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...
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Format: | Article |
Language: | English |
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Public Library of Science (PLoS)
2008-01-01
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Series: | PLoS Neglected Tropical Diseases |
Online Access: | http://europepmc.org/articles/PMC2565693?pdf=render |
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author | Ron P Schuring Jan H Richardus Ewout W Steyerberg David Pahan William R Faber Linda Oskam |
author_facet | Ron P Schuring Jan H Richardus Ewout W Steyerberg David Pahan William R Faber Linda Oskam |
author_sort | Ron P Schuring |
collection | DOAJ |
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. |
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institution | Directory Open Access Journal |
issn | 1935-2727 1935-2735 |
language | English |
last_indexed | 2024-12-12T01:28:34Z |
publishDate | 2008-01-01 |
publisher | Public Library of Science (PLoS) |
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series | PLoS Neglected Tropical Diseases |
spelling | doaj.art-91901f9ed44642d9beecee11b04999e82022-12-22T00:43:02ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352008-01-0128e28310.1371/journal.pntd.0000283Preventing nerve function impairment in leprosy: validation and updating of a prediction rule.Ron P SchuringJan H RichardusEwout W SteyerbergDavid PahanWilliam R FaberLinda OskamBACKGROUND: 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.http://europepmc.org/articles/PMC2565693?pdf=render |
spellingShingle | Ron P Schuring Jan H Richardus Ewout W Steyerberg David Pahan William R Faber Linda Oskam Preventing nerve function impairment in leprosy: validation and updating of a prediction rule. PLoS Neglected Tropical Diseases |
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 |
url | http://europepmc.org/articles/PMC2565693?pdf=render |
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