Management of patients with multidrug-resistant tuberculosis
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/10216/154103 |
Resumo: | The emergence of multidrug-resistant tuberculosis (MDR-TB; defined as resistance to at least rifampicin and isoniazid) represents a growing threat to public health and economic growth. Never before in the history of mankind have more patients been affected by MDR-TB than is the case today. The World Health Organization reports that MDR-TB outcomes are poor despite staggeringly high management costs. Moreover, treatment is prolonged, adverse events are common, and the majority of affected patients do not receive adequate treatment. As MDR-TB strains are often resistant to one or more second-line anti-TB drugs, in-depth genotypic and phenotypic drug susceptibility testing is needed to construct personalised treatment regimens to improve treatment outcomes. For the first time in decades, the availability of novel drugs such as bedaquiline allow us to design potent and well-tolerated personalised MDR-TB treatment regimens based solely on oral drugs. In this article, we present management guidance to optimise the diagnosis, algorithm-based treatment, drug dosing and therapeutic drug monitoring, and the management of adverse events and comorbidities, associated with MDR-TB. We also discuss the role of surgery, physiotherapy, rehabilitation, palliative care and smoking cessation in patients with MDR-TB. We hope that incorporating these recommendations into patient care will be helpful in optimising treatment outcomes, and lead to more MDR-TB patients achieving a relapse-free cure. |
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Management of patients with multidrug-resistant tuberculosisMDR-TB; RESIST-TB; TBNET; TB; XDR-TB; personalised treatmentThe emergence of multidrug-resistant tuberculosis (MDR-TB; defined as resistance to at least rifampicin and isoniazid) represents a growing threat to public health and economic growth. Never before in the history of mankind have more patients been affected by MDR-TB than is the case today. The World Health Organization reports that MDR-TB outcomes are poor despite staggeringly high management costs. Moreover, treatment is prolonged, adverse events are common, and the majority of affected patients do not receive adequate treatment. As MDR-TB strains are often resistant to one or more second-line anti-TB drugs, in-depth genotypic and phenotypic drug susceptibility testing is needed to construct personalised treatment regimens to improve treatment outcomes. For the first time in decades, the availability of novel drugs such as bedaquiline allow us to design potent and well-tolerated personalised MDR-TB treatment regimens based solely on oral drugs. In this article, we present management guidance to optimise the diagnosis, algorithm-based treatment, drug dosing and therapeutic drug monitoring, and the management of adverse events and comorbidities, associated with MDR-TB. We also discuss the role of surgery, physiotherapy, rehabilitation, palliative care and smoking cessation in patients with MDR-TB. We hope that incorporating these recommendations into patient care will be helpful in optimising treatment outcomes, and lead to more MDR-TB patients achieving a relapse-free cure.International Union Against Tuberculosis and Lung Disease20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/154103eng1027-37191815-792010.5588/ijtld.18.0622Lange, CAarnoutse, REAlffenaar, JWCBothamley, GBrinkmann, FCosta, JChesov, Dvan Crevel, RDedicoat, MDominguez, JDuarte, RGrobbel, HPGunther, GGuglielmetti, LHeyckendorf, JKay, AWKirakosyan, OKirk, OKoczulla, RAKudriashov, GGKuksa, Lvan Leth, FMagis-Escurra, CMandalakas, AMMolina-Moya, BPeloquin, CAReimann, MRumetshofer, RSchaaf, HSSchon, TTiberi, SValda, JYablonskii, PKDheda, Kinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T14:19:32Zoai:repositorio-aberto.up.pt:10216/154103Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:58:56.010624Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Management of patients with multidrug-resistant tuberculosis |
title |
