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Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study
BACKGROUND: Since the roll-out of the Xpert MTB/RIF assay, continuous surveillance can provide an estimate of rifampicin-resistant TB (RR-TB) prevalence, provided high drug susceptibility testing (DST) coverage is achieved. We use national data from Rwanda to describe rifampicin DST coverage, estima...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318964/ https://www.ncbi.nlm.nih.gov/pubmed/35653710 http://dx.doi.org/10.1093/inthealth/ihac039 |
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author | Habimana-Mucyo, Yves Dushime, Augustin Migambi, Patrick Habiyambere, Innocent Semuto Ngabonziza, Jean Claude Decroo, Tom |
author_facet | Habimana-Mucyo, Yves Dushime, Augustin Migambi, Patrick Habiyambere, Innocent Semuto Ngabonziza, Jean Claude Decroo, Tom |
author_sort | Habimana-Mucyo, Yves |
collection | PubMed |
description | BACKGROUND: Since the roll-out of the Xpert MTB/RIF assay, continuous surveillance can provide an estimate of rifampicin-resistant TB (RR-TB) prevalence, provided high drug susceptibility testing (DST) coverage is achieved. We use national data from Rwanda to describe rifampicin DST coverage, estimate the prevalence of RR-TB and assess its predictors. METHODS: Routinely collected DST data were entered into an electronic TB case-based surveillance system. DST coverage was calculated among all bacteriologically confirmed pulmonary TB patients notified from 1 July 2019 to 30 June 2020 in Rwanda. The prevalence of RR-TB was estimated among those with DST results. Univariable and multivariable analysis was performed to explore predictors for RR TB. RESULTS: Among 4066 patients with bacteriologically confirmed pulmonary TB, rifampicin DST coverage was 95.6% (4066/4251). RR-TB was diagnosed in 73 patients. The prevalence of RR-TB was 1.4% (53/3659; 95% CI 1.09 to 1.89%) and 4.9% (20/406; 95% CI 3.03 to 7.51%) in new and previously treated TB cases, respectively. Predictors of RR-TB were: (1) living in Kigali City (adjusted OR [aOR] 1.65, 95% CI 1.03 to 2.65); (2) previous TB treatment (aOR 3.64, 95% CI 2.14 to 6.19); and (3) close contact with a known RR-TB patient (aOR 11.37, 95% CI 4.19 to 30.82). CONCLUSIONS: High rifampicin DST coverage for routine reporting allowed Rwanda to estimate the RR-TB prevalence among new and previously treated patients. |
format | Online Article Text |
id | pubmed-10318964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103189642023-07-05 Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study Habimana-Mucyo, Yves Dushime, Augustin Migambi, Patrick Habiyambere, Innocent Semuto Ngabonziza, Jean Claude Decroo, Tom Int Health Original Article BACKGROUND: Since the roll-out of the Xpert MTB/RIF assay, continuous surveillance can provide an estimate of rifampicin-resistant TB (RR-TB) prevalence, provided high drug susceptibility testing (DST) coverage is achieved. We use national data from Rwanda to describe rifampicin DST coverage, estimate the prevalence of RR-TB and assess its predictors. METHODS: Routinely collected DST data were entered into an electronic TB case-based surveillance system. DST coverage was calculated among all bacteriologically confirmed pulmonary TB patients notified from 1 July 2019 to 30 June 2020 in Rwanda. The prevalence of RR-TB was estimated among those with DST results. Univariable and multivariable analysis was performed to explore predictors for RR TB. RESULTS: Among 4066 patients with bacteriologically confirmed pulmonary TB, rifampicin DST coverage was 95.6% (4066/4251). RR-TB was diagnosed in 73 patients. The prevalence of RR-TB was 1.4% (53/3659; 95% CI 1.09 to 1.89%) and 4.9% (20/406; 95% CI 3.03 to 7.51%) in new and previously treated TB cases, respectively. Predictors of RR-TB were: (1) living in Kigali City (adjusted OR [aOR] 1.65, 95% CI 1.03 to 2.65); (2) previous TB treatment (aOR 3.64, 95% CI 2.14 to 6.19); and (3) close contact with a known RR-TB patient (aOR 11.37, 95% CI 4.19 to 30.82). CONCLUSIONS: High rifampicin DST coverage for routine reporting allowed Rwanda to estimate the RR-TB prevalence among new and previously treated patients. Oxford University Press 2022-06-02 /pmc/articles/PMC10318964/ /pubmed/35653710 http://dx.doi.org/10.1093/inthealth/ihac039 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Habimana-Mucyo, Yves Dushime, Augustin Migambi, Patrick Habiyambere, Innocent Semuto Ngabonziza, Jean Claude Decroo, Tom Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title | Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title_full | Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title_fullStr | Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title_full_unstemmed | Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title_short | Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study |
title_sort | continuous surveillance of drug-resistant tb burden in rwanda: a retrospective cross-sectional study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318964/ https://www.ncbi.nlm.nih.gov/pubmed/35653710 http://dx.doi.org/10.1093/inthealth/ihac039 |
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