PMID- 36923548 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230316 IS - 1078-4497 (Print) IS - 1945-337X (Electronic) IS - 1078-4497 (Linking) VI - 39 IP - Suppl 5 DP - 2022 Nov TI - Assessment of Glucagon-like Peptide-1 Receptor Agonists in Veterans Taking Basal/Bolus Insulin Regimens. PG - S18-S23 LID - 10.12788/fp.0317 [doi] AB - BACKGROUND: Clinical use of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) is well established as add-on therapy to oral medications and basal insulin. However, there is little published data regarding the use of GLP-1 RAs for longer than 12 months in patients taking basal/bolus insulin regimens. The primary goal of our study was to assess the long-term efficacy of GLP-1 RAs as add-on therapy to basal/bolus insulin regimens. METHODS: This study was a retrospective record review of all patients on basal/bolus insulin regimens who received additional therapy with a GLP-1 RA. The primary outcome was the change in glycosylated hemoglobin A(1c) (HbA(1c)) at 3, 6, 12, 18, and 24 months after initiation of the GLP-1 RA. Secondary outcomes included change in weight and total daily dose (TDD) of insulin and incidence of hypoglycemia and other adverse effects (AEs). RESULTS: Ninety-two patient records were reviewed. Mean glycemic control changed from baseline -1.1% (95% CI, -1.3 to -0.8; P < .001) at 3 months; -1.0% (95% CI, -1.3 to -0.7; P < .001) at 6 months; -0.9% (95% CI, 1.3 to -0.6; P < .001) at 12 months; -0.9% (95% CI, -1.4 to -0.3; P = .002) at 18 months; and -0.7 (95% CI, -1.4 to 0.1; P = .07) at 24 months. A significant decrease in weight was also observed from baseline through 18 months, and a significant decrease in TDD of insulin was identified from baseline through 12 months. Hypoglycemia was documented in 29.8% of patients at any point during GLP-1 RA therapy, and gastrointestinal AEs were documented in 18.3% of patients. CONCLUSIONS: Adding GLP-1 RAs to complex insulin regimens may help achieve glycemic control while decreasing insulin requirements and mitigating undesirable AEs, such as weight gain. CI - Copyright (c) 2022 Frontline Medical Communications Inc., Parsippany, NJ, USA. FAU - Castek, Shannon L AU - Castek SL AD - Veterans Affairs Puget Sound Health Care System, Seattle, Washington. FAU - Healey, Lindsey C AU - Healey LC AD - Veteran Health Indiana, Indianapolis. FAU - Kania, Deanna S AU - Kania DS AD - Veteran Health Indiana, Indianapolis. AD - Purdue University College of Pharmacy, West Lafayette, Indiana. FAU - Vernon, Veronica P AU - Vernon VP AD - Veteran Health Indiana, Indianapolis. AD - Butler University College of Pharmacy and Health Sciences, Indianapolis. FAU - Dawson, Andrea J AU - Dawson AJ AD - Veteran Health Indiana, Indianapolis. LA - eng PT - Journal Article DEP - 20220926 PL - United States TA - Fed Pract JT - Federal practitioner : for the health care professionals of the VA, DoD, and PHS JID - 9500574 PMC - PMC10010496 COIS- Author disclosures The authors report no actual or potential conflicts of interest or outside sources of funding with regard to this article. EDAT- 2023/03/17 06:00 MHDA- 2023/03/17 06:01 PMCR- 2022/11/01 CRDT- 2023/03/16 02:25 PHST- 2023/03/16 02:25 [entrez] PHST- 2023/03/17 06:00 [pubmed] PHST- 2023/03/17 06:01 [medline] PHST- 2022/11/01 00:00 [pmc-release] AID - fp-39-11s-s18 [pii] AID - 10.12788/fp.0317 [doi] PST - ppublish SO - Fed Pract. 2022 Nov;39(Suppl 5):S18-S23. doi: 10.12788/fp.0317. Epub 2022 Sep 26.