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Safety of Capsule Endoscopy Using Human Body Communication in Patients with Cardiac Devices

机译:胶囊内窥镜检查使用心脏器件患者人体通信的安全性

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Background The MiroCam (IntroMedic, Ltd., Seoul, Korea) is a small-bowel capsule endoscope that uses human body communication to transmit data. The potential interactions between cardiac devices and the capsule endoscope are causes for concern, but no data are available for this matter. Aim This clinical study was designed to evaluate the potential influence of the MiroCam capsules on cardiac devices. Methods Patients with cardiac pacemakers or implantable cardiac defibrillators referred for evaluation of small bowel disease were prospectively enrolled in this study. Before capsule endoscopy, a cardiologist checked baseline electrocardiograms and functions of the cardiac devices. Cardiac rhythms were continuously monitored by 24-h telemetry during capsule endoscopy in the hospital. After completion of procedures, functions of the cardiac devices were checked again for interference. Images from the capsule endoscopy were reviewed and analyzed for technical problems. Results Six patients, three with pacemakers and three with implantable cardiac defibrillators, were included in the study. We identified no disturbances in the cardiac devices and no arrhythmias detected on telemetry monitoring during capsule endoscopy. No significant changes in the programmed parameters of the cardiac devices were noted after capsule endoscopy. There were no imaging disturbances from the cardiac devices on capsule endoscopy. Conclusions Capsule endoscopy using human body communication to transmit data was safely performed in patients with cardiac pacemakers or implantable cardiac defibrillators. Images from the capsule endoscopy were not affected by cardiac devices. A further large-scale study is required to confirm the safety of capsule endoscopy with various types of cardiac devices.
机译:背景技术Mirocam(Intromedic,Ltd,Seoul,韩国)是一种小肠胶囊内窥镜,使用人体通信来传输数据。心脏装置和胶囊内窥镜之间的潜在相互作用是关注的原因,但没有任何数据可用于此问题。目的该临床研究旨在评估Mirocam胶囊对心脏装置的潜在影响。方法本研究预先注册了对评估小肠病评估的心脏起搏器或可植入心脏除颤器的方法。在胶囊内窥镜检查之前,心脏病专家检查了心脏装置的基线心电图和功能。在医院的胶囊内窥镜检查期间,24小时遥测连续监测心脏节律。完成程序后,再次检查心脏装置的功能以进行干扰。综述和分析来自胶囊内窥镜检查的图像进行技术问题。结果研究中包括六名患者,三名与起搏器和三种带有植入心脏除颤器。我们在胶囊内窥镜检查期间识别心脏装置中没有检测到的心律失常,并且在遥测中没有进行心律失常。在胶囊内窥镜检查后,注意到心脏装置的编程参数没有显着变化。胶囊内窥镜检查中心脏装置没有成像障碍。结论在心脏起搏器或可植入心脏除颤器的患者中安全地进行了使用人体通信传播数据的胶囊内窥镜检查。来自胶囊内窥镜检查的图像不受心脏装置的影响。需要进一步的大规模研究来确认胶囊内窥镜检查的安全性,具有各种类型的心脏装置。

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