HYPOGLYCEMIA: INTRODUCTION
Hypoglycemia is most commonly caused by drugs used to treat diabetes mellitus or by exposure to other drugs, including alcohol. However, a number of other disorders, including insulinoma, critical organ failure, sepsis and inanition, hormone deficiencies, non-β-cell tumors, inherited metabolic disorders, and prior gastric surgery, may cause hypoglycemia (Table 339-1). Hypoglycemia is most convincingly documented by Whipple’s triad
: (1) symptoms consistent with hypoglycemia, (2) a low plasma glucose concentration measured with a precise method (not a glucose monitor), and (3) relief of those symptoms after the plasma glucose level is raised. The lower limit of the fasting plasma glucose concentration is normally approximately 70 mg/dL (3.9 mmol/L), but substantially lower venous glucose levels occur normally, late after a meal. Glucose levels <55 mg/dL (3.0 mmol/L) with symptoms that are relieved promptly after the glucose level is raised document hypoglycemia. Hypoglycemia can cause serious morbidity; if severe and prolonged, it can be fatal. It should be considered in any patient with episodes of confusion, an altered level of consciousness, or a seizure.
Table 339-1 Causes of Hypoglycemia
Fasting (Postabsorptive) Hypoglycemia
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Drugs
Especially insulin, sulfonylureas, ethanol
Sometimes quinine, pentamidine
Rarely salicylates, sulfonamides, others
Critical illnesses
Hepatic, renal, or cardiac failure
Sepsis
Inanition
Hormone deficiencies
Cortisol, growth hormone, or both
Glucagon and epinephrine (in insulin-deficient diabetes)
Non-β-cell tumors
Endogenous hyperinsulinism
Insulinoma
Other β cell disorders
Insulin secretagogue (sulfonylurea, other)
Autoimmune (autoantibodies to insulin or the insulin receptor)
Ectopic insulin secretion
Disorders of infancy or childhood
Transient intolerance of fasting
Congenital hyperinsulinism
Inherited enzyme deficiencies
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Reactive (Postprandial) Hypoglycemia
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Alimentary (postgastrectomy)
Noninsulinoma pancreatogenous hypoglycemia syndrome
In the absence of prior surgery
Following Roux-en-Y-gastric bypass
Other causes of endogenous hyperinsulinism
Hereditary fructose intolerance, galactosemia
Idiopathic
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