Your browser doesn't support javascript.
loading
Assessing the performance of group-based trajectory modeling method to discover different patterns of medication adherence.
Diop, Awa; Gupta, Alind; Mueller, Sabrina; Dron, Louis; Harari, Ofir; Berringer, Heather; Kalatharan, Vinusha; Park, Jay J H; Mésidor, Miceline; Talbot, Denis.
Affiliation
  • Diop A; Core Clinical Sciences Inc., Vancouver, British Columbia, Canada.
  • Gupta A; Département de médecine sociale et préventive, Université Laval, Québec, Canada.
  • Mueller S; Department of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Dron L; GIPAM GmbH, Wismar, Germany.
  • Harari O; Cascade Outcomes Research Inc., Vancouver, British Columbia, Canada.
  • Berringer H; Core Clinical Sciences Inc., Vancouver, British Columbia, Canada.
  • Kalatharan V; Core Clinical Sciences Inc., Vancouver, British Columbia, Canada.
  • Park JJH; Department of Mathematics and Statistics, University of Victoria, Victoria, British Columbia, Canada.
  • Mésidor M; Core Clinical Sciences Inc., Vancouver, British Columbia, Canada.
  • Talbot D; Core Clinical Sciences Inc., Vancouver, British Columbia, Canada.
Pharm Stat ; 23(4): 511-529, 2024.
Article in En | MEDLINE | ID: mdl-38327261
ABSTRACT
It is well known that medication adherence is critical to patient outcomes and can decrease patient mortality. The Pharmacy Quality Alliance (PQA) has recognized and identified medication adherence as an important indicator of medication-use quality. Hence, there is a need to use the right methods to assess medication adherence. The PQA has endorsed the proportion of days covered (PDC) as the primary method of measuring adherence. Although easy to calculate, the PDC has however several drawbacks as a method of measuring adherence. PDC is a deterministic approach that cannot capture the complexity of a dynamic phenomenon. Group-based trajectory modeling (GBTM) is increasingly proposed as an alternative to capture heterogeneity in medication adherence. The main goal of this paper is to demonstrate, through a simulation study, the ability of GBTM to capture treatment adherence when compared to its deterministic PDC analogue and to the nonparametric longitudinal K-means. A time-varying treatment was generated as a quadratic function of time, baseline, and time-varying covariates. Three trajectory models are considered combining a cat's cradle effect, and a rainbow effect. The performance of GBTM was compared to the PDC and longitudinal K-means using the absolute bias, the variance, the c-statistics, the relative bias, and the relative variance. For all explored scenarios, we find that GBTM performed better in capturing different patterns of medication adherence with lower relative bias and variance even under model misspecification than PDC and longitudinal K-means.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Models, Statistical / Medication Adherence Limits: Humans Language: En Journal: Pharm Stat Journal subject: FARMACOLOGIA Year: 2024 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Models, Statistical / Medication Adherence Limits: Humans Language: En Journal: Pharm Stat Journal subject: FARMACOLOGIA Year: 2024 Type: Article Affiliation country: Canada