Randomized Study of Basal-Bolus Insulin Therapy in the Inpatient Management of Patients With Type 2 Diabetes (RABBIT 2 Trial)

OBJECTIVE:--We sought to study the optimal management of hyperglycemia in non-intensive care unit patients with type 2 diabetes, as few studies thus far have focused on the subject. RESEARCH DESIGN AND METHODS--We conducted a prospective, multicenter, randomized trial to compare the efficacy and saf...

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Veröffentlicht in:Diabetes care 2007-09, Vol.30 (9), p.2181-2186
Hauptverfasser: Umpierrez, Guillermo E, Smiley, Dawn, Zisman, Ariel, Prieto, Luz M, Palacio, Andres, Ceron, Miguel, Puig, Alvaro, Mejia, Roberto
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Sprache:eng
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Zusammenfassung:OBJECTIVE:--We sought to study the optimal management of hyperglycemia in non-intensive care unit patients with type 2 diabetes, as few studies thus far have focused on the subject. RESEARCH DESIGN AND METHODS--We conducted a prospective, multicenter, randomized trial to compare the efficacy and safety of a basal-bolus insulin regimen with that of sliding-scale regular insulin (SSI) in patients with type 2 diabetes. A total of 130 insulin-naive patients were randomized to receive glargine and glulisine (n = 65) or a standard SSI protocol (n = 65). Glargine was given once daily and glulisine before meals at a starting dose of 0.4 units · kg⁻¹ · day⁻¹ for blood glucose 140-200 mg/dl or 0.5 units · kg⁻¹ · day⁻¹ for blood glucose 201-400 mg/dl. SSI was given four times per day for blood glucose >140 mg/dl. RESULTS:--The mean admission blood glucose was 229 ± 6 mg/dl and A1C 8.8 ± 2%. A blood glucose target of 240 mg/dl. There were no differences in the rate of hypoglycemia or length of hospital stay. CONCLUSIONS:--Treatment with insulin glargine and glulisine resulted in significant improvement in glycemic control compared with that achieved with the use of SSI alone. Our study indicates that a basal-bolus insulin regimen is preferred over SSI in the management of non-critically ill, hospitalized patients with type 2 diabetes.
ISSN:0149-5992
1935-5548
DOI:10.2337/dc07-0295