Literature DB >> 24524662

Anxiety among informal hospice caregivers: an exploratory study.

Karla T Washington1, George Demiris2, Kenneth C Pike3, Robin L Kruse1, Debra Parker Oliver1.   

Abstract

OBJECTIVE: This study examined the prevalence of clinically significant anxiety among informal hospice caregivers and identified the characteristics of caregivers who experienced anxiety of this severity.
METHOD: An exploratory secondary data analysis pooled from three separate studies of informal hospice caregivers (N = 433) was conducted. Researchers employed descriptive statistics to calculate anxiety prevalence and utilized logistic regression to model the associations between the covariates (i.e., caregiver characteristics) and anxiety.
RESULTS: Overall, 31% of informal hospice caregivers reported moderate or higher levels of anxiety. Caregivers associated with the research site in the Northwest were less likely to be anxious than those in the Southeast [χ2(3, N = 433) = 7.07, p = 0.029], and employed caregivers were less likely to be anxious than unemployed caregivers (OR = 0.56, 95% CI = 0.33, 0.96). The likelihood of being anxious decreased with increasing physical quality of life (OR = 0.77, 95% CI = 0.69, 0.85), and younger female caregivers were more likely to be anxious than male caregivers and older females (OR = 0.95, CI = 0.91, 0.99). SIGNIFICANCE OF
RESULTS: A noteworthy number of informal hospice caregivers experience clinically significant levels of anxiety. Increased efforts to screen and address anxiety in this population are recommended.

Entities:  

Keywords:  Anxiety; Caregivers; Family; Hospice care

Mesh:

Year:  2014        PMID: 24524662      PMCID: PMC4133335          DOI: 10.1017/S1478951513001193

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  23 in total

Review 1.  Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008).

Authors:  L Funk; Ki Stajduhar; C Toye; S Aoun; Ge Grande; Cj Todd
Journal:  Palliat Med       Date:  2010-06-24       Impact factor: 4.762

Review 2.  Cancer family caregivers during the palliative, hospice, and bereavement phases: a review of the descriptive psychosocial literature.

Authors:  Anna-Leila Williams; Ruth McCorkle
Journal:  Palliat Support Care       Date:  2011-09

3.  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

4.  Hospice decision making: diagnosis makes a difference.

Authors:  Deborah P Waldrop; Mary Ann Meeker
Journal:  Gerontologist       Date:  2012-03-02

5.  The psychological and physical health of hospice caregivers.

Authors:  Y Chentsova-Dutton; S Shuchter; S Hutchin; L Strause; K Burns; S Zisook
Journal:  Ann Clin Psychiatry       Date:  2000-03       Impact factor: 1.567

6.  Stress variances among informal hospice caregivers.

Authors:  Elaine Wittenberg-Lyles; George Demiris; Debra Parker Oliver; Karla Washington; Stephanie Burt; Sara Shaunfield
Journal:  Qual Health Res       Date:  2012-06-06

7.  Feasibility and preliminary effects of an intervention targeting schema development for caregivers of newly admitted hospice patients.

Authors:  Kathryn B Lindstrom; Bernadette Mazurek Melnyk
Journal:  J Palliat Med       Date:  2013-02-05       Impact factor: 2.947

Review 8.  Overview of generalized anxiety disorder: epidemiology, presentation, and course.

Authors:  Risa B Weisberg
Journal:  J Clin Psychiatry       Date:  2009       Impact factor: 4.384

Review 9.  Dementia caregiver intervention research: in search of clinical significance.

Authors:  Richard Schulz; Alison O'Brien; Sara Czaja; Marcia Ory; Rachel Norris; Lynn M Martire; Steven H Belle; Lou Burgio; Laura Gitlin; David Coon; Robert Burns; Dolores Gallagher-Thompson; Alan Stevens
Journal:  Gerontologist       Date:  2002-10

10.  Predictors of burnout in the family caregivers of Alzheimer's disease: evidence from Turkey.

Authors:  Aysegul Yilmaz; Engin Turan; Duru Gundogar
Journal:  Australas J Ageing       Date:  2009-03       Impact factor: 2.111

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  8 in total

1.  Gender Differences in Caregiving at End of Life: Implications for Hospice Teams.

Authors:  Karla T Washington; Kenneth C Pike; George Demiris; Debra Parker Oliver; David L Albright; Alexandria M Lewis
Journal:  J Palliat Med       Date:  2015-10-20       Impact factor: 2.947

2.  A Problem-Solving Intervention for Hospice Family Caregivers: A Randomized Clinical Trial.

Authors:  George Demiris; Debra Parker Oliver; Karla Washington; Kenneth Pike
Journal:  J Am Geriatr Soc       Date:  2019-04-04       Impact factor: 5.562

3.  Unique characteristics of informal hospice cancer caregiving.

Authors:  Karla T Washington; Kenneth C Pike; George Demiris; Debra Parker Oliver
Journal:  Support Care Cancer       Date:  2014-12-30       Impact factor: 3.603

4.  The Prevalence and Risks for Depression and Anxiety in Hospice Caregivers.

Authors:  Debra Parker Oliver; Karla Washington; Jamie Smith; Aisha Uraizee; George Demiris
Journal:  J Palliat Med       Date:  2016-12-02       Impact factor: 2.947

5.  Sleep Problems, Anxiety, and Global Self-Rated Health Among Hospice Family Caregivers.

Authors:  Karla T Washington; Debra Parker Oliver; Jamie B Smith; Christina S McCrae; Shanky M Balchandani; George Demiris
Journal:  Am J Hosp Palliat Care       Date:  2017-04-10       Impact factor: 2.500

6.  Anxiety, Depression, Quality of Life, Caregiver Burden, and Perceptions of Caregiver-Centered Communication among Black and White Hospice Family Caregivers.

Authors:  Lauren T Starr; Karen Bullock; Karla Washington; Subhash Aryal; Debra Parker Oliver; George Demiris
Journal:  J Palliat Med       Date:  2021-11-18       Impact factor: 2.947

7.  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

8.  Perceived Benefits and Burdens of Participation for Caregivers of Cancer Patients in Hospice Clinical Trials: A Pilot Study.

Authors:  Debra Parker Oliver; Jacquelyn J Benson; Connie Ulrich; Karla T Washington; Abigail J Rolbiecki; Patrick White; Jamie B Smith; Christina Lero; Olivia J Landon; George Demiris
Journal:  J Pain Symptom Manage       Date:  2020-11-06       Impact factor: 5.576

  8 in total

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