Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/121820
Title: Quality of life of adults with congenital heart disease in 15 Countries
Other Titles: Evaluating country-specific characteristics
Authors: Apers, Silke
Kovacs, Adrienne H.
Luyckx, Koen
Thomet, Corina
Budts, Werner
Enomoto, Junko
Sluman, Maayke A.
Wang, Jou-Kou
Jackson, Jamie L.
Khairy, Paul
Cook, Stephen C.
Chidambarathanu, Shanthi
Alday, Luis
Eriksen, Katrine
Dellborg, Mikael
Berghammer, Malin
Mattsson, Eva
Mackie, Andrew S.
Menahem, Samuel
Caruana, Maryanne
Veldtman, Gruschen
Soufi, Alexandra
Romfh, Anitra W.
White, Kamila
Callus, Edward
Kutty, Shelby
Fieuws, Steffen
Moons, Philip
Authors: APPROACH-IS consortium
ISACHD
Keywords: Congenital heart disease -- Patients
Quality of life -- Health aspects
International health
Health surveys
Patient Reported Outcome Measures
Issue Date: 2016
Publisher: Elsevier Inc.
Citation: Apers, S., Kovacs, A. H., Luyckx, K., Thomet, C., Budts, W., Enomoto, J.,...APPROACH-IS consortium and ISACHD. (2016). Quality of life of adults with congenital heart disease in 15 countries: evaluating country-specific characteristics. Journal of the American College of Cardiology, 67(19), 2237-2245.
Abstract: Background: Measuring quality of life (QOL) is fundamental to understanding the impact of disease and treatment on patients’ lives. Objectives: This study aimed to explore QOL in an international sample of adults with congenital heart disease (CHD), the association between patient characteristics and QOL, and international variation in QOL and its relationship to country-specific characteristics.
Objectives: This study aimed to explore QOL in an international sample of adults with congenital heart disease (CHD), the association between patient characteristics and QOL, and international variation in QOL and its relationship to country-specific characteristics.
Methods: We enrolled 4,028 adults with CHD from 15 countries. QOL was assessed using a linear analog scale (LAS) (0 to 100) and the Satisfaction with Life Scale (SWLS) (5 to 35). Patient characteristics included sex, age, marital status, educational level, employment status, CHD complexity, and patient-reported New York Heart Association (NYHA) functional class. Country-specific characteristics included general happiness and 6 cultural dimensions. Linear mixed models were applied.
Results: Median QOL was 80 on the LAS and 27 on the SWLS. Older age, lack of employment, no marriage history, and worse NYHA functional class were associated with lower QOL (p < 0.001). Patients from Australia had the highest QOL (LAS: 82) and patients from Japan the lowest (LAS: 72). Happiness scores and cultural dimensions were not associated with variation in QOL after adjustment for patient characteristics and explained only an additional 0.1% of the variance above and beyond patient characteristics (p = 0.56).
Conclusions: This large-scale, international study found that overall QOL in adults with CHD was generally good. Variation in QOL was related to patient characteristics but not country-specific characteristics. Hence, patients at risk for poorer QOL can be identified using uniform criteria. General principles for designing interventions to improve QOL can be developed.
URI: https://www.um.edu.mt/library/oar/handle/123456789/121820
ISSN: 15583597
Appears in Collections:Scholarly Works - FacM&SMed

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