Updated guidelines on the diagnosis and management of acute PE in adult patients.
Pulmonary hypertension (PH), defined as invasively measured mean pulmonary artery pressure ≥25 mmHg, occurs in many different diseases. The focus of this task force was mainly on patients with pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). This summaries the current state of knowledge and open questions regarding the clinical effects of exercise training, training modalities and mechanisms of action in patients with PH.
This guideline for the initial OP management of PE provides guidance on how to risk-stratify patients with suspected and confirmed PE and subsequently manage them in an OP or ambulatory care setting.
Health disparities have a major impact in the quality of life and clinical care received by minorities in the United States. Pulmonary arterial hypertension (PAH) is a rare cardiopulmonary disorder that affects children and adults and that, if untreated, results in premature death.
PH has been defined as an increase in mean pulmonary arterial pressure (P̄pa) ≥25 mmHg at rest as assessed by right heart catheterisation. These are updated guidelines on the management of PAH.