首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >Botulinum toxin F in the treatment of torticollis clinically resistant to botulinum toxin A.
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Botulinum toxin F in the treatment of torticollis clinically resistant to botulinum toxin A.

机译:肉毒杆菌毒素F在临床上对肉毒杆菌毒素A耐药的斜颈的治疗中。

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摘要

Two reports have shown a Japanese preparation of botulinum toxin type F (BTX-F) to be an effective alternative for patients with torticollis who develop clinical resistance to botulinum toxin type A (BTX-A). A group of patients with torticollis, comprising five secondary non-responders and one primary non-responder, were treated with a preparation of BTX-F produced in the UK (Speywood Pharmaceuticals). A low dose of BTX-F (220 mouse units (MU) in total) was given into clinically affected neck muscles, followed six weeks later by an injection of a total of 520 MU. Antibodies to BTX-A (mouse protection assay) were present in all secondary non-responders but not in the primary non-responder. No patients developed atrophy after injection of Dysport BTX-A (40 MU) into the left extensor digitorum brevis muscle whereas pronounced atrophy occurred in all patients after injection of 40 MU of BTX-F into the right extensor digitorum brevis muscle. Three patients improved subjectively after treatment with 220 MU BTX-F and five (all secondary non-responders) after the subsequent dose of 520 MU (two considerably), with reduced Tsui scores, but group scores were only significantly changed after the higher dose. The primary non-responder remained unchanged after both doses of BTX-F. One patient reported mild dysphagia with 520 MU BTX-F. Mean duration of improvement with 520 MU BTX-F was five (range 4-6)weeks. Thus BTX-F provides benefit for BTX-A non-responders with few side effects but for a shorter period than BTX-A, possibly due to relative underdosing. As with BTX-A, biological sensitivity to BTX-F does not necessarily predict a clinical response.
机译:两项报告显示,日本制备的F型肉毒杆菌毒素(BTX-F)是对临床对A型肉毒杆菌毒素产生耐药性的斜颈患者的有效替代品。用英国生产的BTX-F制剂(Speywood Pharmaceuticals)治疗一组患有斜颈的患者,其中包括5名次要无反应者和1名原发性无反应者。将低剂量的BTX-F(总共220个小鼠单位(MU))注入受临床影响的颈部肌肉,然后在六周后注射总计520 MU。 BTX-A(小鼠保护分析)抗体存在于所有继发性非应答者中,但不存在于主要非应答者中。将Dysport BTX-A(40 MU)注射到左侧短指伸肌短肌中后,没有患者出现萎缩,而所有患者将40 MU的BTX-F注射到右侧伸指短肌短肌中均出现了明显的萎缩。 3例患者在接受220 MU BTX-F治疗后主观改善,5例(所有继发性无反应者)在随后的520 MU剂量(明显改善2例)后有所改善,Tsu评分降低,但组评分仅在高剂量后显着改变。两种剂量的BTX-F后,主要的无反应者均保持不变。一名患者报告了520 MU BTX-F轻度吞咽困难。 520 MU BTX-F的平均改善时间为5周(4-6周)。因此,BTX-F可以为BTX-A无反应者带来好处,副作用少,但周期比BTX-A短,这可能是由于相对剂量不足引起的。与BTX-A一样,对BTX-F的生物敏感性不一定能预测临床反应。

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