Ulcer prevention in long-term users of nonsteroidal anti-inflammatory drugs - Results of a double-blind, randomized,, multicenter, active- and placebo-controlled study of misoprostol vs lansoprazole

被引:213
作者
Graham, DY
Agrawal, NM
Campbell, DR
Haber, MM
Collis, C
Lukasik, NL
Huang, B
机构
[1] Vet Affairs Med Ctr, Dept Med, Houston, TX 77030 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Univ Kansas, Med Ctr, Sch Med, Dept Med, Kansas City, KS 66103 USA
[4] Univ Missouri, Kansas City, MO 64110 USA
[5] Dept Vet Affairs Med Ctr, Sch Med, Kansas City, MO USA
[6] St Lukes Hosp, Kansas City, MO 64111 USA
[7] Med Coll Penn & Hahnemann Univ, Philadelphia, PA 19129 USA
[8] TAP Pharmaceut Prod Inc, Lake Forest, IL USA
[9] Abbott Labs, Abbott Pk, IL 60064 USA
关键词
D O I
10.1001/archinte.162.2.169
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Studies that report prevention of ulcer recurrence among long-term users of nonsteroidal anti-inflammatory drugs (NSAIDs) that do not stratify for Helicobacter pylori status may not be generalizable to the large population of individuals without H pylori. Methods: This was a prospective, double-blind, multicenter, active- and placebo-controlled study among 537 patients without H pylori who were long-term users of NSAIDs and who had a history of endoscopically documented gastric ulcer. Patients were randomized to receive placebo, 200 mug of misoprostol 4 times a day, or 15 or 30 mg of lansoprazole once daily for 12 weeks. Ulcer status was determined by endoscopy at 4, 8, and 12 weeks. Results: Patients receiving lansoprazole (15 or 30 mg) remained free from gastric ulcer longer than those who received placebo (P<.001) but for a shorter time than those who received misoprostol. By week 12, the percentages of gastric ulcer-free patients were as follows: placebo, 51% (95% confidence interval [Cl], 41.1%-61.3%); misoprostol, 93% (95% CI, 87.2%-97.9%); 15-mg lansoprazole, 80% (95% CI, 72.5%-87.3%); and 30-mg lansoprazole, 82% (95% CI, 75.0%-89.6%). A significantly higher proportion of patients in the misoprostol group reported treatment-related adverse events and early withdrawal from the study. When the impact of withdrawals on ulcer development was considered (as failures), therapy was successful for 69% for each of the active treatment groups and 35% for the placebo group. Conclusions: Proton pump inhibitors such as lansoprazole are superior to placebo for the prevention of NSAID-induced gastric ulcers but not superior to misoprostol, 800 mug/d. When the poor compliance and potential adverse effects associated with misoprostol are considered, proton pump inhibitors and full-dose misoprostol are clinically equivalent.
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页码:169 / 175
页数:7
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