"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead

Case report

SGLT-2 Inhibitor-Associated Euglycemic Diabetic Ketoacidosis: A Case Report and a Literature Review


Diabetic ketoacidosis (DKA) is considered a medical emergency, most commonly associated with type 1 diabetes mellitus, and is relatively rare in type 2 diabetes mellitus (T2DM). We discuss a case of a 45-year-old woman with T2DM who presented to the emergency room with worsening lethargy and weakness. Before her presentation, her physician had recently added empagliflozin, a sodium-glucose cotransporter-2 (SGLT-2) inhibitor, to her anti-diabetic drug regimen along with glimepiride and a combination drug of vildagliptin and metformin. Based on the clinical examination and lab findings, DKA was suspected, but her glucose level was below the cutoff value for DKA diagnosis. However, her lab results showed significant metabolic acidosis and ketonemia with no clinical or laboratory features of sepsis. Therefore, the diagnosis of euglycemic diabetic ketoacidosis (eu-DKA) was made. She was successfully treated according to the DKA protocol and discharged in good condition. In this report, our aim is to discuss the relationship between SGLT-2 inhibitors with eu-DKA. Given the absence of significant hyperglycemia, recognition of this entity by clinicians may be delayed. Serum ketones should be obtained in diabetic patients with symptoms of nausea, vomiting, or malaise while taking SGLT-2 inhibitors, and SGLT-2 inhibitors should be discontinued if ketoacidosis is confirmed.


Diabetic ketoacidosis (DKA) is diagnosed by the presence of a triad of hyperglycemia or random blood sugar (RBS) >250 mg/dL, metabolic acidosis (pH <7.3, serum bicarbonate <18 mEq/L), and ketosis [1]. Rarely does the patient present with characteristics of DKA in the presence of blood sugar levels less than 200 mg/dL, and this is defined as euglycemic diabetic ketoacidosis (eu-DKA) [2]. eu-DKA was first described by Munro et al. in 1973 [3]. This case documents one of the rare side effects associated with empagliflozin. Sodium-glucose cotransporter-2 (SGLT-2) inhibitors are a newer generation of anti-diabetic drugs that ultimately inhibit sodium-dependent glucose uptake by the kidneys and increase glucose loss in urine [4]. However, the diagnosis of DKA can sometimes be missed due to the presence of an associated euglycemic effect. Therefore, physicians should be aware when prescribing SGLT-2 inhibitors about this rare side effect and the novel presentation of eu-DKA

Case Presentation

We present here the case of a 45-year-old woman, a known case of type 2 diabetes mellitus (T2DM) for the last five years, poorly controlled with oral hypoglycemic medications including glimepiride, vildagliptin, and metformin. She saw her primary care physician, who added empagliflozin to the prescription five days prior to her presentation at the emergency department. She presented with complaints of increasing lethargy and weakness for the last two days. There were no preceding respiratory, gastrointestinal, or cardiovascular symptoms. She had no fever, cough, sore throat, chest pain, syncope, headache, vomiting, diarrhea, or urinary problems. She denied any history of chronic abdominal pain, weight loss, hypertension, ischemic heart disease, thyroid disease, stroke, substance abuse, or recent travel. She was married, a non-smoker, and a non-alcoholic. Her dietary habits were satisfactory. She had recently recovered from a COVID-19 infection two weeks ago.

On examination, she had no hyperthyroid or hypothyroid features. She had pallor and was slightly drowsy, but easily arousable; dehydrated but without jaundice and lymphadenopathy. Her pulse rate was 106 beats per minute (BPM) and regular, blood pressure (BP) was 110/70 mmHg with no postural drop, respiratory rate was 22 breaths per minute (BPM), peripheral capillary oxygen saturation (SpO2) was 88% at room air, and she was afebrile. Neurological examination showed normal tone, power, and reflexes, but she had bilaterally impaired vibration sense in her lower limbs. The rest of the systemic examination was unremarkable.

