首页   按字顺浏览 期刊浏览 卷期浏览 SENSORY AXONOPATHY IN MILD TO MODERATE PERIPHERAL ARTERIAL DISEASE
SENSORY AXONOPATHY IN MILD TO MODERATE PERIPHERAL ARTERIAL DISEASE

 

作者: Viviane,   Ugalde Mark,   Wineinger C.,   Kappagoda David,   Kilmer William,   Pevec William,   Rosen Deborah,  

 

期刊: American Journal of Physical Medicine and Rehabilitation  (OVID Available online 1998)
卷期: Volume 77, issue 1  

页码: 59-68

 

ISSN:0894-9115

 

年代: 1998

 

出版商: OVID

 

关键词: Peripheral Vascular Disease;Peripheral Neuropathy;Sural Nerve;Nerve Conduction Studies;Peroneal Nerve

 

数据来源: OVID

 

摘要:

The effect of mild to moderate arterial occlusive disease on peripheral nervous system conduction was prospectively investigated in 18 subjects and 18 control subjects, aged 40 to 85 years. Experimental and control subjects underwent a thorough history and physical followed by vascular and electrophysiologic studies. The primary outcome measure was the sensory nerve action potential. Although 33% of the subjects with peripheral arterial disease had experienced paresthesias, the clinical evaluation of sensation was relatively unaffected. Sensory conduction studies revealed 30% absent sural responses and 56% absent superficial peroneal nerve responses in subjects with peripheral arterial disease compared with 3 and 14% absent responses in control subjects, respectively (P = 0.044; 0.025). There were no differences in distal latency or sensory amplitude, although the superficial peroneal amplitude did approach significance (P = 0.06). No significant differences were found in motor distal latency, amplitude, or conduction velocity. Age, leg length, temperature, disease severity, presence of paresthesias, cholesterol levels, and past alcohol or tobacco ingestion did not account for the difference in sensory responses. These results support the presence of a mild sensory axonopathy in subjects with peripheral arterial disease. Electromyographers should be cognizant of absent distal responses from peripheral arterial disease so as not to ascribe the findings to an alternative pathology and should not attribute abnormal motor conduction results to the presence of this degree of peripheral arterial disease.

 

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