Identifying predictors of sodium-glucose cotransporter 2 inhibitor and glucagon-like peptide 1 receptor agonist use in hospital among adults with diabetes.

Ashley Raudanskis, Shohinee Sarma, Tor Biering-Sørensen, Katarina Zorcic, Fahad Razak, Amol Verma, Magnus Thorsten Jensen, Bruce A Perkins, Michael Colacci, Michael Fralick
Author Information
  1. Ashley Raudanskis: Sinai Health System, Division of General Internal Medicine, Toronto, Ontario, Canada.
  2. Shohinee Sarma: Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Boston, MA, United States of America.
  3. Tor Biering-Sørensen: Department of Cardiology, Copenhagen University Hospital - Herlev & Gentofte, Copenhagen, Denmark.
  4. Katarina Zorcic: Sinai Health System, Division of General Internal Medicine, Toronto, Ontario, Canada.
  5. Fahad Razak: Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario; St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  6. Amol Verma: Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario; St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  7. Magnus Thorsten Jensen: Steno Diabetes Center Copenhagen, Copenhagen, Denmark.
  8. Bruce A Perkins: Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Division of Endocrinology and Metabolism, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
  9. Michael Colacci: Sinai Health System, Division of General Internal Medicine, Toronto, Ontario, Canada; Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario.
  10. Michael Fralick: Sinai Health System, Division of General Internal Medicine, Toronto, Ontario, Canada; Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario. Electronic address: mike.fralick@mail.utoronto.ca.

Abstract

AIMS: To identify factors associated with use of novel diabetes medications among patients hospitalized under general internal medicine.
METHODS: We conducted a cohort study of patients with type 2 diabetes mellitus (T2DM) hospitalized in Ontario, Canada between 2015 and 2020. We evaluated the patient- and physician-level factors associated with sodium-glucose cotransporter 2 inhibitor (SGLT2) and glucagon-like peptide 1 receptor agonist (GLP1R) use using a multivariable logistic regression model.
RESULTS: There were 253,152 hospitalizations and 68,126 involved patients who had T2DM. Prior to discharge, 3.7 % (N = 2490) of patients with T2DM received an SGLT2 and 0.2 % (N = 121) received a GLP1R. The strongest predictors for receiving a novel diabetes medication were hemoglobin A1C > 9.0 % (Odds Ratio (OR) = 1.81, 95 % Confidence Interval (CI) 1.28, 2.60) and patients aged 40-60 compared with patients <40 years old (OR = 1.81, 95 % CI 1.33, 2.68). The strongest predictors for not receiving a novel diabetes medication were dementia (OR = 0.47, 95 % CI 0.39, 0.56) and creatinine ≥200 μmol/L (OR = 0.11, 95 % CI 0.08, 0.15). Overall, 46.8 % of patients hospitalized with T2DM not receiving a novel diabetes medication would potentially benefit from an SGLT2 inhibitor.
CONCLUSIONS: Novel diabetes medications were rarely continued or initiated during hospitalization despite a high prevalence of cardiovascular disease, raising the concern for systematic under-utilization after discharge.

Keywords

Word Cloud

Created with Highcharts 10.0.0diabetespatients210novelT2DMmedication95 %CIusehospitalizedcotransporterinhibitorSGLT2peptidereceptorpredictorsreceivingfactorsassociatedmedicationsamongmellitussodium-glucoseglucagon-likeagonistGLP1R68dischargereceivedstrongest81OR = 0DiabetesAIMS:identifygeneralinternalmedicineMETHODS:conductedcohortstudytypeOntarioCanada20152020evaluatedpatient-physician-levelusingmultivariablelogisticregressionmodelRESULTS:253152hospitalizations126involvedPrior37 %N = 24902 %N = 121hemoglobinA1C > 90 %OddsRatioOR = 1ConfidenceInterval2860aged40-60compared<40 yearsoldOR = 133dementia473956creatinine≥200 μmol/L110815Overall468 %potentiallybenefitCONCLUSIONS:Novelrarelycontinuedinitiatedhospitalizationdespitehighprevalencecardiovasculardiseaseraisingconcernsystematicunder-utilizationIdentifyinghospitaladultsGlucagon-like[GLP1R]agonistsSodium-glucose[SGLT2]inhibitorsType[T2DM]

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