The real-world use of OPSUMIT® (macitentan) has been rigorously examined in both the OPUS registry and the OrPHeUS cohort study. These data demonstrate the effective use of OPSUMIT® in a broad range of patients with pulmonary arterial hypertension (PAH), including those with PAH associated with connective tissue disease (CTD), as well as in elderly patients with PAH and those with comorbidities.[1][2][3][4][5]
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Real-world data from OPUS and OrPHeUS support the use of OPSUMIT® in patients with connective tissue disease (CTD)-associated pulmonary arterial hypertension (PAH) and its subtypes, including PAH associated with scleroderma/systemic sclerosis (SSc), systemic lupus erythematosus (SLE) and mixed connective tissue disease (MCTD). Similar clinical outcomes were observed in patients with CTD-PAH and those with idiopathic PAH (IPAH)/heritable PAH (HPAH) at 2 years.[2]
Adapted from McLaughlin et al. 2019[2]
Real-world data from the OPUS registry show that OPSUMIT® can be used effectively in patients with pulmonary arterial hypertension (PAH) and various comorbidities that may complicate treatment choice, including:[3][4]
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Evidence from the combined OPUS registry and OrPHeUS cohort show that OPSUMIT® can be used effectively in both younger (<65 years) and older (≥65 years) patients with pulmonary arterial hypertension (PAH).*[5]
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CHD, congenital heart disease; CI, confidence interval; CTD, connective tissue disease; FC, functional class; HPAH, heritable pulmonary arterial hypertension; IPAH, idiopathic pulmonary arterial hypertension; MCTD, mixed connective tissue disease; PAH, pulmonary arterial hypertension; SLE, systemic lupus erythematosus; SSc, systemic sclerosis; WHO, World Health Organization
OPSUMIT® PRESCRIBING INFORMATION AND ADVERSE EVENT REPORTING