TY - JOUR
T1 - Visual Outcomes Following Plasma Exchange for Optic Neuritis
T2 - An International Multicenter Retrospective Analysis of 395 Optic Neuritis Attacks
AU - Chen, John J.
AU - Flanagan, Eoin P.
AU - Pittock, Sean J.
AU - Stern, Nicole Caroline
AU - Tisavipat, Nanthaya
AU - Bhatti, M. Tariq
AU - Chodnicki, Kevin D.
AU - Tajfirouz, Deena A.
AU - Jamali, Sepideh
AU - Kunchok, Amy
AU - Eggenberger, Eric R.
AU - Nome, Marie A.Di
AU - Sotirchos, Elias S.
AU - Vasileiou, Eleni S.
AU - Henderson, Amanda D.
AU - Arnold, Anthony C.
AU - Bonelli, Laura
AU - Moss, Heather E.
AU - Navarro, Sylvia Elizabeth Villarreal
AU - Padungkiatsagul, Tanyatuth
AU - Stiebel-Kalish, Hadas
AU - Lotan, Itay
AU - Wilf-Yarkoni, Adi
AU - Danesh-Meyer, Helen
AU - Ivanov, Stefan
AU - Huda, Saif
AU - Forcadela, Mirasol
AU - Hodge, David
AU - Poullin, Pascale
AU - Rode, Julie
AU - Papeix, Caroline
AU - Saheb, Samir
AU - Boudot de la Motte, Marine
AU - Vignal, Catherine
AU - Hacohen, Yael
AU - Pique, Julie
AU - Maillart, Elisabeth
AU - Deschamps, Romain
AU - Audoin, Bertrand
AU - Marignier, Romain
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/8
Y1 - 2023/8
N2 - PURPOSE: To evaluate the effectiveness of plasma exchange (PLEX) for optic neuritis (ON). METHODS: We conducted an international multicenter retrospective study evaluating the outcomes of ON following PLEX. Outcomes were compared to raw data from the Optic Neuritis Treatment Trial (ONTT) using a matched subset. RESULTS: A total of 395 ON attack treated with PLEX from 317 patients were evaluated. The median age was 37 years (range 9-75), and 71% were female. Causes of ON included multiple sclerosis (108), myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) (92), aquaporin-4-IgG–positive neuromyelitis optica spectrum disorder (AQP4+NMOSD) (75), seronegative-NMOSD (34), idiopathic (83), and other (3). Median time from onset of vision loss to PLEX was 2.6 weeks (interquartile range [IQR], 1.4-4.0). Median visual acuity (VA) at the time of PLEX was count fingers (IQR, 20/200-hand motion), and median final VA was 20/25 (IQR, 20/20-20/60) with no differences among etiologies except MOGAD-ON, which had better outcomes. In 81 (20.5%) ON attacks, the final VA was 20/200 or worse. Patients with poor outcomes were older (P = .002), had worse VA at the time of PLEX (P < .001), and longer delay to PLEX (P < .001). In comparison with the ONTT subset with severe corticosteroid-unresponsive ON, a final VA of worse than 20/40 occurred in 6 of 50 (12%) PLEX-treated ON vs 7 of 19 (37%) from the ONTT treated with intravenous methylprednisolone without PLEX (P = .04). CONCLUSION: Most ON attacks improved with PLEX, and outcomes were better than attacks with similar severity in the ONTT. The presence of severe vision loss at nadir, older age, and longer delay to PLEX predicted a worse outcome whereas MOGAD-ON had a more favorable prognosis.
AB - PURPOSE: To evaluate the effectiveness of plasma exchange (PLEX) for optic neuritis (ON). METHODS: We conducted an international multicenter retrospective study evaluating the outcomes of ON following PLEX. Outcomes were compared to raw data from the Optic Neuritis Treatment Trial (ONTT) using a matched subset. RESULTS: A total of 395 ON attack treated with PLEX from 317 patients were evaluated. The median age was 37 years (range 9-75), and 71% were female. Causes of ON included multiple sclerosis (108), myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) (92), aquaporin-4-IgG–positive neuromyelitis optica spectrum disorder (AQP4+NMOSD) (75), seronegative-NMOSD (34), idiopathic (83), and other (3). Median time from onset of vision loss to PLEX was 2.6 weeks (interquartile range [IQR], 1.4-4.0). Median visual acuity (VA) at the time of PLEX was count fingers (IQR, 20/200-hand motion), and median final VA was 20/25 (IQR, 20/20-20/60) with no differences among etiologies except MOGAD-ON, which had better outcomes. In 81 (20.5%) ON attacks, the final VA was 20/200 or worse. Patients with poor outcomes were older (P = .002), had worse VA at the time of PLEX (P < .001), and longer delay to PLEX (P < .001). In comparison with the ONTT subset with severe corticosteroid-unresponsive ON, a final VA of worse than 20/40 occurred in 6 of 50 (12%) PLEX-treated ON vs 7 of 19 (37%) from the ONTT treated with intravenous methylprednisolone without PLEX (P = .04). CONCLUSION: Most ON attacks improved with PLEX, and outcomes were better than attacks with similar severity in the ONTT. The presence of severe vision loss at nadir, older age, and longer delay to PLEX predicted a worse outcome whereas MOGAD-ON had a more favorable prognosis.
UR - http://www.scopus.com/inward/record.url?scp=85158108269&partnerID=8YFLogxK
U2 - 10.1016/j.ajo.2023.02.013
DO - 10.1016/j.ajo.2023.02.013
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C2 - 36822570
AN - SCOPUS:85158108269
SN - 0002-9394
VL - 252
SP - 213
EP - 224
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
ER -