Evidence map›Paper›PMID 40785508›Full record

ArticleDiabetes, obesity & metabolism2025

Ketosis and ketoacidosis in hospitalized patients receiving SGLT2 inhibitor therapy.

Frank M Gao, Kartik Kishore, Dinesh Pandey, Hossein Jahanabadi, Meg Stevens, Ashani Lecamwasam, Rinaldo Bellomo, Leonid Churilov, Elif I Ekinci

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Article in Diabetes, obesity & metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Frank M GaoDepartment of Endocrinology, Austin Hospital, Melbourne, Australia.
Kartik KishoreAustralian Centre for Accelerating Diabetes Innovations, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Dinesh PandeyData Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Victoria, Australia.
Hossein JahanabadiData Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Victoria, Australia.
Meg StevensData Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Victoria, Australia.
Ashani LecamwasamDepartment of Medicine, Austin Health, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Rinaldo BellomoData Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Victoria, Australia.
Leonid ChurilovAustralian Centre for Accelerating Diabetes Innovations, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.
Elif I EkinciDepartment of Endocrinology, Austin Hospital, Melbourne, Australia.ORCID 0000-0003-2372-395X

Funding

Australian Government
6 · The paper itself

Abstract

aimsThe use and safety of sodium-glucose co-transporter 2 inhibitors (SGLT2i) in hospital are controversial due to the risk of ketoacidosis. We aimed to describe rates of ketosis, ketoacidosis, and acidosis in patients with type 2 diabetes treated with in-hospital SGLT2i use. MATERIALS AND

methodsSingle-centre retrospective cohort study of adult patients with type 2 diabetes admitted for >24 h. Rates of ketone testing, ketone levels, ketosis precipitants, and ketoacidosis and acidosis frequency were determined from examination of electronic medical records. Outcomes were described relative to the first dose of SGLT2i in hospital.

resultsThere were 1511 patients who received SGLT2i at any stage of admission; of these, 777 (51.4%) had ketone levels checked. Peak ketone levels after the first dose of SGLT2i were >1 mmol/L in 12.6% and >3 mmol/L in 2.8%. Eleven out of 12 patients with ketones >3 mmol/L post-SGLT2i had ketosis in the setting of a procedure or surgery, sepsis, reduced oral intake, or critical illness. No patient admitted with heart failure had a ketone level >2 mmol/L. Biochemical ketoacidosis occurred in 1.7% of SGLT2i users pre-first dose of SGLT2i and 0.7% after the first dose. Acidosis (irrespective of ketone levels) occurred in 16.8% before the first dose of SGLT2i and 5.5% after the first dose.

conclusionsKetosis following inpatient SGLT2i administration was infrequent and generally occurred in the setting of known precipitants. These results suggest that, in hospitalized patients selected by clinicians to receive SGLT2i, clinically significant ketone accumulation is low in prevalence.

Indexed as

Diabetes Mellitus, Type 2Diabetic KetoacidosisHypoglycemic AgentsKetosisSodium-Glucose Transporter 2 InhibitorsAdultAgedFemaleHospitalizationHumansKetonesMaleMiddle AgedRetrospective StudiesHypoglycemic AgentsKetonesSodium-Glucose Transporter 2 Inhibitorsdiabetic ketoacidosisheart failurehospitalizationketosisSGLT2 inhibitorstype 2 diabetes

Identifiers

PMID40785508
PMCPMC12515793

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.