| Literature DB >> 30740318 |
Rhoia Neidenbach1, Koichiro Niwa2, Oeztekin Oto3, Erwin Oechslin4, Jamil Aboulhosn5, David Celermajer6, Joerg Schelling7, Lars Pieper8, Linda Sanftenberg7, Renate Oberhoffer1,9, Fokko de Haan10, Michael Weyand11, Stephan Achenbach12, Christian Schlensak13, Dirk Lossnitzer14, Nicole Nagdyman1, Yskert von Kodolitsch15, Hans-Carlo Kallfelz16, David Pittrow17, Ulrike M M Bauer18, Peter Ewert1, Thomas Meinertz15, Harald Kaemmerer1.
Abstract
Today most patients with congenital heart defects (CHD) survive into adulthood. Unfortunately, despite relevant residua and sequels, follow-up care of adults with congenital heart disease (ACHD) is not performed in specialized and/or certified physicians or centres. Major problems in the long-term course encompass heart failure, cardiac arrhythmias, heart valve disorders, pulmonary vascular disease, infective endocarditis, aortopathy and non-cardiac comorbidities. Many of them manifest themselves differently from acquired heart disease and therapy regimens from general cardiology cannot be transferred directly to CHD. It should be noted that even simple, postoperative heart defects that were until recently considered to be harmless can lead to problems with age, a fact that had not been expected so far. The treatment of ACHD has many special features and requires special expertise. Thereby, it is important that treatment regimens from acquired heart disease are not necessarily transmitted to CHD. While primary care physicians have the important and responsible task to set the course for adequate diagnosis and treatment early and to refer patients to appropriate care in specialized ACHD-facilities, they should actively encourage ACHD to pursue follow-up care in specialized facilities who can provide responsible and advanced advice. This medical update emphasizes the current data on epidemiology, heart failure and cardiac arrhythmia in ACHD.Entities:
Keywords: Congenital heart defect (CHD); endocarditis; heart failure; primary health care; pulmonary hypertension
Year: 2018 PMID: 30740318 PMCID: PMC6331379 DOI: 10.21037/cdt.2018.10.15
Source DB: PubMed Journal: Cardiovasc Diagn Ther ISSN: 2223-3652