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dc.contributor.authorWAREHAM, DWen_US
dc.date.accessioned2017-08-22T08:36:08Z
dc.date.available2017-07-27en_US
dc.date.submitted2017-08-09T10:03:30.372Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/25363
dc.description.abstractThe recent emergence of plasmid-mediated colistin resistance (1) highlights a new problem in the development of bacterial antimicrobial resistance. Colistin, while an old antibiotic, is increasingly turned to as a “drug of last resort” for many recalcitrant Gram-negative infections. With the efficacy of this drug now compromised, the spread of pan-resistant organisms is a very real threat. To meet this challenge clinicians are seeking new treatment options, however with a drug development pipeline that is virtually dry, an urgent rethinking of how we employ our existing arsenal of antibiotics is required to deal with this problem. Un-orthodox combinations of existing antimicrobial drugs are increasingly being used, often with little rationale on how such combinations are selected beyond the thinking that ‘more is likely to be better’ (2). There is a clear need for a precision medicine approach that combines robust laboratory testing methods with effective dosing strategies for individual patients.en_US
dc.format.extent? - ? (4)en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Laboratory and Precision Medicineen_US
dc.titleA Drug to Consider Re-purposing in the Targeted Treatment of Multi-drug Resistant Bacterial Infections?en_US
dc.typeArticle
dc.identifier.doi10.21037/jlpm.2017.06.18en_US
pubs.author-urlhttp://10.0.82.45/jlpm.2017.06.18en_US
pubs.issue49en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublished onlineen_US
pubs.volume2en_US
dcterms.dateAccepted2017-07-27en_US


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