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鞘内长期注射巴氯芬治疗严重致残性痉挛:选择、临床评估及长期疗效

Chronic intrathecal baclofen in severely disabling spasticity: selection, clinical assessment and long-term benefit.

作者信息

Pirotte B, Heilporn A, Joffroy A, Zegers de Beyl D, Wesel P, Brotchi J, Levivier M

机构信息

Service de Neurochirurgie, Hôpital Erasme, Belgium.

出版信息

Acta Neurol Belg. 1995 Dec;95(4):216-25.

PMID:8553795
Abstract

Flexor and extensor spasms associated with severe spasticity frequently cause pain and suffering in neurologically impaired patients, and greatly interfere with comfort and activities. When high doses of oral medications are necessary to keep the symptoms under control and are poorly tolerated, the long-term spinal-selective intrathecal infusion of baclofen by means of implanted drug pump and catheter is a safe, efficient and reversible alternative to destructive surgical procedures. Between September 1991 and March 1995, intrathecal baclofen was infused in 18 selected patients out of a series of 42 severely disabled spastic cases. We report here our preliminary experience with the criteria of selection, the initial intrathecal bolus test and the long-term benefit of the selected patients. Our results confirm the dramatic immediate and long-term benefit reported in other series. After a period of treatment of 1 to 42 months, 13 patients had a complete disappearance of their spastic symptoms without any oral treatment, one patient kept unchanged clonus despite the use of low-dose oral treatment and another one a severe, not improved dysuria although in both of them hypertonia and spasms were abolished. Finally, 2 patients had important joint stiffness slightly impairing the benefit from the treatment. None of the 18 patients had central side-effects related to baclofen. With time, a slight increase in daily dose (inferior to 10%) was necessary in most patients.

摘要

与严重痉挛相关的屈肌和伸肌痉挛常常给神经功能受损的患者带来疼痛和痛苦,极大地影响他们的舒适度和日常活动。当需要大剂量口服药物来控制症状且耐受性较差时,通过植入式药物泵和导管进行长期脊髓选择性鞘内注射巴氯芬,是一种比破坏性手术更安全、有效且可逆的替代方法。1991年9月至1995年3月期间,在42例严重残疾痉挛患者中,为18例选定患者进行了鞘内巴氯芬注射。我们在此报告我们在患者选择标准、初始鞘内推注试验以及选定患者的长期疗效方面的初步经验。我们的结果证实了其他研究系列中所报道的显著的即刻和长期疗效。经过1至42个月的治疗期后,13例患者在未接受任何口服治疗的情况下痉挛症状完全消失,1例患者尽管使用了低剂量口服治疗,阵挛仍无变化,另1例患者严重排尿困难且未改善,尽管这两名患者的张力亢进和痉挛均已消除。最后,2例患者出现重要关节僵硬,轻微影响了治疗效果。18例患者均未出现与巴氯芬相关的中枢性副作用。随着时间推移,大多数患者的每日剂量需要轻微增加(低于10%)。

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