Literature DB >> 27224450

Development of an Assessment to Examine Training of the Hospice Primary Caregiver.

Eleanor L DiBiasio1, Joan M Teno2, Melissa A Clark3, Carol Spence4, David Casarett5.   

Abstract

BACKGROUND: Key to high-quality care of dying hospice patients at home is whether the hospice provides adequate training so the caregiver can safely care for the patient.
OBJECTIVE: The study objective was to develop and validate a survey of hospice training for caregivers to ensure safe, high-quality care in the home setting.
DESIGN: Our survey design was cross-sectional. Bereaved respondents of individuals who died at home under the care of hospice were surveyed three to six months postdeath. MEASUREMENTS: Items were developed based on advice of an expert panel, focus groups of hospice caregivers, and literature review, with 12 items developed for testing and examining 8 key processes of care. We examined the validity and reliability of the assessment using factor analysis, correlational analyses, and multivariable modeling.
RESULTS: Our sample consisted of 262 primary caregivers (mean age 62.4, 76.7% female, 58.8% non-Hispanic white). Six questions focused on providing the caregiver with information, while another six focused on the training that hospice provided. Based on model fit and Cronbach's alpha, we dropped the information items. The items that examined hospice training demonstrated a one-factor solution and a Cronbach's of 0.90. We examined correlations of the multi-item composite with overall rating of quality of care (0.53), overall distress (0.31), and whether the respondent would recommend this hospice to others (0.49). There were no significant sociodemographic correlates of concerns with training.
CONCLUSIONS: Sufficient preliminary reliability and validity warrants further testing of this composite to examine the adequacy of training provided to family members to care safely for the patient.

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Year:  2016        PMID: 27224450      PMCID: PMC4904156          DOI: 10.1089/jpm.2015.0185

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


  17 in total

1.  Psychometric properties of the CAHPS 1.0 survey measures. Consumer Assessment of Health Plans Study.

Authors:  R D Hays; J A Shaul; V S Williams; J S Lubalin; L D Harris-Kojetin; S F Sweeny; P D Cleary
Journal:  Med Care       Date:  1999-03       Impact factor: 2.983

2.  Empowerment through information: supporting rural families of oncology patients in palliative care.

Authors:  L Wilkes; K White; L O'Riordan
Journal:  Aust J Rural Health       Date:  2000-02       Impact factor: 1.662

Review 3.  The national agenda for quality palliative care: the National Consensus Project and the National Quality Forum.

Authors:  Betty Ferrell; Stephen R Connor; Anne Cordes; Constance M Dahlin; Perry G Fine; Nancy Hutton; Mark Leenay; Judy Lentz; Judi Lund Person; Diane E Meier; Ken Zuroski
Journal:  J Pain Symptom Manage       Date:  2007-06       Impact factor: 3.612

4.  Screening for mental health: validity of the MHI-5 using DSM-IV Axis I psychiatric disorders as gold standard.

Authors:  H J Rumpf; C Meyer; U Hapke; U John
Journal:  Psychiatry Res       Date:  2001-12-31       Impact factor: 3.222

5.  Patient-focused, family-centered end-of-life medical care: views of the guidelines and bereaved family members.

Authors:  J M Teno; V A Casey; L C Welch; S Edgman-Levitan
Journal:  J Pain Symptom Manage       Date:  2001-09       Impact factor: 3.612

Review 6.  A systematic review of informal caregivers' needs in providing home-based end-of-life care to people with cancer.

Authors:  Penny E Bee; Pamela Barnes; Karen A Luker
Journal:  J Clin Nurs       Date:  2009-04-08       Impact factor: 3.036

7.  Association between quality of end-of-life care and possible complicated grief among bereaved family members.

Authors:  Kaya Miyajima; Daisuke Fujisawa; Kimio Yoshimura; Masaya Ito; Satomi Nakajima; Joichiro Shirahase; Masaru Mimura; Mitsunori Miyashita
Journal:  J Palliat Med       Date:  2014-07-22       Impact factor: 2.947

8.  Intervention development for enhanced lay palliative caregiver support - the use of focus groups.

Authors:  P Hudson; S Aranda; N McMurray
Journal:  Eur J Cancer Care (Engl)       Date:  2002-12       Impact factor: 2.520

9.  Death from cancer at home: the carers' perspective.

Authors:  R V Jones; J Hansford; J Fiske
Journal:  BMJ       Date:  1993-01-23

10.  Performance of a five-item mental health screening test.

Authors:  D M Berwick; J M Murphy; P A Goldman; J E Ware; A J Barsky; M C Weinstein
Journal:  Med Care       Date:  1991-02       Impact factor: 2.983

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