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万古霉素联合哌拉西林与急性肾损伤风险:一项全球药物警戒数据库分析。

Combination of vancomycin plus piperacillin and risk of acute kidney injury: a worldwide pharmacovigilance database analysis.

机构信息

Université de Paris, Faculté de Médecine, F-75006 Paris, France.

Équipe Mobile d'Infectiologie, AP-HP, APHP.CUP, Hôpital Cochin, F-75014 Paris, France.

出版信息

J Antimicrob Chemother. 2021 Apr 13;76(5):1311-1314. doi: 10.1093/jac/dkab003.

Abstract

BACKGROUND

Excess of acute kidney injury (AKI) secondary to the association of vancomycin plus piperacillin is debated.

OBJECTIVES

To detect a signal for an increased risk of AKI with the vancomycin and piperacillin combination compared with other vancomycin-based regimens.

METHODS

Using VigiBase, the WHO global database of individual case safety reports (ICSR) from 1997 to 2019, we conducted a disproportionality analysis comparing the reporting of AKI cases between different vancomycin-based regimens (vancomycin plus piperacillin, cefepime or meropenem). To take into account a possible notoriety bias, we secondarily restricted the study period to before 2014, the date of the first publication of AKI in patients receiving vancomycin plus piperacillin. Results are expressed using the reporting OR (ROR) and its 95% CI.

RESULTS

From 1997 to 2019, 53 701 ICSR concerning vancomycin have been registered in the database, including 6016 reports of AKI (11.2%), among which 925 (15.4%) were reported with vancomycin/piperacillin, 339 (5.6%) with vancomycin/cefepime and 197 (3.7%) with vancomycin/meropenem. ROR (95% CI) for AKI was 2.6 (2.4-2.8) for vancomycin/piperacillin, 2.5 (2.2-2.9) for vancomycin/cefepime and 0.5 (0.4-0.6) for vancomycin/meropenem versus other vancomycin-containing regimens. After restriction of the study period to 1997-2013, the ROR for AKI remains significant only for vancomycin/piperacillin [ROR (95% CI) = 2.1 (1.8-2.4)].

CONCLUSIONS

We found a disproportionality in reports of AKI in patients receiving vancomycin plus piperacillin compared with vancomycin in other regimens. This suggests a drug-drug interaction between these two antibiotics resulting in an increased risk of AKI.

摘要

背景

万古霉素联合哌拉西林引起的急性肾损伤(AKI)过量存在争议。

目的

与其他万古霉素为基础的方案相比,检测万古霉素联合哌拉西林引起 AKI 风险增加的信号。

方法

利用世卫组织全球个体病例安全报告数据库(VigiBase),我们对 1997 年至 2019 年期间不同万古霉素方案(万古霉素联合哌拉西林、头孢吡肟或美罗培南)的 AKI 病例报告进行了比例失调分析。为了考虑可能的恶名偏见,我们还将研究期限限制在 2014 年之前,即首次发表接受万古霉素联合哌拉西林治疗的患者 AKI 的日期。结果用报告比值比(ROR)及其 95%置信区间表示。

结果

1997 年至 2019 年,数据库中登记了 53701 例万古霉素相关的个体病例安全报告,其中 6016 例 AKI 报告(11.2%),其中 925 例(15.4%)报告为万古霉素/哌拉西林,339 例(5.6%)报告为万古霉素/头孢吡肟,197 例(3.7%)报告为万古霉素/美罗培南。万古霉素/哌拉西林、万古霉素/头孢吡肟和万古霉素/美罗培南治疗 AKI 的 ROR(95%CI)分别为 2.6(2.4-2.8)、2.5(2.2-2.9)和 0.5(0.4-0.6)与其他含万古霉素的方案相比。将研究期限限制在 1997-2013 年,AKI 的 ROR 仅对万古霉素/哌拉西林有意义[ROR(95%CI)=2.1(1.8-2.4)]。

结论

我们发现接受万古霉素联合哌拉西林治疗的患者与其他方案相比,AKI 的报告存在比例失调。这表明这两种抗生素之间存在药物相互作用,导致 AKI 的风险增加。

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