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Dysthyroid optic neuropathy: emerging treatment strategies

PURPOSE: Dysthyroid optic neuropathy (DON) is a rare sight-threatening complication of Graves’ disease. First-line treatment for DON consists of high-dose intravenous methylprednisolone (ivMP), followed by immediate orbital decompression (OD) if the response is poor or absent as recommended by the 2...

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Autores principales: Pelewicz-Sowa, M., Miśkiewicz, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261203/
https://www.ncbi.nlm.nih.gov/pubmed/36802028
http://dx.doi.org/10.1007/s40618-023-02036-0
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author Pelewicz-Sowa, M.
Miśkiewicz, P.
author_facet Pelewicz-Sowa, M.
Miśkiewicz, P.
author_sort Pelewicz-Sowa, M.
collection PubMed
description PURPOSE: Dysthyroid optic neuropathy (DON) is a rare sight-threatening complication of Graves’ disease. First-line treatment for DON consists of high-dose intravenous methylprednisolone (ivMP), followed by immediate orbital decompression (OD) if the response is poor or absent as recommended by the 2021 European Group on Graves’ orbitopathy guidelines. The safety and efficacy of the proposed therapy have been proven. However, consensus regarding possible therapeutic options for patients with contraindications to ivMP/OD or resistant form of disease is missing. This paper aims to provide and summarize all available data regarding possible alternative treatment strategies for DON. METHODS: A comprehensive literature search within an electronic database was performed including data published until December 2022. RESULTS: Overall, 52 articles describing use of emerging therapeutic strategies for DON were identified. Collected evidence indicates that biologics, including teprotumumab and tocilizumab, may be considered as an important possible treatment option for DON patients. Rituximab should be avoided in DON due to conflicting data and risk of adverse events. Orbital radiotherapy could be beneficial for patients with restricted ocular motility classified as poor surgical candidates. CONCLUSION: Only a limited number of studies have been dedicated to the therapy of DON, mostly retrospective with a small sample size. Clear criteria regarding diagnosis and resolution of DON do not exist, which restricts comparison of therapeutic outcomes. Randomized clinical trials and comparison studies with long-term follow-ups are necessary to verify the safety and efficacy of each therapeutic option for DON.
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spelling pubmed-102612032023-06-15 Dysthyroid optic neuropathy: emerging treatment strategies Pelewicz-Sowa, M. Miśkiewicz, P. J Endocrinol Invest Review PURPOSE: Dysthyroid optic neuropathy (DON) is a rare sight-threatening complication of Graves’ disease. First-line treatment for DON consists of high-dose intravenous methylprednisolone (ivMP), followed by immediate orbital decompression (OD) if the response is poor or absent as recommended by the 2021 European Group on Graves’ orbitopathy guidelines. The safety and efficacy of the proposed therapy have been proven. However, consensus regarding possible therapeutic options for patients with contraindications to ivMP/OD or resistant form of disease is missing. This paper aims to provide and summarize all available data regarding possible alternative treatment strategies for DON. METHODS: A comprehensive literature search within an electronic database was performed including data published until December 2022. RESULTS: Overall, 52 articles describing use of emerging therapeutic strategies for DON were identified. Collected evidence indicates that biologics, including teprotumumab and tocilizumab, may be considered as an important possible treatment option for DON patients. Rituximab should be avoided in DON due to conflicting data and risk of adverse events. Orbital radiotherapy could be beneficial for patients with restricted ocular motility classified as poor surgical candidates. CONCLUSION: Only a limited number of studies have been dedicated to the therapy of DON, mostly retrospective with a small sample size. Clear criteria regarding diagnosis and resolution of DON do not exist, which restricts comparison of therapeutic outcomes. Randomized clinical trials and comparison studies with long-term follow-ups are necessary to verify the safety and efficacy of each therapeutic option for DON. Springer International Publishing 2023-02-18 2023 /pmc/articles/PMC10261203/ /pubmed/36802028 http://dx.doi.org/10.1007/s40618-023-02036-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Pelewicz-Sowa, M.
Miśkiewicz, P.
Dysthyroid optic neuropathy: emerging treatment strategies
title Dysthyroid optic neuropathy: emerging treatment strategies
title_full Dysthyroid optic neuropathy: emerging treatment strategies
title_fullStr Dysthyroid optic neuropathy: emerging treatment strategies
title_full_unstemmed Dysthyroid optic neuropathy: emerging treatment strategies
title_short Dysthyroid optic neuropathy: emerging treatment strategies
title_sort dysthyroid optic neuropathy: emerging treatment strategies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10261203/
https://www.ncbi.nlm.nih.gov/pubmed/36802028
http://dx.doi.org/10.1007/s40618-023-02036-0
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