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Safe and Simple Emergency Department Discharge Therapy for Patients with Type 2 Diabetes Mellitus and Severe Hyperglycemia
Affiliation:1. Department of Endocrinology and Metabolism, John H. Stroger Jr. Hospital of Cook County and Rush University Medical Center, Chicago, Illinois.;2. Department of Family Medicine, Lutheran Medical Center, Brooklyn, New York.;3. Department of Emergency Medicine, John H. Stroger Jr. Hospital of Cook County and Rush University Medical Center, Chicago, Illinois.;4. Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan.;5. Department of Preventive Medicine and Biostatistics, Rush University Medical Center, Chicago, Illinois.;6. Division of Endocrinology, Rush University Medical Center, Chicago, Illinois.;1. Department of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA;2. Peter Flom Consulting, New York, NY, USA;3. Department of Medicine, Maine Medical Center Research Institute, Scarborough, ME, USA;4. Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY, USA;5. Department of Obstetrics and Gynecology, Albert Einstein College of Medicine, Bronx, NY, USA;1. Department of Medicine and Geriatrics, Skellefteå County Hospital, S-931 86 Skellefteå, Sweden;2. Karolinska Institutet, Department of Clinical Scienecs, Cardiology Unit, Danderyd University Hospital, Stockholm, Sweden;3. Department of Clinical Science and Education Södersjukhuset, Karolinska Institutet, Stockholm, Sweden S-118 83 Stockholm, Sweden
Abstract:ObjectiveTo investigate the safety and effectiveness of 2 simple discharge regimens for use in patients with type 2 diabetes mellitus (DM2) and severe hyperglycemia, who present to the emergency department (ED) and do not need to be admitted.MethodsWe conducted an 8-week, open-label, randomized controlled trial in 77 adult patients with DM2 and blood glucose levels of 300 to 700 mg/dL seen in a public hospital ED. Patients were randomly assigned to receive glipizide XL, 10 mg orally daily (G group), versus glipizide XL, 10 mg orally daily, plus insulin glargine, 10 U daily (G + G group). The primary outcome was to maintain safe fasting glucose and random glucose levels of < 350 and < 500 mg/dL up to 4 weeks and < 300 and < 400 mg/ dL, respectively, thereafter and to have no return ED visits (responders).ResultsBaseline characteristics were similar between the 2 treatment groups. The primary outcome was achieved in 87% of patients in both treatment groups. The enrollment mean blood glucose values of 440 and 467 mg/dL in the G and G + G groups, respectively, declined by the end of week 1 to 298 and 289 mg/dL and by week 8 to 140 and 135 mg/dL, respectively. Homeostasis model assessment of b-cell function and early insulin response improved 7-fold and 4-fold, respectively, in responders at the end of the 8-week study.ConclusionSulfonylurea with and without use of a small dose of insulin glargine rapidly improved blood glucose levels and b-cell function in patients with DM2. Use of sulfonylurea alone once daily can be considered a safe discharge regimen for such patients and an effective bridge between ED intervention and subsequent follow-up. (Endocr Pract. 2009;15:696-704)
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