Abstract

We are reporting a timely case of atypical euglycemic diabetic ketoacidosis in a type 1 diabetic patient treated with sodium-glucose cotransporter-2 (SGLT-2) inhibitor canagliflozin. The clinical history, physical examination findings and laboratory values are described. Other causes of acidosis such as salicylate toxicity or alcohol intoxication were excluded. Ketoacidosis resolved after increasing dextrose and insulin doses supporting the hypothesis that SGLT-2 inhibitors may lead to hypoinsulinemia. Euglycemic ketoacidosis did not recur in our patient after discontinuing canagliflozin. We recommend reserving SGLT2 inhibitor therapy to type 2 diabetics, discontinuing medication and treating patients presenting with ketoacidosis due to SGLT-2 inhibitors with higher concentrations of dextrose with appropriate doses of insulin to help resolve acidosis.

Highlights

  • Sodium glucose co-transporter 2 (SGLT2) inhibitors are one of the newest anti-diabetic drugs that improve glycemic control by increasing urinary excretion of glucose

  • We present a case of type 1 diabetic patient treated with SGLT2 inhibitor who was admitted to the hospital with diabetes ketoacidosis (DKA)

  • Results revealed two cases where ketoacidosis was seen in Type 2 diabetics after they were started on an sodium-glucose cotransporter-2 (SGLT-2) Inhibtor.[1]

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Summary

INTRODUCTION

Sodium glucose co-transporter 2 (SGLT2) inhibitors are one of the newest anti-diabetic drugs that improve glycemic control by increasing urinary excretion of glucose. SGLT2 inhibitors are indicated for type 2 diabetics as adjunct to diet and exercise.

METHOD
DISCUSSION
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CONCLUSIONS

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