{
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  "id": "maternal:antenatal-corticosteroids",
  "owner": "maternal",
  "kind": "intervention",
  "slug": "antenatal-corticosteroids",
  "name": "Antenatal corticosteroids",
  "aliases": [
    "Antenatal glucocorticoids"
  ],
  "atlases": [
    "maternal"
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  "summary_plain": "Steroid medicines, dexamethasone or betamethasone, given by injection to a pregnant woman who is likely to give birth early. The medicine reaches the baby and helps the lungs mature, which can protect the baby's breathing after an early birth. The mother receives the medicine and the baby is the one who is meant to benefit.",
  "summary_technical": "Glucocorticoids given to women with a high likelihood of preterm birth. WHO 2022 recommends intramuscular dexamethasone or betamethasone, total 24 mg in divided doses (Recommendation 1.9). ACTION-I gave intramuscular dexamethasone 6 mg every 12 hours for up to four doses, against placebo, in 29 hospitals in five low-resource countries. The recipient is the woman and the outcome of interest is the infant's, so each claim on this page states both.",
  "editorial_state": "draft",
  "last_substantive_edit": "2026-10-12",
  "last_evidence_check": null,
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  "external_ids": [],
  "navigation": {
    "maternal": {
      "life-stage": [
        "pregnancy"
      ]
    }
  },
  "payload": {
    "subtype": "medicine",
    "mechanism": "Per WHO 2022, the glucocorticoid crosses the placenta and helps the fetal lungs mature, including faster production of surfactant, which can prevent breathing-related illness and death in preterm newborns.",
    "taxonomy_codes": []
  },
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      "owner": "maternal",
      "subject_entity_id": "maternal:antenatal-corticosteroids",
      "category": "safety",
      "statement": "In ACTION-I, possible maternal bacterial infection (defined as maternal fever of 38 degrees C or more, or clinically suspected or confirmed infection, for which therapeutic antibiotics were used) occurred in 68 of 1416 women (4.8%) given dexamethasone and 89 of 1412 (6.3%) given placebo (relative risk 0.76, 95% CI 0.56 to 1.03). The trial tested whether dexamethasone was not worse than placebo on this outcome, with a prespecified margin of 1.25 on the relative scale, and the result was consistent with that.",
      "context": {
        "id": "maternal:ctx-action-i-women-26w0d-33w6d",
        "label": "Pregnant women at risk of imminent preterm birth at 26w0d to 33w6d, in 29 hospitals in five low-resource countries (ACTION-I)",
        "recipient": "maternal",
        "population": "Pregnant women with a confirmed live fetus, single or multiple pregnancy, who were at risk of preterm birth between 26 weeks 0 days and 33 weeks 6 days of gestation and whose birth was planned or expected within 48 hours. Gestational age came from the earliest ultrasound or one done at admission.",
        "care_setting": "Hospital-based: 29 secondary- and tertiary-level hospitals across six study sites. The hospitals were chosen after a standard assessment so that the WHO conditions for antenatal corticosteroid use could reasonably be met.",
        "geography": "Bangladesh, India, Kenya, Nigeria and Pakistan",
        "life_stage": "Pregnancy, from randomization to birth, with maternal infection followed to 28 days after birth",
        "gestational_age_min_days": 182,
        "gestational_age_max_days": 237,
        "postnatal_age_min_days": null,
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        "postnatal_age_status": null,
        "followup_description": "The maternal primary outcome, possible maternal bacterial infection, ran from randomization to 28 days postpartum and was captured during hospital admission only.",
        "eligibility": {
          "inclusion": [
            "Live fetus, single or multiple pregnancy",
            "Gestational age 26 weeks 0 days to 33 weeks 6 days",
            "Birth planned or expected in the next 48 hours",
            "Written informed consent before randomization"
          ],
          "exclusion": [
            "Clinical signs of severe infection",
            "Major congenital fetal anomalies",
            "Systemic glucocorticoid use now or within the past two weeks",
            "Participation in another trial",
            "Contraindication to steroids",
            "Clinical suspicion or evidence of chorioamnionitis (registry criteria only; the paper lists clinical signs of severe infection)",
            "No earlier ultrasound estimate of gestational age and an immediate ultrasound not possible (registry criteria only; both ANZCTR and CTRI via ICTRP list it, and the paper says gestational age came from the earliest ultrasound or one done at admission)"
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      "evidence_stage": "interventional",
      "certainty": "not_assessed",
      "certainty_method": null,
      "limitations": "This is one prespecified maternal outcome, counted during hospital admission only, in these hospitals and this population. It does not show that antenatal corticosteroids are safe in general, or in places that cannot meet the WHO conditions. The interval includes 1.00, so the data do not show a lower infection risk with dexamethasone. The same trial limits apply: hospitals chosen to meet WHO conditions, early stopping for benefit, and the Author Final Manuscript read in place of the version of record.",
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      "id": "maternal:claim-action-i-neonatal-death",
      "owner": "maternal",
      "subject_entity_id": "maternal:antenatal-corticosteroids",
      "category": "effect",
      "statement": "In the ACTION-I trial, pregnant women at risk of imminent preterm birth, from 26 weeks 0 days to 33 weeks 6 days of pregnancy, received either dexamethasone or a dummy injection. Fewer of their liveborn babies died in the first 28 days of life in the dexamethasone group: 278 of 1417 (19.6%) against 331 of 1406 (23.5%) in the placebo group (relative risk 0.84, 95% CI 0.72 to 0.97). The medicine was given to the mother, and the outcome counted here is the baby's.",
      "context": {
        "id": "maternal:ctx-action-i-liveborn-infants",
        "label": "Liveborn infants of women randomized at 26w0d to 33w6d, followed to 28 completed days of life (ACTION-I)",
        "recipient": "newborn",
        "population": "Liveborn infants of the randomized women. The window of 26 weeks 0 days to 33 weeks 6 days is the mother's gestational age when she entered the trial. It does not limit the infant's gestational age at birth, and the research gives no such limit. Birth occurred before 37 weeks for 90.0% of infants in the dexamethasone group and 90.8% of infants in the placebo group.",
