Effect of Normobaric Hypoxia on Exercise Performance in Pulmonary Hypertension
Patients with pulmonary hypertension exhibited a reduced exercise capacity under hypoxic conditions, although with high inter-individual variability.
Pulmonary Hypertension
PAH Mortality Risk Accurately Predicted by Abridged REVEAL Risk Calculator
An abridged version of the REVEAL risk calculator, the REVEAL Lite 2, represents a simpler and accurate tool for predicting mortality risk in patients with pulmonary arterial hypertension.
Oral Combination Therapy May Not Improve Risk Status in Pulmonary Arterial Hypertension
Oral combination therapy does not appear to help achieve or maintain low risk status in most treatment-naive patients with pulmonary arterial hypertension.
Pulmonary Arterial Compliance May Predict Mortality in SLE-Associated PAH
Pulmonary arterial compliance was found to be strongly associated with all-cause mortality and clinical worsening in patients with systemic lupus erythematosus-associated pulmonary arterial hypertension.
Nasal High Flow Therapy May Reduce Sympathetic Drive in Pulmonary Hypertension and OSA
Nighttime nasal high flow therapy at 20 L/min reduced sympathetic drive in patients with precapillary pulmonary hypertension and obstructive sleep apnea.
Pulmonary Artery Denervation Found to Be Beneficial for Residual CTEPH After Pulmonary Endarterectomy
Pulmonary artery denervation in patients with residual chronic thromboembolic pulmonary hypertension after pulmonary endarterectomy was associated with improved hemodynamics and clinical and functional status compared with medical therapy.
Sex Differences in Liver Transplant Candidates With Portopulmonary Hypertension
Female candidates for liver transplant who have portopulmonary hypertension have higher pulmonary vascular resistance, lower Model for End-Stage Liver Disease scores, and are more likely to have autoimmune liver disease, compared with male candidates.
C-Arm CT With Digital Subtraction Angiography May Enhance CTEPH Diagnostic Work-Up
A combination of C-arm computed tomography with conventional digital subtraction angiography of the pulmonary arteries can enhance the diagnostic work-up of patients with suspected CTEPH.
Pulmonary Arterial Hypertension Associated With CHD: Developments in Treatments, Remaining Gaps According to Experts
PAH associated with CHD is linked to significant reductions in survival and quality of life, especially for patients progressing to Eisenmenger syndrome.
Treprostinil Under Review for Pulmonary Hypertension With Interstitial Lung Disease
The sNDA is supported by data from the multicenter, double-blind, placebo-controlled phase 3 INCREASE study.
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