Key result
Placental transfer occurs for methyldopa, labetalol, and nifedipine with fetal/maternal ratios between 0.1 and 1, indicating no fetal accumulation, though pharmacokinetic data are highly heterogeneous.
Why the study?
Methyldopa, labetalol, and nifedipine are recommended in international guidelines for hypertension during pregnancy, but a complete overview of their pharmacokinetics throughout pregnancy was needed.
What is the pharmacokinetic profile of methyldopa, labetalol, and nifedipine during pregnancy?
Systematic Review
What is the pharmacokinetic profile of methyldopa, labetalol, and nifedipine during pregnancy?
Despite widespread use, there is a lack of robust pharmacokinetic data for methyldopa, labetalol, and nifedipine during pregnancy, highlighting the need for further studies to optimize dosing.
Limited heterogeneous PK data leave dosing uncertain in pregnancy; leaves open need for prospective studies to guide therapy.
PURPOSE: Antihypertensive drugs are among the most prescribed drugs during pregnancy. Methyldopa, labetalol, and nifedipine have been perceived safe to use during pregnancy and are therefore recommended in international guidelines for treatment of hypertension. In this review, we provide a complete overview of what is known on the pharmacokinetics (PK) of the antihypertensive drugs methyldopa, labetalol, and nifedipine throughout pregnancy. METHODS: A systematic search was performed to retrieve studies on the PK of methyldopa, labetalol, and nifedipine used throughout pregnancy. The search was restricted to English and original studies. The systematic search was conducted on July 27, 2021, in Embase, Medline Ovid, Web of Science, Cochrane Library, and Google Scholar. Keywords were methyldopa, labetalol, nifedipine, pharmacokinetics, pregnancy, and placenta. RESULTS: A total of 1459 unique references were identified of which title and abstract were screened. Based on this screening, 67 full-text papers were assessed, to retain 30 PK studies of which 2 described methyldopa, 12 labetalol, and 16 nifedipine. No fetal accumulation is found for any of the antihypertensive drugs studied. CONCLUSION: We conclude that despite decades of prescribing methyldopa, labetalol, and nifedipine throughout pregnancy, descriptions of their PK during pregnancy are hampered by a large heterogeneity in the low number of available studies. Aiming for evidence-based and personalized dosing of antihypertensive medication in the future, further studies on the relationship of both PK and pharmacodynamics (including the optimal blood pressure targeting) during pregnancy and pregnancy-related pathology are urgently needed to prevent undertreatment, overtreatment, and side effects.
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Vusse et al. (2022) conducted a systematic review in Hypertension during pregnancy. Methyldopa, labetalol, and nifedipine was evaluated on Pharmacokinetic parameters and fetal/maternal plasma ratio. Placental transfer occurs for methyldopa, labetalol, and nifedipine with fetal/maternal ratios between 0.1 and 1, indicating no fetal accumulation, though pharmacokinetic data are highly heterogeneous.
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