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作 者:戴红军 王钰君 董从银[2] DAI Hong-jun;WANG Yu-jun;DONG Cong-yin(Shandong First Medical University Affiliated Provincial Hospital,Shandong Jinan 250021;Shandong Jianzhu University,Shandong Jinan 250000)
机构地区:[1]山东第一医科大学附属省立医院,山东济南250021 [2]山东建筑大学,山东济南250000
出 处:《中国医疗器械信息》2023年第13期172-174,共3页China Medical Device Information
摘 要:心脏除颤器和(或)除颤监护仪是临床心脏疾病患者的重要急救设备,其主要通过一定强度的电流刺激心脏恢复正常的窦性心律,以挽救患者生命。然而心脏除颤器和(或)除颤监护仪在应用过程中存有一定潜在危害性,可能出现故障,贻误抢救时机。为确保除颤器的在临床应用的安全性,需定期对其质量展开有效的控制管理。研究使用瑞典奥利科Phase3型除颤器和经皮起搏器质量检测仪检测心脏除颤器和(或)除颤监护仪,并分析其能量失准原因,为临床安全使用提供可靠依据。Cardiac defibrillator and/or defibrillator monitor are important emergency equipment for patients with clinical heart disease.They mainly stimulate the heart to restore normal sinus rhythm through a certain intensity of current to save the patient's life.However,cardiac defibrillators and/or defibrillation monitors have certain potential hazards in the application process,and may malfunction,delaying the rescue opportunity.In order to ensure the safety of defibrillators in clinical application,it is necessary to carry out effective control and management of their quality on a regular basis.In this study,the Swedish Oriko Phase 3 defibrillator and percutaneous pacemaker quality detector were used to detect cardiac defibrillators and/or defibrillation monitors,and to analyze the causes of their energy inaccuracy,so as to provide a reliable basis for safe clinical use.
分 类 号:TH778[机械工程—仪器科学与技术]
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