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find Keyword "肌萎缩侧索硬化" 9 results
  • INTRODUCTION OF AMYOTROPHIC LATERAL SCLEROSIS SELF-ASSESSMENT SCALE

    Objective To introduce a new functional self-assessment scale of amyotrophic lateral sclerosis (ALS). Methods By comparing current different ALS functional scales and combining relative cl inical experience and numeric pain intensity scale, ALS self-assessment scale was set down by International Association of Neural Restoration. Results ALS self-assessment scale included 3 categories with 18 items, adopting 10 points grading system, namely 10 was defined as the normal, 0 as the worst, and the total scores was 180. This scale included: ① Bulbus medullae function: speech, swallowing, sal ivation, and tongue extension. ② Limbs function: left arm movement, left hand movement, right arm movement, right hand movement, left leg movement, right leg movement, trunk movement, head-up, walking, and cl imbing stairs. ③ Others: breathing, muscular tone, pain, and muscle discomfort. Conclusion ALS self-assessment scale is specifically designed for ASL patients. It can evaluate patient’s function comprehensively and is simple and convenient, consuming less time.

    Release date:2016-09-01 09:17 Export PDF Favorites Scan
  • MR Spectroscopy Evaluation and Short-term Outcome of Olfactory Ensheathing Cells Transplantation in Amyotrophic Lateral Sclerosis Patients

    Objective To evaluate proton MR spectroscopy (1H-MRS) for detection of the motor cortex and adjacent brain in amyotrophic lateralsclerosis (ALS) patients with apparent upper motor neuron involvement after olfactory ensheathing cells(OECs) transplantation. Methods From December 2004 to February 2005, 7 patients with clinically definite ALS who could safely undergo MRS were admitted into the perspective study. The neurological status, ALS functional rating scale (ALSFRS), EMG, and 1H-MRS taken before and 2 weeks after operationswere carefully analyzed. The NAA/Cr and Cho/Cr ratios were measured in the cerebral peduncle,genu and posterior limb of the internal capsule, corona radiata and precentral gyrus. Results The ALSFRS in 2 cases mproved obviously whose ALSFRS increased from 30 to 33 and from 29 to 34 respectively. And 5 cases remained stable 2 weeks after OECs transplantation. Statistical analyses for all seven cases showed both theNAA/Cr and Cho/Cr ratios decreased, but in the two cases with ALSFRS improvement the NAA/Cr increased in the certain anatomic position which confirmed the neurological and EMG findings. Conclusion The proton MR spectroscopy is a suitablenoninvasive measure for ALS evaluation. The preliminary study suggests that twoof the seven ALS cases improved apparently shortterm after OECs transplantation. More patients are required for the clinical study and longer followup duration is needed for future research.

    Release date:2016-09-01 09:19 Export PDF Favorites Scan
  • Short-term Outcome of Olfactory Ensheathing Cells Transplantation for Treatment of Amyotrophic Lateral Sclerosis

    Objective To determine whether transplanting olfactory ensheathing cells (OECs) is effective in controlling or reversing the deterioration caused by amyotrophic lateral sclerosis (ALS). Methods Between February 2003 and April 2006, 327 patients (241 males and 86 females) with probable or definite ALS (diagnosed according to the El Escorial criteria) received the OECs transplantation. Their ages ranged from 20 to 84 years (51.6±11.1 years). The duration of symptoms before surgical treatment was 4-8 months to 13 years (2.9±2.0 years). OECs were cultured and injected into pathological regions of the spinal cord and/or bilateral corona radiata of the brain; the patients were divided into three groups, group A (cord only,n=29), group B (cord and brain,n=6), and group C (brain only,n=292) based on the transplant sites. Results The patient’s neurological function was assessed both before and at 4 weeks after transplantation by using the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) of the ALS CNTF Treatment Study (ACTS). The scores were increased from 17.2±8.6 preoperation to 20.1±9.7 postoperation in group A (P<0.05),from 24.2±6.8to 25.7±6.6 (P>0.05) in group B, and from 20.3±8.6 to 22.0±9.4 (P<0.001) in group C.There were no significant difference in increased ALSFRS scores among the threegroups (P>0.05). The total improvement rate of neurological function was 77.1% (252/327). The result of electromyographic examination showed that spontaneouspotential diminished and/or disappeared, the amplitude of the motor unit actionpotential decreased remarkably and the numbers of motor unit action potential greatly increased in 261 cases (79.8%). Sixteen patients (4.9%) experienced thevarious complications including headache, shortterm fever, seizure attack, central nerve system infection, pneumonia, respiratory failure, urinary tract infection, heart failure, and possible pulmonary embolism; of them, there were 4 deaths(1.2%). Conclusion These preliminary results suggest that the OECs transplantation is effective in controlling or reversing the physiological deterioration caused by ALS.

