生物反馈治疗仪

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关于脑电生物反馈治疗仪的临床使用指南

关于脑电生物反馈治疗仪的临床使用指南

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生物反馈治疗仪3篇

生物反馈治疗仪3篇

生物反馈治疗仪生物反馈治疗仪是一种非侵入性的医疗设备,可用于调节身体的自然反应过程以改善健康状况。

本文将介绍生物反馈治疗仪的原理、应用和效果。

一、生物反馈治疗仪的基本原理生物反馈治疗仪基于生物反馈原理,通过监测身体的生理参数并反馈给患者,帮助其掌握和调节身体的反应。

生物反馈可以监测脑电波、心率、呼吸、皮肤温度、肌肉张力等多种生理参数,并将这些数据转换为可视化的信号或声音,并反馈给患者。

患者可以通过观察自己的生理数据变化,逐渐学会如何调节身体反应以达到治疗效果。

二、生物反馈治疗仪的应用1. 健康恢复生物反馈治疗仪可用于恢复患者的健康,包括减轻压力、焦虑、抑郁症状、改善睡眠质量、增强身体免疫力和促进细胞再生等。

通过反馈患者的生理参数,让其清楚地了解自己的身体反应,从而找到最佳的调节方式,以达到恢复健康的目的。

2. 慢性疼痛治疗生物反馈治疗仪还可用于治疗慢性疼痛,如头痛、颈痛、腰痛等。

通过监测患者的肌肉张力,以及提供放松和呼吸练习等反馈,帮助患者减轻疼痛和改善身体状况。

3. 康复训练生物反馈治疗仪还可用于康复训练,如中风康复、运动伤害康复等。

通过监测患者的肌肉活动和身体平衡情况,并提供相应的反馈,帮助患者恢复身体功能和协调性。

三、生物反馈治疗仪的效果生物反馈治疗仪的效果被广泛认可和接受。

近年来,许多研究已经证明,生物反馈治疗仪可以有效地延缓疾病的进展、改善生命质量、减轻疼痛、改善抑郁和焦虑症状等。

生物反馈治疗仪具有无风险、非侵入性、持久效果的优点,可以为患者提供一个全面的治疗解决方案。

四、生物反馈治疗仪的使用注意事项生物反馈治疗仪具有一定的使用注意事项。

首先,及时联系医生,确保设备使用适宜幅度和频率,不要过度使用。

其次,不要使用该设备来替代已有的正规治疗。

最后,使用生物反馈治疗仪时,需保持平静放松的状态,不要过度焦虑或过度激动。

总之,生物反馈治疗仪可作为一项创新的治疗方式,对改善患者健康状况和康复训练具有显著的贡献。

生物反馈治疗仪技术参数

生物反馈治疗仪技术参数

生物反馈治疗仪
(双通道多功能神经康复诊疗系统)
技术参数
一、临床应用要求
主要用于运动功能障碍的治疗及康复训练,同时也可用于包括感觉障碍、痉挛、面瘫、脑血管扩张及微循环治疗(小脑顶核仿生刺激)等。

无临床体征(认知、肌力水平等)限制,可满足病人全过程(急性期、发展期、后遗症期)、多体征的康复需求。

二、主要技术参数
(一)计算机系统:
1、一体化计算机;
2、通讯方式:USB2.0数据接口,并采用光电隔离,传输速率大于10Mbit/s ;超强抗干
扰性能,4000V隔离安全标准;
(二)EM(反馈放大器系统
1、强抗干扰能力,适合任何环境下使用
2、E MG放大器灵敏度:2—10000 口V (10mV
3、通道设置:2通道左右分屏显示,可同时治疗两个病人或同一病人的两个部位,两
个独立的控制时钟,互不干扰和影响。

(三)声音输出系统
在同时治疗两个部位或两个病人时,有两套独立的多媒体声音提示系统,由不同的时钟控制,病人完全不相互干扰
(四)功能电刺激系统
1、二套独立的功能电刺激系统,可独立进行输出、控制及设置
2、电流强度:0—100± 1mA恒流且可调和电子锁定(3K欧姆)
3、最大输出电压:300V
4、刺激频率:10—100Hz;仿真电刺激时可调制到中频(1000HZ以上)
5、刺激脉宽:50—1000 口s
6、刺激波形:单极性、双极性、交替式、多形态
7、刺激持续时间:1 —60S,也可根据需要任意设定
8、系统可自动测量最合适的电流强度,并进行锁定处理。

生物反馈治疗仪

生物反馈治疗仪

生物反馈治疗仪生物反馈治疗仪是一种针对患者自身的生理反应进行治疗的设备。

该设备能够通过测量和分析患者自身的生理反应信号,并将这些信号转化为人类能够理解的反馈信号,从而帮助患者更好地了解自己的身体机能,并且调节自身的生理反应,达到治疗和预防疾病的效果。

本文将对生物反馈治疗仪的原理、分类、功效等方面进行介绍。

一、生物反馈治疗仪的原理生物反馈治疗仪的原理是基于生物反馈理论而设计的。

生物反馈理论是指,通过对身体生理变化的监测和分析,将这些信息反馈给人类,帮助人们认识和调节自身的生理反应机制,从而达到治疗和预防疾病的效果。

生物反馈治疗仪的主要成分包括传感器、仪器放大器、指示器和计算机。

传感器负责测量和监测人类的生理变化信号,例如心率、呼吸、血压、皮肤电反应等。

仪器放大器对上述信号进行放大和处理,使其具有足够的能量和频率,保证信号清晰稳定。

指示器通过可视化图形展示患者的生理反应,例如波形和刻度,帮助患者理解自身的身体机能。

计算机根据测量结果进行分析和计算,将生理反应信号转化为反馈信号,并通过电子音乐、声音、震动等形式进行反馈,使患者能够有针对性地进行调节。

二、生物反馈治疗仪的分类生物反馈治疗仪可以根据测量的生理信号进行分类,主要包括以下几种类型。

1.心理生物反馈治疗仪:主要测量和分析患者的心率、血压、皮肤电反应等生理变化信号,帮助患者更好地了解自身情绪变化。

例如,当患者感到不安、紧张或焦虑时,心理生物反馈治疗仪会通过电子音乐等形式进行反馈,帮助患者放松身心,达到治疗和预防焦虑症的效果。

2.肌肉生物反馈治疗仪:主要测量和分析患者肌肉张力的变化,帮助患者更好地了解自身肌肉的紧张状态。

例如,当患者感到肌肉紧张或痉挛时,肌肉生物反馈治疗仪会通过电子音乐等形式进行反馈,帮助患者放松肌肉、减轻疼痛,达到治疗和预防肌肉疾病的效果。

3.脑电生物反馈治疗仪:主要测量和分析患者脑电波的变化,帮助患者更好地了解自身大脑活动状态。

便携式生物反馈治疗仪原理

便携式生物反馈治疗仪原理

便携式生物反馈治疗仪原理
一、便携式生物反馈治疗仪原理
便携式生物反馈治疗仪是一种利用脑波、体感和呼吸来改善心理健康的设备,常常被用于改善焦虑、失眠、精神分裂症等症状的康复。

