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
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