Hypoglycaemic medication forms a disparate group of therapeutic compou
nds including insulin, the sulphonylureas and biguanides. They are all
designed to prevent hyperglycaemia and in general are well tolerated.
Careful prescribing practice and patient education by the physician c
an do much to reduce the risk of adverse effects from diabetic therapy
. However, the presentation of adverse effects, together with accident
al and non-accidental overdose, is a frequent clinical problem. Furthe
rmore, the possible impairment of hypoglycaemic awareness in patients
prescribed human insulin has added complexity to diabetic management.
The cardinal features of insulin overdose are hypoglycaemia and hypoka
laemia. The sulphonylureas predominantly cause hypoglycaemia, while th
e biguanides may precipitate lactataemia and acidosis. Recognition of
hypoglycaemia is therefore crucial in avoidance of toxicity. Intraveno
us dextrose is the mainstay of therapy following gut decontamination (
for the oral agents). The efficacy of glucagon is dependent on hepatic
glycogen stores and should therefore be used with caution. Diazoxide
is not recommended. More recently, octreotide has been shown to be eff
ective in sulphonylurea overdose. Patients should be admitted and moni
tored with serial blood sugar measurements for a minimum of 1 to 2 day
s as clinically warranted.