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Glucose sensor-augmented continuous subcutaneous insulin infusion in patients with diabetic gastroparesis: An open-label pilot prospective study.
Calles-Escandón, Jorge; Koch, Kenneth L; Hasler, William L; Van Natta, Mark L; Pasricha, Pankaj J; Tonascia, James; Parkman, Henry P; Hamilton, Frank; Herman, William H; Basina, Marina; Buckingham, Bruce; Earle, Karen; Kirkeby, Kjersti; Hairston, Kristen; Bright, Tamis; Rothberg, Amy E; Kraftson, Andrew T; Siraj, Elias S; Subauste, Angela; Lee, Linda A; Abell, Thomas L; McCallum, Richard W; Sarosiek, Irene; Nguyen, Linda; Fass, Ronnie; Snape, William J; Vaughn, Ivana A; Miriel, Laura A; Farrugia, Gianrico.
Afiliação
  • Calles-Escandón J; Endocrinology Section, MetroHealth Regional, Case Western Reserve University, Cleveland, Ohio, United States of America.
  • Koch KL; Section on Gastroenterology, Wake Forest University, Winston-Salem, North Carolina, United States of America.
  • Hasler WL; Division of Gastroenterology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Van Natta ML; Departments of Biostatistics and Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
  • Pasricha PJ; Section of Gastroenterology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
  • Tonascia J; Departments of Biostatistics and Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
  • Parkman HP; Section of Gastroenterology, Temple University School of Medicine, Philadelphia, Pennsylvania, United States of America.
  • Hamilton F; National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, United States of America.
  • Herman WH; Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Basina M; Division of Pediatric Endocrinology, Stanford University School of Medicine, Palo Alto, California, United States of America.
  • Buckingham B; Division of Pediatric Endocrinology, Stanford University School of Medicine, Palo Alto, California, United States of America.
  • Earle K; Division of Endocrinology, California Pacific Medical Center, San Francisco, California, United States of America.
  • Kirkeby K; Division of Endocrinology, California Pacific Medical Center, San Francisco, California, United States of America.
  • Hairston K; Section of Endocrinology, Wake Forest University, Winston-Salem, North Carolina, United States of America.
  • Bright T; Division of Endocrinology, Diabetes, and Metabolism, Texas Tech University School of Medicine, El Paso, Texas, United States of America.
  • Rothberg AE; Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Kraftson AT; Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Siraj ES; Section of Endocrinology, Temple University School of Medicine, Philadelphia, Pennsylvania, United States of America.
  • Subauste A; Division of Endocrinology, University of Mississippi, Jackson, Mississippi, United States of America.
  • Lee LA; Section of Gastroenterology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
  • Abell TL; Division of Gastroenterology, University of Louisville School of Medicine, Louisville, Kentucky, United States of America.
  • McCallum RW; Section of Gastroenterology, Texas Tech University School of Medicine, El Paso, Texas, United States of America.
  • Sarosiek I; Section of Gastroenterology, Texas Tech University School of Medicine, El Paso, Texas, United States of America.
  • Nguyen L; Division of Gastroenterology, Stanford University School of Medicine, Palo Alto, California, United States of America.
  • Fass R; Gastroenterology Division, MetroHealth Regional, Case Western Reserve University, Cleveland, Ohio, United States of America.
  • Snape WJ; Division of Gastroenterology, California Pacific Medical Center, San Francisco, California, United States of America.
  • Vaughn IA; Departments of Biostatistics and Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
  • Miriel LA; Departments of Biostatistics and Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, United States of America.
  • Farrugia G; Section of Gastroenterology, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One ; 13(4): e0194759, 2018.
Article em En | MEDLINE | ID: mdl-29652893
Erratic blood glucose levels can be a cause and consequence of delayed gastric emptying in patients with diabetes. It is unknown if better glycemic control increases risks of hypoglycemia or improves hemoglobin A1c levels and gastrointestinal symptoms in diabetic gastroparesis. This study investigated the safety and potential efficacy of continuous subcutaneous insulin infusion (CSII) and continuous glucose monitoring (CGM) in poorly controlled diabetes with gastroparesis. Forty-five type 1 or 2 patients with diabetes and gastroparesis and hemoglobin A1c >8% from the NIDDK Gastroparesis Consortium enrolled in a 24 week open-label pilot prospective study of CSII plus CGM. The primary safety outcome was combined numbers of mild, moderate, and severe hypoglycemic events at screening and 24 weeks treatment. Secondary outcomes included glycemic excursions on CGM, hemoglobin A1c, gastroparesis symptoms, quality-of-life, and liquid meal tolerance. Combined mild, moderate, and severe hypoglycemic events occurred similarly during the screening/run-in (1.9/week) versus treatment (2.2/week) phases with a relative risk of 1.18 (95% CI 0.85-1.64, P = 0.33). CGM time in hypoglycemia (<70 mg/dL) decreased from 3.9% to 1.8% (P<0.0001), time in euglycemia (70-180 mg/dL) increased from 44.0% to 52.0% (P = 0.02), time in severe hyperglycemia (>300 mg/dL) decreased from 14.2% to 7.0% (P = 0.005), and hemoglobin A1c decreased from 9.4±1.4% to 8.3±1.3% (P = 0.001) on CSII plus CGM. Symptom scores decreased from 29.3±7.1 to 21.9±10.2 with lower nausea/vomiting, fullness/early satiety, and bloating/distention scores (P≤0.001). Quality-of-life scores improved from 2.4±1.1 to 3.1±1.1 (P<0.0001) and volumes of liquid nutrient meals tolerated increased from 420±258 to 487±312 mL (P = 0.05) at 24 weeks. In conclusion, CSII plus CGM appeared to be safe with minimal risks of hypoglycemic events and associated improvements in glycemic control, gastroparesis symptoms, quality-of-life, and meal tolerance in patients with poorly controlled diabetes and gastroparesis. This study supports the safety, feasibility, and potential benefits of improving glycemic control in diabetic gastroparesis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Gastroparesia / Complicações do Diabetes / Insulina Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Gastroparesia / Complicações do Diabetes / Insulina Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: PLoS One Ano de publicação: 2018 Tipo de documento: Article