Visual Outcomes Following Plasma Exchange for Optic Neuritis: An International Multicenter Retrospective Analysis of 395 Optic Neuritis Attacks

dc.contributor.authorChen J.J.
dc.contributor.authorFlanagan E.P.
dc.contributor.authorPittock S.J.
dc.contributor.authorStern N.C.
dc.contributor.authorTisavipat N.
dc.contributor.authorBhatti M.T.
dc.contributor.authorChodnicki K.D.
dc.contributor.authorTajfirouz D.A.
dc.contributor.authorJamali S.
dc.contributor.authorKunchok A.
dc.contributor.authorEggenberger E.R.
dc.contributor.authorNome M.A.D.
dc.contributor.authorSotirchos E.S.
dc.contributor.authorVasileiou E.S.
dc.contributor.authorHenderson A.D.
dc.contributor.authorArnold A.C.
dc.contributor.authorBonelli L.
dc.contributor.authorMoss H.E.
dc.contributor.authorNavarro S.E.V.
dc.contributor.authorPadungkiatsagul T.
dc.contributor.authorStiebel-Kalish H.
dc.contributor.authorLotan I.
dc.contributor.authorWilf-Yarkoni A.
dc.contributor.authorDanesh-Meyer H.
dc.contributor.authorIvanov S.
dc.contributor.authorHuda S.
dc.contributor.authorForcadela M.
dc.contributor.authorHodge D.
dc.contributor.authorPoullin P.
dc.contributor.authorRode J.
dc.contributor.authorPapeix C.
dc.contributor.authorSaheb S.
dc.contributor.authorBoudot de la Motte M.
dc.contributor.authorVignal C.
dc.contributor.authorHacohen Y.
dc.contributor.authorPique J.
dc.contributor.authorMaillart E.
dc.contributor.authorDeschamps R.
dc.contributor.authorAudoin B.
dc.contributor.authorMarignier R.
dc.contributor.otherMahidol University
dc.date.accessioned2023-05-27T17:13:45Z
dc.date.available2023-05-27T17:13:45Z
dc.date.issued2023-08-01
dc.description.abstractPURPOSE: 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.
dc.identifier.citationAmerican Journal of Ophthalmology Vol.252 (2023) , 213-224
dc.identifier.doi10.1016/j.ajo.2023.02.013
dc.identifier.eissn18791891
dc.identifier.issn00029394
dc.identifier.pmid36822570
dc.identifier.scopus2-s2.0-85158108269
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/82858
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleVisual Outcomes Following Plasma Exchange for Optic Neuritis: An International Multicenter Retrospective Analysis of 395 Optic Neuritis Attacks
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85158108269&origin=inward
oaire.citation.endPage224
oaire.citation.startPage213
oaire.citation.titleAmerican Journal of Ophthalmology
oaire.citation.volume252
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationQueen Square Multiple Sclerosis Centre
oairecerif.author.affiliationThe Walton Centre NHS Foundation Trust
oairecerif.author.affiliationCentre de Résonance Magnétique Biologique et Médicale
oairecerif.author.affiliationPermanente Medical Group
oairecerif.author.affiliationFondation Adolphe de Rothschild
oairecerif.author.affiliationUniversity of California, Los Angeles
oairecerif.author.affiliationMayo Clinic Scottsdale-Phoenix, Arizona
oairecerif.author.affiliationHopital Neurologique et Neurochirurgical Pierre Wertheimer
oairecerif.author.affiliationCleveland Clinic Foundation
oairecerif.author.affiliationGreat Ormond Street Hospital for Children NHS Foundation Trust
oairecerif.author.affiliationHôpital Universitaire Pitié Salpêtrière
oairecerif.author.affiliationStanford University
oairecerif.author.affiliationThe University of Auckland
oairecerif.author.affiliationTel Aviv University
oairecerif.author.affiliationMayo Clinic
oairecerif.author.affiliationJohns Hopkins University
oairecerif.author.affiliationAP-HM Assistance Publique - Hôpitaux de Marseille
oairecerif.author.affiliationMayo Clinic in Jacksonville, Florida
oairecerif.author.affiliationJohns Hopkins School of Medicine
oairecerif.author.affiliationS.J.P.)
oairecerif.author.affiliationS.J.)
oairecerif.author.affiliationDepartments of Ophthalmology (M.A.D.N.)
oairecerif.author.affiliationA.K.)
oairecerif.author.affiliationE.M.)

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