Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-17T11:24:23.988Z Has data issue: false hasContentIssue false

P0173 - Sensitivity of comparisons of TTAD across antipsychotics to patient selection criteria and model specification in a retrospective paid claims analysis

Published online by Cambridge University Press:  16 April 2020

J.S. McCombs
Affiliation:
Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, University of Southern California, School of Pharmacy, Los Angeles, CA, USA
D. Stafkey-Mailey
Affiliation:
Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, University of Southern California, School of Pharmacy, Los Angeles, CA, USA
T. Marshall
Affiliation:
Department of Clinical Pharmacy and Pharmaceutical Economics and Policy, University of Southern California, School of Pharmacy, Los Angeles, CA, USA Astellas Pharma US, Los Angeles, CA, USA

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background and Aims:

Investigate how selection criteria and statistical model specifications affect time to all cause discontinuation (TTAD) comparisons across alternative antipsychotics using retrospective database analyses.

Methods:

231,635 episodes of antipsychotic therapy were identified using data from the California Medicaid (Medi-Cal) program. A series of regression models were estimated for TTAD that altered selection criteria and the list of independent variables used in the models.

Results:

Unadjusted TTAD (in days) for typical antipsychotics, olanzapine, risperidone and quetiapine were 92, 175, 182 and 177, respectively. TTAD achieved by patients using conventional antipsychotics was consistently shorter than TTAD achieved with atypical antipsychotics, but estimates varied from -96 days to -44 days depending on selection criteria and model specification (p<0.0001 relative to olanzapine). TTAD using risperidone or quetiapine appeared to be superior to olanzapine in simple models (+11 to +13 days, p<0.000), while virtually no differences across atypical antipsychotics were found when the analysis was restricted to patients with schizophrenia and more complete model specifications were employed. Specifically, screening for schizophrenia reversed risperidone's advantage over olanzapine from +6 days (p<0.0001) to -1.4 days (p>0.05). TTAD results favoring quetiapine over olanzapine were reversed from +7 days (p<0.0001) to – 0.4 days (p>0.05) when covariates for episode type were included in the model.

Conclusions:

Differences in duration of antipsychotic therapy exist across diagnostic groups and episode type. Differences also exist in the diagnostic and episode mix across drugs. Therefore, disaggregated patient samples and expanded model specifications provide more accurate estimates of differences in TTAD.

Type
Poster Session I: Schizophrenia and Psychosis
Copyright
Copyright © European Psychiatric Association 2008
Submit a response

Comments

No Comments have been published for this article.