PMID- 31115873 OWN - NLM STAT- MEDLINE DCOM- 20191202 LR - 20221207 IS - 1179-6901 (Electronic) IS - 1174-5886 (Print) IS - 1174-5886 (Linking) VI - 19 IP - 2 DP - 2019 Jun TI - Timing of GLP-1 Receptor Agonist Initiation for Treatment of Type 2 Diabetes in the UK. PG - 213-225 LID - 10.1007/s40268-019-0273-0 [doi] AB - INTRODUCTION: Patients with type 2 diabetes mellitus (T2DM) who fail to meet glycaemic control are at increased risk of diabetes complications. For patients who cannot maintain glycaemic control with oral medication, one recommended option is to add an injectable glucagon-like peptide-1 receptor agonist (GLP-1 RA) to their treatment regimen. The purpose of this study was to examine time to treatment intensification with GLP-1 RAs, including the duration of time that patients did not maintain glycaemic control with oral medication. METHODS: This was a medical record review conducted in the UK via a physician survey. Patients eligible to have their records reviewed were required to be >/= 18 years of age, have a confirmed T2DM diagnosis, and have initiated GLP-1 RA treatment for T2DM in the past 6 months. All glycated haemoglobin (HbA1c) values within 5 years prior to GLP-1 RA initiation were collected. RESULTS: A total of 113 physicians contributed data for 1096 patients (mean age at the time of GLP-1 RA initiation was 54.9 years, 55.4% were male, and 71.4% were White). Median time from T2DM diagnosis to GLP-1 RA initiation was 6.1 years. Median consecutive time patients taking oral regimens were not under glycaemic control (HbA1c > 7.0%) prior to GLP-1 RA initiation was 13.5 months. Patients treated by general practitioners (GPs) had a significantly longer duration of time with insufficient glycaemic control prior to GLP-1 RA initiation compared with patients treated by diabetes specialists (median time for specialists was 11.0 months vs. 17.0 months for GPs; p = 0.038). CONCLUSIONS: Results suggest that treatment intensification is often delayed despite consistently poor glycaemic control for more than 12 months, contrary to treatment guideline recommendations. Findings from this study highlight that some T2DM patients may benefit from more rapid treatment intensification, which could improve glycaemic control and reduce the risk for many short- and long-term health complications. FAU - Boye, Kristina S AU - Boye KS AD - Eli Lilly and Company, Indianapolis, IN, USA. FAU - Stein, Dara AU - Stein D AD - Patient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA. FAU - Matza, Louis S AU - Matza LS AD - Patient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA. louis.matza@evidera.com. FAU - Jordan, Jessica AU - Jordan J AD - Patient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA. FAU - Yu, Ren AU - Yu R AD - Patient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA. FAU - Norrbacka, Kirsi AU - Norrbacka K AD - Eli Lilly and Company, Indianapolis, IN, USA. FAU - Hassan, Syed Wasi AU - Hassan SW AD - Eli Lilly and Company, Indianapolis, IN, USA. FAU - Garcia-Perez, Luis-Emilio AU - Garcia-Perez LE AD - Eli Lilly and Company, Indianapolis, IN, USA. LA - eng GR - EVA-19867/Eli Lilly and Company/ PT - Journal Article PL - New Zealand TA - Drugs R D JT - Drugs in R&D JID - 100883647 RN - 0 (Blood Glucose) RN - 0 (Glucagon-Like Peptide-1 Receptor) RN - 0 (Glycated Hemoglobin A) RN - 0 (Hypoglycemic Agents) SB - IM MH - Adult MH - Aged MH - Blood Glucose/analysis/drug effects MH - Diabetes Mellitus, Type 2/blood/*drug therapy MH - Female MH - Glucagon-Like Peptide-1 Receptor/*antagonists & inhibitors MH - Glycated Hemoglobin/analysis MH - Humans MH - Hypoglycemic Agents/pharmacology/*therapeutic use MH - Male MH - Middle Aged MH - Physicians/statistics & numerical data MH - Practice Patterns, Physicians'/statistics & numerical data MH - Surveys and Questionnaires/statistics & numerical data MH - Time Factors MH - Time-to-Treatment MH - United Kingdom PMC - PMC6544605 EDAT- 2019/05/23 06:00 MHDA- 2019/12/04 06:00 PMCR- 2019/05/21 CRDT- 2019/05/23 06:00 PHST- 2019/05/23 06:00 [pubmed] PHST- 2019/12/04 06:00 [medline] PHST- 2019/05/23 06:00 [entrez] PHST- 2019/05/21 00:00 [pmc-release] AID - 10.1007/s40268-019-0273-0 [pii] AID - 273 [pii] AID - 10.1007/s40268-019-0273-0 [doi] PST - ppublish SO - Drugs R D. 2019 Jun;19(2):213-225. doi: 10.1007/s40268-019-0273-0.