Literature DB >> 9160459

A rational approach to long-term care: comparing the independent living model with agency-based care for persons with high spinal cord injuries.

J Mattson-Prince.   

Abstract

Two groups of individuals with high level tetraplegia (C1-4) were compared with respect to the model of personal care assistance used. The study was undertaken to determine whether a finite population with severe disability had differences in health status, costs and perceived quality of life, relative to whether they used agencies for their care, or hired, trained and reimbursed care givers independently. A survey, which included demographics as well as portions of RAND-36, LSI-A, PIP, PASI and CHART was used. Telephone interviews were held with 29 individuals who received their care through an agency and 42 who managed care independently. Chi square, 't'-tests, and multiple regression analysis were used to control for potentially confounding group differences. The self-managed group demonstrated significantly better health outcomes, with fewer re-hospitalizations for preventable complications. They experienced better life satisfaction and significantly lower costs. Although those who used an independent model of care-giving received significantly more hours of paid assistance, the average annual cost of care was significantly lower for each individual. In addition to reducing the financial burden on the individual and society, self-managed care seemed to diminish the emotional burden borne by these individuals.

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Year:  1997        PMID: 9160459     DOI: 10.1038/sj.sc.3100453

Source DB:  PubMed          Journal:  Spinal Cord        ISSN: 1362-4393            Impact factor:   2.772


  8 in total

1.  Assessment of physical function and secondary complications after complete spinal cord injury.

Authors:  Shauna Dudley-Javoroski; Richard K Shields
Journal:  Disabil Rehabil       Date:  2006-01-30       Impact factor: 3.033

2.  Preferences of adults with spinal cord injury for widely used health-related quality of life and subjective well-being measures.

Authors:  Alina Ionela Palimaru; William E Cunningham; Marcus Dillistone; Arturo Vargas-Bustamante; Honghu Liu; Ron D Hays
Journal:  J Spinal Cord Med       Date:  2018-05-23       Impact factor: 1.985

3.  Measuring health-related quality of life for persons with mobility impairments: an enabled version of the short-form 36 (SF-36E).

Authors:  Katherine Froehlich-Grobe; Elena M Andresen; Charlene Caburnay; Glen W White
Journal:  Qual Life Res       Date:  2008-04-22       Impact factor: 4.147

Review 4.  Caregiving services in spinal cord injury: a systematic review of the literature.

Authors:  E M Smith; N Boucher; W C Miller
Journal:  Spinal Cord       Date:  2016-02-23       Impact factor: 2.772

5.  A framework for understanding modifications to measures for diverse populations.

Authors:  Anita L Stewart; Angela D Thrasher; Jack Goldberg; Judy A Shea
Journal:  J Aging Health       Date:  2012-04-10

Review 6.  Identifying and classifying quality-of-life tools for assessing pressure ulcers after spinal cord injury.

Authors:  Sander L Hitzig; Christina Balioussis; Ethne Nussbaum; Colleen F McGillivray; B Catharine Craven; Luc Noreau
Journal:  J Spinal Cord Med       Date:  2013-05-22       Impact factor: 1.985

7.  Are persons with physical disabilities who participate in society healthier and happier? Structural equation modelling of objective participation and subjective well-being.

Authors:  Cretien van Campen; Jurjen Iedema
Journal:  Qual Life Res       Date:  2007-02-01       Impact factor: 4.147

Review 8.  Short Form health surveys and related variants in spinal cord injury research: a systematic review.

Authors:  David G T Whitehurst; Lidia Engel; Stirling Bryan
Journal:  J Spinal Cord Med       Date:  2014-01-06       Impact factor: 1.985

  8 in total

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