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Methodological considerations in estimating adherence and persistence for a long-acting injectable medication.

Elizabeth J Campagna1, Erik Muser, Joseph Parks

  • 1University of Colorado Anschutz Medical Campus, 13199 E. Montview Blvd., Ste. 300, MS F443, Aurora, CO 80045. Elizabeth.Campagna@ucdenver.edu.

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Standard adherence measures may misrepresent long-acting injectable antipsychotic (LA-SGA) use. New methods accounting for dosing schedules and formulation differences are crucial for accurate comparisons with oral antipsychotics (O-SGA).

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Area of Science:

  • Pharmacoeconomics and Health Services Research
  • Psychiatric Pharmacy Practice
  • Medication Adherence Research

Background:

  • Medication adherence and persistence are key quality indicators, with non-adherence linked to poor outcomes and increased healthcare costs.
  • Long-acting injectable (LAI) antipsychotics are proposed to improve adherence, but standard adherence measures, developed for oral medications, may not accurately reflect LAI use.
  • Assessing adherence for LAI formulations, particularly second-generation antipsychotics (SGAs), requires specialized methods due to their unique administration and dosing schedules.

Purpose of the Study:

  • To compare the consistency of standard medication adherence/persistence measures against proposed variations tailored for long-acting injectable second-generation antipsychotics (LA-SGAs).
  • To evaluate how data quality and injectable administration methods influence adherence/persistence assessments for LA-SGAs.
  • To use orally administered SGAs (O-SGAs) as a reference for comparing adherence/persistence measurement methods.

Main Methods:

  • Compared standard adherence/persistence measures (MPR, PDC) with two proposed variations for LA-SGAs using administrative claims data.
  • Proposed variations adjusted 'days supply' based on the LA-SGA's labeled dosing schedule and the minimum time between injections.
  • Analyzed data from 195 patients initiating LA-SGAs and 369 patients initiating O-SGAs, using statistical tests (Chi-squared, Kruskal-Wallis) and Kaplan-Meier curves.

Main Results:

  • Standard measures showed no significant difference in MPR between LA-SGAs (0.91) and O-SGAs (0.90).
  • Adjusting for the labeled dosing schedule increased LA-SGA MPR to 0.97, significantly differing from O-SGA MPR.
  • Further adjustments for LA-SGA formulation (0.86 MPR) and PDC values (0.55-0.61 vs. 0.37) revealed significant differences between LA-SGA and O-SGA cohorts.

Conclusions:

  • Standard adherence/persistence measures can yield conflicting conclusions when comparing LA-SGAs and O-SGAs due to differing assumptions about 'days supply'.
  • Adherence measures must account for pharmacological differences, including formulation and duration of therapeutic drug levels, especially with increasing LAI approvals.
  • Payers and researchers should conduct sensitivity analyses with various adherence definitions to ensure reliable comparisons between medication formulations.