AI Article Synopsis

  • Oral prostanoids are recommended for patients with pulmonary arterial hypertension (PAH) who don't respond well to initial treatments, and the study compares several oral therapies targeting the prostacyclin pathway.
  • A meta-analysis of 8 randomized controlled studies (involving 3023 patients) showed that oral treprostinil and beraprost significantly improved the 6-minute walking distance (6MWD) compared to placebo, while selexipag had a non-significant increase.
  • Both oral treprostinil and selexipag reduced the risk of clinical worsening, but no significant differences in effectiveness or safety were found between the two; beraprost caused fewer adverse events than the others.

Article Abstract

Background: Oral prostanoids are recommended in patients with pulmonary arterial hypertension (PAH) and an unsatisfactory response to first-line therapy.

Objective: To compare the effectiveness of oral therapies targeting the prostacyclin pathway in PAH patients.

Methods: An online search of Medline, Cochrane Registry, Scopus and EMBASE libraries (from inception to May, 12,020) was conducted. Eight randomized controlled studies were included in the meta-analysis involving 3023 patients, with 828 receiving oral treprostinil, 607 patients receiving selexipag, 125 patients receiving beraprost, and 1463 patients receiving placebo.

Results: Compared to placebo, oral treprostinil (WMD 9.05, 95% CI 3.0280-15.0839, p = 0.0032) and beraprost (WMD 21.98, 95% CI 5.0536-38.9063, p = 0.0109) were associated with a significant increase in 6-min walking distance (6MWD) at follow-up from baseline, whereas selexipag use was associated with a non-significant increase in 6MWD (WMD 15.41, 95% CI -0.6074; 31.4232, p = 0.0593). Compared to placebo, the risk of clinical worsening was significantly lowered by selexipag (RR 0.47, 95% CI 0.35-0.65, p < 0.001) and oral treprostinil (RR 0.65, 95% CI 0.46-0.90, p 0.012), whereas a non-significant reduction of the outcome was related to beraprost use (RR 0.70, 95% CI 0.36-1.38, p 0.31). No significant difference in 6MWD change and clinical worsening reduction were found among oral treprostinil and selexipag. Beraprost use less frequently caused adverse events as compared to selexipag and oral treprostinil.

Conclusions: No differences in 6MWD change, clinical worsening reduction and adverse events rates were found among oral treprostinil and selexipag, resulting in similar efficacy and safety profiles.

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Source
http://dx.doi.org/10.1016/j.vph.2024.107280DOI Listing

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