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根据体质和性别划分的蜂毒穴位注射反应

Bee venom pharmacopuncture responses according to sasang constitution and gender.

作者信息

Kim Chaeweon, Lee Kwangho

机构信息

Department of Acupuncture & Moxibustion Medicine, Sangji University College of Oriental Medicine, Wonju, Gangwon, Korea.

出版信息

J Pharmacopuncture. 2013 Dec;16(4):43-8. doi: 10.3831/KPI.2013.16.023.

Abstract

OBJECTIVES

The current study was performed to compare the bee venom pharmacopuncture skin test reactions among groups with different sexes and Sasang constitutions.

METHODS

Between July 2012 and June 2013, all 76 patients who underwent bee venom pharmacopuncture skin tests and Sasang constitution diagnoses at Oriental Medicine Hospital of Sangji University were included in this study. The skin test was performed on the patient's forearm intracutaneously with 0.05 ml of sweet bee venom (SBV) on their first visit. If the patients showed a positive response, the test was discontinued. On the other hand, if the patient showed a negative response, the test was performed on the opposite forearm intracutaneously with 0.05 ml of bee venom pharmacopuncture 25% on the next day or the next visit. Three groups were made to compare the differences in the bee venom pharmacopuncture skin tests according to sexual difference and Sasang constitution: group A showed a positive response to SBV, group B showed a positive response to bee venom pharmacopuncture 25%, and group C showed a negative response on all bee venom pharmacopuncture skin tests. Fisher's exact test was performed to evaluate the differences statistically.

RESULTS

The results of the bee venom pharmacopuncture skin tests showed no significant differences according to Sasang constitution (P = 0.300) or sexual difference (P = 0.163).

CONCLUSION

No significant differences on the results of bee venom pharmacopuncture skin tests were observed according to two factors, Sasang constitution and the sexual difference.

摘要

目的

本研究旨在比较不同性别和体质类型人群的蜂毒药针皮肤试验反应。

方法

2012年7月至2013年6月期间,所有在桑济大学韩医院接受蜂毒药针皮肤试验和体质类型诊断的76例患者纳入本研究。首次就诊时,在前臂皮内注射0.05 ml甜蜂毒(SBV)进行皮肤试验。如果患者呈阳性反应,则停止试验。另一方面,如果患者呈阴性反应,则在第二天或下次就诊时,在对侧前臂皮内注射0.05 ml 25%蜂毒药针。根据性别差异和体质类型,分为三组比较蜂毒药针皮肤试验的差异:A组对SBV呈阳性反应,B组对25%蜂毒药针呈阳性反应,C组在所有蜂毒药针皮肤试验中均呈阴性反应。采用Fisher精确检验进行统计学差异评估。

结果

蜂毒药针皮肤试验结果在体质类型(P = 0.300)或性别差异(P = 0.163)方面无显著差异。

结论

根据体质类型和性别差异这两个因素,蜂毒药针皮肤试验结果未观察到显著差异。

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