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分娩过程中疼痛管理的催眠疗法。

Hypnosis for pain management during labour and childbirth.

作者信息

Madden Kelly, Middleton Philippa, Cyna Allan M, Matthewson Mandy, Jones Leanne

机构信息

St Helen's Private Hospital, 186 Macquarie Street, Hobart, Tasmania, Australia, 7000.

出版信息

Cochrane Database Syst Rev. 2016 May 19;2016(5):CD009356. doi: 10.1002/14651858.CD009356.pub3.

Abstract

BACKGROUND

This review is one in a series of Cochrane reviews investigating pain management for childbirth. These reviews all contribute to an overview of systematic reviews of pain management for women in labour, and share a generic protocol. This review updates an earlier version of the review of the same title.

OBJECTIVES

To examine the effectiveness and safety of hypnosis for pain management during labour and childbirth.

SEARCH METHODS

We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (30 September 2015) and the reference lists of primary studies and review articles.

SELECTION CRITERIA

Randomised controlled trials (RCTs) and quasi-RCTS comparing preparation for labour using hypnosis and/or use of hypnosis during labour, with or without concurrent use of pharmacological or non-pharmacological pain relief methods versus placebo, no treatment or any analgesic drug or technique.

DATA COLLECTION AND ANALYSIS

Two review authors independently extracted data and assessed trial quality. Where possible we contacted study authors seeking additional information about data and methodology.

MAIN RESULTS

We included nine trials randomising a total of 2954 women. The risk of bias in trials was variable, there were several well-designed large trials and some trials where little was reported about trial design. Although eight of the nine trials assessed antenatal hypnotherapy, there were considerable differences between these trials in timing and technique. One trial provided hypnotherapy during labour. In this updated review we compared hypnosis interventions with all control groups (main comparison) and also with specific control conditions: standard care (nine RCTs), supportive counselling (two RCTs) and relaxation training (two RCTs).In the main comparison, women in the hypnosis group were less likely to use pharmacological pain relief or analgesia than those in the control groups, (average risk ratio (RR) 0.73, 95% CI 0.57 to 0.94, eight studies, 2916 women; very low-quality evidence; random-effects model). There were no clear differences between women in the hypnosis group and those in the control groups for most of the other primary outcomes. There were no clear differences for sense of coping with labour (MD 0.22, 95% CI -0.14 to 0.58, one study, 420 women; low-quality evidence) or spontaneous vaginal birth (average RR 1.12, 95% CI 0.96 to 1.32, six studies, 2361 women; low-quality evidence; random-effects model). There were no clear differences for satisfaction with pain relief (measured on a seven-point scale two weeks postnatally) for women in the hypnosis group who also received pethidine (MD 0.41, 95% CI -0.45 to 1.27; one study, 72 women), Entonox (MD 0.19, 95% CI -0.19 to 0.57; one study, 357 women), self-hypnosis (MD 0.28, 95% CI -0.32 to 0.88; one study, 160 women), or epidural (MD -0.03, 95% CI -0.40 to 0.34; one study, 127 women), but a slight benefit in favour of hypnosis was seen for women who received water immersion (MD 0.52, 95% CI 0.04 to 1.00; one study, 174 women (all low-quality evidence). There were no clear differences for satisfaction with pain relief when it was measured as the number of women who reported they had adequate pain relief (risk ratio (RR) 1.06, 95% confidence interval (CI) 0.94 to 1.20, one study, 264 women; low-quality evidence). It should be noted that for pharmacological pain relief and spontaneous vaginal birth, there was evidence of considerable statistical heterogeneity, which could not be fully explained by subgroup analysis.For this review's secondary outcomes, no clear differences were found between women in the hypnosis group and women in the control groups for most outcomes where data were available. There was mixed evidence regarding benefits for women in the hypnosis group compared with all control groups for pain intensity, satisfaction with childbirth experience and postnatal depression. For each of these outcomes, data from more than one trial were available for analysis but could not be combined due to differences in measurement methods. There was evidence that fewer women in the hypnosis group stayed in hospital for more than two days after the birth but this finding was based on one small study (RR 0.11, 95% CI 0.02 to 0.83). No clear differences between women in the hypnosis group and the control groups were found for the other secondary outcomes where data were available.In the comparisons of hypnosis with specific types of control conditions: standard care, supportive counselling and relaxation training, there were no clear differences found between women in the hypnosis group and those in the standard care control groups or the relaxation control groups for the primary outcomes. Compared with the women in the supportive counselling control group, women in the hypnosis group were less likely to use pharmacological analgesia (average RR 0.48, 95% CI 0.32 to 0.73, two studies, 562 women). They were also more likely to have a spontaneous vaginal birth (RR 2.42, 95% CI 1.43 to 4.07), although this finding was based on the results of one small study. Overall these new comparisons displayed much less statistical heterogeneity than the comparison including all control groups.

AUTHORS' CONCLUSIONS: There are still only a relatively small number of studies assessing the use of hypnosis for labour and childbirth. Hypnosis may reduce the overall use of analgesia during labour, but not epidural use. No clear differences were found between women in the hypnosis group and those in the control groups for satisfaction with pain relief, sense of coping with labour or spontaneous vaginal birth. Not enough evidence currently exists regarding satisfaction with pain relief or sense of coping with labour and we would encourage any future research to prioritise the measurement of these outcomes. The evidence for the main comparison was assessed using GRADE as being of low quality for all the primary outcomes with downgrading decisions due to concerns regarding inconsistency of the evidence, limitations in design and imprecision. Further research is needed in the form of large, well-designed randomised controlled trials to assess whether hypnosis is of value for pain management during labour and childbirth.

