Management of Euglycemic Diabetic Ketoacidosis in T2DM Patient on SGLT2 Inhibitor
This patient has euglycemic diabetic ketoacidosis (euDKA) secondary to empagliflozin, and you should administer 10% dextrose at 100-125 mL/hour alongside an insulin infusion to suppress ketogenesis while preventing hypoglycemia.
Immediate Recognition and Diagnosis
- This clinical presentation—ketones 2.9 mmol/L with normal blood glucose (5.6 mmol/L) and normal pH (7.41) in a patient on empagliflozin with minimal oral intake—represents euglycemic diabetic ketoacidosis, a well-documented complication of SGLT2 inhibitors 1
- Euglycemic DKA is characterized by blood glucose <13.9 mmol/L (250 mg/dL), arterial pH <7.35, and presence of ketones in blood or urine 1
- While this patient's pH is currently normal at 7.41, the significantly elevated ketones (2.9 mmol/L) with minimal oral intake and missed medications indicate evolving metabolic decompensation requiring immediate intervention 1
Dextrose Administration Protocol
- Administer 10% dextrose intravenously at 100-125 mL/hour (10-12.5 grams/hour) to provide substrate for glucose metabolism and suppress ketogenesis 2
- The dextrose infusion must be started simultaneously with insulin therapy, as insulin alone will drive blood glucose dangerously low while ketones remain elevated 2
- Continue dextrose infusion until ketones normalize (<0.6 mmol/L) and the patient resumes adequate oral intake, even if blood glucose rises to 10-14 mmol/L (180-250 mg/dL) 2
Concurrent Insulin Therapy
- Start an insulin infusion at 0.05-0.1 units/kg/hour to suppress ketogenesis, as insulin is required to halt lipolysis and ketone production regardless of blood glucose level 2
- Monitor blood glucose every 1-2 hours and adjust dextrose concentration (5%, 10%, or even 20%) to maintain blood glucose between 8-12 mmol/L (140-220 mg/dL) while continuing insulin to clear ketones 2
Critical Management Steps
- Immediately discontinue empagliflozin and do not restart it—this patient should never receive SGLT2 inhibitors again 1
- Provide aggressive intravenous fluid resuscitation with normal saline at 250-500 mL/hour initially (adjusted for age and cardiac status) to correct volume depletion from osmotic diuresis 1
- Monitor electrolytes every 2-4 hours, particularly potassium, as insulin therapy will drive potassium intracellularly and may require aggressive repletion 2
Common Pitfalls to Avoid
- Do not withhold dextrose because the blood glucose is "normal"—this is the defining feature of euglycemic DKA and requires dextrose to resolve ketosis 1
- Do not rely on sliding scale insulin alone without basal insulin coverage, as this approach is strongly discouraged and ineffective for metabolic management 3, 4
- Do not delay treatment waiting for pH to drop further—elevated ketones with minimal oral intake in an SGLT2 inhibitor user requires immediate intervention before full metabolic decompensation occurs 1
- Avoid restarting gliclazide until the patient is eating normally, as sulfonylureas increase hypoglycemia risk when combined with insulin therapy and reduced oral intake 2, 3
Monitoring and Transition
- Continue monitoring ketones every 2-4 hours until they normalize to <0.6 mmol/L 1
- Once ketones clear and the patient tolerates oral intake, transition from intravenous insulin to subcutaneous basal-bolus insulin regimen 3
- Resume metformin when oral intake is adequate, but permanently discontinue empagliflozin given this serious adverse event 1
- Consider alternative glucose-lowering agents such as GLP-1 receptor agonists once metabolically stable, as these do not carry the euDKA risk 2