High-dose Ig VENA is well tolerated and efficacious in patients with multifocal motor neuropathy

被引:1
作者
Nobile-Orazio, Eduardo [1 ,7 ]
Cocito, Dario [2 ]
Briani, Chiara [3 ]
Plasmati, Rosaria [4 ]
Schenone, Angelo [5 ]
Gallia, Francesca [1 ]
Marjanovic, Ivan [6 ]
Suffredini, Anna Lotti [6 ]
机构
[1] Milan Univ, Dept Med Biotechnol & Translat Med BIOMETRA, Humanitas Clin & Res Ctr, Neuromuscular & Neuroimmunol Serv, Milan, Italy
[2] Turin Univ, Neurosci Dept, Neurol 2, Turin, Italy
[3] Univ Padua, Dept Neurosci, Padua, Italy
[4] Bellaria Hosp, IRCCS Neurol Sci, Bologna, Italy
[5] Genoa Univ, Dept Neurosci Rehabil Ophthalmol Genet & Maternal, Genoa, Italy
[6] Kedrion Biopharma, Med Affairs, Lucca, Italy
[7] Milan Univ, Dept Med Biotechnol & Translat Med, Humanitas Clin & Res Inst, Neuromuscular & Neuroimmunol Serv, Via Manzoni 56, I-20089 Milan, Italy
关键词
Multifocal motor neuropathy; Ig VENA; High dose; Efficacy; Tolerability; Immunoglobulin therapy; INTRAVENOUS IMMUNOGLOBULIN; THERAPY;
D O I
10.1007/s10072-017-2826-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multifocal motor neuropathy (MMN) is a rare, chronic, motor neuropathy that progressively impairs physical functioning and quality of life. Randomised controlled trials have shown that high-dose intravenous immunoglobulin (IVIg) is superior to placebo in improving muscle strength and disability, but many patients require periodic infusions to maintain long-term improvement. This observational, multicentre, retrospective study investigated the efficacy and tolerability of human normal immunoglobulin (Ig VENA) at high intravenous infusion rates in 20 MMN patients (14 male, 6 female). Thirty days after the first infusion, there was an improvement of at least 1 point in two muscles compared to baseline on the Medical Research Council (MRC) scale and of 1 point in the ONLS (Overall Neuropathy Limitation Scale) scale in 15 patients (75%) and 10 patients (50%), respectively; 45% improved on both scales. At 6 months, 100% of 12 patients had improved on the MRC and 79% of 14 patients had improved on the ONLS scale; 83% improved on both scales. All reported adverse drug reactions (ADR) were mild, transient and possibly related to the study drug. Four patients (20%) reported ADRs, three reported headache and one fever. There were no serious or unexpected ADRs. By confirming that high-dose Ig VENA is efficacious and well tolerated, this study adds to the evidence base for IVIg in MMN and potentially increases clinicians' and patients' choice of therapy.
引用
收藏
页码:899 / 902
页数:4
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