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Early mortality during rifampicin-resistant TB treatment

BACK GROUND: Data suggest that treatment with newer TB drugs (linezolid [LZD], bedaquiline [BDQ] and delamanid [DLM]), used in Khayelitsha, South Africa, since 2012, reduces mortality due to rifampicin-resistant TB (RR-TB). METHODS: This was a retrospective cohort study to assess 6-month mortality a...

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Autores principales: Mohr-Holland, E., Daniels, J., Reuter, A., Rodriguez, C. A., Mitnick, C., Kock, Y., Cox, V., Furin, J., Cox, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Union 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802559/
https://www.ncbi.nlm.nih.gov/pubmed/35086627
http://dx.doi.org/10.5588/ijtld.21.0494
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author Mohr-Holland, E.
Daniels, J.
Reuter, A.
Rodriguez, C. A.
Mitnick, C.
Kock, Y.
Cox, V.
Furin, J.
Cox, H.
author_facet Mohr-Holland, E.
Daniels, J.
Reuter, A.
Rodriguez, C. A.
Mitnick, C.
Kock, Y.
Cox, V.
Furin, J.
Cox, H.
author_sort Mohr-Holland, E.
collection PubMed
description BACK GROUND: Data suggest that treatment with newer TB drugs (linezolid [LZD], bedaquiline [BDQ] and delamanid [DLM]), used in Khayelitsha, South Africa, since 2012, reduces mortality due to rifampicin-resistant TB (RR-TB). METHODS: This was a retrospective cohort study to assess 6-month mortality among RR-TB patients diagnosed between 2008 and 2019. RESULTS: By 6 months, 236/2,008 (12%) patients died; 12% (78/651) among those diagnosed in 2008–2011, and respectively 8% (49/619) and 15% (109/738) with and without LZD/BDQ/DLM in 2012–2019. Multivariable analysis showed a small, non-significant mortality reduction with LZD/BDQ/DLM use compared to the 2008–2011 period (aOR 0.79, 95% CI 0.5–1.2). Inpatient treatment initiation (aOR 3.2, 95% CI 2.4–4.4), fluoroquinolone (FQ) resistance (aOR 2.7, 95% CI 1.8–4.2) and female sex (aOR 1.5, 95% CI 1.1–2.0) were also associated with mortality. When restricted to 2012–2019, use of LZD/BDQ/DLM was associated with lower mortality (aOR 0.58, 95% CI 0.39–0.87). CONCLUSIONS: While LZD/BDQ/DLM reduced 6-month mortality between 2012 and 2019, there was no significant effect overall. These findings may be due to initially restricted LZD/BDQ/DLM use for those with high-level resistance or treatment failure. Additional contributors include increased treatment initiation among individuals who would have otherwise died before treatment due to universal drug susceptibility testing from 2012, an effect that also likely contributed to higher mortality among females (survival through to care-seeking).
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spelling pubmed-88025592022-02-05 Early mortality during rifampicin-resistant TB treatment Mohr-Holland, E. Daniels, J. Reuter, A. Rodriguez, C. A. Mitnick, C. Kock, Y. Cox, V. Furin, J. Cox, H. Int J Tuberc Lung Dis Original Articles BACK GROUND: Data suggest that treatment with newer TB drugs (linezolid [LZD], bedaquiline [BDQ] and delamanid [DLM]), used in Khayelitsha, South Africa, since 2012, reduces mortality due to rifampicin-resistant TB (RR-TB). METHODS: This was a retrospective cohort study to assess 6-month mortality among RR-TB patients diagnosed between 2008 and 2019. RESULTS: By 6 months, 236/2,008 (12%) patients died; 12% (78/651) among those diagnosed in 2008–2011, and respectively 8% (49/619) and 15% (109/738) with and without LZD/BDQ/DLM in 2012–2019. Multivariable analysis showed a small, non-significant mortality reduction with LZD/BDQ/DLM use compared to the 2008–2011 period (aOR 0.79, 95% CI 0.5–1.2). Inpatient treatment initiation (aOR 3.2, 95% CI 2.4–4.4), fluoroquinolone (FQ) resistance (aOR 2.7, 95% CI 1.8–4.2) and female sex (aOR 1.5, 95% CI 1.1–2.0) were also associated with mortality. When restricted to 2012–2019, use of LZD/BDQ/DLM was associated with lower mortality (aOR 0.58, 95% CI 0.39–0.87). CONCLUSIONS: While LZD/BDQ/DLM reduced 6-month mortality between 2012 and 2019, there was no significant effect overall. These findings may be due to initially restricted LZD/BDQ/DLM use for those with high-level resistance or treatment failure. Additional contributors include increased treatment initiation among individuals who would have otherwise died before treatment due to universal drug susceptibility testing from 2012, an effect that also likely contributed to higher mortality among females (survival through to care-seeking). The Union 2022-02 2022-02-01 /pmc/articles/PMC8802559/ /pubmed/35086627 http://dx.doi.org/10.5588/ijtld.21.0494 Text en © 2022 The Union https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Articles
Mohr-Holland, E.
Daniels, J.
Reuter, A.
Rodriguez, C. A.
Mitnick, C.
Kock, Y.
Cox, V.
Furin, J.
Cox, H.
Early mortality during rifampicin-resistant TB treatment
title Early mortality during rifampicin-resistant TB treatment
title_full Early mortality during rifampicin-resistant TB treatment
title_fullStr Early mortality during rifampicin-resistant TB treatment
title_full_unstemmed Early mortality during rifampicin-resistant TB treatment
title_short Early mortality during rifampicin-resistant TB treatment
title_sort early mortality during rifampicin-resistant tb treatment
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802559/
https://www.ncbi.nlm.nih.gov/pubmed/35086627
http://dx.doi.org/10.5588/ijtld.21.0494
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