نتایج جستجو برای: pulmonary artery hypertension

تعداد نتایج: 527701  

2009
Beodeul Kang Deok-Kyu Cho Ki Hyun Byun Lucy Youngmin Eun Yun-Hyeong Cho

We describe a 54-year-old woman with isolated pulmonary arterial hypertension accompanied by hyperthyroidism due to Graves' disease. Her pulmonary artery hypertension resolved spontaneously after restoration of euthyroidism. This case suggests that hyperthyroidism should be considered a reversible cause of pulmonary arterial hypertension.

Journal: :The European respiratory journal 2013
Benjamin D Fox Avi Shimony David Langleben Andrew Hirsch Lawrence Rudski Robert Schlesinger Mark J Eisenberg Dominique Joyal Marie Hudson Kim Boutet Alexandrina Serban Ariel Masetto Murray Baron

Our study aimed to determine the prevalence of occult left-heart disease in patients with scleroderma and pulmonary hypertension. In patients with pulmonary hypertension (mean pulmonary artery pressure (mean PAP)≥25 mmHg), differentiation between pre- and post-capillary pulmonary hypertension has been made according to pulmonary artery wedge pressure (PAWP) less than or more than 15 mmHg, respe...

Journal: :Arteriosclerosis, Thrombosis, and Vascular Biology 2019

Journal: :Journal of the American College of Cardiology 2013

2012
Sanjay Tyagi Sumod Kurien Anuj Goel

precapillary pulmonary resistance. Pulmonary hypertension is deemed present when the mean pulmonary artery pressure exceeds 25 mm Hg at rest, or 30 mm Hg with exercise. The presence of pulmonary arterial hypertension further requires normal left heart filling pressures (i.e. a normal left ventricular end diastolic pressure directly measured, or indirectly approximated by a pulmonary artery occl...

2011
Tyler JM Jordan Brian A Scansen Agnieszka M Kent Lora S Hitchcock Duncan S Russell

CASE SERIES SUMMARY Two cats were evaluated for progressive exercise intolerance, dyspnea and unilateral infiltrate of the left lung. Computed tomography angiography (CTA) revealed absence of the right pulmonary artery in both cats with systemic arterial collateral vessels perfusing the right segmental pulmonary arteries. In one case, the collateral vessels arose from the esophageal artery, whi...

Journal: :The European respiratory journal 2007
F Perros P Dorfmüller R Souza I Durand-Gasselin V Godot F Capel S Adnot S Eddahibi M Mazmanian E Fadel P Hervé G Simonneau D Emilie M Humbert

Pulmonary hypertension is characterised by a progressive increase in pulmonary arterial resistance due to endothelial and smooth muscle cell proliferation resulting in chronic obstruction of small pulmonary arteries. There is evidence that inflammatory mechanisms may contribute to the pathogenesis of human and experimental pulmonary hypertension. The aim of the study was to address the role of ...

Journal: :Chest 1976
B L Meyer D B Bogart J E Carley B Y Wong M I Dunn

Pulsus alternans of the pulmonary artery without systemic pulsus alternans is uncommon and is associated with multiple diseases. Two cases of pulmonary hypertension with pulmonary arterial pulsus alternans and right-sided heart failure are described. Primary pulmonary hypertension was demonstrated at autopsy in both cases. These two case reports constitute another previously unreported cause fo...

Journal: :Chest 1985
J Ohar C Polatty A Robichaud A Fowler G Vetrovec F Glauser

The use of systemic vasodilator drugs in reducing pulmonary artery pressures in patients with pulmonary hypertension is controversial. The effect of hydralazine in four patients with pulmonary hypertension resulting from interstitial lung disease (group 1) and nifedipine in four patients with pulmonary hypertension secondary to progressive systemic sclerosis (group 2) was investigated. Hydralaz...

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