Literature DB >> 17040156

Caregiving at the end of life.

Randy S Hebert1, Richard Schulz.   

Abstract

This paper provides a review of family caregiving for adult patients with serious, lifethreatening illness. Areas covered include the (1) epidemiology of family caregiving, (2) cross-cultural issues in caregiving, (3) impact of caregiving on families, (4) similarities and differences involved in providing care for patients with various illnesses, and (5) interventions for family caregivers. The importance of family caregiving to palliative care practice is emphasized.

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Mesh：

Year:  2006        PMID： 17040156     DOI： 10.1089/jpm.2006.9.1174

Source DB:  PubMed          Journal:  J Palliat Med        ISSN： 1557-7740            Impact factor:   2.947


  20 in total

1.  [Evaluation of the German version of the caregiver reaction assessment questionnaire for informal caregivers of patients with neovascular age-related macular degeneration].

Authors:  H Weyer-Wendl; M Tamm; P Walter
Journal:  Ophthalmologe       Date:  2016-03       Impact factor: 1.059

2.  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 3.  Informal caregiving of hospice patients.

Authors:  Colin G Pottie; Karen A Burch; Lori P Montross Thomas; Scott A Irwin
Journal:  J Palliat Med       Date:  2014-07       Impact factor: 2.947

4.  Events Leading to Hospital-Related Disenrollment of Home Hospice Patients: A Study of Primary Caregivers' Perspectives.

Authors:  Veerawat Phongtankuel; Shawn Paustian; Manney Carrington Reid; Amanda Finley; Angela Martin; John Delfs; Rosemary Baughn; Ronald D Adelman
Journal:  J Palliat Med       Date:  2016-11-28       Impact factor: 2.947

5.  Caring for Chronically Ill Older Adults: A View Over the Last 75 Years.

Authors:  Karl Pillemer; Sara J Czaja; M Cary Reid
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2020-11-13       Impact factor: 4.077

6.  Psychosocial, cultural, and spiritual health disparities in end-of-life and palliative care: where we are and where we need to go.

Authors:  Bronwynne C Evans; Ebere Ume
Journal:  Nurs Outlook       Date:  2012 Nov-Dec       Impact factor: 3.250

7.  Cumulative adversity and depressive symptoms among older adults in Israel: the differential roles of self-oriented versus other-oriented events of potential trauma.

Authors:  Dov Shmotkin; Howard Litwin
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2009-03-14       Impact factor: 4.328

8.  Trajectory and determinants of the quality of life of family caregivers of terminally ill cancer patients in Taiwan.

Authors:  Siew Tzuh Tang; Chung-Yi Li; Cheryl Chia-Hui Chen
Journal:  Qual Life Res       Date:  2008-02-15       Impact factor: 4.147

9.  Cognitive and behavioral treatments for anxiety and depression in a patient with an implantable cardioverter defibrillator (ICD): a case report and clinical discussion.

Authors:  Adam T Hirsh; Samuel F Sears; Jamie B Conti
Journal:  J Clin Psychol Med Settings       Date:  2009-04-30

10.  Reaction to Caregiving by Hospice Caregivers Upon Enrollment.

Authors:  David L Albright; Debra Parker Oliver; George Demiris
Journal:  Am J Hosp Palliat Care       Date:  2014-04-16       Impact factor: 2.500
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