What are the management guidelines for a pregnant woman with hypertension, preeclampsia, or eclampsia?

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Management of Hypertension, Preeclampsia, and Eclampsia in Pregnancy

All pregnant women with severe hypertension (≥160/110 mmHg) require immediate treatment in a monitored setting with IV labetalol, IV hydralazine, or oral nifedipine, and those with severe preeclampsia must receive magnesium sulfate for seizure prophylaxis followed by expedited delivery after maternal stabilization. 1, 2

Immediate Management of Severe Hypertension (≥160/110 mmHg)

Severe hypertension requires urgent treatment within 15 minutes to prevent maternal cerebral hemorrhage. 1, 3

First-Line Antihypertensive Agents:

  • IV labetalol: 20 mg IV bolus, then 40 mg after 10 minutes, then 80 mg every 10 minutes (maximum cumulative dose 220 mg) 2, 3
  • IV hydralazine: 5-10 mg IV every 20 minutes as needed 3, 4
  • Oral nifedipine: Acceptable alternative if IV agents unavailable 1

Blood Pressure Targets:

  • Target diastolic BP: 85 mmHg 1
  • Target systolic BP: 110-140 mmHg 1, 2
  • Minimum acceptable: <160/105 mmHg 2, 3
  • Goal: Decrease mean BP by 15-25% to maintain uteroplacental perfusion while preventing maternal complications 2

Critical Medication Warnings:

  • Avoid short-acting oral nifedipine when combined with magnesium sulfate due to risk of uncontrolled hypotension and fetal compromise 2
  • Sodium nitroprusside only as last resort due to risk of fetal cyanide poisoning 2, 4
  • ACE inhibitors, ARBs, and direct renin inhibitors are absolutely contraindicated due to severe fetotoxicity 2
  • Diuretics are contraindicated as they further reduce plasma volume which is already contracted in preeclampsia 2, 3

Management of Non-Severe Hypertension (140-159/90-109 mmHg)

Blood pressures consistently ≥140/90 mmHg in clinic (or ≥135/85 mmHg at home) should be treated to reduce the likelihood of developing severe hypertension and complications. 1

Acceptable Oral Agents:

  • First-line: Methyldopa, labetalol, oxprenolol, nifedipine 1
  • Second/third-line: Hydralazine, prazosin 1
  • Reduce or cease antihypertensives if diastolic BP falls <80 mmHg 1

Preeclampsia-Specific Management

Initial Assessment and Hospitalization:

All women with newly diagnosed preeclampsia must be assessed in hospital initially; stable patients may transition to outpatient management only if they can reliably report problems and monitor BP. 1

Magnesium Sulfate for Seizure Prophylaxis:

Administer magnesium sulfate immediately to all patients with:

  • Preeclampsia with proteinuria AND severe hypertension 1
  • Any hypertension with neurological signs or symptoms (severe headache, visual disturbances) 1, 2
  • All cases of severe preeclampsia 2, 5

Dosing regimen: 2, 3

  • Loading dose: 4-5 g IV over 5 minutes (diluted in 250 mL of 5% dextrose or 0.9% normal saline)
  • Maintenance: 1-2 g/hour continuous IV infusion
  • Continue until delivery and for at least 24 hours postpartum 1

In low-resource settings: 4 g IV or 10 g IM loading dose, followed by 5 g IM every 4 hours 1

Monitoring Requirements for Magnesium Sulfate:

  • Hourly urine output via Foley catheter: target ≥100 mL/4 hours (or >35 mL/hour) 2, 3
  • Deep tendon reflexes before each dose to monitor for toxicity 2
  • Respiratory rate monitoring (magnesium toxicity causes respiratory depression) 2
  • Oxygen saturation on room air (maternal early warning if <95%) 2

Comprehensive Maternal Monitoring in Preeclampsia

Laboratory Assessment:

Obtain at least twice weekly (more frequently with clinical deterioration): 1

  • Complete blood count (hemoglobin, platelet count)
  • Liver transaminases (AST/ALT)
  • Creatinine
  • Uric acid (associated with worse maternal and fetal outcomes) 1

Clinical Monitoring:

  • Continuous BP monitoring 1, 5
  • Repeated assessments for proteinuria if not already present 1
  • Clinical assessment including clonus 1
  • Assessment for maternal agitation, confusion, or unresponsiveness 2
  • Monitor for non-remitting headache and shortness of breath 2

Proteinuria Assessment:

Screen with automated dipstick urinalysis; if positive, quantify with urine protein/creatinine ratio. 1

  • Abnormal ratio: ≥30 mg/mmol (0.3 mg/mg) 1, 3
  • Alternative: ≥300 mg/24 hours or ≥1+ on dipstick 3

Fetal Monitoring in Preeclampsia

Initial Assessment:

Perform ultrasound at diagnosis to assess: 1

  • Fetal biometry
  • Amniotic fluid volume
  • Umbilical artery Doppler

Serial Surveillance:

