Science and Research

[Pulmonary arterial hypertension in congenital heart disease - Part I]

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.

  • Kaemmerer, H.
  • Diller, G. P.
  • Dähnert, I.
  • Eichstaedt, C. A.
  • Eicken, A.
  • Freiberger, A.
  • Freilinger, S.
  • Geiger, R.
  • Gorenflo, M.
  • Grünig, E.
  • Hager, A.
  • Herberg, U.
  • Huntgeburth, M.
  • Kaemmerer, A. S.
  • Kozlik-Feldmann, R.
  • Lammers, A.
  • Nagdyman, N.
  • Michel, S.
  • Schmidt, K. H.
  • Uebing, A.
  • von Scheidt, F.
  • Apitz, C.

Keywords

  • Adult
  • Humans
  • *Pulmonary Arterial Hypertension/complications/diagnosis
  • *Heart Defects, Congenital/complications/diagnosis/therapy
  • *Cardiology
  • Germany
Publication details
DOI: 10.1055/a-2146-7434
Journal: Pneumologie
Pages: 956-961 
Number: 11
Work Type: Original
Location: TLRC
Disease Area: PH
Partner / Member: Thorax
Access-Number: 37963485

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