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鞘内注射甲氨蝶呤治疗多发性硬化症。

Intrathecal methotrexate treatment in multiple sclerosis.

机构信息

Multiple Sclerosis Research Center of New York, 4th Floor, New York, NY 10019, USA.

出版信息

J Neurol. 2010 Nov;257(11):1806-11. doi: 10.1007/s00415-010-5614-4. Epub 2010 Jun 10.

Abstract

This study reports on the feasibility of using intrathecal methotrexate (ITMTX) in treatment unresponsive multiple sclerosis (MS) patients with progressive forms of the disease. A retrospective, open-label, chart review analysis was conducted following patients (n = 121) with MS for up to eight treatments given every 8-11 weeks. Patients were considered for ITMTX treatment if they were unresponsive to or intolerant of FDA-approved treatments. There was a 1 year follow-up after their eighth or last treatment (if discontinued earlier). Patients underwent neurological assessments and expanded disability status scale (EDSS) evaluations. No serious adverse effects were noted during the study period. In 87 secondary progressive MS patients, EDSS scores were stable or improved in 89%, with significantly improved mean EDSS post-treatment compared to baseline (P = 0.014). Of 34 primary progressive patients, EDSS scores were stable in 82%, with no significant progression in EDSS post-treatment compared to baseline. ITMTX may have a beneficial role in progressive forms of MS and is well tolerated with no serious adverse events.

摘要

本研究报告了鞘内注射甲氨蝶呤(ITMTX)治疗对疾病进展型多发性硬化(MS)无反应的患者的可行性。对 121 名 MS 患者进行了回顾性、开放性、图表审查分析,这些患者最多接受了 8 次治疗,每 8-11 周一次。如果患者对 FDA 批准的治疗无反应或不耐受,则考虑使用 ITMTX 治疗。在第八次或最后一次治疗后(如果更早停止)进行了为期 1 年的随访。患者接受了神经系统评估和扩展残疾状况量表(EDSS)评估。在研究期间未观察到严重不良事件。在 87 名继发进展性 MS 患者中,89%的患者 EDSS 评分稳定或改善,治疗后平均 EDSS 明显优于基线(P=0.014)。在 34 名原发进展性患者中,82%的患者 EDSS 评分稳定,治疗后 EDSS 与基线相比无明显进展。ITMTX 可能对进展型 MS 具有有益作用,且耐受性良好,无严重不良事件。

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