Self-reported Barriers to Adherence and Persistence to Treatment With Injectable Medications for Type 2 Diabetes

Clin Ther. 2016 Jul;38(7):1653-1664.e1. doi: 10.1016/j.clinthera.2016.05.009. Epub 2016 Jun 28.

Abstract

Purpose: This study explored the barriers that adult Americans experience when taking injectable medications for type 2 diabetes, from the time of filling the initial prescription through the decision to discontinue the medication.

Methods: An Internet-based survey was conducted in 2 waves among adult patients (N = 2000) who had received a physician prescription for insulin, liraglutide, or exenatide once weekly (QW), regardless of whether the prescription was filled by a pharmacy. In wave 1, patients were surveyed on their medication history and experience and, if relevant, the medication discontinuation process. Those still taking their injectable medication at the time of wave 1 were contacted 6 months later (wave 2, n = 585) to assess any changes in their medication experience.

Findings: Among patients who delayed filling their prescription by ≥1 week, cost was a common reason for delay for refilling of liraglutide (63%) and exenatide QW (49%). The most commonly reported barrier to maintaining injectable medication was injection concerns (42%) such as aversion to needles, pain, or needle size. Lack of perceived need was the most common reason for discontinuation for basal (47%) and prandial/premixed (44%) insulin. For liraglutide, the most common reason for discontinuation was experiencing an adverse event (33%); for exenatide QW, it was injection concerns (38%).

Implications: The diverse barriers we identified underscore the need for better patient-prescriber communication to ensure that newly prescribed injectable medications are consistent with a patient's ability or willingness to manage them, to appropriately set expectations about medications, and to address new barriers that arise during the course of treatment.

Keywords: adherence; discontinuation; injectable medication; persistence; type 2 diabetes.

MeSH terms

  • Cross-Sectional Studies
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Exenatide
  • Female
  • Humans
  • Hypoglycemic Agents / therapeutic use*
  • Insulin / therapeutic use*
  • Liraglutide / therapeutic use*
  • Male
  • Medication Adherence
  • Middle Aged
  • Peptides / therapeutic use*
  • Retrospective Studies
  • Self Report
  • Surveys and Questionnaires
  • Venoms / therapeutic use*

Substances

  • Hypoglycemic Agents
  • Insulin
  • Peptides
  • Venoms
  • Liraglutide
  • Exenatide