Literature DB >> 22441884

[Family caregivers of palliative cancer patients: health-related quality of life and care-related burden].

Norbert Köhler1, Andrea Perner, Daniela Anders, Elmar Brähler, Kirsten Papsdorf, Heide Götze.   

Abstract

Family caregivers of palliative cancer patients are usually much burdened. In order to avoid the failure of home care, family caregivers need support. The current study evaluates support needs in family caregivers of palliative cancer patients. 53 family caregivers of palliative cancer patients answered the questionnaire. Health-related quality of life was assessed using the EORTC QLQ-C30 questionnaire. Home care burden was assessed using the "Burden Scale for Family Caregivers" (BSFC). Family caregivers suffered of reduced social and emotional function. Female and older caregivers reported a stronger home care burden than male and younger caregivers. For female and older family caregivers of palliative cancer patients, home care is very burdensome. Thus, female caregivers need, above all, psychosocial support, whereas older caregivers need the most support in a physical and social level. © Georg Thieme Verlag KG Stuttgart · New York.

Entities:  

Mesh:

Year:  2012        PMID: 22441884     DOI: 10.1055/s-0032-1304601

Source DB:  PubMed          Journal:  Psychother Psychosom Med Psychol        ISSN: 0937-2032


  7 in total

1.  Specialized home palliative care for adults and children: differences and similarities.

Authors:  Gesa Groh; Berend Feddersen; Monika Führer; Gian Domenico Borasio
Journal:  J Palliat Med       Date:  2014-06-13       Impact factor: 2.947

2.  Health-related quality of life of significant others of patients with malignant CNS versus non-CNS tumors: a comparative study.

Authors:  Florien W Boele; Jan J Heimans; Neil K Aaronson; Martin J B Taphoorn; Tjeerd J Postma; Jaap C Reijneveld; Martin Klein
Journal:  J Neurooncol       Date:  2013-07-04       Impact factor: 4.130

3.  Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care.

Authors:  Heide Götze; Elmar Brähler; Lutz Gansera; Nina Polze; Norbert Köhler
Journal:  Support Care Cancer       Date:  2014-05-09       Impact factor: 3.603

4.  Quality of life discordance between terminal cancer patients and family caregivers: a multicenter study.

Authors:  Yong Joo Lee; Jung Eun Kim; Youn Seon Choi; In Cheol Hwang; Sun Wook Hwang; Young Sung Kim; Hyo Min Kim; Hong Yup Ahn; So Jin Kim
Journal:  Support Care Cancer       Date:  2016-02-02       Impact factor: 3.603

5.  Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers.

Authors:  Maja Holm; Ida Carlander; Carl-Johan Fürst; Yvonne Wengström; Kristofer Årestedt; Joakim Öhlen; Anette Henriksson
Journal:  BMC Palliat Care       Date:  2015-04-24       Impact factor: 3.234

6.  Older people living alone (OPLA) - non-kin-carers' support towards the end of life: qualitative longitudinal study protocol.

Authors:  Sabine Pleschberger; Elisabeth Reitinger; Birgit Trukeschitz; Paulina Wosko
Journal:  BMC Geriatr       Date:  2019-08-13       Impact factor: 3.921

7.  Dyadic coping and its association with emotional functioning in couples confronted with advanced cancer: Results of the multicenter observational eQuiPe study.

Authors:  Janneke van Roij; Natasja Raijmakers; Jeroen Kloover; Evelien Kuip; Tineke Smilde; Lilly-Ann van der Velden; Gary Rodin; Lonneke van de Poll-Franse
Journal:  Psychooncology       Date:  2022-05-23       Impact factor: 3.955

  7 in total

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