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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Clinical trial: the incidence of NSAID-associated endoscopic gastric ulcers in patients treated with PN 400 (naproxen plus esomeprazole magnesium) vs. enteric-coated naproxen alone.
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Clinical trial: the incidence of NSAID-associated endoscopic gastric ulcers in patients treated with PN 400 (naproxen plus esomeprazole magnesium) vs. enteric-coated naproxen alone.

机译:临床试验:与单独肠溶衣的萘普生相比,用PN 400(萘普生加埃索美拉唑镁)治疗的患者与NSAID相关的内镜胃溃疡的发生率。

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BACKGROUND: Gastroprotective co-therapy may reduce the risk of nonsteroidal anti-inflammatory drug (NSAID)-associated gastric ulcers, but adherence is suboptimal. AIM: To compare the incidence of gastric ulcers with PN 400 [enteric-coated (EC) naproxen 500 mg and immediate-release esomeprazole 20 mg], or EC naproxen. METHODS: Two randomized, double-blind, multicentre studies (PN400-301, PN400-302). Patients [stratified by low-dose aspirin (< or =325 mg) use] aged > or =50 years or 18-49 years with a history of ulcer, received PN 400 BID (301, n = 218; 302, n = 210) or EC naproxen 500 mg BID (301, n = 216; 302, n = 210) for 6 months. The primary endpoint was the cumulative incidence of endoscopic gastric ulcers. RESULTS: The cumulative incidence of gastric ulcers was significantly lower with PN 400 vs. EC naproxen (301: 4.1% vs. 23.1%, P < 0.001; 302: 7.1% vs. 24.3%, P < 0.001). PN 400 was associated with a lower combined incidence of gastric ulcers vs. EC naproxen in low-dose aspirin users (n = 201) (3.0% vs. 28.4%, P < 0.001) and non-users (n = 653) (6.4% vs. 22.2%, P < 0.001). The incidence of, and discontinuations due to, upper gastrointestinal (UGI) AEs was significantly lower with PN 400 relative to EC naproxen (P < 0.01, both studies). CONCLUSIONS: PN 400 significantly reduces the incidence of gastric ulcers, regardless of low-dose aspirin use, in at-risk patients, and is associated with improved UGI tolerability relative to EC naproxen (ClinicalTrials.gov, NCT00527782).
机译:背景:胃保护性联合疗法可降低非甾体抗炎药(NSAID)相关性胃溃疡的风险,但依从性欠佳。目的:为了比较PN 400 [肠溶性(EC)萘普生500 mg和速释埃索美拉唑20 mg]或EC萘普生的胃溃疡发生率。方法:两项随机,双盲,多中心研究(PN400-301,PN400-302)。年龄≥50岁或有溃疡病史的≥50岁或18-49岁的低剂量阿司匹林(<或= 325 mg使用量分层)患者,接受PN 400 BID(301,n = 218; 302,n = 210 )或EC萘普生500 mg BID(301,n = 216; 302,n = 210)持续6个月。主要终点是内镜胃溃疡的累积发生率。结果:PN 400与EC萘普生相比,胃溃疡的累积发生率显着降低(301:4.1%vs. 23.1%,P <0.001; 302:7.1%vs. 24.3%,P <0.001)。 PN 400与低剂量阿司匹林使用者(n = 201)(3.0%vs. 28.4%,P <0.001)和非使用者(n = 653)的胃溃疡联合EC萘普生的发生率较低相关%对22.2%,P <0.001)。 PN 400相对于EC萘普生,上消化道(UGI)AE的发生率和中断率均显着降低(P <0.01,两项研究)。结论:PN 400可显着降低高危患者的胃溃疡发生率,无论使用低剂量阿司匹林,且相对于EC萘普生而言,其与UGI耐受性提高有关(ClinicalTrials.gov,NCT00527782)。

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