        "care_setting": "Hospital-based: 29 secondary- and tertiary-level hospitals across six study sites. The hospitals were chosen after a standard assessment so that the WHO conditions for antenatal corticosteroid use could reasonably be met.",
        "geography": "Bangladesh, India, Kenya, Nigeria and Pakistan",
        "life_stage": "Neonatal period, birth to 28 days",
        "gestational_age_min_days": null,
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        "followup_description": "Infants entered the analysis at birth and were followed until 28 days after birth or death, whichever came first. Neonatal death means death of a liveborn within 28 completed days of life. The postnatal age bounds give age at entry, not the length of follow-up.",
        "eligibility": {
          "inclusion": [
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          ],
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      "certainty": "not_assessed",
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      "limitations": "One placebo-controlled trial in 29 secondary- and tertiary-level hospitals in five low-resource countries. The hospitals were chosen so that the WHO conditions for steroid use could reasonably be met, so the result does not describe lower-level facilities or the community. The trial stopped early for benefit, short of its planned sample. About 90% of the infants were born before 37 weeks. The authors report that 45% of women received fewer than four doses, and name the difficulty of standardizing care across sites and the use of third-trimester ultrasound to confirm gestational age for many participants as limits. The relative risk is model-based, adjusted for site and for multiple births, with intervals adjusted for multiplicity. Figures come from the PubMed abstract and the Author Final Manuscript; the version of record was not fetched (HTTP 403) and the figures were not checked against it.",
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      "statement": "In ACTION-I, 393 of 1532 fetuses and infants (25.7%) in the dexamethasone group were stillborn or died as newborns, against 444 of 1519 (29.2%) in the placebo group (relative risk 0.88, 95% CI 0.78 to 0.99). The trial defined this as one count across the fetal period after enrolment and the first 28 completed days of life, and the atlas does not split it into fetal and newborn parts.",
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      "category": "recommendation",
      "statement": "WHO recommends antenatal corticosteroid therapy for women with a high likelihood of preterm birth from 24 weeks to 34 weeks of gestation, but only when five conditions are met: gestational age can be assessed accurately, preterm birth is highly likely within 7 days of starting treatment, there is no clinical evidence of maternal infection, adequate childbirth care is available (including capacity to recognize and safely manage preterm labour and birth), and the preterm newborn can receive adequate care, including resuscitation, kangaroo mother care, thermal care, feeding support, infection treatment and respiratory support including continuous positive airway pressure (CPAP) as needed. WHO introduces that list with the word including, so the items are examples of adequate newborn care and the list is not complete. WHO's Remarks add that antenatal corticosteroids should not be routinely given where ultrasound for gestational age assessment cannot be performed. WHO classes this as a context-specific recommendation, from its 2022 update that replaced its 2015 advice. The woman is treated and the newborn is the intended beneficiary.",
      "context": {
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        "population": "Women with a high likelihood of preterm birth within 7 days of starting therapy, from 24 weeks to 34 weeks 0 days of gestation. The woman receives the treatment and the preterm newborn is the intended beneficiary. The recommendation sets the lower limit at 24 weeks, and the Remarks set 34 weeks 0 days as the upper limit.",
        "care_setting": "Health-care facilities that can meet the five conditions, including accurate gestational age assessment, adequate childbirth care and adequate care of the preterm newborn. The Remarks say harm cannot be excluded where the conditions cannot be met, such as lower-level health facilities and the community level. They also say antenatal corticosteroids should not be routinely administered where ultrasound for gestational age assessment cannot be performed.",
        "geography": "Global (WHO guideline; no country is excluded, but the conditions must be met)",
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            "The preterm newborn can receive adequate care, including resuscitation, kangaroo mother care, thermal care, feeding support, infection treatment and respiratory support including continuous positive airway pressure (CPAP) as needed. WHO introduces the list with the word including, so it gives examples"
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      "limitations": "WHO's four recommendation categories are not GRADE strong or conditional labels. WHO rates certainty for each outcome with GRADE and gives no single certainty rating for a recommendation, so certainty is not assessed here. The Remarks say harm cannot be excluded where the conditions cannot be met, such as lower-level health facilities and the community level. The guideline group chose 34 weeks 0 days as the upper limit because of uncertainty in the balance of benefit and harm at later gestational ages. WHO says the recommendations may be updated when new evidence appears. On 2026-10-11 title searches of WHO IRIS found no later WHO antenatal corticosteroid guideline; that is a search result, not proof of absence.",
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      "statement": "WHO recommends against antenatal corticosteroid therapy for women who have chorioamnionitis and are likely to give birth preterm. Chorioamnionitis is inflammation of the membranes around the fetus (the chorion and amnion) and connected tissues, often associated with infection rising into the womb during pregnancy (MeSH definition). WHO's Remarks say timely birth should be the priority, that treatment should not be started at the expense of timely birth when the maternal or fetal condition calls for it, and that the guideline group acknowledged a concern about the risk of exacerbating maternal infection, particularly in low- and middle-income settings where the baseline risk of maternal infectious illness is higher. The group felt this potential risk may outweigh the known benefits of the steroid in the majority of populations where steroid use is essential for improving newborn survival.",
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