Cited by 118Diabetes Treatment and ManagementDiabetes Management and ResearchPharmacovigilance and Adverse Drug Reactions

Sodium‐glucose co‐transporter‐2 inhibitors and diabetic ketoacidosis: A n updated review of the literature

Bonora, Benedetta Maria, Avogaro, Angelo, Fadini, Gian Paolo·2018·Diabetes, Obesity and Metabolism

Abstract

Sodium-glucose cotransporter-2 inhibitors (SGLT2is) are increasingly used for the treatment of type 2 diabetes (T2D) and can improve glucose control also in type 1 diabetes (T1D). In May 2015, regulatory agencies issued a warning that SGLT2is may cause diabetic ketoacidosis (DKA). We report details on 2 new cases of SGLT2i-associated DKA and review the literature for similar cases within randomized controlled trials (RCTs), cohort studies and single reports. We searched the medical literature for reports of SGLT2i-associated DKA cases. A quantitative analysis of frequency and clinical characteristics is reported. The 2 narrative cases illustrate that SGLT2i-associated DKA can occur in patients with T1D incorrectly diagnosed as T2D, perhaps without the presence of obvious DKA precipitating factors. The incidence of SGLT2i-associated DKA was less than 1/1000 in randomized controlled trials and 1.6/1000 person-years in cohort studies. We retrieved detailed data on 105 SGLT2i-associated DKA case reports, wherein 35% showed glucose levels of less than 200 mg/dL and 22% were not associated with typical triggers. In case reports and in pharmacovigilance databases, duration of SGLT2i treatment before DKA onset was extremely variable. Fatal SGLT2i-associated DKA episodes were found only in pharmacovigilance databases and represented 1.6% of all reported cases. DKA is a rare adverse event during SGLT2i therapy. Predisposing and precipitating factors are still incompletely understood, a…

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  • Up to a third of people treated with SGLT2 inhibitors who developed DKA present with glucose levels <200 mg/dL.

    “Up to a third of people treated with SGLT2 inhibitors who developed DKA present with glucose levels <200 mg/dL (11.1 mmol/L) (239), and in one study 71% presented with glucose levels #250 mg/dL (13.9 mmol/L) (240)”

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References 66 · Cited by 118

Authors
Bonora, B. M., Avogaro, A., & Fadini, G. P.
Affiliations
University of Padua (IT)
Corresponding author
Fadini, Gian Paolo
Venue
Diabetes, Obesity and Metabolism
Publisher
Wiley
Published
2017-07-06
Volume
20
Issue
1
Pages
25-33
ISSN
  • 1462-8902 (ISSN-L)
  • 1463-1326
OpenAlex
W2615244338
Cited by
118
References
66
Citations by year
2026: 6 · 2025: 19 · 2024: 12 · 2023: 12 · 2022: 10 · 2021: 13 · 2020: 18 · 2019: 16 · 2018: 11 · 2017: 1
FWCI
1.84
Type
journal article
Language
en
Open access
closed
Locations
  • Diabetes Obesity and Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • Padua Research Archive (University of Padova) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
Keywords
SGLT2 inhibitors, diabetic ketoacidosis, type 1 diabetes misdiagnosis, adverse drug reactions, pharmacovigilance, drug safety, type 2 diabetes
MeSH terms
Sodium-Glucose Transporter 2 Inhibitors, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Diagnostic Errors, Humans, Hyperglycemia, Hypoglycemia, Hypoglycemic Agents, Diabetic Ketoacidosis, Membrane Transport Modulators, Sodium-Glucose Transporter 2, Pharmacovigilance

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