Patient preferences for treatment in type 2 diabetes: the Italian discrete-choice experiment analysis

Acta Diabetol. 2019 Mar;56(3):289-299. doi: 10.1007/s00592-018-1236-6. Epub 2018 Oct 10.

Abstract

Aims: Several drug classes are now available to achieve a satisfactory metabolic control in patients with type 2 diabetes (T2DM), but patients' preferences may differ.

Methods: In a discrete-choice experiment, we tested T2DM patients' preferences for recent antidiabetic drugs, in the event that their treatment might require intensification. The following attributes were considered: (a) route of administration; (b) type of delivery; (c) timing; (d) risk of adverse events; (e) effects on body weight. Twenty-two possible scenarios were built, transferred into 192 paired choices and proposed to 491 cases naïve to injectable treatments and 171 treated by GLP-1 receptor agonists (GLP-1RAs). Analyses were performed by descriptive statistics and random effects logit regression model.

Results: Preferences according to dosing frequency, risk of nausea and urinary tract infections (UTls) were similar across groups, age, sex and BMI. Administration route and delivery type accounted for 1/3 of relative importance; the risk of UTIs, nausea and dosing frequency for ≈ 20% each, and weight loss for only 6%. Two significant interactions emerged (p < 0.01): type of delivery × group, and weight change × BMI class. Irrespective of previous treatment, the three preferred choices were injectable, coupled with weekly dosing and a ready-to-use device (first two choices). In a regression model, being naïve or non-naïve changed the ranking of preferences (p < 0.001), and the order was systematically shifted towards injectable medications in non-naïve subjects.

Conclusion: Easy-to-deliver, injectable treatment is preferred in T2DM, independently of treatment history, and previous experience with GLP-1RAs strengthens patients' willingness to accept injectable drugs.

Keywords: Adverse events; Dose frequency; Glucagon-like peptide-1 receptor agonists; Injectable drugs; Nausea; Oral treatment; Route of delivery; Sodium–glucose co-transporter 2 inhibitors; Urogenital-tract infections; Weight loss.

MeSH terms

  • Aged
  • Body Weight / drug effects
  • Choice Behavior
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / epidemiology*
  • Dosage Forms*
  • Dose-Response Relationship, Drug
  • Drug Administration Routes
  • Drug Administration Schedule
  • Female
  • Glucagon-Like Peptide-1 Receptor / agonists
  • Humans
  • Hypoglycemic Agents / administration & dosage*
  • Hypoglycemic Agents / adverse effects
  • Hypoglycemic Agents / classification
  • Italy / epidemiology
  • Male
  • Middle Aged
  • Patient Preference / statistics & numerical data*
  • Surveys and Questionnaires
  • Weight Loss / drug effects

Substances

  • Dosage Forms
  • Glucagon-Like Peptide-1 Receptor
  • Hypoglycemic Agents