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Isolation and Chemical Characterization of Lipid A from Gram-negative Bacteria
Published on: September 16, 2013
Impact of piperacillin/tazobactam on nephrotoxicity in patients with Gram-negative bacteraemia
Ronald G Hall1, Eunice Yoo2, Andrew Faust3
1Texas Tech University Health Sciences Center, Department of Pharmacy Practice, 5920 Forest Park Road, Suite 400, Dallas, TX 75235, USA; VA North Texas Health Care System, 4500 S. Lancaster Road, Dallas, TX 75216, USA; University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA; Dose Optimization and Outcomes Research (DOOR) Program, 5920 Forest Park Road, Suite 400, Dallas, TX 75235, USA.
Abstract:
Piperacillin/tazobactam (TZP) has been associated with nephrotoxicity in patients receiving vancomycin. Its impact on nephrotoxicity in patients with Gram-negative bacteraemia (GNB) is unclear. This study evaluated the impact of TZP on nephrotoxicity in patients with GNB. This retrospective cohort included patients aged ≥18 years receiving ≥48 h of therapy for bacteraemia due to Escherichia coli, Pseudomonas aeruginosa, Enterobacter, Klebsiella, Acinetobacter or Stenotrophomonas maltophilia from 1/01/2008-8/31/2011. Patients with baseline serum creatinine (SCr) ≥3.5 mg/dL, polymicrobial infection or recurrent bacteraemia were excluded. Nephrotoxicity was defined as a ≥0.5 mg/dL increase in SCr or ≥50% increase from baseline for ≥2 consecutive days. Any variable demonstrating a 10% change in exposure effect was retained in the final model. All variables biologically reasonable causes of nephrotoxicity were also considered for inclusion. The median age of the cohort (n = 292) was 76 years; 38.0% had a cancer diagnosis and ICU residence was common (21.9%). There was no difference in nephrotoxicity incidence based on days of TZP received (0 days, 13.6%; 1-2 days, 14.7%; 3-4 days, 6.9%; ≥5 days, 16.7%; P = 0.71). In multivariable analysis, baseline SCr, total body weight and vasopressor use were independently associated with nephrotoxicity. Duration of TZP was not associated with nephrotoxicity in multivariable analysis (1-2 days, OR = 0.91, 95% CI 0.39-2.12; 3-4 days, OR = 0.48, 95% CI 0.10-2.46; ≥5 days, OR = 0.57, 95% CI 0.11-3.02). In this cohort of GNB patients, duration of TZP was not associated with nephrotoxicity.
Insights
Piperacillin/tazobactam (TZP) did not increase nephrotoxicity in Gram-negative bacteraemia patients. Study found no link between TZP duration and kidney injury, suggesting it
Area of Science:
- Pharmacology
- Nephrology
- Infectious Diseases
Background:
- Piperacillin/tazobactam (TZP) is linked to nephrotoxicity when co-administered with vancomycin.
- The impact of TZP on kidney injury in Gram-negative bacteraemia (GNB) patients remains unclear.
Purpose of the Study:
- To evaluate the association between piperacillin/tazobactam (TZP) use and nephrotoxicity in patients with Gram-negative bacteraemia (GNB).
Main Methods:
- Retrospective cohort study of 292 adult patients with GNB treated with TZP.
- Nephrotoxicity defined as a ≥0.5 mg/dL or ≥50% increase in serum creatinine.
- Multivariable analysis adjusted for baseline SCr, body weight, and vasopressor use.
Main Results:
- No significant difference in nephrotoxicity incidence was observed across different durations of TZP exposure.
- Multivariable analysis revealed baseline SCr, body weight, and vasopressor use as independent predictors of nephrotoxicity.
- Duration of TZP therapy was not associated with an increased risk of nephrotoxicity in GNB patients.
Conclusions:
- In patients with Gram-negative bacteraemia, the duration of piperacillin/tazobactam (TZP) therapy was not associated with an increased risk of nephrotoxicity.
- Factors such as baseline kidney function, body weight, and vasopressor use are more critical in predicting nephrotoxicity in this population.
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