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SGLT2 Inhibitors Increase the Risk of Diabetic Ketoacidosis Developing in the Community and during Hospital Admission

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Version 2 2024-06-05, 07:55
Version 1 2019-04-11, 15:31
journal contribution
posted on 2024-06-05, 07:55 authored by PS Hamblin, R Wong, EI Ekinci, S Fourlanos, S Shah, AR Jones, MJL Hare, GL Calder, DS Epa, EM George, R Giri, MA Kotowicz, M Kyi, N Lafontaine, RJ Macisaac, BJ Nolan, DN O'Neal, D Renouf, S Varadarajan, J Wong, S Xu, LA Bach
CONTEXT: Diabetic ketoacidosis (DKA) has been associated with the use of sodium glucose cotransporter 2 inhibitors (SGLT2is). OBJECTIVE: To determine the incidence, characteristics, and outcomes of DKA in SGLT2i users vs nonusers with type 2 diabetes. DESIGN: Retrospective, multicenter, controlled cohort study. SETTING: All public hospitals in Melbourne and Geelong (combined population of 5 million), Australia, from 1 September 2015 to 31 October 2017. PATIENTS: Consecutive cases of DKA that developed in the community, or during the course of hospital admission, in patients with type 2 diabetes. MAIN OUTCOME MEASURES: In SGLT2i users vs nonusers: (i) OR of DKA developing during hospital admission, and (ii) incidence of DKA. RESULTS: There were 162 cases of DKA (37 SGLT2i users and 125 non-SGLT2i users) with a physician-adjudicated diagnosis of type 2 diabetes. Of these, DKA developed during the course of inpatient admission in 14 (38%) SGLT2i users vs 2 (2%) non-SGLT2i users (OR, 37.4; 95% CI, 8.0 to 175.9; P < 0.0001). The incidence of DKA was 1.02 per 1000 (95% CI, 0.74 to 1.41 per 1000) in SGLT2i users vs 0.69 per 1000 (95% CI, 0.58 to 0.82 per 1000) in non-SGLT2i users (OR, 1.48; 95% CI, 1.02 to 2.15; P = 0.037). Fifteen SGLT2i users (41%) had peak blood glucose <250 mg/dL (14 mmol/L) compared with one (0.8%) non-SGLT2i user (P < 0.001). CONCLUSIONS: SGLT2i users were more likely to develop DKA as an inpatient compared with non-SGLT2i users. SGLT2i use was associated with a small but significant increased risk of DKA.

History

Journal

Journal of Clinical Endocrinology and Metabolism

Volume

104

Pagination

3077-3087

Location

United States

Open access

  • Yes

ISSN

0021-972X

eISSN

1945-7197

Language

English

Publication classification

C1 Refereed article in a scholarly journal

Copyright notice

2019, Endocrine Society

Issue

8

Publisher

ENDOCRINE SOC