Horey Dell, Kealy Michelle, Davey Mary-Ann, Small Rhonda, Crowther Caroline A
Faculty of Health Sciences, La Trobe University, Bundoora, Australia.
Cochrane Database Syst Rev. 2013 Jul 30;2013(7):CD010041. doi: 10.1002/14651858.CD010041.pub2.
Pregnant women who have previously had a caesarean birth and who have no contraindication for vaginal birth after caesarean (VBAC) may need to decide whether to choose between a repeat caesarean birth or to commence labour with the intention of achieving a VBAC. Women need information about their options and interventions designed to support decision-making may be helpful. Decision support interventions can be implemented independently, or shared with health professionals during clinical encounters or used in mediated social encounters with others, such as telephone decision coaching services. Decision support interventions can include decision aids, one-on-one counselling, group information or support sessions and decision protocols or algorithms. This review considers any decision support intervention for pregnant women making birth choices after a previous caesarean birth.
To examine the effectiveness of interventions to support decision-making about vaginal birth after a caesarean birth.Secondary objectives are to identify issues related to the acceptability of any interventions to parents and the feasibility of their implementation.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (30 June 2013), Current Controlled Trials (22 July 2013), the WHO International Clinical Trials Registry Platform Search Portal (ICTRP) (22 July 2013) and reference lists of retrieved articles. We also conducted citation searches of included studies to identify possible concurrent qualitative studies.
All published, unpublished, and ongoing randomised controlled trials (RCTs) and quasi-randomised trials with reported data of any intervention designed to support pregnant women who have previously had a caesarean birth make decisions about their options for birth. Studies using a cluster-randomised design were eligible for inclusion but none were identified. Studies using a cross-over design were not eligible for inclusion. Studies published in abstract form only would have been eligible for inclusion if data were able to be extracted.
Two review authors independently applied the selection criteria and carried out data extraction and quality assessment of studies. Data were checked for accuracy. We contacted authors of included trials for additional information. All included interventions were classified as independent, shared or mediated decision supports. Consensus was obtained for classifications. Verification of the final list of included studies was undertaken by three review authors.
Three randomised controlled trials involving 2270 women from high-income countries were eligible for inclusion in the review. Outcomes were reported for 1280 infants in one study. The interventions assessed in the trials were designed to be used either independently by women or mediated through the involvement of independent support. No studies looked at shared decision supports, that is, interventions designed to facilitate shared decision-making with health professionals during clinical encounters.We found no difference in planned mode of birth: VBAC (risk ratio (RR) 1.03, 95% confidence interval (CI) 0.97 to 1.10; I² = 0%) or caesarean birth (RR 0.96, 95% CI 0.84 to 1.10; I² = 0%). The proportion of women unsure about preference did not change (RR 0.87, 95% CI 0.62 to 1.20; I² = 0%).There was no difference in adverse outcomes reported between intervention and control groups (one trial, 1275 women/1280 babies): permanent (RR 0.66, 95% CI 0.32 to 1.36); severe (RR 1.02, 95% CI 0.77 to 1.36); unclear (0.66, 95% CI 0.27, 1.61). Overall, 64.8% of those indicating preference for VBAC achieved it, while 97.1% of those planning caesarean birth achieved this mode of birth. We found no difference in the proportion of women achieving congruence between preferred and actual mode of birth (RR 1.02, 95% CI 0.96 to 1.07) (three trials, 1921 women).More women had caesarean births (57.3%), including 535 women where it was unplanned (42.6% all caesarean deliveries and 24.4% all births). We found no difference in actual mode of birth between groups, (average RR 0.97, 95% CI 0.89 to 1.06) (three trials, 2190 women).Decisional conflict about preferred mode of birth was lower (less uncertainty) for women with decisional support (standardised mean difference (SMD) -0.25, 95% CI -0.47 to -0.02; two trials, 787 women; I² = 48%). There was also a significant increase in knowledge among women with decision support compared with those in the control group (SMD 0.74, 95% CI 0.46 to 1.03; two trials, 787 women; I² = 65%). However, there was considerable heterogeneity between the two studies contributing to this outcome ( I² = 65%) and attrition was greater than 15 per cent and the evidence for this outcome is considered to be moderate quality only. There was no difference in satisfaction between women with decision support and those without it (SMD 0.06, 95% CI -0.09 to 0.20; two trials, 797 women; I² = 0%). No study assessed decisional regret or whether women's information needs were met.Qualitative data gathered in interviews with women and health professionals provided information about acceptability of the decision support and its feasibility of implementation. While women liked the decision support there was concern among health professionals about their impact on their time and workload.
