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Eur J Cardiothorac Surg 2009;36:105-111. doi:10.1016/j.ejcts.2009.03.023
Copyright © 2009, European Association for Cardio-thoracic Surgery. Published by Elsevier. All rights reserved.

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Ophélie Loup
Thierry Carrel
Alexander Kadner
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Quality of life of grown-up congenital heart disease patients after congenital cardiac surgery

Ophélie Loupa, Catherina von Weissenfluha, Brigitta Gahla, Markus Schwerzmannb, Thierry Carrela, Alexander Kadnera,*

a Department of Cardiovascular Surgery, University Hospital Berne, Freiburgstrasse, 3010 Bern, Switzerland
b Department of Cardiology, University Hospital Berne, Bern, Switzerland

Received 4 September 2008; received in revised form 9 March 2009; accepted 11 March 2009.

* Corresponding author. Tel.: +41 31 632 2111; fax: +41 31 632 2919. (Email: a.kadner{at}web.de).

Background: Due to better early and long-term outcome, the increasing population of grown-ups with congenital heart disease (GUCH) brings up unexpected quality of life (QoL) issues. The cardiac lesion by itself is not always the major problem for these patients, since issues pertaining to QoL and psychosocial aspects often predominate. This study analyses the QoL of GUCH patients after cardiac surgery and the possible impact of medical and psychosocial complications. Patients and methods: A questionnaire package containing the SF-36 health survey (health related QoL), the HADS test (anxiety/depression aspects) and an additional disease specific questionnaire was sent to 345 patients (mean 26 ± 11 years) operated for isolated transposition of the great arteries (TGA), tetralogy of Fallot (TOF), and ventricular septal defect (VSD). The scores were compared with age- and gender-matched standard population data and in relation to the underlying congenital heart disease (CHD). Results: In all SF-36 and HADS health dimensions the GUCH patients showed excellent scores (116 ± 20), which are comparable to the standard population (100 ± 15), regardless of the initial CHD (p = 0.12). Eighty-two percent of the patients were found to be in NYHA class I and 83% patients declared that they do not consider their QoL to be limited by their malformation. Complications like reoperations (p = 0.21) and arrhythmias (p = 0.10) do not show significant impact on the QoL. The additional questionnaire revealed that 76% of adult patients have a fulltime job, 18% receive a full or partial disability pension, 21% reported problems with insurances, most of them regarding health insurances (67%), and 4.4% of adult patients declared to have renounced the idea of having children due to their cardiac malformation. Conclusion: QoL in GUCH patients following surgical repair of isolated TOF, TGA and VSD is excellent and comparable to standard population, this without significant difference between the diagnosis groups. However, these patients are exposed to a high rate of complications and special psychosocial problems, which are not assessed by standardized questionnaires, such as the SF-36 and HADS. These findings highlight the great importance for a multidisciplinary and specialized follow-up for an adequate management of these complex patients.

Key Words: Congenital • GUCH • Quality of life • Reoperation • Cyanotic • Acyanotic




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Copyright © 2009 European Association for Cardio-Thoracic Surgery. Published by Elsevier. All rights reserved.