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Total parenteral nutrition associated with severe insulin resistance following hematopoietic stem cell transplantation in patients with hemophagocytic syndrome: report on two cases.
Suresh, Deepa; Athanassaki, Ioanna; Jeha, George S; Heptulla, Rubina A.
Afiliação
  • Suresh D; Department of Pediatrics, Division of Diabetes and Endocrinology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA. suresh@bcm.edu
Pediatr Diabetes ; 11(1): 70-3, 2010 Feb.
Article em En | MEDLINE | ID: mdl-19460123
ABSTRACT
Hyperglycemia secondary to total parenteral nutrition (TPN) is reported in adults. In addition, insulin resistance and type 2 diabetes as late consequences of hematopoietic stem cell transplantation (HSCT) are well described. Both situations are generally manageable with traditional insulin dosing. We present two children who developed severe insulin resistance requiring intravenous insulin therapy at doses up to 13 units/kg/h. Both children were on TPN after undergoing HSCT for hemophagocytic syndrome. We believe that our report will alert physicians to such a condition and help with early recognition that is a key to successful intervention. These cases aim to increase awareness and stimulate research to unravel the associated underling mechanisms.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Nutrição Parenteral Total / Transplante de Células-Tronco Hematopoéticas / Linfo-Histiocitose Hemofagocítica / Insulina Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans Idioma: En Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Resistência à Insulina / Nutrição Parenteral Total / Transplante de Células-Tronco Hematopoéticas / Linfo-Histiocitose Hemofagocítica / Insulina Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans Idioma: En Ano de publicação: 2010 Tipo de documento: Article