The main aetiology of acute gastrointestinal haemorrhage in cirrhotic
patients is variceal bleeding. Prognosis is determined by early or lat
e rebleeding rates and the severity of underlying liver disease, mostl
y estimated by Child Pugh score. Diagnosis and therapy of variceal ble
eding is currently based on endoscopic sclerotherapy and more recently
on banding ligation, However, the management of acute variceal bleedi
ng remains controversial and vasoactive drugs are an alternative treat
ment, At present, most of these studies showed encouraging but conflic
ting results. These trials show that the cyclic octapeptide analogue (
octreotid) of somatostatin or the triglycyl analogue (terlipressin) of
vasopressin are safer and more effective than their natural drugs res
pectively.Clinically, drug choice depends on four factors: results of
trials comparing vasoactive treatment to classical sclerotherapy: comp
arison of these two kinds of treatment show similar results concerning
haemostatic rate as well as mortality especially for somatostatin or
its synthetic analogue; results of trials comparing synthetic analogue
of vasopressin to cyclic analogue of somatostatin in variceal bleedin
g: current study designs demonstrate an arithmetic difference (p=0.06)
with a better early haemostatic rate after octreotid associated with
comparable final haemostasis (after 24 hours) and mortality; results o
f combination of both treatments (i.e. sclerotherapy associated with v
asoactive drug versus sclerotherapy): such association decreases varic
eal rebleeding without improvement of survival rate; and finally, impo
rtance of adverse drug effects on hepatic and renal functions: few stu
dies show scanty and conflicting adverse drug effect especially on fre
e water clearance which must be studied by further clinical trials to
confirm their benefit in emergency management of variceal bleeding.