Goldstein Jay L, Huang Bidan, Amer Fouad, Christopoulos Nikos G
Department of Medicine, University of Illinois at Chicago, 840 South Wood Street (m/c 787), Room 1020, 10th Floor, Chicago, IL 60612, USA.
Clin Ther. 2004 Oct;26(10):1637-43. doi: 10.1016/j.clinthera.2004.10.002.
Concomitant aspirin use is a risk factor for nonsteroidal anti-inflammatory drug (NSAID)-associated upper gastrointestinal toxicity. In high-risk individuals, such as those with a history of NSAID-related gastric ulcer bleeding, gastroprotective therapy with a proton pump inhibitor has been reported to reduce the risk of recurrent aspirin-associated gastroduodenal ulcer bleeding.
This analysis compared the efficacy of misoprostol, lansoprazole, and placebo in reducing the risk of gastric or duodenal ulcer recurrence in patients taking NSAIDs and low-dose aspirin.
This post hoc subanalysis was based on a previous multicenter, prospective, randomized, double-blind, placebo-controlled, 12-week study in patients who had a history of gastric ulcer, were Helicobacter pylori negative, required chronic NSAID therapy, and were free of gastric or duodenal ulcer on baseline endoscopy. The study treatments were misoprostol 200 microg QID or lansoprazole 15 or 30 mg OD. The subanalysis included data from patients in the intent-to-treat cohort who took aspirin at an amount <or=325 mg/d. The end point was the cumulative rate of gastric ulcers, as assessed by serial endoscopy at 4, 8, and 12 weeks.
Of 535 intent-to-treat patients from the primary study, 70 (40 men, 30 women; mean [SD] age, 64.7 [10.0] years; age range, 40-83 years) met the criteria for inclusion in the subanalysis. The proportions of patients who were free of gastric ulcers at the end of 12 weeks were 96% in the misoprostol group, 93% in the lansoprazole 15-mg group, 100% in the lansoprazole 30-mg group, and 35% in the placebo group (P <or= 0.008, each active treatment vs placebo). Adverse events considered possibly or probably related to treatment occurred in 5 (20.0%) misoprostol recipients (4 episodes of diarrhea, 1 episode of abdominal pain), 1 (14.3%) recipient of lansoprazole 30 mg (1 episode of pharyngitis), and 3 (13.6%) placebo recipients (1 episode each of abdominal pain, palpitations, and dyspepsia).
In this subgroup analysis in patients at high risk for recurrence of gastric ulcer, use of cotherapy with misoprostol 200 microg QID or lansoprazole 15 or 30 mg OD significantly lowered the risk for gastric ulcer recurrence.
同时使用阿司匹林是与非甾体抗炎药(NSAID)相关的上消化道毒性的一个危险因素。在高危个体中,如那些有NSAID相关胃溃疡出血病史的患者,据报道使用质子泵抑制剂进行胃保护治疗可降低阿司匹林相关胃十二指肠溃疡出血复发的风险。
本分析比较了米索前列醇、兰索拉唑和安慰剂在降低服用NSAIDs和低剂量阿司匹林患者胃或十二指肠溃疡复发风险方面的疗效。
这项事后亚组分析基于之前一项针对有胃溃疡病史、幽门螺杆菌阴性、需要长期NSAID治疗且基线内镜检查时无胃或十二指肠溃疡的患者进行的多中心、前瞻性、随机、双盲、安慰剂对照的12周研究。研究治疗药物为米索前列醇200微克每日四次或兰索拉唑15毫克或30毫克每日一次。亚组分析纳入了意向性治疗队列中服用阿司匹林剂量≤325毫克/天的患者的数据。终点是通过在第4、8和12周进行的系列内镜检查评估的胃溃疡累积发生率。
在原研究的535名意向性治疗患者中,70名(40名男性,30名女性;平均[标准差]年龄,64.7[10.0]岁;年龄范围,40 - 83岁)符合纳入亚组分析的标准。在12周结束时无胃溃疡的患者比例在米索前列醇组为96%,兰索拉唑15毫克组为93%,兰索拉唑30毫克组为100%,安慰剂组为35%(每种活性治疗与安慰剂相比,P≤0.008)。被认为可能或很可能与治疗相关的不良事件发生在5名(20.0%)米索前列醇接受者身上(4次腹泻发作,1次腹痛发作),1名(14.3%)兰索拉唑30毫克接受者身上(1次咽炎发作),以及3名(13.6%)安慰剂接受者身上(各1次腹痛、心悸和消化不良发作)。
在这项针对胃溃疡复发高危患者的亚组分析中,使用米索前列醇200微克每日四次或兰索拉唑15毫克或30毫克每日一次的联合治疗显著降低了胃溃疡复发的风险。