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长期鞘内注射巴氯芬治疗脊髓源性严重痉挛的剂量与用法

The dosage and administration of long-term intrathecal baclofen therapy for severe spasticity of spinal origin.

作者信息

Kawano Osamu, Masuda Muneaki, Takao Tsuneaki, Sakai Hiroaki, Morishita Yuichiro, Hayashi Tetsuo, Ueta Takayoshi, Maeda Takeshi

机构信息

Department of Orthopaedic Surgery, Spinal Injuries Center, Fukuoka, Japan.

出版信息

Spinal Cord. 2018 Oct;56(10):996-999. doi: 10.1038/s41393-018-0153-4. Epub 2018 Jun 12.

DOI:10.1038/s41393-018-0153-4
PMID:29895878
Abstract

STUDY DESIGN

Retrospective chart audit.

OBJECTIVE

To indicate the appropriate baclofen dosage to control severe spasticity of spinal origin and to develop the optimal administration protocol for long-term intrathecal baclofen (ITB) therapy.

SETTING

Department of Orthopaedic Surgery, Spinal Injuries Center, Japan.

METHODS

Thirty-four people with spasticity of various spinal origins who were consistently treated at our hospital were included. The median follow-up period was 6 years and 11 months. Measures of Ashworth score were taken before and after surgical implant of baclofen pump. We decided not to increase the baclofen dosage after the Ashworth score reached 1. We recorded the control of spasticity, changes in the baclofen dose, and the incidence of complications.

RESULTS

The average Ashworth score was 3.31 (1.75-4.0) before implant surgery, 1.38 (1.0-2.25) after implant surgery, and 1.39 (1.0-2.25) at the final follow-up, while the average baclofen dose (therapeutic/optimal dose) was 230.6 μg/day (50-450). The incidence of each complication was as follows: 8.8% (n = 3) catheter-related, 2.9% (n = 1) pump-related and 5.9% (n = 2) drug tolerance. No patients experienced withdrawal syndrome. Dose fluctuation with changes in the pathology of the original disease was observed in three cases.

CONCLUSIONS

The usage of the Ashworth score as a guide for dose adjustment was found to be a good objective indicator for ITB therapy. The administration based on this objective indicator made it possible to effectively manage patients with a relatively low dose of baclofen and a low rate of drug-related complications.

摘要

研究设计

回顾性病历审核。

目的

确定控制脊髓源性严重痉挛的合适巴氯芬剂量,并制定长期鞘内注射巴氯芬(ITB)治疗的最佳给药方案。

地点

日本脊柱损伤中心骨科。

方法

纳入34例我院持续治疗的各种脊髓源性痉挛患者。中位随访期为6年11个月。在植入巴氯芬泵前后测量Ashworth评分。当Ashworth评分达到1分时,我们决定不再增加巴氯芬剂量。我们记录了痉挛的控制情况、巴氯芬剂量的变化以及并发症的发生率。

结果

植入手术前平均Ashworth评分为3.31(1.75 - 4.0),植入手术后为1.38(1.0 - 2.25),末次随访时为1.39(1.0 - 2.25),而平均巴氯芬剂量(治疗/最佳剂量)为230.6μg/天(50 - 450)。各并发症的发生率如下:导管相关8.8%(n = 3),泵相关2.9%(n = 1),药物耐受性5.9%(n = 2)。无患者出现戒断综合征。3例患者观察到随着原发病病理变化出现剂量波动。

结论

发现使用Ashworth评分作为剂量调整指南是ITB治疗的良好客观指标。基于该客观指标给药能够以相对低剂量的巴氯芬和较低的药物相关并发症发生率有效管理患者。

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