Management of patients with multidrug-resistant tuberculosis

Detalhes bibliográficos
Autor(a) principal: Lange, C
Data de Publicação: 2019
Outros Autores: 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
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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spelling 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
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instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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