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Oral antihypertensive therapy for severe hypertension in pregnancy and postpartum: a systematic review.

Firoz, T; Magee, LA; MacDonell, K; Payne, BA; Gordon, R; Vidler, M; von Dadelszen, P; Community Level Interventions for Pre-eclampsia (CLIP) Working G, CLIP (2014) Oral antihypertensive therapy for severe hypertension in pregnancy and postpartum: a systematic review. Bjog : An International Journal Of Obstetrics & Gynaecology, 121 (10). pp. 1210-1218. https://doi.org/10.1111/1471-0528.12737
SGUL Authors: von Dadelszen, Peter

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Abstract

BACKGROUND: Pregnant and postpartum women with severe hypertension are at increased risk of stroke and require blood pressure (BP) reduction. Parenteral antihypertensives have been most commonly studied, but oral agents would be ideal for use in busy and resource-constrained settings. OBJECTIVES: To review systematically, the effectiveness of oral antihypertensive agents for treatment of severe pregnancy/postpartum hypertension. SEARCH STRATEGY: A systematic search of MEDLINE, EMBASE and the Cochrane Library was performed. SELECTION CRITERIA: Randomised controlled trials in pregnancy and postpartum with at least one arm consisting of a single oral antihypertensive agent to treat systolic BP ≥ 160 mmHg and/or diastolic BP ≥ 110 mmHg. DATA COLLECTION AND ANALYSIS: Cochrane RevMan 5.1 was used to calculate relative risk (RR) and weighted mean difference by random effects. MAIN RESULTS: We identified 15 randomised controlled trials (915 women) in pregnancy and one postpartum trial. Most trials in pregnancy compared oral/sublingual nifedipine capsules (8-10 mg) with another agent, usually parenteral hydralazine or labetalol. Nifedipine achieved treatment success in most women, similar to hydralazine (84% with nifedipine; relative risk [RR] 1.07, 95% confidence interval [95% CI] 0.98-1.17) or labetalol (100% with nifedipine; RR 1.02, 95% CI 0.95-1.09). Less than 2% of women treated with nifedipine experienced hypotension. There were no differences in adverse maternal or fetal outcomes. Target BP was achieved ~ 50% of the time with oral labetalol (100 mg) or methyldopa (250 mg) (47% labetelol versus 56% methyldopa; RR 0.85 95% CI 0.54-1.33). CONCLUSIONS: Oral nifedipine, and possibly labetalol and methyldopa, are suitable options for treatment of severe hypertension in pregnancy/postpartum.

Item Type: Article
Additional Information: © 2014 The Authors BJOG An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd on behalf of Royal College of Obstetricians and Gynaecologists. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Keywords: Antihypertensive therapy, hypertensive disorders of pregnancy, oral agents, pregnancy, severe hypertension, Administration, Oral, Antihypertensive Agents, Female, Humans, Hydralazine, Hypertension, Pregnancy-Induced, Labetalol, Methyldopa, Nifedipine, Postpartum Period, Pregnancy, Pregnancy Complications, Cardiovascular, Randomized Controlled Trials as Topic, Treatment Outcome, Vasodilator Agents, Community Level Interventions for Pre-eclampsia (CLIP) Working Group, Humans, Hypertension, Pregnancy-Induced, Pregnancy Complications, Cardiovascular, Labetalol, Methyldopa, Hydralazine, Nifedipine, Antihypertensive Agents, Vasodilator Agents, Treatment Outcome, Administration, Oral, Postpartum Period, Pregnancy, Female, Randomized Controlled Trials as Topic, Obstetrics & Reproductive Medicine, 11 Medical And Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Bjog : An International Journal Of Obstetrics & Gynaecology
Language: eng
Dates:
DateEvent
16 May 2014Published
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 3.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDBill and Melinda Gates Foundationhttp://dx.doi.org/10.13039/100000865
PubMed ID: 24832366
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/107507
Publisher's version: https://doi.org/10.1111/1471-0528.12737

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