NSAID-induced gastropathy is the most frequent side effect due to NSAI
D use, The resulting clinical event is usually of little significance
and only in a small percentage of cases results in serious side effect
s, Nevertheless, the large worldwide use of NSAIDs makes, even a rare
side effect, numerically consistent, The pathogenesis of NSAID-induced
gastropathy is related to two main mechanisms: an initial topical eff
ect which is pH dependent and a systemic effect which is, more slowly
developing, and mainly to the inhibition of prostaglandin The therapy
of NSAID-gastropathy is almost completely identified with the therapy
of NSAID ulceration because of its frequent relation to the developmen
t of potentially serious complications, In the case of symptomatic ulc
er development the first therapeutic step is NSAID suspension and, in
such a case all ''antiulcer'' drugs are efficient, When the NSAID can
not be discontinued, omeprazole seems to be the most efficient drug; H
-2 blockers can promote ulcer healing but at a slower rate; sucralfate
shows an efficacy similar to H-2 blockers; misoprostol is useful in t
he prevention of NSAID-gastropathy, However, it is not so efficient in
the treatment of established lesions and shows poor efficacy in the r
eduction of dyspeptic symptoms, For each one of these drugs it is nece
ssary to obtain further data.