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

被引:23
作者
Hiragi, Shusuke [1 ,2 ]
Yamada, Hiroyuki [1 ]
Tsukamoto, Tatsuo [1 ,3 ]
Yoshida, Kazuki [4 ,5 ]
Kondo, Naoya [1 ]
Matsubara, Takeshi [1 ]
Yanagita, Motoko [1 ]
Tamura, Hiroshi [2 ]
Kuroda, Tomohiro [2 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Nephrol, Kyoto, Japan
[2] Kyoto Univ Hosp, Div Med Informat & Adm Planning, Kyoto, Japan
[3] Kitano Hosp, Tazuke Kofukai Med Res Inst, Dept Nephrol & Dialysis, Osaka, Japan
[4] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[5] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
基金
日本学术振兴会;
关键词
acetaminophen; acute kidney injury; adverse drug event; self-controlled case series; hospital information system; ACUTE-RENAL-FAILURE; VACCINE SAFETY; DISEASE; DRUGS; RECOMMENDATIONS; MANAGEMENT; MECHANISM; PAIN;
D O I
10.2147/CLEP.S158110
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
收藏
页码:264 / 274
页数:11
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