Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-27T19:51:01.388Z Has data issue: false hasContentIssue false

Outcome Measures for Use with Home Care Clients

Published online by Cambridge University Press:  29 November 2010

John N. Morris
Affiliation:
Hebrew Rehabilitation Center for Aged
Iain Carpenter
Affiliation:
The University of Kent
Katherine Berg
Affiliation:
Brown University
Richard N. Jones
Affiliation:
Hebrew Rehabilitation Center for Aged
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Prior to the past decade, much research examining outcomes of home care programs, including efforts at delaying institutional placement, maintaining function, and supporting independence, was atheoretical in character. Outcomes hoped for were often unobserved. New policy developments require comprehensive assessment of need and aggregation of this assessment information. As more and more patients leave hospitals with complex clinical problems and extensive rehabilitative goals there has been a corresponding explosion of home care services. Social care models, while they still exist, are becoming a smaller component of the overall home care market. In this changing environment, questions are now being asked concerning the appropriateness of the care programs in home care and other post-acute care settings. There are also concerns that need to be addressed about movement of clients between post-acute settings. In this paper, we describe a set of proposed functional, behavioural, and social outcome measures that are germane to evaluating the efficacy of programmatic efforts within the post-acute continuum. Data were collected with a standardized data collection instrument, the Resident Assessment Instrument for Home Care (RAI-HC). We provide data summarizing these proposed outcomes and evidence of known groups validity in a cross-national sample of home care clients. Data highlight the differing characteristics of clients across these agencies and provide evidence that this standardized data collection instrument can capture data that is reliable and valid for describing populations and evaluating program effectiveness.

Résumé

RÉSUMÉ

Avant les années 1990, la plupart des recherches portant sur l'évaluation des résultats des programmes de soins à domicile, notamment sur les efforts pour retarder le placement, maintenir le fonctionnement et assurer l'autonomie des aîné(e)s, ne reposaient pas sur des fondements théoriques. Les résultats attendus des programmes étaient rarement mentionnés. L'élaboration de nouvelles politiques exige maintenant une évaluation complète des besoins et une agrégation des données recueillies. Depuis qu'un nombre croissant de patients quittent l'hôpital avec des problèmes cliniques complexes et que les objectifs de réhabilitation deviennent plus étendus, on assiste à une explosion des services de soins à domicile. Les modèles de soins sociaux, bien que toujours en cours, ne constituent désormais qu'une mince part du marché des soins offerts à domicile. Dans cet environnement en mutation, la pertinence des programmes de soins dans les établissements ou des autres soins dispensés suite à une maladie grave soulève de nouvelles interrogations. On s'interroge également sur les déplacements des clients entre les diverses installations de soins suite à des maladies graves. Cet article décrit un ensemble de mesures fonctionnelles, comportementales et sociales proposées en lien avec l'évaluation des effets des programmes de soins faisant suite à une longue maladie. L'instrument normalisé de collecte de données utilisé est le Resident Assessment Instrument for Home Care (RAI-HC). L'article présente un résumé des mesures proposées et témoigne de la validité de groupes identifiés à partir d'un échantillon national des clients de soins à domicile. Les données soulignent les différentes caractéristiques des clients entre les organismes et attestent que le RAI-HC permet de recueillir des données fiables et valides pour décrire les populations et évaluer l'efficacité des programmes.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - ND
This is an Open Access article, distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work.
Copyright
Copyright © Canadian Association on Gerontology 2000

Footnotes

*

Work on this project was supported in part by a contract from the Agency for Health Care Policy & Research, Rockville, M.D. Grant Number U18 HS09455-03 Quality Outcomes in Subacute and Home Care Programs (Q-SPAN) awarded to John Morris, Ph.D.

