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The dangers of immediate-release nifedipine in the emergency treatment of hypertension

Journal of Human Hypertension volume 22, pages 301–302 (2008)Cite this article

Most authorities recommend that in the emergency treatment of hypertension, the aim is to produce a gradual but sustained fall in systemic blood pressure over hours to days.1 For example, the European Society of Hypertension recommends that in hypertensive urgencies (defined as severe elevations in BP >180/120 mm Hg without evidence of target organ damage), blood pressure should be lowered over 24–48 h using orally administered drugs.2 Although the dangers of immediate-release nifedipine are well described these preparations remain in widespread clinical use. This review summarises recent reports of such adverse events. Rapid fall in pressure can compromise cerebral and myocardial perfusion with dramatic consequences. There are numerous case reports in the literature of such calamities following administration of sublingual nifedipine capsules, including reports of cerebrovascular ischaemia, severe hypotension, acute myocardial infarction, conduction disturbances, fetal distress and death.3, 4 Given that sublingual absorption of nifedipine is poor and most of the drug is absorbed by the intestinal mucosa,5 it is to be expected that other immediate-release preparations carry similar risks. There are no large randomized clinical trials showing the frequency of adverse events with immediate-release nifedipine. The few small trials that do exist are outlined in Table 1.

Table 1 Summary of adverse events reported with immediate-release nifedipine
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  1. Department of Clinical Pharmacology, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK

    T J Burton & I B Wilkinson

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  1. T J Burton
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  2. I B Wilkinson
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Correspondence to T J Burton.

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Burton, T., Wilkinson, I. The dangers of immediate-release nifedipine in the emergency treatment of hypertension. J Hum Hypertens 22, 301–302 (2008). https://doi.org/10.1038/sj.jhh.1002324

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