Full metadata record
DC FieldValueLanguage
dc.contributor.authorSyue, Ling-Shanen_US
dc.contributor.authorChen, Yen-Hsuen_US
dc.contributor.authorKo, Wen-Chienen_US
dc.contributor.authorHsueh, Po-Renen_US
dc.date.accessioned2017-04-21T06:55:42Z-
dc.date.available2017-04-21T06:55:42Z-
dc.date.issued2016-04en_US
dc.identifier.issn0924-8579en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ijantimicag.2015.12.021en_US
dc.identifier.urihttp://hdl.handle.net/11536/133673-
dc.description.abstractThe continuing increase in multidrug-resistant organisms (MDROs) worldwide has created new challenges in treating complicated intra-abdominal infections (cIAIs). A number of novel antimicrobial agents have been developed against resistant pathogens. To target extended-spectrum beta-lactamase (ESBL)-producing pathogens, novel beta-lactam antibiotics, such as ceftolozane/tazobactam, ceftazidime/avibactam, aztreonam/avibactam, imipenem/relebactam and S-649266, are antimicrobial alternatives for cIAIs. Two new drugs, eravacycline and plazomicin, have activity against Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae, carbapenem-resistant Acinetobacter baumannii and ESBL-producers. New lipoglycopeptides and oxazolidinones provide feasible options against resistant Gram-positive pathogens. These novel antimicrobials may play a role in improving the clinical outcomes of cIAIs caused by MDROs. (C) 2016 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectIntra-abdominal infectionsen_US
dc.subjectAntimicrobial resistanceen_US
dc.subjectCeftolozaneen_US
dc.subjectAvibactamen_US
dc.subjectEravacyclineen_US
dc.subjectPlazomicinen_US
dc.titleNew drugs for the treatment of complicated intra-abdominal infections in the era of increasing antimicrobial resistanceen_US
dc.identifier.doi10.1016/j.ijantimicag.2015.12.021en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTSen_US
dc.citation.volume47en_US
dc.citation.issue4en_US
dc.citation.spage250en_US
dc.citation.epage258en_US
dc.contributor.department生醫工程研究所zh_TW
dc.contributor.departmentInstitute of Biomedical Engineeringen_US
dc.identifier.wosnumberWOS:000373854500002en_US
Appears in Collections:Articles