Laryngeal Spasm in Scorpion Envenoming Syndrome
Journal: Indian Journal of Mednodent and Allied Sciences (Vol.2, No. 1)Publication Date: 2014-02-01
Authors : Polisetti Ravi Babu; K. Radha Krishna Murthy;
Page : 41-48
Keywords : Stridor; Acute pancreatitis; Autonomic storm; Disseminated intravascular coagulation; Free fatty acids; Hyperglycemia; Hypocalcemia; Laryngeal spasm; Scorpion sting; Suppressed insulin secretion;
Abstract
Death due to scorpion envenoming syndrome is a common event all over the world in tropical and sub-tropical countries. Scorpion envenoming syndrome results in a severe autonomic storm with a massive release of catecholamines, increased levels of angiotensin II, glucagon, cortisol, thyroid hormones, either hypoinsulinemia or hyperinsulinemia, hyperglycemia and increased free fatty acid levels. Under these conditions, scorpion envenoming syndrome with laryngeal spasm, fasciculations, clonus and tetany like skeletal muscle contractions, myocardial damage, disseminated intravascular coagulation, cardiovascular disturbances, peripheral circulatory failure, cardiac pulmonary oedema, adult respiratory distress syndrome, and many other clinical manifestations cause multi-systemorgan-failure and death. Under these altered conditions, scorpion envenoming essentially results in a syndrome of fuel ? energy defi cits and an inability to use the existing metabolic substrates by vital organs causing MSOF and death. Based on our animal experiments in which insulin administration reversed the metabolic and ECG changes induced by scorpion envenoming and treating the poisonous scorpion sting victims with insulin, we consider that insulin has a primary metabolic role in preventing and reversing laryngeal spasm, fasciculations, clonus and tetany like contractions, the cardiovascular, neurological manifestations and pulmonary oedema. Administration of insulinglucose infusion to scorpion sting victims is the physiological basis for the control of the metabolic response when that has become a determinant to survival. Continuous infusion of regular crystalline insulin at the rate of 0.3 U/g glucose and glucose at the rate of 0.1 g/kg body weight/hour, for 48?72 hours, potassium supplementation and maintenance of fl uid, electrolytes and acid?base balance.
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