94,p = 0.78)。昂丹司琼与安慰剂或哌替啶在心动过缓风险方面无显著差异,但与安慰剂相比,昂丹司琼发生低血压的风险较低(RR:0.26,95% CI:0.08 - 0.79,p = 0.020)。昂丹司琼与哌替啶相比,低血压发生率无差异。
昂丹司琼可有效预防PAS并降低低血压风险。