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Safety of Proton Pump Inhibitors Based on a Large, Multi-Year, Randomized Trial of Patients Receiving Rivaroxaban or Aspirin

机译:质子泵抑制剂的安全基于大,多年,随机试验,患者接受Rivaroxaban或阿司匹林的患者

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BACKGROUND & AIMS: Proton pump inhibitors (PPIs) are effective at treating acid-related disorders. These drugs are well tolerated in the short term, but long-term treatment was associated with adverse events in observational studies. We aimed to confirm these findings in an adequately powered randomized trial. METHODS: We performed a 3 x 2 partial factorial double-blind trial of 17,598 participants with stable cardiovascular disease and peripheral artery disease randomly assigned to groups given pantoprazole (40 mg daily, n = 8791) or placebo (n = 8807). Participants were also randomly assigned to groups that received rivaroxaban (2.5 mg twice daily) with aspirin (100 mg once daily), rivaroxaban (5 mg twice daily), or aspirin (100 mg) alone. We collected data on development of pneumonia, Clostridium difficile infection, other enteric infections, fractures, gastric atrophy, chronic kidney disease, diabetes, chronic obstructive lung disease, dementia, cardiovascular disease, cancer, hospitalizations, and all-cause mortality every 6 months. Patients were followed up for a median of 3.01 years, with 53,152 patient-years of follow-up. RESULTS: There was no statistically significant difference between the pantoprazole and placebo groups in safety events except for enteric infections (1.4% vs 1.0% in the placebo group; odds ratio, 1.33; 95% confidence interval, 1.01-1.75). For all other safety outcomes, proportions were similar between groups except for C difficile infection, which was approximately twice as common in the pantoprazole vs the placebo group, although there were only 13 events, so this difference was not statistically significant. CONCLUSIONS: In a large placebo-controlled randomized trial, we found that pantoprazole is not associated with any adverse event when used for 3 years, with the possible exception of an increased risk of enteric infections. ClinicalTrials.gov Number: NCT01776424.
机译:背景和目的:质子泵抑制剂(PPI)可有效治疗酸相关的病症。这些药物在短期内耐受良好,但长期治疗与观察研究的不良事件有关。我们旨在在充分供电的随机试验中确认这些发现。方法:我们进行了3×2部分因子双盲试验,17,598名参与者,随机分配给给定泮托拉唑(每日40毫克,N = 8791)或安慰剂(n = 8807)的组。参与者也被随机分配给接受罗马昔巴班(每日2.5毫克)的群体(每日每日每日2.5毫克),蓖麻昔扎班(每日5毫克),或单独服用阿司匹林(100mg)。我们收集了关于肺炎的发展数据,艰难艰难的感染,其他肠溶感染,骨折,胃萎缩,慢性肾病,糖尿病,糖尿病,患有每6个月的患者,心血管疾病,癌症,住院治疗和所有原因死亡率。患者随访3.01岁的中位数,53,152名患者随访。结果:除了肠道感染外,泮托拉唑和安慰剂组之间没有统计学显着差异,除了肠道感染(安慰剂组中1.4%vs 1.0%;差距,1.33; 95%置信区间,1.01-1.75)。对于所有其他安全结果,除C艰难梭菌感染外,比例相似,除了泮托拉唑与安慰剂组中大约是常见的两倍,尽管只有13个事件,但这种差异没有统计学意义。结论:在大型安慰剂对照随机试验中,我们发现在使用3年时,泮托拉唑与任何不良事件无关,可能发生肠道感染的风险增加。 ClinicalTrials.gov数字:NCT01776424。

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