将可用性评估纳入医疗器械评估

P. Tremoulet
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引用次数: 0

摘要

ECRI是一家致力于在全球推进有效、循证医疗保健的非营利组织,半个多世纪以来一直在评估医疗设备。项目官员制定评估标准,然后进行实验室测试,以评估设备性能、安全性和可靠性。为了帮助将可用性评估纳入ECRI的评估中,一位人为因素顾问根据被评估的设备类型、使用环境的性质(如手术室、重症监护患者区、护理站)、目标用户群体、,以及可用于支持评价的资源。该顾问还开发了一个决策树,帮助ECRI项目官员从七份免费提供的标准化可用性问卷中进行选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating Usability Assessments into Medical Device Evaluations
ECRI, a non-profit dedicated to advancing effective, evidence-based healthcare globally, has been evaluating medical devices for over a half century. Project officers develop evaluation criteria and then perform laboratory tests to assess device performance, safety, and reliability. To help incorporate usability assessments into ECRI’s evaluations, a human factors consultant provided guidance on selecting assessment technique(s) based upon the type of device being evaluated, the nature of the environment in which it is used (e.g. operating room, intensive care patient area, nursing station), the target user population, and the resources available to support the evaluation. The consultant also developed a decision-tree to help ECRI project officers select among seven freely-available standardized usability questionnaires.
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