The minimum data set: No longer just for clinical assessment

M. J. Rantz, M. Zwygart-Stauffacher, L. L. Popejoy, D. R. Mehr, V. T. Grando, D. D. Wipke-Tevis, L. L. Hicks, V. S. Conn, R. Porter, M. Maas

Research output: Contribution to journalReview article

10 Scopus citations

Abstract

Minimum Data Set (MDS) data, available in every nursing home in the United States, are now integral to reimbursement for Medicare nationwide and Medicaid in some states. MDS data are also used for clinical assessment, improvement in clinical practice, and evaluation of care outcomes. The Resident Assessment Instrument process, Quality Indicators (QIs), Resource Utilization Groups, and implications for prospective payment are discussed in this article. Suggestions are presented for using QI information for quality improvement efforts as well as how all data may be incorporated into improving clinical practice and outcomes of care.

Original languageEnglish (US)
Pages (from-to)354-360
Number of pages7
JournalAnnals of Long-Term Care
Volume7
Issue number9
StatePublished - Oct 4 1999

ASJC Scopus subject areas

  • Gerontology
  • Geriatrics and Gerontology

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