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Meta-analysis of randomized controlled trials of bosentan for treatment of pulmonary arterial hypertension

  • Lee, Young Ho (Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine) ;
  • Song, Gwan Gyu (Division of Rheumatology, Department of Internal Medicine, Korea University College of Medicine)
  • Received : 2012.11.29
  • Accepted : 2013.01.17
  • Published : 2013.11.01

Abstract

Background/Aims: We assessed the efficacy and safety of bosentan in patients with pulmonary arterial hypertension (PAH). Methods: We surveyed randomized controlled trials (RCTs) of the efficacy and safety of bosentan in patients with PAH using MEDLINE, EMBASE, the Cochrane Controlled Trials Register, and manual searches. Meta-analysis of RCTs was performed to determine treatment efficacy and safety outcomes. Results are presented as odds ratios (ORs) or weighted mean differences (WMDs). Results: Meta-analysis of seven RCTs including a total of 410 patients and 296 controls revealed that the 6-minute work distance was significantly higher in the bosentan group than in the placebo group (WMD, 46.19; 95% confidence interval [CI], 21.20 to 71.19; $p=2.9{\times}10^{-5}$). Compared with the placebo, bosentan significantly reduced the mean pulmonary arterial pressure in patients with PAH (WMD, -6.026; 95% CI, -8.785 to -3.268, $p=1.8{\times}10^{-6}$). The bosentan therapy group worsened less clinically than the placebo group (OR, 0.252; 95% CI, 0.140 to 0.454; $p=4.6{\times}10^{-7}$). The incidence of serious adverse events did not differ between the bosentan and placebo groups (OR, 0.948; 95% CI, 0.556 to 1.614; p = 0.843). However, the results of the abnormal liver function test (LFT) were significantly higher in the bosentan group than in the placebo group (OR, 2.312; 95% CI, 1.020 to 5.241; p = 0.045). Conclusions: This meta-analysis shows that bosentan can treat PAH effectively. However, bosentan increased the incidence of abnormal LFT results compared with the placebo.

Keywords

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