PMID- 30165844 OWN - NLM STAT- MEDLINE DCOM- 20181115 LR - 20190318 IS - 1472-6963 (Electronic) IS - 1472-6963 (Linking) VI - 18 IP - 1 DP - 2018 Aug 30 TI - Valuing injection frequency and other attributes of type 2 diabetes treatments in Australia: a discrete choice experiment. PG - 675 LID - 10.1186/s12913-018-3484-0 [doi] LID - 675 AB - BACKGROUND: Multiple pharmacotherapy options are available to control blood glucose in Type 2 Diabetes Mellitus (T2DM). Patients and prescribers may have different preferences for T2DM treatment attributes, such as mode and frequency of administration, based on their experiences and beliefs which may impact adherence. As adherence is a pivotal issue in diabetes therapy, it is important to understand what patients value and how they trade-off the risks and benefits of new treatments. This study aims to investigate the key drivers of choice for T2DM treatments, with a focus on injection frequency, and explore patients' associated willingness-to-pay. METHODS: A discrete choice experiment (DCE) was used to present patients with a series of trade-offs between different treatment options, injectable and oral medicines that were made up of 10 differing levels of attributes (frequency and mode of administration, weight change, needle type, storage, nausea, injection site reactions, hypoglycaemic events, instructions with food and cost). A sample of 171 Australian consenting adult T2DM patients, of which 58 were receiving twice-daily injections of exenatide and 113 were on oral glucose-lowering treatments, completed the national online survey. An error components model was used to estimate the relative priority and key drivers of choice patients place on different attributes and to estimate their willingness to pay for new treatments. RESULTS: Injection frequency, weight change, and nausea were shown to be important attributes for patients receiving injections. Within this cohort, a once-weekly injection generated an additional benefit over a twice-daily injection, equivalent to a weighted total willingness to pay of AUD$22.35 per month. CONCLUSIONS: Based on the patient preferences, the importance of frequency of administration and other non-health benefits can be valued. Understanding patient preferences has an important role in health technology assessment, as the identification of the value as well as the importance weighting for each treatment attribute may assist with funding decisions beyond clinical trial outcomes. FAU - Fifer, Simon AU - Fifer S AD - Community and Patient Preference Research (CaPPRe), Level 5, 478 George St, Sydney, NSW, 2000, Australia. simon.fifer@cappre.com.au. AD - Community and Patient Preference Research Pty Ltd, PO Box 1156, Darlinghurst, NSW, 1300, Australia. simon.fifer@cappre.com.au. FAU - Rose, John AU - Rose J AD - Business Intelligence & Data Analytics (BIDA) Research Centre, University of Technology of Sydney, Ultimo, NSW, 2007, Australia. FAU - Hamrosi, Kim K AU - Hamrosi KK AD - Community and Patient Preference Research (CaPPRe), Level 5, 478 George St, Sydney, NSW, 2000, Australia. FAU - Swain, Dan AU - Swain D AD - Swain Health Economics, 15 Tidal Cr, Moonee Beach, Coffs Harbour, NSW, 2450, Australia. LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20180830 PL - England TA - BMC Health Serv Res JT - BMC health services research JID - 101088677 RN - 0 (Blood Glucose) RN - 0 (Hypoglycemic Agents) RN - 0 (Peptides) RN - 0 (Venoms) RN - 9P1872D4OL (Exenatide) SB - IM MH - Administration, Oral MH - Adolescent MH - Adult MH - Aged MH - Australia MH - Blood Glucose/metabolism MH - Choice Behavior MH - Clinical Decision-Making MH - Diabetes Mellitus, Type 2/*drug therapy/economics MH - Drug Administration Schedule MH - Exenatide MH - Female MH - Financing, Personal MH - Humans MH - Hypoglycemic Agents/*administration & dosage/economics/therapeutic use MH - Injections MH - Male MH - Middle Aged MH - Patient Preference/statistics & numerical data MH - Peptides/*administration & dosage/economics MH - Pilot Projects MH - Venoms/*administration & dosage/economics MH - Young Adult PMC - PMC6117901 OTO - NOTNLM OT - Consumer surplus OT - Diabetes OT - Discrete choice experiment OT - Health technology assessment OT - Patient preference OT - Reimbursement OT - Willingness to pay COIS- ETHICS APPROVAL AND CONSENT TO PARTICIPATE: Ethics: The study was conducted under the Australian Market and Social Research Society (AMSRS) Code of Professional Behaviour which covered the ethical requirements and standard conditions of conducting and reporting market and social research. Patient involvement and consent: The development of the research question and design of the study is based on the creating real life treatment decisions patients pay face when selecting between treatments. The content and associated attributes used in the DCE study was informed by initial qualitative research with patients and a review of patient literature, however no direct patient input was used in finalising the included attributes. This information provided context to the study to firstly better understand patient' priorities, experiences and preferences for treatment with type 2 diabetes and secondly ensure that the relevant attributes of treatment were included in the DCE. A pilot was conducted with patients and feedback received. Revisions were consequently made to the study design and content. All patients were asked to provide consent to participate by selecting an option in the online survey. To be able to ensure the results of the study are available to anyone, particularly patients, who are interested in knowing more about preferences for treatment of type 2 diabetes we are electing to submit to a journal with open access. CONSENT FOR PUBLICATION: Not applicable. COMPETING INTERESTS: DS was an employee of AstraZeneca at the time of the study. PUBLISHER'S NOTE: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. EDAT- 2018/09/01 06:00 MHDA- 2018/11/16 06:00 PMCR- 2018/08/30 CRDT- 2018/09/01 06:00 PHST- 2018/04/16 00:00 [received] PHST- 2018/08/20 00:00 [accepted] PHST- 2018/09/01 06:00 [entrez] PHST- 2018/09/01 06:00 [pubmed] PHST- 2018/11/16 06:00 [medline] PHST- 2018/08/30 00:00 [pmc-release] AID - 10.1186/s12913-018-3484-0 [pii] AID - 3484 [pii] AID - 10.1186/s12913-018-3484-0 [doi] PST - epublish SO - BMC Health Serv Res. 2018 Aug 30;18(1):675. doi: 10.1186/s12913-018-3484-0.