Her laboratory results revealed increased white blood cell (WBC) count and raised glycosylated hemoglobin (HbA1c) levels (Table 1). Analysis of arterial blood gas (ABG) and serum electrolytes revealed a decrease in pH, with hypobicarbonatemia, hypokalemia, and hypocarbia. A euglycemic state was indicated in basal metabolic tests with an elevated anion gap and ketosis. The patient also had no history of methanol, ethanol, and paraldehyde ingestion. Chest X-ray was unremarkable. Therefore, based on the clinical and laboratory findings, the diagnosis of eu-DKA due to the use of the SGLT-2 inhibitor was made.

Investigations Day 1 - Before diagnosis   Day 4 - After recovery Reference ranges
Complete blood count
Hemoglobin  10.2 g/dL 10.1 g/dL 12-16 g/dL
WBC  15.7 × 103 µL 11.4 × 103 µL 4-11 × 103 µL
Platelets  215 × 10µL 215 × 10µL 150-400 × 103 µL
MCV  91 fL 91 fL 80-100 fL
HbA1c  10.4% 10.4% 4.8-5.7%
Sodium  140 mEq/L 140 mEq/L 135-145 mEq/L
Potassium  2 mEq/L 3.2 mEq/L 3.5-5 mEq/L
Chloride 98 mEq/L 101 mEq/L 95-105 mEq/L
Arterial blood gas analysis
 pH  7.03 7.4 7.35-7.45
 Bicarbonate  5.9 mmol/L 23.2 mmol/L 24-28 mmol/L
PCO2  19 mmHg 41 mmHg 35-45 mmHg
Basic metabolic panel
RBS  142 mg/dL 133 mg/dL <140 mg/dL
Ketones  >10 mmol/L Negative ≤1.5 mmol/L
Lactate  13.8 mg/dL 13.2 mg/dL 4.5-19.8 mg/dL
Anion gap 36 15.4 8-16
Liver function tests
 AST  26 IU 29 IU 5-40 IU
 ALT 29 IU 31 IU 5-40 IU
Renal function tests
Creatinine        0.5 mg/dL 0.54 mg/dL 0.5-1.30 mg/dL
 Urea  14 mg/dL 14 mg/dL 10-50 mg/dL
Urinary ketones  +++ Negative <0.6

According to the local DKA protocol, the patient was treated with IV fluids, insulin, and potassium replacement. Four days later, the patient improved clinically. Her ABG, electrolyte levels, and basal metabolism returned to their normal values. After treatment, the patient was discharged in a stable condition.


The SGLT-2 inhibitors are a relatively new class of oral hypoglycemic agents that can be used as an adjunctive agent or alternative monotherapy for patients who fail initial therapy with lifestyle interventions, metformin, and/or sulfonylureas. Due to the obvious cardiovascular and renal benefits, they are preferred in patients with atherosclerotic cardiovascular disease, heart failure, or chronic kidney disease. These drugs dramatically reduce blood glucose and HbA1c level [5,6]. Additional benefits include promoting weight loss, decreasing blood pressure, reducing hypoglycemic episodes, and lowering exogenous insulin requirements [4]. However, several studies have estimated a three-fold increased risk of DKA compared to dipeptidyl peptidase-4 enzyme inhibitors [6]. We discuss the link between SGLT-2 inhibitors and eu-DKA.

