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Zeder, K; Sassmann, T; Foris, V; Douschan, P; Olschewski, H; Kovacs, G.
Severe pulmonary hypertension in chronic obstructive pulmonary disease - From clinical perspective to histological evidence
INT J CARDIOL CONGEN. 2024; 17: 100519 Doi: 10.1016/j.ijcchd.2024.100519 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Zeder Katarina Eleonora
Co-authors Med Uni Graz
Douschan Philipp
Foris Vasile
John Teresa
Kovacs Gabor
Olschewski Horst
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Abstract:
Severe pulmonary hypertension (PH) in chronic obstructive pulmonary disease (COPD) is currently defined by an elevated mean pulmonary arterial pressure and strongly elevated pulmonary vascular resistance >5 wood units. Clinically, these patients show a male predominance, and usually present with very severe dyspnea, severe hypoxemia, strongly decreased exercise capacity and poor prognosis, even though the clinical picture is frequently associated with less severe airflow obstruction. Explanted lung samples of patients with COPD and severe PH show severe remodeling of small pulmonary arterioles, predominantly in the intima and media of the vessels. In this concise review, we discuss the clinical and histopathological evidence of severe PH in COPD.

Find related publications in this database (Keywords)
Pulmonary hypertension
Chronic obstructive pulmonary disease
Remodeling
Diagnosis
Survival
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