Literature DB >> 3853574

The needs of families who care for patients with cancer at home: are we meeting them?

C Hinds.   

Abstract

A diagnosis of cancer in a family member has an impact on the entire unit. A study was conducted to determine needs perceived by families as they met the care requirements of such patients, to assess how families coped with these needs and to determine the resources they utilized. Families were selected from a stratified random sampling of patients who were receiving treatment at a local cancer clinic. Classification was by sex and site of disease. Families were interviewed in their homes. Descriptive statistics were used to summarize the data. Chi-square test of independence was conducted on selective qualitative variables. Eighty-three family members consisting of 43 males and 40 females with average ages 53 and 54 years respectively participated in the investigation. Families needed assistance with the physical care of patients. As many as 31% of them were coping poorly with this area of care. There were also several unmet needs in the psychosocial domain. The need most frequently expressed by families was for a place where they could turn to discuss their fears. Nineteen (23%) of the families knew of community services they could call on for assistance. Only seven (8%) of the families had utilized these services. These results suggest that fresh approaches might be needed in order to achieve our goal of family-focused care.

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Year:  1985        PMID: 3853574     DOI: 10.1111/j.1365-2648.1985.tb00550.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  14 in total

1.  Patients with cancer and family caregivers: management of symptoms caused by cancer or cancer therapy at home.

Authors:  Daniela Maria Hazelwood; Sabine Koeck; Martin Wallner; Kathryn Hoehn Anderson; Hanna Mayer
Journal:  HeilberufeScience       Date:  2012-11-01

2.  Caring for elderly people at home: the consequences to caregivers.

Authors:  E Grunfeld; R Glossop; I McDowell; C Danbrook
Journal:  CMAJ       Date:  1997-10-15       Impact factor: 8.262

3.  Caregivers of adults with cancer: Multidimensional correlates of psychological distress.

Authors:  J R Rodrigue; R G Hoffmann
Journal:  J Clin Psychol Med Settings       Date:  1994-09

4.  Pain catastrophizing, pain intensity, and dyadic adjustment influence patient and partner depression in metastatic breast cancer.

Authors:  Hoda Badr; Megan J Shen
Journal:  Clin J Pain       Date:  2014-11       Impact factor: 3.442

5.  [Patient-controlled analgesia (PCA) in outpatients with cancer pain. Analysis of 1,692 treatment days].

Authors:  C Schiessl; J Bidmon; R Sittl; N Griessinger; J Schüttler
Journal:  Schmerz       Date:  2007-02       Impact factor: 1.107

Review 6.  Care for the cancer caregiver: a systematic review.

Authors:  Allison J Applebaum; William Breitbart
Journal:  Palliat Support Care       Date:  2012-10-10

7.  Fatigue affecting family caregivers of cancer patients.

Authors:  S Jensen; B Given
Journal:  Support Care Cancer       Date:  1993-11       Impact factor: 3.603

8.  Developing the Cambridge palliative audit schedule (CAMPAS): a palliative care audit for primary health care teams.

Authors:  M S Rogers; S I Barclay; C J Todd
Journal:  Br J Gen Pract       Date:  1998-05       Impact factor: 5.386

9.  Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers.

Authors:  Allison J Applebaum; Carol J Farran; Allison M Marziliano; Anna R Pasternak; William Breitbart
Journal:  Palliat Support Care       Date:  2013-08-07

10.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

Authors:  Eva Grunfeld; Doug Coyle; Timothy Whelan; Jennifer Clinch; Leonard Reyno; Craig C Earle; Andrew Willan; Raymond Viola; Marjorie Coristine; Teresa Janz; Robert Glossop
Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262

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