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Pulmonary hypertension in left heart disease [PDF]
Archives of Medical Science, 2018 Pulmonary hypertension in left heart disease (PH-LHD) is the most prevalent form of PH. It is classified as group 2 PH as per WHO classification. As the prevalence of left heart disease such as congestive heart failure is increasing, the number of ...
Pratishtha Mehra +6 more
doaj +7 more sources
Life, 2023 Advances in the diagnosis and treatment of pulmonary hypertension (PH) have gradually improved the disease course. This retrospective cohort study aims to explore the diagnostic hemodynamic profile and survival of PH patients and their temporal changes ...
Georgios E. Papadopoulos +12 more
doaj +1 more source
European Journal of Medical Research, 2023 The etiology of pulmonary arterial hypertension (PAH) is complex, especially the investigation of rare pathogeny is difficult. Congenital portosystemic venous shunt (CPSS) is a rare congenital anomaly in which the portal blood completely or partially ...
Yunyan Li +5 more
doaj +1 more source
Cardiothoracic imaging findings of Proteus syndrome
Scientific Reports, 2021 In this work, we sought to delineate the prevalence of cardiothoracic imaging findings of Proteus syndrome in a large cohort at our institution. Of 53 individuals with a confirmed diagnosis of Proteus syndrome at our institution from 10/2001 to 10/2019 ...
S. Mojdeh Mirmomen +6 more
doaj +1 more source
Canadian Respiratory Journal, 2022 Background. Following COVID-19, patients often present with ongoing symptoms comparable to chronic fatigue and subjective deterioration of exercise capacity (EC), which has been recently described as postacute COVID-19 syndrome. Objective.
Georg Evers +11 more
doaj +1 more source
Pulmonary capillary recruitment and distention in mammalian lungs: species similarities
European Respiratory Review, 2022 Pulmonary arterial pressure rises minimally during exercise. The pulmonary microcirculation accommodates increasing blood flow via recruitment of pulmonary capillaries and, at higher flows, by distention of already perfused capillaries.
David Langleben +4 more
doaj +1 more source
Idiopathic pulmonary arterial hypertension and co-existing lung disease: is this a new phenotype?
Pulmonary Circulation, 2020 Patients classified as idiopathic pulmonary arterial hypertension (defined as Group 1 on European Respiratory Society (ERS)/European Cardiac Society (ESC) criteria) may have evidence of minor co-existing lung disease on thoracic computed tomography.
Andrew J. Peacock +16 more
doaj +1 more source
ESC Heart Failure, 2021 Aims Pulmonary arterial hypertension (PAH) is common amongst patients with congenital heart disease (CHD). It is a severe and complex condition that adversely affects quality of life and prognosis.
Andrew Constantine +5 more
doaj +1 more source
Isolated major aortopulmonary collateral as the sole pulmonary blood supply to an entire lung segment [PDF]
, 2017 Congenital systemic-to-pulmonary collateral arteries or major aortopulmonary collaterals are associated with cyanotic congenital heart disease with decreased pulmonary blood flow.
Grady, R. Mark +2 more
core +3 more sources
Interdisciplinary three-step strategy to treat aortic stenosis and coronary artery disease in a patient with end-stage chronic obstructive pulmonary disease [PDF]
, 2012 Background: Valvular aortic stenosis is a common disease in the elderly, often in multimorbid patients. It is often associated with coronary artery disease and peripheral artery disease.
Michel, Sebastian +6 more
core +1 more source