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鞘内持续输注巴氯芬对非卧床脑瘫儿童影响的对照研究。

Controlled study of the effects of continuous intrathecal baclofen infusion in non-ambulant children with cerebral palsy.

机构信息

Department of Paediatrics, Derbyshire Children's Hospital, Derby, and Queens Medical Centre, Nottingham, UK.

出版信息

Dev Med Child Neurol. 2011 Aug;53(8):736-41. doi: 10.1111/j.1469-8749.2011.04009.x. Epub 2011 Jun 27.

Abstract

AIM

To measure changes in children with severe spastic cerebral palsy (CP) after continuous intrathecal baclofen (ITB) infusion over 18 months and to compare the results with those of a comparison group awaiting treatment.

METHOD

Thirty-eight children with severe spastic CP considered suitable for ITB were assessed when first seen, just before insertion of an intrathecal pump, and 9 months and 18 months later. Eighteen children waited around 9 months for a pump (group 1: nine males, nine females; mean age 9y 11mo [SD 3y 7mo], nine in Gross Motor Function Classification System [GMFCS] level IV, nine in level V). This baseline period was used as a control for comparison with the first and second 9-month periods after the pump for the remaining 20 children (group 2: 11 males, nine females; mean age 10y 2mo [SD 3y 1mo], nine in GMFCS level IV, 11 in level V). The main outcome measure was the Pediatric Evaluation of Disability Inventory (PEDI); other assessments were of function, ease of care, quality of life, and costs of new equipment.

RESULTS

No significant change was found in the PEDI between group 1 while awaiting treatment and group 2 in the two periods afterwards, nor in the Lifestyle Assessment Questionnaire or the cost of new equipment. Significant changes were found in group 2 in the first 9 months according to the modified Ashworth score (difference between mean values for groups -1.7, standard error 0.58; p=0.008), Penn Spasm score (-1.3, 0.37; p=0.001), mean joint range of movement (8.3°, 2.8; p=0.005), and Caregiver Questionnaire (-19.7, 5.1; p=0.01), and in the second 9 months for the Modified Ashworth Scale score (-0.62, 0.12; p=0.001).

INTERPRETATION

ITB in children with severe spastic CP over the first 18 months improves their quality of life in terms of comfort and ease of care. It has less effect on function, participation in society, or the overall cost of new equipment.

摘要

目的

测量在连续鞘内巴氯芬(ITB)输注 18 个月后严重痉挛性脑瘫(CP)儿童的变化,并将结果与等待治疗的对照组进行比较。

方法

38 名严重痉挛性 CP 患儿在首次就诊时、植入鞘内泵前和 9 个月和 18 个月后进行评估。18 名儿童等待约 9 个月的泵(第 1 组:9 名男性,9 名女性;平均年龄 9y11mo[SD3y7mo],9 名在粗大运动功能分类系统[GMFCS] 4 级,9 名在 5 级)。此基线期用作与泵后前 9 个月和后 9 个月期间的第 2 组(第 2 组:11 名男性,9 名女性;平均年龄 10y2mo[SD3y1mo],9 名在 GMFCS 4 级,11 名在 5 级)的比较对照。主要结局测量指标为儿科残疾评估量表(PEDI);其他评估指标为功能、护理便利性、生活质量和新设备成本。

结果

在等待治疗的第 1 组和随后的 2 组中,PEDI 或生活方式评估问卷或新设备成本均未发现显著变化。第 2 组在第 1 个 9 个月中根据改良 Ashworth 评分(组间平均值差异-1.7,标准误差 0.58;p=0.008)、Penn 痉挛评分(-1.3,0.37;p=0.001)、平均关节活动范围(8.3°,2.8;p=0.005)和照顾者问卷(-19.7,5.1;p=0.01)有显著变化,在第 2 个 9 个月中改良 Ashworth 量表评分(-0.62,0.12;p=0.001)也有显著变化。

结论

在严重痉挛性 CP 儿童中,在最初 18 个月内使用 ITB 可改善他们的舒适度和护理便利性,从而提高他们的生活质量。它对功能、参与社会或新设备的总体成本影响较小。

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