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A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre
CONTEXT: Pure neuritic leprosy is a risk factor for grade 2 disability owing to the early nerve damage. AIMS: To study the clinical patterns of neuritic leprosy, to determine the percentage of patients manifesting grade 2 disability at the time of diagnosis and to identify any risk factors for the s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362753/ https://www.ncbi.nlm.nih.gov/pubmed/30788282 http://dx.doi.org/10.4103/idoj.IDOJ_118_18 |
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author | Kolleri, Jouhar Jabeen Sasidharanpillai, Sarita Vadakkayil, Bindu Chathoth, Anuradha Thalian |
author_facet | Kolleri, Jouhar Jabeen Sasidharanpillai, Sarita Vadakkayil, Bindu Chathoth, Anuradha Thalian |
author_sort | Kolleri, Jouhar Jabeen |
collection | PubMed |
description | CONTEXT: Pure neuritic leprosy is a risk factor for grade 2 disability owing to the early nerve damage. AIMS: To study the clinical patterns of neuritic leprosy, to determine the percentage of patients manifesting grade 2 disability at the time of diagnosis and to identify any risk factors for the same. SETTINGS AND DESIGN: Retrospective descriptive study from previous case records of pure neuritic leprosy patients who attended a tertiary centre from 1(st) July 2007 to 30(th) June 2017. SUBJECTS AND METHODS: Data on patients who satisfied the World Health Organization (WHO) cardinal criteria for diagnosis of leprosy, who had no skin lesion of leprosy and had acid-fast bacilli negative status on skin smears were collected using a pre-set proforma. STATISTICAL ANALYSIS USED: The Chi-square test was used to assess statistical significance and logistic regression model was applied to avoid the effects of confounding factors. RESULTS: A diagnostic delay of >1 year was observed in 44% patients. At the time of diagnosis, grade 2 disability was documented in 60 (80%) of patients. No statistically significant risk factor was identified for grade 2 disability. LIMITATIONS: Retrospective nature and the study conducted in a tertiary care centre not reflecting the status in the community were the limitations. CONCLUSIONS: Grade 2 disability noted in 80% of patients points to the inherent nature of disease to cause early nerve damage. Diagnostic delay of >1 year documented in 44% of patients underscores the diagnostic challenges in the absence of skin lesions. |
format | Online Article Text |
id | pubmed-6362753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63627532019-02-20 A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre Kolleri, Jouhar Jabeen Sasidharanpillai, Sarita Vadakkayil, Bindu Chathoth, Anuradha Thalian Indian Dermatol Online J Original Article CONTEXT: Pure neuritic leprosy is a risk factor for grade 2 disability owing to the early nerve damage. AIMS: To study the clinical patterns of neuritic leprosy, to determine the percentage of patients manifesting grade 2 disability at the time of diagnosis and to identify any risk factors for the same. SETTINGS AND DESIGN: Retrospective descriptive study from previous case records of pure neuritic leprosy patients who attended a tertiary centre from 1(st) July 2007 to 30(th) June 2017. SUBJECTS AND METHODS: Data on patients who satisfied the World Health Organization (WHO) cardinal criteria for diagnosis of leprosy, who had no skin lesion of leprosy and had acid-fast bacilli negative status on skin smears were collected using a pre-set proforma. STATISTICAL ANALYSIS USED: The Chi-square test was used to assess statistical significance and logistic regression model was applied to avoid the effects of confounding factors. RESULTS: A diagnostic delay of >1 year was observed in 44% patients. At the time of diagnosis, grade 2 disability was documented in 60 (80%) of patients. No statistically significant risk factor was identified for grade 2 disability. LIMITATIONS: Retrospective nature and the study conducted in a tertiary care centre not reflecting the status in the community were the limitations. CONCLUSIONS: Grade 2 disability noted in 80% of patients points to the inherent nature of disease to cause early nerve damage. Diagnostic delay of >1 year documented in 44% of patients underscores the diagnostic challenges in the absence of skin lesions. Medknow Publications & Media Pvt Ltd 2019 /pmc/articles/PMC6362753/ /pubmed/30788282 http://dx.doi.org/10.4103/idoj.IDOJ_118_18 Text en Copyright: © 2019 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Kolleri, Jouhar Jabeen Sasidharanpillai, Sarita Vadakkayil, Bindu Chathoth, Anuradha Thalian A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title | A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title_full | A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title_fullStr | A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title_full_unstemmed | A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title_short | A 10-year Retrospective Descriptive Study on Pure Neuritic Leprosy from a Tertiary Referral Centre |
title_sort | 10-year retrospective descriptive study on pure neuritic leprosy from a tertiary referral centre |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362753/ https://www.ncbi.nlm.nih.gov/pubmed/30788282 http://dx.doi.org/10.4103/idoj.IDOJ_118_18 |
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