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首次发作的严重视神经炎的治疗结果

Treatment outcomes of first-ever episode of severe optic neuritis.

作者信息

Galetta Kristin, Ryan Sophia, Manzano Giovanna, Chibnik Lori B, Balaban Denis, Prasad Sashank, Chwalisz Bart K, Salazar-Camelo Andrea, Conway Sarah, Levy Michael, Matiello Marcelo

机构信息

Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology, Mayo Clinic Alix School of Medicine, Rochester MN.

Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA; Department of Neurology, Mount Sinai Health System, New York, NY; Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology, Mayo Clinic Alix School of Medicine, Rochester MN.

出版信息

Mult Scler Relat Disord. 2022 Oct;66:104020. doi: 10.1016/j.msard.2022.104020. Epub 2022 Jul 2.

Abstract

BACKGROUND

Severe optic neuritis (ON) is an acute inflammatory attack of the optic nerve(s) leading to severe visual loss that may occur in isolation or as part of a relapsing neuroinflammatory disease, such neuromyelitis optica spectrum disorder (NMOSD), myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD), or more rarely multiple sclerosis (MS). In cases of first-ever severe ON of uncertain etiology best treatment strategies remain unclear.

METHODS

We reviewed records of all patients with a documented diagnosis of ON between 2004 and 2019 at Mass General Brigham (MGB) and Johns Hopkins University (JHU) hospitals. Out of 381 patients identified, 90 (23.6%) satisfied the study criteria for severe ON with visual acuity (VA) equal to or worse than 20/200 (logMAR=1) at nadir in the affected eye and had sufficient follow-up data. Treatment strategies with corticosteroids only or treatment escalation with therapeutic plasma exchange (PLEX) after steroids were compared and evaluated for differences in visual outcomes at follow-up.

RESULTS

Of the 90 patients with severe optic neuritis, 71(78.9%) received corticosteroids only, and 19 (17.0%) underwent PLEX following corticosteroids. Of the 71 patients who received steroids without escalation to PLEX, 30 patients (42.2%) achieved complete recovery (VA 20/20 on the affected eye), whereas 35 (49.3%) had a partial recovery and 6 (8.4%) had no recovery. Among the 19 corticosteroid non-responders patients who underwent escalation treatment, 13 (68.4%) made complete recovery, 6 (31.6%) had partial visual recoveries (p=0.0434). The median delta logMAR of patients who underwent escalation of care was -1.2 compared with 2.0 for the ones who did not (p=0.0208). A change of delta logmar 2.0 is equivalent of going from hand motion to light perception and the positive delta value refers to intra-attack worsening. Other than not responding to steroids, patients who underwent PLEX tended to have more severe ON with significantly worse nadir visual acuity compared with those who received corticosteroids alone (logMAR 3.12 (min 2.0 - max 5.0) vs. 2.17 (min 1.3 - max 3.0); p=0.004).

CONCLUSION

In our cohort of first-ever severe optic neuritis of unknown etiology, patients that did not respond adequately to corticosteroids benefited from treatment escalation to PLEX, followed in most cases by Rituximab, regardless of final etiology. Randomized controlled trials are needed to confirm the best treatment strategies.

摘要

背景

严重视神经炎(ON)是视神经的急性炎症发作,可导致严重视力丧失,其可单独发生,或作为复发性神经炎症性疾病的一部分出现,如视神经脊髓炎谱系障碍(NMOSD)、髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD),或更罕见的多发性硬化症(MS)。在病因不明的首次严重ON病例中,最佳治疗策略仍不明确。

方法

我们回顾了2004年至2019年在麻省总医院布莱根分院(MGB)和约翰霍普金斯大学(JHU)医院确诊为ON的所有患者的记录。在381例确诊患者中,90例(23.6%)符合严重ON的研究标准,即患眼最低点视力(VA)等于或低于20/200(logMAR = 1),且有足够的随访数据。比较并评估了仅使用皮质类固醇的治疗策略或在使用类固醇后升级为治疗性血浆置换(PLEX)的治疗策略在随访时视力结果的差异。

结果

在90例严重视神经炎患者中,71例(78.9%)仅接受了皮质类固醇治疗,19例(17.0%)在接受皮质类固醇治疗后进行了PLEX。在71例未升级为PLEX而仅接受类固醇治疗的患者中,30例(42.2%)实现了完全恢复(患眼VA为20/20),而35例(49.3%)部分恢复,6例(8.4%)未恢复。在19例接受升级治疗的皮质类固醇无反应患者中,13例(68.4%)完全恢复,6例(31.6%)部分视力恢复(p = 0.0434)。接受升级治疗的患者的中位logMAR变化值为-1.2,而未接受升级治疗的患者为2.0(p = 0.0208)。logMAR变化值2.0相当于从手动感知变为光感,正变化值表示发作期病情恶化。除了对类固醇无反应外,接受PLEX的患者往往患有更严重的ON,最低点视力明显比仅接受皮质类固醇治疗的患者差(logMAR 3.12(最小值2.0 - 最大值5.0)对2.17(最小值1.3 - 最大值3.0);p = 0.004)。

结论

在我们的首次病因不明的严重视神经炎队列中,对皮质类固醇治疗反应不佳的患者从升级为PLEX治疗中获益,大多数情况下随后使用利妥昔单抗,无论最终病因如何。需要进行随机对照试验以确认最佳治疗策略。

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