PMID- 23464623 OWN - NLM STAT- MEDLINE DCOM- 20140311 LR - 20161125 IS - 1463-1326 (Electronic) IS - 1462-8902 (Linking) VI - 15 IP - 9 DP - 2013 Sep TI - Preferences for medication attributes among patients with type 2 diabetes mellitus in the UK. PG - 802-9 LID - 10.1111/dom.12091 [doi] AB - AIM: To examine preferences for oral medication attributes among participants with early and advanced type 2 diabetes mellitus (T2DM) in the UK using a discrete choice experiment (DCE). METHODS: A web-based DCE was administered where participants indicated which medication they preferred from two different hypothetical oral anti-diabetic (OAD) medication profiles, each composed of differing levels of seven attributes (efficacy, hypoglycaemic events, weight change, gastrointestinal/nausea side effects, urinary tract infection and genital infection, blood pressure and cardiovascular risk) for 20 sets of pair-wise comparisons. A random effects multinomial logit regression model was used to estimate the preference weight (PW) for each of the attribute levels, and the relative importance (RI) of each attribute was calculated. Analyses were conducted for the overall sample and for medication and gender subgroups. RESULTS: The final sample included 100 participants with a mean age of 62.9 (SD 11.1) years and comparable numbers of participants of each gender (51% male, 49% female). The majority of the participants were White-British (92%). The total PW and corresponding RI were highest for four of the seven attributes: hypoglycaemic events (PW = 1.98; RI = 24.7%), weight change (PW = 1.65; RI = 20.6%), gastrointestinal/nausea side effects (PW = 1.49; RI = 18.6%) and efficacy (PW = 1.44; RI = 18.0%). The RI values differed for some attributes across gender and number of current T2DM medication subgroups. CONCLUSION: The results suggest that hypoglycaemia, weight change, gastrointestinal side effects and efficacy are of primary importance to patients in their OAD preferences in T2DM. These four attributes comprised over 80% of the RI. CI - (c) 2013 Blackwell Publishing Ltd. FAU - Gelhorn, H L AU - Gelhorn HL AD - United BioSource Corporation, Bethesda, MD, USA. heather.gelhorn@unitedbiosource.com FAU - Stringer, S M AU - Stringer SM FAU - Brooks, A AU - Brooks A FAU - Thompson, C AU - Thompson C FAU - Monz, B U AU - Monz BU FAU - Boye, K S AU - Boye KS FAU - Hach, T AU - Hach T FAU - Lund, S S AU - Lund SS FAU - Palencia, R AU - Palencia R LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130407 PL - England TA - Diabetes Obes Metab JT - Diabetes, obesity & metabolism JID - 100883645 RN - 0 (Hypoglycemic Agents) SB - IM MH - Administration, Oral MH - Adult MH - Cardiovascular Diseases/*chemically induced/psychology MH - *Choice Behavior MH - Decision Making MH - Diabetes Mellitus, Type 2/*drug therapy/psychology MH - Female MH - Gastrointestinal Diseases/*chemically induced/psychology MH - Humans MH - Hypoglycemia/*chemically induced/psychology MH - Hypoglycemic Agents/adverse effects/*therapeutic use MH - Internet MH - Logistic Models MH - Male MH - Medication Adherence MH - Middle Aged MH - *Patient Preference MH - Pilot Projects MH - Risk Factors MH - Surveys and Questionnaires MH - United Kingdom/epidemiology MH - Weight Gain/drug effects MH - Weight Loss/drug effects OTO - NOTNLM OT - discrete choice experiment OT - patient preference OT - type 2 diabetes EDAT- 2013/03/08 06:00 MHDA- 2014/03/13 06:00 CRDT- 2013/03/08 06:00 PHST- 2012/12/17 00:00 [received] PHST- 2013/01/20 00:00 [revised] PHST- 2013/03/03 00:00 [accepted] PHST- 2013/03/08 06:00 [entrez] PHST- 2013/03/08 06:00 [pubmed] PHST- 2014/03/13 06:00 [medline] AID - 10.1111/dom.12091 [doi] PST - ppublish SO - Diabetes Obes Metab. 2013 Sep;15(9):802-9. doi: 10.1111/dom.12091. Epub 2013 Apr 7.