  • Repeat ultrasound every 2 weeks if initial assessment normal 1, 2
  • More frequent monitoring (amniotic fluid and Doppler) if fetal growth restriction present 1, 2
  • Continuous fetal heart rate monitoring 2, 5

Delivery Timing: Gestational Age-Based Algorithm

≥37 Weeks:

Deliver immediately after maternal stabilization, regardless of severity. 1, 3

  • Induction of labor is associated with improved maternal outcome 2
  • Do not delay delivery based on non-reactive NST 3

34-37 Weeks:

  • Without severe features: Expectant management with close monitoring is appropriate 5, 3
  • With severe features: Deliver after maternal stabilization 3

<34 Weeks:

Conservative expectant management at a center with Maternal-Fetal Medicine expertise, unless maternal or fetal deterioration occurs. 2, 3

<24 Weeks:

Expectant management is associated with high maternal morbidity with limited perinatal benefit—counsel regarding pregnancy termination. 2

Absolute Indications for Immediate Delivery (Any Gestational Age)

Deliver immediately regardless of gestational age if any of the following develop: 1, 2

  • Inability to control BP despite ≥3 classes of antihypertensives in appropriate doses 1, 2
  • Progressive thrombocytopenia 1, 2
  • Progressively abnormal renal or liver enzyme tests 1, 2
  • Pulmonary edema 1, 2
  • Severe intractable headache, repeated visual scotomata, or convulsions 1, 2
  • Non-reassuring fetal status 1, 2
  • Maternal oxygen saturation deterioration (<90%) 2, 3
  • Placental abruption 2, 3

HELLP Syndrome Recognition and Management

HELLP syndrome is defined by hemolysis, elevated liver enzymes, and low platelets, with a maternal mortality rate of 3.4%. 2, 3

Hallmark Symptoms:

  • Epigastric or right upper quadrant pain (suggests hepatic capsule distension) 2, 3
  • Renal dysfunction with oliguria and elevated creatinine 2
  • Thrombocytopenia and elevated liver enzymes 2

Critical Considerations:

  • Monitor glucose intraoperatively as severe hypoglycemia can occur 2, 3
  • Immediate delivery is indicated after maternal stabilization 3

Management of Pulmonary Edema

Drug of choice: IV nitroglycerin (glycerol trinitrate) 2, 3

  • Starting dose: 5 mcg/min
  • Gradually increase every 3-5 minutes to maximum 100 mcg/min 2, 3
  • Plasma volume expansion is NOT recommended routinely 1, 2, 3

Eclampsia Management

Eclampsia (seizures in the setting of preeclampsia) requires immediate magnesium sulfate administration and expedited delivery after maternal stabilization. 2, 5

  • Magnesium sulfate is the definitive treatment for eclamptic seizures 6
  • Administer loading dose immediately, followed by maintenance infusion 2
  • Deliver after maternal stabilization regardless of gestational age 2

Gestational Hypertension Considerations

At least 25% of gestational hypertension cases will progress to preeclampsia; therefore, it is not a benign disorder. 1

Management:

  • Hospital assessment required if severe hypertension (≥160/110 mmHg) or preeclampsia develops 1
  • No specific test can predict which cases will progress to preeclampsia at time of diagnosis 1
  • Risk is highest among those presenting <34 weeks 1
  • Optimal delivery timing: 38-39 weeks for gestational hypertension without preeclampsia features (based on retrospective data, awaiting randomized trial confirmation) 1

Prevention Strategies

Low-dose aspirin (75-162 mg/day) starting in the first trimester until labor or 36-37 weeks reduces risk of preterm preeclampsia in high-risk women. 1, 6

  • Screening with maternal risk factors, BP, placental growth factor (PlGF), and uterine artery Doppler can identify candidates 1
  • Calcium supplementation recommended for prevention 6

Critical Pitfalls to Avoid

Do not underestimate disease severity—all preeclampsia cases should be treated as potentially severe, as rapid progression to life-threatening complications can occur even with initially mild presentations. 1, 3

  • Blood pressure alone is not a reliable indicator of disease severity—serious organ dysfunction can develop at relatively mild levels of hypertension 5, 3
  • Do not use serum uric acid or level of proteinuria as indication for delivery 2, 3
  • Do not attempt to diagnose "mild versus severe" preeclampsia clinically—all cases may become emergencies rapidly 1, 2
  • Do not reduce antihypertensives if diastolic BP falls <80 mmHg 2, 3
  • Home BP monitoring is mandatory in white-coat hypertension management 1

Transfer and Coordination

Medicalized transport to a specialized obstetric center should be systematically considered for all patients with severe preeclampsia. 2

Before Transfer:

  • Coordinate with obstetric and anesthetic-intensivist teams at receiving facility 2
  • Initiate magnesium sulfate and blood pressure control prior to transport 2
  • Involve emergency medical assistance service regulating doctor 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Severe Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Initial Management of Pre-eclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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