What is the recommended management of hypertension in pregnancy?

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Management of Hypertension in Pregnancy

For pregnant women with gestational hypertension, pre-existing hypertension with superimposed gestational hypertension, or hypertension with subclinical organ damage, initiate antihypertensive treatment at BP ≥140/90 mmHg; for all other pregnant women with chronic hypertension, treatment should begin at BP ≥150/95 mmHg. 1, 2, 3

Blood Pressure Thresholds for Treatment

The treatment threshold depends on the specific hypertensive disorder:

  • Lower threshold (≥140/90 mmHg): Start treatment at this level for women with gestational hypertension (with or without proteinuria), pre-existing hypertension with superimposed gestational hypertension, or hypertension with subclinical organ damage or symptoms at any time during pregnancy 1, 2, 3

  • Higher threshold (≥150/95 mmHg): For all other pregnant women with chronic hypertension without the above features, treatment begins at this higher threshold 1, 3

  • Target BP during treatment: Aim for diastolic BP of 85 mmHg and systolic BP between 110-140 mmHg to ensure adequate uteroplacental perfusion while protecting the mother 2, 3

First-Line Pharmacological Agents

Methyldopa, labetalol, and long-acting nifedipine are the three preferred first-line agents for chronic blood pressure control during pregnancy. 2, 3

Methyldopa

  • Remains the drug of choice based on the longest safety data, including 7.5-year follow-up studies showing no adverse effects on child development 1, 4
  • Important caveat: Should be avoided postpartum due to risk of postnatal depression 3
  • May interfere with laboratory tests for pheochromocytoma (falsely elevated urinary catecholamines) 4

Labetalol

  • Has efficacy comparable to methyldopa and can be given orally or intravenously 1, 5
  • Critical warning: Should not be used concomitantly with calcium channel blockers due to risk of severe hypotension 3, 5
  • Small amounts (0.004% of maternal dose) are excreted in breast milk 5

Nifedipine (long-acting)

  • A 2019 randomized controlled trial of 894 women demonstrated that nifedipine retard achieved blood pressure control within 6 hours in 84% of women, significantly more than methyldopa (76%, p=0.03) 6
  • Particularly useful for acute management of severe hypertension when given as immediate-release formulation 3

Management of Severe Hypertension (Emergency)

BP ≥170/110 mmHg constitutes a hypertensive emergency requiring immediate hospitalization and treatment within 15 minutes to prevent maternal stroke. 1, 3

First-line agents for acute severe hypertension:

  • Oral immediate-release nifedipine: Preferred first-line option 3
  • Intravenous labetalol: Equally effective alternative 1, 3
  • Oral methyldopa: Can be used but has slower onset 1

Important changes in practice:

  • Intravenous hydralazine is no longer the drug of choice as it is associated with more perinatal adverse effects than other drugs 1
  • Sodium nitroprusside (0.25-5.0 mg/kg/min IV) is reserved for hypertensive crises, but prolonged use risks fetal cyanide poisoning 1
  • Nitroglycerin (glyceryl trinitrate) IV infusion is the drug of choice specifically for pre-eclampsia associated with pulmonary edema 1

Non-Pharmacological Management

For pregnant women with SBP 140-150 mmHg or DBP 90-99 mmHg, non-pharmacological management is recommended initially 1:

  • Close supervision with limitation of activities and some bed rest in left lateral position 1
  • Normal diet without salt restriction is advised, particularly close to delivery, as salt restriction may induce low intravascular volume 1
  • Low-dose aspirin (75-100 mg/day) should be used prophylactically in women with history of early-onset (<28 weeks) pre-eclampsia, administered at bedtime starting before 16 weeks gestation and continued until delivery 1
  • Calcium supplementation of at least 1 g daily almost halved the risk of pre-eclampsia, with greatest effect in high-risk women, though evidence is conflicting 1
  • Weight reduction is not recommended during pregnancy in obese women as it can lead to reduced neonatal weight 1

Timing of Delivery

  • Gestational hypertension with proteinuria and adverse conditions (visual disturbances, coagulation abnormalities, fetal distress): Induction of delivery is indicated 1, 2
  • Pre-eclampsia at term (37 weeks): Recommend delivery 2, 3
  • Gestational hypertension without preeclampsia: Delivery can be delayed until 39+6 weeks if BP remains controlled 3

Contraindicated Medications

ACE inhibitors, angiotensin receptor blockers (ARBs), and direct renin inhibitors are strictly contraindicated in pregnancy due to severe fetotoxicity, particularly in the second and third trimesters 1, 7, 8

  • If taken inadvertently during first trimester, switch to another medication immediately and perform close monitoring including fetal ultrasound 1
  • Atenolol should also be avoided due to concerns with fetal growth 8

Postpartum Management

  • Switch from methyldopa to an alternative agent due to postnatal depression risk 3
  • BP typically rises over the first 5 postpartum days; women may become hypertensive again after initial normalization 3
  • Annual medical review lifelong is recommended for cardiovascular risk assessment, as women with gestational hypertension or preeclampsia have significantly increased lifetime cardiovascular risk 2, 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Pregnancy-Induced Hypertension

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Hypertension in Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Pregnancy-Induced hypertension.

Hormones (Athens, Greece), 2015

Research

Hypertension in pregnancy.

Advances in chronic kidney disease, 2007

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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