Management of patients with multidrug-resistant tuberculosis |
spellingShingle |
Management of patients with multidrug-resistant tuberculosis Lange, C MDR-TB; RESIST-TB; TBNET; TB; XDR-TB; personalised treatment |
title_short |
Management of patients with multidrug-resistant tuberculosis |
title_full |
Management of patients with multidrug-resistant tuberculosis |
title_fullStr |
Management of patients with multidrug-resistant tuberculosis |
title_full_unstemmed |
Management of patients with multidrug-resistant tuberculosis |
title_sort |
Management of patients with multidrug-resistant tuberculosis |
author |
Lange, C |
author_facet |
Lange, C Aarnoutse, RE Alffenaar, JWC Bothamley, G Brinkmann, F Costa, J Chesov, D van Crevel, R Dedicoat, M Dominguez, J Duarte, R Grobbel, HP Gunther, G Guglielmetti, L Heyckendorf, J Kay, AW Kirakosyan, O Kirk, O Koczulla, RA Kudriashov, GG Kuksa, L van Leth, F Magis-Escurra, C Mandalakas, AM Molina-Moya, B Peloquin, CA Reimann, M Rumetshofer, R Schaaf, HS Schon, T Tiberi, S Valda, J Yablonskii, PK Dheda, K |
author_role |
author |
author2 |
Aarnoutse, RE Alffenaar, JWC Bothamley, G Brinkmann, F Costa, J Chesov, D van Crevel, R Dedicoat, M Dominguez, J Duarte, R Grobbel, HP Gunther, G Guglielmetti, L Heyckendorf, J Kay, AW Kirakosyan, O Kirk, O Koczulla, RA Kudriashov, GG Kuksa, L van Leth, F Magis-Escurra, C Mandalakas, AM Molina-Moya, B Peloquin, CA Reimann, M Rumetshofer, R Schaaf, HS Schon, T Tiberi, S Valda, J Yablonskii, PK Dheda, K |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Lange, C Aarnoutse, RE Alffenaar, JWC Bothamley, G Brinkmann, F Costa, J Chesov, D van Crevel, R Dedicoat, M Dominguez, J Duarte, R Grobbel, HP Gunther, G Guglielmetti, L Heyckendorf, J Kay, AW Kirakosyan, O Kirk, O Koczulla, RA Kudriashov, GG Kuksa, L van Leth, F Magis-Escurra, C Mandalakas, AM Molina-Moya, B Peloquin, CA Reimann, M Rumetshofer, R Schaaf, HS Schon, T Tiberi, S Valda, J Yablonskii, PK Dheda, K |
dc.subject.por.fl_str_mv |
MDR-TB; RESIST-TB; TBNET; TB; XDR-TB; personalised treatment |
topic |
MDR-TB; RESIST-TB; TBNET; TB; XDR-TB; personalised treatment |
description |
The emergence of multidrug-resistant tuberculosis (MDR-TB; defined as resistance to at least rifampicin and isoniazid) represents a growing threat to public health and economic growth. Never before in the history of mankind have more patients been affected by MDR-TB than is the case today. The World Health Organization reports that MDR-TB outcomes are poor despite staggeringly high management costs. Moreover, treatment is prolonged, adverse events are common, and the majority of affected patients do not receive adequate treatment. As MDR-TB strains are often resistant to one or more second-line anti-TB drugs, in-depth genotypic and phenotypic drug susceptibility testing is needed to construct personalised treatment regimens to improve treatment outcomes. For the first time in decades, the availability of novel drugs such as bedaquiline allow us to design potent and well-tolerated personalised MDR-TB treatment regimens based solely on oral drugs. In this article, we present management guidance to optimise the diagnosis, algorithm-based treatment, drug dosing and therapeutic drug monitoring, and the management of adverse events and comorbidities, associated with MDR-TB. We also discuss the role of surgery, physiotherapy, rehabilitation, palliative care and smoking cessation in patients with MDR-TB. We hope that incorporating these recommendations into patient care will be helpful in optimising treatment outcomes, and lead to more MDR-TB patients achieving a relapse-free cure. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019 2019-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10216/154103 |
url |
https://hdl.handle.net/10216/154103 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1027-3719 1815-7920 10.5588/ijtld.18.0622 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
International Union Against Tuberculosis and Lung Disease |
publisher.none.fl_str_mv |
International Union Against Tuberculosis and Lung Disease |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799135912023556096 |