Bardhan K D, Bjarnason I, Scott D L, Griffin W M, Fenn G C, Shield M J, Morant S V
District General Hospital, Rotherham.
Br J Rheumatol. 1993 Nov;32(11):990-5. doi: 10.1093/rheumatology/32.11.990.
This double-blind study assessed the acute development of NSAID-associated gastroduodenal (GD) damage and its prevention by misoprostol. Patients requiring chronic NSAID therapy were stratified into two groups depending on initial endoscopic appearance, Group I: normal (n = 223); Group II: non-ulcer lesions (n = 78). After 2 weeks of therapy with NSAID and either misoprostol 400-800 micrograms daily or placebo the incidence of severe mucosal damage (including ulcers) was significantly reduced by misoprostol (odds ratio; 95% CI). Group I: 4.52; 1.94, 10.51 (P = 0.018); Group II: 10.93; 1.09, 109.60 (P = 0.014); Groups I and II combined: 5.95; 3.23, 10.94 (P = 0.0003). Misoprostol exerted a significant protective effect against progression of minor to severe damage in Group II (P < 0.001). Endoscopic findings did not correlate significantly with gastrointestinal symptoms and misoprostol did not interfere with the NSAID efficacy. Significant GD damage occurs early in the course of NSAID treatment and misoprostol significantly reduces the incidence of such damage.
这项双盲研究评估了非甾体抗炎药(NSAID)相关的胃十二指肠(GD)损伤的急性发展情况以及米索前列醇对其的预防作用。需要长期接受NSAID治疗的患者根据初始内镜检查结果分为两组,第一组:正常(n = 223);第二组:非溃疡病变(n = 78)。在用NSAID以及每日400 - 800微克米索前列醇或安慰剂治疗2周后,米索前列醇显著降低了严重黏膜损伤(包括溃疡)的发生率(优势比;95%置信区间)。第一组:4.52;1.94,10.51(P = 0.018);第二组:10.93;1.09,109.60(P = 0.014);第一组和第二组合并:5.95;3.23,10.94(P = 0.0003)。米索前列醇对第二组中轻微损伤进展为严重损伤具有显著的保护作用(P < 0.001)。内镜检查结果与胃肠道症状无显著相关性,且米索前列醇不影响NSAID的疗效。显著的GD损伤在NSAID治疗过程早期就会出现,米索前列醇可显著降低此类损伤的发生率。