Outcomes in Patients Receiving Treatment for Pulmonary Arterial Hypertension Associated With Repaired Congenital Heart Disease
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39999520
PubMed Central
PMC11908551
DOI
10.1016/j.jacadv.2025.101626
PII: S2772-963X(25)00043-2
Knihovny.cz E-zdroje
- Klíčová slova
- COMPASS-2, GRIPHON, SERAPHIN, congenital heart disease, pooled analysis, pulmonary arterial hypertension,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Pulmonary arterial hypertension (PAH) is a common complication among patients with congenital heart disease (CHD). Despite advances in PAH treatment, evidence for the benefits of PAH therapies in CHD-PAH is limited. OBJECTIVES: This analysis aimed to evaluate outcomes in patients with repaired PAH-CHD receiving an approved PAH drug. METHODS: This was a pooled analysis including CHD-PAH patients whose CHD was repaired ≥1 year prior from 3 randomized, placebo-controlled, event-driven studies: GRIPHON (NCT01106014), SERAPHIN (NCT00660179), and COMPASS-2 (NCT00303459). The primary endpoint was time to first confirmed morbidity/mortality (M/M) event. HRs with 95% CIs were determined with random effects models. RESULTS: The analysis included 1,982 patients with PAH, 177 (8.9%) with CHD-PAH. In the overall PAH cohort, the mean age was 48 and 49 years in treatment and placebo groups; 80% and 77% were female. In the CHD-PAH cohort, the mean age was 41 and 39 years; 70% and 66% were female. Overall, ≥98% in each group were World Health Organization functional class II and III at baseline. There was a significant reduction in risk of M/M events vs placebo in the overall PAH and CHD-PAH cohorts: 37% reduction in the overall PAH cohort (HR: 0.63; 95% CI: 0.52-0.77) and 50% reduction in the CHD-PAH population (HR: 0.50; 95% CI: 0.26-0.94). CONCLUSIONS: Treatment with approved PAH drugs provided a similar reduction in M/M risk in patients with repaired CHD-PAH when compared with the overall PAH population. This pooled analysis provides important evidence to guide medical management in this patient population.
Cardiology and Center of Cardiovascular Medicine Medical University of Vienna Vienna Austria
CARE Hospitals Hyderabad India
Centre of Postgraduate Medical Education European Health Centre Otwock Poland
Charles University and General University Hospital Prague Czech Republic
David Geffen School of Medicine at University of California Los Angeles Los Angeles California USA
Duke University Health System Durham North Carolina USA
Hannover Medical School Hannover Germany; German Center of Lung Research Hannover Germany
Ignacio Chavez National Heart Institute Mexico Mexico
Johnson and Johnson Titusville New Jersey USA
Mater Misericordiae University Hospital Dublin Ireland
Université Paris Saclay APHP Hôpital Bicêtre Le Kremlin Bicêtre France
University of Michigan Health System Ann Arbor Michigan USA
University of Texas Southwestern Medical Center Dallas Texas USA
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