Diabetes en niños y adolescentes | 30 JUL 12

Tratamiento intensificado sin bomba de insulina en pediatría

La ventaja particular del uso del tratamiento insulinico intensificado es que trata de imitar el modelo fisiológico de secreción de insulina, incrementa la flexibilidad en el tiempo de la ingesta y provee más oportunidades de corregir durante el día.
Autor/a: Dra. Valeria Hirschler* 
INDICE:  1. Artículo | 2. Referencias
Referencias

Referencias

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2. Verge CF, Stenger D, Bonifacio E, et al. Combined use of autoantibodies (IA-2 autoantibody, GAD autoantibody, insulin autoantibody, cytoplasmic islet cell antibodies) in type 1 diabetes: combinatorial islet autoantibody workshop. Diabetes 1998;47(12):1857–66.

3. DCCT Research Group. The effects of intensive diabetes treatment on the development and progression of long-term complication in insulin-dependent diabetes mellitus. The Diabetes Control and Complications Trial. N Engl J Med 1993;329: 977–86.

4. The DCCT Research Group. The effect of intensive diabetes treatment on the development and progression of long-term complications in adolescents with insulin-dependent diabetes mellitus: the Diabetes Control and Complications Trial. J Pediatr 1994;125:177–88.

5. DCCT Research Group, EDIC Research Group. Beneficial effects of intensive therapy of diabetes during adolescence: outcomes after the conclusion of the diabetes control and complications trial (DCCT). J Pediatr 2001;139(6):804–12.

6. Writing Team for the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. Sustained effect of intensive treatment of type 1 diabetes mellitus on development and progressionof diabetic nephropathy: the Epidemiology of Diabetes Interventions and Complications (EDIC) study. JAMA 2003;290:2159–67.

7. Lind M, Oden A, Fahlen M, et al. The shape of the metabolic memory of HbA1c: re-analysing the DCCT with respect to time-dependent effects. Diabetologia 2010;53:1093–8.

8. Silverstein J, Klingensmith G, Copeland K, et al. Care of children and adolescents with type 1 diabetes. A statement of the American Diabetes Association. Diabetes Care 2005;28(1):186–212.

9. Rewers M, Pihoker C, Donaghue K, et al. Assessment and monitoring of glycemic control in children and adolescents with diabetes. Pediatr Diabetes 2009; 10(Suppl 12):71–81.

10. Tamborlane WV, Sikes KA.Insulin therapy in children and adolescents. Endocrinol Metab Clin North Am. 2012, 41:145-60.

11. Greenbaum CJ. Insulin resistance in type 1 diabetes. Diabetes Metab Res Rev 2002;18(3):192–200.

12. Cengiz E, Sherr JL, Erkin-Cakmak A, et al. A bridge to insulin pump therapy: bid regimen with NPH and detemir insulin during initial treatment of youth with type 1 diabetes (T1D). Endocr Pract 2011;6:1–17.

13. Rosenstock J, Dailey G, Massi-Benedetti M, et al. Reduced hypoglycemia risk with insulin glargine: A meta-analysis comparing insulin glargine with human NPH insulin in type 2 diabetes. Diabetes Care 2005;28(4):950–5.
14. Garg SK, Ellis SL, Ulrich H. Insulin glulisine: a new rapid-acting insulin analogue for the treatment of diabetes. Expert Opin Pharmacother 2005;6(4):1–9.

15. Owens DR, Bolli GB. Beyond the era of NPH insulin—long-acting insulin analogs: chemistry comparative pharmacology, and clinical application. Diabetes Technol Ther 2008;10:333–49

16. Mooradian A, Bernbaum M, Albert SG. Narrative review: a rational approach to starting insulin therapy. Ann Intern Med 2006;145(2):125–34.

17. Vajo Z, Fawcett J, Duckworth WC. Recombinant DNA technology in the treatment of diabetes: insulin analogs. Endocr Rev 2001;22:706–17.

18. Angostad HJ, Danne T, Deeb LC, et al. Insulin treatment in children and adolescents with diabetes. Pediatr Diabetes 2009;10(Suppl 12):82–99.

 

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