Literature DB >> 12001403

What determines the quality of life of terminally ill cancer patients from their own perspective?

S Robin Cohen1, Anne Leis.   

Abstract

BACKGROUND: Although several instruments have been developed to measure the quality of life (QOL) of palliative care patients, a rigorous research study has not specifically asked patients themselves what is important to their QOL. It is, therefore, not clear whether these instruments measure what is most important to these patients' QOL.
PURPOSE: To understand the primary determinants of the QOL of palliative care patients with cancer.
METHOD: The study used a qualitative paradigm. Participants were interviewed concerning what was important to their QOL. A systematic content analysis of the transcripts was carried out by all the investigators.
RESULTS: Five broad domains were found to be importnat determinants of patient QOL: (1) the patient's own state, including physical and cognitive functioning, psychological state, and physical condition; (2) quality of palliative care; (3) physical environment; (4) relationships; and (5) outlook.
CONCLUSIONS: Existing instruments cover many of these domains, but no single instrument includes all of the relevant content. The McGill Quality of Life Questionnaire, which we developed previously, has been revised based on these data.

Entities:  

Mesh:

Year:  2002        PMID: 12001403

Source DB:  PubMed          Journal:  J Palliat Care        ISSN: 0825-8597            Impact factor:   2.250


  15 in total

1.  Development of a computer-administered mobility questionnaire.

Authors:  Jorunn L Helbostad; Line M Oldervoll; Peter M Fayers; Marit S Jordhøy; Kenneth C H Fearon; Florian Strasser; Stein Kaasa
Journal:  Support Care Cancer       Date:  2010-03-26       Impact factor: 3.603

2.  Religious coping is associated with the quality of life of patients with advanced cancer.

Authors:  Nalini Tarakeshwar; Lauren C Vanderwerker; Elizabeth Paulk; Michelle J Pearce; Stanislav V Kasl; Holly G Prigerson
Journal:  J Palliat Med       Date:  2006-06       Impact factor: 2.947

3.  The Quality of Dying and Death Questionnaire (QODD): empirical domains and theoretical perspectives.

Authors:  Lois Downey; J Randall Curtis; William E Lafferty; Jerald R Herting; Ruth A Engelberg
Journal:  J Pain Symptom Manage       Date:  2009-09-25       Impact factor: 3.612

Review 4.  Psychosocial interventions for cancer survivors: A meta-analysis of effects on positive affect.

Authors:  John M Salsman; James E Pustejovsky; Stephen M Schueller; Rosalba Hernandez; Mark Berendsen; Laurie E Steffen McLouth; Judith T Moskowitz
Journal:  J Cancer Surviv       Date:  2019-11-19       Impact factor: 4.442

Review 5.  Environmental Design for End-of-Life Care: An Integrative Review on Improving the Quality of Life and Managing Symptoms for Patients in Institutional Settings.

Authors:  Rana Sagha Zadeh; Paul Eshelman; Judith Setla; Laura Kennedy; Emily Hon; Aleksa Basara
Journal:  J Pain Symptom Manage       Date:  2017-09-19       Impact factor: 3.612

6.  Validation of the "Quality of Life in Life-Threatening Illness--Family Carer Version" (QOLLTI-F) in German-speaking carers of advanced cancer patients.

Authors:  Sophie Schur; Alexandra Ebert-Vogel; Michaela Amering; Eva Katharina Masel; Marie Neubauer; Andrea Schrott; Ingrid Sibitz; Herbert Watzke; Beate Schrank
Journal:  Support Care Cancer       Date:  2014-05-09       Impact factor: 3.603

7.  Kinesitherapy alleviates fatigue in terminal hospice cancer patients-an experimental, controlled study.

Authors:  Tomasz Buss; Krystyna de Walden-Gałuszko; Aleksandra Modlińska; Magdalena Osowicka; Monika Lichodziejewska-Niemierko; Justyna Janiszewska
Journal:  Support Care Cancer       Date:  2009-08-12       Impact factor: 3.603

Review 8.  Somatically ill persons' self-nominated quality of life domains: review of the literature and guidelines for future studies.

Authors:  Elsbeth F Taminiau-Bloem; Mechteld R M Visser; Carol Tishelman; Margot A Koeneman; Florence J van Zuuren; Mirjam A G Sprangers
Journal:  Qual Life Res       Date:  2010-01-03       Impact factor: 4.147

9.  An evaluation of Canada's Compassionate Care Benefit from a family caregiver's perspective at end of life.

Authors:  Valorie A Crooks; Allison Williams
Journal:  BMC Palliat Care       Date:  2008-08-28       Impact factor: 3.234

10.  Implementing a home-based exercise program for patients with advanced, incurable diseases after discharge and their caregivers: lessons we have learned.

Authors:  Waldemar Siemens; Anja Wehrle; Jan Gaertner; Michael Henke; Peter Deibert; Gerhild Becker
Journal:  BMC Res Notes       Date:  2015-09-30
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