A. Lizarraga, Salman F Bhai, G. Wolfe, L. Herbelin, S. Nations, Morgan McCreary, D. Saperstein, R. Barohn
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The objective of the study was to evaluate if different patterns of QST abnormalities could distinguish between PN types. \nMethods: \nThis single-center retrospective cohort study evaluated the frequency of QST abnormalities to vibratory, cold and heat detection thresholds in a large population of PN cases evaluated at the University of Texas Southwestern Medical Center peripheral neuropathy clinic between 1995-2000. PN was categorized by etiology. \nResults: \nA total of 559 QST studies were performed in this study. The average age of patients (n=557) was 60 years with a male-to-female ratio of 1:1. The most common diagnosis was cryptogenic sensory polyneuropathy (CSPN, n=294), followed by Charcot–Marie–Tooth disease (n=84)). Meta-regression of vibration and cold indicate that the expected proportion of abnormal responses is less for the vibration test (p = 0.0002), relative to the cold test. However, no differences were observed between diagnoses. \nConclusions: \nThough abnormal QST thresholds were seen in most patients with PN, patterns of QST abnormalities do not distinguish between different types of PN. The routine clinical utility of QST is likely limited.","PeriodicalId":309700,"journal":{"name":"RRNMF Neuromuscular Journal","volume":"55 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quantitative sensory testing in a large cohort of neuropathy patients\",\"authors\":\"A. Lizarraga, Salman F Bhai, G. Wolfe, L. Herbelin, S. Nations, Morgan McCreary, D. Saperstein, R. 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PN was categorized by etiology. \\nResults: \\nA total of 559 QST studies were performed in this study. The average age of patients (n=557) was 60 years with a male-to-female ratio of 1:1. The most common diagnosis was cryptogenic sensory polyneuropathy (CSPN, n=294), followed by Charcot–Marie–Tooth disease (n=84)). Meta-regression of vibration and cold indicate that the expected proportion of abnormal responses is less for the vibration test (p = 0.0002), relative to the cold test. However, no differences were observed between diagnoses. \\nConclusions: \\nThough abnormal QST thresholds were seen in most patients with PN, patterns of QST abnormalities do not distinguish between different types of PN. 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引用次数: 0
摘要
背景:定量感觉测试(QST)是一种主观但可靠且可量化的方法,用于检测患者对不同感觉刺激的阈值。QST用于测量小纤维和大纤维神经功能,并可与周围神经病变(PN)的其他诊断方式结合使用。然而,QST区分不同类型PN的效用尚未得到探讨。该研究的目的是评估不同类型的QST异常是否可以区分PN类型。方法:这项单中心回顾性队列研究评估了1995-2000年间在德克萨斯大学西南医学中心周围神经病变诊所评估的大量PN病例中,QST异常到振动、冷和热检测阈值的频率。PN按病因分类。结果:本研究共进行了559项QST研究。患者平均年龄(n=557)为60岁,男女比例为1:1。最常见的诊断是隐源性感觉多神经病变(CSPN, n=294),其次是charcott - marie - tooth病(n=84)。振动和冷态的元回归表明,相对于冷态试验,振动试验的预期异常响应比例更小(p = 0.0002)。然而,在诊断之间没有观察到差异。结论:虽然大多数PN患者的QST阈值异常,但QST异常模式并不能区分不同类型的PN。QST的常规临床应用可能是有限的。
Quantitative sensory testing in a large cohort of neuropathy patients
Background:
Quantitative sensory testing (QST) is a subjective but reliable and quantifiable method to detect patient thresholds to different sensory stimuli. QST is used to measure small- and large-fiber nerve function and can be used in conjunction with other diagnostic modalities in the evaluation of peripheral neuropathy (PN). The utility of QST to distinguish among different types of PN, however, has not been explored. The objective of the study was to evaluate if different patterns of QST abnormalities could distinguish between PN types.
Methods:
This single-center retrospective cohort study evaluated the frequency of QST abnormalities to vibratory, cold and heat detection thresholds in a large population of PN cases evaluated at the University of Texas Southwestern Medical Center peripheral neuropathy clinic between 1995-2000. PN was categorized by etiology.
Results:
A total of 559 QST studies were performed in this study. The average age of patients (n=557) was 60 years with a male-to-female ratio of 1:1. The most common diagnosis was cryptogenic sensory polyneuropathy (CSPN, n=294), followed by Charcot–Marie–Tooth disease (n=84)). Meta-regression of vibration and cold indicate that the expected proportion of abnormal responses is less for the vibration test (p = 0.0002), relative to the cold test. However, no differences were observed between diagnoses.
Conclusions:
Though abnormal QST thresholds were seen in most patients with PN, patterns of QST abnormalities do not distinguish between different types of PN. The routine clinical utility of QST is likely limited.