Abstract

BackgroundAcute kidney injury (AKI) occurs frequently in hospitalized patients and has been associated with the administration of certain medications. Concerns have been raised in recent reports that the antibiotic combination of vancomycin and piperacillin/tazobactam (combV/P) may be more associated with AKI than monotherapy with either drug.MethodsTo compare the incidence of and risk factors for AKI in patients receiving combV/P versus monotherapy with either drug, a retrospective study was conducted in non-critically ill inpatients at a large urban teaching hospital. AKI was defined as either: (1) Increase in serum creatinine ≥0.5 mg/dl OR (2) ≥1.5-fold creatinine increase from admission baseline. In addition to standard multivariable regression adjustment, propensity score weighting was used as a robust approach to reduce the effects of covariate confounding when estimating the adjusted odds of AKI.ResultsA total of 228 patients were evaluated. The overall incidence of AKI was 11.8 % (27 of 228 patients). AKI occurred in 4 of 101 patients in the vanc group (4.0 %), 4 of 26 patients in the piptazo group (15.4 %), and 19 of 101 patients in the combV/P group (18.8 %). The univariable odds of AKI was significantly lower in the vanc group compared to both the combV/P group (OR 0.178, 95 % CI 0.058–0.544, p = 0.003) and piptazo (OR 0.227, 95 % CI 0.053–0.978, p = 0.047) group. A multivariable model accounting for baseline characteristics again showed that vanc monotherapy was associated with lower odds of AKI than combV/P (OR 0.14, 95 % CI 0.04–0.52, p = 0.004). Male sex was also associated with lower odds of AKI (OR 0.28, 95 % CI 0.10–0.79, p = 0.02) in the multivariable model. In the propensity score analysis using inverse probability of treatment weighting (IPTW), vanc monotherapy and male sex were again associated with lower odds of AKI (OR 0.17; 95 % CI 0.04–0.62, p = 0.008 and OR 0.28, 95 % CI 0.09–0.89, p = 0.03, respectively).ConclusionThis study substantiates recent reports that combV/P may be more associated with AKI than vanc monotherapy in hospital inpatients. AKI also appears to be more likely in females during therapy with these antimicrobials. While severity of illness is difficult to account for, these findings are further justification for narrowing antibiotic coverage when possible after this combination has been initiated in hospitalized patients.

Highlights

  • Acute kidney injury (AKI) occurs frequently in hospitalized patients and has been associated with the administration of certain medications

  • While studies focusing on intensive care unit (ICU) patients suggest that AKI may be associated with comb V/P, ICU patients have many confounders that increase their risk for AKI, including hypotension and shock [11]

  • A total of 1172 patients were reviewed. 944 patients met exclusion criteria (586 patients were excluded due to ICU or intermediate care unit transfer, 353 patients received antibiotics for less than 48 h, and 5 patients were excluded due to hemodialysis receipt).a total of 228 patients were identified after review of 26 months of inpatient admissions: 101 patients on vanc monotherapy, 26 patients on piptazo monotherapy, and 101 patients on combination of vancomycin and piperacillin/tazobactam (combV/P)

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Summary

Introduction

Acute kidney injury (AKI) occurs frequently in hospitalized patients and has been associated with the administration of certain medications. Concerns have been raised in recent reports that the antibiotic combination of vancomycin and piperacillin/tazobactam (combV/P) may be more associated with AKI than monotherapy with either drug. Two antibiotics that are commonly used in hospitalized patients are vancomycin (vanc) for gram positive coverage and piperacillin/tazobactam (piptazo) for gram negative coverage. These two antimicrobials are often used in combination [8]. Given that nephrotoxicity has been associated with each of these antimicrobials [9, 10], we sought to determine if the risk of AKI is higher during combination vanc + piptazo therapy (combV/P) than during monotherapy with either agent in non-critically ill hospitalized patients. Similar evidence from the non-critically ill hospitalized population has been heretofore lacking but is needed given that typically less than 10 % of hospitalized patients are admitted to intensive care units [12]

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