Adverse Patient Events in Anesthesia Delivery – Review and Analysis of Potentially Avoidable Events

机译：麻醉分娩中的不良患者事件–潜在可避免事件的回顾和分析

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The paper examines the MDR (Medical Device Reporting) reportable events reported to Food and Drug Administration (FDA) from medical device manufacturers and caregivers in the US market. A review of all MDRs reported between October 2014 and September 2019 is performed. The MDRs under analysis are related to adverse patient events, in particular to deaths and serious injuries. The study will provide a trend of patient safety as a result of the adverse patient events reported in the five considered years.

机译：本文研究了美国市场上医疗器械制造商和护理人员向食品药品监督管理局（FDA）报告的MDR（医疗器械报告）可报告事件。对2014年10月至2019年9月期间报告的所有MDR进行了审查。分析中的MDR与患者不良事件有关，特别是与死亡和重伤有关。由于在所考虑的五年中报告了不利的患者事件，该研究将提供患者安全的趋势。

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《IEEE International Symposium on Medical Measurements and Applications》|2020年|1-5|共5页
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Lorenzo Dinia; Fabio Mangini; Ilaria Mileti; Eduardo Palermo; Fabrizio Frezza;
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Patient Safety; Anesthesia; MDR Events; Risk; FDA;

机译：患者安全;麻醉; MDR事件;风险; FDA;

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Adverse Patient Events in Anesthesia Delivery – Review and Analysis of Potentially Avoidable Events

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