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地塞米松经声透入治疗后血清中的水平。

Serum dexamethasone levels after decadron phonophoresis.

机构信息

Department of Physical Education, Brigham Young University, Provo, UT.

出版信息

J Athl Train. 1999 Oct;34(4):338-41.

Abstract

OBJECTIVE

To determine serum levels of dexamethasone at several intervals after administration of Decadron (dexamethasone sodium phosphate) phonophoresis.

DESIGN AND SETTING

This study was designed as a 2-factor analysis of variance with repeated measures on 1 factor (blood draws). Independent variables were group (gel/sham, gel/ ultrasound, dexamethasone/sham, dexamethasone/ultrasound) and blood draws (pretreatment, posttreatment, 15 minutes, and 30 minutes). The dependent variable was the serum level of dexamethasone.

SUBJECTS

Forty healthy college students (21 males, 19 females; mean age = 22 +/- 1.3 years) with no known drug allergies or current medication use were randomly assigned to 1 of 4 treatment groups. The treatment site was the left forearm.

MEASUREMENTS

After the pretreatment blood draw, a 10- minute ultrasound treatment was administered, followed by a posttreatment blood draw. Two additional blood draws followed at 15-minute intervals. A total of 4 serum samples (5 cc each) from each subject were centrifuged, and the pipetted serum was frozen for later analysis by double antibody radioimmunoassay.

RESULTS

No significant amounts of serum dexamethasone were detected in 12 consecutive samples. Testing of additional samples was, therefore, discontinued.

CONCLUSIONS

Decadron phonophoresis as used in this experiment did not result in detectable serum levels of dexamethasone. More study is needed to validate the efficacy of Decadron phonophoresis on serum dexamethasone levels.

摘要

目的

测定地塞米松磷酸钠经 Decadron(地塞米松)声透皮给药后不同时间点的血清水平。

设计和设置

本研究采用双因素方差分析,对 1 个因素(采血)进行重复测量。自变量为组(凝胶/假、凝胶/超声、地塞米松/假、地塞米松/超声)和采血(预处理、后处理、15 分钟和 30 分钟)。因变量为地塞米松的血清水平。

受试者

40 名健康大学生(21 名男性,19 名女性;平均年龄=22 +/- 1.3 岁),无已知药物过敏或当前用药史,随机分为 4 个治疗组之一。治疗部位为左前臂。

测量

预处理采血后,给予 10 分钟的超声治疗,随后进行后处理采血。15 分钟后再进行两次采血。从每个受试者中抽取 4 份血清样本(每份 5cc),离心后吸取血清,冷冻备用,以后用双抗体放射免疫法分析。

结果

在连续 12 个样本中未检测到明显量的血清地塞米松。因此,停止了对额外样本的测试。

结论

在本实验中使用的地塞米松声透皮给药未导致可检测的血清地塞米松水平。需要进一步研究以验证地塞米松声透皮给药对血清地塞米松水平的疗效。

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