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术前系统阿片类药物需求、鞘内试验剂量和非心理因素作为鞘内泵治疗结果的预测因素:一位临床医生在腰椎后路减压术后疼痛方面的经验。

Role of pretrial systemic opioid requirements, intrathecal trial dose, and non-psychological factors as predictors of outcome for intrathecal pump therapy: one clinician's experience with lumbar postlaminectomy pain.

机构信息

Department of Anesthesiology, Henry Ford Hospital, Detroit, MI 48202, USA.

出版信息

Neuromodulation. 2011 Mar-Apr;14(2):165-75; discussion 175. doi: 10.1111/j.1525-1403.2011.00333.x. Epub 2011 Mar 1.

Abstract

OBJECTIVE

Non-psychological parameters may predict pump success.

METHODS

Review was performed on 35 implants for gender, age, pretrial/trial dose, baseline visual analog scale (VAS), and pain location. One-year outcomes were % change VAS/intrathecal dose and medication change. Spearman coefficients correlated pretrial/trial dose, age, baseline VAS, and % change in VAS/intrathecal dose. Wilcoxon Rank-Sum tests correlated gender/pain location and % change in VAS/intrathecal dose. Pretrial/trial dose, baseline VAS, and medication change was tested using Wilcoxon Rank-Sums. Chi-square was used to correlate medication change with gender/pain location. A two-sample t-test compared age and medication change.

RESULTS

Positive correlation between % change VAS and trial dose was noted. Greater age correlated with lower VAS and % dose change. Marginally significant difference in % dose change by pain location was present with higher doses for leg pain.

CONCLUSION

Trial dose, age, and partially pain location are good predictors of pain relief.

摘要

目的

非心理参数可能预测泵的成功。

方法

对 35 例植入物进行了性别、年龄、术前/试验剂量、基线视觉模拟评分(VAS)和疼痛部位的回顾。一年的结果是 VAS/鞘内剂量的变化百分比和药物变化。Spearman 系数相关术前/试验剂量、年龄、基线 VAS 和 VAS/鞘内剂量的变化百分比。Wilcoxon 秩和检验相关性别/疼痛部位和 VAS/鞘内剂量的变化百分比。使用 Wilcoxon 秩和检验对术前/试验剂量、基线 VAS 和药物变化进行测试。卡方检验用于比较药物变化与性别/疼痛部位的关系。两样本 t 检验比较年龄和药物变化。

结果

VAS 的变化百分比与试验剂量呈正相关。年龄越大,VAS 和剂量变化百分比越低。腿部疼痛的疼痛部位的剂量变化百分比有显著差异,剂量较高。

结论

试验剂量、年龄和部分疼痛部位是疼痛缓解的良好预测指标。

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