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Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study
BACKGROUND: The multidrug therapy (MDT) for leprosy treatment adopted by Brazil in the 1990s was important for reducing leprosy in the country; however, recurrent cases remained problematic. Mechanisms involved in leprosy recurrence are heterogeneous and can be sorted into three groups: insufficient...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532254/ https://www.ncbi.nlm.nih.gov/pubmed/31118048 http://dx.doi.org/10.1186/s12879-019-4100-6 |
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author | Gonçalves, Franciely Gomes Belone, Andréa de Faria Fernandes Rosa, Patrícia Sammarco Laporta, Gabriel Zorello |
author_facet | Gonçalves, Franciely Gomes Belone, Andréa de Faria Fernandes Rosa, Patrícia Sammarco Laporta, Gabriel Zorello |
author_sort | Gonçalves, Franciely Gomes |
collection | PubMed |
description | BACKGROUND: The multidrug therapy (MDT) for leprosy treatment adopted by Brazil in the 1990s was important for reducing leprosy in the country; however, recurrent cases remained problematic. Mechanisms involved in leprosy recurrence are heterogeneous and can be sorted into three groups: insufficient therapy, bacillary persistence and new infections. This study aimed to analyse the time interval of leprosy recurrence in relation to the therapeutic scheme in the state of Acre. The hypotheses were as follows: 1) treatments (a) rifampicin, ofloxacin and minocycline (ROM) and (b) dapsone (DDS) have a short leprosy recurrence time, 2) treatments based on MDT have a long leprosy recurrence time, 3) there is a dose-response relationship between MDT and the time interval between leprosy episodes. METHODS: This retrospective cohort study included 201 patients with a second episode of clinical leprosy at the reference centers for leprosy control in the state of Acre. Exposure was the type of therapeutic scheme as follows: 1) ROM, 2) DDS, 3) MDT(0–9 doses), 4) MDT(10–19 doses), 5) MDT(20–29 doses), and 6) MDT(30+ doses). Outcome was the time interval between release from treatment and a diagnosis of a recurrent leprosy case. Incidence rate ratios and relative risk Poisson regressions adjusted by age and sex were calculated with 95% confidence intervals. RESULTS: The 201 patients studied during this retrospective follow-up resulted in a total of 224 cases of recurrent leprosy. Incidence rate ratios within this therapeutic scheme were as follows: 3.3 (2.39, 4.2; ROM/MDT(30+)), 1.12 (0.33, 1.92; DDS/MDT(30+)), 2.17 (1.39, 2.94; MDT(0–9)/MDT(30+)), 1.94 (1.13, 2.75; MDT(10–19)/MDT(30+)) and 1.26 (0.47, 2.05; MDT(20–29)/MDT(30+)). Relative risk Poisson regressions showed a protective effect of MDT(30+) in comparison with ROM (0.22; 0.07, 0.72), MDT(0–9) (0.42; 0.21, 0.85), and MDT(10–19) (0.44; 0.21, 0.92). No differences among MDT(30+) and DDS (0.71; 0.36, 1.41) and MDT(20–29) (0.76; 0.38, 1.49) were observed. CONCLUSIONS: New infection is an important—yet neglected—mechanism in leprosy recurrence in the state of Acre and can challenge the leprosy elimination plan in Brazil. MDT with few doses might be associated with leprosy recurrence due to insufficient therapy or bacillary persistence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4100-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6532254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65322542019-05-29 Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study Gonçalves, Franciely Gomes Belone, Andréa de Faria Fernandes Rosa, Patrícia Sammarco Laporta, Gabriel Zorello BMC Infect Dis Research Article BACKGROUND: The multidrug therapy (MDT) for leprosy treatment adopted by Brazil in the 1990s was important for reducing leprosy in the country; however, recurrent cases remained problematic. Mechanisms involved in leprosy recurrence are heterogeneous and can be sorted into three groups: insufficient therapy, bacillary persistence and new infections. This study aimed to analyse the time interval of leprosy recurrence in relation to the therapeutic scheme in the state of Acre. The hypotheses were as follows: 1) treatments (a) rifampicin, ofloxacin and minocycline (ROM) and (b) dapsone (DDS) have a short leprosy recurrence time, 2) treatments based on MDT have a long leprosy recurrence time, 3) there is a dose-response relationship between MDT and the time interval between leprosy episodes. METHODS: This retrospective cohort study included 201 patients with a second episode of clinical leprosy at the reference centers for leprosy control in the state of Acre. Exposure was the type of therapeutic scheme as follows: 1) ROM, 2) DDS, 3) MDT(0–9 doses), 4) MDT(10–19 doses), 5) MDT(20–29 doses), and 6) MDT(30+ doses). Outcome was the time interval between release from treatment and a diagnosis of a recurrent leprosy case. Incidence rate ratios and relative risk Poisson regressions adjusted by age and sex were calculated with 95% confidence intervals. RESULTS: The 201 patients studied during this retrospective follow-up resulted in a total of 224 cases of recurrent leprosy. Incidence rate ratios within this therapeutic scheme were as follows: 3.3 (2.39, 4.2; ROM/MDT(30+)), 1.12 (0.33, 1.92; DDS/MDT(30+)), 2.17 (1.39, 2.94; MDT(0–9)/MDT(30+)), 1.94 (1.13, 2.75; MDT(10–19)/MDT(30+)) and 1.26 (0.47, 2.05; MDT(20–29)/MDT(30+)). Relative risk Poisson regressions showed a protective effect of MDT(30+) in comparison with ROM (0.22; 0.07, 0.72), MDT(0–9) (0.42; 0.21, 0.85), and MDT(10–19) (0.44; 0.21, 0.92). No differences among MDT(30+) and DDS (0.71; 0.36, 1.41) and MDT(20–29) (0.76; 0.38, 1.49) were observed. CONCLUSIONS: New infection is an important—yet neglected—mechanism in leprosy recurrence in the state of Acre and can challenge the leprosy elimination plan in Brazil. MDT with few doses might be associated with leprosy recurrence due to insufficient therapy or bacillary persistence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4100-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-22 /pmc/articles/PMC6532254/ /pubmed/31118048 http://dx.doi.org/10.1186/s12879-019-4100-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Gonçalves, Franciely Gomes Belone, Andréa de Faria Fernandes Rosa, Patrícia Sammarco Laporta, Gabriel Zorello Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title | Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title_full | Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title_fullStr | Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title_full_unstemmed | Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title_short | Underlying mechanisms of leprosy recurrence in the Western Amazon: a retrospective cohort study |
title_sort | underlying mechanisms of leprosy recurrence in the western amazon: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532254/ https://www.ncbi.nlm.nih.gov/pubmed/31118048 http://dx.doi.org/10.1186/s12879-019-4100-6 |
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