dc.date.accessioned2019-02-06T14:59:06Z
dc.date.available2019-02-06T14:59:06Z
dc.date.created2019-02-06T14:59:06Z
dc.date.issued2015
dc.identifierhttps://hdl.handle.net/20.500.12866/5535
dc.identifierhttps://doi.org/10.1016/S0140-6736(14)62450-8
dc.description.abstractBedaquiline and delamanid, novel classes of anti-tuberculosis drugs, have been recently approved for the treatment of multidrug-resistant tuberculosis. Antimicrobial resistance invariably follows the introduction of new drugs, and appropriate drug-susceptibility testing assays are needed to detect resistance and tailor treatment regimens that contain new agents. Given that phenotypic drug-susceptibility testing is slow, technically demanding, and, in some cases, unreliable, future assays are likely to be based on rapid molecular techniques. To design such assays, research to unravel the genetic basis of resistance is urgently required (appendix). The question is how to ensure that this research occurs in a timely way, before the emergence and spread of resistance.
dc.languageeng
dc.publisherElsevier
dc.relationLancet
dc.relation1474-547X
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectHumans
dc.subjectAntitubercular Agents/therapeutic use
dc.subjectDiarylquinolines/therapeutic use
dc.subjectDrug Approval
dc.subjectMutation/genetics
dc.subjectNitroimidazoles/therapeutic use
dc.subjectOxazoles/therapeutic use
dc.subjectTuberculosis, Multidrug-Resistant/genetics/prevention & control
dc.titleDrug-resistance mechanisms and tuberculosis drugs
dc.typeinfo:eu-repo/semantics/article


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