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Original Articles

Congestive heart failure patients’ perceptions of quality of life: the integration of physical and psychosocial factors

, , , , &
Pages 83-91 | Received 04 Nov 2002, Accepted 30 Apr 2003, Published online: 19 Oct 2010
 

Abstract

Congestive heart failure (CHF) lowers survival and worsens the quality of life (QOL) of over four million older Americans. Both clinicians and standardized instruments used to assess the QOL of patients with CHF focus primarily on physical symptoms rather than capturing the full range of psychosocial concerns. The purpose of this study was to gather descriptions of the components of QOL as understood by patients living with CHF. Focus groups were conducted with patients with known CHF, New York Heart Association (NYHA) class I–IV, and left ventricular fraction of <40%. Focus groups were audiotaped, transcribed, and reviewed for common and recurrent themes using the methods of constant comparisons. We conducted three focus groups (n = 15) stratified by NYHA stage with male patients ranging in age from 47–82 years of age. Five patients were classified with NYHA stage III/IV and ten with NYHA stage I/II. Thirty attributes of QOL were identified which fell into five broad domains: symptoms, role loss, affective response, coping, and social support. Expectedly, patients reported the importance of physical symptoms; however, participants also identified concern for family, the uncertainty of prognosis, and cognitive function as dimensions of QOL. Changes in patients’ lives attributed to CHF were not always considered deficiencies; rather, methods of coping with CHF were identified as important attributes representing possible opportunities for personal growth. Clinicians must understand the full range of concerns affecting the QOL of their older patients with CHF. The findings suggest that psychosocial aspects and patient uncertainty about their prognosis are important components of QOL among CHF patients.

Acknowledgements

This research is supported in part, by the Department of Veterans Affairs, Veterans Health Administration, HSR&D Service, grant IIR 20-034 to the first author and the views expressed in this manuscript are those of the authors and do not necessarily represent the views of the Department of Veterans Affairs. An earlier version of this study was presented at the 52nd Annual Meeting of the Gerontological Society of America in Washington DC, 2000.

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