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

ConclusionPatients 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.
Source: European Heart Journal - Category: Cardiology Source Type: research