其原理是通过测量用户的脑波,从而分析出当前的心理健康状态,通过控制用户的体感和呼吸,调整和调节用户的心理状态,以达到改善心理健康的目的。

1、脑波分析
脑波分析是便携式生物反馈治疗仪的核心部分。

它首先用传感器测量用户的脑波,然后通过计算机软件分析用户的脑波,来分析用户当前的心理健康状况。

用户的脑波将根据不同的状态显示不同的波形,计算机软件可以将这些波形进行分类,由此分析出用户当前的心理健康状况。

2、体感控制
体感控制是便携式生物反馈治疗仪的另一部分。

通过体感控制,可以通过体感刺激,改变用户的情绪,以实现心理健康的改善。

该技术可以利用体感刺激来改善用户的情绪,通过刺激人体皮肤来引起神经的兴奋,通过调节神经的兴奋度来改变用户的情绪,用人体感觉上的刺激来改变用户的心理状态。

3、呼吸训练
呼吸训练是便携式生物反馈治疗仪的最后一部分。

通过呼吸训练,可以通过呼吸来调整用户的心理状态。

例如,用户可以放慢呼吸,放
松身体,改变情绪,有助于减轻压力,改善心理健康。

总之,便携式生物反馈治疗仪是一种利用脑波、体感和呼吸来改善心理健康的设备,其原理是通过测量用户的脑波,从而分析出当前的心理健康状态,通过控制用户的体感和呼吸,调整和调节用户的心理状态,以达到改善心理健康的目的。

家用版大脑生物反馈治疗仪用户手册说明书

家用版大脑生物反馈治疗仪用户手册说明书

家用版大脑生物反馈治疗仪用户手册广州市润杰医疗器械有限公司(已通过质量管理体系认证ISO 9001:2008 和 ISO 13485:2003)技术支持如果您的系统出现问题,并且无法从使用手册中获得帮助,请您直接联系我司,我司技术支持工程师将竭诚为您服务。

联系方式:020-******** 32215212 82115619 82115176传真:************联系地址:广州市经济技术开发区科学城彩频路 11 号广东软件科学园 F 栋 602公司名称:广州市润杰医疗器械有限公司邮编:510500网址:版权声明本手册为广州市润杰医疗器械有限公司的知识产权,我们非常小心的整理此手册。

但我们对于本手册的内容不保证完全正确。

因为我们的产品一直在持续的改良及更新,故我们保留随时修改而不另行通知的权利。

目录第一章产品简介第二章产品说明第三章产品指标及注意事项第四章电极的连接与安装第五章操作界面介绍第一章产品简介一、运行环境1、硬件环境电脑笔记本一台,CPU 双核以上,内存 2G 以上,带独立显卡;显示器分辨率达到1024*768 或以上;放大器一套。

注意:4D训练游戏需要显卡和显示器都必须支持4D 功能,显示器分辨率要达到1920*1080。

2、软件环境操作系统支持 Windows xp 或Win7。

二、功能及性能生物反馈疗法(Biofeedback therapy)又称生物回授疗法,或称植物神经学习法,是在行为疗法的基础上发展起来的一种新的心理治疗技术。

生物反馈仪采用生物反馈的原理,通过采集与分析人体的生理指标如脑电、心率变异性和肌电来确定人体的精神心理状态,并将这些信号以容易理解的视觉、听觉形式展现出来,使个体了解自身的生理变化,通过反复的训练与治疗,帮助个体达到认知、调控自身的生理变化,从而达到缓解和治疗心理紧张、焦虑、抑郁、失眠等精神心理症状的目的。

脑电生物反馈技术通过EEG传感器,采集和放大由脑细胞产生的微弱电信号,不同位置的神经元细胞产生不同节律的波形。

生物反馈治疗仪在康复中应用

生物反馈治疗仪在康复中应用

生物反馈治疗仪的应用范围
神经康复:用于 治疗脑卒中、脑 外伤等神经系统 疾病引起的瘫痪、 肌肉萎缩等症状
精神心理康复: 用于治疗焦虑症、 抑郁症、失眠等 精神心理疾病
疼痛康复:用于 治疗慢性疼痛、 颈肩腰腿痛等疼 痛性疾病
儿童康复:用于 治疗孤独症、多 动症、语言障碍 等儿童发育行为 疾病
生物反馈治疗仪在康复中 的应用
章节副标题
生物反馈治疗仪的原理
章节副标题

生物反馈技术的定义
生物反馈是一种利用现代生理科学仪器,将人体内部生理机能的变化情况通过视觉、 听觉等方式反映出来,使个体能够有意识地控制和调节自身生理机能的技术。
生物反馈技术通过调节自主神经系统和内分泌系统的功能,帮助个体更好地应对压 力和焦虑等情绪问题,提高身心健康水平。
心理治疗
生物反馈治疗仪 在康复中可以用 于心理治疗,通 过调节患者的情 绪和心理状态, 改善焦虑、抑郁
等心理问题。
生物反馈治疗仪 可以帮助患者了 解自己的心理状 态,通过自我调 节和认知行为疗 法等手段,提高 心理自我调节能
力。
生物反馈治疗仪 还可以结合其他 心理治疗方法, 如放松训练、正 念疗法等,提高 治疗效果,促进
与传统康复方法 相比,生物反馈 治疗仪在运动康 复中具有更高的 疗效和安全性。
生物反馈治疗仪的优势与 局限性
章节副标题
优势
实时监测:生物反馈治疗仪可以实时监测 患者的生理参数,为医生提供准确的诊断 依据。
安全性高:生物反馈治疗仪采用非侵入式 监测方式,不会对患者造成创伤或副作用。
操作简便:生物反馈治疗仪操作简单,易 于掌握,适合在家庭和康复机构中使用。
心理治疗的实际案例
患者情况:一位 中年女性,患有 焦虑症和抑郁症

生物肌电反馈治疗仪产品技术要求康进

生物肌电反馈治疗仪产品技术要求康进

2.性能指标2.1肌反仪性能指标2.1.1测量范围:1uV-999uV 误差≤±10%或≤2uV2.1.2最高分辨率:≤0.2uV2.1.3系统噪声:≤1μV2.1.4 通频带:20Hz~500Hz(-3dB)2.1.5差模输入阻抗:大于5MΩ2.1.6共模抑制比:大于 100dB2.1.7肌电信号以曲线及电压值的方式进行显示2.1.8当测得肌电信号变化达到 0.2uV 时,肌电信号的曲线及电压值会出现变化2.1.9带计算机的肌反仪,肌电测量部分与计算机应有效的隔离,计算机应符合相应的安全标准。

GB17625.1-2012、GB4943.1-2011、GB/T9254-20082.1.10:有 50HZ 的工频陷波滤波器。

衰减后的幅值应不大于 5uV(峰峰值)2.1.11:AD 数据:16 位2.1.12:AD 采集率:9000HZ2.2刺激仪性能指标2.2.1额定负载阻抗:刺激仪金属电极的额定负载应为500Ω,允差值为±10%。

2.2.2电刺激强度:参数:0mA~100mA 可调,1mA 调节, 误差:±20%2.2.3 脉冲宽度:参数:20-1000us,10us 可调,误差:±20%2.2.4 频率:参数:频率 2-250Hz,1HZ 可调,误差:±10%2.2.5输出指示:刺激仪在有输出时,应有明显的指示2.2.6定时功能:刺激仪应能设定 1-60min 的定时工作,定时精度应优于±1.5min2.2.7负载检测功能:刺激仪应能在负载脱落情况下停止输出,重新接入负载后需要手动恢复输出。

