Hospital Pengajar University Putra Malaysia, University Putra Malaysia, Selangor, Malaysia.
Department of Neurology, Kuala Lumpur Hospital, Kuala Lumpur, Malaysia.
J Clin Neurosci. 2019 Nov;69:114-119. doi: 10.1016/j.jocn.2019.08.016. Epub 2019 Aug 12.
We determined the clinical progression, disability and outcome of 11 Multifocal Motor Neuropathy (MMN) patients from Malaysia. Mean patient age was 46.8 (SD 13.3), with mean disease duration of 108.0 months (SD 80.2). All reported unilateral limb weakness at onset. At diagnosis, after mean 49.9 months (SD 73.5) delay, 7 (63.6%) had more than 2 limbs involvement. Nine (90%) of 10 patients received induction IVIg dose of 2.0 gm/kg responded, demonstrated improvement in MRCSS of > 2 points or mRS score of > 1 point. We observed 38.5% drop in IVIg dose to mean 1.12 gm/kg/month after 12 months of treatment, and a further 34.8% drop upon 24th month treatment to mean dose of 0.73 gm/kg/month. This was in parallel with initial improvement in MRCSS and mRS, observed among 88.9% and 77.8% of the patients, and later further improvement (33.3%) or stabilization (66.7%) of mRS score toward 2nd year. During the same period, 50% of patients reported deterioration in ONLS, 33.3% in grip strength and 16.7% in MMN-RODS. Beyond 36th month, average annual IVIg dose increased at 0.12 gm/kg/year (SD 0.09) or 11.2%, up to the 84th months. Despite that, progressive deterioration was observed in term of number of limbs involvement, definite motor conduction blocks on electrophysiology study, and both clinical as well as functional scores. Although IVIg dose reduction for maintenance treatment in MMN is recommended, careful clinical assessment is required to prevent under-treatment. Use of reliable and responsive modern outcome measures is important to quantify clinically relevant change to guide therapy.
我们确定了 11 名来自马来西亚的多灶性运动神经病(MMN)患者的临床进展、残疾和结局。患者平均年龄为 46.8(SD 13.3)岁,平均病程为 108.0(SD 80.2)个月。所有患者均报告首发时单侧肢体无力。诊断时,平均延迟 49.9(SD 73.5)个月后,7 例(63.6%)有超过 2 个肢体受累。10 例患者中有 9 例(90%)接受了 2.0 gm/kg 的诱导 IVIg 剂量,结果均有反应,MRCSS 评分改善>2 分或 mRS 评分>1 分。我们观察到,治疗 12 个月后,IVIg 剂量降至平均 1.12 gm/kg/月,下降了 38.5%,治疗 24 个月后进一步下降了 34.8%,降至平均 0.73 gm/kg/月。这与患者中 88.9%和 77.8%的初始 MRCSS 和 mRS 改善平行,随后 33.3%或稳定(66.7%)mRS 评分至第 2 年。同期,50%的患者报告 ONLS 恶化,33.3%的患者报告握力下降,16.7%的患者报告 MMN-RODS 恶化。超过 36 个月后,平均每年 IVIg 剂量增加 0.12 gm/kg/年(SD 0.09)或 11.2%,直至第 84 个月。尽管如此,在肢体受累数量、电生理研究中明确的运动传导阻滞以及临床和功能评分方面,仍观察到进行性恶化。虽然建议在 MMN 中进行维持治疗的 IVIg 剂量减少,但需要进行仔细的临床评估,以防止治疗不足。使用可靠和敏感的现代结局测量方法对于量化对指导治疗有临床意义的变化很重要。