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对于1型复杂性区域疼痛综合征患者而言,有意义的疼痛减轻是指什么?

What is a meaningful pain reduction in patients with complex regional pain syndrome type 1?

作者信息

Forouzanfar Tymour, Weber Wilhelm E J, Kemler Marius, van Kleef Maarten

机构信息

Pain Management and Research Center, University Hospital Maastricht, P.O. Box 5800, 6202 AZ Maastricht, The Netherlands.

出版信息

Clin J Pain. 2003 Sep-Oct;19(5):281-5. doi: 10.1097/00002508-200309000-00001.

Abstract

OBJECTIVE

To investigate the degree of pain reduction in patients with complex regional pain syndrome type 1 (CRPS 1) that can be defined as "successful."

DESIGN

All patients rated their pain on a visual analog scale (VAS; 0-10) before treatment and on three occasions after treatment, at 6 months, 1 year, and 2 years. Patients also rated a Global Perceived Effect (GPE) for their pain relief at the same time periods. The GPE items were classified as "successful" or "unsuccessful." The mean absolute and relative pain reduction (using the VAS) was calculated for both "successful" and "unsuccessful" GPE classifications for each time period. Sensitivity and specificity analyses were performed.

PATIENTS

Sixty-one patients with CRPS 1.

RESULTS

The patients defined a relative pain reduction of 58% (SD, 23.4) or more as "successful," whereas in "successful" and "unsuccessful" patient groups the pain was reduced significantly on the VAS. Furthermore, sensitivity and specificity analyses showed that a cut-off point of 50% relative pain reduction and a 3-cm absolute pain reduction on the VAS have the highest likelihood that patients will report their treatment "successful" on the GPE.

CONCLUSIONS

Relative pain reduction of 50% or more and an absolute pain reduction of at least 3 cm on the VAS are accurate in predicting a successful pain reduction after a given treatment.

摘要

目的

研究1型复杂性区域疼痛综合征(CRPS 1)患者疼痛减轻程度,将其定义为“成功”。

设计

所有患者在治疗前以及治疗后6个月、1年和2年这三个时间点,使用视觉模拟量表(VAS;0 - 10)对疼痛进行评分。患者同时对同一时期疼痛缓解的整体感知效果(GPE)进行评分。GPE项目分为“成功”或“不成功”。计算每个时间段“成功”和“不成功”GPE分类的平均绝对和相对疼痛减轻程度(使用VAS)。进行敏感性和特异性分析。

患者

61例CRPS 1患者。

结果

患者将相对疼痛减轻58%(标准差,23.4)或更多定义为 “成功”,而在“成功”和“不成功”患者组中,VAS评分的疼痛均显著减轻。此外,敏感性和特异性分析表明,VAS上相对疼痛减轻50%且绝对疼痛减轻3 cm的截断点,患者在GPE上报告治疗“成功”的可能性最高。

结论

VAS上相对疼痛减轻50%或更多且绝对疼痛减轻至少于3 cm,对于预测特定治疗后疼痛减轻是否成功是准确可靠的。

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