Treatment response in patients with idiopathic pulmonary arterial hypertension and a severely reduced diffusion capacity
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DOI: 10.1086/690016
Abstract: Patients with idiopathic pulmonary arterial hypertension (IPAH) and a reduced diffusion capacity of the lung for carbon monoxide (DLCO) have a worse survival compared to IPAH patients with a preserved DLCO. Whether this poor survival… read more here.
Keywords: severely reduced; ipah patients; capacity; dlco ... See more keywords
Differences in disease severity and prognosis of exercise-induced right-to-left shunt between idiopathic pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension patients
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DOI: 10.3389/fcvm.2022.976730
Abstract: Objective Whether exercise-induced venous-to-systemic shunt (EIS) during cardiopulmonary exercise testing (CPET) has different manifestations or characteristics in idiopathic pulmonary arterial hypertension (IPAH) and chronic thromboembolic pulmonary hypertension (CTEPH) patients remains unknown. We explored the differences… read more here.
Keywords: prognosis; without eis; hypertension; exercise induced ... See more keywords
Peripheral Blood T Cells of Patients with IPAH Have a Reduced Cytokine-Producing Capacity
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DOI: 10.3390/ijms23126508
Abstract: Pulmonary arterial hypertension (PAH) is rare disease that is categorized as idiopathic (IPAH) when no underlying cause can be identified. Lungs of most patients with IPAH contain increased numbers of T cells and dendritic cells… read more here.
Keywords: ipah; reduced cytokine; peripheral blood; ipah patients ... See more keywords