Clinical practice guidelines for congenital hyperinsulinism
- PMID: 28804205
- PMCID: PMC5537210
- DOI: 10.1297/cpe.26.127
Clinical practice guidelines for congenital hyperinsulinism
Abstract
Congenital hyperinsulinism is a rare condition, and following recent advances in diagnosis and treatment, it was considered necessary to formulate evidence-based clinical practice guidelines reflecting the most recent progress, to guide the practice of neonatologists, pediatric endocrinologists, general pediatricians, and pediatric surgeons. These guidelines cover a range of aspects, including general features of congenital hyperinsulinism, diagnostic criteria and tools for diagnosis, first- and second-line medical treatment, criteria for and details of surgical treatment, and future perspectives. These guidelines were generated as a collaborative effort between The Japanese Society for Pediatric Endocrinology and The Japanese Society of Pediatric Surgeons, and followed the official procedures of guideline generation to identify important clinical questions, perform a systematic literature review (April 2016), assess the evidence level of each paper, formulate the guidelines, and obtain public comments.
Keywords: congenital hyperinsulinism; guidelines; hypoglycemia.
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References
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- Ludwig A, Ziegenhorn K, Empting S, Meissner T, Marquard J, Holl R, et al. Diabetes Patienten-Verlaufsdokumentationssystem (DPV) GroupGlucose metabolism and neurological outcome in congenital hyperinsulinism. Semin Pediatr Surg 2011;20: 45–9(MEDIUM). doi: 10.1053/j.sempedsurg.2010.10.005 - DOI - PubMed
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