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刺激腕部穴位内关预防术后恶心呕吐:一项网状Meta分析。

Stimulation of the wrist acupuncture point PC6 for preventing postoperative nausea and vomiting: a network meta-analysis.

作者信息

Lee Anna, Zhang Jack Zhenhe, Xie Jing, Cheng Vesa, Wong Man Kin Henry, Yau Derek King Wai

机构信息

Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Shatin, Hong Kong.

Centre for Biostatistics and Clinical Trials (BaCT), Peter MacCallum Cancer Centre, Melbourne, Australia.

出版信息

Cochrane Database Syst Rev. 2025 Sep 12;9(9):CD003281. doi: 10.1002/14651858.CD003281.pub5.

Abstract

RATIONALE

Postoperative nausea and vomiting (PONV) are common complications following surgery and anaesthesia. Antiemetic drugs are only partially effective in preventing PONV. Stimulating the PC6 acupoint(s) on the wrist offers an alternative approach, but the effectiveness of the various common techniques is unclear.

OBJECTIVES

To update and compare the effects and safety of PC6 acupoint stimulation with or without antiemetic drug(s) versus sham or antiemetic drug(s) for preventing postoperative nausea (PON) and postoperative vomiting (POV) in people undergoing surgery, and to identify the most effective techniques using network meta-analyses (NMAs).

SEARCH METHODS

We searched CENTRAL, MEDLINE, Embase, ISI Web of Science, CINAHL, WHO Global Index Medicus, major trial registries, and reference lists of articles for studies up to 6 June 2025, with no language restrictions.

ELIGIBILITY CRITERIA

Parallel randomised controlled trials of techniques that compared any combinations of PC6 acupoint stimulation, drug therapy, and sham for preventing PONV in children and adults were eligible. Interventions included invasive techniques (e.g. needle acupuncture) and noninvasive techniques (e.g. acupressure wristbands). Drug therapy included antiemetics that belonged to one of the following substance classes: 5-HT receptor antagonists, D receptor antagonists, corticosteroids, and antihistamines. The sham group included sham PC6 interventions and/or placebo saline antiemetic interventions.

OUTCOMES

Critical outcomes: incidence of PON and POV. Important outcomes: need for rescue antiemetic therapy when prophylaxis failed and adverse events (side effects).

RISK OF BIAS

We assessed the risk of bias in the included studies using RoB 1.

SYNTHESIS METHODS

We performed frequentist NMAs using random-effects models to report risk ratios (RRs) with 95% confidence intervals (95% CIs). We compared the relative effects (with sham as reference) of six broad classes of PC6 acupoint stimulation techniques and their combined use with antiemetic drugs on the outcomes. We summarised the safety data narratively due to heterogeneous reporting of adverse events (side effects). We assessed the certainty of evidence of the NMA treatment effect on outcomes according to the CINeMA and GRADE approaches.

INCLUDED STUDIES

This update included 77 trials, conducted between 1986 and 2022, involving 9847 participants. The majority were adults across several countries (USA, South Korea, India, China, Turkey, and Iran). There were 58 (33.9%) sham groups, 16 (9.4%) invasive PC6 acupoint stimulation groups, 50 (29.3%) noninvasive PC6 acupoint stimulation groups, 32 (18.7%) antiemetic(s) groups, 4 (2.3%) combined invasive PC6 acupoint stimulation and antiemetic(s) groups, 10 (5.8%) combined noninvasive PC6 acupoint stimulation and antiemetic(s) groups, and one (0.6%) combined invasive and noninvasive PC6 acupoint stimulation group for the NMAs. The high risk of bias was primarily due to selective reporting.

