医学
患者安全
不良事件报告系统
医疗急救
事件(粒子物理)
业务
不利影响
事故报告
药物不良事件
急诊医学
作者
Scott R. Schoem,Udayan K. Shah
标识
DOI:10.1016/j.otohns.2009.10.017
摘要
Primum non nocere— “Above all do no harm.” Since the first year of medical school, we have all heard and spoken this dictum countless times. Translating this dictum into action may present challenges in our daily practice. Every day, clinicians must distinguish between scientific evidence, clinical experience, and marketing claims by industry vendors of improved efficacy and safety regarding medical devices. Adverse event reporting and device failure notification are generally laid out well in hospital practice settings. Reporting beyond the local level takes on a new dimension for most surgeons. Perceived stigma from peers and corporations, lack of confidentiality, and cynicism regarding protective actions for patients should not limit one from “raising the alarm” when concerns arise about device safety or performance. This commentary aims to explain the process for reporting device-related adverse events.
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