Epsilon
Aminocaproic Acid
e-
Aminocaproic acid is an inhibitor of fibrinolysis, whichis useful in the
management of post-partum haemorrhage, haematuria, hereditary angioedema,
subarachnoid haemor-rhage, prevention of haemorrhage after dental extraction in
haemophiliacs, and prevention of rebleeding following trau-matic hyphaema. It
is a synthetic amino acid which is similar in structure to lysine and
ornithine.
Aminocaproic
acid is readily absorbed from the gastroin-testinal tract. Peak plasma levels
are reached within 2 hours of a single oral dose. After prolonged
administration, it distributes throughout both the intravascular and
extravascular compart-ments. It readily penetrates red blood cells. It does not
appear to be bound to plasma proteins. Aminocaproic acid is readily excreted in
the urine. 80% of a single dose is excreted in 12 hours.
Side
effects include nausea, vomiting, diarrhoea, conjunc-tival hyperaemia, and delirium.
Hypotension and bradycardia may be seen after too rapid intravenous
administration. Overdose results in rash, vomiting, diarrhoea, myopathy,
prolongation of bleeding time, seizures, thrombosis formation, hepatic failure,
and acute renal failure. Severe cases of myop-athy may be associated with
muscle necrosis, myoglobinuria, rhabdomyolysis, and prolonged elevations of
muscle enzymes.
Treatment
involves stabilisation and supportive measures. Bleeding time, hepatic
function, and renal function should be monitored. Serial bleeding time tests
are indicated for patients receiving aminocaproic acid. Myopathy may occur,
producing high plasma creatine kinase levels, and mild hyperbilirubinaemia.
Serial creatinine phosphokinase (CPK) levels are important in monitoring a
patient using aminocaproic acid. This is especially true if the therapy is in
excess of 2 weeks and a total dose greater than 500 grams. In general,
aminocaproic acid-associated renal failure and myopathy have improved with
discontinuation of therapy. Aminocaproic acid can be removed by dialysis.
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