1

Hebrew Rehabilitation Center for Aged, 1200 Centre Street, Boston, MA 02131, ([email protected])

References

Bellelli, G., Frisoni, G.B., Bianchetti, A., & Trabucchi, M. (1997). The Bedford Alzheimer Nursing Severity scale for the severely demented: validation study. Alzheimer Disease and Associated Disorders, 11(2), 7177.CrossRefGoogle ScholarPubMed
Carpenter, G., & Bernabei, R. (1995). Database needs and practical models: is a minimum dataset and common database possible and/or desirable. In Rubenstein, L., Wieland, D., & Bernabei, R. (Eds.), Geriatric assessment technology: The state of the art. Milan: Editrice Kurtis.Google Scholar
Department of Health. (1995). NHS responsibilities for meeting continuing health care needs. London: Department of Health.Google Scholar
Kemper, P. (1988). The evaluation of the National Long Term Care Demonstration. 10. Overview of the findings. Health Services Research, 2(6), 420427.Google Scholar
Lafferty, G. (1996). Community based alternatives to hospital rehabilitation services: a review of the evidence and suggestions for approaching future evaluations. Reviews in Clinical Gerontology, 6, 183194.CrossRefGoogle Scholar
Leicester, M.C., & Pollock, A.M. (1996). Community care in South Thames (West) Region: is needs assessment working? Public Health, 110(2), 109113.CrossRefGoogle ScholarPubMed
Lipsitz, L.A., Nakajima, I., Gagnon, M., Hirayama, T., Connelly, C.M., & Izumo, H. (1994). Muscle strength and fall rates among residents of Japanese and American nursing homes: an international cross-cultural study. Journal of the American Geriatrics Society, 42(9), 953959.CrossRefGoogle Scholar
Ljunggren, G., Phillips, C.D., & Sgadari, A. (1997). Comparisons of restraint use in nursing homes in eight countries. Age and Ageing, 26(suppl. 2), 4347.CrossRefGoogle ScholarPubMed
Morris, J., Bernabei, R., Ikegami, N., Gilgen, R., Fries, B., Steel, K., & Carpenter, I. (1997a). RAI-Home Care (RAI-HC)(C) Assessment Manual. Washington, DC: InterRAI Corporation.Google Scholar
Morris, J.N., Fries, B.E., Mehr, D.R., Hawes, C., Phillips, C., Mor, V., & Lipsitz, L.A. (1994). MDS Cognitive Performance Scale. Journals of Gerontology, 49(4), M174–M182.CrossRefGoogle ScholarPubMed
Morris, J.N., Fries, B.E., Steel, K., Ikegami, N., Bernabei, R., Carpenter, G.I., Gilgen, R., Hirdes, J.P., & Topinkova, E. (1997b). Comprehensive clinical assessment in community setting: applicability of the MDS-HC. Journal of the American Geriatrics Society, 45(8), 10171024.CrossRefGoogle ScholarPubMed
Morris, J.N., Hawes, C., Fries, B.E., Phillips, C. D., Mor, V., Katz, S., Murphy, K., Drugovich, M.L., & Friedlob, A.S. (1990). Designing the national resident assessment instrument for nursing homes. Gerontologist, 30(3), 293307.CrossRefGoogle ScholarPubMed
Phillips, C, Hawes, C., Mor, V., Fries, B., & Morris, J. (1996). Evaluation of the Nursing Home Resident Assessment Instrument. Washington: Health Care Financing Administration.Google Scholar
Rossi, P.H., Wright, J.D., & Anderson, A.B. (1983). Handbook of survey research. New York: Academic Press.Google Scholar
Spector, P.E. (1992). Summated rating scale construction: an introduction. Newbury Park, CA: Sage Publications.CrossRefGoogle Scholar
Spector, W.D., & Kemper, P. (1994). Disability and cognitive impairment criteria: targeting those who need the most home care. Gerontologist, 34(5), 640651.CrossRefGoogle ScholarPubMed
Weissert, W.G., Cready, C.M., & Pawelak, J.E. (1988). The past and future of homeand community-based long-term care. Milbank Quarterly, 66(2), 309388.CrossRefGoogle Scholar