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U-500 Regular Insulin: Clinical Experience and Pharmacokinetics in Obese, Severely Insulin Resistant Type 2 Diabetic Patients

  1. Mayer B. Davidson, MD (mayerdavidson{at}cdrewu.edu),
  2. Maria D. Navar, MSN, NP,
  3. Diana Echeverry, MD and
  4. Petra Duran, BS
  1. 1Charles Drew University Los Angeles, California

    Abstract

    Objective: To describe the clinical experience and the pharmacokinetics of U-500 regular insulin in severely insulin resistant obese type 2 diabetic patients.

    Research design and methods: Patients requiring >200 units of insulin with A1C levels >8.0% were switched to U-500 regular insulin. For the pharmacokinetic study, fasting subjects received 100 units of U-500 regular insulin subcutaneously and samples drawn before and every 30-60 minutes for glucose, insulin and C-peptides until glucose fell below 100 mg/dl.

    Results: U-500 regular insulin doses were adjusted using the same approach as for adjusting NPH insulin doses. Mean values at baseline and at minimum A1C levels, respectively, were, respectively: A1C (%) — 9.9, 7.1; units/kg — 3.2, 3.3; weight (kg) — 98.6, 102.8. Pharmacokinetically, insulin concentrations rose briskly by 30 minutes and remained elevated for at least 7 hours.

    Conclusions: Uncontrolled severely insulin resistant obese type 2 diabetic patients can be satisfactorily controlled with U-500 regular insulin.

    Footnotes

      • Received August 10, 2009.
      • Accepted November 1, 2009.

    This Article

    1. Diabetes Care November 12, 2009
    1. All Versions of this Article:
      1. dc09-1490v1
      2. 33/2/281 most recent
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