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  "kind": "intervention",
  "slug": "induction-of-labour",
  "name": "Induction of labour",
  "aliases": [],
  "atlases": [
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  "summary_plain": "Induction means starting labour with medicines or other methods instead of waiting for it to begin on its own. It is usually done when the due date has passed or when a problem with the pregnancy puts the mother or baby at risk. Two large trials asked a different question: is it better to induce healthy women at a set time than to wait? ARRIVE looked at first-time mothers at 39 weeks. SWEPIS compared induction at 41 weeks with waiting until 42 weeks. They measured different things and found different results, so read each on its own page.",
  "summary_technical": "A procedure with several methods: medicines (oxytocin, dinoprostone) and mechanical ripening of the cervix (a balloon device). Each method has its own record; this record is about the strategy of inducing labour at a chosen time. Sources: MedlinePlus Childbirth, NIH Labor and Delivery (cite only), ARRIVE (Grobman et al., NEJM 2018: abstract and registry record) and SWEPIS (Wennerholm et al., BMJ 2019: abstract and PMC full text, with its erratum). Neither trial compares methods of induction. The oxytocin record keeps induction apart from the use of oxytocin after birth to prevent bleeding.",
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      "statement": "In ARRIVE, caesarean delivery was the principal secondary outcome. It occurred in 18.6% of women in the induction group and 22.2% with expectant management (relative risk 0.84, 95% confidence interval 0.76 to 0.93), a significantly lower frequency with induction. The women were low-risk first-time mothers randomly assigned at 38 weeks 0 days to 38 weeks 6 days of gestation to induction at 39 weeks 0 days to 39 weeks 4 days or to expectant management.",
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        "label": "Low-risk first-time mothers randomised at 38 weeks 0 days to 38 weeks 6 days: caesarean delivery (ARRIVE)",
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        "population": "Low-risk nulliparous women (no previous pregnancy beyond 20 weeks per the registry) with a singleton pregnancy who were randomly assigned at 38 weeks 0 days to 38 weeks 6 days of gestation either to labour induction at 39 weeks 0 days to 39 weeks 4 days or to expectant management. The gestational bounds are the gestational age at randomisation.",
        "care_setting": "Multicentre trial in the United States; the abstract does not say what kind of site took part.",
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        "followup_description": "To delivery (caesarean delivery was the principal secondary outcome).",
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      "limitations": "This is a secondary outcome. The abstract and registry were read, not the full text, so adjustment, missing data and other methods are not described here. The abstract gives no number of women in each group for this outcome, so none is computed. The result concerns low-risk first-time mothers and does not apply to other women. The primary composite outcome measured in babies is a separate claim in a separate context, and it did not differ significantly between the groups.",
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      "statement": "ARRIVE randomly assigned low-risk first-time mothers at 38 weeks 0 days to 38 weeks 6 days of gestation either to labour induction at 39 weeks 0 days to 39 weeks 4 days or to expectant management. The primary outcome, a composite of perinatal death or severe neonatal complications, occurred in 4.3% of neonates in the induction group and 5.4% in the expectant-management group (relative risk 0.80, 95% confidence interval 0.64 to 1.00). The authors report that induction did not result in a significantly lower frequency of the composite adverse perinatal outcome.",
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        "label": "Fetuses and babies of low-risk first-time mothers randomised at 38 weeks 0 days to 38 weeks 6 days: perinatal death or severe neonatal complications (ARRIVE)",
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        "care_setting": "Multicentre trial in the United States; the abstract does not say what kind of site took part.",
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