Case Series
Author Details :
Volume : 9, Issue : 2, Year : 2022
Article Page : 269-272
https://doi.org/10.18231/j.ijca.2022.051
Abstract
Congenital hyperinsulinism (CHI) is one of the common causes of recurrent or persistent hypoglycemia. It is marked by islet cell dysfunction leading to insufficient suppression of insulin secretion in the presence of serious hypoglycemia. CHI is genetic in origin, where children present with symptoms of hypoglycemia like irritability, listlessness, nausea, vomiting, tachypnoea, seizure or with long-term sequelae such as developmental delay and focal neurologic deficits, thus making it a medical emergency. Surgical management becomes essential in most of the cases with challenging perioperative management. We successfully managed three such cases with favorable postoperative outcome.
Keywords: Congenital hyperinsulinism, Pancreatectomy, Perioperative management
How to cite : Kaushik P, Hayaran N, Goel I, Perioperative management of congenital hyperinsulinism (CHI). Indian J Clin Anaesth 2022;9(2):269-272
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