2.2.8急停功能;刺激仪在工作的过程中需要进行紧急停止的功能2.2.9上升 /下降时间:0s~20s, 1s 调节,误差±1S2.3存储功能: 治疗仪能自动记忆存贮“当前的数据”,方便下次调用2.4语音提示功能: 刺激仪在开始工作时有语音提示,使用者可以跟随语音完成训练,语音也可以关闭,使用者根据屏幕显示也能完成训练。

生物刺激反馈仪评估治疗型技术参数

生物刺激反馈仪评估治疗型技术参数

生物刺激反馈仪(评估治疗型)技术参数数量:1台设备要求:1.所投设备必须为最新型号,最高端设备。

2.所投品牌每年必须有设备相关的、独立的学术会议,以保证科室学术交流需要。

3.所投设备必须在江苏省内有10家以上三级甲等医院的装机,以保证客户对该品牌的认可度。

硬件要求:4.主机:显示器与主机集成化一体机设计(显示器、信号采集模块与工控机封装于同一机箱内),稳定性和兼容性更有保障,抗电磁干扰性能突出。

5.电容触摸屏,可外接键盘鼠标,触摸屏尺寸≥15英寸。

6.★主机多功能物理通道≥4个,其中≥4个电刺激通道(STIM),≥3个肌电采集通道(EMG)。

7.使用物理旋钮调节电流强度,操作方便,每个通道均设置各自的独立旋钮控制,可实现多通道不同强度刺激。

8.肌电采集范围:2-2500μV(r.m.s)9.分辨率:≤0.5μV(r.m.s)10.通频带:不窄于20Hz~500Hz (-3dB)11.刺激电流强度:0-100mA范围内可调,步进0.5mA可调节。

12.★电刺激脉冲宽度:至少在50-900μs范围内均可调,步进10us可调节。

13.电刺激脉冲频率:至少在1-250Hz范围内均可调,步进1Hz可调节。

14.上升/下降时间:至少在0s~18s范围内可调。

15.一键式开机,直接进入软件操作界面,一键式关机。

软件参数:16.筛查模式用于短时间内筛查出盆底肌异常者,快速筛查耗时小于等于1分钟,标准筛查耗时小于等于2分40秒。

快速筛查和标准筛查指标包括:前静息平均值、前静息变异性、快速收缩上升时间、快速收缩最大值、快速收缩下降时间、持续收缩平均值、持续收缩变异性、后静息平均值、后静息变异性。

17.盆底表面肌电标准评估(Glazer评估),对盆底肌肉进行全面且标准化的评估,耗时约6分钟。

评估指标包括:前静息平均值,前静息变异性,快速收缩上升时间,快速收缩最大值,快速收缩下降时间,持续收缩平均值,持续收缩变异性,耐久收缩平均值、耐久收缩变异性、耐久收缩后前10秒比值、后静息平均值,后静息变异性。

生物反馈治疗仪

生物反馈治疗仪

生物反馈治疗仪肌电生物反馈治疗仪(神经功能组织重建仪)生物反馈治疗仪就是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉脑血管、帮助病人重建并恢复肌肉正常运动功能,训练治疗,以达到改善肌肉功能,中枢神经系统损伤得运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪治疗原理:生物反馈治疗仪就是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉训练治疗,以达到改善肌肉功能,帮助病人重建并恢复肌肉正常运动功能,脑血管、中枢神经系统损伤得运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪结合生物反馈与神经功能重建得最新康复理念,集肌电、直肠、盆底得评估、治疗、训练于一身得康复专家。

什么就是生物反馈生物反馈 (biofeedback) 又称生物回授。

它在不同得场合下具有不同得涵义,既可以指有机体内发生得一种过程;又可以表示一种方法;还可以表示一种特殊得治疗手段。

生物反馈疗法运用生物反馈疗法,就就是把求治者体内生理机能用现代电子仪器予以描记,并转换为声、光等反馈信号,因而使其根据反馈信号,学习调节自己体内不遂意得内脏机能及其她躯体机能、达到防治身心疾病得目得,由于此疗法训练目得明确、直观有效、指标精确,因而求治者无任何痛苦与副作用。

