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Clinical features and survival in Takayasu’s arteritis-associated pulmonary hypertension: a nationwide study

Xin Jiang, Yongjian Zhu, Yu‐Ping Zhou, Fu-Hua Peng, Lan Wang, Wei Ma, Yunshan Cao, Xin Pan, Gangcheng Zhang, Feng Zhang, Fenling Fan, Bingxiang Wu, Wei Huang, Zhenwen Yang, Cheng Hong, Mengtao Li, Yining Wang, Xi‐Qi Xu, Duolao Wang, Shuyang Zhang, Zhi‐Cheng Jing

2021European Heart Journal37 citationsDOI

Abstract

AIMS: This study aimed to assess the clinical characteristics and long-term survival outcome in patients with Takayasu's arteritis-associated pulmonary hypertension (TA-PH). METHODS AND RESULTS: We conducted a nationally representative cohort study of TA-PH using data from the National Rare Diseases Registry System of China. Patients with pulmonary artery involvement who fulfilled the diagnostic criteria of Takayasu's arteritis and pulmonary hypertension were included. The primary outcome was the time from diagnosis of TA-PH to the occurrence of all-cause death. Between January 2007 and January 2019, a total of 140 patients were included, with a mean age of 41.4 years at diagnosis, and a female predominance (81%). Patients with TA-PH had severely haemodynamic and functional impairments at diagnosis. Significant improvements have been found in N-terminal pro-B-type natriuretic peptide (NT-proBNP) and haemodynamic profiles in patients with TA-PH receiving drugs approved for pulmonary arterial hypertension. The overall 1-, 3-, and 5-year survival rates in TA-PH were 94.0%, 83.2%, and 77.2%, respectively. Predictors associated with an increased risk of all-cause death were syncope [adjusted hazard ratio (HR) 5.38 (95% confidence interval 1.77-16.34), P = 0.003], NT-proBNP level [adjusted HR 1.04 (1.03-1.06), P < 0.001], and mean right atrial pressure [adjusted HR 1.07 (1.01-1.13), P = 0.015]. CONCLUSION: Patients with TA-PH were predominantly female and had severely compromised haemodynamics. More than 80% of patients in our cohort survived for at least 3 years. Medical treatment was based on investigators' personal opinions, and no clear risk-to-benefit ratio can be derived from the presented data.

Topics & Concepts

MedicineInternal medicineHazard ratioPulmonary hypertensionPulmonary arteryCardiologyArteritisTakayasu's arteritisHemodynamicsCohortConfidence intervalCohort studyBlood pressureSurgeryVasculitisDiseaseVasculitis and related conditionsRenal Diseases and GlomerulopathiesRenal and Vascular Pathologies
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