Key result
Macitentan linked to a ~19% lower risk of PAH-related hospitalization vs. other ERAs.
Why the study?
Few studies have evaluated macitentan alongside other endothelin receptor antagonists in patients with pulmonary arterial hypertension.
Does macitentan reduce PAH-related hospitalization in adults with pulmonary arterial hypertension compared to other ERAs?
Observational (n=897)
Does macitentan reduce PAH-related hospitalization in adults with pulmonary arterial hypertension compared to other ERAs?
Answers are grounded in this paper and cite their sources.
In a real-world cohort of patients with pulmonary arterial hypertension, macitentan was associated with significantly lower risks of PAH-related and all-cause hospitalizations, as well as reduced ICU utilization, compared to other endothelin receptor antagonists.
BACKGROUND: Few studies have evaluated macitentan alongside other endothelin receptor antagonists (ERAs) in patients with pulmonary arterial hypertension (PAH). This retrospective, observational, real-world, comparative effectiveness analysis assessed outcomes in PAH with macitentan versus other ERAs. METHODS: Adults (≥18 years) were included from the de-identified Optum Clinformatics Data Mart database (January 2014-December 2023). Index date was first ERA prescription. Patients were continuously enrolled in the database for ≥12 months before index (baseline), with pulmonary hypertension/PAH diagnosis and right-heart catheterization during baseline. Primary endpoint was time to first PAH-related hospitalization (Cox proportional-hazards). Secondary endpoints included healthcare resource utilization. RESULTS: Overall, 518 patients receiving macitentan and 379 other ERAs (ambrisentan, n = 370; bosentan, n = 9) were included. Mean age was 67 years and ∼70 % were female. Patients on macitentan versus other ERAs had higher baseline Charlson Comorbidity Index (P < 0.007). Risks of PAH-related and all-cause hospitalization were 19 % and 20 % lower, respectively, for macitentan versus other ERAs (hazard ratios: 0.81, P = 0.034; 0.80, P = 0.020, respectively). There were fewer all-cause and PAH-related intensive care unit (ICU) stays for macitentan versus other ERAs (P = 0.009, P = 0.013, respectively). Overall duration of all-cause ICU stay per patient per year was significantly shorter for macitentan versus other ERAs (7.0 vs 7.7 days; P = 0.003), as was the duration of all-cause ICU stay per visit (2.4 vs 3.7 days; P = 0.003). CONCLUSION: Macitentan was associated with a significantly reduced risk of PAH-related and all-cause hospitalization, with lower ICU healthcare resource utilization, versus other ERAs.
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Paoli et al. (2025) conducted an observational in pulmonary arterial hypertension (PAH) (n=897). macitentan vs. other ERAs (ambrisentan, bosentan) was evaluated on time to first PAH-related hospitalization (HR 0.81, p=0.034). Macitentan was associated with a 19% lower risk of PAH-related hospitalization compared with other endothelin receptor antagonists (HR 0.81; P=0.034).
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