Although SGLT-2 inhibitors are relatively safer drugs, they have been associated with side effects, such as urinary tract infection, genital mycotic infections, and volume depletion. eu-DKA has also been observed in rare cases [7]. Given the absence of significant hyperglycemia, the recognition of the problem may be delayed by both patients and clinicians. As noted in our case report, hyperglycemia was not present in our patient despite high anion gap metabolic acidosis and increased plasma and urinary ketones. Farjo et al. also studied a case of eu-DKA with empagliflozin in a 57-year-old man with T2DM with an RBS of 120 mg/dL after empagliflozin [8]. Hypoglycemia is associated with the use of SGLT-2 inhibitors, which in turn stimulate glucagon release and decrease glucose-dependent insulin release, thus altering the insulin-to-glucagon ratio and ketosis. Ketosis may be improved by reduced carbohydrate intake, starvation, acute illness, and decreasing exogenous insulin, as suggested by Burke et al. in their review [9]. Although SGLT-2 inhibitors increase glucose excretion in urine, this effect may be counterbalanced by its effect of increasing endogenous glucose production and glucagon release, which can eventually lead to ketosis [10,11]. In Pakistan, a case of eu-DKA after empagliflozin treatment was also reported [1]. Several similar cases have been reported in the literature. Some of them have been demonstrated in Table 2.

Study name Age, years Type of DM Sex SGLT-2 inhibitor Blood analysis Arterial blood gas Basal metabolic panel Renal function tests
Mistry and Eschler (2021) [12] 47     T2DM   Female Empagliflozin HbA1C: 13.6% pH: 7.24. Serum bicarbonate: 11 mmol/L, β-hydroxybutyrate: 6.78 mmol/L Plasma glucose: 187 mg/dL, anion gap: 22 mmol/L Not reported
34 T2DM Male Canagliflozin HbA1C: 8.2% pH: 7.27, serum bicarbonate: 12 mmol/L, β-hydroxybutyrate: 5 mmol/L Serum glucose: 251 mg/dL, anion gap: 24 mmol/L Not reported
Brown and McColl (2018) [13] 53 T2DM Male Dapagliflozin WBC count: 12 × 103 µL pH: 7.24, β-hydroxybutyrate: 6.2 mmol/L Blood glucose: 162 mg/dL, lactate: 4.5 mmol/L, anion gap: 30 Not reported
Chou et al. (2018) [14] 61 T2DM Female Dapagliflozin Not reported pH: 6.986, CO2: 20.9 mmHg, serum bicarbonate: 7.0  mEq/L Blood glucose: 180 mg/dL, blood ketones: 8.0  mmol/L, urine ketones: positive, serum lactate: 9.0  mg/dL, anion gap: 20  mEq/L Blood urea nitrogen: 25 mg/dL, serum creatinine: 0.8 mg/dL
Diaz-Ramos et al. (2019) [15] 44 T2DM Female Canagliflozin Not reported pH: 7.27, PCO2:  29 mm/Hg Serum glucose: 163 mg/dL, serum bicarbonate: 14 mmol/L, anion gap:  18 mmol/L, urinary ketones: positive, serum acetone: positive Not reported
Gajjar and Luthra (2019) [16] 28 T2DM Female Dapagliflozin HbA1c: 10% pH: 7.27, bicarbonate: 18 mmol/L, β-hydroxybutyrate: 5.29 mmol/L Serum glucose: 111 mg/dL, anion gap: 20 Creatinine: 0.4 mg/dL
Lee and Ahn (2020) [17] 76 T2DM Female Dapagliflozin WBC count: 11,800/μL, Hb: 13 g/dL, platelet count:  173,000/μL, erythrocyte sedimentation rate: 12 mm/hour, HbA1C: 8.1% pH: 6.904, pCO2: 12.0 mmHg, serum bicarbonate: 3.1  mmol/L Serum glucose: 410  mg/dL, insulin, 3.3  μIU/mL, anion gap; 37, serum lactate: 1.1 mmol/L, serum ketone: 2.7 mg/dL Blood urea nitrogen: 41.7 mg/dL, creatinine: 3.2 mg/dL
Turner et al. (2016) [18] 62 T2DM Female Canagliflozin HbA1c: 11.1 % pH: 7.08, CO2: <5 mEq/L Serum glucose: 213 mg/dL, anion gap: >17, serum lactate: 0.8 mmol/L Blood urea nitrogen: 22 mg/dL, creatinine: 1.3 mg/dL
Steinmetz-Wood et al. (2020) [19] 47 T2DM Male Empagliflozin HbA1c: 9.1% pH: 6.94, serum bicarbonate: 5 mmol/L, β-hydroxybutyrate: 8.9 mmol/L Serum glucose: 269 mg/dL, urinary ketones: +++, anion gap: 28 Creatinine: 1.21 mg/dL