据国内有关报道证实:生物反馈疗法对多种与社会心理应激有关得身心疾病都有较好得疗效。

运用于生物反馈治疗得设备有:肌电反馈仪、皮肤湿度反馈仪、脑电反馈仪、脑电反馈仪及脉练,以保证结果得可靠性与科学性。

搏反馈仪等。

仪器得操作者需经过专业训生物反馈治疗仪生物反馈治疗仪得作用生物反馈治疗技术就是根据条件反射理论发展起来得,于20世纪60年代末首先在美国用于临床。

生物反馈就是用电子仪器测定神经-肌肉与自主神经得正常或异常活动情况,并把这些信息放大成视觉与听觉信号,反映给受试人。

医生帮助受试人了解原来不能感觉得机体得变化,通过学习控制这些反映信息,学会调节心理生理变化,来治疗与预防特定疾病。

治疗焦虑障碍用脑电生物反馈等治疗后,多数人能控制焦虑与惊恐发作,不再影响其工作与生活,能更好地平稳发挥脑功能。

生物反馈治疗仪说明书

生物反馈治疗仪说明书

MYOTRAC INFINITIDual SEMGThe Manufacturer: Thought Technology Ltd.2180 Belgrave AvenueMontreal, Quebec, CanadaH4A 2L8Product Name: MyoTrac Infiniti System Product #: T9800Device Name: MyoTrac Infiniti Encoder Device #: SA9800•Type BF Equipment •Internally powered equipment•Continuous operation•Read Instruction Manual•The pins of the connectors identified with the ESD warning symbol should not be touched unless ESB precautionary procedures are used.CAUTION•US Federal Law restricts this device to sale by, or on order of, a physician or any otherpractitioner licensed by the law of the state in which he or she practices to use or order theuse of this device.WARNING•Do not operate Active Sensors within 10 feet of an operating cellular phone, similar radio transmitting device, other powerful radio interference producing sources such as arcwelders, radio thermal treatment equipment, x-ray machines, or any other equipment thatproduces electrical sparks. Portable and mobile RF communication equipment can affectthis equipment.•With the MyoTrac Infiniti Encoder SA9800 use only with supplied power supply. GlobTek Part Number WR92B2500LF9P-Y-MED (WR95/WR93/WR97) or GS889•The PC used with MyoTrac Infiniti must be placed outside the patient/client environment(more than 3 meters or 10 feet) or the PC must comply with EN60601-1 (system safety).•After use, the Batteries or the Battery pack must be disposed of in accordance with local, state and federal regulations and laws.•After use, the Disposable Electrodes may be a biohazard. Handle, and when applicable, dispose of these materials in accordance with accepted medical practice and any applicablelocal, state and federal laws and regulations.•Reusable electrodes present a potential risk of cross-infection especially when used onabraded skin, unless they are restricted to a single patient or sterilized between patients. Ifsterilizing electrodes, employ only gas sterilization.•Radiated radio frequency electromagnetic fields can cause performance degradation in the MyoScan-Pro EMG sensor. In the worst case, an RF field strength of 22mV/M can causean increase of 1μV in the signal reading from a MyoScan-Pro sensor. Be sure to keep inmind that a very relaxed muscle should provide an EMG reading of approximately 1-3μV.•This device is capable of generating current densities exceeding 2mA r.m.s./cm² this may require special attention of the operator.•Avoid accidental contact between connected but unused applied parts and other conductive parts including those connected to protective earth.•Explosion Hazard; Do not use in the presence of a flammable anesthetic mixture with air, or with Oxygen or Nitrous Oxide.•Not to be immersed in water.•Take care in arranging patient and sensor cables to avoid risk of patient entanglement or strangulation.•The operator is responsible for ensuring the safety of any devices controlled or triggered by Infiniti equipment or software, or by any software or hardware receiving data from Infinitiequipment. Infiniti equipment must not be configured or connected in such a way thatfailure in its data acquisition, processing or control functions can trigger patient feedbackstimulus that poses an unacceptable level of risk.•Use of any equipment in a biofeedback or stimulation context should be immediatelyterminated upon any sign of treatment-related distress or discomfort.•Not to be connected to a patient undergoing MRI, Electro surgery or defibrillation.•Not for use with patients with undiagnosed pain conditions.•Only use the unit for which it was prescribed.•Do not immerse the unit in water or any other liquid substance.•Do not use if you have symptoms of bladder infection.•Do not use with diminished mental capacity or physical competence limiting the use of the device.•Caution should be used for patients with suspected or diagnosed heart problems.•Caution should be used for patients with suspected or diagnosed epilepsy.•Electrode placement and stimulation settings should be based on the guidance of theprescribing practitioner.•If damage is evident of the unit or accessories, discontinue use and contact your supplierfor further information on repair.•The system should not be used adjacent to or stacked with other equipment, if usedadjacent or stacked the unit should be observed to verify normal operation in theconfiguration in which it will be used.•Use of accessories, transducers or cables other than those specified by ThoughtTechnology ltd may result in increased emissions or decreased immunity of the equipmentto electromagnetic energy.ATTENTION•Sensors and equipment damaged by static electricity are not covered under warranty. Toprevent static discharge from damaging the sensor and/or encoders, use anti-static mats orsprays in your working area. A humidifier may also be used to prevent static environmentsby conditioning hot, dry air. It is recommended that all staff involved with the unit receive anexplanation of the ESD symbol and the precautions described above as a minimum.•Do not apply any electrode gel or equivalent directly on the sensor snaps. Always useelectrodes as a medium between the sensor and the client.•Not for diagnostic purposes, not defibrillator proof, not for critical patient monitoring.•To prevent voiding warranty by breaking connector pins, carefully align white guiding dot onsensor plug with slot on sensor input.•Make sure to remove electrodes from sensor snaps immediately after use.•Do not plug third party sensors directly into instrument inputs. Plug only ThoughtTechnology Active Sensor cable connectors into instrument inputs. All electrodes and thirdparty sensors must be connected to active sensors, either directly or through an adapter.•Remove batteries when the device is not being used for an extended period of time. Pleasedispose of battery following local regulations.INTENDED PURPOSE•Biofeedback, Relaxation & Muscle Re-Education purposes•Relaxation of muscle spasms•Prevention or retardation of disuse atrophy•Increasing local blood circulation•Muscle re-education•Maintaining or increasing range of motionNOTE•No preventative inspections required; maintenance must be performed by qualified personnel.Factory re-calibration can be requested.•The supplier will make available, upon request, circuit diagrams, component parts lists anddescription or other information required for the repair of product by qualified personnel.•The operator must be familiar with typical characteristics of signals acquired by thisequipment, and be able to detect anomalies in the acquired signal that could interfere withtreatment effectiveness. Depending on the importance of signal integrity, it may be advisableto continuously monitor the raw signals, in time and/or frequency domain, while the device isbeing used for biofeedback or other purposes. If anomalies are observed on acquired signals,and if you suspect a problem with electromagnetic interference, contact Thought Technologyfor a technical note on identification and remediation.•This product conforms to standards EN60601-1, EN60601-2-10 and EN60601-2-40; someencoder labeling may indicate superceded standards.MAINTENANCE AND CALIBRATION•Wipe encoder with a clean cloth•Factory testing and calibration ensure equipment accuracy and frequency response. Contact Thought Technology for factory re-calibration if necessary.STORAGE•Store in its original case at up to 90% humidity / 30C°TRANSPORTATION•Transport in its original caseManual # SA9814 Rev 4Guidance and manufacturer’s declaration – electromagnetic immunity The MyoTrac Infiniti is intended for use in the electromagnetic environment specified below. The customer or the user of the MyoTrac Infiniti should assure that it is used in such an environment, and that precautions regarding that environment are heeded.Immunity test IEC 60601test level Compliance level Electromagnetic environment –guidanceElectrostatic discharge (ESD) IEC 61000-4-2 ±6 kV contact±8 kV air±6 kV contact±8 kV airFloors should be wood, concrete orceramic tile. If floors are covered withsynthetic material, the relative humidityshould be at least 30 %.Electrical fast transient/burst IEC 61000-4-4 ±2 kV for powersupply lines±1 kV for input/outputlines±2 kV for powersupply lines±1 kV for input/outputlinesMains power quality should be that of atypical commercial or hospitalenvironment.SurgeIEC 61000-4-5 ±1 kV differentialmode±2 kV common mode±1 kV differentialmode±2 kV common modeMains power quality should be that of atypical commercial or hospitalenvironment.Voltage dips, short interruptions and voltage variations on power supply input linesIEC 61000-4-11 <5 % U T(>95 % dip in U T)for 0,5 cycle40 % U T(60 % dip in U T)for 5 cycles70 % U T(30 % dip in U T)for 25 cycles<5 % U T(>95 % dip in U T)for 5 sec<5 % U T(>95 % dip in U T)for 0,5 cycle40 % U T(60 % dip in U T)for 5 cycles70 % U T(30 % dip in U T)for 25 cycles<5 % U T(>95 % dip in U T)for 5 secMains power quality should be that of atypical commercial or hospitalenvironment. If the user of theMyoTrac Infiniti requirescontinued operation during powermains interruptions, it is recommendedthat the MyoTrac Infiniti bepowered from an uninterruptible powersupply or a battery.Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 3 A/m 3 A/m Power frequency magnetic fieldsshould be at levels characteristic of atypical location in a typical commercialor hospital environment.NOTE U T is the a.c. mains voltage prior to application of the test level.NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the MyoTrac Infiniti is used exceeds the applicable RF compliance level above, the MyoTrac Infiniti should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the MyoTrac Infiniti.Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.Guidance and manufacturer’s declaration – electromagnetic emissionsThe MyoTrac Infiniti is intended for use in the electromagnetic environment specified below. The customer or the user of the MyoTrac Infiniti should assure that it is used in such an environment.Emissions test Compliance Electromagnetic environment – guidanceRF emissions CISPR 11 Group 1 The MyoTrac Infiniti uses RF energy only for its internal function.Therefore, its RF emissions are very low and are not likely tocause any interference in nearby electronic equipment.RF emissionsCISPR 11Class BHarmonic emissionsIEC 61000-3-2Not applicableVoltage fluctuations/ flicker emissions IEC 61000-3-3 Not applicableThe MyoTrac Infiniti is suitable for use in all establishments,including domestic establishments and those directly connected tothe public low-voltage power supply network that suppliesbuildings used for domestic purposes.Table of ContentsAbout This Guide (9)Chapter 1 (10)Introduction to your MYOTRAC INFINITI™ Dual SEMG Encoder (10)System Requirements (11)MyoTrac Infiniti Components (12)Connection to the Client (15)Connection to the PC (19)Screen Elements (20)Thought Support (20)Settings Menu (21)Chapter 2 (25)SEMG sessions on your MYOTRAC INFINITI™ Dual SEMG Encoder (25)Open SEMG Sessions (25)Script SEMG Sessions (27)Chapter 3 (28)Data Management on your MYOTRAC INFINITI™ Dual SEMG Encoder (28)MyoTrac Infiniti Review (29)Chapter 4 (30)Display Options on your MYOTRAC INFINITI™ Dual SEMG Encoder (30)Displays (30)Chapter 5 (34)Flow on your MYOTRAC INFINITI™ Dual SEMG Encoder (34)Chapter 6 (35)Reference (35)Technical Support and Order Placing (36)Technical Support (36)Product Numbers & Accessories (37)Placing Orders (38)Specifications (39)MyoTrac Infiniti Hardware Copyright Notice (44)About This Guide Welcome to the MYOTRAC INFINITI™ encoder. This guide is designed to help you get up and running quickly with your new encoder. It will describe the operation of the encoder, and how it interfaces to the host personal computer (PC).It walks you through:•Physical Operation of the encoder.• EMG sessions.• Data management.• Display options.After you have become familiar with the key concepts of your new encoder, you can use the rest of this guide as a reference for less common tasks, and also as a source of information if you have problems operating it.Chapter 1 Introduction to your MYOTRAC INFINITI™ Dual SEMG EncoderThis chapter explains the physical interface with the MyoTrac Infiniti Encoder, how to use it for the first time, and how to transfer data to the host PC.Getting to know your MyoTrac Infiniti Dual SEMG EncoderWhat is a MyoTrac Infiniti Dual SEMG Encoder?The MyoTrac Infiniti is the cutting edge in handheld, dual channel Surface Electromyography(SEMG). With it you will be able to deliver targeted and customized treatment directly to the client’s clinically relevant areas.A simple first approach has been adopted in the design of the MyoTrac Infiniti to make it as easyand fast as possible to get the clinical results desired from this powerful device.Customizing the MyoTrac Infiniti to your clinical needs couldn’t be easier; all users input is directed through a series of intuitive and guided screens using touch screen technology.The partnership of the MyoTrac Infiniti with the BioGraph Infiniti PC software enhances yet further the power and flexibility of the MyoTrac Infiniti. This link enables you to transfer session data to the PC for further viewing, analysis and reporting, in real time or post session.System RequirementsTo install the BioGraph Infiniti software, your computer system must meet or exceed the following requirements.