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用于预防剖宫产术接受区域麻醉的女性恶心和呕吐的干预措施。

Interventions for preventing nausea and vomiting in women undergoing regional anaesthesia for caesarean section.

机构信息

Department of Anaesthesia, Royal Women's Hospital, Parkville, Australia.

Cochrane Pregnancy and Childbirth Group, Department of Women's and Children's Health, University of Liverpool, Liverpool, UK.

出版信息

Cochrane Database Syst Rev. 2021 May 18;5(5):CD007579. doi: 10.1002/14651858.CD007579.pub3.

Abstract

BACKGROUND

Nausea and vomiting are distressing symptoms which are experienced commonly during caesarean section under regional anaesthesia and in the postoperative period.  OBJECTIVES: To assess the efficacy of pharmacological and non-pharmacological interventions versus placebo or no intervention given prophylactically to prevent nausea and vomiting in women undergoing regional anaesthesia for caesarean section.

SEARCH METHODS

For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform (ICTRP) (16 April 2020), and reference lists of retrieved studies.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) of studies and conference abstracts, and excluded quasi-RCTs and cross-over studies.

DATA COLLECTION AND ANALYSIS

Review authors independently assessed the studies for inclusion, assessed risk of bias and carried out data extraction. Our primary outcomes are intraoperative and postoperative nausea and vomiting. Data entry was checked. Two review authors independently assessed the certainty of the evidence using the GRADE approach.

MAIN RESULTS

Eighty-four studies (involving 10,990 women) met our inclusion criteria. Sixty-nine studies, involving 8928 women, contributed data. Most studies involved women undergoing elective caesarean section. Many studies were small with unclear risk of bias and sometimes few events. The overall certainty of the evidence assessed using GRADE was moderate to very low. 5-HT antagonists: We found intraoperative nausea may be reduced by 5-HT antagonists (average risk ratio (aRR) 0.55, 95% confidence interval (CI) 0.42 to 0.71, 12 studies, 1419 women, low-certainty evidence). There may be a reduction in intraoperative vomiting but the evidence is very uncertain (aRR 0.46, 95% CI 0.29 to 0.73, 11 studies, 1414 women, very low-certainty evidence). There is probably a reduction in postoperative nausea (aRR 0.40, 95% CI 0.30 to 0.54, 10 studies, 1340 women, moderate-certainty evidence), and these drugs may show a reduction in postoperative vomiting (aRR 0.47, 95% CI 0.31 to 0.69, 10 studies, 1450 women, low-certainty evidence). Dopamine antagonists: We found dopamine antagonists may reduce intraoperative nausea but the evidence is very uncertain (aRR 0.38, 95% CI 0.27 to 0.52, 15 studies, 1180 women, very low-certainty evidence). Dopamine antagonists may reduce intraoperative vomiting (aRR 0.41, 95% CI 0.28 to 0.60, 12 studies, 942 women, low-certainty evidence) and postoperative nausea (aRR 0.61, 95% CI 0.48 to 0.79, 7 studies, 601 women, low-certainty evidence). We are uncertain if dopamine antagonists reduce postoperative vomiting (aRR 0.63, 95% CI 0.44 to 0.92, 9 studies, 860 women, very low-certainty evidence). Corticosteroids (steroids): We are uncertain if intraoperative nausea is reduced by corticosteroids (aRR 0.56, 95% CI 0.37 to 0.83, 6 studies, 609 women, very low-certainty evidence) similarly for intraoperative vomiting (aRR 0.52, 95% CI 0.31 to 0.87, 6 studies, 609 women, very low-certainty evidence). Corticosteroids probably reduce postoperative nausea (aRR 0.59, 95% CI 0.49 to 0.73, 6 studies, 733 women, moderate-certainty evidence), and may reduce postoperative vomiting (aRR 0.68, 95% CI 0.49 to 0.95, 7 studies, 793 women, low-certainty evidence). Antihistamines: Antihistamines may have little to no effect on intraoperative nausea (RR 0.99, 95% CI 0.47 to 2.11, 1 study, 149 women, very low-certainty evidence) or intraoperative vomiting (no events in the one study of 149 women). Antihistamines may reduce postoperative nausea (aRR 0.44, 95% CI 0.30 to 0.64, 4 studies, 514 women, low-certainty evidence), however, we are uncertain whether antihistamines reduce postoperative vomiting (average RR 0.48, 95% CI 0.29 to 0.81, 3 studies, 333 women, very low-certainty evidence). Anticholinergics: Anticholinergics may reduce intraoperative nausea (aRR 0.67, 95% CI 0.51 to 0.87, 4 studies, 453 women, low-certainty evidence) but may have little to no effect on intraoperative vomiting (aRR 0.79, 95% CI 0.40 to 1.54, 4 studies; 453 women, very low-certainty evidence). No studies looked at anticholinergics in postoperative nausea, but they may reduce postoperative vomiting (aRR 0.55, 95% CI 0.41 to 0.74, 1 study, 161 women, low-certainty evidence). Sedatives: We found that sedatives probably reduce intraoperative nausea (aRR 0.65, 95% CI 0.51 to 0.82, 8 studies, 593 women, moderate-certainty evidence) and intraoperative vomiting (aRR 0.35, 95% CI 0.24 to 0.52, 8 studies, 593 women, moderate-certainty evidence). However, we are uncertain whether sedatives reduce postoperative nausea (aRR 0.25, 95% CI 0.09 to 0.71, 2 studies, 145 women, very low-certainty evidence) and they may reduce postoperative vomiting (aRR 0.09, 95% CI 0.03 to 0.28, 2 studies, 145 women, low-certainty evidence). Opioid antagonists: There were no studies assessing intraoperative nausea or vomiting. Opioid antagonists may result in little or no difference to the number of women having postoperative nausea (aRR 0.75, 95% CI 0.39 to 1.45, 1 study, 120 women, low-certainty evidence) or postoperative vomiting (aRR 1.25, 95% CI 0.35 to 4.43, 1 study, 120 women, low-certainty evidence). Acupressure: It is uncertain whether acupressure/acupuncture reduces intraoperative nausea (aRR 0.55, 95% CI 0.41 to 0.74, 9 studies, 1221 women, very low-certainty evidence). Acupressure may reduce intraoperative vomiting (aRR 0.52, 95% CI 0.33 to 0.80, 9 studies, 1221 women, low-certainty evidence) but it is uncertain whether it reduces postoperative nausea (aRR 0.46, 95% CI 0.27 to 0.75, 7 studies, 1069 women, very low-certainty evidence) or postoperative vomiting (aRR 0.52, 95% CI 0.34 to 0.79, 7 studies, 1069 women, very low-certainty evidence). Ginger: It is uncertain whether ginger makes any difference to the number of women having intraoperative nausea (aRR 0.66, 95% CI 0.36 to 1.21, 2 studies, 331 women, very low-certainty evidence), intraoperative vomiting (aRR 0.62, 95% CI 0.38 to 1.00, 2 studies, 331 women, very low-certainty evidence), postoperative nausea (aRR 0.63, 95% CI 0.22 to 1.77, 1 study, 92 women, very low-certainty evidence) and postoperative vomiting (aRR 0.20, 95% CI 0.02 to 1.65, 1 study, 92 women, very low-certainty evidence). Few studies assessed our secondary outcomes including adverse effects or women's views.

