Results 21 to 30 of about 27,650 (185)

Pulmonary venous remodeling in COPD‐pulmonary hypertension and idiopathic pulmonary arterial hypertension [PDF]

Pulmonary Circulation, 2017
Pulmonary vascular arterial remodeling is an integral and well‐understood component of pulmonary hypertension (PH). In contrast, morphological alterations of pulmonary veins in PH are scarcely described. Explanted lungs (n = 101) from transplant recipients with advanced chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary arterial ...
Andersen, Kasper Hasseriis, Andersen, Claus Bøgelund, Gustafsson, Finn, Carlsen, Jørn   +3 more
openaire   +3 more sources

Elevated serum circ_0068481 levels as a potential diagnostic and prognostic indicator in idiopathic pulmonary arterial hypertension

Pulmonary Circulation, 2019
Circular RNAs have continuous, stable, and covalently closed circular structures and are not easily degraded by nucleases, thus they are ideal serum biomarkers for detecting diseases.
Ying Zhang, Yongbin Chen, Hua Yao, Zhenbang Lie, Guo Chen, Hong Tan, Yingling Zhou   +6 more
doaj   +1 more source

Inhaled iloprost as third add-on therapy in idiopathic pulmonary arterial hypertension

Pulmonary Circulation, 2021
Triple combination therapy is suggested in current pulmonary arterial hypertension guidelines in case of unsatisfactory treatment with oral double combination therapy.
Caio J.C.S. Fernandes, Taysa A.F. da Silva, Jose L. Alves Jr, Carlos V.P. Jardim, Rogerio de Souza   +4 more
doaj   +1 more source

Anticoagulation in pulmonary arterial hypertension: a decision analysis

Pulmonary Circulation, 2019
Systemic anticoagulation may be beneficial in pulmonary arterial hypertension, but there is no randomized clinical trial data to guide therapeutic decision making, and current guidelines do not account for patient preferences or quality of life. Decision
Arun Jose, Mark H. Eckman, Jean M. Elwing   +2 more
doaj   +1 more source

Oxygen therapy may worsen the survival rate in rats with monocrotaline-induced pulmonary arterial hypertension. [PDF]

PLoS ONE, 2018
Although oxygen therapy rapidly improves arterial oxygen saturation in idiopathic pulmonary arterial hypertension, the effects of chronic administration of oxygen are unknown.
Naoto Fujita, Natsuki Yamasaki, Kanako Eto, Makoto Asaeda, Wataru Kuwahara, Hidetaka Imagita   +5 more
doaj   +1 more source

Phenotyping of idiopathic pulmonary arterial hypertension: a registry analysis [PDF]

The Lancet Respiratory Medicine, 2022
Among patients meeting diagnostic criteria for idiopathic pulmonary arterial hypertension (IPAH), there is an emerging lung phenotype characterised by a low diffusion capacity for carbon monoxide (DLCO) and a smoking history. The present study aimed at a detailed characterisation of these patients.We analysed data from two European pulmonary ...
Hoeper, Marius M., Dwivedi, Krit, Pausch, Christine, Lewis, Robert A., Olsson, Karen M., Huscher, Doerte, Pittrow, David, Gruenig, Ekkehard, Staehler, Gerd, Vizza, Carmine Dario, Gall, Henning, Distler, Oliver, Opitz, Christian, Gibbs, John Simon R., Delcroix, Marion, Park, Da-Hee, Ghofrani, Hossein Ardeschir, Ewert, Ralf, Kaemmerer, Harald, Kabitz, Hans-Joachim, Skowasch, Dirk, Behr, Juergen, Milger, Katrin, Lange, Tobias J., Wilkens, Heinrike, Seyfarth, Hans-Juergen, Held, Matthias, Dumitrescu, Daniel, Tsangaris, Iraklis, Vonk-Noordegraaf, Anton, Ulrich, Silvia, Klose, Hans, Claussen, Martin, Eisenmann, Stephan, Schmidt, Kai-Helge, Swift, Andrew J., Thompson, Alfred A. Roger, Elliot, Charlie A., Rosenkranz, Stephan, Condliffe, Robin, Kiely, David G., Halank, Michael   +41 more
openaire   +3 more sources

Pregnancy outcome in a pregnant patient with idiopathic Pulmonary Arterial Hypertension: a case report and review of the literature

Journal of Medical Case Reports, 2018
Background Idiopathic pulmonary arterial hypertension is a rare and progressive condition which is aggravated by the physiologic changes during pregnancy.
Farid Rashidi, Hossein Sate
doaj   +1 more source

Association between splenectomy and portal hypertension in the development of pulmonary hypertension

Pulmonary Circulation, 2020
Both portal hypertension and splenectomy are risk factors for pulmonary hypertension. However, the interactions between portal hypertension and splenectomy in the development of pulmonary hypertension remain unclear.
Li Huang, Wen Li, Tao Yang, Changming Xiong, Xinhai Ni, Qing Gu, Jianguo He   +6 more
doaj   +1 more source

Circulating angiopoietins in idiopathic pulmonary arterial hypertension [PDF]

European Heart Journal, 2010
To determine the diagnostic utility of circulating angiopoietin-1 (Ang-1) and its antagonist angiopoietin-2 (Ang-2) as potential biomarkers of disease severity or response to treatment in idiopathic pulmonary arterial hypertension (IPAH). Imbalances in angiogenic factors including vascular endothelial cell growth factor (VEGF) and the angiopoetin-Tie2 ...
Philipp, Kümpers, Nils, Nickel, Alexander, Lukasz, Heiko, Golpon, Volker, Westerkamp, Karen M, Olsson, Danny, Jonigk, Lavinia, Maegel, Clemens L, Bockmeyer, Sascha, David, Marius M, Hoeper   +10 more
openaire   +2 more sources

Impact of right ventricular dyssynchrony on prognosis of patients with idiopathic pulmonary arterial hypertension

Pulmonary Circulation, 2019
Idiopathic pulmonary arterial hypertension is a progressive disease with high mortality with an increasing burden of right ventricular. Right ventricular dyssynchrony was observed in idiopathic pulmonary arterial hypertension, but the association with ...
Xiao-Ling Cheng, Bing-Yang Liu, Wei-Chun Wu, Wen Li, Li Huang, Tao Yang, Zhi-Hong Liu, Hao Wang, Jian-Guo He, Chang-Ming Xiong   +9 more
doaj   +1 more source