TY - JOUR
T1 - Racial-ethnic differences in incident olanzapine use after an FDA advisory for patients with schizophrenia
AU - Dusetzina, Stacie B.
AU - Cook, Benjamin L.
AU - Busch, Alisa B.
AU - Alexander, G. Caleb
AU - Huskamp, Haiden A.
N1 - Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2013/1/1
Y1 - 2013/1/1
N2 - Objective: Prior investigations suggest that olanzapine use declined rapidly after a U.S. Food and Drug Administration (FDA) communication and consensus statement warning of the drug's increased metabolic risks, but whether declines differed by racial-ethnic groups is unknown. Methods: Changes in olanzapine use over time by raceethnicity was assessed among 7,901 Florida Medicaid enrollees with schizophrenia. Results: Prior to the advisory, 57% of secondgeneration antipsychotic fills among Hispanics were for olanzapine, compared with 40% for whites or blacks (adjusted risk difference [ARD]=.17, 95% confidence interval [CI]=.13-.20). Olanzapine use declined among all racial-ethnic groups. Although Hispanics had greater olanzapine use than whites in each period, the differences in absolute risk were only 3% by the latest study period (ARD=.03, CI=.01-.04). Conclusions: After the FDA communication and consensus statement were issued, differences in olanzapine use between white and Hispanic enrollees narrowed considerably. Identifying high-use subgroups for targeted delivery of drug safety information may help eliminate any existing differences in prescribing.
AB - Objective: Prior investigations suggest that olanzapine use declined rapidly after a U.S. Food and Drug Administration (FDA) communication and consensus statement warning of the drug's increased metabolic risks, but whether declines differed by racial-ethnic groups is unknown. Methods: Changes in olanzapine use over time by raceethnicity was assessed among 7,901 Florida Medicaid enrollees with schizophrenia. Results: Prior to the advisory, 57% of secondgeneration antipsychotic fills among Hispanics were for olanzapine, compared with 40% for whites or blacks (adjusted risk difference [ARD]=.17, 95% confidence interval [CI]=.13-.20). Olanzapine use declined among all racial-ethnic groups. Although Hispanics had greater olanzapine use than whites in each period, the differences in absolute risk were only 3% by the latest study period (ARD=.03, CI=.01-.04). Conclusions: After the FDA communication and consensus statement were issued, differences in olanzapine use between white and Hispanic enrollees narrowed considerably. Identifying high-use subgroups for targeted delivery of drug safety information may help eliminate any existing differences in prescribing.
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U2 - 10.1176/appi.ps.201200002
DO - 10.1176/appi.ps.201200002
M3 - Article
C2 - 23280461
AN - SCOPUS:84878874725
SN - 1075-2730
VL - 64
SP - 83
EP - 87
JO - Hospital and Community Psychiatry
JF - Hospital and Community Psychiatry
IS - 1
ER -