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Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis
BACKGROUND: The causes, clinical presentations and treatment outcomes of optic neuritis are distinct among different populations. Early diagnosis based on clinical presentations plays an important role in treating optic neuritis patients. OBJECTIVE: The study aimed to determine clinical characterist...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131319/ https://www.ncbi.nlm.nih.gov/pubmed/30258505 http://dx.doi.org/10.2174/1874364101812010247 |
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author | Hansapinyo, Linda Vivattanaseth, Chayanee |
author_facet | Hansapinyo, Linda Vivattanaseth, Chayanee |
author_sort | Hansapinyo, Linda |
collection | PubMed |
description | BACKGROUND: The causes, clinical presentations and treatment outcomes of optic neuritis are distinct among different populations. Early diagnosis based on clinical presentations plays an important role in treating optic neuritis patients. OBJECTIVE: The study aimed to determine clinical characteristics, treatment outcomes and predictive factors of treatment outcomes in optic neuritis patients with and without demyelinating disease. METHODS: A retrospective descriptive study of optic neuritis patients carried out between January 2009 and December 2016 was done. Univariate analysis and multivariate logistic regression analysis were used to evaluate the predictive factors of treatment outcomes. RESULTS: Among 150 patients with optic neuritis, 58 patients were diagnosed with Neuromyelitis Optica Spectrum Disease (NMOSD), 23 patients were diagnosed with Multiple Sclerosis (MS) and 69 patients were idiopathic. The age at presentation in the NMOSD group was significantly younger than the MS group and the idiopathic group. The female:male ratio was significantly lower in the idiopathic group than in the NMOSD group. The initial Best Corrected Visual Activity (BCVA) of 20/20-20/60 (p = 0.001) and the idiopathic group (p =0.030) was associated with good visual outcomes. Initial BCVA of < 20/200 (p = 0.009) and the NMOSD group (p < 0.001) was associated with poor visual outcomes. CONCLUSION: NMOSD is a more common cause of optic neuritis than MS in Thai population. Female patients with poor initial VA, poor response to steroids treatment, and presenting recurrent attacks are highly suspicious for NMOSD. Optic neuritis without associated demyelinating disease has a better visual outcome and lower recurrence rate. |
format | Online Article Text |
id | pubmed-6131319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-61313192018-09-26 Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis Hansapinyo, Linda Vivattanaseth, Chayanee Open Ophthalmol J Ophthalmology BACKGROUND: The causes, clinical presentations and treatment outcomes of optic neuritis are distinct among different populations. Early diagnosis based on clinical presentations plays an important role in treating optic neuritis patients. OBJECTIVE: The study aimed to determine clinical characteristics, treatment outcomes and predictive factors of treatment outcomes in optic neuritis patients with and without demyelinating disease. METHODS: A retrospective descriptive study of optic neuritis patients carried out between January 2009 and December 2016 was done. Univariate analysis and multivariate logistic regression analysis were used to evaluate the predictive factors of treatment outcomes. RESULTS: Among 150 patients with optic neuritis, 58 patients were diagnosed with Neuromyelitis Optica Spectrum Disease (NMOSD), 23 patients were diagnosed with Multiple Sclerosis (MS) and 69 patients were idiopathic. The age at presentation in the NMOSD group was significantly younger than the MS group and the idiopathic group. The female:male ratio was significantly lower in the idiopathic group than in the NMOSD group. The initial Best Corrected Visual Activity (BCVA) of 20/20-20/60 (p = 0.001) and the idiopathic group (p =0.030) was associated with good visual outcomes. Initial BCVA of < 20/200 (p = 0.009) and the NMOSD group (p < 0.001) was associated with poor visual outcomes. CONCLUSION: NMOSD is a more common cause of optic neuritis than MS in Thai population. Female patients with poor initial VA, poor response to steroids treatment, and presenting recurrent attacks are highly suspicious for NMOSD. Optic neuritis without associated demyelinating disease has a better visual outcome and lower recurrence rate. Bentham Open 2018-08-31 /pmc/articles/PMC6131319/ /pubmed/30258505 http://dx.doi.org/10.2174/1874364101812010247 Text en © 2018 Hansapinyo and Vivattanaseth. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: (https://creativecommons.org/licenses/by/4.0/legalcode). This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Ophthalmology Hansapinyo, Linda Vivattanaseth, Chayanee Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title | Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title_full | Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title_fullStr | Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title_full_unstemmed | Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title_short | Clinical Characteristics, Treatment Outcomes and Predictive Factors in Optic Neuritis |
title_sort | clinical characteristics, treatment outcomes and predictive factors in optic neuritis |
topic | Ophthalmology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131319/ https://www.ncbi.nlm.nih.gov/pubmed/30258505 http://dx.doi.org/10.2174/1874364101812010247 |
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