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Long-term follow-up of facilitated subcutaneous immunoglobulin therapy in multifocal motor neuropathy
被引:1
|作者:
Al-Zuhairy, Ali
[1
]
Sindrup, Soren H.
[2
]
Jakobsen, Johannes
[1
]
机构:
[1] Copenhagen Univ Hosp, Dept Neurol, Rigshosp, Blegdamsvej 9, DK-2100 Copenhagen, Denmark
[2] Odense Univ Hosp, Dept Neurol, Odense, Denmark
关键词:
Peripheral neuropathy;
Multifocal motor neuropathy;
Immunoglobulin;
Treatment;
Facilitated subcutaneous immunoglobulin;
Clinical long-term study;
INTRAVENOUS IMMUNOGLOBULIN;
WALKING ABILITY;
IMMUNODEFICIENCY;
EFFICACY;
STRENGTH;
INFUSION;
D O I:
10.1016/j.jns.2021.117495
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objective: To assess the feasibility, efficacy and patient satisfaction of long-term facilitated subcutaneous immunoglobulin therapy (fSCIG) in multifocal motor neuropathy (MMN). Methods: Twelve patients previously participating in a randomized trial investigating the short-term efficacy of fSCIG were offered to switch to fSCIG maintenance therapy following a variable interval on conventional subcutaneous immunoglobulin. Results: Eight patients were switched to fSCIG maintenance therapy, seven of whom were invited for a follow-up assessment after 18 months (range 13-23 months) of treatment. The age at follow-up was 57 years (range 45-70 years) and patients received a median weekly dose immunoglobulin G of 32.5 g (range 20.0-50.0 g), the dose being unaltered compared to baseline values following completion of the fSCIG trial. In five patients the infusion was biweekly, whereas two patients were infused weekly. The follow-up mean isometric strength normalized to pre-trial values was 107.7% (95% CI 86.4-129.0%) being non-inferior to baseline values (104.7%, 95% CI 97.6-111.8%, P = 0.015). The mean ODSS was 2.0 (95% CI 0.8-3.2) which is identical to the baseline score following completion of the fSCIG trial, the P-value for non-inferiority being <0.0001. The secondary variables of impairment, function and quality of life at follow-up all were non-inferior to baseline values (P <= 0.046). Conclusion: fSCIG seems feasible and effective for long-term maintenance treatment in patients with MMN.
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