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

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Anna Lee, Jack Zhenhe Zhang, Jing Xie, Vesa Cheng, Man Kin Henry Wong, Derek King Wai Yau
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Stimulating the PC6 acupoint(s) on the wrist offers an alternative approach, but the effectiveness of the various common techniques is unclear.</p><p><strong>Objectives: </strong>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).</p><p><strong>Search methods: </strong>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.</p><p><strong>Eligibility criteria: </strong>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<sub>3</sub> receptor antagonists, D<sub>2</sub> receptor antagonists, corticosteroids, and antihistamines. The sham group included sham PC6 interventions and/or placebo saline antiemetic interventions.</p><p><strong>Outcomes: </strong>Critical outcomes: incidence of PON and POV. Important outcomes: need for rescue antiemetic therapy when prophylaxis failed and adverse events (side effects).</p><p><strong>Risk of bias: </strong>We assessed the risk of bias in the included studies using RoB 1.</p><p><strong>Synthesis methods: </strong>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.</p><p><strong>Included studies: </strong>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.</p><p><strong>Synthesis of results: </strong>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.</p><p><strong>Authors' conclusions: </strong>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. 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引用次数: 0

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-HT3 receptor antagonists, D2 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.

刺激腕穴PC6预防术后恶心呕吐:网络荟萃分析。
理由:术后恶心和呕吐(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PC6穴位提供了另一种方法,但各种常用技术的有效性尚不清楚。目的:更新和比较PC6穴位刺激加或不加止吐药物与假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,并利用网络荟萃分析(nma)确定最有效的技术。检索方法:我们检索了CENTRAL、MEDLINE、Embase、ISI Web of Science、CINAHL、WHO Global Index Medicus、主要试验注册库和截至2025年6月6日的研究文章参考文献列表,无语言限制。资格标准:比较PC6穴位刺激、药物治疗和假药预防儿童和成人PONV的任何组合的平行随机对照试验均符合资格。干预措施包括侵入性技术(如针刺)和非侵入性技术(如指压腕带)。药物治疗包括止吐药,属于以下物质类别之一:5-HT3受体拮抗剂、D2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:关键结局:PON和POV的发生率。重要结局:当预防失败时需要紧急止吐治疗和不良事件(副作用)。偏倚风险:我们使用RoB 1评估纳入研究的偏倚风险。综合方法:我们使用随机效应模型进行频率nma,以95%置信区间(95% ci)报告风险比(rr)。我们比较了六大类PC6穴位刺激技术及其与止吐药物联合使用的相对效果(以假药为参照)。由于不良事件(副作用)的异质报告,我们对安全性数据进行了叙述性总结。我们根据CINeMA和GRADE方法评估了NMA治疗效果对结果的证据确定性。纳入的研究: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。大多数是来自几个国家(美国、韩国、印度、中国、土耳其和伊朗)的成年人。假手术组58例(33.9%),有创PC6穴位刺激组16例(9.4%),无创PC6穴位刺激组50例(29.3%),止吐组32例(18.7%),有创PC6穴位刺激与止吐联合组4例(2.3%),无创PC6穴位刺激与止吐联合组10例(5.8%),有创与无创PC6穴位刺激联合组1例(0.6%)。高偏倚风险主要是由于选择性报道。来自NMA(63项研究,7534名参与者)的证据表明,联合侵入性PC6和止吐技术可能比假手术更能减少PON (RR 0.21, 95% CI 0.10至0.45;仅间接证据的中等可信度)。证据还表明,与假手术相比,有创PC6、无创PC6和止吐药可降低PON(有创PC6: RR 0.49, 95% CI 0.38至0.64,低置信度;无创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(RR 0.65, 95% CI 0.45 - 0.96,低置信度),与假手术相比,无创PC6和止吐药联合使用可减少PON。来自NMA(75项研究,8627名参与者)的证据表明,与假手术相比,联合侵入性PC6和止吐技术可能导致POV中度降低(RR 0.37, 95% CI 0.18至0.76;仅间接证据的低可信度)。证据还表明,与假手术相比,有创PC6、无创PC6、止吐剂和无创PC6联合止吐剂可降低POV(有创PC6: RR 0.47, 95% CI 0.34 ~ 0.64,低置信度;无创PC6: RR 0.58, 95% CI 0.49 ~ 0.70,低置信度;止吐剂:RR 0.62, 95% CI 0.47 ~ 0.81,极低置信度;无创PC6联合止吐剂:RR 0.52, 95% CI 0.33 ~ 0.83,非常低置信度)。直接证据表明,与假手术相比,非侵入性PC6和侵入性PC6联合使用可能导致POV几乎没有差异(RR 1.02, 95% CI 0.43至2.44;低置信度)。救急止吐药物的需求:来自NMA(55项研究,6614名参与者)的证据表明,与假手术相比,当预防性技术失败时,联合使用无创PC6和止吐药可能减少对救急止吐药物的需求(RR 0.44, 95% CI 0.28 ~ 0)。 70年;间接证据的中等可信度)。止吐药、无创PC6和有创PC6与假止吐药相比,可减少抢救止吐药的需要:RR 0.56, 95% CI 0.40 ~ 0.80,非常低置信度;无创PC6: RR 0.60, 95% CI 0.51 ~ 0.70,低置信度;侵袭性PC6: RR 0.61, 95% CI 0.44 ~ 0.84,低置信度)。联合使用有创PC6和止吐药(RR 0.31, 95% CI 0.04 - 2.49;仅间接证据可信度低)以及联合使用无创PC6和有创PC6可能导致与假手术相比,对抢救止吐药的需求很少或没有差异(RR 1.41, 95% CI 0.64 - 3.09;仅直接证据可信度低)。不良事件(副作用)纳入的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穴位刺激的轻微副作用(如皮肤刺激、红肿),但证据非常不确定。发表偏倚在NMA漏斗图中不明显。作者的结论是:nma提示,与假手术相比,有创和无创PC6穴位刺激联合止吐药可降低PON和POV,并可能降低抢救止吐药的使用。刺激PC6穴位可能会引起轻微的副作用,但证据非常不确定。资助:这篇更新的Cochrane综述部分由美国国立卫生研究院国家补充和替代医学中心的Cochrane补充医学领域奖学金2020资助(资助号R24 AT001293)。注册:议定书(2001):doi.org/10.1002/14651858.CD003281原始审查(2004):doi.org/10.1002/14651858.CD003281.pub2更新审查(2009):doi.org/10.1002/14651858.CD003281.pub3更新审查(2015):doi.org/10.1002/14651858.CD003281.pub4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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