右美托咪定在儿童扁桃体切除术中的应用:一项荟萃分析的系统综述。

IF 3.3 3区 医学 Q1 ANESTHESIOLOGY
Julia M Olsen, Makoto Sumie, Alan Yang, Marina Englesakis, Naoko Niimi, Paolo Campisi, Jason Hayes, William C K Ng, Jason T Maynes, Petros Pechlivanoglou, Kazuyoshi Aoyama
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引用次数: 0

摘要

目的:我们旨在评估静脉注射右美托咪定(DEX)对儿童扁桃体切除术患者围手术期阿片类药物需求的影响,以及对围手术期呼吸不良事件(PRAE)、出现性谵妄(ED)和术后恶心和呕吐的影响。方法:对截至2024年5月7日的7个数据库进行系统评价和meta分析。我们纳入了18岁或以下接受扁桃体切除术的患者的随机对照试验,比较静脉注射DEX和阿片类药物与阿片类药物。我们的主要结局是围手术期阿片类药物需求,以口服吗啡当量(OME)表示。次要结局包括围手术期呼吸不良事件(PRAE)、出现性谵妄(ED)和术后恶心和呕吐(PONV)的发生率。我们使用Cochrane风险偏倚2工具,并使用推荐评估、发展和评价分级(GRADE)来评估证据的确定性。我们使用两两随机效应模型,以95%置信区间(ci)计算DEX对各结局影响的风险比(rr)或平均差异(md)。为了探讨DEX的剂量依赖效应,我们使用随机效应元回归模型。结果:我们在系统综述中纳入了16项试验,其中我们分析了7项阿片类药物需求,4项PRAE, 3项ED和12项PONV。右美托咪定与较低的围手术期阿片类药物需求相关(MD, -0.25 mg·kg-1 OME;95% CI, -0.36 ~ -0.13;中度确定性),相当于围手术期OME相对降低40%,ED的可能性降低(RR, 0.24;95% CI, 0.08 ~ 0.71;温和的确定性)。尽管DEX对OME没有剂量依赖性,但DEX剂量每增加0.5µg·kg-1, ED的RR降低87%。右美托咪定没有降低持续或严重咳嗽作为PRAE的一部分的发生率,但它降低了PONV (RR, 0.48;95% CI, 0.35 ~ 0.66;i2 = 0%;低确定性)。结论:右美托咪定可能通过减少围手术期阿片类药物的需求和剂量依赖性地降低ED的发生率来改善扁桃体切除术儿童的围手术期。本系统综述的meta分析的局限性包括试验中PRAE的定义不一致,以及由于观察到的效应大小的可变性而存在异质性。研究注册:PROSPERO (CRD42023392579);首次提交于2023年7月1日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dexmedetomidine in pediatric tonsillectomy: a systematic review with meta-analysis.

Purpose: We aimed to evaluate the effects of intravenous dexmedetomidine (DEX) on perioperative opioid requirements, and secondarily on perioperative respiratory adverse events (PRAE), emergence delirium (ED), and postoperative nausea and vomiting in pediatric patients undergoing tonsillectomy.

Methods: We conducted a systematic review with meta-analysis, searching seven databases up to 7 May 2024. We included randomized controlled trials of patients aged 18 yr or younger undergoing tonsillectomy, comparing intravenous DEX and opioids with opioids. Our primary outcome was perioperative opioid requirements, expressed as oral morphine equivalents (OME). The secondary outcomes included the incidences of perioperative respiratory adverse events (PRAE), emergence delirium (ED), and postoperative nausea and vomiting (PONV), We used the Cochrane Risk of Bias 2 tool and assessed the certainty of the evidence with the Grading of Recommendations Assessment, Development, and Evaluation (GRADE). We used a pairwise random effects model to compute the risk ratios (RRs) or mean differences (MDs) with 95% confidence intervals (CIs) of the effects of DEX on each outcome. To explore dose-dependent effects of DEX, we used a random effects meta-regression model.

Results: We included 16 trials in our systematic review, of which we analyzed 7 for opioid requirements, 4 for PRAE, 3 for ED, and 12 for PONV. Dexmedetomidine was associated with lower perioperative opioid requirements (MD, -0.25 mg·kg-1 OME; 95% CI, -0.36 to -0.13; moderate certainty), equivalent to a 40% relative reduction of perioperative OME, and a lower likelihood of ED (RR, 0.24; 95% CI, 0.08 to 0.71; moderate certainty). Despite DEX not having a dose-dependent effect on OME, the RR of ED decreased 87% for each 0.5 µg·kg-1 increment in DEX dose. Dexmedetomidine did not reduce the incidence of sustained or severe cough as a part of PRAE, but it reduced PONV (RR, 0.48; 95% CI, 0.35 to 0.66; I2 = 0%; low certainty).

Conclusion: Dexmedetomidine may improve the perioperative course of children undergoing tonsillectomy by decreasing perioperative opioid requirements and dose-dependently lowering the incidence of ED. Limitations of the present systematic review with meta-analysis include an inconsistent definition of PRAE in trials and heterogeneity due to variability of observed effect sizes.

Study registration: PROSPERO ( CRD42023392579 ); first submitted 1 July 2023.

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来源期刊
CiteScore
8.50
自引率
7.10%
发文量
161
审稿时长
6-12 weeks
期刊介绍: The Canadian Journal of Anesthesia (the Journal) is owned by the Canadian Anesthesiologists’ Society and is published by Springer Science + Business Media, LLM (New York). From the first year of publication in 1954, the international exposure of the Journal has broadened considerably, with articles now received from over 50 countries. The Journal is published monthly, and has an impact Factor (mean journal citation frequency) of 2.127 (in 2012). Article types consist of invited editorials, reports of original investigations (clinical and basic sciences articles), case reports/case series, review articles, systematic reviews, accredited continuing professional development (CPD) modules, and Letters to the Editor. The editorial content, according to the mission statement, spans the fields of anesthesia, acute and chronic pain, perioperative medicine and critical care. In addition, the Journal publishes practice guidelines and standards articles relevant to clinicians. Articles are published either in English or in French, according to the language of submission.
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