The Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
The Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Gastroenterology. 2019 Sep;157(3):682-691.e2. doi: 10.1053/j.gastro.2019.05.056. Epub 2019 May 29.
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.
We performed a 3 × 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.
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.
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.
质子泵抑制剂(PPIs)在治疗酸相关疾病方面非常有效。这些药物在短期治疗中具有良好的耐受性,但在观察性研究中,长期治疗与不良事件相关。我们旨在通过一项充分有力的随机试验来证实这些发现。
我们对 17598 名患有稳定心血管疾病和外周动脉疾病的参与者进行了一项 3×2 部分因子双盲试验,将他们随机分为接受泮托拉唑(每天 40 毫克,n=8791)或安慰剂(n=8807)的两组。参与者还被随机分为接受利伐沙班(每天两次 2.5 毫克)联合阿司匹林(每天一次 100 毫克)、利伐沙班(每天两次 5 毫克)或阿司匹林(每天 100 毫克)单独治疗的组。我们每 6 个月收集一次肺炎、艰难梭菌感染、其他肠道感染、骨折、胃萎缩、慢性肾脏病、糖尿病、慢性阻塞性肺病、痴呆、心血管疾病、癌症、住院和全因死亡率的发展数据。患者的中位随访时间为 3.01 年,随访时间为 53152 患者年。
除肠道感染外(安慰剂组为 1.0%,而安慰剂组为 1.4%;比值比,1.33;95%置信区间,1.01-1.75),泮托拉唑组与安慰剂组在安全性事件方面没有统计学上的显著差异。对于所有其他安全性结果,两组之间的比例相似,除艰难梭菌感染外,泮托拉唑组的比例约为安慰剂组的两倍,尽管只有 13 例事件,因此这一差异没有统计学意义。
在一项大型安慰剂对照随机试验中,我们发现泮托拉唑在使用 3 年时与任何不良事件无关,除了肠道感染的风险增加外。临床试验编号:NCT01776424。