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[急性多巴胺能反应性试验在帕金森病及帕金森综合征诊断中的应用]

[Acute dopaminergic responsiveness test in diagnosis of Parkinson's disease and Parkinsonian disorders].

作者信息

Li Wei, Feng Tao, Wang Yong-jun, Lin Jin-xi, Xu Xiao-tong

机构信息

Department of Neurology, Beijing Tiantan Hospital , Capital Medicine University , Beijing 100050, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2008 Aug 26;88(33):2347-9.

Abstract

OBJECTIVE

To investigate the features of acute dopaminergic responsiveness test in patients with Parkinsonian disorders, and to find a convenient approach of differential diagnosis of Parkinsonian disorders.

METHODS

Sixty inpatients with Parkinson disease (PD) or Parkinson's syndrome, including vascular Parkinsonism (VP), multiple system atrophy (MSA), etc, were given the Levodopa and Benserazide tablets, containing levodopa of the doses of 62.5, 125 187.5, 250, and 375 mg in a pattern of gradual acute DOPA test. The third part of the unified Parkinson's disease rating scale (UPDRS) was used to evaluate the development of PD symptom before and 1 hour after taking the medicine. The differences among the improvement rates were compared with one-way ANOVA test and post hoc multiple comparison by SSPS 11.5.

RESULTS

The improvement rates after taking the Levodopa and Benserazide tablets were 11.3% for the dose of 62.5 mg, 23.1% for 125 mg, 29.4% for 187.5 mg, 31.2% for 250 mg, and 34.3% for 375 mg. When the dose was 65 mg there was no significant difference between the diagnoses of PD and Parkinsonism, however, when the doses were 125, 187.5, 250, and 375 mg, and the improvement rates > or = 23.1%, 29.4%, 31.2%, and 34.3% were used as the indicators of diagnosis of PD, there were significant differences between the diagnoses of PD and Parkinson's syndrome.

CONCLUSION

Easy and convenient, acute dopaminergic responsiveness test is not associated with sex, age, and H-Y ranking, and is an important approach in differential diagnosis of Parkinsonian disorders.

摘要

目的

探讨帕金森病相关疾病患者急性多巴胺能反应性试验的特点,寻找一种便捷的帕金森病相关疾病鉴别诊断方法。

方法

对60例帕金森病(PD)或帕金森综合征患者,包括血管性帕金森综合征(VP)、多系统萎缩(MSA)等,给予复方左旋多巴片,按逐渐递增剂量的急性多巴试验方式,分别给予含左旋多巴62.5、125、187.5、250和375mg的剂量。采用统一帕金森病评定量表(UPDRS)第三部分评估服药前及服药1小时后帕金森病症状的改善情况。用SPSS 11.5软件进行单因素方差分析及事后多重比较,比较改善率之间的差异。

结果

服用复方左旋多巴片后的改善率分别为:62.5mg剂量时为11.3%;125mg剂量时为23.1%;187.5mg剂量时为29.4%;250mg剂量时为31.2%;375mg剂量时为34.3%。当剂量为65mg时,PD与帕金森综合征的诊断之间无显著差异,然而,当剂量为125、187.5、250和375mg,且以改善率≥23.1%、29.4%、31.2%和34.3%作为PD诊断指标时,PD与帕金森综合征的诊断之间存在显著差异。

结论

急性多巴胺能反应性试验简便易行,与性别、年龄及H-Y分级无关,是帕金森病相关疾病鉴别诊断的重要方法。

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