<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T02:52:17Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/107149" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/107149</identifier><datestamp>2025-03-18T15:36:07Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Cidal activity of oral third-generation cephalosporins against Streptococcus pneumoniae in relation to cefotaxime intrinsic activity</dc:title>
   <dc:creator>Cafini, Fabio</dc:creator>
   <dc:creator>Aguilar, Lorenzo</dc:creator>
   <dc:creator>Alou Cervera, Luis</dc:creator>
   <dc:creator>Giménez, María José</dc:creator>
   <dc:creator>Sevillano Fernández, David</dc:creator>
   <dc:creator>Torrico, Martha</dc:creator>
   <dc:creator>González Hidalgo, Natalia</dc:creator>
   <dc:creator>Granizo, Juan José</dc:creator>
   <dc:creator>Martín Herrero, José Emilio</dc:creator>
   <dc:creator>Prieto Prieto, José</dc:creator>
   <dc:subject>611.02</dc:subject>
   <dc:subject>Ceftriaxone</dc:subject>
   <dc:subject>Cefotaxime</dc:subject>
   <dc:subject>Cefixime</dc:subject>
   <dc:subject>Cefpodoxime</dc:subject>
   <dc:subject>Initial Inoculum</dc:subject>
   <dc:subject>Microbiología médica</dc:subject>
   <dc:subject>2414 Microbiología</dc:subject>
   <dc:description>This study explores the killing kinetics within 12 h of four oral third-generation cephalosporins against ten Streptococcus pneumoniae strains exhibiting cefotaxime minimum inhibitory concentrations (MICs) from 0.03 to 2 microg/ml. Killing curves were performed with concentrations achievable in serum after standard doses (0.015-4 microg/ml). Reductions of 90% were achieved with all compounds at serum-achievable concentrations for strains exhibiting cefotaxime MIC &lt; or = 0.5 microg/ml. Against strains with cefotaxime MIC > or = 1 microg/ml, only cefditoren reached a 90% reduction with concentrations of 0.5-1 microg/ml doses. At 4 microg/ml, cefditoren and cefotaxime reached 99.9% reduction in seven of the ten strains studied. At serum-achievable concentrations, cefdinir and cefixime were not bactericidal against strains exhibiting cefotaxime MIC > or = 0.25 microg/ml and > or = 0.5 microg/ml, respectively. Cefditoren showed the best killing kinetic profiles and this observation may be important when choosing an oral third-generation cephalosporin as initial or sequential therapy</dc:description>
   <dc:description>GlaxoSmithKline S.A.</dc:description>
   <dc:description>Depto. de Medicina</dc:description>
   <dc:description>Fac. de Medicina</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-07-29T08:31:50Z</dc:date>
   <dc:date>2024-07-29T08:31:50Z</dc:date>
   <dc:date>2008-02-26</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>VoR</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/107149</dc:identifier>
   <dc:identifier>0934-9723</dc:identifier>
   <dc:identifier>10.1007/s10096-008-0493-7</dc:identifier>
   <dc:identifier>1435-4373</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Cafini F, Aguilar L, Alou L, Giménez MJ, Sevillano D, Torrico M, González N, Granizo JJ, Martín-Herrero JE, Prieto J. Cidal activity of oral third-generation cephalosporins against Streptococcus pneumoniae in relation to cefotaxime intrinsic activity. Eur J Clin Microbiol Infect Dis. 2008 Aug;27(8):679-83.</dc:relation>
   <dc:rights>restricted access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Springer</dc:publisher>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>