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Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study

PURPOSE: We investigated the efficacy and safety of adalimumab (ADA) treatment for chronic recurrent Vogt-Koyanagi-Harada (VKH) patients with sunset glow fundus (SGF). METHODS: Medical records of 50 chronic recurrent VKH patients with SGF who received ADA treatment for more than 6 months were retros...

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Autores principales: Takeuchi, Masaru, Nakai, Shunsaku, Usui, Yoshihiko, Namba, Kenichi, Suzuki, Kayo, Harada, Yosuke, Kusuhara, Sentaro, Kaburaki, Toshikatsu, Tanaka, Rie, Takeuchi, Masaki, Mizuki, Nobuhisa, Nakai, Kei, Goto, Hiroshi, Herbort, Carl P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811924/
https://www.ncbi.nlm.nih.gov/pubmed/36618573
http://dx.doi.org/10.4103/sjopt.sjopt_204_22
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author Takeuchi, Masaru
Nakai, Shunsaku
Usui, Yoshihiko
Namba, Kenichi
Suzuki, Kayo
Harada, Yosuke
Kusuhara, Sentaro
Kaburaki, Toshikatsu
Tanaka, Rie
Takeuchi, Masaki
Mizuki, Nobuhisa
Nakai, Kei
Goto, Hiroshi
Herbort, Carl P.
author_facet Takeuchi, Masaru
Nakai, Shunsaku
Usui, Yoshihiko
Namba, Kenichi
Suzuki, Kayo
Harada, Yosuke
Kusuhara, Sentaro
Kaburaki, Toshikatsu
Tanaka, Rie
Takeuchi, Masaki
Mizuki, Nobuhisa
Nakai, Kei
Goto, Hiroshi
Herbort, Carl P.
author_sort Takeuchi, Masaru
collection PubMed
description PURPOSE: We investigated the efficacy and safety of adalimumab (ADA) treatment for chronic recurrent Vogt-Koyanagi-Harada (VKH) patients with sunset glow fundus (SGF). METHODS: Medical records of 50 chronic recurrent VKH patients with SGF who received ADA treatment for more than 6 months were retrospectively reviewed. RESULTS: The mean age of chronic recurrent VKH patients with SGF was 55.9 ± 14.4 years, and the male/female ratio was 26/24. Before ADA treatment, the mean daily dose of systemic corticosteroids was 16.5 ± 12.7 mg, and 22 patients (44%) were under immunosuppressors. LogMAR visual acuity (VA), flare counts, subfoveal choroidal thickness (SFCT), indocyanine green angiography scores, and corticosteroid and cyclosporine doses were significantly reduced by ADA treatment at 6 months compared to baseline. Among all parameters, flare count was significantly related to LogMAR VA. LogMAR VA was significantly related to flare counts but not to SFCT nor to ICGA scores. ADA treatment was continued in 94%. CONCLUSION: ADA was shown to be effective in achieving remission of chronic recurrent VKH disease with SGF refractory to conventional treatments, and was generally well tolerated with few serious adverse events.
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spelling pubmed-98119242023-01-05 Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study Takeuchi, Masaru Nakai, Shunsaku Usui, Yoshihiko Namba, Kenichi Suzuki, Kayo Harada, Yosuke Kusuhara, Sentaro Kaburaki, Toshikatsu Tanaka, Rie Takeuchi, Masaki Mizuki, Nobuhisa Nakai, Kei Goto, Hiroshi Herbort, Carl P. Saudi J Ophthalmol Original Article PURPOSE: We investigated the efficacy and safety of adalimumab (ADA) treatment for chronic recurrent Vogt-Koyanagi-Harada (VKH) patients with sunset glow fundus (SGF). METHODS: Medical records of 50 chronic recurrent VKH patients with SGF who received ADA treatment for more than 6 months were retrospectively reviewed. RESULTS: The mean age of chronic recurrent VKH patients with SGF was 55.9 ± 14.4 years, and the male/female ratio was 26/24. Before ADA treatment, the mean daily dose of systemic corticosteroids was 16.5 ± 12.7 mg, and 22 patients (44%) were under immunosuppressors. LogMAR visual acuity (VA), flare counts, subfoveal choroidal thickness (SFCT), indocyanine green angiography scores, and corticosteroid and cyclosporine doses were significantly reduced by ADA treatment at 6 months compared to baseline. Among all parameters, flare count was significantly related to LogMAR VA. LogMAR VA was significantly related to flare counts but not to SFCT nor to ICGA scores. ADA treatment was continued in 94%. CONCLUSION: ADA was shown to be effective in achieving remission of chronic recurrent VKH disease with SGF refractory to conventional treatments, and was generally well tolerated with few serious adverse events. Wolters Kluwer - Medknow 2022-12-27 /pmc/articles/PMC9811924/ /pubmed/36618573 http://dx.doi.org/10.4103/sjopt.sjopt_204_22 Text en Copyright: © 2022 Saudi Journal of Ophthalmology https://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
Takeuchi, Masaru
Nakai, Shunsaku
Usui, Yoshihiko
Namba, Kenichi
Suzuki, Kayo
Harada, Yosuke
Kusuhara, Sentaro
Kaburaki, Toshikatsu
Tanaka, Rie
Takeuchi, Masaki
Mizuki, Nobuhisa
Nakai, Kei
Goto, Hiroshi
Herbort, Carl P.
Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title_full Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title_fullStr Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title_full_unstemmed Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title_short Adalimumab treatment for chronic recurrent Vogt-Koyanagi-Harada disease with sunset glow fundus: A multicenter study
title_sort adalimumab treatment for chronic recurrent vogt-koyanagi-harada disease with sunset glow fundus: a multicenter study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811924/
https://www.ncbi.nlm.nih.gov/pubmed/36618573
http://dx.doi.org/10.4103/sjopt.sjopt_204_22
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