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dc.contributor.authorTiberi, Sen_US
dc.contributor.authorBuchanan, Ren_US
dc.contributor.authorCaminero, JAen_US
dc.contributor.authorCentis, Ren_US
dc.contributor.authorArbex, MAen_US
dc.contributor.authorSalazar, Men_US
dc.contributor.authorPotter, Jen_US
dc.contributor.authorMigliori, GBen_US
dc.date.accessioned2017-05-11T11:10:34Z
dc.date.available2017-01-19en_US
dc.date.issued2017-03en_US
dc.date.submitted2017-02-15T13:19:09.440Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/23032
dc.description.abstractTuberculosis (TB) continues to cause more deaths worldwide than any other single infectious disease. Even though tuberculosis appears to be decreasing in incidence globally for some time, the proportion of drug resistance is increasing, contributing to greater complexity, morbidity and mortality as well as cost. Since the advent of rifampicin in the 1960s, and the implementation of standard quadruple anti-tuberculosis regimen in the late 1970s, no new drugs have been changed the first line regimen. This regimen is effective however it is pill burden, and duration has not received investment and innovation. Drug-resistant regimens are long and frequently poorly tolerated due to significant toxicity. This review is an update on what is new in the treatment of drug-susceptible and drug-resistant tuberculosis, new TB drugs currently being used and studied in clinical trials are also mentioned. Fortunately, there have been many significant advances in this field in recent years. The horizon is changing with the new WHO shorter multidrug-resistant tuberculosis regimens and with the increasing availability of new or repurposed drugs like bedaquiline, delamanid, clofazimine and linezolid. These drugs pose new challenges relating to their rational use to prevent selection of resistant strains of Mycobacterium tuberculosis even before a new regimen has been studied. The availability of these new drugs is offering hope and new possibilities for saving patients who had few or no treatment options. Their use and combination into effective regimens need to be studied; trials are in progress. It is hoped that soon we will be able to treat sensitive and drug-resistant cases with a universal regimen, this would revolutionise treatment and take us another step closer towards elimination.en_US
dc.format.extente41 - e51en_US
dc.languagefreen_US
dc.relation.ispartofPresse Meden_US
dc.rights© 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAntitubercular Agentsen_US
dc.subjectDisease Managementen_US
dc.subjectDrug Repositioningen_US
dc.subjectDrug Resistance, Multiple, Bacterialen_US
dc.subjectDrug Therapy, Combinationen_US
dc.subjectForecastingen_US
dc.subjectHumansen_US
dc.subjectMycobacterium tuberculosisen_US
dc.subjectPractice Guidelines as Topicen_US
dc.subjectSelection, Geneticen_US
dc.subjectTherapies, Investigationalen_US
dc.subjectTreatment Outcomeen_US
dc.subjectTuberculosisen_US
dc.subjectTuberculosis, Multidrug-Resistanten_US
dc.subjectWorld Health Organizationen_US
dc.titleThe challenge of the new tuberculosis drugs.en_US
dc.typeArticle
dc.rights.holderCopyright © 2017 Elsevier Masson SAS. All rights reserved.
dc.identifier.doi10.1016/j.lpm.2017.01.016en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28256383en_US
pubs.issue2 Pt 2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume46en_US
dcterms.dateAccepted2017-01-05en_US
qmul.funderPopulation Health Scientist Doctoral Fellowship::Medical Research Councilen_US


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