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      Membrane sweeping for induction of labour

      systematic-review

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          Abstract

          Background

          Induction of labour involves stimulating uterine contractions artificially to promote the onset of labour. There are several pharmacological, surgical and mechanical methods used to induce labour. Membrane sweeping is a mechanical technique whereby a clinician inserts one or two fingers into the cervix and using a continuous circular sweeping motion detaches the inferior pole of the membranes from the lower uterine segment. This produces hormones that encourage effacement and dilatation potentially promoting labour. This review is an update to a review first published in 2005.

          Objectives

          To assess the effects and safety of membrane sweeping for induction of labour in women at or near term (≥ 36 weeks' gestation).

          Search methods

          We searched Cochrane Pregnancy and Childbirth’s Trials Register (25 February 2019), ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (25 February 2019), and reference lists of retrieved studies.

          Selection criteria

          Randomised and quasi‐randomised controlled trials comparing membrane sweeping used for third trimester cervical ripening or labour induction with placebo/no treatment or other methods listed on a predefined list of labour induction methods. Cluster‐randomised trials were eligible, but none were identified.

          Data collection and analysis

          Two review authors independently assessed studies for inclusion, risk of bias and extracted data. Data were checked for accuracy. Disagreements were resolved by discussion, or by including a third review author. The certainty of the evidence was assessed using the GRADE approach.

          Main results

          We included 44 studies (20 new to this update), reporting data for 6940 women and their infants. We used random‐effects throughout.

          Overall, the risk of bias was assessed as low or unclear risk in most domains across studies. Evidence certainty, assessed using GRADE, was found to be generally low, mainly due to study design, inconsistency and imprecision. Six studies (n = 1284) compared membrane sweeping with more than one intervention and were thus included in more than one comparison.

          No trials reported on the outcomes uterine hyperstimulation with/without fetal heart rate (FHR) change, uterine rupture or neonatal encephalopathy.

          Forty studies (6548 participants) compared membrane sweeping with no treatment/sham

          Women randomised to membrane sweeping may be more likely to experience:

          · spontaneous onset of labour (average risk ratio (aRR) 1.21, 95% confidence interval (CI) 1.08 to 1.34, 17 studies, 3170 participants, low‐certainty evidence).

          but less likely to experience:

          · induction (aRR 0.73, 95% CI 0.56 to 0.94, 16 studies, 3224 participants, low‐certainty evidence);

          There may be little to no difference between groups for:

          · caesareans (aRR 0.94, 95% CI 0.85 to 1.04, 32 studies, 5499 participants, moderate‐certainty evidence);

          · spontaneous vaginal birth (aRR 1.03, 95% CI 0.99 to 1.07, 26 studies, 4538 participants, moderate‐certainty evidence);

          · maternal death or serious morbidity (aRR 0.83, 95% CI 0.57 to 1.20, 17 studies, 2749 participants, low‐certainty evidence);

          · neonatal perinatal death or serious morbidity (aRR 0.83, 95% CI 0.59 to 1.17, 18 studies, 3696 participants, low‐certainty evidence).

          Four studies reported data for 480 women comparing membrane sweeping with vaginal/intracervical prostaglandins

          There may be little to no difference between groups for the outcomes:

          · spontaneous onset of labour (aRR, 1.24, 95% CI 0.98 to 1.57, 3 studies, 339 participants, low‐certainty evidence);

          · induction (aRR 0.90, 95% CI 0.56 to 1.45, 2 studies, 157 participants, low‐certainty evidence);

          · caesarean (aRR 0.69, 95% CI 0.44 to 1.09, 3 studies, 339 participants, low‐certainty evidence);

          · spontaneous vaginal birth (aRR 1.12, 95% CI 0.95 to 1.32, 2 studies, 252 participants, low‐certainty evidence);

          · maternal death or serious morbidity (aRR 0.93, 95% CI 0.27 to 3.21, 1 study, 87 participants, low‐certainty evidence);

          · neonatal perinatal death or serious morbidity (aRR 0.40, 95% CI 0.12 to 1.33, 2 studies, 269 participants, low‐certainty evidence).

