[Euglycemic ketoacidosis - rare condition on the rise]
Daniela Kampmeyer1, Friedhelm Sayk1
1Medizinische Klinik 1, UKSH, Campus Lübeck.
Abstract:
SGLT2 inhibitors have been developed as antidiabetics. Large randomized prospective studies have shown prognostic benefit in patients with heart and/or renal insufficiency regarding cardiovascular and general endpoints - even in absence of type 2 diabetes mellitus. This extends the indication to large groups of multimorbid patients. SGLT2 inhibitors induce ketogenesis comparable to fasting conditions. This may - in presence of additional catabolic factors - deteriorate into life-threatening ketoacidosis - probably due to increased reabsorption of ketone bodies from urine as well as the blockage of SGLT2 receptors on α-cells of the pancreas. Euglycaemic ketoacidosis (eKA) under SGLT2 inhibition occurs in about 2:1000 years of treatment. The diagnosis is challenging: in eKA, blood sugar levels are often normal, and ketone detection in urinalysis can be falsely negative, while glucosuria is excessive compared to euglycemic blood-glucose. The management corresponds to classical diabetic ketoacidosis, but special features of blood glucose target, hydration and potassium management should be considered. SGLT2 inhibitors should be paused if a longer fasting period is expected ("sick-day-break"). Due to the soaring number of prescriptions, a significant increase in the prevalence of eKA is expected. Immediate diagnosis and therapy are essential in emergency and intensive care medicine.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors can cause euglycemic ketoacidosis (eKA), a dangerous condition mimicking diabetic ketoacidosis. Early diagnosis and treatment are crucial for managing this rare but serious side effect.
Area of Science:
- Pharmacology
- Endocrinology
- Cardiology
Background:
- SGLT2 inhibitors are antidiabetic drugs with proven cardiovascular and renal benefits, even in non-diabetic patients.
- These drugs induce ketogenesis, similar to fasting states.
- This mechanism can lead to life-threatening euglycemic ketoacidosis (eKA) under certain conditions.
Purpose of the Study:
- To highlight the risk of euglycemic ketoacidosis (eKA) associated with SGLT2 inhibitors.
- To discuss the diagnostic challenges and management strategies for SGLT2 inhibitor-induced eKA.
- To emphasize the importance of prompt diagnosis and therapy in emergency settings.
Main Methods:
- Review of randomized prospective studies on SGLT2 inhibitors.
- Analysis of case reports and clinical data on euglycemic ketoacidosis.
- Discussion of pathophysiological mechanisms and diagnostic criteria.
Main Results:
- SGLT2 inhibitors can cause euglycemic ketoacidosis (eKA) at a rate of approximately 2:1000 patient-years.
- Diagnosis is challenging due to normal blood glucose levels and potentially misleading ketone and glucose tests.
- Management requires careful attention to blood glucose targets, hydration, and potassium levels.
Conclusions:
- SGLT2 inhibitors, while beneficial, carry a risk of inducing euglycemic ketoacidosis (eKA).
- Physicians must be aware of the diagnostic difficulties and specific management needs for eKA.
- Prompt recognition and treatment are vital, especially with increasing SGLT2 inhibitor prescriptions.
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