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International Consensus on Risk Management of Diabetic Ketoacidosis in Patients With Type 1 Diabetes Treated With Sodium-Glucose Cotransporter (SGLT) Inhibitors.
Danne, Thomas; Garg, Satish; Peters, Anne L; Buse, John B; Mathieu, Chantal; Pettus, Jeremy H; Alexander, Charles M; Battelino, Tadej; Ampudia-Blasco, F Javier; Bode, Bruce W; Cariou, Bertrand; Close, Kelly L; Dandona, Paresh; Dutta, Sanjoy; Ferrannini, Ele; Fourlanos, Spiros; Grunberger, George; Heller, Simon R; Henry, Robert R; Kurian, Martin J; Kushner, Jake A; Oron, Tal; Parkin, Christopher G; Pieber, Thomas R; Rodbard, Helena W; Schatz, Desmond; Skyler, Jay S; Tamborlane, William V; Yokote, Koutaro; Phillip, Moshe.
Afiliación
  • Danne T; Diabetes Centre for Children and Adolescents, Kinder- und Jugendkrankenhaus Auf der Bult, Hannover, Germany.
  • Garg S; University of Colorado Denver and Barbara Davis Center for Diabetes, Aurora, CO.
  • Peters AL; Keck School of Medicine of the University of Southern California, Los Angeles, CA.
  • Buse JB; University of North Carolina School of Medicine, Chapel Hill, NC.
  • Mathieu C; Department of Endocrinology, UZ Gasthuisberg, KU Leuven, Leuven, Belgium.
  • Pettus JH; Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Diego, San Diego, CA.
  • Alexander CM; Alexander Associates LLC, Gwynedd Valley, PA.
  • Battelino T; Department of Pediatric Endocrinology, Diabetes and Metabolic Diseases, University Children's Hospital, University Medical Centre Ljubljana, and Faculty of Medicine, University of Ljubljana, Slovenia.
  • Ampudia-Blasco FJ; Clinic University Hospital of Valencia, Valencia, Spain.
  • Bode BW; Atlanta Diabetes Associates, Atlanta, GA.
  • Cariou B; Clinique d'endocrinologie, L'institut du thorax, CHU Nantes, CIC 1413 INSERM, Nantes, France.
  • Close KL; The diaTribe Foundation, San Francisco, CA.
  • Dandona P; Division of Endocrinology, Diabetes and Metabolism, University at Buffalo, The State University of New York, Buffalo, NY.
  • Dutta S; JDRF International, New York, NY.
  • Ferrannini E; National Research Council (CNR) Institute of Clinical Physiology, Pisa, Italy.
  • Fourlanos S; Department of Diabetes and Endocrinology, Royal Melbourne Hospital, Melbourne, Australia.
  • Grunberger G; Grunberger Diabetes Institute, Bloomfield Hills, MI.
  • Heller SR; Academic Unit of Diabetes, Endocrinology & Metabolism, University of Sheffield, Sheffield, U.K.
  • Henry RR; Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Diego, San Diego, CA.
  • Kurian MJ; Close Concerns, San Francisco, CA.
  • Kushner JA; McNair Interests, Houston, TX.
  • Oron T; Jesse Z and Sara Lea Shafer Institute of Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Parkin CG; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Pieber TR; CGParkin Communications, Inc., Boulder City, NV chris@cgparkin.org.
  • Rodbard HW; Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Schatz D; Endocrine and Metabolic Consultants, Rockville, MD.
  • Skyler JS; Division of Endocrinology, Department of Pediatrics, University of Florida, Gainesville, FL.
  • Tamborlane WV; Division of Endocrinology, Diabetes and Metabolism, Miller School of Medicine, University of Miami, Miami, FL.
  • Yokote K; Department of Pediatrics, Yale School of Medicine, New Haven, CT.
  • Phillip M; Department of Diabetes, Metabolism and Endocrinology, Chiba University Graduate School of Medicine, Chiba, Japan.
Diabetes Care ; 42(6): 1147-1154, 2019 Jun.
Article en En | MEDLINE | ID: mdl-30728224
ABSTRACT
Sodium-glucose cotransporter (SGLT) inhibitors are new oral antidiabetes medications shown to effectively reduce glycated hemoglobin (A1C) and glycemic variability, blood pressure, and body weight without intrinsic properties to cause hypoglycemia in people with type 1 diabetes. However, recent studies, particularly in individuals with type 1 diabetes, have demonstrated increases in the absolute risk of diabetic ketoacidosis (DKA). Some cases presented with near-normal blood glucose levels or mild hyperglycemia, complicating the recognition/diagnosis of DKA and potentially delaying treatment. Several SGLT inhibitors are currently under review by the U.S. Food and Drug Administration and European regulatory agencies as adjuncts to insulin therapy in people with type 1 diabetes. Strategies must be developed and disseminated to the medical community to mitigate the associated DKA risk. This Consensus Report reviews current data regarding SGLT inhibitor use and provides recommendations to enhance the safety of SGLT inhibitors in people with type 1 diabetes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cetoacidosis Diabética / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Guideline / Risk_factors_studies Límite: Humans Idioma: En Revista: Diabetes Care Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cetoacidosis Diabética / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Guideline / Risk_factors_studies Límite: Humans Idioma: En Revista: Diabetes Care Año: 2019 Tipo del documento: Article País de afiliación: Alemania