          One study, reported data for 104 women, comparing membrane sweeping with intravenous oxytocin +/‐ amniotomy

          There may be little to no difference between groups for:

          · spontaneous onset of labour (aRR 1.32, 95% CI 88 to 1.96, 1 study, 69 participants, low‐certainty evidence);

          · induction (aRR 0.51, 95% CI 0.05 to 5.42, 1 study, 69 participants, low‐certainty evidence);

          · caesarean (aRR 0.69, 95% CI 0.12 to 3.85, 1 study, 69 participants, low‐certainty evidence);

          · maternal death or serious morbidity was reported on, but there were no events.

          Two studies providing data for 160 women compared membrane sweeping with vaginal/oral misoprostol

          There may be little to no difference between groups for:

          · caesareans (RR 0.82, 95% CI 0.31 to 2.17, 1 study, 96 participants, low‐certainty evidence).

          One study providing data for 355 women which compared once weekly membrane sweep with twice‐weekly membrane sweep and a sham procedure

          There may be little to no difference between groups for:

          · induction (RR 1.19, 95% CI 0.76 to 1.85, 1 study, 234 participants, low‐certainty);

          · caesareans (RR 0.93, 95% CI 0.60 to 1.46, 1 study, 234 participants, low‐certainty evidence);

          · spontaneous vaginal birth (RR 1.00, 95% CI 0.86 to 1.17, 1 study, 234 participants, moderate‐certainty evidence);

          · maternal death or serious maternal morbidity (RR 0.78, 95% CI 0.30 to 2.02, 1 study, 234 participants, low‐certainty evidence);

          · neonatal death or serious neonatal perinatal morbidity (RR 2.00, 95% CI 0.18 to 21.76, 1 study, 234 participants, low‐certainty evidence);

          We found no studies that compared membrane sweeping with amniotomy only or mechanical methods.

          Three studies, providing data for 675 women, reported that women indicated favourably on their experience of membrane sweeping with one study reporting that 88% (n = 312) of women questioned in the postnatal period would choose membrane sweeping in the next pregnancy.

          Two studies reporting data for 290 women reported that membrane sweeping is more cost‐effective than using prostaglandins, although more research should be undertaken in this area.

          Authors' conclusions

          Membrane sweeping may be effective in achieving a spontaneous onset of labour, but the evidence for this was of low certainty. When compared to expectant management, it potentially reduces the incidence of formal induction of labour. Questions remain as to whether there is an optimal number of membrane sweeps and timings and gestation of these to facilitate induction of labour.

          Plain language summary

          Membrane sweeping for induction of labour

          What is the question?

          The aim of this Cochrane Review is to find out if membrane sweeping is a safe and effective way of inducing labour at or near term and if it is more effective than the formal methods of induction.

          Why is this important?

          Most commonly, formal induction of labour is offered to women when continuing with a pregnancy is considered probably more harmful for the mother or baby than the adverse effects of induction. The most common reason for formal induction of labour is post‐term pregnancy (pregnancies that continue past 42 weeks' gestation).

          Membrane sweeping is a relatively simple, low‐cost procedure that seeks to reduce the use of formal induction of labour and it can be performed without the need for hospitalisation. It involves the clinician inserting one or two fingers into the lower part of the uterus (the cervix) and using a continuous circular sweeping motion to free the membrane from the lower uterus. Formal induction of labour involves artificially stimulating the uterus with drugs such as prostaglandins or oxytocin or by breaking the amniotic sack that holds the baby (breaking the waters).

          What evidence did we find?

          We searched for evidence on 25 February 2019. We included 44 randomised studies that reported findings for 6940 women from a wide range of countries including high‐, middle‐ and low‐income countries.

          Studies compared membrane sweeping with no intervention or sham intervention, and also compared membrane sweeping with vaginal or intracervical prostaglandins, oral misoprostol, oxytocin and repeated membrane sweeping.

          Of the seven studies that reported financial funding, two studies reported funding from pharmaceutical companies. Overall, the certainty of the evidence was found to be low.

          Key results

          Compared with no intervention or a sham sweep (40 studies involving 6548 women), allocated to membrane sweeping may be more likely to have spontaneous onset of labour, but we found no clear difference in unassisted vaginal births. Women may also be less likely to have formal induction of labour. We also found no clear differences between the groups for caesarean section, instrumental vaginal births or serious illness or death of the mother or baby.

          Compared with vaginal or intracervical prostaglandins (four studies involving 480 women), we found no difference in any outcomes although data were limited.

