Literature DB >> 32580342

Facts about the General Medical Care of Adults with Congenital Heart Defects: Experience of a Tertiary Care Center.

Lavinia Seidel1, Kathrin Nebel1, Stephan Achenbach2, Ulrike Bauer3, Peter Ewert1, Sebastian Freilinger1, Ulrike Gundlach2, Harald Kaemmerer1, Nicole Nagdyman1, Renate Oberhoffer1,4, Lars Pieper5, Wibke Reinhard6, Linda Sanftenberg7, Jörg Schelling8, Michael Weyand9, Rhoia Neidenbach1.   

Abstract

Background: Due to the increase in survival rates for congenital heart disease (CHD) in the last decades, over 90% of patients today reach adulthood. Currently, there are more than 300,000 adults with CHD (ACHD) living in Germany. They have an increased need for specialized medical care, since almost all ACHD have chronic heart disease and suffer from specific chronic symptoms, risks, and sequelae. Primary care physicians (PCPs) play a crucial role in referring patients to ACHD specialists or specialized institutions. This cross-sectional study is intended to clarify the real-world care of ACHD from the PCP's perspective.
Methods: This analysis, initiated by the German Heart Centre Munich, was based on a 27-item questionnaire on actual ACHD health care practice in Germany from the PCP's perspective.
Results: In total, 767 questionnaires were considered valid for inclusion. The majority of the PCPs were general practitioners (95.9%), and 84.1% had cared for ACHD during the past year. A majority (69.2%) of the PCPs had cared for patients with simple CHD, while 50.6% and 33.4% had cared for patients with moderate and severe CHD, respectively, in all age groups. PCPs treated almost all typical residual symptoms and sequelae, and advised patients regarding difficult questions, including exercise capacity, pregnancy, genetics, and insurance matters. However, 33.8% of the PCPs did not even know about the existence of certified ACHD specialists or centers. Only 23.9% involved an ACHD-specialized physician in their treatment. In cases of severe cardiac issues, 70.8% of the PCPs referred patients to ACHD-certified centers. Although 52.5% of the PCPs were not sufficiently informed about existing structures, 64.2% rated the current care situation as either "very good" or "good". Only 26.3% (n = 190) of the responding physicians were aware of patient organizations for ACHD. Conclusions: The present study showed that the majority of PCPs are not informed about the ACHD care structures available in Germany. The need for specialized ACHD follow-up care is largely underestimated, with an urgent need for optimization to reduce morbidity and mortality. For the future, solutions must be developed to integrate PCPs more intensively into the ACHD care network.

Entities:  

Keywords:  adults with congenital heart disease; general practitioners; medical health care characteristics in congenital heart defects; primary health care; real world data

Year:  2020        PMID: 32580342     DOI: 10.3390/jcm9061943

Source DB:  PubMed          Journal:  J Clin Med        ISSN: 2077-0383            Impact factor:   4.241


  5 in total

1.  Medical treatment of pulmonary hypertension in adults with congenital heart disease: updated and extended results from the International COMPERA-CHD Registry.

Authors:  Christian Opitz; Ekkehard Grünig; Stephan Rosenkranz; Ann-Sophie Kaemmerer; Matthias Gorenflo; Dörte Huscher; David Pittrow; Peter Ewert; Christine Pausch; Marion Delcroix; Hossein A Ghofrani; Marius M Hoeper; Rainer Kozlik-Feldmann; Andris Skride; Gerd Stähler; Carmine Dario Vizza; Elena Jureviciene; Dovile Jancauskaite; Lina Gumbiene; Ralf Ewert; Ingo Dähnert; Matthias Held; Michael Halank; Dirk Skowasch; Hans Klose; Heinrike Wilkens; Katrin Milger; Christian Jux; Martin Koestenberger; Laura Scelsi; Eva Brunnemer; Michael Hofbeck; Silvia Ulrich; Anton Vonk Noordegraaf; Tobias J Lange; Leonhard Bruch; Stavros Konstantinides; Martin Claussen; Judith Löffler-Ragg; Hubert Wirtz; Christian Apitz; Rhoia Neidenbach; Sebastian Freilinger; Attila Nemes
Journal:  Cardiovasc Diagn Ther       Date:  2021-12

2.  Endangered patients with congenital heart defect during transition-Germany-wide evaluation of medical data from National Register for Congenital Heart Defects (NRCHD).

Authors:  Julia Remmele; Sandra Schiele; Renate Oberhoffer-Fritz; Peter Ewert; Ulrike M M Bauer; Paul Christian Helm
Journal:  Cardiovasc Diagn Ther       Date:  2021-12

3.  Lessons from the short- and mid-term outcome of medical rehabilitation in adults with congenital heart disease.

Authors:  Sebastian Freilinger; Dario Andric; Caroline Andonian; Jürgen Beckmann; Christa Bongarth; Hans Peter Einwang; Peter Ewert; Michael Hofbeck; Ann-Sophie Kaemmerer; Nicole Nagdyman; Renate Oberhoffer; Yskert von Kodolitsch; Harald Kaemmerer; Rhoia Neidenbach
Journal:  Cardiovasc Diagn Ther       Date:  2021-12

4.  Systematic assessment of health care perception in adults with congenital heart disease in Germany.

Authors:  Rhoia Neidenbach; Stephan Achenbach; Caroline Andonian; Ulrike M M Bauer; Peter Ewert; Sebastian Freilinger; Ulrike Gundlach; Ann-Sophie Kaemmerer; Nicole Nagdyman; Kathrin Nebel; Renate Oberhoffer; Lars Pieper; Wibke Reinhard; Linda Sanftenberg; Fabian von Scheidt; Jörg Schelling; Lavinia Seidel; Michael Weyand; Harald Kaemmerer
Journal:  Cardiovasc Diagn Ther       Date:  2021-04

5.  Morbidity and mortality in adults with congenital heart defects in the third and fourth life decade.

Authors:  Siegfried Geyer; Claudia Dellas; Matthias J Müller; Kambiz Norozi; Jonas Caroline; Nicole Sedlak; Jonas Bock; Thomas Paul
Journal:  Clin Res Cardiol       Date:  2022-03-01       Impact factor: 6.138

  5 in total

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