Evidence map›Paper›PMID 40843859›Full record

ArticleMedicines (Basel, Switzerland)2025

Duration of DKA and Insulin Use in People with and Without SGLT2 Inhibitor Medications.

Yeung-Ae Park, Anya Kitt Lee, Rahul D Barmanray, Frank Gao, Spiros Fourlanos, Chris Gilfillan

Abstract read
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Article in Medicines (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yeung-Ae ParkDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne 3050, Australia.ORCID 0000-0003-4632-9306
Anya Kitt LeeMonash School of Medicine, Monash University, Melbourne 3168, Australia.
Rahul D BarmanrayDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne 3050, Australia.ORCID 0000-0002-1433-2239
Frank GaoAustralian Centre for Accelerating Diabetes Innovations (ACADI), University of Melbourne, Melbourne 3010, Australia.
Spiros FourlanosDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne 3050, Australia.
Chris GilfillanDepartment of Endocrinology and Diabetes, Eastern Health, Melbourne 3128, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesSodium-glucose co-transporter 2 inhibitors (SGLT2i) are associated with increased rates of diabetic ketoacidosis (DKA). The difference in the management and outcomes of SGLT2i-associated DKA (SGLT2i DKA) from non-SGLT2i-associated DKA (non-SGLT2i DKA) remains unclear due to a lack of specific reporting on dextrose and insulin. This study aims to compare the management and outcome of SGLT2i and non-SGLT2i diabetic ketoacidosis.

methodsIn this retrospective cohort study, patients admitted to the Intensive Care Unit (ICU) for diabetic ketosis between 1 January 2020 to 31 December 2021 at a tertiary hospital were identified. For each SGLT2i diabetic ketosis, two non-SGLT2i diabetic ketosis admissions closest to the SGLT2i admission date were evaluated for comparison. Clinical data including biochemistry, ICU length of stay (LOS), time to normalize acidemia and ketonemia, dextrose and insulin requirements, were evaluated.

resultsIn the SGLT2i group (

conclusionsThe greater insulin requirement in SGLT2i DKA compared to non-SGLT2i DKA may be explained by the greater proportion of precipitating intercurrent illnesses and demographic differences in SGLT2i DKA, highlighting that SGLT2i DKA (predominantly comprising T2D) and non-SGLT2i DKA (predominantly comprising T1D) represent distinct clinical entities. Our findings in comparison to the literature imply that in SGLT2i DKA, the need for prolonged IV insulin infusion may be reduced through intensive management using intravenous 10% dextrose and VRIII. Prospective studies are warranted to evaluate the efficacy of different management strategies for SGLT2i DKA.

Indexed as

diabetesdiabetic ketoacidosisinsulin resistancesodium–glucose co-transporter 2 inhibitorstreatment outcome

Identifiers

PMID40843859
PMCPMC12371971

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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.