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Progression of leprosy disability after discharge: is multidrug therapy enough?

OBJECTIVE: To evaluate the risk factors related to worsening of physical disabilities after treatment discharge among patients with leprosy administered 12 consecutive monthly doses of multidrug therapy (MDT/WHO). METHODS: Cohort study was carried out at the Leprosy Laboratory in Rio de Janeiro, Bra...

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Autores principales: Sales, Anna Maria, Campos, Dayse Pereira, Hacker, Mariana Andrea, da Costa Nery, José Augusto, Düppre, Nádia Cristina, Rangel, Emanuel, Sarno, Euzenir Nunes, Penna, Maria Lucia Fernandes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285222/
https://www.ncbi.nlm.nih.gov/pubmed/23937704
http://dx.doi.org/10.1111/tmi.12156
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author Sales, Anna Maria
Campos, Dayse Pereira
Hacker, Mariana Andrea
da Costa Nery, José Augusto
Düppre, Nádia Cristina
Rangel, Emanuel
Sarno, Euzenir Nunes
Penna, Maria Lucia Fernandes
author_facet Sales, Anna Maria
Campos, Dayse Pereira
Hacker, Mariana Andrea
da Costa Nery, José Augusto
Düppre, Nádia Cristina
Rangel, Emanuel
Sarno, Euzenir Nunes
Penna, Maria Lucia Fernandes
author_sort Sales, Anna Maria
collection PubMed
description OBJECTIVE: To evaluate the risk factors related to worsening of physical disabilities after treatment discharge among patients with leprosy administered 12 consecutive monthly doses of multidrug therapy (MDT/WHO). METHODS: Cohort study was carried out at the Leprosy Laboratory in Rio de Janeiro, Brazil. We evaluated patients with multibacillary leprosy treated (MDT/WHO) between 1997 and 2007. The Cox proportional hazards model was used to estimate the relationship between the onset of physical disabilities after release from treatment and epidemiological and clinical characteristics. RESULTS: The total observation time period for the 368 patients was 1 570 person-years (PY), averaging 4.3 years per patient. The overall incidence rate of worsening of disability was 6.5/100 PY. Among those who began treatment with no disability, the incidence rate of physical disability was 4.5/100 PY. Among those who started treatment with Grade 1 or 2 disabilities, the incidence rate of deterioration was 10.5/100 PY. The survival analysis evidenced that when disability grade was 1, the risk was 1.61 (95% CI: 1.02–2.56), when disability was 2, the risk was 2.37 (95% CI 1.35–4.16), and when the number of skin lesions was 15 or more, an HR = 1.97 (95% CI: 1.07–3.63). Patients with neuritis showed a 65% increased risk of worsening of disability (HR = 1.65 [95% CI: 1.08–2.52]). CONCLUSION: Impairment at diagnosis was the main risk factor for neurological worsening after treatment/MDT. Early diagnosis and prompt treatment of reactional episodes remain the main means of preventing physical disabilities.
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spelling pubmed-42852222015-01-26 Progression of leprosy disability after discharge: is multidrug therapy enough? Sales, Anna Maria Campos, Dayse Pereira Hacker, Mariana Andrea da Costa Nery, José Augusto Düppre, Nádia Cristina Rangel, Emanuel Sarno, Euzenir Nunes Penna, Maria Lucia Fernandes Trop Med Int Health Leprosy OBJECTIVE: To evaluate the risk factors related to worsening of physical disabilities after treatment discharge among patients with leprosy administered 12 consecutive monthly doses of multidrug therapy (MDT/WHO). METHODS: Cohort study was carried out at the Leprosy Laboratory in Rio de Janeiro, Brazil. We evaluated patients with multibacillary leprosy treated (MDT/WHO) between 1997 and 2007. The Cox proportional hazards model was used to estimate the relationship between the onset of physical disabilities after release from treatment and epidemiological and clinical characteristics. RESULTS: The total observation time period for the 368 patients was 1 570 person-years (PY), averaging 4.3 years per patient. The overall incidence rate of worsening of disability was 6.5/100 PY. Among those who began treatment with no disability, the incidence rate of physical disability was 4.5/100 PY. Among those who started treatment with Grade 1 or 2 disabilities, the incidence rate of deterioration was 10.5/100 PY. The survival analysis evidenced that when disability grade was 1, the risk was 1.61 (95% CI: 1.02–2.56), when disability was 2, the risk was 2.37 (95% CI 1.35–4.16), and when the number of skin lesions was 15 or more, an HR = 1.97 (95% CI: 1.07–3.63). Patients with neuritis showed a 65% increased risk of worsening of disability (HR = 1.65 [95% CI: 1.08–2.52]). CONCLUSION: Impairment at diagnosis was the main risk factor for neurological worsening after treatment/MDT. Early diagnosis and prompt treatment of reactional episodes remain the main means of preventing physical disabilities. BlackWell Publishing Ltd 2013-09 2013-08-13 /pmc/articles/PMC4285222/ /pubmed/23937704 http://dx.doi.org/10.1111/tmi.12156 Text en © 2013 The Authors. Tropical Medicine and International Health published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Leprosy
Sales, Anna Maria
Campos, Dayse Pereira
Hacker, Mariana Andrea
da Costa Nery, José Augusto
Düppre, Nádia Cristina
Rangel, Emanuel
Sarno, Euzenir Nunes
Penna, Maria Lucia Fernandes
Progression of leprosy disability after discharge: is multidrug therapy enough?
title Progression of leprosy disability after discharge: is multidrug therapy enough?
title_full Progression of leprosy disability after discharge: is multidrug therapy enough?
title_fullStr Progression of leprosy disability after discharge: is multidrug therapy enough?
title_full_unstemmed Progression of leprosy disability after discharge: is multidrug therapy enough?
title_short Progression of leprosy disability after discharge: is multidrug therapy enough?
title_sort progression of leprosy disability after discharge: is multidrug therapy enough?
topic Leprosy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285222/
https://www.ncbi.nlm.nih.gov/pubmed/23937704
http://dx.doi.org/10.1111/tmi.12156
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