...
首页> 外文期刊>Pakistan journal of medical sciences. >The clinical & neurophysiological study of leprosy
【24h】

The clinical & neurophysiological study of leprosy

机译:麻风的临床和神经生理学研究

获取原文

摘要

Objectives: The aim of this study was to evaluate neurological and neurophysiological features of leprosy.Methods: Seventy seven hospitalized leprosy patients (52 male, 25 female) were examined neurological and neurophysiologically between 2010 and 2012. Standard procedures were performed for evaluating sensory and motor conduction studies to all patients. Motor studies were carried out on median, ulnar, tibial and common peroneal nerves. Sensory studies were carried out on median, ulnar and sural nerves. Sympathetic skin response (SSR) recordings on both hands and feet, and the heart rate (R-R) interval variation (RRIV) recordings on precordial region were done in order to evaluate the autonomic dysfunction.Results: The mean age was 59.11±14.95 years ranging between 17 and 80 years. The mean duration of disease was 35.58±18.30 years. Clinically, the patients had severe deformity and disability. In neurophysiological examinations, sensory, motor conduction studies of the lower extremities were found to be more severely affected than upper, and sensory impairment predominated over motor. Abnormal SSRs were recorded in 63 (81.8%) cases of leprosy. Abnormal RRIVs were recorded in 41 (53.2%) cases and abnormal RRIVs with hyperventilation were recorded in 55 (71.4%) cases of leprosy. Significant differences were found between SSR and sensory conduction parameters of median, ulnar nerves as well as motor conduction parameters of median, ulnar and peroneal nerves (p < 0.05).Conclusion: Peripheral nervous system dysfunction is accompanied by autonomic nervous system dysfunction in leprosy patients. Sympathetic involvement may predominate over parasympathetic involvement.doi: http://dx.doi.org/10.12669/pjms.303.5354How to cite this:Cabalar M, Yayla V, Ulutas S, Senadim S, Oktar AC. The clinical & neurophysiological study of leprosy. Pak J Med Sci 2014;30(3):501-506. doi: http://dx.doi.org/10.12669/pjms.303.5354This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
机译:目的:本研究旨在评估麻风病的神经和神经生理特征。方法:在2010年至2012年之间对77例住院麻风病患者(男52例,女25例)进行了神经学和神经生理学检查。执行了评估感觉和运动的标准程序对所有患者进行传导研究。在正中,尺骨,胫骨和腓总神经上进行了运动研究。对正中,尺神经和腓肠神经进行了感觉研究。进行手足交感性皮肤反应(SSR)记录和心前区心律(RR)间隔变化(RRIV)记录,以评估自主神经功能障碍。结果:平均年龄为59.11±14.95岁在17至80年之间。平均病程为35.58±18.30年。临床上,患者有严重的畸形和残疾。在神经生理学检查中,发现下肢的感觉,运动传导研究比上肢受到的影响更大,并且感觉障碍比运动更为重要。在63例(81.8%)麻风病例中记录到SSR异常。麻风患者中有41例(53.2%)记录了RRIVs异常,而通气过度的RRIVs则有55例(71.4%)。 SSR与正中,尺神经的感觉传导参数以及正中,尺神经和腓神经的运动传导参数之间存在显着差异(p <0.05)。结论:麻风病人的周围神经系统功能障碍伴有自主神经系统功能障碍。交感神经的参与可能比副交感神经的参与更为重要。doi:http://dx.doi.org/10.12669/pjms.303.5354引用方式:凯巴拉M,Yayla V,Ulutas S,Senadim S,Oktar AC。麻风的临床和神经生理学研究。 Pak J Med Sci 2014; 30(3):501-506。 doi:http://dx.doi.org/10.12669/pjms.303.5354这是根据知识共享署名许可(http://creativecommons.org/licenses/by/3.0)条款发布的开放获取文章,允许在任何媒体中无限制地使用,分发和复制,但要正确引用原始作品。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号