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How Patient Perceptions Shape Responses and Outcomes in Inherited Cardiac Conditions - 13/03/20

Doi : 10.1016/j.hlc.2019.11.003 
Claire O’Donovan, MSc a, Jodie Ingles, PhD b, c, d, Elizabeth Broadbent, PhD a, Jonathan R. Skinner, MD, FHRS e, f, , Nadine A. Kasparian, PhD g, h, i
a Department of Psychological Medicine, The University of Auckland, Auckland, New Zealand 
b Agnes Ginges Centre for Molecular Cardiology at Centenary Institute, The University of Sydney, Sydney, NSW, Australia 
c Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia 
d Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia 
e Green Lane Paediatric and Congenital Cardiac Services, Starship Children’s Hospital, Auckland, New Zealand 
f Department of Paediatrics Child and Youth Health, The University of Auckland, Auckland, New Zealand 
g Discipline of Paediatrics, School of Women’s and Children’s Health, UNSW Medicine, The University of New South Wales, Sydney, NSW, Australia 
h Department of Cardiology, Boston Children’s Hospital, Boston, MA, USA 
i Harvard Medical School, Boston, MA, USA 

Corresponding author at: Green Lane Paediatric and Congenital Cardiac Services, Starship Children's Hospital, Private Bag 92024, Auckland 1142, New Zealand. Tel.: +64 9 3074949; fax: +64 9 6310785Green Lane Paediatric and Congenital Cardiac ServicesStarship Children's HospitalPrivate Bag 92024, Auckland 1142New Zealand

Abstract

At least one-third of adults living with an inherited cardiac condition report clinically-significant levels of psychological distress. Poorer health-related quality of life compared with population norms is also consistently reported. These outcomes are associated with younger patient age, having an implantable cardioverter defibrillator, and receipt of uncertain clinical test results, and can influence self-management behaviours, such as adherence to potentially critical life-preserving medications. According to the Common Sense Model of Illness, people use information from multiple sources to ‘make sense’ of their health condition, and how they conceptualise the condition can strongly influence adaptation and coping responses. Previous studies with people with inherited cardiac conditions show that illness perceptions, such as greater perceived consequences and a poorer understanding of the condition, are associated with greater psychological distress and poorer adherence to medication. The Common Sense Model provides one potential framework for identifying patients who may be more vulnerable to adverse health outcomes, and for developing early interventions to reduce the physical and psychosocial burden of these conditions. Interventions based on the Common Sense Model have successfully improved physical and psychosocial outcomes associated with other cardiac conditions, and could be tailored for use with patients with an inherited cardiac condition (ICC).

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Keywords : Inherited cardiac conditions, Anxiety, Depression, Health-related quality of life, Illness perceptions, Common Sense Model of Illness


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© 2019  Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 29 - N° 4

P. 641-652 - aprile 2020 Ritorno al numero
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