•IBM PC compatible(Intel/Pentium/Celeron family or AMDK6/Athlon/Duron family, CPU P4 speed 3GHz or higher), Desktop or Laptop withtwo monitor capability•Windows 2000/XP Professional or Home edition.•50 - 60 gigabytes hard disk space for video recording and processing. (Thesoftware needs 2.5 gigabytes to installand run on available hard drive space) •Memory, 512 MB of RAM or more•CD ROM or DVD drive•SVGA graphic card (1024 x 768) or higher resolution adapter & monitor•32 bit Sound Blaster compatible sound card & speakers• 1 to 4 USB ports, depending on thedesired number of MyoTrac Infinitiencoders•Mouse or compatible pointing device •MS Word 97 or higher (for printingpurposes)•Compact Flash Reader (For use with compact flash card only)•Webcam 30 frames per second (for video purposes only)NOTE: When using certain more complex screens, you must adhere to the Recommended Computer Requirements.••IBM PC compatible(Intel/Pentium/Celeron family or AMDK6/Athlon/Duron family, CPU P3speed 1.8 GHz), Desktop or Laptop •Windows 2000/XP Professional or Home edition.•10 - 20 gigabytes hard disk space •(The software needs 2.5 gigabytes to install and run on available hard drivespace)•Memory, 256 MB of RAM or more •CD ROM or DVD drive•SVGA graphic card (1024 x 768) or higher resolution adapter & monitor •16 Bit Sound Blaster compatible sound card & speakers• 1 to 4 USB ports, depending on the desired number of MyoTrac Infinitiencoders•Mouse or compatible pointing device •Word 97 or higher (for printingpurposes)NOTE: For most recent computer requirements contact Thought Technology Ltd for MAR473Update informationPeriodically updates may become available for the BioGraph Infiniti software and for the MyoTrac Infiniti Hardware. Please contact your local distributor or visit our website for further information on how to obtain updates.MyoTrac Infiniti Components•Compact Flash for increased memory capacity and one method for transfer of data to the PC.•USB for real time transfer of data to the PC.•Touch screen enables graphically guided navigation through the software.•Rugged Ergonomic Case, easy to hold or attach to the subject and will withstand the rigors of daily use.•Battery Charging jack for wall connection enables fast built-in battery charging.•Headphone Jack for stereo sound feedback (or use the built-in speaker).•Push button On/Off switch to prevent accidental switching.• 2 Channels of Surface EMG.PowerThere are three basic methods to power the MyoTrac Infiniti unit: Inserting batteries into the battery compartment of the unit, plugging it into the wall using the supplied AC adapter, or plugging it into a powered up computer using a USB cable.The MyoTrac Infiniti is available with battery charging capabilities. It will work with four standard Alkaline AAA batteries available in all consumer electrical stores. It is also possible to run the unit on removable, externally rechargeable batteries. A rechargeable battery pack is supplied with the MyoTrac Infiniti and can be charged while still inside the unit.Note: When changing batteries it is recommended to plug the unit into external power, either USB or wall transformer so that data is not lost. Failure to supply external power will result in data and script loss.The battery compartment cover slides open by pushing up using the notch provided. Place four AAA batteries in the slots, observing the polarity as illustrated. Please note that a diagram of the correct battery polarity is embossed on the inside surface of the compartment.Alternatively it is possible to use a rechargeable battery pack (Thought Technology Part Number MI1028). This battery pack is plugged into the connector in the battery compartment marked BATT. The pack then fits into the normal battery area. Note: only use battery packs from Thought Technology or authorized representative, as use of other battery packs will damage the device.A wall mounted AC power adapter, supplied with the MyoTrac Infiniti, is used to connect the unit toan electrical outlet. This can be used in conjunction with the batteries or without.The unit can also be powered from the computer via the USB cable. The cable is connected to the unit on one side and on the other side to the USB port of the computer. This can be used inconjunction with the batteries or without.Charging the BatteriesNote: exact power supply subject to change without notice.Internal ChargerIf your MyoTrac Infiniti was supplied with a wall mounted AC adapter it is possible to charge the battery pack while it is inserted in the device.Note: Only use Thought Technology Ltd supplied wall mounted chargers with this device. Failure to do so could result in potential injury. Use only GlobTek Part Number WR9אB2500LCP-Y-MED where א= 2 for North America, א=3 for Europe, א=5 for United Kingdom and א=7 for Australia with the exception of Japan where the part number is GS 889.To start the charging plug in either the wall mounted AC adaptor or the USB cable. A full charging cycle from fully empty to fully charged will take approximately 2hrs for AC adaptor and 5.5hrs for the USB cable. The unit can be used while plugged in to either power source. The charging cycle does not need to be completed in full; it can be stopped at anytime by removing the connector.When the unit is turned off while plugged into an external power source, the screen displays a battery symbol. Charging action is shown with an animation of the battery filling up. When the battery is fully charged, the symbol shows a full battery.If the unit is plugged into an external power source while it is turned off, it will start charging within one minute.The state of the battery charging is available by going to the power menu in the settings menu of the device. It indicates the current mode of power and whether the unit is currently charging the batteries.Note: The rechargeable batteries must be fully charged prior to initial use. In order for the batteries to reach full capacity it may be necessary to charge them several times (~2-8) after initial use.MemoryRecorded data can be saved using three methods - choose the one which most closely matches your usage needs. To select saving method, select the Settings menu from the main menu, and tap on the Save icon.•Internal Memory – Limited size, only the statistical summaries are recorded. Specifically, the statistics for 13 open sessions or 9 training sessions (work/rest) or 6 assessment sessions(work/rest + fast-flick + endurance) can be recorded. Data can be lost if the batteries areremoved from the unit for longer than a few minutes.•Compact Flash Card – Most flexible method of data saving: save all the raw data for review on the encoder or for download to the PC. Available in most electronics stores in a range ofmemory sizes. Since all EMG data is recorded, the amount of data that is saved to thecompact flash card depends on the size of the card:hours64MB 1.75128MB 3.5 hours256MB 7 hours512MB 14 hourshours1GB 27.5hours2GB 55.5The encoder is delivered with a protective insert in the compact flash slot. To remove it, push the button next to the slot once to eject the card. The CF card can then be inserted; you willnotice that the CF card can only be inserted one way into the encoder to protect from incorrect insertion. When inserted properly it will be flush with the encoder rear. Follow the procedure above to remove this card when no longer required, and re-insert the protective insert. CFcards require a CF card reader to transfer data to the PC. The CF cards and reader can bepurchased from most computer stores. Before its first use in the encoder, a CF card requires PC formatting using the file manager, then format the card using the BioGraph Infiniti MainApplication. Formatting and transferring CF data to the PC is covered in depth in theBioGraph Infiniti software manual.•Real Time PC Transfer – Connect to the PC via the USB and save and display the data on the PC in real time. See the following section “Connection to the PC”.Attention: Do not remove the CF card without first stopping recording. If the CF card is removed during recording, you will lose all the data for the current session.TappingLike using a mouse on a computer screen the MyoTrac Infiniti allows you to use your finger or a stylus to tap the buttons directly on the screen. The first time you start your handheld unit, or if the power has been disconnected for a while, you will be guided through a set of welcome screens including calibration, time and date setting. The calibration aligns the internal circuitry of theencoder with its touch sensitive screen so that when you tap a button on the screen, the handheld unit can detect exactly which button is being pressed. It is recommended to use a stylus when calibrating the device as it will provide a more accurate calibration than using a finger.Note:Always use a finger or stylus for tapping the screen. Never use a pen, pencil or othermarking or sharp object on the screen.Damage resulting from misuse of the screen is notcovered by the warranty.The software is designed so that once the screen has been calibrated it is possible to use all the buttons with a finger. In many cases the touch sensitive area is greater than the graphicalconstraints of the button allowing for easier operation using a finger. As necessary wipe screen with a dry cloth to clean. Screen protectors are available from good stationary suppliers and are a good way to extending the life of your screen.Connection to the ClientDepending on the type of session you are going to record there are different ways to connect the two channels to the client. Either plug the extender cable into the device directly and connect to the client with EMG electrodes, or plug them into the pre-amplifier and the pre-amplifier into the MyoTrac Infiniti.Attention: When you insert the extender cable (lead wire) into the electrode connector, MAKE SURE THAT NO BARE METAL OF THE PINS IS EXPOSED.Before applying electrodes, be sure the skin surface is cleaned and dried. Make sure theelectrodes are placed firmly to the skin and make good contact between the skin and electrodes.Please consult the clinical guide for information on electrode selection for different placements. The illustration below shows the division of the body into six areas of treatment.Arms and ShouldersHead and NeckAbdominalsBack and ButtocksLegs and HipsWhen connecting a sensor or extender cables, be sure to properly line up the guiding dot on the top of the plug with the notch in the encoder's input socket. Forcing the plug into the jack in any other position may damage your equipment.Using the MyoTrac Infiniti with AC Power Adapter or Connected to a PCThe MyoTrac Infiniti is designed for safe operation on ungrounded AC power sources. However, if you are using the MyoTrac Infiniti while it is connected to an ungrounded AC power source, for best results you may need to follow some simple guidelines for skin preparation and electrode placement. These measures will help to avoid falsely elevated EMG readings while the muscle is at rest.If you notice elevated resting EMG levels not related to the patient’s condition, and if this occurs only when the unit is connected to AC power (directly via the supplied AC adapter or indirectly via a USB connection to the PC), and if it is necessary to run the MyoTrac Infiniti on ungrounded power(i.e. no 3rd ground pin on the AC wall socket or on the PC power supply), try the followingtechniques to improve the readings.First, if you are using a PC with only 2 prongs on the wall plug and you have a grounded outlet (3 pin wall sockets with a working ground), plug the ac adapter into the MyoTrac-Infiniti and into the grounded outlet to provide a ground for the system.If you have no opportunity to ground either the PC or the AC adapter, use the following electrode placement tips:•If the EMG site is located on an extremity or limb, be sure to place the REF (black colored) electrode more proximally (on or closer to the trunk of the body) than the sense electrodes(yellow and blue), and at least ten centimeters away from either sense electrode.•Prepare the skin under all three electrodes, using a product designed for skin preparation prior to electrode application (mild abrasives such as NuPrep are effective).•If you are using Ag/AgCl (silver/silver chloride) electrodes, put some conductive electrode paste or cream on them before applying them to the skin, or try using gel-type rather than dry Ag/AgCl electrodes.Resting EMG readings will not be affected by connection to AC power, in the following cases:•Running the MyoTrac Infiniti stand-alone, with no AC power adapter and no connection to the PC (only on its rechargeable batteries).。

