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1.
Diabetes Technol Ther ; 14(9): 762-4, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22694194

ABSTRACT

BACKGROUND: Efficacy and feasibility of sensor-augmented pump (SAP) therapy were evaluated in very young children with type 1 diabetes (T1D). SUBJECTS AND METHODS: SAP (Dexcom [San Diego, CA] Seven Plus™ usage combined with insulin pump) therapy was retrospectively evaluated in 28 children (15 boys) younger than 7 years (mean age, 5.8 ± 1.2 years; range, 3-7 years), with T1D. Glycosylated hemoglobin (HbA1c) was evaluated at baseline and at the end of the study, as were efficacy and feasibility of the system, using a rating scale (with 3 being the most positive). RESULTS: SAP has been used for at least 6 months by 85% of patients, with an overall good satisfaction (92%). The greatest perceived benefit was the reduced fear of hypoglycemia (score of 3, 81%). HbA1c significantly improved only in patients with baseline HbA1c >7.5% (P = 0.026). CONCLUSIONS: SAP therapy is effective and feasible in preschool children with T1D. In patients with high HbA1c at baseline it provide a 0.9% decrease, sustained for at least 6 months.


Subject(s)
Biosensing Techniques , Blood Glucose/metabolism , Diabetes Mellitus, Type 1/blood , Glycated Hemoglobin/metabolism , Hypoglycemic Agents/administration & dosage , Insulin Infusion Systems , Blood Glucose/drug effects , Child , Child, Preschool , Diabetes Mellitus, Type 1/drug therapy , Diabetes Mellitus, Type 1/physiopathology , Dose-Response Relationship, Drug , Drug Administration Schedule , Feasibility Studies , Female , Glycated Hemoglobin/drug effects , Humans , Italy , Male , Retrospective Studies , Treatment Outcome
2.
J Pediatr Endocrinol Metab ; 24(7-8): 561-3, 2011.
Article in English | MEDLINE | ID: mdl-21932600

ABSTRACT

Congenital adrenal hyperplasia (CAH) is an autosomal recessive enzymatic defect caused by mutations or deletions of the cytochrome P450 21-hydroxylase CYP21 gene. Oral therapy with glucocorticoids and mineralcorticoids is administered to prevent adrenal crisis and to control hyperandrogenism. During puberty this type of therapy is difficult to manage owing to physiological and hormonal changes and poor compliance. We describe a case of a pubertal boy affected by CAH, in whom continuous subcutaneous infusion of hydrocortisone led to improved metabolic control and compliance.


Subject(s)
Adrenal Hyperplasia, Congenital/drug therapy , Anti-Inflammatory Agents/administration & dosage , Hydrocortisone/administration & dosage , Adolescent , Adolescent Behavior/psychology , Adrenal Hyperplasia, Congenital/physiopathology , Adrenal Hyperplasia, Congenital/psychology , Anti-Inflammatory Agents/therapeutic use , Drug Delivery Systems , Glycosuria/etiology , Glycosuria/prevention & control , Humans , Hydrocortisone/therapeutic use , Infusions, Subcutaneous , Male , Medication Adherence/psychology , Puberty, Precocious/etiology , Treatment Outcome
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