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Management of Hypertension in Pregnancy
Classification
Hypertensive disorders of pregnancy are classified into four main categories:
- Chronic hypertension — pre-existing hypertension (before 20 weeks or pre-pregnancy)
- Gestational hypertension — new-onset hypertension ≥20 weeks, without proteinuria, resolving within 3 months postpartum
- Preeclampsia/eclampsia — new-onset hypertension ≥20 weeks with proteinuria (or end-organ dysfunction)
- Chronic hypertension with superimposed preeclampsia
Blood Pressure Thresholds and Targets
| Category | Definition |
|---|
| Mild/moderate hypertension | SBP 140–159 / DBP 90–104 mmHg |
| Severe hypertension | SBP ≥160 / DBP ≥105 mmHg |
Treatment targets:
- Severe hypertension (SBP ≥160 or DBP ≥105 mmHg): antihypertensive therapy is clearly indicated to prevent stroke and cardiovascular complications.
- Mild-to-moderate hypertension: evidence supports treating to a DBP target of 85 mmHg (CHIPS trial). Tight control reduces episodes of severe hypertension without adverse fetal outcomes.
- Avoid BP falling too low — excessive lowering may compromise uteroplacental perfusion.
— Creasy & Resnik's Maternal-Fetal Medicine, p. 490; Comprehensive Clinical Nephrology, p. 2160
Antihypertensive Drug Selection
First-Line Oral Agents
| Medication | Starting Dose | Max Daily Dose | Notes |
|---|
| Methyldopa | 250 mg twice daily | 2000 mg | Most extensive safety data; sedation, rare hemolytic anemia |
| Labetalol | 200 mg twice daily | 1200 mg | α+β blockade preserves uteroplacental flow; avoid in asthma |
| Long-acting nifedipine | 30 mg once daily | 120 mg | Once-daily dosing; side effect: edema, headache |
| Hydralazine (oral) | 50 mg three times daily | 300 mg | Tachycardia; second-line orally |
First-Line IV Agents (Acute/Severe Hypertension)
- IV Labetalol — good safety data; preferred initial IV agent
- IV Nicardipine — extensive safety data as a tocolytic; effective for acute BP control
- IV Hydralazine — historically used but now second-line IV due to increased risk of maternal hypotension and placental abruption
Second-Line Agents
- Metoprolol — potential once-daily dosing; less safety data than labetalol
- Verapamil / Diltiazem — no adverse fetal effects but limited data
- Clonidine — comparable to methyldopa in mechanism; fewer data
Agents to Avoid or Use Cautiously
| Drug | Reason |
|---|
| ACE inhibitors | Fetal renal dysplasia, oligohydramnios, pulmonary hypoplasia (2nd/3rd trimester) — contraindicated |
| ARBs | Same risks as ACE inhibitors — contraindicated |
| Atenolol | Associated with fetal growth restriction |
| Diuretics | Impair plasma volume expansion; avoid in preeclampsia; acceptable for volume overload only |
| Nitroprusside | Risk of fetal cyanide toxicity if used >4 hours |
| Spironolactone | Theoretical risk of inadequate male fetal virilization (antiandrogenic); eplerenone preferred if mineralocorticoid blockade needed |
— Comprehensive Clinical Nephrology, p. 2160; Creasy & Resnik's Maternal-Fetal Medicine, p. 490
Preeclampsia
Diagnosis
- Hypertension ≥140/90 mmHg after 20 weeks plus proteinuria (≥300 mg/24h), or end-organ involvement (thrombocytopenia, renal insufficiency, impaired liver function, pulmonary edema, new-onset headache/visual disturbance)
Risk Factors
Nulliparity, new partner, family history, multiple gestation, prior preeclampsia, chronic hypertension, diabetes, CKD, obesity, antiphospholipid syndrome, extremes of maternal age
Pathophysiology (key points)
- Impaired trophoblast invasion → high-resistance spiral arteries → placental ischemia
- Excess placental sFlt-1 (soluble VEGF receptor) neutralizes VEGF and PlGF → widespread endothelial dysfunction
- sFlt-1/PlGF ratio: elevated before onset; a low ratio has 99% NPV for ruling out preeclampsia within the next week
Management of Preeclampsia
- Definitive treatment = delivery (only cure)
- Antihypertensive therapy as above for BP control
- Magnesium sulfate for seizure prophylaxis (eclampsia prevention) in severe preeclampsia
- Monitor for HELLP syndrome (Hemolysis, Elevated Liver enzymes, Low Platelets)
- Fetal surveillance: growth scans, umbilical artery Doppler, fetal well-being monitoring
Delivery Timing
- ≥37 weeks with preeclampsia without severe features: deliver
- ≥34 weeks with severe features or deteriorating maternal/fetal condition: deliver
- <34 weeks with severe features: corticosteroids for fetal lung maturation, then individualize based on maternal/fetal stability
Eclampsia
- Defined as seizures in a woman with preeclampsia
- Management: IV magnesium sulfate (first-line for acute seizure control and prevention of recurrence), BP control, prompt delivery
Chronic Hypertension in Pregnancy
- Screen for secondary causes (renal artery stenosis, primary hyperaldosteronism, OSA, pheochromocytoma) — especially if hypertension is severe or resistant
- Switch to pregnancy-safe antihypertensives before conception where possible; stop ACE inhibitors/ARBs immediately when pregnancy is confirmed
- Counsel about increased risks: superimposed preeclampsia, preterm birth, IUGR
- Follow closely with BP monitoring and urine protein surveillance
Gestational Hypertension
- New-onset hypertension after 20 weeks, without proteinuria, resolving by 12 weeks postpartum
- 15–25% progress to preeclampsia — requires close monitoring
- Associated with increased risk of future hypertension and cardiovascular disease in the mother
- Offspring at increased risk for preterm delivery and IUGR
Non-Pharmacologic Measures
Aerobic exercise, dietary sodium restriction, and weight loss — while beneficial in non-pregnant hypertensive patients — have not been thoroughly evaluated in pregnancy and are not recommended as primary strategies.
Key Take-Aways
| Situation | Action |
|---|
| SBP ≥160 or DBP ≥105 | Treat urgently (IV labetalol or nicardipine; oral nifedipine) |
| Mild-to-moderate HTN | Treat to DBP ~85 mmHg (CHIPS trial) |
| Preeclampsia | Deliver at appropriate gestational age + MgSO₄ + antihypertensives |
| ACE inhibitors / ARBs | Stop immediately upon pregnancy confirmation |
| Eclampsia | IV magnesium sulfate + urgent delivery |
— Comprehensive Clinical Nephrology, pp. 2159–2161; Creasy & Resnik's Maternal-Fetal Medicine, pp. 489–491