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    TMP-SMX Effect(s) on Renal Function and Population Factors that may increase the risk of AKI

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    PHR_2021_Group62_Poster.pdf
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    Description:
    Poster
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    PHR_2021_Group62_Report.pdf
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    Report
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    Author
    Myslinski, Britt T.
    Root, Kyle
    Guzman, Alex
    Affiliation
    College of Pharmacy, The University of Arizona
    Issue Date
    2021
    Keywords
    Chart review
    acute kidney injury
    Retrospective chart review
    nephrotoxic drugs
    trimethoprim/sulfamethoxazole
    MeSH Subjects
    Trimethoprim, Sulfamethoxazole Drug Combination
    Advisor
    Nix, David
    
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    Rights
    Copyright © is held by the author.
    Collection Information
    This item is part of the Pharmacy Student Research Projects collection, made available by the College of Pharmacy and the University Libraries at the University of Arizona. For more information about items in this collection, please contact Jennifer Martin, Librarian and Clinical Instructor, Pharmacy Practice and Science, jenmartin@email.arizona.edu.
    Publisher
    The University of Arizona.
    Abstract
    Specific Aims: To explore what patient specific factors may predispose an individual to experiencing a true Acute Kidney Injury (AKI) with Sulfamethoxazole Trimethoprim (TMP/SMX) in the first 10 days of treatment. The findings then can be used by providers to better differentiate a true AKI from pseudo renal failure when they notice an increase in serum creatinine (sCr) due to TMP/SMX. Subjects: Patients will be included in the study if they are: adults (18 years of age or older), who at the time of TMP/SMX initiation had stable renal function and received a TMP/SMX dose of ≥ 160mg/800mg for at least 72 hours. Methods: Using the facility’s electronic health record system (Cerner) we generated a report of patients who received a minimum daily dose of TMP ≥320 mg and were discharged between March 01 2020 and August 31 2020. Main Results: Of the 102 patients screened from Banner University Medical Center Tucson that we screened 23 patients met our inclusion criteria. AKI was found in 8 of the 23 subjects and was more common with increased comorbidities, nephrotoxic drugs, and contrast agents, supporting current literature. Conclusions: In our 8 subjects with AKI, we found that occurrence of AKI occurred in the setting of multiple comorbidities and/or with nephrotoxic agents.
    Description
    Class of 2021 Abstract, Report and Poster
    Collections
    Pharmacy Student Research Projects

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