Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/95194
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dc.contributor.authorSime, F.B.en
dc.contributor.authorRoberts, M.S.en
dc.contributor.authorTiong, I.S.en
dc.contributor.authorGardner, J.H.en
dc.contributor.authorLehman, S.en
dc.contributor.authorPeake, S.L.en
dc.contributor.authorHahn, U.en
dc.contributor.authorWarner, M.S.en
dc.contributor.authorRoberts, J.A.en
dc.date.issued2015en
dc.identifier.citationAntimicrobial Agents and Chemotherapy, 2015; 59(9):5463-5469en
dc.identifier.issn0066-4804en
dc.identifier.issn1098-6596en
dc.identifier.urihttp://hdl.handle.net/2440/95194-
dc.description.abstractWhile guidelines recommend empirical cefepime therapy in febrile neutropenia, the mortality benefit of cefepime has been controversial. In light of this, recent reports on pharmacokinetic changes for several antibiotics in febrile neutropenia and the consequent suboptimal exposure call for a pharmacokinetic/pharmacodynamic evaluation of current dosing. This study aimed to assess pharmacokinetic/pharmacodynamic target attainment from a 2-g intravenous (i.v.) every 8 h (q8h) cefepime regimen in febrile neutropenic patients with hematological malignancies. Cefepime plasma concentrations were measured in the 3rd, 6th, and 9th dosing intervals at 60% of the interval and/or trough point. The selected pharmacokinetic/pharmacodynamic targets were the proportion of the dosing interval (60% and 100%) for which the free drug concentration remains above the MIC (fT>MIC). Target attainment was assessed in reference to the MIC of isolated organisms if available or empirical breakpoints if not. The percentage of fT>MIC was also estimated by log-linear regression analysis. All patients achieved >60% fT>MIC in the 3rd and 6th dosing intervals. A 100% fT>MIC was not attained in 6/12, 4/10, and 4/9 patients in the 3rd, 6th, and 9th dose intervals, respectively, or in 14/31 (45%) of the dosing intervals investigated. On the other hand, 29/31 (94%) of trough concentrations were at or above 4 mg/liter. In conclusion, for patients with normal renal function, a high-dose 2-g i.v. q8h cefepime regimen appears to provide appropriate exposure if the MIC of the organism is ≤4 mg/liter but may fail to cover less susceptible organisms.en
dc.description.statementofresponsibilityFekade Bruck Sime, Michael S. Roberts, Ing Soo Tiong, Julia H. Gardner, Sheila Lehman, Sandra L. Peake, Uwe Hahn, Morgyn S. Warner, Jason A. Robertsen
dc.language.isoenen
dc.publisherAmerican Society for Microbiologyen
dc.rightsCopyright © 2015, American Society for Microbiology. All Rights Reserveden
dc.subjectHumans; Hematologic Neoplasms; Cephalosporins; Anti-Bacterial Agents; Microbial Sensitivity Tests; Aged; Middle Aged; Female; Male; Febrile Neutropenia; Cefepimeen
dc.titleAdequacy of high-dose cefepime regimen in febrile neutropenic patients with hematological malignanciesen
dc.typeJournal articleen
dc.identifier.rmid0030035611en
dc.identifier.doi10.1128/AAC.00389-15en
dc.identifier.pubid192272-
pubs.library.collectionMedicine publicationsen
pubs.library.teamDS07en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidTiong, I.S. [0000-0001-7417-4343]en
dc.identifier.orcidPeake, S.L. [0000-0001-6682-7973]en
dc.identifier.orcidWarner, M.S. [0000-0002-4053-1610]en
Appears in Collections:Medicine publications

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