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Other considerations: Perspective and obligations of our societies and governmental organizations

机译:其他考虑因素:我们社团和政府组织的透视和义务

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Recurrent episodes of transmitted infection during gastrointestinal endoscopy have resulted in heightened visibility of the various organizations providing education, guidance, and regulatory oversight for endoscopes and the practice of endoscopy. They include the Food and Drug Administration, the Centers for Disease Control and Prevention, state health departments, accrediting organizations, and national medical societies representing practitioners and nurses. The Food and Drug Administration is responsible for ensuring the safety of manufacturer's products, without constraining the availability of critical medical services, such as gastrointestinal endoscopy. Their ongoing oversight of postmarket surveillance studies, and the results of such studies, will significantly influence the expectations for reprocessing in years to come. As a nonregulatory body, the Centers for Disease Control and Prevention primarily provides investigational expertise pertaining to infectious outbreaks and guidance to the medical industry regarding best practices, with input from the medical experts in their Hospital Infection Control and Professional Advisory Committee. National societies of nurses, reprocessing professionals, and physicians all provide education and guidance to the field, each with viewpoints ostensibly protective of patients and their membership. The Association for the Advancement of Medical Instrumentation, which publishes standards detailing the proper production quality for medical instruments and the procedures in which they are used, is in the midst of rewriting their guidance for reprocessing of gastrointestinal endoscopes. Despite reservations about process, Advancement of Medical Instrumentation deliberations emphasize the original guidance of the Spaulding Criteria for sterilization of semicritical devices, including endoscopes, when feasible and practicable. This is likely the future state for reprocessing in gastrointestinal endoscopy.
机译:胃肠内窥镜检查期间反复发生的传播性感染,提高了为内窥镜和内窥镜检查实践提供教育、指导和监管的各种组织的知名度。它们包括食品和药物管理局、疾病控制和预防中心、国家卫生部门、认证机构以及代表从业者和护士的国家医学会。食品和药物管理局负责确保制造商产品的安全,同时不限制关键医疗服务的可用性,如胃肠内窥镜检查。他们对上市后监测研究的持续监督,以及此类研究的结果,将对未来几年的再加工预期产生重大影响。作为一个非监管机构,疾病控制和预防中心主要提供与传染病暴发有关的调查专业知识,并向医疗行业提供有关最佳实践的指导,其医院感染控制和专业咨询委员会的医学专家提供了意见。由护士、再处理专业人员和医生组成的全国性协会都为该领域提供教育和指导,每个协会的观点表面上都保护患者及其成员。医疗器械进步协会(Association for Advanced of Medical Instrumentation)发布了详细说明医疗器械正确生产质量及其使用程序的标准,该协会正在重新编写胃肠道内窥镜再加工指南。尽管对过程有所保留,但医疗仪器的进步讨论强调了在可行和可行的情况下,半关键设备(包括内窥镜)灭菌的斯伯丁标准的原始指导。这可能是胃肠内窥镜再处理的未来状态。

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