摘要

背景

本综述是Cochrane关于分娩疼痛管理系列综述之一。这些综述均有助于对分娩期妇女疼痛管理的系统评价进行概述,并共享通用方案。本综述更新了同一标题的早期版本。

目的

探讨催眠用于分娩期疼痛管理的有效性和安全性。

检索方法

我们检索了Cochrane妊娠与分娩组试验注册库(2015年9月30日)以及原始研究和综述文章的参考文献列表。

选择标准

随机对照试验(RCT)和半随机对照试验,比较使用催眠进行分娩准备和/或分娩期间使用催眠,无论是否同时使用药物或非药物镇痛方法,与安慰剂、不治疗或任何镇痛药物或技术。

数据收集与分析

两名综述作者独立提取数据并评估试验质量。如有可能,我们联系研究作者以获取有关数据和方法的更多信息。

主要结果

我们纳入了9项试验,共随机分配2954名妇女。试验中的偏倚风险各不相同,有几项设计良好的大型试验,也有一些试验对试验设计的报告很少。虽然9项试验中有8项评估了产前催眠疗法,但这些试验在时间安排和技术上存在很大差异。一项试验在分娩期间提供催眠疗法。在本次更新的综述中,我们将催眠干预与所有对照组(主要比较)以及特定对照条件进行了比较:标准护理(9项RCT)、支持性咨询(2项RCT)和放松训练(2项RCT)。在主要比较中,催眠组的妇女使用药物镇痛或止痛的可能性低于对照组(平均风险比(RR)0.73,95%CI 0.57至0.94,8项研究,2916名妇女;极低质量证据;随机效应模型)。在大多数其他主要结局方面,催眠组妇女与对照组妇女之间没有明显差异。在应对分娩的感觉方面没有明显差异(MD 0.22,95%CI -0.14至0.58,1项研究,420名妇女;低质量证据)或自然阴道分娩方面(平均RR 1.12,95%CI 0.96至1.32,6项研究,2361名妇女;低质量证据;随机效应模型)。对于同时接受哌替啶治疗的催眠组妇女,产后两周对疼痛缓解的满意度没有明显差异(MD 0.41,95%CI -0.45至1.27;1项研究,72名妇女)、接受恩托诺克斯治疗的妇女(MD 0.19,95%CI -0.19至0.57;1项研究,357名妇女)、自我催眠的妇女(MD 0.28,95%CI -0.32至0.88;1项研究,160名妇女)或接受硬膜外麻醉的妇女(MD -0.03,95%CI -0.40至0.34;1项研究,127名妇女),但对于接受水浸浴的妇女,发现有利于催眠的轻微益处(MD 0.52,95%CI 0.04至1.00;1项研究,174名妇女(均为低质量证据)。当以报告疼痛缓解充分的妇女数量来衡量疼痛缓解满意度时,没有明显差异(风险比(RR)1.06,95%置信区间(CI)0.94至1.20,1项研究,264名妇女;低质量证据)。应该注意的是,对于药物镇痛和自然阴道分娩,有证据表明存在相当大的统计异质性,亚组分析无法完全解释。对于本综述的次要结局,在大多数可获得数据的结局方面,催眠组妇女与对照组妇女之间没有明显差异。与所有对照组相比,催眠组妇女在疼痛强度、对分娩经历的满意度和产后抑郁方面的益处证据不一。对于这些结局中的每一个,有多个试验的数据可供分析,但由于测量方法的差异无法合并。有证据表明,催眠组中在产后住院超过两天的妇女较少,但这一发现基于一项小型研究(RR 0.11,95%CI 0.02至0.83)。在可获得数据的其他次要结局方面,催眠组妇女与对照组妇女之间没有明显差异。在催眠与特定类型对照条件(标准护理、支持性咨询和放松训练)的比较中,催眠组妇女与标准护理对照组或放松对照组妇女在主要结局方面没有明显差异。与支持性咨询对照组的妇女相比,催眠组的妇女使用药物镇痛的可能性较小(平均RR 0.48,95%CI 0.32至0.73,2项研究,562名妇女)。她们自然阴道分娩的可能性也更大(RR 2.42,95%CI 1.43至4.07),尽管这一发现基于一项小型研究的结果。总体而言,这些新的比较显示的统计异质性远低于包括所有对照组的比较。

作者结论

目前评估催眠用于分娩的研究仍然相对较少。催眠可能会减少分娩期间镇痛药物的总体使用,但不会减少硬膜外麻醉的使用。在疼痛缓解满意度、应对分娩的感觉或自然阴道分娩方面,催眠组妇女与对照组妇女之间没有明显差异。目前关于疼痛缓解满意度或应对分娩的感觉没有足够的证据,我们鼓励未来的任何研究优先测量这些结局。主要比较的证据使用GRADE评估,由于证据不一致、设计局限性和不精确性等问题,所有主要结局的证据质量均为低质量。需要以大型、设计良好的随机对照试验的形式进行进一步研究,以评估催眠对分娩期疼痛管理是否有价值。

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