Study of Adherence to Treatment with Sitagliptin in Real-World: A Population-Based Study from the French National Healthcare System Claims Databases (SNDS)

Author(s)

Portugues C1, Soubeiga A1, Berthod C2, Charpentier G3, Franc S4, Chomette E5, Mistretta F1, Lajoinie A1
1RCTs, Lyon, 69, France, 2Service de consultations non programmées de pédiatrie du Val d’Ouest (Lyon) ; Équipe Évaluation et Modélisation des Effets Thérapeutiques, UMR CNRS 5558 – LBBE "Biométrie et Biologie Évolutive", Université Claude Bernard-Lyon 1, Lyon, FRANCE, Lyon, France, 3Centre d’Études et de Recherches pour l’Intensification du Traitement du Diabète (CERITD), FRANCE ; Association française des diabétiques (AFD), France, Evry, France, 4Service d'endocrino-diabétologie, Centre Hospitalier Sud Francilien (CHSF), Corbeil-Essonnes, FRANCE ; Centre d’Études et de Recherches pour l’Intensification du Traitement du Diabète (CERITD), FRANCE, Corbeil-Essonnes, France, 5D.I.M (Département d'Information Médicale) Groupe Vivalto Santé, FRANCE, Paris, France

OBJECTIVES: We assessed the real-world adherence of patients treated with sitagliptin between 2014 and 2016 over a 2-year period using electronic drug dispensing records.

METHODS: This study was carried out on a 1/97th sample of the French National Healthcare System Claims Databases (i.e. the EGB database). Beneficiaries with at least 3 dispensations of sitagliptin from 01/01/2014 to 31/12/2016 were followed for 2 years, or until death or treatment withdrawal. Adherence was assessed through the Medication Possession Ratio (MPR) - with a maximum set at 100% - and the Proportion of Days Covered (PDC). The following parameters have been defined: period covered by a dispensation; grace period (i.e. uncovered period without considering discontinuation): 7 days; minimum timeframe to consider a withdrawal: 180 days.

RESULTS: A total of 4,406 patients were included in the study population, aged 68.1 ± 42.1 years. The median exposure time available for the study population was 728 days [Q1-Q3: 394-730; mean: 572 ± 230]. During that period, 86% of patients (n = 3,803) had at least one discontinuation, with an average number of 5 ± 4 discontinuations per patient and an average duration of 22 ± 17 days. Median adherence was estimated (i) at 94% according to the MPR [Q1-Q3: 82-100], i.e. 76% of adherent patients (MPR ≥ 80%), and (ii) at 86% [Q1-Q3 : 75-92] according to the PDC, i.e. 68% of adherent patients (PDC ≥ 80%).

CONCLUSIONS: Almost 3/4 of patients are adherent to sitagliptin with MPR, and 2/3 with PDC. According to the literature, the MPR method would lead to an overestimation of adherence due to double counting of days covered by two dispensations; external validation is necessary to verify these hypotheses. In addition, our results raise the question of frequent discontinuations in this pathology where daily glycaemic control plays a major role in preventing complications.

Conference/Value in Health Info

2020-11, ISPOR Europe 2020, Milan, Italy

Value in Health, Volume 23, Issue S2 (December 2020)

Code

PDB84

Topic

Epidemiology & Public Health, Real World Data & Information Systems

Topic Subcategory

Health & Insurance Records Systems, Safety & Pharmacoepidemiology

Disease

Diabetes/Endocrine/Metabolic Disorders

Explore Related HEOR by Topic


Your browser is out-of-date

ISPOR recommends that you update your browser for more security, speed and the best experience on ispor.org. Update my browser now

×