Persistence with macitentan versus other endothelin receptor antagonists in patients with pulmonary arterial hypertension: experience from a real-world data repository in the USA

نویسندگان

چکیده

Abstract Background Pulmonary arterial hypertension (PAH) is a progressive and fatal disease as such, it imperative that patients remain on therapy to delay progression maintain functional status. Previous research has demonstrated differences in overall survival the real-world by endothelin receptor antagonists (ERA) treatments with lower risk of death macitentan than ambrisentan bosentan. However, data persistence ERAs are limited. Purpose To compare versus bosentan) PAH. Methods This retrospective, non-interventional, observational study identified between 10/21/2013–3/31/2021 (study period) from Decision Resources Group (DRG) Real World Data Repository. The repository links medical prescription claims commercial, Medicaid, Medicare plans electronic health records (EHRs) provide longitudinal patient-level representative over 300 million US. Patients selected must have been dispensed an ERA 4/14/14–3/31/20 AND 1) either inpatient diagnosis pulmonary (PH), or 2) right heart catheterization any PH diagnosis, 3) were taking phosphodiesterase 5 inhibitor (PDE5i). primary outcome was defined time index drug discontinuation (90-day gap after end last prescription's days supply). Descriptive analysis comprised means, standard deviations, medians, interquartile ranges for continuous variables frequencies percentages categorical variables. Three-sample proportion tests conducted at baseline detect three cohorts identify potentially confounding Hazard ratios (HR) pairwise comparisons (macitentan vs ambrisentan; calculated using inverse probability treatment weighting (IPTW)-adjusted Cox proportional regression model, adjust potential confounders (see Table receiving specific ERA. analyzed Kaplan-Meier method. Results A total 4,526 included, whom 1,205 received macitentan, 2,592 729 Study population characteristics general PAH (Table 1). Unadjusted showed median shortest (12.6 months) followed bosentan (13.6 greatest (15.8 months; log-rank p-value: 0.061). Compared other had greater discontinuation: (10%) (18%) 2). Conclusions Persistence significantly macitentan-treated those Further examining variability key sub-groups well impact improved long-term outcomes warranted. Funding Acknowledgement Type funding sources: Private company. Main source(s): Janssen Scientific Affairs, LLC

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Endothelin receptor antagonists for pulmonary arterial hypertension.

BACKGROUND Pulmonary arterial hypertension (PAH) is a devastating disease, which leads to right heart failure and premature death. Pulmonary arterial hypertension can be classified into five categories according to Venice classification: (1) Idiopathic PAH; (2) Familial PAH; (3) PAH associated with collagen vascular disease, congenital systemic-to-pulmonary shunts, portal hypertension, HIV infe...

متن کامل

Slow Receptor Dissociation Kinetics Differentiate Macitentan from Other Endothelin Receptor Antagonists in Pulmonary Arterial Smooth Muscle Cells

Two endothelin receptor antagonists (ERAs), bosentan and ambrisentan, are currently approved for the treatment of pulmonary arterial hypertension (PAH), a devastating disease involving an activated endothelin system and aberrant contraction and proliferation of pulmonary arterial smooth muscle cells (PASMC). The novel ERA macitentan has recently concluded testing in a Phase III morbidity/mortal...

متن کامل

The Importance of Electrocardiography in Pediatric Patients with Pulmonary Arterial Hypertension in Follow- up

Background: Right Ventricular (RV) hypertrophy is an adaptive response to chronic RV pressure overload in patients with pulmonary hypertension. We investigated the relationships between RV hypertrophy indicators, including electrocardiography, the percentage oxygen saturation (SaO2%), body mass index (BMI), and blood uric acid levels in patients with...

متن کامل

Effect of treatment with epoprostenol and endothelin receptor antagonists on the development of thyrotoxicosis in patients with pulmonary arterial hypertension.

Thyroid disease is known to be associated with pulmonary arterial hypertension (PAH). We investigated the prevalence of thyroid disease in patients with idiopathic PAH (IPAH) or heritable PAH (HPAH), and the factors affecting the pathogenesis of thyroid disease. We retrospectively evaluated 59 patients with IPAH or HPAH who had been diagnosed with PAH before the age of 20 years. Thyrotoxicosis ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: European Heart Journal

سال: 2022

ISSN: ['2634-3916']

DOI: https://doi.org/10.1093/eurheartj/ehac544.2194