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估1. 引言1.1 背景介绍随着生物反馈治疗仪的不断发展和完善,越来越多的研究表明其在产后盆底康复治疗中的潜在作用。

通过生物反馈治疗仪,患者可以清晰地看到自己盆底肌群的收缩和放松情况,从而更好地进行盆底康复训练。

生物反馈治疗仪还可以帮助患者更准确地掌握盆底肌群的力度和协调性,进一步提高治疗效果。

基于以上背景,本研究旨在评估生物反馈治疗仪在产后盆底康复治疗中的疗效,为改善产后盆底功能障碍患者的生活质量提供更有效的康复方案。

1.2 问题意义产后盆底功能障碍是困扰许多产妇的常见问题,包括尿失禁、盆底肌无力等症状。

这些问题不仅会给产妇的生活质量带来影响,还可能导致其他严重的健康问题。

目前,传统的盆底功能康复治疗方法效果不佳,需要更有效的治疗手段来帮助产妇恢复盆底功能。

1.3 研究目的本研究旨在探讨生物反馈治疗仪在产后盆底康复治疗中的疗效评估。

通过对生物反馈治疗仪在产后盆底康复中的应用进行深入研究,我们希望能够评估其对盆底肌群功能恢复的影响,探讨其在产后盆底康复治疗中的作用机制,为临床提供更为有效的康复治疗方案。

