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氯胺酮和艾司氯胺酮预防阿片类药物引起咳嗽的疗效和安全性:一项随机对照试验的系统评价和荟萃分析

Efficacy and safety of ketamine and esketamine for preventing opioid-induced cough: a systematic review and meta-analysis of randomized controlled trials.

作者信息

Hung Kuo-Chuan, Yu Ting-Sian, Hsu Chih-Wei, Liu Wei-Cheng, Wu Jheng-Yan, Liao Shu-Wei, Lin Chien-Ming, Chen I-Wen

机构信息

Department of Anesthesiology, Chi Mei Medical Center, Tainan City, Taiwan.

School of Medicine, College of Medicine, National Sun Yat-Sen University, Kaohsiung City, Taiwan.

出版信息

Syst Rev. 2025 Jul 1;14(1):131. doi: 10.1186/s13643-025-02886-0.

DOI:10.1186/s13643-025-02886-0
PMID:40598615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12211305/
Abstract

BACKGROUND

Opioid-induced cough (OIC) is a common side effect during anesthetic induction. This systematic review and meta-analysis aimed to evaluate the efficacy and safety of ketamine/esketamine in preventing OIC during anesthetic induction.

METHODS

We systematically searched Medline, Embase, Cochrane Library, and Google Scholar from inception through December 2024 for randomized controlled trials that examined the efficacy of ketamine/esketamine in preventing OIC (Registration: INPLASY2024120102). Studies were included if they: (1) evaluated surgical patients receiving short-acting opioids (e.g., fentanyl) during anesthetic induction; (2) compared ketamine or esketamine against placebo/no treatment; and (3) reported OIC incidence. Studies were assessed using the Cochrane Risk of Bias 2.0 tool. Random-effects meta-analysis was performed using risk ratios (RR) for dichotomous outcomes and mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI). The primary outcome was the overall incidence of OIC within 3 min after opioids administration.

RESULTS

Twelve trials involving ketamine (nine trials) and esketamine (three trials) were analyzed. Notably, both agents significantly reduced the overall incidence of OIC compared to placebo (RR: 0.30; 95% CI: 0.22-0.41; p < 0.00001, I = 61%, moderate certainty). All studies demonstrated low risk of bias across all domains for primary outcome. These agents also demonstrated efficacy against mild cough (RR: 0.41, 95% CI: 0.28-0.59, high certainty) and moderate-to-severe cough (RR: 0.26, 95% CI: 0.18-0.38, moderate certainty). The intervention delayed cough onset by 2.77 s (95% CI: 1.25-4.29, moderate certainty) and showed mild improvement in oxygen saturation (MD: 0.55%, 95% CI: 0.15-0.95, high certainty) without significant effects on heart rate or blood pressure. Subgroup analyses confirmed consistent benefits across adult and pediatric populations, as well as between ketamine and esketamine.

CONCLUSIONS

Our findings suggest that ketamine and esketamine are effective in reducing OIC during anesthetic induction. However, given the short delay in cough onset and mild improvements in oxygen saturation, the clinical significance of these findings may be limited in routine practice. Their use may be most beneficial in selected patients at risk of OIC-related complications. Further research is warranted to assess their value in high-risk populations and their role in combination prevention strategies.

摘要

背景

阿片类药物诱发的咳嗽(OIC)是麻醉诱导期间的常见副作用。本系统评价和荟萃分析旨在评估氯胺酮/艾氯胺酮在预防麻醉诱导期间OIC方面的疗效和安全性。

方法

我们系统检索了从创刊至2024年12月的Medline、Embase、Cochrane图书馆和谷歌学术,以查找检验氯胺酮/艾氯胺酮预防OIC疗效的随机对照试验(注册号:INPLASY2024120102)。纳入的研究需满足以下条件:(1)评估在麻醉诱导期间接受短效阿片类药物(如芬太尼)的手术患者;(2)将氯胺酮或艾氯胺酮与安慰剂/不治疗进行比较;(3)报告OIC发生率。使用Cochrane偏倚风险2.0工具对研究进行评估。采用随机效应荟萃分析,对二分结局使用风险比(RR),对连续结局使用平均差(MD),并给出95%置信区间(CI)。主要结局是阿片类药物给药后3分钟内OIC的总体发生率。

结果

分析了12项涉及氯胺酮(9项试验)和艾氯胺酮(3项试验)的试验。值得注意的是,与安慰剂相比,两种药物均显著降低了OIC的总体发生率(RR:0.30;95%CI:0.22 - 0.41;p < 0.00001,I = 61%,中等确定性)。所有研究在主要结局的所有领域均显示出低偏倚风险。这些药物对轻度咳嗽也有效(RR:0.41,95%CI:0.28 - 0.59,高确定性)和中重度咳嗽(RR:0.26,95%CI:0.18 - 0.38,中等确定性)。干预使咳嗽发作延迟了2.77秒(95%CI:1.25 - 4.29,中等确定性),并使氧饱和度有轻度改善(MD:0.55%,95%CI:0.15 - 0.95,高确定性),对心率或血压无显著影响。亚组分析证实了在成人和儿科人群以及氯胺酮和艾氯胺酮之间的一致益处。

结论

我们的研究结果表明,氯胺酮和艾氯胺酮在减少麻醉诱导期间的OIC方面是有效的。然而,鉴于咳嗽发作延迟时间短且氧饱和度改善轻微,这些发现的临床意义在常规实践中可能有限。它们的使用可能对有OIC相关并发症风险的特定患者最有益。有必要进一步研究以评估它们在高危人群中的价值及其在联合预防策略中的作用。

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