Literature DB >> 12597468

What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness.

R Harding1, I J Higginson.   

Abstract

Informal carers in cancer and palliative care are known to have high needs and psychological morbidity, yet a literature review identified few targeted interventions. This systematic review of interventions for carers of patients using home cancer and palliative care services searched Medline, CancerLit, Psycinfo and Cinahl databases. The terms used were carer(s), caregiver(s), palliative and cancer. Papers that reported interventions for adults actively providing informal care for noninstitutionalized cancer and palliative care patients were reviewed. Twenty-two interventions were identified, comprising home nursing care (four), respite services (three), social networks and activity enhancement (two), problem solving and education (three) and group work (10). Of these, nine were delivered solely to carers (i.e., were targeted services). Only six of the carers' interventions had been evaluated, two of these had used a randomized control trial (RCT; grades IB), three employed a single group methodology (two prospective grades IIIC and one retrospective grade IIIC) and one was evaluated using facilitator feedback. There was a lack of outcome evaluation designs, small sample sizes and a reliance on intervention descriptions and formative evaluations. Methodological challenges may mean alternatives to 'pure' RCTs should be considered. The current evidence contributes more to understanding feasibility and acceptability than to effectiveness. Practitioners and evaluators must prioritize the further development of intervention studies.

Entities:  

Mesh:

Year:  2003        PMID: 12597468     DOI: 10.1191/0269216303pm667oa

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  88 in total

1.  A qualitative exploration of the role of primary care in supporting colorectal cancer patients.

Authors:  Susan Hall; Nicola Gray; Susan Browne; Sue Ziebland; Neil C Campbell
Journal:  Support Care Cancer       Date:  2012-03-09       Impact factor: 3.603

2.  What are the perceived needs and challenges of informal caregivers in home cancer palliative care? Qualitative data to construct a feasible psycho-educational intervention.

Authors:  R Harding; E Epiphaniou; D Hamilton; S Bridger; V Robinson; R George; T Beynon; I J Higginson
Journal:  Support Care Cancer       Date:  2011-11-10       Impact factor: 3.603

3.  A Problem Solving Intervention for hospice caregivers: a pilot study.

Authors:  George Demiris; Debra Parker Oliver; Karla Washington; Lynne Thomas Fruehling; Donna Haggarty-Robbins; Ardith Doorenbos; Hope Wechkin; Donna Berry
Journal:  J Palliat Med       Date:  2010-08       Impact factor: 2.947

4.  Preferred place of care and place of death of the general public and cancer patients in Japan.

Authors:  Akemi Yamagishi; Tatsuya Morita; Mitsunori Miyashita; Saran Yoshida; Nobuya Akizuki; Yutaka Shirahige; Miki Akiyama; Kenji Eguchi
Journal:  Support Care Cancer       Date:  2012-01-24       Impact factor: 3.603

5.  Developing primary palliative care.

Authors:  Scott A Murray; Kirsty Boyd; Aziz Sheikh; Keri Thomas; Irene J Higginson
Journal:  BMJ       Date:  2004-11-06

6.  Using mixed methods to assess how cancer patients' needs in relation to their relatives are met in the Danish health care system: a report from the population-based study "The Cancer Patient's World".

Authors:  Lone Ross; Morten Aagaard Petersen; Anna Thit Johnsen; Louise Hyldborg Lundstrøm; Line Lund; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2012-04-25       Impact factor: 3.603

7.  A noninferiority trial of a problem-solving intervention for hospice caregivers: in person versus videophone.

Authors:  George Demiris; Debra Parker Oliver; Elaine Wittenberg-Lyles; Karla Washington; Ardith Doorenbos; Tessa Rue; Donna Berry
Journal:  J Palliat Med       Date:  2012-04-26       Impact factor: 2.947

8.  [Palliative medicine].

Authors:  H P Zenner
Journal:  HNO       Date:  2013-03       Impact factor: 1.284

9.  Experience of meaning in life in bereaved informal caregivers of palliative care patients.

Authors:  Monika Brandstätter; Monika Kögler; Urs Baumann; Veronika Fensterer; Helmut Küchenhoff; Gian Domenico Borasio; Martin Johannes Fegg
Journal:  Support Care Cancer       Date:  2014-01-03       Impact factor: 3.603

Review 10.  Minor children of palliative patients: a systematic review of psychosocial family interventions.

Authors:  Franziska Kühne; Thomas Krattenmacher; Volker Beierlein; Johann Christian Grimm; Corinna Bergelt; Georg Romer; Birgit Möller
Journal:  J Palliat Med       Date:  2012-08       Impact factor: 2.947

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