AACE Clinical Case Reports (Nov 2018)

Diabetic Ketoacidosis in a Patient with Type 1 Diabetes Mellitus Treated with Low Insulin in Combination with Empagliflozin

  • Josá G. Jiménez-Montero, MD, FACE,
  • Christopher J. Mora-Aguilar,
  • Chih Hao Chen-Ku, MD, FACE

Journal volume & issue
Vol. 4, no. 6
pp. e505 – e508

Abstract

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ABSTRACT: Objective: To report an episode of diabetic ketoacidosis (DKA) in a patient with type 1 diabetes mellitus treated with low doses of neutral protamine Hagedorn insulin. The patient had recently initiated treatment with a sodium-glucose cotransporter-2 inhibitor as well.Methods: We describe the clinical presentation, laboratory data, and management of a diabetic patient with DKA.Results: A 50-year-old diabetic male presented with weight loss, fatigue, nausea, recurrent vomiting, muscle pain, malaise, and shortness of breath 2 weeks after initiation of empagliflozin and reduction in insulin dose. On admission to the emergency department, the glucose concentration was 541 mg/dL, pH 7.087, bicarbonate 4.5 mmol/L, blood urea nitrogen 50 mg/dL, creatinine 2.0 mg/dL, and beta-hydroxybutirate 4.1 mmol/L. The estimated osmolality was 319.9 mOsm/L and the anion gap was 25.6 mEq/L. Empagliflozin was discontinued; the patient was treated with balanced electrolyte solutions and continuous insulin infusion with resolution of acute kidney injury and metabolic acidosis. C-peptide level was <0.1 ng/mL and anti-glutamic acid decarboxylase-65 was 6 IU/mL (reference range is <5 IU/mL).Conclusion: In this patient, who was misdiagnosed with type 2 diabetes mellitus, the insulin dose reduction provoked DKA. When selecting sodium-glucose cotrans-porter-2 inhibitors in diabetics, physicians must assure adequate insulin provision as well as strict monitoring of blood glucose and urine ketones.Abbreviations: DKA = diabetic ketoacidosis; NPH = neutral protamine Hagedorn; SGLT2 = sodium-glucose cotransporter-2; T1DM = type 1 diabetes mellitus; T2DM = type 2 diabetes mellitus