This rare and unique form of DKA may be due to an altered physiological process. Usually, a decrease in insulin or insulin resistance causes a surge of glucagon release, leading to increased glucose levels and lipolysis, i.e., fatty acid oxidation and, hence, ketosis (Figure 1). A recent meta-analysis was able to develop a dose-dependent association between eu-DKA and SGLT-2 inhibitors. Patients taking high doses of SGLT-2 inhibitors have an increased risk of developing eu-DKA [20].


The case report discusses a rare and life-threatening side effect of SGLT-2 inhibitors. Given the potential adverse consequences of eu-DKA, it is important that emergency physicians should consider the reasonable suspicion of eu-DKA in patients on SGLT-2 inhibitors, especially if the patient presents with nausea, vomiting, lethargy, dyspnea, and severe dehydration. Ketone studies and blood gas analyses would be performed on these patients, regardless of their blood glucose levels for early diagnosis and better prognostic outcomes. Patients taking SGLT-2 inhibitors should be educated to perform urine dipstick tests to check for ketonuria and seek immediate medical attention if positive.


  1. Rashid O, Farooq S, Kiran Z, Islam N: Euglycaemic diabetic ketoacidosis in a patient with type 2 diabetes started on empagliflozin. BMJ Case Rep. 2016, 2016:bcr2016215340. 10.1136/bcr-2016-215340
  2. Barski L, Eshkoli T, Brandstaetter E, Jotkowitz A: Euglycemic diabetic ketoacidosis. Eur J Intern Med. 2019, 63:9-14. 10.1016/j.ejim.2019.03.014
  3. Munro JF, Campbell IW, McCuish AC, Duncan LJ: Euglycaemic diabetic ketoacidosis. Br Med J. 1973, 2:578-80. 10.1136/bmj.2.5866.578
  4. John M, Gopinath D, Jagesh R: Sodium-glucose cotransporter 2 inhibitors with insulin in type 2 diabetes: clinical perspectives. Indian J Endocrinol Metab. 2016, 20:22-31. 10.4103/2230-8210.172268
  5. Douros A, Lix LM, Fralick M, et al.: Sodium-glucose cotransporter-2 inhibitors and the risk for diabetic ketoacidosis: a multicenter cohort study. Ann Intern Med. 2020, 173:417-25. 10.7326/M20-0289
  6. Davidson JA, Kuritzky L: Sodium glucose co-transporter 2 inhibitors and their mechanism for improving glycemia in patients with type 2 diabetes. Postgrad Med. 2014, 126:33-48. 10.3810/pgm.2014.10.2819
  7. Roach P, Skierczynski P: Euglycemic diabetic ketoacidosis in a patient with type 2 diabetes after treatment with empagliflozin. Diabetes Care. 2016, 39:e3. 10.2337/dc15-1797
  8. Farjo PD, Kidd KM, Reece JL: A case of euglycemic diabetic ketoacidosis following long-term empagliflozin therapy. Diabetes Care. 2016, 39:e165-6. 10.2337/dc16-0728
  9. Burke KR, Schumacher CA, Harpe SE: SGLT2 inhibitors: a systematic review of diabetic ketoacidosis and related risk factors in the primary literature. Pharmacotherapy. 2017, 37:187-94. 10.1002/phar.1881
  10. Nasa P, Chaudhary S, Shrivastava PK, Singh A: Euglycemic diabetic ketoacidosis: a missed diagnosis. World J Diabetes. 2021, 12:514-23. 10.4239/wjd.v12.i5.514
  11. Ferrannini E, Muscelli E, Frascerra S, et al.: Metabolic response to sodium-glucose cotransporter 2 inhibition in type 2 diabetic patients. J Clin Invest. 2014, 124:499-508. 10.1172/JCI72227
