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Screening for Clinical Laboratory Errors with Medicare Claims Data: Results for Digoxin
To whom correspondence should be addressed at: University of Alabama at Birmingham, B55 MJH 1825 University Blvd., Birmingham, AL 35294-2010 A statistical model is demonstrated for finding outpa tient clinical laboratories having high frequencies of bad patient outcomes, after testing, that may indicate testing errors. A sample of Medicare Part A and Part B claims for 30,685 digoxin tests for 1985 through 1987 was analyzed. Deaths or digoxin-related hospitaliza tions within 14 days of digoxin testing are defined as "adverse events" potentially influenced by test informa tion. Approximately 3.3% of digoxin tests were followed by adverse events with two-thirds resulting in hospital ization or death. Adverse events were (a) lower in states with stronger laboratory regulations, (b) 15% higher whenever the site of testing switched, (c) unre lated to testing in low volume physician office labora tories, and (d) unrelated to frequency of digoxin testing in previous 6 months. Results a and b are consistent with findings for prothrombin testing but c and d are not. Differences are consistent with technical charac teristics of the tests.
American Journal of Medical Quality, Vol. 11, No. 1,
25-32 (1996) |
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