AUTHORS' CONCLUSIONS: This review indicates that 5-HT antagonists, dopamine antagonists, corticosteroids, sedatives and acupressure probably or possibly have efficacy in reducing nausea and vomiting in women undergoing regional anaesthesia for caesarean section. However the certainty of evidence varied widely and was generally low. Future research is needed to assess side effects of treatment, women's views and to compare the efficacy of combinations of different medications.

摘要

背景

在剖宫产术下进行区域麻醉以及术后期间,恶心和呕吐是令人痛苦的症状,经常发生。

目的

评估在接受区域麻醉行剖宫产术的妇女中,预防性使用药理学和非药理学干预措施与安慰剂或无干预相比,预防恶心和呕吐的疗效。

检索方法

本次更新,我们检索了 Cochrane 妊娠与分娩组试验注册库、ClinicalTrials.gov 和世卫组织国际临床试验注册平台(ICTRP)(2020 年 4 月 16 日),并查阅了纳入研究的参考文献。

纳入排除标准

我们纳入了随机对照试验(RCT)研究和会议摘要,排除了准随机对照试验和交叉研究。

数据收集与分析

综述作者独立评估研究纳入情况、评估偏倚风险并提取数据。我们的主要结局是术中及术后恶心和呕吐。数据录入经过了核对。两名综述作者使用 GRADE 方法独立评估证据的确定性。

