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dc.contributor.authorAslan, Abdullah Tarik
dc.contributor.authorPashayev, Tural
dc.contributor.authorDağ, Osman
dc.contributor.authorAkova, Murat
dc.date.accessioned2019-12-10T11:10:00Z
dc.date.available2019-12-10T11:10:00Z
dc.date.issued2018
dc.identifier.issn2328-8957
dc.identifier.urihttps://doi.org/10.1093/ofid/ofy210.1242
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253424/
dc.identifier.urihttp://hdl.handle.net/11655/14786
dc.description.abstractBackground VAN has been shown to cause increased incidence of AKI when combined with TZP. The reason is unknown. TEI is a glycopeptide which may be less nephrotoxic. We compared both glycopeptides in combination with TZP or MER for causing AKI. Methods A retrospective cohort study was performed between May 2015 and December 2017 in a large tertiary care setting. Evaluation of AKI was made by using RIFLE criteria. Patients ≥18 years were included if they had a baseline serum creatinine available and received one of the combinations tested for at least 48 hours. Exclusion criteria were renal replacement therapy, pregnancy, <48 hours antibiotic therapy and no follow-up. Results Overall 456 patients were screened and 379 included in the study. After controlling for residual differences (age, Charlson comorbidity index score, presence of AKI, GFR value, presence of sepsis or septic shock, residing in intensive care unit at the time of antibiotic therapy and number of days of antibiotic therapy), AKI incidence was significantly higher in patients receiving TZP-VAN than those receiving TZP-TEI and also in patients receiving TZP-VAN than those with MER-VAN. No difference in AKI was detected between patients with MER-VAN and with MER-TEI (table). Mortality at 7 and 30 days and resolution of AKI at discharge were similar in all groups., Conclusion TZP causes increased nephrotoxicity when combined with VAN. Combination with TEI may offset this side effect. Additionally, the higher AKI incidence with TZP-VAN than MER-VAN may suggest a particular nephrotoxic synergy between TZP and VAN. Randomized controlled trials should confirm this observation. Disclosures All authors: No reported disclosures.
dc.relation.isversionof10.1093/ofid/ofy210.1242
dc.rightsinfo:eu-repo/semantics/openAccess
dc.title1411. Tecioplanin (Tei) Vs. Vancomycin (Van) In Combination With Piperacillin-Tazobactam (Tzp) Or Meropenem (Mer) As A Cause Of Acute Kidney Injury (Aki)
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalOpen Forum Infectious Diseases
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume5
dc.identifier.issueSuppl 1
dc.identifier.startpageS434
dc.identifier.endpageS435
dc.description.indexPubMed


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