Comparison of risk of acute kidney injury between patients receiving the combination of teicoplanin and piperacillin/tazobactam versus vancomycin and piperacillin/tazobactam

被引:7
作者
Shao, Chi-Hao [1 ]
Tai, Chih-Hsun [2 ]
Lin, Fang-Ju [1 ,2 ,3 ]
Wu, Chien-Chih [2 ,3 ]
Wang, Jann-Tay [4 ]
Wang, Chi-Chuan [1 ,2 ,3 ]
机构
[1] Natl Taiwan Univ, Coll Med, Grad Inst Clin Pharm, Taipei, Taiwan
[2] Natl Taiwan Univ Hopsital, Dept Pharm, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Internal Med, Div Infect Dis, Taipei, Taiwan
关键词
Teicoplanin; Vancomycin; Piperacillin/tazobactam; Acute kidney injury; LOADING REGIMEN; NEPHROTOXICITY; TAZOBACTAM; MANAGEMENT; GUIDELINES; SCORE;
D O I
10.1016/j.jfma.2021.02.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/purpose: To compare the risk of acute kidney injury (AKI) among patients receiving teicoplanin (TA) plus piperacillin/tazobactam (TZP) versus vancomycin (VAN) plus TZP. Methods: This was a retrospective cohort study using electronic health records. Patients were included if a combination of glycopeptide and TZP or other selected 3-lactams were used during hospitalization. In the main analysis, two study groups were identified: TA + TZP and VAN + TZP. We used 1:1 propensity score matching to control for potential confounders, and hazard ratio (HR) of AKI between study groups was calculated. We further compared the risk of AKI between patients receiving VAN + TZP and VAN + 3-lactams as an auxiliary analysis to verify the validity of the study design. Results: The final sample contained 211 pairs of patients receiving either TA + TZP or VAN + TZP. The median dosage of TA and VAN were 10.3 and 26.7 mg/kg/day, respectively. The median trough level of VAN was 12.3 mg/L. The AKI risk in the TA + TZP group was similar to that in the VAN + TZP group (12.3% vs. 11.4%; HR = 1.25 [0.72-2.18], p = 0.44). The auxiliary analysis showed a higher risk of AKI in the VAN + TZP group than in the VAN + 3-lactam group (13.2% vs. 9.6%; HR = 1.63 [1.04-2.55], p = 0.03). Conclusion: Our study results showed that the risk of AKI were similar for patients receiving TA + TZP and VAN + TZP. However, low VAN and high TA dose may play a role in this finding. Further investigation on the association between AKI and TA + TZP is required. Copyright (C) 2021, Formosan Medical Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:117 / 125
页数:9
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