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Safety and efficacy of saxagliptin for glycemic control in non-critically ill hospitalized patients
  1. Rajesh Garg,
  2. Brooke Schuman,
  3. Shelley Hurwitz,
  4. Cheyenne Metzger,
  5. Shreya Bhandari
  1. Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA
  1. Correspondence to Dr Rajesh Garg; rgarg{at}partners.org

Abstract

Objective To evaluate whether saxagliptin is non-inferior to basal-bolus insulin therapy for glycemic control in patients with controlled type 2 diabetes mellitus (T2DM) admitted to hospital with non-critical illnesses.

Research design and methods This was an open-label, randomized controlled clinical trial. Patients received either saxagliptin or basal-bolus insulin, both with correctional insulin doses. The main study outcome was the mean daily blood glucose (BG) after the first day of randomization.

Results Of 66 patients completing the study, 33 (age 69±10 years, 40% men) were randomized to saxagliptin and 33 (age 67±10 years, 52% men) to basal-bolus insulin therapy. The mean daily BG was 149.8±22.0 mg/dL in the saxagliptin group and 146.9±30.5 mg/dL in the insulin group (p=0.59). With an observed group difference of 2.9 mg/dL and an a priori margin of 20 mg/dL, inferiority of saxagliptin was rejected in favor of non-inferiority (p=0.007). There was no significant difference in the percentage of high or low BG values. The insulin group received a higher number of insulin injections (2.3±1.7/day vs 1.2±1.9/day; p<0.001) as well as a higher daily insulin dose (13.3±12.9 units/day vs 2.4±3.3 units/day; p<0.001) than did the saxagliptin group. Continuous BG monitoring showed that glycemic variability was lower in the saxagliptin group as compared to the insulin group. Patient satisfaction scores were similar in the two groups.

Conclusions We conclude that saxagliptin use is non-inferior to basal-bolus insulin in non-critically ill hospitalized patients with T2DM controlled on 0–2 oral agents without insulin. Saxagliptin use may decrease glycemic variability in these patients.

Trial registration number NCT02182895.

  • Inpatient Diabetes Management

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Footnotes

  • Contributors RG designed the study, obtained funding, led the program, supervised the data collection, analyzed the data, and wrote the manuscript; BS, CM, and SB helped in conducting the study, collected the data, and reviewed the manuscript; SH conducted all statistical analysis and collaborated on writing the manuscript.

  • Funding This work was supported by AstraZeneca Company through an investigator-initiated research grant.

  • Competing interests RG received research support from AstraZeneca for this study. Other authors have no conflict of interest.

  • Patient consent Obtained.

  • Ethics approval Partners Institutional Review Board.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.