关键词: hypoglycemia pediatrics review, systematic type 1 diabetes

Mesh : Adolescent Age of Onset Blood Glucose / drug effects metabolism Child Diabetes Complications / drug therapy epidemiology Diabetes Mellitus, Type 1 / complications drug therapy epidemiology Glycated Hemoglobin A / analysis Humans Hypoglycemia / epidemiology etiology pathology Hypoglycemic Agents / therapeutic use Incidence Insulin / therapeutic use Prospective Studies Retrospective Studies Risk Factors Severity of Illness Index

来  源:   DOI:10.1111/pedi.12876   PDF(Sci-hub)

Abstract:
In 1993, the Diabetes Control and Complications Trial (DCCT) found that intensive antihyperglycemic therapy was effective in the primary and secondary prevention of microvascular complications in patients with type 1 diabetes (T1D) but was associated with a 3-fold greater rate of severe hypoglycemia (SH) than conventional therapy. The aim of this analysis was to determine whether, in the real-world setting, the incidence of SH in pediatric patients with T1D has changed since 1993.
A systematic literature search of PubMed for prospective or retrospective observational studies (≥250 participants) on SH epidemiology or related topics in pediatric patients with T1D, published between October 1993 and June 2016, identified 35 articles (involving >55 000 participants). SH incidence data were analyzed in approximate 5-year blocks: 1993-2000, 2001-2005, 2006-2010, and 2011-2016. Information on factors that might influence the incidence of SH was also collected.
A trend for a marked reduction in the incidence of SH in the post-DCCT setting (from 62.0 per 100 patient-years to 1.21-30 per 100 patient-years) was apparent. Factors that could have influenced this temporal trend in SH incidence included the increased use of new types of, and methods of administering, insulin, in particular rapid-acting insulin analogs and continuous subcutaneous insulin infusion.
SH in pediatric patients with T1D has declined in incidence since the DCCT but remains a common problem. The optimal use of new insulin therapies/regimens/technologies, improved education, and dedicated specialized management teams are needed to help reduce the risk of SH in this population.
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