Abstract
Objective: Hypertension affects approximately 10% of pregnancies worldwide, contributing significantly to maternal morbidity and mortality. Severe hypertension in pregnancy is defined as systolic blood pressure exceeding 160 mmHg and diastolic blood pressure greater than 110 mmHg, persisting for more than 15 minutes. This condition represents an obstetric emergency that necessitates immediate and appropriate management.
Methods: A quasi-experimental study was conducted at a tertiary care centre in Rawalpindi. The study included 70 patients, divided into two groups: Group 1 (n = 35) received oral nifedipine, while Group 2 (n = 35) was treated with intravenous labetalol. Treatment was initiated with 5 mg of oral nifedipine and 20 mg of intravenous labetalol as part of a gradual dose-escalation protocol designed to reduce pharmacological risks while ensuring effective blood pressure control.
Results: The findings revealed that therapeutic blood pressure was achieved significantly faster in the nifedipine group (mean time: 22.3 ± 11.5 minutes) compared to the labetalol group (mean time: 33.5 ± 13.3 minutes, p=0.03). Additionally, fewer doses were required in the nifedipine group than in the labetalol group. The rate of treatment failure was notably higher among patients treated with intravenous labetalol.
Conclusion: Oral nifedipine proved to be as efficacious and safe as intravenous labetalol, with the added advantage of convenience in low-resource settings.
Keywords: Pregnancy-induced hypertension, nifedipine, labetalol, failed treatment, Preeclampsia
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