Quality of Life in Adult Congenital Heart Disease: What Do We Already Know and What Do We Still Need To Know?

2013 ◽  
Vol 15 (10) ◽  
Author(s):  
Silke Apers ◽  
Koen Luyckx ◽  
Philip Moons
2013 ◽  
Vol 23 (4) ◽  
pp. 473-485 ◽  
Author(s):  
Theodora Fteropoulli ◽  
Jan Stygall ◽  
Shay Cullen ◽  
John Deanfield ◽  
Stanton P. Newman

AbstractAimsThis review explores the quality of life of adult congenital heart disease patients and the relationship between disease severity and quality of life.MethodsWe searched seven electronic databases and the bibliography of articles. The 31 selected studies fulfilled the following criteria: adult population; quantitative; assessment of quality of life and/or impact of disease severity on quality of life using validated measures; English language. Data extraction forms were used to summarise the results.ResultsThere are evident methodological limitations within the reviewed studies such as heterogeneous populations, designs, and quality of life conceptualisations and measurements. Despite these problems, findings suggest that the quality of life of adult congenital heart disease patients is compromised in the physical domain compared with their healthy counterparts, whereas no differences were found in relation to the psychosocial and environmental/occupational domain. Some severity variables appear to be significant correlates of quality of life and could be considered in a future standardised classification of disease severity.ConclusionThe methodological limitations of past research in relation to the definition and measurement of quality of life, the study designs, and disease severity classifications need to be addressed in future studies in order to provide robust evidence and valid conclusions in this area of study. This will enable the development of targeted interventions for the improvement of quality of life in the adult population of congenital heart disease patients.


Congenital heart disease (CHD) is the most common congenital anomaly, affecting around 1–2% of newborns. Over the last generation, advances in medical, interventional, and surgical techniques have revolutionized the care of CHD patients. Most patients of all levels of CHD complexity are now expected to survive into adulthood. Few interventional or surgical treatments for CHD are truly curative and serial diagnostic evaluation, repeat intervention, and lifelong follow up is required to ensure optimal cardiac status and quality of life. Cardiac MRI (CMR) and echocardiography are the standard techniques utilized for routine interval assessment and follow-up of patients with all forms of ACHD.


2012 ◽  
Vol 157 (1) ◽  
pp. 70-74 ◽  
Author(s):  
Luc M. Beauchesne ◽  
Judith Therrien ◽  
Nanette Alvarez ◽  
Lynn Bergin ◽  
Gary Burggraf ◽  
...  

2009 ◽  
Vol 32 (4) ◽  
pp. 450-456 ◽  
Author(s):  
AARON F. PULVER ◽  
MICHAEL D. PUCHALSKI ◽  
DAVID J. BRADLEY ◽  
L. LUANN MINICH ◽  
JASON T. SU ◽  
...  

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