          We found insufficient data to draw any conclusions in the studies comparing membrane sweep with intravenous oxytocin, with or without breaking the waters, or with vaginal/oral misoprostol. Similarly for the comparison between different frequencies of membrane sweeping.

          What does this mean?

          Membrane sweeping appears to be effective in promoting labour but current evidence suggests this did not, overall, follow‐on to unassisted vaginal births. Membrane sweeping may reduce formal induction of labour. Only three studies reported on women’s satisfaction with membrane sweeping. Women reported feeling positive about membrane sweeping. While acknowledging that it may be uncomfortable, they felt the benefits outweighed the harms and most would recommend it to other women. Further research is needed to confirm our review findings and to identify the ideal time for membrane sweep and whether having more than one sweep would be beneficial. Further information on women’s views is also needed.

          Related collections

          Most cited references54

          • Record: found
          • Abstract: found
          • Article: not found

          Induction of labour for improving birth outcomes for women at or beyond term

          Beyond term, the risks of stillbirth or neonatal death increase. It is unclear whether a policy of labour induction can reduce these risks. This Cochrane review is an update of a review that was originally published in 2006 and subsequently updated in 2012 To assess the effects of a policy of labour induction at or beyond term compared with a policy of awaiting spontaneous labour or until an indication for birth induction of labour is identified) on pregnancy outcomes for infant and mother. We searched Cochrane Pregnancy and Childbirth’s Trials Register, ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform ( ICTRP ) (9 October 2017), and reference lists of retrieved studies. Randomised controlled trials (RCTs) conducted in pregnant women at or beyond term, comparing a policy of labour induction with a policy of awaiting spontaneous onset of labour (expectant management). We also included trials published in abstract form only. Cluster‐RCTs, quasi‐RCTs and trials using a cross‐over design are not eligible for inclusion in this review. We included pregnant women at or beyond term. Since a risk factor at this stage of pregnancy would normally require an intervention, only trials including women at low risk for complications were eligible. We accepted the trialists' definition of 'low risk'. The trials of induction of labour in women with prelabour rupture of membranes at or beyond term were not considered in this review but are considered in a separate Cochrane review. Two reviewers independently assessed trials for inclusion, assessed risk of bias and extracted data. Data were checked for accuracy. We assessed the quality of evidence using the GRADE approach. In this updated review, we included 30 RCTs (reporting on 12,479 women). The trials took place in Norway, China, Thailand, the USA, Austria, Turkey, Canada, UK, India, Tunisia, Finland, Spain, Sweden and the Netherlands. They were generally at a moderate risk of bias. Compared with a policy of expectant management, a policy of labour induction was associated with fewer (all‐cause) perinatal deaths (risk ratio (RR) 0.33, 95% confidence interval (CI) 0.14 to 0.78; 20 trials, 9960 infants; moderate‐quality evidence). There were two perinatal deaths in the labour induction policy group compared with 16 perinatal deaths in the expectant management group. The number needed to treat to for an additional beneficial outcome (NNTB) with induction of labour in order to prevent one perinatal death was 426 (95% CI 338 to 1337). There were fewer stillbirths in the induction group (RR 0.33, 95% CI 0.11 to 0.96; 20 trials, 9960 infants; moderate‐quality evidence); there was one stillbirth in the induction policy arm and 10 in the expectant management group. For women in the policy of induction arms of trials, there were fewer caesarean sections compared with expectant management (RR 0.92, 95% CI 0.85 to 0.99; 27 trials, 11,738 women; moderate‐quality evidence); and a corresponding marginal increase in operative vaginal births with induction (RR 1.07, 95% CI 0.99 to 1.16; 18 trials, 9281 women; moderate‐quality evidence). There was no evidence of a difference between groups for perineal trauma (RR 1.09, 95% CI 0.65 to 1.83; 4 trials; 3028 women; low‐quality evidence), postpartum haemorrhage (RR 1.09 95% CI 0.92 to 1.30, 5 trials; 3315 women; low‐quality evidence), or length of maternal hospital stay (average mean difference (MD) ‐0.34 days, 95% CI ‐1.00 to 0.33; 5 trials; 1146 women; Tau² = 0.49; I² 95%; very low‐quality evidence). Rates of neonatal intensive care unit (NICU) admission were lower (RR 0.88, 95% CI 0.77 to 1.01; 13 trials, 8531 infants; moderate‐quality evidence) and fewer babies had Apgar scores less than seven at five minutes in the induction groups compared with expectant management (RR 0.70, 95% CI 0.50 to 0.98; 16 trials, 9047 infants; moderate‐quality evidence). There was no evidence of a difference for neonatal trauma (RR 1.18, 95% CI 0.68 to 2.05; 3 trials, 4255 infants; low‐quality