PMID- 28660256 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 2509-4262 (Print) IS - 2509-4254 (Electronic) IS - 2509-4262 (Linking) VI - 1 IP - 2 DP - 2017 TI - A Comparison of Inpatient Cost Per Day in General Surgery Patients with Type 2 Diabetes Treated with Basal-Bolus versus Sliding Scale Insulin Regimens. PG - 109-115 LID - 10.1007/s41669-017-0020-9 [doi] AB - BACKGROUND: The identification of cost-effective glycaemic management strategies is critical to hospitals. Treatment with a basal-bolus insulin (BBI) regimen has been shown to result in better glycaemic control and fewer complications than sliding scale regular insulin (SSI) in general surgery patients with type 2 diabetes mellitus (T2DM), but the effect on costs is unknown. OBJECTIVE: We conducted a post hoc analysis of the RABBIT Surgery trial to examine whether total inpatient costs per day for general surgery patients with T2DM treated with BBI (n = 103) differed from those for patients with T2DM treated with SSI (n = 99) regimens. METHODS: Data were collected from patient clinical and hospital billing records. Charges were adjusted to reflect hospital costs. General linearized models were used to estimate the risk-adjusted effects of BBI versus SSI treatment on average total inpatient costs per day. RESULTS: Risk-adjusted average total inpatient costs per day were $US5404. Treatment with BBI compared with SSI reduced average total inpatient costs per day by $US751 (14%; 95% confidence interval [CI] 20-4). Being treated in a university medical centre, being African American or having a bowel procedure or higher-volume pharmacy use significantly reduced costs per day. CONCLUSIONS: In general surgery patients with T2DM, a BBI regimen significantly reduced average total hospital costs per day compared with an SSI regimen. BBI has been shown to improve outcomes in a randomized controlled trial. Those results, combined with our findings regarding savings, suggest that hospitals should consider adopting BBI regimens in patients with T2DM undergoing surgery. FAU - Phillips, Victoria L AU - Phillips VL AD - Department of Health Policy and Management, Rollins School of Public Health of Emory University, 1518 Clifton Road, Atlanta, GA 30322 USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 FAU - Byrd, Anwar L AU - Byrd AL AD - Department of Medicine, Division of Endocrinology, Emory University School of Medicine, Atlanta, GA USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 FAU - Adeel, Saira AU - Adeel S AD - Department of Medicine, Division of Endocrinology, Emory University School of Medicine, Atlanta, GA USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 FAU - Peng, Limin AU - Peng L AD - Department of Biostatistics, Rollins School of Public Health, Atlanta, GA USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 FAU - Smiley, Dawn D AU - Smiley DD AD - Department of Medicine, Division of Endocrinology, Emory University School of Medicine, Atlanta, GA USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 FAU - Umpierrez, Guillermo E AU - Umpierrez GE AD - Department of Medicine, Division of Endocrinology, Emory University School of Medicine, Atlanta, GA USA. ISNI: 0000 0001 0941 6502. GRID: grid.189967.8 LA - eng GR - M01 RR000039/RR/NCRR NIH HHS/United States GR - UL1 RR025008/RR/NCRR NIH HHS/United States GR - UL1 TR000454/TR/NCATS NIH HHS/United States PT - Journal Article DEP - 20170421 PL - Switzerland TA - Pharmacoecon Open JT - PharmacoEconomics - open JID - 101700780 PMC - PMC5468101 COIS- This study is adjunct to the RABBIT 2 Surgery trial (ClinicalTrials.gov identification: NCT00596687) [10]. Pilot data from this study were presented in abstract form at the 73rd Scientific Sessions of the American Diabetes Association, Chicago, IL. The Emory University Institutional Review Board (IRB) approved this study and informed consent was obtained for all patients in accordance with IRB guidelines. CONFLICT OF INTEREST: Victoria L Phillips, Anwar L Byrd, Saira Adeel, Limin Peng, Dawn D Smiley and Guillermo E Umpierrez, have no conflicts of interest, financial or otherwise, in relation to the manuscript. FUNDING: This investigator-initiated study was supported by an unrestricted grant from Sanofi (Bridgewater, NJ, USA). The sponsor had no input into the results presented here. DATA AVAILABILITY STATEMENT: The dataset contains complete medical records for the sample. Upon request, the authors will provide a de-identified dataset. Given the nature of the data, the Institutional Review Board require the authors to catalogue researchers accessing the data. EDAT- 2017/07/01 06:00 MHDA- 2017/07/01 06:01 PMCR- 2017/04/21 CRDT- 2017/06/30 06:00 PHST- 2017/06/30 06:00 [entrez] PHST- 2017/07/01 06:00 [pubmed] PHST- 2017/07/01 06:01 [medline] PHST- 2017/04/21 00:00 [pmc-release] AID - 20 [pii] AID - 10.1007/s41669-017-0020-9 [doi] PST - ppublish SO - Pharmacoecon Open. 2017;1(2):109-115. doi: 10.1007/s41669-017-0020-9. Epub 2017 Apr 21.