Background: Despite optimized medical therapy, severe idiopathic pulmonary arterial hypertension (IPAH) is a devastating disease with a poor outcome. Autoantibodies have been detected in IPAH that can contribute to worsening of the disease. Objectives: The objective of this prospective, open-label, single-arm, multicenter trial was to evaluate the safety and efficacy of immunoadsorption (IA) as an add-on to optimized medical treatment for patients with IPAH. Methods: A total of 10 IPAH patients received IA over 5 days. Their clinical parameters, including hemodynamics measured by right heart catheter, were assessed at baseline and after 3 and 6 months. The primary endpoint was the change in pulmonary vascular resistance (PVR). Secondary end...
There are several classifications of Pulmonary Hypertension, one of them being Pulmonary Arterial Hy...
AbstractBackground and objectivesBecause there is no cure for idiopathic pulmonary artery hypertensi...
To characterise the different types of pulmonary hypertension (PH) among idiopathic inflammatory myo...
Background: Despite optimized medical therapy, severe idiopathic pulmonary arterial hypertension (IP...
RATIONALE: Autoimmunity is thought to play a role in idiopathic pulmonary arterial hypertension (IPA...
Dilated cardiomyopathy (DCM) which is a common cause of heart failure is often related to elevated l...
Rationale: Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IP...
Background: Antiproliferative strategies have emerged as a potential therapeutic option for pulmonar...
of anti-endothelial cell antibodies in idiopathic pulmonary arterial hypertension To the Editors: Pu...
ObjectivesThe goal of this study was to investigate the feasibility, safety, and initial clinical ou...
Contains fulltext : 177244.pdf (publisher's version ) (Open Access)To characterise...
<p>Background—By its inhibitory effect on platelet-derived growth factor signaling, imatinib c...
Background-: By its inhibitory effect on platelet-derived growth factor signaling, imatinib could be...
Background: The majority of patients with idiopathic pulmonary arterial hypertension (IPAH) in funct...
Pulmonary arterial hypertension (PAH) is a progressive life-threatening disease. The notion that aut...
There are several classifications of Pulmonary Hypertension, one of them being Pulmonary Arterial Hy...
AbstractBackground and objectivesBecause there is no cure for idiopathic pulmonary artery hypertensi...
To characterise the different types of pulmonary hypertension (PH) among idiopathic inflammatory myo...
Background: Despite optimized medical therapy, severe idiopathic pulmonary arterial hypertension (IP...
RATIONALE: Autoimmunity is thought to play a role in idiopathic pulmonary arterial hypertension (IPA...
Dilated cardiomyopathy (DCM) which is a common cause of heart failure is often related to elevated l...
Rationale: Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IP...
Background: Antiproliferative strategies have emerged as a potential therapeutic option for pulmonar...
of anti-endothelial cell antibodies in idiopathic pulmonary arterial hypertension To the Editors: Pu...
ObjectivesThe goal of this study was to investigate the feasibility, safety, and initial clinical ou...
Contains fulltext : 177244.pdf (publisher's version ) (Open Access)To characterise...
<p>Background—By its inhibitory effect on platelet-derived growth factor signaling, imatinib c...
Background-: By its inhibitory effect on platelet-derived growth factor signaling, imatinib could be...
Background: The majority of patients with idiopathic pulmonary arterial hypertension (IPAH) in funct...
Pulmonary arterial hypertension (PAH) is a progressive life-threatening disease. The notion that aut...
There are several classifications of Pulmonary Hypertension, one of them being Pulmonary Arterial Hy...
AbstractBackground and objectivesBecause there is no cure for idiopathic pulmonary artery hypertensi...
To characterise the different types of pulmonary hypertension (PH) among idiopathic inflammatory myo...