What is the management and treatment for a pregnant patient with pregnancy-induced hypertension?

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Management of Pregnancy-Induced Hypertension

For pregnant women with pregnancy-induced hypertension, initiate antihypertensive treatment when blood pressure reaches ≥140/90 mmHg, targeting a diastolic BP of 85 mmHg and systolic BP of 110-140 mmHg, using methyldopa, labetalol, or long-acting nifedipine as first-line agents. 1, 2

Blood Pressure Thresholds and Treatment Initiation

  • Start pharmacological treatment at BP ≥140/90 mmHg in women with gestational hypertension (new-onset hypertension after 20 weeks), pre-existing hypertension with superimposed gestational hypertension, or hypertension with subclinical organ damage or symptoms. 3, 1, 2

  • For women with chronic hypertension without these specific features, treatment begins at BP ≥150/95 mmHg. 3, 2

  • Non-pharmacological management alone is appropriate for BP 140-150/90-99 mmHg without concerning features, including close supervision, limitation of activities, bed rest in left lateral position, normal diet without salt restriction, and calcium supplementation of at least 1 g daily. 3, 2

Urgent Management of Severe Hypertension

  • BP ≥160/110 mmHg constitutes a hypertensive emergency requiring immediate treatment within 15 minutes in a monitored setting to prevent maternal stroke. 3, 1, 2

  • First-line agents for acute severe hypertension include:

    • Oral immediate-release nifedipine 3, 1, 2
    • Intravenous labetalol 3, 1, 2
    • Intravenous hydralazine 3, 1
  • Position the patient in left lateral decubitus to relieve inferior vena cava compression and improve venous return. 4

First-Line Antihypertensive Medications for Chronic Control

  • Methyldopa, labetalol, and long-acting nifedipine are the three preferred agents for ongoing BP control during pregnancy, with methyldopa having the longest safety data including 7.5-year infant follow-up. 3, 1, 2

  • Metoprolol is also recommended as an alternative. 3

  • Reduce or cease antihypertensive drugs if diastolic BP falls below 80 mmHg to avoid compromising uteroplacental perfusion. 3

Absolutely Contraindicated Medications

  • ACE inhibitors, angiotensin receptor blockers (ARBs), and direct renin inhibitors are strictly contraindicated due to severe fetotoxicity, particularly in the second and third trimesters. 3, 2, 5

  • If taken inadvertently during the first trimester, switch immediately to another medication and perform close monitoring including fetal ultrasound. 3

Critical Drug Interaction Warning

  • Do not administer magnesium sulfate concomitantly with calcium channel blockers due to risk of severe hypotension. 4, 2

  • Do not use labetalol concomitantly with calcium channel blockers for the same reason. 2

Indications for Hospitalization

Admit immediately for:

  • BP ≥160/110 mmHg (severe hypertension) 3, 1, 2
  • Development of preeclampsia features (proteinuria ≥0.3 g/day) 3
  • Neurological signs or symptoms (severe headache, visual disturbances, clonus) 3, 1, 2
  • Inability to control BP with ≥3 antihypertensive drug classes 1, 2

Preeclampsia-Specific Management

  • All women with preeclampsia should be assessed in hospital when first diagnosed; some may be managed as outpatients once stable if they can reliably report problems and monitor their BP. 3

  • Administer magnesium sulfate for seizure prophylaxis in women with preeclampsia who have proteinuria and severe hypertension, or hypertension with neurological signs or symptoms. 3, 1, 2

  • In low-resource settings, all women with preeclampsia should receive MgSO4: loading dose of 4 g IV or 10 g IM, followed by 5 g IM every 4 hours or 1 g/h infusion until delivery and for at least 24 hours postpartum. 3

  • Plasma volume expansion is not recommended routinely in women with preeclampsia. 3

Maternal Monitoring Protocol

For women with preeclampsia, perform:

  • BP monitoring continuously or at least 4 times daily 3, 6
  • Repeated assessments for proteinuria if not already present 3
  • Clinical assessment including clonus 3
  • Blood tests at least twice weekly (and with any clinical status change) for hemoglobin, platelet count, liver transaminases, creatinine, and uric acid 3
  • Weekly creatinine clearance determination 6
  • Weight and urine protein 3 times weekly 6

Fetal Monitoring Protocol

Fetal monitoring should include:

  • Assessment of fetal biometry, amniotic fluid, and umbilical artery Doppler ultrasound at first diagnosis 3
  • Repeat at 2-week intervals if initial assessment was normal 3
  • More frequent amniotic fluid and Doppler assessments in the presence of fetal growth restriction 3
  • Serial sonography to monitor fetal growth 6

Timing of Delivery

  • For gestational hypertension without preeclampsia: delivery can be delayed until 39+6 weeks if BP remains controlled, fetal monitoring is reassuring, and preeclampsia has not developed. 1, 2

  • For preeclampsia at term (≥37 weeks): recommend delivery. 1

  • Deliver earlier if: rapid weight gain, decreasing creatinine clearance, appearance of significant proteinuria, suspected fetal growth retardation, or development of severe headache or visual disturbances. 6

  • Administer antenatal corticosteroids between 24+0 and 34+0 weeks if delivery is likely within 7 days. 1

Important Clinical Pitfalls

  • Do not attempt to diagnose "mild versus severe" preeclampsia clinically as all cases may become emergencies, often rapidly. 3

  • At least 25% of women with gestational hypertension will progress to preeclampsia, with highest risk among those presenting before 34 weeks. 3, 1

  • Salt restriction may induce low intravascular volume and should be avoided, particularly close to delivery. 3

  • Weight reduction is not recommended during pregnancy in obese women as it can lead to reduced neonatal weight and slower subsequent growth. 3

Prevention Strategies

  • Low-dose aspirin (75-100 mg/day) should be administered at bedtime in women with a history of early-onset (<28 weeks) preeclampsia, starting pre-pregnancy or from diagnosis of pregnancy but before 16 weeks gestation, and continued until delivery. 3

  • Calcium supplementation of at least 1 g daily during pregnancy almost halved the risk of preeclampsia, with greatest effect in high-risk women, though evidence is conflicting. 3

  • Fish oil supplementation and vitamin/nutrient supplements have no role in prevention. 3

Postpartum Management

  • Record BP shortly after birth and again within 6 hours, continuing antihypertensive treatment as needed to maintain BP <140/90 mmHg. 1

  • Switch from methyldopa to an alternative agent postpartum due to risk of postnatal depression. 2

  • BP typically rises over the first 5 postpartum days; women may become hypertensive again after initial normalization. 2

Long-Term Cardiovascular Risk

  • Women with gestational hypertension or preeclampsia have significantly increased lifetime cardiovascular risk, with relative risk of ischemic heart disease more than doubled. 1, 2

  • Women with early-onset preeclampsia, stillbirth, or fetal growth retardation are at highest risk. 2

  • Recommend annual medical review lifelong for cardiovascular risk assessment, lifestyle modifications, regular blood pressure control, and control of metabolic factors. 1, 2

  • Earlier onset in the first pregnancy correlates with greater recurrence risk in subsequent pregnancies. 2

References

Guideline

Management of Hypertension in Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Hypertension in Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Seizures and Hypotension in Pregnant Women

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Pregnancy-Induced hypertension.

Hormones (Athens, Greece), 2015

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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