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多发性硬化症、利妥昔单抗和 COVID-19。

Multiple sclerosis, rituximab, and COVID-19.

机构信息

Department of Neurology, Los Angeles Medical Center, Southern California Permanente Medical Group, Los Angeles, CA, USA.

Department of Research & Evaluation, Southern California Permanente Medical Group, Pasadena, CA, USA.

出版信息

Ann Clin Transl Neurol. 2021 Apr;8(4):938-943. doi: 10.1002/acn3.51342. Epub 2021 Mar 30.

DOI:10.1002/acn3.51342
PMID:33783140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8045943/
Abstract

We conducted a retrospective cohort study in Kaiser Permanente Southern California from 1 January 2020 to 30 September 2020. We found that rituximab-treated persons with multiple sclerosis (pwMS, n = 1895) were more likely be hospitalized (n = 8, 33.3%), but not die (n = 0) from COVID-19, compared to the 4.81 million non-MS population (5.8% and 1.4%, respectively). Time in months (adjusted OR = 0.32, 95% CI = 0.15-0.69, p = 0.0033) and receiving 1000 mg compared to lower doses at last infusion (adjusted OR = 6.28, 95% CI = 1.38-28.5, p = 0.0173) were independent predictors of COVID-19 severity. Rituximab-treated pwMS should be counseled to take extra precautions in the 5 months following each infusion. Using extended dosing intervals and lower doses could be considered.

摘要

我们在 Kaiser Permanente Southern California 进行了一项回顾性队列研究,时间为 2020 年 1 月 1 日至 2020 年 9 月 30 日。我们发现,与 481 万非多发性硬化症人群(分别为 5.8%和 1.4%)相比,接受利妥昔单抗治疗的多发性硬化症患者(pwMS,n=1895)更有可能因 COVID-19 住院(n=8,33.3%),但不会死亡(n=0)。随访期间每增加一个月(调整后的比值比[OR] = 0.32,95%置信区间[CI] = 0.15-0.69,p=0.0033)以及最后一次输注时接受 1000mg 剂量而非较低剂量(调整后的 OR = 6.28,95% CI = 1.38-28.5,p=0.0173)与 COVID-19 严重程度独立相关。应建议接受利妥昔单抗治疗的 pwMS 在每次输注后的 5 个月内采取额外的预防措施。可以考虑延长给药间隔和降低剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60aa/8045943/fa2518bba2a5/ACN3-8-938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60aa/8045943/fa2518bba2a5/ACN3-8-938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60aa/8045943/fa2518bba2a5/ACN3-8-938-g001.jpg

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