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鞘内持续注入巴氯芬治疗脑源性痉挛

Continuous intrathecal baclofen infusion for spasticity of cerebral origin.

作者信息

Albright A L, Barron W B, Fasick M P, Polinko P, Janosky J

机构信息

Department of Neurosurgery, Children's Hospital of Pittsburgh, PA 15213.

出版信息

JAMA. 1993 Nov 24;270(20):2475-7.

PMID:8230625
Abstract

OBJECTIVE

To determine if continuous intrathecal baclofen infusion (CIBI) would provide continuous relief of spasticity in patients with spasticity of cerebral origin, especially children with cerebral palsy.

DESIGN

Prospective, unblinded trial, before and after CIBI.

SETTING

Children's Hospital of Pittsburgh (Pa).

PATIENTS

Thirty-seven patients, 5 to 27 years of age, with spasticity of cerebral origin.

INTERVENTION

Continuous intrathecal baclofen infusion for 3 to 48 months.

MAIN OUTCOME MEASURES

Muscle tone, range of motion, upper extremity timed tasks, activities of daily living (ADLs).

RESULTS

Six and 12 months after CIBI, muscle tone was significantly decreased in the upper (P = .04) and lower (P = .001) extremities. There was a significant relationship between baclofen dosage and muscle tone in the upper (P = .02) and lower (P = .001) extremities. Hamstring motion, upper extremity function, and ADLs were significantly improved in 25 patients who were capable of self-care.

CONCLUSION

Spasticity of cerebral origin can be effectively treated with CIBI. Because baclofen dosages can be titrated for the desired clinical response, CIBI is particularly useful for patients who need some spasticity to stand and ambulate.

摘要

目的

确定鞘内持续注入巴氯芬(CIBI)是否能持续缓解脑源性痉挛患者,尤其是脑瘫患儿的痉挛症状。

设计

CIBI治疗前后的前瞻性、非盲法试验。

地点

匹兹堡儿童医院(宾夕法尼亚州)。

患者

37例年龄在5至27岁的脑源性痉挛患者。

干预措施

鞘内持续注入巴氯芬3至48个月。

主要观察指标

肌张力、活动范围、上肢定时任务、日常生活活动能力(ADL)。

结果

CIBI治疗6个月和12个月后,上肢(P = 0.04)和下肢(P = 0.001)的肌张力显著降低。上肢(P = 0.02)和下肢(P = 0.001)的巴氯芬剂量与肌张力之间存在显著相关性。25例能够自理的患者的绳肌活动、上肢功能和ADL均有显著改善。

结论

CIBI可有效治疗脑源性痉挛。由于巴氯芬剂量可根据所需临床反应进行滴定,CIBI对需要一定痉挛才能站立和行走的患者特别有用。

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