SYNTHESIS OF RESULTS

Postoperative nausea The evidence from the NMA (63 studies; 7534 participants) suggests that the combined invasive PC6 and antiemetics technique probably results in a larger reduction in PON than sham (RR 0.21, 95% CI 0.10 to 0.45; moderate confidence from indirect evidence only). The evidence also suggests that invasive PC6, noninvasive PC6, and antiemetic(s) may reduce PON, compared to sham (invasive PC6: RR 0.49, 95% CI 0.38 to 0.64, low confidence; noninvasive PC6: RR 0.67, 95% CI 0.58 to 0.76, low confidence; antiemetic(s): RR 0.73, 95% CI 0.59 to 0.91, very low confidence). The combined use of noninvasive PC6 and antiemetic(s) may reduce PON, compared to sham, based on indirect evidence (RR 0.65, 95% CI 0.45 to 0.96; low confidence). Postoperative vomiting The evidence from the NMA (75 studies; 8627 participants) suggests that the combined invasive PC6 and antiemetics technique may result in a moderate reduction in POV, compared to sham (RR 0.37, 95% CI 0.18 to 0.76; low confidence from indirect evidence only). The evidence also suggests that invasive PC6, noninvasive PC6, antiemetic(s), and combined noninvasive PC6 and antiemetic(s) may reduce POV, compared to sham (invasive PC6: RR 0.47, 95% CI 0.34 to 0.64, low confidence; noninvasive PC6: RR 0.58, 95% CI 0.49 to 0.70, low confidence; antiemetic(s): RR 0.62, 95% CI 0.47 to 0.81, very low confidence; combined noninvasive PC6 and antiemetic(s): RR 0.52, 95% CI 0.33 to 0.83, very low confidence). The combined use of noninvasive PC6 and invasive PC6 may result in little to no difference in POV, compared to sham, based on direct evidence (RR 1.02, 95% CI 0.43 to 2.44; low confidence). Need for rescue antiemetic drug(s) The evidence from the NMA (55 studies; 6614 participants) suggests that combined use of noninvasive PC6 and antiemetic(s) probably reduces the need for rescue antiemetic drug(s) when prophylactic techniques fail, compared to sham (RR 0.44, 95% CI 0.28 to 0.70; moderate confidence from indirect evidence). Antiemetic(s), noninvasive PC6, and invasive PC6 may reduce the need for rescue antiemetics, compared to sham (antiemetic(s): RR 0.56, 95% CI 0.40 to 0.80, very low confidence; noninvasive PC6: RR 0.60, 95% CI 0.51 to 0.70, low confidence; invasive PC6: RR 0.61, 95% CI 0.44 to 0.84, low confidence). The combined use of invasive PC6 and antiemetic(s) (RR 0.31, 95% CI 0.04 to 2.49; low confidence from indirect evidence only) and the combined use of noninvasive PC6 and invasive PC6 may result in little or no difference in the need for rescue antiemetic drug(s), compared to sham (RR 1.41, 95% CI 0.64 to 3.09; low confidence from direct evidence only). Adverse events (side effects) None of the included studies reported serious or long-term complications. Thirty-nine studies, involving 5334 participants, reported minor side effects that go away (e.g. skin irritation, redness, and swelling) with PC6 acupoint stimulation, but the evidence is very uncertain. Publication bias was not apparent in the NMA funnel plots.

AUTHORS' CONCLUSIONS: NMAs suggest that both invasive and noninvasive PC6 acupoint stimulation combined with antiemetics may reduce PON and POV, compared to sham, and likely lower rescue antiemetic use. PC6 acupoint stimulation may cause minor side effects, but the evidence is very uncertain.

FUNDING

This updated Cochrane review was partially funded by the Cochrane Complementary Medicine Field Bursary 2020 from the National Center for Complementary and Alternative Medicine, National Institutes of Health (Grant Number R24 AT001293).

REGISTRATION

Protocol (2001): doi.org/10.1002/14651858.CD003281 Original review (2004): doi.org/10.1002/14651858.CD003281.pub2 Update review (2009): doi.org/10.1002/14651858.CD003281.pub3 Update review (2015): doi.org/10.1002/14651858.CD003281.pub4.

摘要

原理

术后恶心呕吐(PONV)是手术和麻醉后常见的并发症。止吐药物在预防PONV方面仅部分有效。刺激手腕上的内关穴(PC6)提供了另一种方法,但各种常见技术的有效性尚不清楚。

目的

更新并比较使用或不使用止吐药物刺激PC6穴位与假刺激或止吐药物预防手术患者术后恶心(PON)和术后呕吐(POV)的效果和安全性,并使用网状Meta分析(NMA)确定最有效的技术。

检索方法

我们检索了截至2025年6月6日的CENTRAL、MEDLINE、Embase、ISI科学网、CINAHL、世界卫生组织全球医学索引、主要试验注册库以及文章的参考文献列表,无语言限制。

纳入标准

比较PC6穴位刺激、药物治疗和假刺激的任何组合预防儿童和成人PONV的平行随机对照试验符合要求。干预措施包括侵入性技术(如针刺)和非侵入性技术(如穴位按压腕带)。药物治疗包括属于以下物质类别之一的止吐药:5-羟色胺受体拮抗剂、多巴胺受体拮抗剂、皮质类固醇和抗组胺药。假手术组包括假PC6干预和/或安慰剂生理盐水止吐干预。

结局指标

关键结局指标:PON和POV的发生率。重要结局指标:预防失败时急救止吐治疗的需求和不良事件(副作用)。

偏倚风险

我们使用RoB 1评估纳入研究的偏倚风险。

合成方法

我们使用随机效应模型进行频率NMA,以报告风险比(RRs)及其95%置信区间(95% CIs)。我们比较了六类PC6穴位刺激技术及其与止吐药物联合使用对结局的相对效果(以假刺激为对照)。由于不良事件(副作用)报告的异质性,我们对安全性数据进行了叙述性总结。我们根据CINeMA和GRADE方法评估NMA治疗效果对结局的证据确定性。

