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    Home»Archives»EFFICACY AND SAFETY PROFILE OF INTRAVENOUS LABETALOL IN THE MANAGEMENT OF SEVERE HYPERTENSION IN PRE-ECLAMPSIA: A PROSPECTIVE EVALUATION IN A NIGERIAN TERTIARY HOSPITAL
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    EFFICACY AND SAFETY PROFILE OF INTRAVENOUS LABETALOL IN THE MANAGEMENT OF SEVERE HYPERTENSION IN PRE-ECLAMPSIA: A PROSPECTIVE EVALUATION IN A NIGERIAN TERTIARY HOSPITAL

    By Ogbiti Mark Imhonikhe, Ezugwu Obinna Patrick, Igene Charles Imonitie, Eigbedion Andrew Oseghale, Afekhobe Jedidiah Suleiman Buraimoh, Salami Isenalumhe Ade, Yaya O.B. and Ekeng OffiongJune 17, 2025No Comments2 Mins Read
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    ABSTRACT
    Severe hypertension in pre-eclampsia remains a leading cause of maternal and perinatal morbidity
    and mortality worldwide, particularly in low-resource settings where access to timely and effective
    treatment can be challenging. Rapid blood pressure control is essential to prevent complications,
    and intravenous Labetalol, a combined alpha- and beta-adrenergic blocker, is widely recommended
    for emergency management in pregnancy. However, there is limited evidence on its efficacy and
    safety among populations in sub-Saharan Africa. This prospective cohort study was conducted at
    a tertiary hospital in Nigeria to evaluate the effectiveness and tolerability of intravenous Labetalol
    in women with pre-eclampsia complicated by severe hypertension, defined as systolic blood
    pressure of 160 mmHg or higher and/or diastolic blood pressure of 110 mmHg or higher, beyond
    28 weeks of gestation. A total of 38 women received escalating bolus doses of intravenous
    Labetalol ranging from 20 mg up to a maximum cumulative dose of 300 mg until target blood
    pressure levels (130–150 mmHg systolic and 80–100 mmHg diastolic) were achieved. The study

    found that 84.2% of participants attained adequate blood pressure control, with a median time to
    control of 20 minutes and a median of 2 doses required. Notably, 31.6% of women achieved control
    with a single dose. No episodes of hypotension were recorded, though some participants
    experienced mild adverse effects including maternal tachycardia (7.9%) and dizziness (13.2%).
    Neonatal bradycardia was observed in 10.5% of cases, but there were no early neonatal deaths.
    These findings suggest that intravenous Labetalol is both effective and well-tolerated for acute
    management of severe hypertension in pre-eclamptic women in this setting. Given the potential
    for neonatal bradycardia, close monitoring of newborns is recommended. This study supports the
    continued use of intravenous Labetalol as a first-line treatment for severe hypertension in pre
    eclampsia within resource-limited tertiary maternity care facilities.
    Keywords: Pre-eclampsia, Severe hypertension, Labetalol, Antihypertensive therapy, Maternal
    safety, Neonatal outcomes, Nigeria

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    Ogbiti Mark Imhonikhe, Ezugwu Obinna Patrick, Igene Charles Imonitie, Eigbedion Andrew Oseghale, Afekhobe Jedidiah Suleiman Buraimoh, Salami Isenalumhe Ade, Yaya O.B. and Ekeng Offiong

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