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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Union
2022
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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). |
format | Online Article Text |
id | pubmed-8802559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Union |
record_format | MEDLINE/PubMed |
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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