具体地,我们的研究目的包括以下几个方面:2. 正文2.1 产后盆底康复治疗的现状产后盆底康复治疗是指针对产后妇女因分娩过程中盆底肌肉和神经受损而导致的盆底功能障碍进行的康复治疗。

产后盆底康复治疗旨在帮助产后妇女恢复盆底肌肉的力量和功能,缓解尿失禁、排便困难、盆腔脏器脱垂等产后盆底问题。

目前,产后盆底康复治疗的方法主要包括康复体育锻炼、盆底肌电刺激、盆底康复理疗等。

康复体育锻炼是通过指导产后妇女进行适当的盆底肌肉锻炼来增强盆底肌肉力量。

盆底肌电刺激是利用电刺激技术帮助产后妇女恢复盆底肌肉功能。

盆底康复理疗则是采用按摩、热敷、牵引等物理疗法帮助产后妇女缓解盆底问题。

2.2 生物反馈治疗仪的原理和应用生物反馈治疗仪是一种通过监测和反馈患者生理功能状态的设备,通过显示和反馈生理参数,帮助患者调节自身生理功能,达到治疗和康复的目的。

生物反馈治疗仪教学内容

生物反馈治疗仪教学内容

生物反馈治疗仪生物反馈治疗仪是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉训练治疗,以达到改善肌肉功能,帮助病人重建并恢复肌肉正常运动功能,脑血管、中枢神经系统损伤的运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪治疗原理:生物反馈治疗仪是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉训练治疗,以达到改善肌肉功能,帮助病人重建并恢复肌肉正常运动功能,脑血管、中枢神经系统损伤的运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪结合生物反馈和神经功能重建的最新康复理念,集肌电、直肠、盆底的评估、治疗、训练于一身的康复专家。

什么是生物反馈生物反馈 (biofeedback) 又称生物回授。

它在不同的场合下具有不同的涵义,既可以指有机体内发生的一种过程;又可以表示一种方法;还可以表示一种特殊的治疗手段。

生物反馈疗法运用生物反馈疗法,就是把求治者体内生理机能用现代电子仪器予以描记,并转换为声、光等反馈信号,因而使其根据反馈信号,学习调节自己体内不遂意的内脏机能及其他躯体机能、达到防治身心疾病的目的,由于此疗法训练目的明确、直观有效、指标精确,因而求治者无任何痛苦和副作用。

据国内有关报道证实:生物反馈疗法对多种与社会心理应激有关的身心疾病都有较好的疗效。

运用于生物反馈治疗的设备有:肌电反馈仪、皮肤湿度反馈仪、脑电反馈仪、脑电反馈仪及脉搏反馈仪等。

仪器的操作者需经过专业训练,以保证结果的可靠性和科学性。

生物反馈治疗仪的作用生物反馈治疗技术是根据条件反射理论发展起来的,于20世纪60年代末首先在美国用于临床。

生物反馈是用电子仪器测定神经-肌肉和自主神经的正常或异常活动情况,并把这些信息放大成视觉和听觉信号,反映给受试人。

医生帮助受试人了解原来不能感觉的机体的变化,通过学习控制这些反映信息,学会调节心理生理变化,来治疗与预防特定疾病。

治疗焦虑障碍用脑电生物反馈等治疗后,多数人能控制焦虑和惊恐发作,不再影响其工作和生活,能更好地平稳发挥脑功能。

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估一、生物反馈治疗仪原理及应用生物反馈治疗是一种通过仪器来帮助患者了解、感知和调节自身生理功能的治疗方法。

通过给患者反馈身体生理指标的变化情况,让患者学会控制和调整自己的生理功能,从而达到治疗的目的。

生物反馈治疗仪是一种非侵入性的治疗工具,可以用于盆底康复治疗中。

它通过监测盆底肌肉的收缩和放松情况,给予患者及时的反馈,帮助患者掌握正确的盆底肌训练方法,达到治疗盆底功能紊乱的目的。

1.产后盆底功能紊乱产后盆底功能紊乱是指女性在生育后盆底肌肉和组织发生一系列改变,表现为盆底肌肉无力、尿潴留、尿失禁等症状。

而且随着年龄的增加,盆底功能紊乱的发生率也逐渐增加,给女性的生活和工作带来很大的困扰。

生物反馈治疗仪在产后盆底康复治疗中起着非常重要的作用。

通过生物反馈治疗仪的监测和反馈,可以帮助患者更好地掌握盆底肌肉的训练方法,达到有效康复的目的。

与传统的盆底康复治疗方法相比,生物反馈治疗仪更加科学、直观、有效。

1.临床观察方法为了评估生物反馈治疗仪在产后盆底康复治疗中的疗效,我们选择了一组产后盆底功能紊乱患者进行观察。

我们将患者分为生物反馈治疗组和传统康复治疗组,分别进行治疗,并对患者的盆底功能进行评估。

2.观察指标我们采用盆底功能评估量表、盆底肌肉力量测试、尿失禁情况记录等方法来观察患者的盆底功能情况。

通过对患者进行长期跟踪观察,评估生物反馈治疗仪在产后盆底康复治疗中的疗效。

3.观察结果经过一段时间的观察,我们发现生物反馈治疗组的患者在盆底功能方面有明显的改善。

盆底功能评估量表的总分明显提高,盆底肌肉力量明显增强,尿失禁情况明显减少。

而传统康复治疗组的患者在这些指标上改善不明显。

四、结论与展望在未来的临床工作中,我们可以进一步拓展生物反馈治疗仪在产后盆底康复治疗中的应用范围,探索更多的治疗手段和方法,为产后盆底功能紊乱患者带来更好的康复效果。

相信随着科技的进步和医学水平的提高,生物反馈治疗仪在产后盆底康复治疗中的应用将会得到更广泛的推广和应用。

生物反馈治疗仪多功能神经康复诊疗系统技术参数

生物反馈治疗仪多功能神经康复诊疗系统技术参数

生物反馈治疗仪(多功能神经康复诊疗系统)技术参数
数量:2台预算:6.4万元
1、嵌入式计算机系统、医用隔离电源(4000V隔离安全标准)
2、嵌入式彩色液晶显示器
3、内置扬声器
★4、EMG放大器灵敏度:2~1000μV
5、刺激波形:方波
6、输出电流:0mA~50mA可调,恒流且安全锁定;
7、刺激频率:1Hz~250Hz
8、脉冲宽度:50~600μs
9、最大刺激持续时间:60S
10、多媒体语音系统
11、支持人工外触发功能
12、具有自动检测、自动报警功能
★13、六种治疗模式,包括:
(1)PBF1、PBF2模式(小肌群,大肌群)
(2)NBF模式(多媒体生物反馈)
(3)TENS1模式(感觉型障碍及神经促通治疗)
(4)TENS2模式
(5)ESFN(小脑顶核仿生电刺激,又称脑循环治疗)
14、可通过NBF模式分析表面肌电峰值、平均值及面积,方便对训练过程效果进行观察及评

