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SGLT2 Inhibitors Increase the Risk of Diabetic Ketoacidosis Developing in the Community and During Hospital Admission.
Hamblin, Peter S; Wong, Rosemary; Ekinci, Elif I; Fourlanos, Spiros; Shah, Sonali; Jones, Alicia R; Hare, Matthew J L; Calder, Genevieve L; Epa, Dilan Seneviratne; George, Elizabeth M; Giri, Rinky; Kotowicz, Mark A; Kyi, Mervyn; Lafontaine, Nicole; MacIsaac, Richard J; Nolan, Brendan J; O'Neal, David N; Renouf, Debra; Varadarajan, Suresh; Wong, Jennifer; Xu, Sylvia; Bach, Leon A.
Afiliación
  • Hamblin PS; Department of Endocrinology and Diabetes, Western Health, St. Albans, Victoria, Australia.
  • Wong R; Department of Medicine, Western Precinct, University of Melbourne, St Albans, Victoria, Australia.
  • Ekinci EI; Department of Endocrinology and Diabetes, Eastern Health, Box Hill, Victoria, Australia.
  • Fourlanos S; Department of Endocrinology, Austin Health, Heidelberg, Victoria, Australia.
  • Shah S; Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Australia.
  • Jones AR; Department of Diabetes and Endocrinology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Hare MJL; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
  • Calder GL; Department of Endocrinology and Diabetes, Monash Health, Clayton, Victoria, Australia.
  • Epa DS; Department of Endocrinology and Diabetes, Western Health, St. Albans, Victoria, Australia.
  • George EM; Department of Endocrinology and Diabetes, Alfred Health, Melbourne, Victoria, Australia.
  • Giri R; Department of Diabetes and Endocrinology, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
  • Kotowicz MA; Department of Diabetes and Endocrinology, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
  • Kyi M; Department of Endocrinology and Diabetes, University Hospital Geelong, Barwon Health, Geelong, Victoria, Australia.
  • Lafontaine N; Werribee Mercy Hospital, Werribee, Victoria, Australia.
  • MacIsaac RJ; Diabetes Technology Research Group, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
  • Nolan BJ; Department of Endocrinology and Diabetes, University Hospital Geelong, Barwon Health, Geelong, Victoria, Australia.
  • O'Neal DN; School of Medicine, Faculty of Health, Deakin University, Geelong, Victoria, Australia.
  • Renouf D; Department of Diabetes and Endocrinology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Varadarajan S; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
  • Wong J; Department of Endocrinology and Diabetes, Eastern Health, Box Hill, Victoria, Australia.
  • Xu S; Department of Diabetes and Endocrinology, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
  • Bach LA; Department of Medicine, St. Vincent's Hospital Melbourne, University of Melbourne, Fitzroy, Victoria, Australia.
J Clin Endocrinol Metab ; 104(8): 3077-3087, 2019 08 01.
Article en En | MEDLINE | ID: mdl-30835263
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cetoacidosis Diabética / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Endocrinol Metab Año: 2019 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cetoacidosis Diabética / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Endocrinol Metab Año: 2019 Tipo del documento: Article País de afiliación: Australia