Literature DB >> 18852581

Physical and emotional symptom burden of patients with end-stage heart failure: what to measure, how and why.

Cristina Opasich1, Alessandra Gualco, Stefania De Feo, Massimo Barbieri, Giovanni Cioffi, Anna Giardini, Giuseppina Majani.   

Abstract

OBJECTIVE: Much of our understanding about symptom burden near the end of life is based on studies of cancer patients. The aim of this study was to explore physical and emotional symptom experience among end-stage chronic heart failure patients, looking for those symptoms mostly related to their global health status.
METHODS: Forty-six patients with end-stage heart failure compiled the following: Edmonton Symptom Assessment Scale (ESAS) and Kansas City Cardiomyopathy Questionnaire (KCCQ).
RESULTS: End-stage heart failure patients have many complaints and poor global health status. The most distressing symptoms reported were general discomfort and tiredness followed by anorexia and dyspnea. The KCCQ summary scores were highly correlated with ESAS (r = -0.78; P = 0.0001). Among the domains explored by the KCCQ, social functioning and self-efficacy showed the lowest correlation coefficients with ESAS (r = -0.50; P = 0.001 and r = -0.31; P = 0.003, respectively); concerning the physical limitation domain, the symptom score and the quality-of-life domain, the correlation coefficients were as follows: r = -0.71 (P = 0.0001), r = -0.75 (P = 0.0001) and r = -0.74 (P = 0.0001), respectively. In the multiple regression analysis of ESAS and KCCQ scores, general discomfort, depression and anxiety were the symptoms that mostly related with the results in the domains explored by the KCCQ. No independent predictor was found among symptoms and quality of life.
CONCLUSION: General discomfort together with depression and anxiety were the symptoms that were mostly related with the physical limitation domain of global health status, but did not influence the social functioning and the self-efficacy domains. When ESAS is used together with KCCQ, comprehensive and quantitative information on a patient's physical, emotional and social distress is provided.

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Year:  2008        PMID: 18852581     DOI: 10.2459/JCM.0b013e32830c1b45

Source DB:  PubMed          Journal:  J Cardiovasc Med (Hagerstown)        ISSN: 1558-2027            Impact factor:   2.160


  11 in total

1.  Health care providers' use and knowledge of the Edmonton Symptom Assessment System (ESAS): is there a need to improve information and training?

Authors:  Daniela Carli Buttenschoen; Jarad Stephan; Sharon Watanabe; Cheryl Nekolaichuk
Journal:  Support Care Cancer       Date:  2013-09-13       Impact factor: 3.603

Review 2.  Old and new tools to assess dyspnea in the hospitalized patient.

Authors:  Barbro Kjellström; Martje H L van der Wal
Journal:  Curr Heart Fail Rep       Date:  2013-09

Review 3.  Are all outcomes in chronic heart failure rated equally? An argument for a patient-centred approach to outcome assessment.

Authors:  Sungwon Chang; Phillip J Newton; Sally Inglis; Tim Luckett; Henry Krum; Peter Macdonald; Patricia M Davidson
Journal:  Heart Fail Rev       Date:  2014-03       Impact factor: 4.214

4.  Double jeopardy: the influence of excessive daytime sleepiness and impaired cognition on health-related quality of life in adults with heart failure.

Authors:  Barbara Riegel; Sarah J Ratcliffe; William S Weintraub; Steven L Sayers; Lee R Goldberg; Sheryl Potashnik; Terri E Weaver; Susan J Pressler
Journal:  Eur J Heart Fail       Date:  2012-04-17       Impact factor: 15.534

5.  Examining the effects of an outpatient palliative care consultation on symptom burden, depression, and quality of life in patients with symptomatic heart failure.

Authors:  Lorraine S Evangelista; Dawn Lombardo; Shaista Malik; Jennifer Ballard-Hernandez; Marjan Motie; Solomon Liao
Journal:  J Card Fail       Date:  2012-12       Impact factor: 5.712

6.  On-going palliative care enhances perceived control and patient activation and reduces symptom distress in patients with symptomatic heart failure: a pilot study.

Authors:  Lorraine S Evangelista; Solomon Liao; Marjan Motie; Nathalie De Michelis; Dawn Lombardo
Journal:  Eur J Cardiovasc Nurs       Date:  2014-01-17       Impact factor: 3.908

7.  Expanding the Palliative Care Domains to Meet the Needs of a Community-Based Supportive Care Model.

Authors:  Eric W Anderson; Monica S Frazer; Sandra E Schellinger
Journal:  Am J Hosp Palliat Care       Date:  2017-04-20       Impact factor: 2.500

Review 8.  A palliative approach for heart failure end-of-life care.

Authors:  Jane Maciver; Heather J Ross
Journal:  Curr Opin Cardiol       Date:  2018-03       Impact factor: 2.161

9.  The feasibility of a randomised controlled trial to compare the cost-effectiveness of palliative cardiology or usual care in people with advanced heart failure: Two exploratory prospective cohorts.

Authors:  Miriam J Johnson; Paula McSkimming; Alex McConnachie; Claudia Geue; Yvonne Millerick; Andrew Briggs; Karen Hogg
Journal:  Palliat Med       Date:  2018-04-24       Impact factor: 4.762

10.  Palliative care needs in patients hospitalized with heart failure (PCHF) study: rationale and design.

Authors:  Ross T Campbell; Colette E Jackson; Ann Wright; Roy S Gardner; Ian Ford; Patricia M Davidson; Martin A Denvir; Karen J Hogg; Miriam J Johnson; Mark C Petrie; John J V McMurray
Journal:  ESC Heart Fail       Date:  2015-03-19
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