Volume 47, Issue 2 p. 215-219

Misclassification and Selection Bias When Identifying Alzheimer's Disease Solely from Medicare Claims Records

Robert Newcomer PhD

Corresponding Author

Robert Newcomer PhD

Department of Social and Behavioral Science and the Institute for Health & Aging, University of California, San Francisco

Department of Social & Behavioral Sciences, University of California, 3333 California St., Suite 455, San Francisco, CA 94143-0612.Search for more papers by this author
Ted Clay MS

Ted Clay MS

Clay Software and Statistics, Ashland, Oregon.

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Jay S. Luxenberg MD

Jay S. Luxenberg MD

Department of Medicine, University of California, San Francisco, and the Jewish Home for the Aged, San Francisco

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Robert H. Miller PhD

Robert H. Miller PhD

Department of Social and Behavioral Science and the Institute for Health & Aging, University of California, San Francisco

Institute for Health Policy Studies, University of California, San Francisco

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First published: 27 April 2015
Citations: 99

The data base used in this work has been supported by Contract No. 50–89-0069 from the Health Care Financing Administration; the analysis and preparation of the manuscript was supported by the University of California.

Abstract

BACKGROUND: Medicare claims as the basis for health condition adjustments is becoming a method of choice in capitation reimbursement. A recent study has found that claims-based beneficiary classification for Alzheimer's disease produces lower prevalence estimates and higher average costs than previous healthcare cost studies in this population. These sets of studies differ in data sources, period length, and in their specification of dementia.

OBJECTIVES: Participants in the Medicare Alzheimer's Disease Demonstration (MADDE) provide a sample of persons known to have some form of dementia. This group is used to test the adequacy of claims data for identifying eligible cases and any bias in expenditure differences between those flagged or not flagged by a claim in a given period.

DESIGN: A prospective cohort design using up to 36 months of claims data.

SETTING: The demonstration enrolled 4166 participants in treatment, and 3942 in a control group in eight communities across the US. Cases were combined in this analysis.

PARTICIPANTS: Persons with available Medicare Part A & B claims data: those receiving care under fee for service reimbursement were used in the analysis. A total of 5379 MADDE cases received fee for service care during 1991 and 1992, the period of primary interest in the analysis.

MEASUREMENT: Client health and functional status interviews and Medicare Part A & B claims.

RESULTS: Less than 20% of MADDE participants were classified with Dementia of the Alzheimer type (DAT) from a single year of claims although 68% had a DAT diagnosis from a referring physician. Annualized expenditures were 1.7 times higher among those with DAT from claims compared with those known otherwise to have dementia but who had not been identified with this condition from Medicare claims.

CONCLUSION: Underclassification of dementia from claims records can be partially remedied by increasing the period during which claims are compiled, but additional diagnostic sources will likely be needed to increase prevalence counts closer to 100% of true cases. Risk adjustment based on a single year of reported claims expenditures may overpay providers, at least in the short term, because payment incentives will likely increase prevalence reporting. J Am Geriatr Soc 47:215–219, 1999.