V. Savarino et al., VARIABILITY IN INDIVIDUAL-RESPONSE TO VARIOUS DOSES OF OMEPRAZOLE - IMPLICATIONS FOR ANTIULCER THERAPY, Digestive diseases and sciences, 39(1), 1994, pp. 161-168
This study was carried out in order to perform a combined prospective
assessment of the individual pharmacodynamic response and of duodenal
ulcer healing in patients treated with three different doses of omepra
zole. Ninety-nine patients with endoscopically proven duodenal ulcers
were subdivided into three parallel groups of 33 cases, who were rando
mly assigned to receive orally at 0800 hr, in single blind fashion, ei
ther 10 mg, 20 mg, or 40 mg of omeprazole. All of them underwent conti
nuous intragastric pH monitoring both in basal conditions and on the f
ifth day of each dose regimen; ulcer healing was then assessed endosco
pically after four weeks of treatment. All three doses of omeprazole c
aused pH values to increase significantly (P < 0.001) over the whole 2
4-hr period. In patients treated with omeprazole 10 mg, the individual
responses showed the highest variability: the acid inhibition, expres
sed in terms of time spent above pH 3.0, lasted for more than 16 hr in
42% of cases, for more than 8 hr in 28%, and for less than 6 hr in 30
%. In patients treated with omeprazole 20 mg, the pharmacological resp
onse was more marked and uniform and lasted for more than 16 hr in 79%
of cases; however, it is worth noting it lasted for less than 6 hr in
three patients (10%). Inpatients treated with omeprazole 40 mg, the i
ndividual response was excellent (more than 16 hr) in 94% of cases, an
d it lasted for less than 6 hr in only one patient (3%). The mean dura
tions of antisecretory effect of 10, 20 and 40 mg of omeprazole were 1
3.21, 19.10, and 21.45 hr, and the respective four-week healing rates
were 68%, 87%, and 98%. Thus, the longer-lasting the acid inhibition,
the higher the healing rate (P < 0.05). A dose of omeprazole as low as
10 mg produces a consistent acid inhibition in 70% of cases, and this
Can be associated with frequent, but unpredictable, clinical benefit.
The acid suppression obtained with omeprazole 20 mg is remarkable in
the majority of patients, but is poor in 10% of cases, and this findin
g may result in clinical nonresponse. The 40-mg dose of omeprazole pro
duces the most uniform response and is only occasionally unsuccessful
in the clinical setting.