引产的机械方法。
Mechanical methods for induction of labour.
作者信息
Boulvain M, Kelly A, Lohse C, Stan C, Irion O
机构信息
Unité de Développement en Obstétrique, Maternité Hôpitaux Universitaires de Genève, Département de Gynécologie et d'Obstétrique, Boulevard de la Cluse, 32, Geneva 14, Switzerland, CH-1211.
出版信息
Cochrane Database Syst Rev. 2001(4):CD001233. doi: 10.1002/14651858.CD001233.
BACKGROUND
Mechanical methods were the first methods developed to ripen the cervix or to induce labour. Devices which were used include various type of catheters and of laminaria tents, introduced into the cervical canal or into the extra-amniotic space. Mechanical methods were never completely abandoned, but were substituted by pharmacological methods during recent decades. Potential advantages of mechanical methods, compared with pharmacological methods, may include simplicity of preservation, lower cost and reduction of the side effects. However, special attention should be paid to contraindications (e.g. low-lying placenta), risk of infection and maternal discomfort when inserting these devices. This is one of a series of reviews of methods of cervical ripening and labour induction using standardised methodology.
OBJECTIVES
To determine the effects of mechanical methods for third trimester cervical ripening or induction of labour in comparison with placebo/no treatment, prostaglandins (vaginal, intracervical, misoprostol) and oxytocin.
SEARCH STRATEGY
The Cochrane Pregnancy and Childbirth Group Trials Register, the Cochrane Controlled Trials Register and bibliographies of relevant papers. Last searched April 2001.
SELECTION CRITERIA
The criteria for inclusion were the following: (1) clinical trials comparing mechanical methods used for third trimester cervical ripening or labour induction with placebo/no treatment or other methods listed above it on a predefined list of labour induction methods; (2) random allocation to the treatment or control group; (3) adequate or unclear method for allocation concealment; (4) violations of allocated management not sufficient to materially affect conclusions; (5) clinically meaningful outcome measures reported; (6) data available for analysis according to the random allocation; (7) missing data insufficient to materially affect the conclusions.
DATA COLLECTION AND ANALYSIS
A strategy has been developed to deal with the large volume and complexity of trial data relating to labour induction. This involved a two-stage method of data extraction. The initial data extraction was done centrally, and incorporated into a series of primary reviews arranged by methods of induction of labour, following a standardised methodology. The data will be extracted from the primary reviews into a series of secondary reviews, arranged by category of woman.
MAIN RESULTS
In total, 58 studies were considered; 45 studies have been included and 13 were excluded. Studies generally included women with unfavourable cervix and intact membranes. Comparing mechanical methods with placebo/no treatment, only one study with 48 participants reported on vaginal delivery not achieved in 24 hours (69% with mechanical methods versus 77% with placebo/no treatment; relative risk (RR) 0.90; 95% confidence interval (CI): 0.64-1.26). Hyperstimulation with fetal heart rate changes was not reported. The risk of caesarean section, reported in six studies including 416 women, was similar between groups (34%; RR 1.00; 95% CI: 0.76-1.30). There were no reported cases of severe neonatal and maternal morbidity. Comparing mechanical methods with vaginal PGE2, only one trial (109 women) reported on vaginal delivery not achieved in 24 hours (73% versus 42%; relative risk (RR) 1.74; 95% CI: 1.21-2.49). Compared with intracervical PGE2, only one trial (100 women) reported on vaginal delivery not achieved in 24 hours (68% versus 40%; relative risk (RR) 1.70; 95% CI: 1.15-2.51). Compared with with misoprostol, the effectiveness of mechanical methods was similar (34% versus 30%; relative risk (RR) 1.15; 95% CI: 0.80-1.66). The use of mechanical method reduced the risk of hyperstimulation with fetal heart rate changes when compared with prostaglandins: vaginal PGE2 (0% versus 6%; RR 0.14; 95% CI: 0.04-0.53), intracervical PGE2 (0% versus 1%; RR 0.21; 95% CI: 0.04-1.20) and misoprostol (4% versus 9%; RR 0.41; 95% CI: 0.20-0.87). There was no difference in the risk of caesarean section between mechanical methods and prostaglandins. Serious neonatal (three cases) and maternal morbidity (one case) were infrequently reported. When compared with oxytocin, use of mechanical methods reduced the risk of caesarean section (4 trials; 198 women; 17% versus 32%; RR 0.55; 95% CI: 0.33-0.91). The likelihood of vaginal delivery in 24 hours and of hyperstimulation with fetal heart rate changes was not reported. There were no reported cases of serious maternal morbidity and severe neonatal morbidity was not reported. These results are similar whatever specific mechanical method was used, except with extra-amniotic infusion. When comparing extra-amniotic infusion with any prostaglandins, women were more likely to not achieve vaginal delivery within 24 hours (57% versus 42%; RR 1.33; 95% CI: 1.02-1.75), the risk of caesarean section was increased (31% versus 22%; RR 1.48; 95% CI: 1.14-1.90), without a reduction of the risk of hyperstimulation.
