中国药物警戒 ›› 2013, Vol. 10 ›› Issue (7): 435-437.

• 药械安全性研究 • 上一篇    下一篇

气管切开插管不良事件及相关进口产品召回简析

骆庆峰,叶成红,邓洁   

  1. 国家食品药品监督管理局医疗器械技术审评中心,北京 100044
  • 收稿日期:2013-05-10 修回日期:2016-03-09 出版日期:2013-07-08 发布日期:2016-03-09
  • 作者简介:骆庆峰,男,博士,助理研究员,医疗器械技术审评。

Analysis of Adverse Events of Tracheostomy Tube and Imported Products Recall

LUO Qing-feng ,YE Cheng-hong, DENG Jie   

  1. Center for Medical Device Evalution, SFDA, Beijing 100044, China
  • Received:2013-05-10 Revised:2016-03-09 Online:2013-07-08 Published:2016-03-09

摘要: 气管切开插管发生不良事件将严重影响临床抢救和治疗。本文介绍了产品结构,简述其常见不良事件。回顾我国近期相关进口产品召回行动,以及企业采取的纠正措施。简要分析导致产品召回的可能原因,提出降低气管切开插管风险的对策,向企业、医护人员、监管部门提出建议,明确完善产品注册申报资料的具体要求。希望能够为生产、监管和技术审评相关人员提供参考。

关键词: 气管切开插管, 不良事件, 召回

Abstract: The adverse events of tracheostomy tube will seriously affect the clinical rescue and treatment. This paper describes product structure and common adverse events, reviews the recall action of imported product and corrective measures of enterprises. This paper also briefly analyzes the possible causes leading to product recalls, advances the measure to reduce the risk of tracheostomy tube, then makes recommendations to the enterprises, health care workers, regulatory authorities, proposes the specific requirements of the product registration documentation. This article intends to provide reference for personnel engaged in production, and technical review, and so on.

Key words: tracheostomy tube, adverse events, recall

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