Dry Powder Formulation of Treprostinil Appears Safe, Tolerable in PAH
Use of the dry powder formulation of treprostinil, known as LIQ861, has demonstrated safety and tolerability in patients with pulmonary arterial hypertension beyond 2 weeks.
Use of the dry powder formulation of treprostinil, known as LIQ861, has demonstrated safety and tolerability in patients with pulmonary arterial hypertension beyond 2 weeks.
The use of spectral-detector computed tomography offers a highly accurate method to diagnose chronic thromboembolic pulmonary hypertension.
Following the use of balloon pulmonary angioplasty, patients with inoperable chronic thromboembolic pulmonary hypertension had decreased mean pulmonary artery pressure, pulmonary vascular resistance, and mean right arterial pressure.
The risk for coronary artery disease in patients with asthma-COPD overlap syndrome who used statins was lower regardless of the duration of treatment.
Comprehensive assessments of exercise capacity and quality of life can be used to predict 2-year mortality in patients with pulmonary arterial hypertension.
The presence of primary hypertension does not appear to have an effect on the prognosis of postmenopausal osteoporosis.
Hypertension and diabetes are especially prevalent comorbidities in obese patients with chronic obstructive pulmonary disease.
Researchers evaluated stroke risk and its effect on quality of life after surgical aortic valve replacement vs transfemoral transcatheter aortic valve.
Treatment with treprostinil has demonstrated potential antithrombotic mechanisms of action in pediatric patients with pulmonary arterial hypertension.
Results indicate that recurrent vascular event rate and changes in vascular status were different between patients with intracranial arterial dissection and those with intracranial atherosclerotic stenosis.