作者
Athénaïs Boucly,Laurent Savale,Xavier Jaïs,Fabrice Bauer,Emmanuel Bergot,Laurent Bertoletti,Antoine Beurnier,Arnaud Bourdin,Hélène Bouvaist,Sophie Bulifon,Céline Chabanne,Ari Chaouat,Vincent Cottin,Claire Dauphin,Bruno Degano,P. De Groote,Nicolas Favrolt,Yuanchao Feng,Delphine Horeau-Langlard,Mitja Jevnikar,Étienne-Marie Jutant,Zhiying Liang,Pascal Magro,Pierre Mauran,Pamela Moceri,Jean‐François Mornex,S. Palat,Florence Parent,François Picard,Jérémie Pichon,P. Poubeau,Grégoire Prévôt,Sébastien Renard,Martine Reynaud‐Gaubert,Marianne Riou,P. Roblot,Olivier Sanchez,Andrei Seferian,Cécile Tromeur,Jason Weatherald,Gérald Simonneau,David Montani,Marc Humbert,Olivier Sitbon
摘要
Rationale: The relationship between the initial treatment strategy and survival in pulmonary arterial hypertension (PAH) remains uncertain. Objectives: To evaluate the long-term survival of patients with PAH categorized according to the initial treatment strategy. Methods: A retrospective analysis of incident patients with idiopathic, heritable, or anorexigen-induced PAH enrolled in the French Pulmonary Hypertension Registry (January 2006 to December 2018) was conducted. Survival was assessed according to the initial strategy: monotherapy, dual therapy, or triple-combination therapy (two oral medications and a parenteral prostacyclin). Measurements and Main Results: Among 1,611 enrolled patients, 984 were initiated on monotherapy, 551 were initiated on dual therapy, and 76 were initiated on triple therapy. The triple-combination group was younger and had fewer comorbidities but had a higher mortality risk. The survival rate was higher with the use of triple therapy (91% at 5 yr) as compared with dual therapy or monotherapy (both 61% at 5 yr) (P < 0.001). Propensity score matching of age, sex, and pulmonary vascular resistance also showed significant differences between triple therapy and dual therapy (10-yr survival, 85% vs. 65%). In high-risk patients (n = 243), the survival rate was higher with triple therapy than with monotherapy or dual therapy, whereas there was no difference between monotherapy and double therapy. In intermediate-risk patients (n = 1,134), survival improved with an increasing number of therapies. In multivariable Cox regression, triple therapy was independently associated with a lower risk of death (hazard ratio, 0.29; 95% confidence interval, 0.11-0.80; P = 0.017). Among the 148 patients initiated on a parenteral prostacyclin, those on triple therapy had a higher survival rate than those on monotherapy or dual therapy. Conclusions: Initial triple-combination therapy that includes parenteral prostacyclin seems to be associated with a higher survival rate in PAH, particularly in the youngest high-risk patients.