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      Co-administration of vancomycin and piperacillin-tazobactam is associated with increased renal dysfunction in adult and pediatric burn patients

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          Abstract

          Background

          Burn patients are prone to infections which often necessitate broad antibiotic coverage. Vancomycin is a common antibiotic after burn injury and is administered alone (V), or in combination with imipenem-cilastin (V/IC) or piperacillin-tazobactam (V/PT). Sparse reports indicate that the combination V/PT is associated with increased renal dysfunction. The purpose of this study was to evaluate the short-term impact of the three antibiotic administration types on renal dysfunction.

          Methods

          All pediatric and adult patients admitted to our centers between 2004 and 2016 with a burn injury were included in this retrospective review if they met the criteria of exposition to either V, V/IC, or V/PT for at least 48 h, had normal baseline creatinine, and no pre-existing renal dysfunction. Creatinine was monitored for 7 days after initial exposure; the absolute and relative increase was calculated, and patient renal outcomes were classified according to the Kidney Disease Improving Global Outcomes (KDIGO) criteria depending on creatinine increases and estimated creatinine clearance. Secondary endpoints (demographic and clinical data, incidences of septicemia, and renal replacement therapy) were analyzed. Antibiotic doses were modeled in logistic and linear multivariable regression models to predict categorical KDIGO events and relative creatinine increase.

          Results

          Out of 1449 patients who were screened, 718 met the inclusion criteria, 246 were adults, and 472 were children. Between the study cohorts V, V/IC, and V/PT, patient characteristics at admission were comparable. V/PT administration was associated with a statistically higher serum creatinine, and lower creatinine clearance compared to patients receiving V alone or V/IC in adults and children after burn injury. The incidence of KDIGO stages 1, 2, and 3 was higher after V/PT treatment. In children, the incidence of KDIGO stage 3 following administration of V/PT was greater than after V/IC. In adults, the incidence of renal replacement therapy was higher after V/PT compared with V or V/IC. Multivariate modeling demonstrated that V/PT is an independent predictor of renal dysfunction.

          Conclusion

          Co-administration of vancomycin and piperacillin-tazobactam is associated with increased renal dysfunction in pediatric and adult burn patients when compared to vancomycin alone or vancomycin plus imipenem-cilastin. The mechanism of this increased nephrotoxicity remains elusive and warrants further scientific evaluation.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13054-017-1899-3) contains supplementary material, which is available to authorized users.

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          Most cited references41

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          Prediction of Creatinine Clearance from Serum Creatinine

          A formula has been developed to predict creatinine clearance (C cr ) from serum creatinine (S cr ) in adult males: Ccr = (140 – age) (wt kg)/72 × S cr (mg/100ml) (15% less in females). Derivation included the relationship found between age and 24-hour creatinine excretion/kg in 249 patients aged 18–92. Values for C cr were predicted by this formula and four other methods and the results compared with the means of two 24-hour C cr’s measured in 236 patients. The above formula gave a correlation coefficient between predicted and mean measured Ccr·s of 0.83; on average, the difference between predicted and mean measured values was no greater than that between paired clearances. Factors for age and body weight must be included for reasonable prediction.
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            Creatinine kinetics and the definition of acute kidney injury.

            Acute kidney injury (AKI) is a common and devastating medical condition, but no widely accepted definition exists. A recent classification system by the Acute Dialysis Quality Initiative (RIFLE) defines AKI largely by percentage increases in serum creatinine (SCr) over baseline. The Acute Kidney Injury Network defines the first stage by either an absolute or a percentage increase in SCr. To examine the implications of various definitions, we solved differential equations on the basis of mass balance principles. We simulated creatinine kinetics after AKI in the setting of normal baseline kidney function and stages 2, 3, and 4 chronic kidney disease (CKD). The percentage changes in SCr after severe AKI are highly dependent on baseline kidney function. Twenty-four hours after a 90% reduction in creatinine clearance, the rise in SCr was 246% with normal baseline kidney function, 174% in stage 2 CKD, 92% in stage 3 CKD, and only 47% in stage 4 CKD. By contrast, the absolute increase was nearly identical (1.8 to 2.0 mg/dl) across the spectrum of baseline kidney function. Time to reach a 50% increase in SCr was directly related to baseline kidney function: From 4 h (normal baseline) up to 27 h for stage 4 CKD. By contrast, the time to reach a 0.5-mg/dl increase in SCr was virtually identical after moderate to severe AKI (>50% reduction in creatinine clearance). We propose an alternative definition of AKI that incorporates absolute changes in SCr over a 24- to 48-h time period.
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              Management of multidrug-resistant organisms in health care settings, 2006.

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                Author and article information

                Contributors
                (409) 770-6744 , gabrielhundeshagen@gmail.com
                dherndon@utmb.edu
                kdcapek@utmb.edu
                lubransk@utmb.edu
                cdvoigt@gmail.com
                killion@bcm.edu
                j.cambiaso.daniel@gmail.com
                misljivi@UTMB.EDU
                ajdecres@UTMB.EDU
                rmlcak@UTMB.EDU
                mkinsky@utmb.edu
                ccfinner@utmb.edu
                wbnorbur@utmb.edu
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                20 December 2017
                20 December 2017
                2017
                : 21
                : 318
                Affiliations
                [1 ]ISNI 0000 0001 1547 9964, GRID grid.176731.5, Department of Surgery, , University of Texas Medical Branch, ; 301 University Blvd., Galveston, TX 77555 USA
                [2 ]ISNI 0000 0004 0449 5549, GRID grid.412705.5, Shriners Hospitals for Children, ; 815 Market St., Galveston, TX 77550 USA
                [3 ]ISNI 0000 0001 2190 4373, GRID grid.7700.0, Department of Hand, Plastic and Reconstructive Surgery, Burn Trauma Center, BG Trauma Center Ludwigshafen, , University of Heidelberg, ; Ludwig-Guttmann-Str. 13, 67071 Ludwigshafen, Germany
                [4 ]ISNI 0000 0001 2160 926X, GRID grid.39382.33, Department of Plastic Surgery, , Baylor College of Medicine, ; 1 Baylor Plaza, Houston, TX 77030 USA
                [5 ]ISNI 0000 0000 8988 2476, GRID grid.11598.34, Division of Plastic, Aesthetic and Reconstructive Surgery, Department of Surgery, , Medical University of Graz, ; Graz, Austria
                [6 ]ISNI 0000 0001 1547 9964, GRID grid.176731.5, Department of Anesthesiology, , University of Texas Medical Branch, ; 301 University Blvd., Galveston, TX 77555 USA
                Author information
                http://orcid.org/0000-0002-6173-8602
                Article
                1899
                10.1186/s13054-017-1899-3
                5738705
                f7a865ac-32cd-4499-99ce-88af59fa2120
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 August 2017
                : 28 November 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: T32 GM008256
                Award ID: GM060338
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006108, National Center for Advancing Translational Sciences;
                Award ID: UL1TR000071
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100011781, Shriners Hospitals for Children;
                Award ID: 84080, 71008, 80100, 71000
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Emergency medicine & Trauma
                Emergency medicine & Trauma

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