REVIEWER'S CONCLUSIONS: There is insufficient evidence to evaluate the effectiveness, in terms of likelihood of vaginal delivery in 24 hours, of mechanical methods compared with placebo/no treatment or with prostaglandins. The risk of hyperstimulation was reduced when compared with prostaglandins (intracervical, intravaginal or misoprostol). Compared to oxytocin in women with unfavourable cervix, mechanical methods reduce the risk of caesarean section. There is no evidence to support the use of extra-amniotic infusion.
背景
机械方法是最早用于宫颈成熟或引产的方法。所使用的器械包括各种类型的导管和海藻棒,将其插入宫颈管或羊膜外间隙。机械方法从未被完全摒弃,但在最近几十年被药物方法所取代。与药物方法相比,机械方法的潜在优势可能包括保存简单、成本较低以及副作用减少。然而,在插入这些器械时,应特别注意禁忌症(如前置胎盘)、感染风险和产妇不适。这是一系列使用标准化方法对宫颈成熟和引产方法进行综述之一。
目的
确定与安慰剂/不治疗、前列腺素(阴道、宫颈内、米索前列醇)和缩宫素相比,机械方法用于孕晚期宫颈成熟或引产的效果。
检索策略
考克兰妊娠与分娩组试验注册库、考克兰对照试验注册库以及相关论文的参考文献。最近一次检索时间为2001年4月。
入选标准
入选标准如下:(1)临床试验将用于孕晚期宫颈成熟或引产的机械方法与安慰剂/不治疗或预先定义的引产方法列表中上述其他方法进行比较;(2)随机分配至治疗组或对照组;(3)分配隐藏方法充分或不明确;(4)违反分配管理不足以实质性影响结论;(5)报告了具有临床意义的结局指标;(6)可根据随机分配进行数据分析;(7)缺失数据不足以实质性影响结论。
数据收集与分析
已制定一项策略来处理与引产相关的大量且复杂的试验数据。这涉及两阶段的数据提取方法。初始数据提取在中心进行,并按照标准化方法纳入一系列按引产方法排列的主要综述中。数据将从主要综述中提取到一系列按女性类别排列的次要综述中。
主要结果
总共考虑了58项研究;纳入45项研究,排除13项。研究通常纳入宫颈条件不佳且胎膜完整的女性。将机械方法与安慰剂/不治疗进行比较,仅有一项纳入48名参与者的研究报告了24小时内未实现阴道分娩的情况(机械方法组为69% vs安慰剂/不治疗组为77%;相对风险(RR)0.90;95%置信区间(CI):0.64 - 1.26)。未报告伴有胎儿心率变化的子宫过度刺激情况。在包括416名女性的六项研究中报告的剖宫产风险,两组相似(34%;RR 1.00;95% CI:0.76 -