    Release date:2016-09-01 09:23 Export PDF Favorites Scan
  • 肌萎缩侧索硬化患者营养支持及护理

    目的 探讨肌萎缩侧索硬化(ALS)患者营养支持方式及护理要点。 方法 对2009年5月-2011年10月收治的20例ALS患者,根据营养评估结果,分别采用不同的营养支持方式,其中8例行经口进食,7例行胃造瘘管喂养,5例行鼻饲管喂养。 结果 经1个月治疗,20例行不同喂养方式的ALS患者,体重平均增加2.35、2.72、2.42 kg,体质量指数平均增加0.81、0.93、0.84 kg/m?,营养状况均较入院前有所改善。 结论 ALS患者经过合理的营养支持及护理,营养状况得到一定改善,其对症的营养支持方式及护理,是改善患者营养状况的关键。

    Release date:2016-09-08 09:16 Export PDF Favorites Scan
  • 散发性肌萎缩侧索硬化遗传学研究进展

    【摘要】 肌萎缩侧索硬化是一种成年起病、选择性侵犯运动神经元的神经系统慢性进展性变性疾病。约90%的患者为散发性,病因及发病机制尚未完全清楚,目前研究认为是多因素包括遗传因素和环境因素共同作用的结果。尽管目前未发现某一个单独的基因可导致散发性肌萎缩侧索硬化的发生,但近年随着全基因组关联研究方法的采用,发现了部分基因与之相关。现就近来散发性肌萎缩侧索硬化的分子遗传学研究进展作一综述。

    Release date:2016-09-08 09:25 Export PDF Favorites Scan
  • 尿酸与神经变性疾病

    目前研究发现尿酸水平与一些神经变性疾病,如帕金森病(PD)、阿尔茨海默病(AD)及肌萎缩侧索硬化(ALS)的发病呈负相关,较高的血及脑脊液尿酸水平可延缓PD、亨廷顿病、多系统萎缩的进展,而低尿酸水平是否促进ALS和AD病情进展还存在争议。尿酸主要通过抗氧化应激作用发挥对神经元的保护作用。调节尿酸水平可能成为神经变性疾病治疗的新策略。

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  • 肌萎缩侧索硬化患者行经皮内镜下胃造瘘术术后并发症的观察及护理

    目的对肌萎缩侧索硬化(ALS)患者经皮内镜下胃造瘘术(PEG)术后并发症的观察及护理进行总结和分析。 方法回顾性分析2013年4月-2014年4月被确诊为ALS且行PEG手术的8例患者的临床资料,观察并发症发生情况并总结护理经验。 结果8例患者中1例并发腹膜炎及造瘘口疼痛自动出院;其余7例中并发造瘘口缘端感染及造瘘口疼痛1例,术后瘘口出血及造瘘口疼痛1例,造瘘口渗漏及造瘘口疼痛1例,术后造瘘口疼痛1例,3例无术后并发症。7例患者经治疗及护理后均好转并带管出院,最长保留胃造瘘管者在造瘘后第370天因留置时间到期更换胃造瘘管。 结论PEG是ALS患者出现吞咽障碍后最主要的营养支持手段,术前的充分评估及术后的密切观察、护理是减少并发症的主要手段。

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  • 肌萎缩侧索硬化中氧化应激与其他发病机制的关系

    肌萎缩侧索硬化(amyotrophic lateral sclerosis,ALS)是由于运动神经元死亡及神经功能障碍导致的一种神经退行性疾病,其病因及发病机制至今未完全明确。目前认为,氧化应激在 ALS 发病过程中起着关键的作用,但运动神经元的死亡不止是氧化应激一个因素导致的,而是各种机制共同作用的结果,包括谷氨酸信号失调导致的兴奋性毒性、线粒体功能障碍、内质网应激、蛋白质聚积、神经纤维网及沿着微管的细胞内交通中断、运动神经元附近非神经细胞介入和 RNA 加工缺陷等。该文将简要介绍在 ALS 中,氧化应激与上述机制的关系。

    Release date:2017-06-22 02:01 Export PDF Favorites Scan
  • CACNA1H基因变异与神经系统疾病

    T型钙离子通道是一种低电压依赖性介导钙离子跨膜转运的膜蛋白,由于其特殊的电生理特性,在调节神经元兴奋性中具有重要作用。目前研究发现CACNA1H突变所致T型钙离子通道异常与多种神经系统疾病发生密切相关,如特发性全面性癫痫,孤独症谱系疾病,肌萎缩侧索硬化等,虽然其作为易感基因在疾病发生发展中的作用已得到一定证实,但致病机制尚不明确,本综述针对T型钙通道在神经系统中的电生理学作用,及CACNA1H突变与部分神经系统疾病之间关系进行探讨,旨在为突变致病机制的研究提供思路,并为后续精准治疗提供依据。

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