纳入研究

本次更新纳入了1986年至2022年间进行的77项试验,涉及9847名参与者。大多数是来自多个国家(美国、韩国、印度、中国、土耳其和伊朗)的成年人。NMA中有58个(33.9%)假手术组、16个(9.4%)侵入性PC6穴位刺激组、50个(29.3%)非侵入性PC6穴位刺激组、32个(18.7%)止吐药组、4个(2.3%)侵入性PC6穴位刺激与止吐药联合组、10个(5.8%)非侵入性PC6穴位刺激与止吐药联合组以及1个(0.6%)侵入性和非侵入性PC6穴位刺激联合组。高偏倚风险主要归因于选择性报告。

结果合成

术后恶心:NMA(63项研究;7534名参与者)的证据表明,侵入性PC6与止吐药联合技术可能比假刺激更能降低PON(RR 0.21,95% CI 0.10至0.45;仅间接证据,中等置信度)。证据还表明,与假刺激相比,侵入性PC6、非侵入性PC6和止吐药可能降低PON(侵入性PC6:RR 0.49,95% CI 0.38至0.64,低置信度;非侵入性PC6:RR 0.67,95% CI 0.58至0.76,低置信度;止吐药:RR 0.73,95% CI 0.59至0.91,极低置信度)。基于间接证据,与假刺激相比,非侵入性PC6与止吐药联合使用可能降低PON(RR 0.65,95% CI 0.45至0.96;低置信度)。术后呕吐:NMA(75项研究;8627名参与者)的证据表明,与假刺激相比,侵入性PC6与止吐药联合技术可能适度降低POV(RR 0.37,95% CI 0.18至0.76;仅间接证据,低置信度)。证据还表明,与假刺激相比,侵入性PC6、非侵入性PC6、止吐药以及非侵入性PC6与止吐药联合使用可能降低POV(侵入性PC6:RR 0.47,95% CI 0.34至0.64,低置信度;非侵入性PC6:RR 0.58,95% CI 0.49至0.70,低置信度;止吐药:RR 0.62,95% CI 0.47至0.81,极低置信度;非侵入性PC与止吐药联合:RR 0.52,95% CI 0.33至0.83,极低置信度)。基于直接证据,与假刺激相比,非侵入性PC6与侵入性PC6联合使用在POV方面可能几乎没有差异(RR 1.02,95% CI 0.43至2.44;低置信度)。急救止吐药的需求:NMA(55项研究;6614名参与者)的证据表明,与假刺激相比,非侵入性PC6与止吐药联合使用在预防技术失败时可能减少急救止吐药的需求(RR 0.44,95% CI 0.28至0.70;间接证据,中等置信度)。与假刺激相比,止吐药、非侵入性PC6和侵入性PC6可能减少急救止吐药的需求(止吐药:RR 0.56,95% CI 0.40至0.,极低置信度;非侵入性PC6:RR 0.60,95% CI 0.51至0.70,低置信度;侵入性PC6:RR 0.61,95% CI 0.44至0.84,低置信度)。侵入性PC6与止吐药联合使用(RR 0.31,95% CI 0.04至2.49;仅间接证据,低置信度)以及非侵入性PC6与侵入性PC6联合使用在急救止吐药需求方面与假刺激相比可能几乎没有差异(RR 1.41,95% CI 0.64至3.09;仅直接证据,低置信度)。不良事件(副作用):纳入研究均未报告严重或长期并发症。39项研究,涉及5334名参与者,报告了PC6穴位刺激后会消失的轻微副作用(如皮肤刺激、发红和肿胀),但证据非常不确定。NMA漏斗图中未显示明显的发表偏倚。

作者结论

NMA表明,与假刺激相比,侵入性和非侵入性PC6穴位刺激联合止吐药可能降低PON和POV,并可能减少急救止吐药的使用。PC6穴位刺激可能会引起轻微副作用,但证据非常不确定。

资助

本更新版Cochrane系统评价部分由美国国立卫生研究院补充和替代医学国家中心的2020年Cochrane补充医学领域助学金资助(资助编号R24 AT001293)。

注册信息

方案(2001年):doi.org/10.1002/14651858.CD003281;原始评价(20~年):doi.org/10.1002/14651858.CD003281.pub2;更新评价(2009年):doi.org/10.1002/14651858.CD003281.pub3;更新评价(2015年):doi.org/10.1002/14651858.CD003281.pub4。

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