Combination of a cyclo-oxygenase-2 inhibitor and a proton-pump inhibitor for prevention of recurrent ulcer bleeding in patients at very high risk: a double-blind, randomised trial

被引:207
作者
Chan, Francis Ka Leung
Wong, Vincent Wai Sun
Suen, Bing Yee
Wu, Justin Che Yuen
Ching, Jessica Yuet Ling
Hung, Lawrence Cheung Tsui
Hui, Aric Josun
Leung, Vincent King Sun
Lee, Vivian Wing Yan
Lai, Larry Hin
Wong, Grace Lai Hung
Chow, Dorothy Kai Lai
To, Ka Fa
Leung, Wai Keung
Chiu, Philip Wai Yan
Lee, Yuk Tong
Lau, James Yun Wong
Chan, Henry Lik Yuen
Ng, Enders Kwok Wai
Sung, Joseph Jao Yiu
机构
[1] Chinese Univ Hong Kong, Dept Med & Therapeut, Prince Wales Hosp, Inst Digest Dis, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Sch Pharm, Shatin, Hong Kong, Peoples R China
[3] United Christian Hosp, Med Unit, Hong Kong, Peoples R China
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0140-6736(07)60749-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Guidelines on pain management recommend that patients at risk of ulcers receive either a cyclo-oxygenase (COX 2) inhibitor or a non-steroidal anti-inflammatory drug (NSAID) with a proton-pump inhibitor (PPI). These two treatments have similar effectiveness, but they are insufficient for protection of patients at very high risk for ulcer bleeding. We aimed to test the hypothesis that in patients with previous ulcer bleeding induced by non-selective NSAIDs, combined treatment with the COX 2 inhibitor celecoxib and the PPI esomeprazole would be better than celecoxib alone for prevention of recurrent ulcer bleeding. Methods 441 consecutively presenting patients who were taking non-selective NSAIDs for arthritis were recruited to our single-centre, prospective, randomised, double-blind trial after admission to hospital with upper-gastrointestinal bleeding. Patients were enrolled after their ulcers had healed and a histological test for Helicobacter pylori was negative. All patients were given 200 mg celecoxib twice daily. 137 patients were randomly assigned to receive 20 mg esomeprazole twice daily (combined-treatment group), and 136 to receive a placebo (control group) for 12 months. The primary endpoint was recurrent ulcer bleeding during treatment or within 1 month of the end of treatment. Analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00365313. Findings Combination treatment was more effective than celecoxib alone for prevention of ulcer bleeding in patients at high risk. The 13-month cumulative incidence of the primary endpoint was 0% in the combined-treatment group and 12 (8.9%) in the controls (95% Cl difference, 4.1 to 13.7; p=0.0004). The median follow-up was 13 months (range 0.4-13.0). Discontinuation of treatment and the incidence of adverse events were similar in the two treatment groups. Interpretation Patients at very high risk for recurrent ulcer bleeding who need anti-inflammatory analgesics should receive combination treatment with a COX 2 inhibitor and a PPI. Our findings should encourage guideline committees to review their recommendations for patients at very high risk of recurrent ulcer bleeding.
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页码:1621 / 1626
页数:6
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