<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>41(11)</volume><submitter>Chin KM</submitter><funding>Actelion Pharmaceuticals Ltd, a Johnson &amp;amp; Johnson Company</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Historically, patients recently (≤ 6 months) diagnosed with pulmonary arterial hypertension (PAH; incident) have had poorer survival than those with a longer (> 6 months) time from PAH diagnosis (prevalent). Despite guideline recommendations for initial combination therapy for most patients with PAH, many are initiated and maintained on monotherapy. Real-world evidence to evaluate the benefit of early combination treatment in newly-diagnosed patients is lacking.&lt;h4>Methods&lt;/h4>Patients with PAH initiating combination therapy with the endothelin receptor antagonist macitentan and the phosphodiesterase-5 inhibitor tadalafil (M+T) were identified from the combined dataset of the US, multicenter OPUS (prospective, observational drug registry; NCT02126943) and OrPHeUS (retr</pubmed_abstract><journal>Advances in therapy</journal><pagination>4205-4227</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11480149</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Macitentan and Tadalafil Combination Therapy in Incident and Prevalent Pulmonary Arterial Hypertension: Real-World Evidence from the OPUS/OrPHeUS Studies.</pubmed_title><pmcid>PMC11480149</pmcid><pubmed_authors>Senatore A</pubmed_authors><pubmed_authors>Ong R</pubmed_authors><pubmed_authors>Channick R</pubmed_authors><pubmed_authors>McLaughlin VV</pubmed_authors><pubmed_authors>MacDonald G</pubmed_authors><pubmed_authors>Martin N</pubmed_authors><pubmed_authors>Chin KM</pubmed_authors><pubmed_authors>Kim NH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Macitentan and Tadalafil Combination Therapy in Incident and Prevalent Pulmonary Arterial Hypertension: Real-World Evidence from the OPUS/OrPHeUS Studies.</name><description>&lt;h4>Introduction&lt;/h4>Historically, patients recently (≤ 6 months) diagnosed with pulmonary arterial hypertension (PAH; incident) have had poorer survival than those with a longer (> 6 months) time from PAH diagnosis (prevalent). Despite guideline recommendations for initial combination therapy for most patients with PAH, many are initiated and maintained on monotherapy. Real-world evidence to evaluate the benefit of early combination treatment in newly-diagnosed patients is lacking.&lt;h4>Methods&lt;/h4>Patients with PAH initiating combination therapy with the endothelin receptor antagonist macitentan and the phosphodiesterase-5 inhibitor tadalafil (M+T) were identified from the combined dataset of the US, multicenter OPUS (prospective, observational drug registry; NCT02126943) and OrPHeUS (retr</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-07-15T05:33:07.268Z</modification><creation>2025-04-04T19:38:08.868Z</creation></dates><accession>S-EPMC11480149</accession><cross_references><pubmed>39316293</pubmed><doi>10.1007/s12325-024-02964-0</doi></cross_references></HashMap>