evidence), for induction compared with expectant management. Neonatal encephalopathy, neurodevelopment at childhood follow‐up, breastfeeding at discharge and postnatal depression were not reported by any trials. In subgroup analyses, no clear differences between timing of induction ( 287 days) gestation for the intervention arm. A policy of labour induction at or beyond term compared with expectant management is associated with fewer perinatal deaths and fewer caesarean sections; but more operative vaginal births. NICU admissions were lower and fewer babies had low Apgar scores with induction. No important differences were seen for most of the other maternal and infant outcomes. Most of the important outcomes assessed using GRADE had a rating of moderate or low‐quality evidence ‐ with downgrading decisions generally due to study limitations such as lack of blinding (a condition inherent in comparisons between a policy of acting and of waiting), or imprecise effect estimates. One outcome (length of maternal stay) was downgraded further to very low‐quality evidence due to inconsistency. Although the absolute risk of perinatal death is small, it may be helpful to offer women appropriate counselling to help choose between scheduled induction for a post‐term pregnancy or monitoring without (or later) induction). The optimal timing of offering induction of labour to women at or beyond term warrants further investigation, as does further exploration of risk profiles of women and their values and preferences. Individual participant meta‐analysis is likely to help elucidate the role of factors, such as parity, in influencing outcomes of induction compared with expectant management. Induction of labour in women with normal pregnancies at or beyond term What is the issue? A normal pregnancy lasts about 40 weeks from the start of the woman's last menstrual period, but anything from 37 to 42 weeks is considered as being at term (within the normal range). If a pregnancy goes too long, a woman and her clinician may wish to intervene to bring the birth on, for example, by induction. Why is this important? Births after 42 weeks' gestation may slightly increase risks for babies, including a greater risk of death (before or shortly after birth). However induction of labour may also have risks for mothers and their babies, especially if women are not ready to labour. No tests can predict if babies would be better to stay inside their mother or if labour should be induced to make the birth happen sooner. Many hospitals therefore have policies for how long pregnancies should continue. This update (originally published in 2006 and subsequently updated in 2012) looks to see if inducing labour at a set time at or beyond term, could reduce risks for the babies. What evidence did we find? We searched for evidence up 9 October 2017 and identified 30 trials with over 12,000 women. The trials took place in Norway, China, Thailand, the USA, Austria, Turkey, Canada, UK, India, Tunisia, Finland, Spain, Sweden and the Netherlands. The evidence was mostly of moderate quality. The trials compared a policy to induce labour at or later than term (usually after 41 completed weeks of gestation (> 287 days)) with waiting for labour to start and/or waiting for a period before inducing labour. We found that there were fewer deaths of babies in hospitals with a policy to induce when a pregnancy was continuing beyond term (moderate‐quality evidence). Fewer caesarean births were required with induction compared with waiting, but more assisted vaginal births were required with induction. There were fewer admissions to the intensive care nursery and fewer low Apgar scores at five minutes after birth (a simple test to test babies' health) in the induction groups compared with waiting (moderate‐quality evidence). We found that there were no clear differences between a policy to induce at or later than term or waiting in the risks of mothers having trauma to their perineum or bleeding after birth (both low‐quality evidence), in the length of their hospital stay (very‐low quality evidence), or in their babies having trauma (low‐quality evidence), None of the trials provided information on breastfeeding at discharge from hospital, postnatal depression, or whether the babies had encephalopathy (early abnormal neurological function), or child development. What does this mean? A policy of labour induction compared with expectant management is associated with fewer deaths of babies and fewer caesarean sections; but more assisted vaginal births. Although the chances of babies dying are small, it may help to offer women appropriate counselling to make an informed choice between induction of labour for pregnancies at, or later than, term ‐ or waiting for labour to start and/or waiting before inducing labour. The best time to offer induction of labour to women at or beyond term is not yet clear and warrants further investigation. The risk profiles of women as well as their values and preferences could also be considered.
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            • Record: found
            • Abstract: found
            • Article: not found

            Systematic review: elective induction of labor versus expectant management of pregnancy.

