Showing 282 results for "chronic thromboembolic pulmonary hypertension"

The Treatment Options for CTEPH

In this video from the Fondazione Internazionale Menarini, Dr. Vittorio Pengo discusses his presentation of the pathophysiology and treatment of chronic thromboembolic pulmonary hypertension (CTEPH). MORE: Find out how doctors diagnosed pulmonary hypertension and CTEPH. Dr. Pengo explains that CTEPH is a treatable disease that occurs in 0.5…

Chicago Man Describes His CTEPH Journey

In this video from Living Healthy Chicago, Jack Wilk shares the story of his chronic thromboembolic pulmonary hypertension (CTEPH) diagnosis. A study finds that international diagnosis and management practices for CTEPH are inadequate. Read more here.  Jack first started to notice symptoms five years ago when he began to get…

Low Levels of Bad Cholesterol Associated with Increased Mortality in PAH, Study Suggests

Patients with pulmonary arterial hypertension (PAH) have low levels of low-density lipoprotein cholesterol (LDL-C) – or “bad cholesterol” – which is associated with an increased mortality risk, according to a new study. PAH treatment may increase LDL-C levels. The study, “Low-Density Lipoprotein Cholesterol And Survival In Pulmonary Arterial Hypertension,”…

Actelion Reports Its PAH Treatment, Macitentan, Aiding CTEPH Patients in Phase 2 Study

Actelion announced that a Phase 2 clinical trial evaluating its pulmonary hypertension treatment, macitentan, in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH) has met its primary endpoint. At week 16, treatment resulted in a significant reduction in pulmonary vascular resistance (PVR) compared to placebo. MERIT is a 24-week, randomized and…

In Certain CTEPH Patients, Vascular Remodeling May Lead to Hypoxemia

Patients with chronic thromboembolic pulmonary hypertension (CTEPH) who are successfully treated with pulmonary endarterectomy (PEA) may be at increased risk of having low levels of oxygen in the blood due to severe pulmonary arteriopathy, a condition characterized by pulmonary artery remodeling, according to a study from Chiba University in Japan. The…

Bosentan Improved Endothelial Function in PAH, but Not in CTEPH Patients, Study Finds

Researchers at the Nagoya University Graduate School of Medicine in Japan demonstrated that the endothelin receptor antagonist bosentan can improve endothelial dysfunction parameters in patients with pulmonary arterial hypertension (PAH), but not in patients with inoperable chronic thromboembolic pulmonary hypertension (CTEPH). The findings were published in the Pulmonary…

PAH Drug, Riociguat, Found Not to Alter the Effectiveness of Oral Contraceptives

Riociguat treatment administered at steady state (2.5 mg, three times a day) to women with pulmonary arterial hypertension (PAH) did not alter the effectiveness of oral contraceptives or make their use unsafe, researchers reported. The study, “Pharmacokinetic interaction study between riociguat and the combined oral contraceptives levonorgestrel and ethinylestradiol in…