Hiragi Shusuke, Yamada Hiroyuki, Tsukamoto Tatsuo, Yoshida Kazuki, Kondo Naoya, Matsubara Takeshi, Yanagita Motoko, Tamura Hiroshi, Kuroda Tomohiro
Department of Nephrology, Graduate School of Medicine, Kyoto University.
Division of Medical Informatics and Administration Planning, Kyoto University Hospital, Kyoto.
Clin Epidemiol. 2018 Mar 6;10:265-276. doi: 10.2147/CLEP.S158110. eCollection 2018.
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).
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.
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.
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.
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.
对乙酰氨基酚(APAP)常用于镇痛,且被认为对肾脏而言比非甾体类抗炎药(NSAIDs)更安全。然而,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。
采用自控病例系列(SCCS)方法研究APAP与AKI之间的关联,这是一种通过比较每位患者的风险期和参照期来控制个体间混杂因素的新策略。
我们通过查阅2011年5月至2016年7月电子存储的医院信息系统数据,对1871例接受APAP治疗并随后发生AKI的患者(女性占39.9%)进行了SCCS研究。我们使用条件泊松回归比较每位患者的风险期和参照期。作为一个随时间变化的混杂因素,我们对肝肾功能、全身炎症反应以及NSAIDs暴露情况进行了调整。
在260549人日的观察期内,我们共识别出5650例AKI事件。参照期和暴露期未经调整的发病率分别为2.01/100人日和3.12/100人日。经SCCS调整后的发病率比为1.03(95%置信区间[CI]:0.95 - 1.12)。当我们将终点限定为2期AKI和3期AKI水平的肌酐升高时,发病率比分别为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。
我们的研究结果为APAP给药与AKI发生之间的关系增添了流行病学信息。结果表明APAP与AKI之间关联不大,这大概支持了全科医生认为APAP对肾脏更安全的观点。