Literature DB >> 16911057

Relatives in end-of-life care--part 1: a systematic review of the literature the five last years, January 1999-February 2004.

Birgitta Andershed1.   

Abstract

AIM: To review systematically research conducted during the past five years focusing on the relatives' situation and needs in end-of-life care. BACKGROUND AND AIM: That relatives make a large contribution in the care of the dying is well-known. In this situation, relatives often have to solve many new practical problems in the care as well as dealing with the sorrow of both themselves and the dying person. In recent years, palliative care has been developed in many countries and many new studies have been carried out.
METHODS: A systematic search of the literature was performed in the CINAHL and Medline databases. Of the 94 papers analysed, there were 59 qualitative and 35 quantitative studies with differing designs. The studies were carried out in 11 countries and were published in 34 different journals.
RESULTS: The results were categorized in two main themes with several subthemes: (1) being a close relative--the situation: (i) exposed position--new responsibility, (ii) balance between burden and capacity and (iii) positive values; (2) being a close relative--needs: (i) good patient care, (ii) being present, (iii) knowing and communicating and (iv) support from and trusting relationship with the professional. The relative's feelings of security and trust in the professional were found to be of great importance.
CONCLUSION: More than twice as many studies had a descriptive/explorative design, which is of importance in the assessment of evidence. However, different studies complement one another and in summary, it can be said that analytic evidence is unequivocal: good patient care, communication, information and the attitude of the professional are of decisive importance regarding relatives' situation. These results are also in accord with earlier review studies. RELEVANCE TO CLINICAL PRACTICE: Staff members have a great deal of responsibility for assuring that the patient feels as good as possible, facilitating relatives' involvement based on the family's wishes and limiting the stress and difficulties experienced by the family. The results showed that the relative's satisfaction could depend on the attitude of the professional as well as on good communication, good listening and good information. This can also be viewed as a prerequisite for the professional to get to know the family and to provide 'care in the light'.

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Year:  2006        PMID: 16911057     DOI: 10.1111/j.1365-2702.2006.01473.x

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  39 in total

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Journal:  Support Care Cancer       Date:  2013-07-26       Impact factor: 3.603

2.  Psychometric Properties of a Spanish-Language Version of a Short-Form FAMCARE: Applications to Caregivers of Patients With Alzheimer's Disease and Related Dementias.

Authors:  Jeanne A Teresi; Katja Ocepek-Welikson; Mildred Ramirez; Katherine A Ornstein; Suzanne Bakken; Albert Siu; José A Luchsinger
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3.  Measuring caregiver outcomes in palliative care: a construct validation study of two instruments for use in economic evaluations.

Authors:  Renske Hoefman; Hareth Al-Janabi; Nikki McCaffrey; David Currow; Julie Ratcliffe
Journal:  Qual Life Res       Date:  2014-11-08       Impact factor: 4.147

4.  Family caregiver involvement for long-term care residents at the end of life.

Authors:  Sharon W Williams; Sheryl Zimmerman; Christianna S Williams
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2012-08-28       Impact factor: 4.077

5.  Guidelines for the psychosocial and bereavement support of family caregivers of palliative care patients.

Authors:  Peter Hudson; Cheryl Remedios; Rachel Zordan; Kristina Thomas; Di Clifton; Michael Crewdson; Christopher Hall; Tom Trauer; Amanda Bolleter; David M Clarke; Catherine Bauld
Journal:  J Palliat Med       Date:  2012-03-02       Impact factor: 2.947

6.  Making sense of continuous sedation in end-of-life care for cancer patients: an interview study with bereaved relatives in three European countries.

Authors:  S M Bruinsma; J Brown; A van der Heide; L Deliens; L Anquinet; S A Payne; J E Seymour; J A C Rietjens
Journal:  Support Care Cancer       Date:  2014-07-15       Impact factor: 3.603

7.  Differences of Quality in End-of-Life Care across Settings: Results from the U.S. National Health and Aging Trends Study of Medicare Beneficiaries.

Authors:  Shuo Xu; Mangdong Liu; Oejin Shin; Vanessa Parker; Rosalba Hernandez
Journal:  J Palliat Med       Date:  2020-03-09       Impact factor: 2.947

8.  Family perceptions of quality of hospice care in the nursing home.

Authors:  Deborah Hwang; Joan M Teno; Melissa Clark; Renée Shield; Cindy Williams; David Casarett; Carol Spence
Journal:  J Pain Symptom Manage       Date:  2014-05-09       Impact factor: 3.612

9.  Performance of the Family Satisfaction with the End-of-Life Care (FAMCARE) measure in an ethnically diverse cohort: psychometric analyses using item response theory.

Authors:  Jeanne A Teresi; Katherine Ornstein; Katja Ocepek-Welikson; Mildred Ramirez; Albert Siu
Journal:  Support Care Cancer       Date:  2013-10-05       Impact factor: 3.603

10.  A systematic review of psychosocial interventions for family carers of palliative care patients.

Authors:  Peter L Hudson; Cheryl Remedios; Kristina Thomas
Journal:  BMC Palliat Care       Date:  2010-08-05       Impact factor: 3.234

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