PMID- 26549576 OWN - NLM STAT- MEDLINE DCOM- 20160829 LR - 20220408 IS - 1473-4877 (Electronic) IS - 0300-7995 (Linking) VI - 32 IP - 2 DP - 2016 TI - A discrete-choice experiment to quantify patient preferences for frequency of glucagon-like peptide-1 receptor agonist injections in the treatment of type 2 diabetes. PG - 251-62 LID - 10.1185/03007995.2015.1117433 [doi] AB - OBJECTIVE: Understanding patients' preferences for attributes of injectable antihyperglycemic regimens may improve patient satisfaction and medication adherence. Our objective was to quantify the preferences of patients with type 2 diabetes mellitus (T2DM) for reducing the frequency of glucagon-like peptide-1 receptor agonist injections from once daily to once weekly. METHODS: A total of 643 respondents with a self-reported physician diagnosis of type 2 diabetes completed a web-based discrete-choice experiment survey. The sample included four prespecified subgroups: currently using exenatide once weekly (n = 150), liraglutide once daily (n = 153), insulin (but not exenatide once weekly or liraglutide) (n = 156), and no injectable treatment (n = 184). Device attributes included type of injection device, needle size and pain, injection frequency, refrigeration, and injection-site reactions. Random-parameters logit was used to estimate the relative impact of device attributes on treatment choice for each subgroup. RESULTS: In all subgroups, changing injection frequency from daily to weekly (independent of the effect of injection frequency on preferences for other attributes) was the most important predictor of treatment choice. Switching from a longer and thicker needle to a shorter and thinner needle and eliminating injection-site reactions were also statistically significant predictors of device choice (P < 0.05). Exenatide once weekly users and those not currently using injections were more likely to choose a treatment with characteristics similar to exenatide once weekly. CONCLUSIONS: The treatment attribute most important to patients choosing among hypothetical injectable treatments for T2DM was injection frequency: patients preferred weekly over daily injections. LIMITATIONS: The primary limitations of this study are that it included only a limited number of attributes that may not reflect the full complexity of patient choices, diagnosis was self-reported, and patients were recruited from an Internet panel and may not be representative of the T2DM patient population. FAU - Hauber, A Brett AU - Hauber AB AD - a a RTI Health Solutions, Research Triangle Park , NC , USA. FAU - Nguyen, Hiep AU - Nguyen H AD - b b AstraZeneca, Fort Washington , PA , USA. FAU - Posner, Joshua AU - Posner J AD - a a RTI Health Solutions, Research Triangle Park , NC , USA. FAU - Kalsekar, Iftekhar AU - Kalsekar I AD - c c Johnson and Johnson , New Brunswick , NJ , USA (was with AstraZeneca at the time this study was developed). FAU - Ruggles, James AU - Ruggles J AD - b b AstraZeneca, Fort Washington , PA , USA. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20151130 PL - England TA - Curr Med Res Opin JT - Current medical research and opinion JID - 0351014 RN - 0 (Glucagon-Like Peptide-1 Receptor) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 0 (Peptides) RN - 0 (Venoms) RN - 839I73S42A (Liraglutide) RN - 9P1872D4OL (Exenatide) SB - IM MH - Adult MH - Aged MH - Choice Behavior MH - Diabetes Mellitus, Type 2/*drug therapy MH - Drug Administration Schedule MH - Exenatide MH - Female MH - Glucagon-Like Peptide-1 Receptor/*agonists MH - Humans MH - Hypoglycemic Agents/*administration & dosage MH - Injections MH - Insulin/therapeutic use MH - Liraglutide/administration & dosage MH - Male MH - Middle Aged MH - Patient Preference MH - Peptides/*administration & dosage MH - Venoms/*administration & dosage OTO - NOTNLM OT - Conjoint analysis OT - Discrete-choice experiment OT - GLP-1 receptor agonist OT - Injection OT - Preference OT - Type 2 diabetes mellitus EDAT- 2015/11/10 06:00 MHDA- 2016/08/30 06:00 CRDT- 2015/11/10 06:00 PHST- 2015/11/10 06:00 [entrez] PHST- 2015/11/10 06:00 [pubmed] PHST- 2016/08/30 06:00 [medline] AID - 10.1185/03007995.2015.1117433 [doi] PST - ppublish SO - Curr Med Res Opin. 2016;32(2):251-62. doi: 10.1185/03007995.2015.1117433. Epub 2015 Nov 30.