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Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule
BACKGROUND: To validate and update a prediction rule for estimating the risk of leprosy-related nerve function impairment (NFI). METHODOLOGY/PRINCIPAL FINDINGS: Prospective cohort using routinely collected data, in which we determined the discriminative ability of a previously published rule and an...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565693/ https://www.ncbi.nlm.nih.gov/pubmed/18846229 http://dx.doi.org/10.1371/journal.pntd.0000283 |
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author | Schuring, Ron P. Richardus, Jan H. Steyerberg, Ewout W. Pahan, David Faber, William R. Oskam, Linda |
author_facet | Schuring, Ron P. Richardus, Jan H. Steyerberg, Ewout W. Pahan, David Faber, William R. Oskam, Linda |
author_sort | Schuring, Ron P. |
collection | PubMed |
description | BACKGROUND: To validate and update a prediction rule for estimating the risk of leprosy-related nerve function impairment (NFI). METHODOLOGY/PRINCIPAL FINDINGS: Prospective cohort using routinely collected data, in which we determined the discriminative ability of a previously published rule and an updated rule with a concordance statistic (c). Additional risk factors were analyzed with a Cox proportional hazards regression model. The population consisted of 1,037 leprosy patients newly diagnosed between 2002 and 2003 in the health care facilities of the Rural Health Program in Nilphamari and Rangpur districts in northwest Bangladesh. The primary outcome was the time until the start of treatment. An NFI event was defined as the decision to treat NFI with corticosteroids after diagnosis. NFI occurred in 115 patients (13%; 95% confidence interval 11%–16%). The original prediction rule had adequate discriminative ability (c = 0.79), but could be improved by substituting one predicting variable: ‘long-standing nerve function impairment at diagnosis’ by ‘anti-PGL-I antibodies’. The adjusted prediction rule was slightly better (c = 0.81) and identified more patients with NFI (80%) than the original prediction rule (72%). CONCLUSIONS/SIGNIFICANCE: NFI can well be predicted by using the risk variables ‘leprosy classification’ and ‘anti-PGL-I antibodies’. The use of these two variables that do not include NFI offer the possibility of predicting NFI, even before it occurs for the first time. Surveillance beyond the treatment period can be targeted to those most likely to benefit from preventing permanent disabilities. |
format | Text |
id | pubmed-2565693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25656932008-10-10 Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule Schuring, Ron P. Richardus, Jan H. Steyerberg, Ewout W. Pahan, David Faber, William R. Oskam, Linda PLoS Negl Trop Dis Research Article BACKGROUND: To validate and update a prediction rule for estimating the risk of leprosy-related nerve function impairment (NFI). METHODOLOGY/PRINCIPAL FINDINGS: Prospective cohort using routinely collected data, in which we determined the discriminative ability of a previously published rule and an updated rule with a concordance statistic (c). Additional risk factors were analyzed with a Cox proportional hazards regression model. The population consisted of 1,037 leprosy patients newly diagnosed between 2002 and 2003 in the health care facilities of the Rural Health Program in Nilphamari and Rangpur districts in northwest Bangladesh. The primary outcome was the time until the start of treatment. An NFI event was defined as the decision to treat NFI with corticosteroids after diagnosis. NFI occurred in 115 patients (13%; 95% confidence interval 11%–16%). The original prediction rule had adequate discriminative ability (c = 0.79), but could be improved by substituting one predicting variable: ‘long-standing nerve function impairment at diagnosis’ by ‘anti-PGL-I antibodies’. The adjusted prediction rule was slightly better (c = 0.81) and identified more patients with NFI (80%) than the original prediction rule (72%). CONCLUSIONS/SIGNIFICANCE: NFI can well be predicted by using the risk variables ‘leprosy classification’ and ‘anti-PGL-I antibodies’. The use of these two variables that do not include NFI offer the possibility of predicting NFI, even before it occurs for the first time. Surveillance beyond the treatment period can be targeted to those most likely to benefit from preventing permanent disabilities. Public Library of Science 2008-08-27 /pmc/articles/PMC2565693/ /pubmed/18846229 http://dx.doi.org/10.1371/journal.pntd.0000283 Text en Schuring et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schuring, Ron P. Richardus, Jan H. Steyerberg, Ewout W. Pahan, David Faber, William R. Oskam, Linda Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title | Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title_full | Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title_fullStr | Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title_full_unstemmed | Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title_short | Preventing Nerve Function Impairment in Leprosy: Validation and Updating of a Prediction Rule |
title_sort | preventing nerve function impairment in leprosy: validation and updating of a prediction rule |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565693/ https://www.ncbi.nlm.nih.gov/pubmed/18846229 http://dx.doi.org/10.1371/journal.pntd.0000283 |
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