15、训练中采用柱状图指引,以0-200分级表达,增加训练者参与的趣味性
16、治疗过程包括休息、用力、刺激、维持(功能位)四种状态构成的“闭环”显示及治疗
过程的时间进度条,使整个治疗过程更加目标化
★17、支持处方预置及后台设置系统,可避免仪器使用中的误操作
18、资质要求:所投设备具有医疗器械注册证,投标商具有医疗器械经营许可证或医疗器械生产许可证。

19、整机保修期≥2年
20、提供耗材及零配件供货价格供业主参考
21、供货期:合同签订后10日以内。

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估

生物反馈治疗仪在产后盆底康复治疗中的疗效评估【摘要】生物反馈治疗仪在产后盆底康复治疗中起着重要作用。

本文通过介绍生物反馈治疗仪的原理和机制,分析产后盆底康复治疗的重要性,总结生物反馈治疗仪在产后盆底康复治疗中的应用情况,并评估其临床疗效。

探讨影响疗效的因素,为临床实践提供参考。

研究显示,生物反馈治疗仪在产后盆底康复治疗中具有显著效果,但仍存在一些局限性。

未来发展方向应注重技术创新和临床研究,不断优化治疗方案,提高疗效。

生物反馈治疗仪是一种有效的产后盆底康复治疗工具,在未来的临床实践中有着广阔的应用前景。

【关键词】生物反馈治疗仪、产后盆底康复治疗、疗效评估、原理、机制、重要性、临床应用、影响因素、作用、发展方向、结论、研究背景、研究目的、研究意义1. 引言1.1 研究背景产后盆底功能障碍是指产后妇女由于分娩过程中器官损伤或疼痛等原因导致盆底肌群松弛、膀胱直肠脱垂、尿失禁等问题,严重影响了患者的生活质量。

随着人口老龄化和生育率的下降,产后盆底功能障碍的患病率逐渐增加,成为妇科临床常见的问题之一。

本研究旨在探讨生物反馈治疗仪在产后盆底康复治疗中的疗效评估,为临床医生提供更多的治疗选择,帮助产后妇女更好地恢复盆底功能,提高生活质量。

通过对生物反馈治疗仪的原理和机制、产后盆底康复治疗的重要性以及临床疗效评估等方面进行深入分析,旨在为未来的研究和临床实践提供有益的参考和指导。

1.2 研究目的研究目的是探究生物反馈治疗仪在产后盆底康复治疗中的疗效评估,为临床提供更科学、有效的治疗方法。

通过对生物反馈治疗仪的原理和机制进行深入分析,了解其对盆底肌群的作用及调节机制。

通过对产后盆底康复治疗的重要性进行阐述,探讨生物反馈治疗仪在这一领域的广泛应用情况,为后续的临床实践提供理论依据。

通过对临床疗效评估和影响因素分析的研究,进一步验证生物反馈治疗仪在产后盆底康复治疗中的有效性和可行性,为未来临床实践提供参考。

通过本研究的目的和内容,旨在为产后盆底康复治疗提供更加科学、系统的治疗方案,提高患者的康复效果和生活质量。

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肌电生物反馈治疗仪(神经功能组织重建仪)生物反馈治疗仪就是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉
训练治疗,以达到改善肌肉功能,帮助病人重建并恢复肌肉正常运动功能,脑血管、中枢神经系统损伤得运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪治疗原理:
生物反馈治疗仪就是利用肌电生物反馈技术并结合多种电刺激模式进行肌肉训练治疗,以达到改善肌肉功能,帮助病人重建并恢复肌肉正常运动功能,脑血管、中枢神经系统损伤得运动功能障碍及盆底肌肉功能障碍等。

生物反馈治疗仪结合生物反馈与神经功能重建得最新康复理念,集肌电、直肠、盆底得评估、治疗、训练于一身得康复专家。

什么就是生物反馈
生物反馈 (biofeedback) 又称生物回授。

它在不同得场合下具有不同得涵义,既可以指有机体内发生得一种过程;又可以表示一种方法;还可以表示一种特殊得治疗手段。

生物反馈疗法
运用生物反馈疗法,就就是把求治者体内生理机能用现代电子仪器予以描记,并转换为声、光等反馈信号,因而使其根据反馈信号,学习调节自己体内不遂意得内脏机能及其她躯体机能、达到防治身心疾病得目得,由于此疗法训练目得明确、直观有效、指标精确,因而求治者无任何痛苦与副作用。

据国内有关报道证实:生物反馈疗法对多种与社会心理应激有关得身心疾病都有较好得疗效。

运用于生物反馈治疗得设备有:肌电反馈仪、皮肤湿度反馈仪、脑电反馈仪、脑电反馈仪及脉搏反馈仪等。

仪器得操作者需经过专业训练,以保证结果得可靠性与科学性。

生物反馈治疗仪得作用
生物反馈治疗技术就是根据条件反射理论发展起来得,于20世纪60年代末首先在美国用于临床。

生物反馈就是用电子仪器测定神经-肌肉与自主神经得正常或异常活动情况,并把这些信息放大成视觉与听觉信号,反映给受试人。

医生帮助受试人了解原来不能感觉得机体得变化,通过学习控制这些反映信息,学会调节心理生理变化,来治疗与预防特定疾病。

治疗焦虑障碍
用脑电生物反馈等治疗后,多数人能控制焦虑与惊恐发作,不再影响其工作与生活,能更好地平稳发挥脑功能。

治疗睡眠障碍
生物反馈疗法,使失眠伴紧张情绪病人控制全身肌肉松弛水平,快速进入睡眠。

可增加失眠不伴焦虑病人睡眠波,产生强烈得困倦感。

治疗纤维肌痛综合征
生物反馈治疗技术可作为纤维肌痛综合征综合性治疗措施,能改变患者得慢波活动。

治疗慢性疼痛
生物反馈治疗紧张性头痛与偏头痛,使患者得肌肉放松,头痛得症状减轻或消失。

治疗高血压病
用生物反馈治疗原发性高血压,病人收缩压、舒张压均下降;比药物治疗合并放松训练治疗效果好。

治疗脑卒中后偏瘫
就是一种有效得辅助治疗手段,生物反馈训练可使病人得受累肌肉重新获得运动能量;能有效地协调单个或多个肌肉活动;治疗上肢协调功能与下肢功能;可减轻痉挛与控制其感受器功能紊乱,也可结合其它方法治疗。

治疗哮喘
对于形成条件反射式得哮喘发作,生物反馈可建立良好得条件反射来对抗,减轻哮喘症状。

用肌电生物反馈与诱导反馈,可掌握平静腹式呼吸等。

适用科室
1、康复理疗科:偏瘫患者肌体功能康复;
2、妇产科:尿失禁、产后康复、术后盆底功能恢复;
3、神经内/外科:上下神经元损伤后得重建治疗;
4、神经肌肉功能障碍得恢复治疗;
5、肛肠科:功能性便秘、大便失禁、术后排便功能恢复;
6、小儿外科:儿童脑性瘫痪得康复治疗;
7、骨外科:各类骨折后得神经肌肉功能康复治疗。

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