The Journal of Clinical Hypertension (Aug 2022)

Comparative efficacy and safety of fimasartan in patients with hypertension: A network meta‐analysis of randomized controlled trials

  • Suk Min Seo,
  • Sang Hyun Ihm,
  • Jeong‐Eun Yi,
  • Seung Hee Jeong,
  • Bong‐Seog Kim

DOI
https://doi.org/10.1111/jch.14536
Journal volume & issue
Vol. 24, no. 8
pp. 971 – 983

Abstract

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Abstract Hypertension is a prevalent risk factor for cardiovascular disease. Angiotensin II receptor blockers are widely prescribed to patients with hypertension, while new drugs are continuously developed. However, data on comparative efficacy and safety of novel agents, such as fimasartan, are scarce. Here, we aimed to collect clinical evidence on different angiotensin II receptor blockers using a network meta‐analysis. Randomized controlled trials whose follow‐up time is within 12 weeks were identified from eight databases via a systematic literature review. Of the 7909 possibly relevant studies, 61 studies with 14,249 adult patients were included in the analysis. These studies were further subjected to quality appraisal using Cochran's Risk of Bias, and sitting systolic blood pressure was considered the primary endpoint. A Bayesian random effect generalized linear model was used for the network meta‐analysis, and the treatment rank probability was determined. Olmesartan (standardized mean difference ‐0.987 [‐1.29, ‐0.729]) and fimasartan (standardized mean difference ‐0.966 [‐1.21, ‐0.745]) showed the highest rank probabilities (37% and 35%) in the 4‐week group, considering the primary endpoint. Furthermore, the odds ratio of adverse events for all agents did not differ significantly from that of the placebo. The treatment rank of angiotensin II receptor blockers varied depending on the outcome type and follow‐up period considerably. Fimasartan rapidly lowered blood pressure in 4 weeks, which was further maintained until 12 weeks, indicating its competent efficacy and tolerability. Our findings may help medical practitioners and patients to select the best angiotensin II receptor blocker against hypertension.

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