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  "id": "maternal:antihypertensive-treatment-non-severe-hypertension-pregnancy",
  "owner": "maternal",
  "kind": "intervention",
  "slug": "antihypertensive-treatment-non-severe-hypertension-pregnancy",
  "name": "Antihypertensive drug treatment for non-severe hypertension in pregnancy",
  "aliases": [],
  "atlases": [
    "maternal"
  ],
  "summary_plain": "Using blood pressure medicines in pregnancy when blood pressure is raised but not yet severe, instead of waiting until it becomes severe. This is a treatment strategy, not one drug. Different sources use different cut-offs and targets, so each target is kept with the claim that reports it.",
  "summary_technical": "Strategy of drug treatment for non-severe hypertension in pregnancy. CHAP treated mild chronic hypertension to a goal below 140/90 mm Hg, compared with treatment only if severe hypertension developed (systolic 160 or diastolic 105 mm Hg or higher); first-line drugs were labetalol or extended-release nifedipine. NICE NG133 1.3.9 gives a target of 135/85 mmHg whenever medicines are used to treat hypertension in pregnancy, and its management tables for gestational hypertension and pre-eclampsia say 135/85 mmHg or less. WHO 2020 recommends offering drug treatment for non-severe hypertension (140 to 159 systolic and/or 90 to 109 diastolic) with no numeric target. WHO also says calcium channel blockers should be avoided, and WHO’s evidence summary lists nifedipine among the calcium channel blockers, while CHAP used extended-release nifedipine as first line; the atlas records this difference and does not reconcile it. The WHO 2020 recommendation predates the CHAP report (2022). Targets belong to each claim’s context.",
  "editorial_state": "draft",
  "last_substantive_edit": "2026-10-11",
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  "navigation": {
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      "life-stage": [
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      "category": "effect",
      "statement": "In the CHAP trial, any pre-eclampsia (with or without severe features) occurred in 295 of 1208 women in the treated group (24.4%) and 373 of 1200 women in the control group (31.1%), a risk ratio of 0.79 (95% CI 0.69 to 0.89).",
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        "id": "maternal:ctx-chap-women-mild-chronic-htn-singleton-lt23w",
        "label": "Pregnant women with mild chronic hypertension and a singleton pregnancy before 23 weeks, United States (CHAP trial)",
        "recipient": "maternal",
        "population": "Pregnant women with known or new chronic hypertension and a viable singleton fetus before 23 weeks of gestation. Mild means below the severe thresholds, but the sources word the limit differently. The abstract says blood pressure below 160/100 mm Hg. The Methods required, at randomization, a systolic pressure of 140 to 159 or a diastolic pressure of 90 to 104 mm Hg for patients who “had not received an antihypertensive drug within 24 hours before measurement”, and below 160 and below 105 mm Hg for patients who “had been receiving antihypertensive therapy”. Women with lower pressures were also eligible. The registry gives a minimum age of 12 years and adds that the minimum age varies by center; the manuscript states no age limit.",
        "care_setting": "Recruiting sites of the CHAP Trial Consortium in the United States. The Methods say more than 70 recruiting sites; the Results say 2419 women were randomized at 61 sites. The manuscript does not say whether the sites were clinics or hospitals.",
        "geography": "United States",
        "life_stage": "Pregnancy, enrolled before 23 weeks of gestation and followed until 6 weeks after birth",
        "gestational_age_min_days": null,
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        "postnatal_age_min_days": null,
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        "followup_description": "Followed until 6 weeks after birth. Pre-eclampsia in the primary composite counted up to 2 weeks after birth.",
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            "Known chronic hypertension confirmed by a documented blood-pressure elevation and previous or current antihypertensive therapy, including lifestyle measures; or new chronic hypertension (systolic 140 mm Hg or higher or diastolic 90 mm Hg or higher on at least two occasions at least 4 hours apart before 20 weeks)",
            "A viable singleton fetus before 23 weeks of gestation",
            "Blood pressure below the severe-hypertension thresholds at randomization, as described in the population text"
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            "Known secondary hypertension",
            "Multiple fetuses",
            "Other serious illnesses or complications, named in advance, that might call for treatment at a lower blood pressure",
            "Obstetric conditions that increase fetal risk",
            "Contraindications to the first-line drugs recommended for use in pregnant women"
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      "certainty": "not_assessed",
      "certainty_method": null,
      "limitations": "This is a secondary outcome, reported without adjustment for multiplicity, so the authors say it should not be used to infer definitive effects. The risk ratio is not described as adjusted in the abstract or the table. The time window for this outcome is not stated in the manuscript text (follow-up ran to 6 weeks after birth; the primary composite counted pre-eclampsia up to 2 weeks after birth). It overlaps with the severe-features part of the primary composite, so the two must not be added. Open-label design, one country.",
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      "statement": "In the CHAP trial in the United States, women with mild chronic hypertension who enrolled before 23 weeks of pregnancy and were treated to a blood-pressure goal below 140/90 mm Hg had fewer of the combined serious pregnancy problems than women whose treatment was held back unless their blood pressure became severe. The combined outcome (pre-eclampsia with severe features, a medically indicated preterm birth before 35 weeks, placental abruption, or the death of the fetus or newborn) occurred in 353 of 1170 women with outcome data in the treated group (30.2%) and 427 of 1155 in the control group (37.0%). A separate analysis that fills in missing outcomes gave an adjusted risk ratio of 0.82 (95% CI 0.74 to 0.92).",
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        "label": "Pregnancies of women with mild chronic hypertension and their fetuses and newborns, United States (CHAP primary composite)",
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        "population": "The same women as the maternal CHAP context, with the outcomes of their pregnancies. The primary composite combines a maternal event (pre-eclampsia with severe features up to 2 weeks after birth), pregnancy events (medically indicated preterm birth before 35 weeks and placental abruption) and a fetal or neonatal event (fetal or neonatal death). It is used only for the composite as the trial defined it and is never split by recipient.",
        "care_setting": "Recruiting sites of the CHAP Trial Consortium in the United States; see the maternal CHAP context.",
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        "care_setting": "Maternity care; the recommendation does not name a setting.",
        "geography": "England. NICE's terms and conditions present the information on its websites as support for people in England who make decisions about funding care (clause 6) and say it is not written as a basis for decisions outside the United Kingdom (clause 8). The guideline page states no jurisdiction of its own.",
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            "reuse_basis": "The page bytes are not committed. Public text is cite_only (Ben's decision of 2026-10-13 (medical-atlas-core issue 2)): public pages state the facts in the atlas's own words, with a citation and a link, and use no NICE wording. NICE reuse terms, read on 2026-10-11 and recorded in research/setup/notes.md: the NICE UK Open Content Licence covers use in a UK setting only, international use outside personal research and study needs a licence and a fee, and the NICE terms and conditions make content available for artificial intelligence purposes only through an approval process, a licence and a fee for international use. This pipeline uses AI agents to read the page, so Ben decided on 2026-10-13 that public pages cite and link NICE and use none of its wording.",
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