  12. Mistry S, Eschler DC: Euglycemic diabetic ketoacidosis caused by SGLT2 inhibitors and a ketogenic diet: a case series and review of literature. AACE Clin Case Rep. 2021, 7:17-9. 10.1016/j.aace.2020.11.009
  13. Brown F, McColl T: Euglycemic diabetic ketoacidosis secondary to dapagliflozin use: a case report. J Emerg Med. 2018, 54:109-11. 10.1016/j.jemermed.2017.10.001
  14. Chou YM, Seak CJ, Goh ZN, Seak JC, Seak CK, Lin CC: Euglycemic diabetic ketoacidosis caused by dapagliflozin: a case report. Medicine (Baltimore). 2018, 97:e11056. 10.1097/MD.0000000000011056
  15. Diaz-Ramos A, Eilbert W, Marquez D: Euglycemic diabetic ketoacidosis associated with sodium-glucose cotransporter-2 inhibitor use: a case report and review of the literature. Int J Emerg Med. 2019, 12:27. 10.1186/s12245-019-0240-0
  16. Gajjar K, Luthra P: Euglycemic diabetic ketoacidosis in the setting of SGLT2 inhibitor use and hypertriglyceridemia: a case report and review of literature. Cureus. 2019, 11:e4384. 10.7759/cureus.4384
  17. Lee IH, Ahn DJ: Dapagliflozin-associated euglycemic diabetic ketoacidosis in a patient with type 2 diabetes mellitus: a case report. Medicine (Baltimore). 2020, 99:e20228. 10.1097/MD.0000000000020228
  18. Turner J, Begum T, Smalligan RD: Canagliflozin-induced diabetic ketoacidosis: case report and review of the literature. J Investig Med High Impact Case Rep. 2016, 4:2324709616663231. 10.1177/2324709616663231
  19. Steinmetz-Wood S, Gilbert M, Menson K: A case of diabetic ketoacidosis in a patient on an SGLT2 inhibitor and a ketogenic diet: a critical trio not to be missed. Case Rep Endocrinol. 2020, 2020:8832833. 10.1155/2020/8832833
  20. Dutta S, Kumar T, Singh S, Ambwani S, Charan J, Varthya SB: Euglycemic diabetic ketoacidosis associated with SGLT2 inhibitors: a systematic review and quantitative analysis. J Family Med Prim Care. 2022, 11:927-40. 10.4103/jfmpc.jfmpc_644_21

Case report

SGLT-2 Inhibitor-Associated Euglycemic Diabetic Ketoacidosis: A Case Report and a Literature Review

Author Information

Rabia Salman Mahfooz Corresponding Author

Internal Medicine, Shalamar Institute of Health Sciences, Lahore, PAK

Muhammad Khuzzaim Khan

College of Medicine, Dow University of Health Sciences, Civil Hospital Karachi, Karachi, PAK

Hussam Al Hennawi

Internal Medicine, Jefferson Abington Hospital, Abington, USA

Anwar Khedr

Internal Medicine, BronxCare Health System, New York, USA

Ethics Statement and Conflict of Interest Disclosures

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


RSM and MKK contributed to the concept and design of the manuscript. RSM and HAH contributed to the review of literature and extraction of data. RSM and AK contributed to the design and construction of tables and figures. RSM drafted the manuscript. All authors critically revised the work and gave final approval and agreed to be accountable for all aspects of the work, ensuring integrity and accuracy.

Case report

SGLT-2 Inhibitor-Associated Euglycemic Diabetic Ketoacidosis: A Case Report and a Literature Review

Figures etc.


Scholarly Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.