AUTHORS' CONCLUSIONS: Evidence is limited to independent and mediated decision supports. Research is needed on shared decision support interventions for women considering mode of birth in a pregnancy after a caesarean birth to use with their care providers.
既往有剖宫产史且无剖宫产术后阴道分娩(VBAC)禁忌证的孕妇,可能需要决定是选择再次剖宫产还是尝试引产以实现VBAC。孕妇需要了解她们的选择,旨在支持决策制定的干预措施可能会有所帮助。决策支持干预措施可以独立实施,或在临床会诊时与卫生专业人员共同实施,或用于与他人的中介性社会交流中,如电话决策指导服务。决策支持干预措施可包括决策辅助工具、一对一咨询、小组信息或支持会议以及决策方案或算法。本综述考虑了针对既往有剖宫产史的孕妇做出分娩选择的任何决策支持干预措施。
研究支持剖宫产术后阴道分娩决策的干预措施的有效性。次要目的是确定与任何干预措施对父母的可接受性以及实施可行性相关的问题。
我们检索了Cochrane妊娠与分娩组试验注册库(2013年6月30日)、当前对照试验(2013年7月22日)、世界卫生组织国际临床试验注册平台搜索门户(ICTRP)(2013年7月22日)以及检索文章的参考文献列表。我们还对纳入研究进行了引文检索,以识别可能同时进行的定性研究。
所有已发表、未发表和正在进行的随机对照试验(RCT)以及半随机试验,只要报告了任何旨在支持既往有剖宫产史的孕妇做出分娩选择的干预措施的数据。采用整群随机设计的研究符合纳入标准,但未找到此类研究。采用交叉设计的研究不符合纳入标准。仅以摘要形式发表的研究,如果能够提取数据则符合纳入标准。
两位综述作者独立应用选择标准,并对研究进行数据提取和质量评估。检查数据的准确性。我们联系了纳入试验的作者以获取更多信息。所有纳入的干预措施分为独立、共同或中介决策支持。分类达成了共识。由三位综述作者对纳入研究的最终列表进行了核实。
三项涉及来自高收入国家2270名女性的随机对照试验符合纳入本综述的标准。一项研究报告了1280名婴儿的结局。试验中评估的干预措施旨在供女性独立使用或通过独立支持的参与进行中介。没有研究关注共同决策支持,即旨在促进在临床会诊期间与卫生专业人员共同决策的干预措施。我们发现计划分娩方式没有差异:VBAC(风险比(RR)1.03,95%置信区间(CI)0.97至1.10;I² = 0%)或剖宫产(RR 0.96,95% CI 0.84至1.10;I² = 0%)。不确定偏好的女性比例没有变化(RR 0.87,95% CI 0.62至1.20;I² = 0%)。干预组和对照组报告的不良结局没有差异(一项试验,1275名女性/1280名婴儿):永久性(RR 0.66,95% CI 0.32至1.36);严重(RR 1.02,95% CI 0.77至1.36);不明确(0.66,95% CI 0.27,1.61)。总体而言,表示偏好VBAC的女性中有64.8%实现了这一目标,而计划剖宫产的女性中有97.1%实现了这种分娩方式。我们发现女性在首选分娩方式与实际分娩方式之间达成一致的比例没有差异(RR 1.02,95% CI 0.96至1.07)(三项试验,1921名女性)。更多女性进行了剖宫产(57.3%),其中535名女性是计划外剖宫产(占所有剖宫产分娩的42.6%,占所有分娩的24.4%)。我们发现两组之间的实际分娩方式没有差异(平均RR 0.97,95% CI 0.89至1.06)(三项试验,2190名女性)。有决策支持的女性在首选分娩方式上的决策冲突较低(不确定性较小)(标准化均值差(SMD)-0.25,95% CI -0.47至-0.02;两项试验,787名女性;I² = 48%)。与对照组相比,有决策支持的女性的知识也有显著增加(SMD 0.74,95% CI 0.46至1.03;两项试验,787名女性;I² = 65%)。然而,促成这一结果的两项研究之间存在相当大的异质性(I² = 65%),失访率大于15%,这一结果的证据仅被认为是中等质量。有决策支持的女性与没有决策支持的女性之间的满意度没有差异(SMD 0.06,95% CI -0.09至0.20;两项试验,797名女性;I² = 0%)。没有研究评估决策后悔或女性的信息需求是否得到满足。对女性和卫生专业人员进行访谈收集的定性数据提供了有关决策支持的可接受性及其实施可行性的信息。虽然女性喜欢决策支持,但卫生专业人员担心其对他们的时间和工作量的影响。
证据仅限于独立和中介决策支持。对于考虑剖宫产术后妊娠分娩方式的女性与她们的护理提供者一起使用的共同决策支持干预措施,需要进行研究。