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Acetaminophen administration and the risk of acute kidney injury: a self-controlled case series study

机译:对乙酰氨基酚的使用和急性肾损伤的风险:自我控制的病例系列研究

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Background: Acetaminophen (APAP) is frequently used for analgesia and is considered safer than nonsteroidal anti-inflammatory drugs (NSAIDs) for the kidneys. However, there is little epidemiological evidence of the association between APAP and acute kidney injury (AKI). Objectives: To examine the association between APAP and AKI using the self-controlled case series (SCCS) method, which is a novel strategy to control between-person confounders by comparing the risk and reference periods in each patient. Methods: We performed SCCS in 1,871 patients (39.9% female) who were administered APAP and subsequently developed AKI, by reviewing electronically stored hospital information system data from May 2011 to July 2016. We used conditional Poisson regression to compare each patient’s risk and reference period. As a time-varying confounder, we adjusted the status of liver and kidney functions, systemic inflammation, and exposure to NSAIDs. Results: We identified 5,650 AKI events during the 260,549 person-day observation period. The unadjusted incidences during the reference and exposure periods were 2.01/100 and 3.12/100 person-days, respectively. The incidence rate ratio adjusted with SCCS was 1.03 (95% confidence interval [CI]: 0.95–1.12). When we restricted endpoints as stage 2 AKI- and stage 3 AKI-level creatinine elevations, the incidence rate ratios were 1.20 (95% CI 0.91–1.58) and 1.20 (95% CI 0.62–2.31), respectively, neither of which was statistically significant. Conclusion: Our findings added epidemiological information for the relationship between APAP administration and AKI development. The results indicated scarce association between APAP and AKI, presumably supporting the general physicians’ impression that APAP is safer for kidney.
机译:背景:对乙酰氨基酚(APAP)通常用于镇痛,并且被认为比非甾体抗炎药(NSAIDs)更安全。但是,几乎没有流行病学证据表明APAP与急性肾损伤(AKI)之间存在关联。目的:使用自控病例序列(SCCS)方法检查APAP与AKI之间的关联,这是一种通过比较每个患者的风险和参考期来控制人与人混杂因素的新策略。方法:我们回顾了2011年5月至2016年7月以电子方式存储的医院信息系统数据,对接受APAP治疗并随后发展为AKI的1,871例患者(占女性的39.9%)进行了SCCS。我们使用条件Poisson回归比较了每个患者的风险和参考期。作为随时间变化的混杂因素,我们调整了肝和肾功能,全身性炎症以及接触非甾体抗炎药的状况。结果:在260,549人日的观察期内,我们确定了5,650个AKI事件。参考期和暴露期的未调整发病率分别为2.01 / 100和3.12 / 100人日。用SCCS调整的发生率比率为1.03(95%置信区间[CI]:0.95-1.12)。当我们将终点限制为第2阶段AKI和第3阶段AKI水平的肌酐升高时,其发生率分别为1.20(95%CI 0.91-1.58)和1.20(95%CI 0.62-2.31),两者均无统计学意义重大。结论:我们的发现为APAP给药与AKI的发展之间的关系增加了流行病学信息。结果表明,APAP和AKI之间缺乏联系,大概支持了一般医生的印象,即APAP对肾脏更安全。

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