Department of Medicine, Nakornprathom Hospital, Nakornprathom, Thailand.
J Gastroenterol. 2013 Jul;48(7):830-8. doi: 10.1007/s00535-012-0717-6. Epub 2012 Dec 4.
There are conflicting and inconsistent data regarding the gastrointestinal (GI) protective effect of cyclooxygenase-2 (COX-2) inhibitors and of non-steroidal anti-inflammatory drugs (NSAIDs) plus proton-pump inhibitors (PPI).
To compare the adverse GI effects between COX-2 inhibitors and NSAIDs plus PPI.
We performed a systematic review of randomized trials comparing GI adverse effects between COX-2 inhibitors and NSAID plus PPI. Trials were identified in MEDLINE, EMBASE, and the Cochrane Library. Primary outcomes were major GI complications including hemorrhage, perforation, and obstruction.
A total of nine trials involving 7,616 participants from 2002 to 2011 were included. All trials were randomized, double blinded, and placebo-controlled with moderate to high quality. COX-2 inhibitors were found to have significantly reduced the risk of major GI events, including perforation, obstruction, and bleeding (relative risk or RR 0.38, 95 % confidence interval or CI 0.25-0.56, p < 0.001); however, the benefit was significant only for patients who were at high risk for NSAID-related GI complications and long-term users. Additionally, the risk of diarrhea (RR 0.56, 95 % CI 0.35-0.9, p 0.02) and withdrawal (RR 0.77, 95 % CI 0.62-0.94, p 0.01) was significantly lower in use of COX-2 inhibitors, while the rate of dyspepsia was higher (RR 1.58, 95 % CI 1.26-1.98, p < 0.001).
COX-2 inhibitors significantly reduced the risk of perforation, obstruction, bleeding, diarrhea, and withdrawal due to GI adverse events, while the risk of dyspepsia was lower with NSAIDs plus PPI.
环氧化酶-2(COX-2)抑制剂和非甾体抗炎药(NSAIDs)加质子泵抑制剂(PPI)的胃肠道(GI)保护作用存在相互矛盾和不一致的数据。
比较 COX-2 抑制剂和 NSAIDs 加 PPI 之间的不良 GI 作用。
我们对比较 COX-2 抑制剂和 NSAIDs 加 PPI 之间 GI 不良事件的随机试验进行了系统评价。在 MEDLINE、EMBASE 和 Cochrane 图书馆中确定了试验。主要结局是包括出血、穿孔和梗阻在内的主要 GI 并发症。
共有 9 项 2002 年至 2011 年期间涉及 7616 名参与者的试验被纳入。所有试验均为随机、双盲、安慰剂对照,质量为中等到高度。COX-2 抑制剂可显著降低主要 GI 事件的风险,包括穿孔、梗阻和出血(相对风险或 RR 0.38,95%置信区间或 CI 0.25-0.56,p<0.001);然而,这种益处仅对 NSAID 相关 GI 并发症高危和长期使用者有意义。此外,COX-2 抑制剂的使用腹泻(RR 0.56,95%CI 0.35-0.9,p0.02)和停药(RR 0.77,95%CI 0.62-0.94,p0.01)的风险显著降低,而消化不良的发生率更高(RR 1.58,95%CI 1.26-1.98,p<0.001)。
COX-2 抑制剂可显著降低因 GI 不良事件导致的穿孔、梗阻、出血、腹泻和停药的风险,而 NSAIDs 加 PPI 的消化不良风险较低。