Prior Authorization for Antidepressants in Medicaid
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Date
2009
Author(s)
Adams, Alyce S.
Gilden, Daniel
Publisher
American Medical Association (AMA)
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Citation
Adams, Alyce S., Fang Zhang, Robert F. LeCates, Amy Johnson Graves, Dennis Ross-Degnan, Daniel Gilden, Thomas J. McLaughlin, Christine Lu, Connie M. Trinacty, and Stephen B. Soumerai. 2009. “Prior Authorization for Antidepressants in Medicaid.” Archives of Internal Medicine 169 (8) (April 27): 750. doi:10.1001/archinternmed.2009.39.
Abstract
Background Prior authorization is a popular, but understudied, strategy for reducing medication costs. We evaluated the impact of a controversial prior authorization policy in Michigan Medicaid on antidepressant use and health outcomes among dual Medicaid and Medicare enrollees with a Social Security Disability Insurance designation of permanent disability.
Methods We linked Medicaid and Medicare (2000-2003) claims for dual enrollees in Michigan and a comparison state, Indiana. Using interrupted time-series and longitudinal data analysis, we estimated the impact of the policy on antidepressant medication use, treatment initiation, disruptions in therapy, and adverse health events among continuously enrolled (Michigan, n = 28 798; Indiana, n = 21 769) and newly treated (Michigan, n = 3671; Indiana, n = 2400) patients.
Results In Michigan, the proportion of patients starting nonpreferred agents declined from 53% prepolicy to 20% postpolicy. The prior authorization policy was associated with a small sustained decrease in therapy initiation overall (9 per 10 000 population; P = .007). We also observed a short-term increase in switching among established users of nonpreferred agents overall (risk ratio, 2.88; 95% confidence interval, 1.87-4.42) and among those with depression (2.04; 1.22-3.42). However, we found no evidence of increased disruptions in treatment or adverse events (ie, hospitalization, emergency department use) among newly treated patients.
Conclusions Prior authorization was associated with increased use of preferred agents with no evidence of disruptions in therapy or adverse health events among new users. However, unintended effects on treatment initiation and switching among patients already taking the drug were also observed, lending support to the state's previous decision to discontinue prior approval for antidepressants in 2003.
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