Literature DB >> 29542418

Diabetic Ketoacidosis in Patients with Type 2 Diabetes on Sodium-Glucose Cotransporter-2 Inhibitors - A Case Series.

Purva V Sharma1, Yash B Jobanputra1, Karen Lewin2, Stuart Bagatell1, Daniel M Lichtstein1.   

Abstract

BACKGROUND: Diabetic ketoacidosis (DKA) is a serious complication of diabetes seen commonly in autoimmune Type 1 diabetes mellitus (DM), however patients with Type 2 diabetes are also at risk. Diabetic ketoacidosis may be precipitated by the catabolic stress of acute illness such as trauma, surgery, or infections. Recent studies have suggested that sodium-glucose cotransporter-2 (SGLT-2) inhibitors precipitate DKA in Type 2 diabetes. We present a case series of four patients on SGLT-2 inhibitors who presented with DKA.
METHODS: Medical records were reviewed and patients who were admitted with diabetic ketoacidosis in the last one year at our institute were identified. The charts of such patients were reviewed and we were able to identify 4 patients who were admitted with DKA and were on SGLT-2 inhibitors at the time of admission for the management of their diabetes.
RESULTS: The age group of the four patients was between 45-65 years. Interestingly, all four patients were female. The admission blood glucose levels of these patients ranged from 203 to 400(mg/dl). The pH at the time of admission was in the acidotic range with anion gap ranging from 19 to 24. Two of these four patients had symptoms of a localized infection at the time of admission, which was confirmed by laboratory and radiological evaluation. Three of these patients required management in the intensive care unit.
CONCLUSION: Ketoacidosis is a rare but serious side effect of SGLT2 inhibitors. It is being increasingly reported as these drugs are now commonly being prescribed in the primary care setting. Awareness that DKA can occur in the setting of relative euglycemia is critical to recognize this life-threatening complication of diabetes. More research is needed to better understand the underlying pathophysiology and precipitating factors leading to ketoacidosis in SGLT-2 inhibitor treated patients. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Canagliflozin; SGLT-2 inhibitors; diabetes mellitus; diabetic ketoacidosis; empagliflozin; type 2 diabetes.

Mesh:

Substances:

Year:  2018        PMID: 29542418     DOI: 10.2174/1574887113666180314101436

Source DB:  PubMed          Journal:  Rev Recent Clin Trials        ISSN: 1574-8871


  5 in total

1.  The Limited Role of Glucagon for Ketogenesis During Fasting or in Response to SGLT2 Inhibition.

Authors:  Megan E Capozzi; Reilly W Coch; Jepchumba Koech; Inna I Astapova; Jacob B Wait; Sara E Encisco; Jonathan D Douros; Kimberly El; Brian Finan; Kyle W Sloop; Mark A Herman; David A D'Alessio; Jonathan E Campbell
Journal:  Diabetes       Date:  2020-01-31       Impact factor: 9.461

2.  Sodium-Glucose Cotransporter 2 Inhibitors in the Era of COVID-19 Pandemic: Is the Benefit to Risk Ratio Still Favorable?

Authors:  Theocharis Koufakis; Symeon Metallidis; Pantelis Zebekakis; Ramzi A Ajjan; Kalliopi Kotsa
Journal:  J Diabetes Sci Technol       Date:  2020-06-02

3.  Fracture risk in patients with type 2 diabetes aged ≥50 years related to HbA1c, acute complications, BMI and SGLT2i-use in the DPV registry.

Authors:  Alexander J Eckert; Julia K Mader; Marcus Altmeier; Steffen Mühldorfer; Anton Gillessen; Dhayana Dallmeier; Viral N Shah; Christoph Heyer; Bettina Hartmann; Reinhard W Holl
Journal:  J Diabetes Complications       Date:  2020-06-27       Impact factor: 2.852

Review 4.  Novel Molecular Evidence Related to COVID-19 in Patients with Diabetes Mellitus.

Authors:  Yu-Huang Liao; Jing-Quan Zheng; Cai-Mei Zheng; Kuo-Cheng Lu; You-Chen Chao
Journal:  J Clin Med       Date:  2020-12-07       Impact factor: 4.241

5.  Relationship of concomitant anti-diabetic drug administration with sodium-glucose co-transporter 2 inhibitor-related ketosis.

Authors:  Cheng-Wei Lin; Shih-Yuan Hung; I-Wen Chen
Journal:  J Int Med Res       Date:  2022-03       Impact factor: 1.671

  5 in total

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