Table 3.
Recommended management options for treating hypertension in pregnancy
| Drug Treatment | Dose[26, 27] |
FDA Class |
Safety | Side Effects | Breast feeding* |
|---|---|---|---|---|---|
| First line agents | |||||
| Methyldopa (F), (I–A) Drug of choice according to all groups |
0.5–3 gm/day in 2divided doses |
B | Proven safety and efficacy |
Some concern with depression, hepatic disturbances, hemolytic anemia -may not lower BP adequately |
Compatible with breast milk |
| Labetalol (M), (I–A) |
200–1200 mg/day p.o. in 2–3 divided doses 20–40mg iv (max 220mg total) |
C | Safety similar to methyldopa may be more efficacious than methyldopa; |
May be associated with fetal growth restriction. Neonatal hypoglycemia with larger doses |
Usually compatible with breast milk |
| Second-line agents | |||||
| Nifedipine Long-acting (Ra), (I–A) |
10–30 mg p.o. |
C | widely used |
May inhibit labor; Rarely, profound hypotension if short- acting agent is used with magnesium |
Usually compatible with breast milk |
| Verapamil | 80mg tds p.o. |
C | Similar efficacy to other oral agents |
Risk of interaction with magnesium – bradycardia |
Usually compatible with breast milk |
| Clonidine Alternative option |
0.1–0.6 mg/day in 2 divided doses |
C | Safety similar to methyldopa Limited data regarding fetal safety |
Efficacy similar to methyldopa |
Possible breast milk effects |
| Hydrochlorothiazide Useful in chronic hypertension |
12.5–25 mg/day |
B | Volume contraction, electrolyte abnormalities – rare with small doses |
May reduce breast milk production |
|
| Hydralazine (F, Re) Not recommended by ESH [24, 23] |
50–300 mg/d in 2–4 divided doses |
D | Efficacious intraveno us agent |
Possible maternal polyneuropathy, drug-induced lupus, neonatal lupus and thrombocytopenia; Tachyphylaxis |
Usually compatible with breast milk |
| Atenolol | (Atenolol not recommended) (I–D) Atenolol has risk of growth restriction when started in first or second trimester and is not recommended if breast feeding |
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| Diazoxide | 30–50 mg iv every 5–15 min; iv bolus for acute BP lowering in severe hypertension [19] |
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| Prazosin | 0.5–5mg tds; consider as a second line agent by SOMANZ [19] Not recommended by SOGC[16] (I–D) Associated with postural hypotension and palpitations |
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| Oxprenolol (beta blocker with ISA) |
20–160mg tds; a first line agent by SOMANZ[19] Contraindicated in heart block |
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| Nitroprusside | Only considered for life-threatening severe hypertension Cyanide and thiocyanate toxicity, must be carefully monitored. Also risk of cardio-neurogenic syncope |
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| Contraindicated[26] | ACE inhibitors, angiotensin II receptor blockers (Pr, Re), (II-2E), FDA Class D |
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| Direct renin inhibitors | |||||
| Spironolactone not recommended due to potential foetal antiandrogen effects | |||||
| Other Management Strategies | |||||
| Low dose aspirin | Use advised in women at high risk Used prophylactically in women with a history of preeclampsia at <28 Weeks |
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| Fish oil supplementation |
Not recommended | ||||
| Calcium supplementation |
May have role in decreasing incidence of preeclampsia Role in low calcium intake populations |
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| Vitamin C and E | Not recommended | ||||
| Steroid therapy | Only for fetal lung maturation | ||||
According to either the World Health Organization and/or Thomson lactation ratings. FDA, Food and Drug Administration; ISA, intrinsic sympathomimetic activity. The abbreviations in parentheses represent the types of studies that provided the evidence base for the recommendations from the NHBPEP. (M)- meta-analysis, an analysis of a compendium of experimental studies; (Ra)- randomized controlled trials; (Re)- retrospective analyses, also known as case-control studies; (F)- prospective follow-up, also known as cohort studies, including historical cohort studies and long-term follow-up; (Pr)- previous review or position statements; and the key codes from the evidence base used by the SOGC. An explanation of these can be found in the appendices.