            The rates of induction of labor and elective induction of labor are increasing. Whether elective induction of labor improves outcomes or simply leads to greater complications and health care costs is commonly debated in the literature. To compare the benefits and harms of elective induction of labor and expectant management of pregnancy. MEDLINE (through February 2009), Web of Science, CINAHL, Cochrane Central Register of Controlled Trials (through March 2009), bibliographies of included studies, and previous systematic reviews. Experimental and observational studies of elective induction of labor reported in English. Two authors abstracted study design; patient characteristics; quality criteria; and outcomes, including cesarean delivery and maternal and neonatal morbidity. Of 6117 potentially relevant articles, 36 met inclusion criteria: 11 randomized, controlled trials (RCTs) and 25 observational studies. Overall, expectant management of pregnancy was associated with a higher odds ratio (OR) of cesarean delivery than was elective induction of labor (OR, 1.22 [95% CI, 1.07 to 1.39]; absolute risk difference, 1.9 percentage points [CI, 0.2 to 3.7 percentage points]) in 9 RCTs. Women at or beyond 41 completed weeks of gestation who were managed expectantly had a higher risk for cesarean delivery (OR, 1.21 [CI, 1.01 to 1.46]), but this difference was not statistically significant in women at less than 41 completed weeks of gestation (OR, 1.73 [CI, 0.67 to 4.5]). Women who were expectantly managed were more likely to have meconium-stained amniotic fluid than those who were electively induced (OR, 2.04 [CI, 1.34 to 3.09]). There were no recent RCTs of elective induction of labor at less than 41 weeks of gestation. The 2 studies conducted at less than 41 weeks of gestation were of poor quality and were not generalizable to current practice. RCTs suggest that elective induction of labor at 41 weeks of gestation and beyond is associated with a decreased risk for cesarean delivery and meconium-stained amniotic fluid. There are concerns about the translation of these findings into actual practice; thus, future studies should examine elective induction of labor in settings where most obstetric care is provided.
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              • Record: found
              • Abstract: found
              • Article: not found

              Does induction of labour increase the risk of caesarean section? A systematic review and meta-analysis of trials in women with intact membranes.

              Recent literature on the effect of induction of labour (compared with expectant management) has provided conflicting results. Reviews of observational studies generally report an increase in the rate of caesarean section, whereas reviews of post-dates and term prelabour rupture of membrane (PROM trials suggest either no difference or a reduction in risk.
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                Author and article information

                Contributors
                elaine1finucane@gmail.com , elainemay.finucane@nuigalway.ie
                Journal
                Cochrane Database Syst Rev
                Cochrane Database Syst Rev
                14651858
                10.1002/14651858
                The Cochrane Database of Systematic Reviews
                John Wiley & Sons, Ltd (Chichester, UK )
                1469-493X
                27 February 2020
                February 2020
                5 March 2020
                : 2020
                : 2
                : CD000451
                Affiliations
                University Maternity Hospital Limerick Ennis Road Limerick Ireland
                University of Dublin deptDepartment of Obstetrics and Gynaecology Trinity College Coombe Women's Hospital Dolphin's Barn Dublin 8 Ireland
                National University of Ireland Galway deptSchool of Nursing and Midwifery Aras Moyola Galway Ireland
                University of Liverpool deptCochrane Pregnancy and Childbirth Group, Department of Women's and Children's Health First Floor, Liverpool Women's NHS Foundation Trust Crown Street Liverpool UK L8 7SS
                University of Limerick deptDepartment of Obstetrics and Gynaecology Limerick Ireland
                Galway University deptMaternity Department, Saolta Women's and Children's Directorate Newcastle Road Galway Ireland
                University of Geneva/GHOL‐Nyon Hospital deptDepartment of Gynecology and Obstetrics NYON Switzerland
                Article
                PMC7044809 PMC7044809 7044809 CD000451.pub3 CD000451
                10.1002/14651858.CD000451.pub3
                7044809
                32103497
                210a329e-188a-42b1-9914-f64fcfe693f5
                Copyright © 2020 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
                History
                Categories
                Induction of labour
                Pregnancy & childbirth

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