Epidemiological changes in Eisenmenger syndrome in the Nordic region in 1977–2012

ObjectiveImproved diagnostic tools, timely closure of the shunt and a better understanding of the complexity of Eisenmenger syndrome (ES) have led to improved care and treatment in tertiary centres. These may have decreased the incidence of ES and improved survival of patients with ES, although evid...

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Veröffentlicht in:Heart (British Cardiac Society) 2017-09, Vol.103 (17), p.1353-1358
Hauptverfasser: Hjortshøj, Cristel Sørensen, Jensen, Annette Schophuus, Sørensen, Keld, Nagy, Edit, Johansson, Bengt, Kronvall, Thomas, Dellborg, Mikael, Estensen, Mette-Elise, Holmstrøm, Henrik, Turanlahti, Maila, Thilén, Ulf, Søndergaard, Lars
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Sprache:eng
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Zusammenfassung:ObjectiveImproved diagnostic tools, timely closure of the shunt and a better understanding of the complexity of Eisenmenger syndrome (ES) have led to improved care and treatment in tertiary centres. These may have decreased the incidence of ES and improved survival of patients with ES, although evidence is still lacking. The aim of this study was to investigate temporal changes in incidence, prevalence and mortality in patients with ES for 35 years in the Nordic region.MethodsThis was a retrospective population-based study including 714 patients with ES. Survival analysis was performed based on all-cause mortality and accounting for immortal time bias.ResultsThe incidence of ES decreased from 2.5/million inhabitants/year in 1977 to 0.2/million inhabitants/year in 2012. Correspondingly, prevalence decreased from 24.6 to 11.9/million inhabitants. The median survival was 38.4 years, with 20-year, 40-year and 60-year survival of 72.5%, 48.4%, and 21.3%, respectively. Complex lesions and Down syndrome were independently associated with worse survival (HR 2.2, p
ISSN:1355-6037
1468-201X
1468-201X
DOI:10.1136/heartjnl-2016-310979