V. Corleto et al., EFFICACY OF LONG-TERM THERAPY WITH LOW-DOSES OF OMEPRAZOLE IN THE CONTROL OF GASTRIC-ACID SECRETION IN ZOLLINGER-ELLISON SYNDROME PATIENTS, Alimentary pharmacology & therapeutics, 7(2), 1993, pp. 167-173
Thirteen patients with Zollinger-Ellison syndrome were investigated: 8
without, and 5 with, previous gastric surgery. After 7-34 months of t
reatment with famotidine, 8 out of 13 patients were resistant to this
drug. Omeprazole 60 mg/day was administered to these 8 patients; after
one month, the dose was reduced to 40 mg/day, and after another month
to 20 mg/day. Basal acid secretion was inhibited by every dose of ome
prazole. The patients were then treated with a low dose (20 mg/day) of
omeprazole for a longer period. Periodic clinical and endoscopic asse
ssments, and measurement of basal acid secretion showed the efficacy o
f this low dose of omeprazole in our Zollinger-Ellison syndrome patien
ts. The drug was discontinued after 12-32 months of omeprazole treatme
nt, and gastric acid recovery was evaluated. Four patients recovered 5
0 % of their 'initial basal acid secretion' after 5 days, while two pa
tients who had been treated with omeprazole for a longer time (30-32 m
onths) recovered only 38 and 40%, respectively, of their 'initial basa
l acid secretion' at the tenth day. Our results indicate that the omep
razole dosage to be used in the treatment of Zollinger-Ellison syndrom
e must be chosen principally on the basis of basal acid secretion dete
rmination. A low daily dose of omeprazole is able to control acid secr
etion in Zollinger-Ellison syndrome for a long period (10-30 months).
The slow recovery of gastric secretory function demonstrates the prolo
nged inhibitory effects of omeprazole.