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Published on: August 30, 2018
Nephrotoxicity of concomitant piperacillin/tazobactam and teicoplanin compared with monotherapy
J D Workum1,2, C Kramers2, E Kolwijck3,4
1Department of Intensive Care, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, The Netherlands.
Objectives:
Piperacillin/tazobactam combined with vancomycin has been associated with a decline in renal function when compared with monotherapy. Teicoplanin is a glycopeptide similar to vancomycin. We investigated whether piperacillin/tazobactam combined with teicoplanin is associated with a decline in renal function as well.
Methods:
We conducted a single-centre retrospective cohort study with data from our electronic health records from 9 August 2013 to 15 November 2019, including all adult patients that received either piperacillin/tazobactam, teicoplanin or piperacillin/tazobactam + teicoplanin. The incidence of acute kidney injury (AKI) at 48-72 h served as the primary outcome, whereas change in serum creatinine served as a secondary outcome.
Results:
Of the 4202 included patients, 3188 (75.9%) received piperacillin/tazobactam, 791 (18.8%) received teicoplanin and 223 (5.3%) received piperacillin/tazobactam + teicoplanin. The incidence of AKI at 48-72 h after commencement of antibiotic therapy was 5.4% for piperacillin/tazobactam, 3.4% for teicoplanin and 11.7% for piperacillin/tazobactam + teicoplanin (P < 0.001). However, mean serum creatinine at 48-72 h was slightly higher in the piperacillin/tazobactam + teicoplanin group therapy compared with baseline [+1.61% (95% CI -2.25 to 5.70)], indicating a slight decrease in renal function, and decreased for piperacillin/tazobactam [-1.98% (95% CI -2.73 to -1.22)] and teicoplanin [-8.01% (95% CI -9.54 to -6.45)]. After correcting for significant confounders in a multivariate linear regression analysis, these patterns remained.
Conclusions:
Our study suggests that piperacillin/tazobactam + teicoplanin is associated with a higher prevalence of AKI compared with monotherapy. However, as the overall decline in renal function with piperacillin/tazobactam + teicoplanin is very small, its clinical relevance is likely limited. Therefore, piperacillin/tazobactam + teicoplanin can probably be safely combined.
Insights
Combining piperacillin/tazobactam with teicoplanin may increase acute kidney injury (AKI) risk. However, the overall impact on renal function is minimal, suggesting this combination is likely safe for patients.
Area of Science:
- Pharmacology
- Nephrology
- Infectious Diseases
Background:
- Piperacillin/tazobactam combined with vancomycin is linked to reduced renal function.
- Teicoplanin, a vancomycin analog, is used in similar clinical scenarios.
- The renal safety of combining piperacillin/tazobactam with teicoplanin requires investigation.
Purpose of the Study:
- To evaluate the association between piperacillin/tazobactam plus teicoplanin combination therapy and renal function decline.
- To compare the incidence of acute kidney injury (AKI) between monotherapy and combination therapy.
Main Methods:
- A retrospective cohort study analyzed data from 4202 adult patients.
- Patients received piperacillin/tazobactam, teicoplanin, or the combination therapy.
- Primary outcome was AKI incidence at 48-72 hours; secondary outcome was serum creatinine change.
Main Results:
- The incidence of AKI was 11.7% for piperacillin/tazobactam + teicoplanin, versus 5.4% for piperacillin/tazobactam and 3.4% for teicoplanin.
- A slight increase in serum creatinine was observed with the combination therapy (+1.61%), while monotherapy showed a decrease.
- These trends persisted after adjusting for confounders.
Conclusions:
- Piperacillin/tazobactam + teicoplanin is associated with a higher AKI prevalence than monotherapy.
- The clinical significance of the observed renal function decline with combination therapy appears limited.
- The combination of piperacillin/tazobactam and teicoplanin is likely safe for clinical use.
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