主要结果

84 项研究(涉及 10990 名妇女)符合纳入标准。69 项研究,涉及 8928 名妇女,提供了数据。大多数研究涉及择期剖宫产的妇女。许多研究规模较小,偏倚风险不明确,有时事件较少。使用 GRADE 评估的证据总体确定性为中到极低。5-HT 拮抗剂:我们发现 5-HT 拮抗剂可能减少术中恶心(平均风险比(RR)0.55,95%置信区间(CI)0.42 至 0.71,12 项研究,1419 名妇女,低确定性证据)。可能减少术中呕吐,但证据非常不确定(RR 0.46,95%CI 0.29 至 0.73,11 项研究,1414 名妇女,极低确定性证据)。术后恶心可能减少(RR 0.40,95%CI 0.30 至 0.54,10 项研究,1340 名妇女,中等确定性证据),这些药物可能减少术后呕吐(RR 0.47,95%CI 0.31 至 0.69,10 项研究,1450 名妇女,低确定性证据)。多巴胺拮抗剂:我们发现多巴胺拮抗剂可能减少术中恶心,但证据非常不确定(RR 0.38,95%CI 0.27 至 0.52,15 项研究,1180 名妇女,极低确定性证据)。多巴胺拮抗剂可能减少术中呕吐(RR 0.41,95%CI 0.28 至 0.60,12 项研究,942 名妇女,低确定性证据)和术后恶心(RR 0.61,95%CI 0.48 至 0.79,7 项研究,601 名妇女,低确定性证据)。我们不确定多巴胺拮抗剂是否减少术后呕吐(RR 0.63,95%CI 0.44 至 0.92,9 项研究,860 名妇女,极低确定性证据)。皮质类固醇(类固醇):我们不确定皮质类固醇是否减少术中恶心(RR 0.56,95%CI 0.37 至 0.83,6 项研究,609 名妇女,极低确定性证据),同样也不确定术中呕吐(RR 0.52,95%CI 0.31 至 0.87,6 项研究,609 名妇女,极低确定性证据)。皮质类固醇可能减少术后恶心(RR 0.59,95%CI 0.49 至 0.73,6 项研究,733 名妇女,中等确定性证据),并可能减少术后呕吐(RR 0.68,95%CI 0.49 至 0.95,7 项研究,793 名妇女,低确定性证据)。抗组胺药:抗组胺药可能对术中恶心(RR 0.99,95%CI 0.47 至 2.11,1 项研究,149 名妇女,极低确定性证据)或术中呕吐(149 名妇女的一项研究中无事件发生)没有影响。抗组胺药可能减少术后恶心(RR 0.44,95%CI 0.30 至 0.64,4 项研究,514 名妇女,低确定性证据),但我们不确定抗组胺药是否减少术后呕吐(平均 RR 0.48,95%CI 0.29 至 0.81,3 项研究,333 名妇女,极低确定性证据)。抗胆碱能药:抗胆碱能药可能减少术中恶心(RR 0.67,95%CI 0.51 至 0.87,4 项研究,453 名妇女,低确定性证据),但可能对术中呕吐没有影响(RR 0.79,95%CI 0.40 至 1.54,4 项研究;453 名妇女,极低确定性证据)。没有研究观察抗胆碱能药对术后恶心的作用,但它们可能减少术后呕吐(RR 0.55,95%CI 0.41 至 0.74,1 项研究,161 名妇女,低确定性证据)。镇静剂:我们发现镇静剂可能减少术中恶心(RR 0.65,95%CI 0.51 至 0.82,8 项研究,593 名妇女,中等确定性证据)和术中呕吐(RR 0.35,95%CI 0.24 至 0.52,8 项研究,593 名妇女,中等确定性证据)。然而,我们不确定镇静剂是否减少术后恶心(RR 0.25,95%CI 0.09 至 0.71,2 项研究,145 名妇女,极低确定性证据),也可能减少术后呕吐(RR 0.09,95%CI 0.03 至 0.28,2 项研究,145 名妇女,低确定性证据)。阿片受体拮抗剂:没有研究评估术中恶心或呕吐。阿片受体拮抗剂可能对术后恶心或呕吐的发生没有差异(RR 0.75,95%CI 0.39 至 1.45,1 项研究,120 名妇女,低确定性证据)或术后呕吐(RR 1.25,95%CI 0.35 至 4.43,1 项研究,120 名妇女,低确定性证据)。穴位按压:目前尚不清楚穴位按压/针灸是否减少术中恶心(RR 0.55,95%CI 0.41 至 0.74,9 项研究,1221 名妇女,极低确定性证据)。穴位按压可能减少术中呕吐(RR 0.52,95%CI 0.33 至 0.80,9 项研究,1221 名妇女,低确定性证据),但不确定其是否减少术后恶心(RR 0.46,95%CI 0.27 至 0.75,7 项研究,1069 名妇女,极低确定性证据)或术后呕吐(RR 0.52,95%CI 0.34 至 0.79,7 项研究,1069 名妇女,极低确定性证据)。姜:目前尚不清楚姜是否对术中恶心(RR 0.66,95%CI 0.36 至 1.21,2 项研究,331 名妇女,极低确定性证据)、术中呕吐(RR 0.62,95%CI 0.38 至 1.00,2 项研究,331 名妇女,极低确定性证据)、术后恶心(RR 0.63,95%CI 0.22 至 1.77,1

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