Laboratory of Drug Informatics, Gifu Pharmaceutical University; Gifu, 1-25-4, Daigaku-Nishi, Gifu, 501-1196, Japan.
Present Address: Department of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.
BMC Pharmacol Toxicol. 2021 Aug 30;22(1):47. doi: 10.1186/s40360-021-00513-x.
Acute kidney injury (AKI) is associated with significant increases in short- and long-term morbidity and mortality. Drug-induced AKI is a major concern in the present healthcare system. Our spontaneous reporting system (SRS) analysis assessed links between AKI, along with patients' age, as healthcare-associated risks and administered anti-infectives. We also generated anti-infective-related AKI-onset profiles.
We calculated reporting odds ratios (RORs) for reports of anti-infective-related AKI (per Medical Dictionary for Regulatory Activities) in the Japanese Adverse Drug Event Report database and evaluated the effect of anti-infective combination therapy. The background factors of cases with anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were matched using propensity score. We evaluated time-to-onset data and hazard types using the Weibull parameter.
Among 534,688 reports (submission period: April 2004-June 2018), there were 21,727 AKI events. The reported number of AKI associated with glycopeptide antibacterials, fluoroquinolones, third-generation cephalosporins, triazole derivatives, and carbapenems were 596, 494, 341, 315, and 313, respectively. Crude RORs of anti-infective-related AKI increased among older patients and were higher in anti-infective combination therapies [anti-infectives, ≥ 2; ROR, 1.94 (1.80-2.09)] than in monotherapies [ROR, 1.29 (1.22-1.36)]. After propensity score matching, the adjusted RORs of anti-infective monotherapy and combination therapy (≥ 2 anti-infectives) were 0.67 (0.58-0.77) and 1.49 (1.29-1.71), respectively. Moreover, 48.1% of AKI occurred within 5 days (median, 5.0 days) of anti-infective therapy initiation.
RORs derived from our new SRS analysis indicate potential AKI risks and number of administered anti-infectives.
急性肾损伤 (AKI) 与短期和长期发病率和死亡率的显著增加有关。药物性 AKI 是当前医疗保健系统中的一个主要关注点。我们的自发报告系统 (SRS) 分析评估了 AKI 与患者年龄之间的联系,以及与医疗相关的风险和给予的抗感染药物之间的联系。我们还生成了抗感染药物相关 AKI 发病特征。
我们计算了在日本不良药物事件报告数据库中,按监管活动医学词典 (Medical Dictionary for Regulatory Activities) 报告的抗感染药物相关 AKI(每例)的报告比值比 (ROR),并评估了抗感染药物联合治疗的效果。使用倾向评分匹配了抗感染药物单药治疗和联合治疗(≥ 2 种抗感染药物)病例的背景因素。我们使用 Weibull 参数评估了发病时间数据和危险类型。
在 534688 例报告(报告期:2004 年 4 月至 2018 年 6 月)中,有 21727 例 AKI 事件。与糖肽类抗菌药物、氟喹诺酮类药物、第三代头孢菌素、三唑衍生物和碳青霉烯类药物相关的 AKI 报告数量分别为 596、494、341、315 和 313。年龄较大的患者的抗感染药物相关 AKI 粗 ROR 增加,抗感染药物联合治疗(≥ 2 种抗感染药物)的 ROR 高于单药治疗(ROR,1.94(1.80-2.09))。在倾向评分匹配后,抗感染药物单药和联合治疗(≥ 2 种抗感染药物)的调整 ROR 分别为 0.67(0.58-0.77)和 1.49(1.29-1.71)。此外,48.1%的 AKI 发生在抗感染治疗开始后 5 天(中位数,5.0 天)内。
我们的新 SRS 分析得出的 ROR 表明存在潜在的 AKI 风险和给予的抗感染药物数量。