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用于诊断不宁腿综合征的“左旋多巴试验”的验证

Validation of the "L-DOPA test" for diagnosis of restless legs syndrome.

作者信息

Stiasny-Kolster Karin, Kohnen Ralf, Möller Jens Carsten, Trenkwalder Claudia, Oertel Wolfgang H

机构信息

Department of Neurology, Center of Nervous Diseases, Philipps-University, Marburg, Germany.

出版信息

Mov Disord. 2006 Sep;21(9):1333-9. doi: 10.1002/mds.20969.

Abstract

We developed and validated a standardized test procedure to evaluate the accuracy of the supportive diagnostic criterion "response to dopaminergic treatment" in restless legs syndrome (RLS). Forty-eight patients who fulfilled at least three of the four essential criteria for RLS, thus including uncertain clinical cases for a nonexpert, were recruited. Patients received a preliminary diagnosis of RLS or non-RLS. All patients underwent a polysomnography (PSG) and were then asked to perform the diagnostic L-DOPA test at home, which consisted in the application of one single dose of 100/25 mg L-DOPA/benserazide and a subsequent observational period of 2 hours. Before, and in 15-minute intervals after, drug intake, the patients rated the severity of the "symptoms in the legs" and the "urge to move the legs" using a 100-mm visual analogue scale. Considering a 50% improvement as a positive test result, we found a sensitivity of 88% ("symptoms in the legs") and 80% ("urge to move the legs") with a specificity of 100% for both test items. A rate of 90% or 83% of all patients could be correctly diagnosed by the L-DOPA test. Both scales were able to predict the response to dopaminergic agents in the subsequent course of the treatment by 100%. The periodic leg movements arousal index as assessed by polysomnography was less appropriate for the prediction of the correct diagnosis. We recommend the L-DOPA test for diagnostic decision making in all patients with an unclear RLS diagnosis according to the essential diagnostic criteria of the International RLS Study Group.

摘要

我们开发并验证了一种标准化测试程序,以评估不安腿综合征(RLS)中支持性诊断标准“对多巴胺能治疗的反应”的准确性。招募了48名至少符合RLS四项基本标准中的三项的患者,因此包括了非专业人员难以确定的临床病例。患者接受了RLS或非RLS的初步诊断。所有患者均接受了多导睡眠图(PSG)检查,然后被要求在家中进行诊断性左旋多巴测试,该测试包括服用一剂100/25 mg左旋多巴/苄丝肼,随后观察2小时。在服药前以及服药后每隔15分钟,患者使用100毫米视觉模拟量表对“腿部症状”和“腿部移动冲动”的严重程度进行评分。将改善50%作为阳性测试结果,我们发现两项测试项目的敏感性分别为88%(“腿部症状”)和80%(“腿部移动冲动”),特异性均为100%。左旋多巴测试能够正确诊断所有患者中的90%或83%。两种量表都能够100%预测后续治疗中对多巴胺能药物的反应。通过多导睡眠图评估的周期性腿部运动唤醒指数不太适合预测正确诊断。我们建议根据国际RLS研究组的基本诊断标准,对所有RLS诊断不明确的患者进行左旋多巴测试以进行诊断决策。

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