Kaemmerer H, Diller GP, Dähnert I, Eichstaedt CA, Eicken A, Freiberger A, Freilinger S, Geiger R, Gorenflo M, Grünig E, Hager A, Herberg U, Huntgeburth M, Kaemmerer AS, Kozlik-Feldmann R, Lammers A, Nagdyman N, Michel S, Schmidt KH, Uebing A, Von Scheidt F, Apitz C (2023)
Publication Type: Journal article
Publication year: 2023
Book Volume: 77
Pages Range: 956-961
Journal Issue: 11
DOI: 10.1055/a-2146-7434
The number of adults with congenital heart disease (CHD) is steadily rising and amounts to approximately 360,000 in Germany. CHD is often associated with pulmonary arterial hypertension (PAH), which may develop early in untreated CHD. Despite timely treatment of CHD, PAH often persists or recurs in older age and is associated with significant morbidity and mortality.The revised European Society of Cardiology/European Respiratory Society 2022 guidelines for the diagnosis and treatment of PH represent a significant contribution to the optimized care of those affected. However, the topic of "adults with congenital heart defects" is addressed only relatively superficially in these guidelines. Therefore, this article addresses the perspective of congenital cardiology in greater depth.
APA:
Kaemmerer, H., Diller, G.P., Dähnert, I., Eichstaedt, C.A., Eicken, A., Freiberger, A.,... Apitz, C. (2023). Pulmonary arterial hypertension in congenital heart disease - Part I Pulmonale arterielle Hypertonie bei Erwachsenen mit angeborenen Herzfehlern – Teil I. Pneumologie, 77(11), 956-961. https://doi.org/10.1055/a-2146-7434
MLA:
Kaemmerer, Harald, et al. "Pulmonary arterial hypertension in congenital heart disease - Part I Pulmonale arterielle Hypertonie bei Erwachsenen mit angeborenen Herzfehlern – Teil I." Pneumologie 77.11 (2023): 956-961.
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