期刊文献+

MAUDE数据库中种植牙不良事件病例报告分析

Analysis of Adverse Event Case Reports of Dental Implants in the MAUDE Database
下载PDF
导出
摘要 目的:统计并分析人工种植牙不良事件特征,为进一步实施种植牙监测工作提供有力支持。方法:对美国食品药品监督管理局MAUDE数据库2011年1月1日~2021年12月31日人工种植牙不良事件状况进行统计分析,采用描述性的方式,通过Excel电子表格软件对收集到的830份报告进行数据分析,对种植牙安全性作一步探讨。结果:种植牙不良事件报告的主要来源是制造企业,文章统计时间段内2015年发生数最多,共245例,占29.52%。涉及种植体的报告有308例,占37.11%,涉及基台(包括基台固定螺丝)522例,占62.89%。基台(基台固定螺丝)不良事件表现主要为断裂、与种植体分离失败、松动、基台无法嵌入种植体等;种植体不良事件表现主要为骨融合失败、植入物的断裂、移位、松动、变形、脱落等。不良事件主要伤害表现为二次手术造成患者再次痛苦;牙周的发炎、感染、疼痛、不适等。结论:重视种植牙不良事件监测工作,为公众用械安全提供保障。 Objective:Statistics and analysis of adverse event characteristics of artificial dental implants,provide strong support for further implementation of dental implants monitoring work.Methods:By conducting statistical analysis on the adverse events of artificial dental implants in the FDA MAUDE database from January 1,2011 to December 31,2021,using a descriptive approach,data analysis was conducted on 830 collected reports using Excel to further explore the safety of dental implants.Results:There were 308 reports involving implants,accounting for 37.11%,and 522 reports involving abutments(including abutment fixing screws),accounting for 62.89%.The main adverse events of the abutment(abutment fixing screws) are fracture,failure to separate from the implants,loosening,and inability to embed the abutment into the implants;The main manifestations of adverse events of implants are bone fusion failure,fracture,displacement,loosening,deformation,and detachment of the implants.The main manifestation of adverse events is secondary surgery causing patient pain again;Periodontal inflammation,infection,pain,discomfort,etc.Conclusion:Pay attention to the monitoring of adverse events during dental implants,and provide guarantees for the safety of public use of equipment.
作者 吕静 LV Jing(Dandong Market Supervision Service Center(Dandong Center for ADR Monitoring),Liaoning Dandong 118002)
出处 《中国医疗器械信息》 2023年第13期4-6,15,共4页 China Medical Device Information
关键词 种植牙 基台 种植体 医疗器械不良事件 分析 dental implants abutment implant adverse events of medical devices analysis
  • 相关文献

参考文献10

二级参考文献73

  • 1罗晨晨.不同形态牙合面固位螺钉对种植牙单冠稳定性的影响[J].中国口腔种植学杂志,2009,14(2):44-44. 被引量:3
  • 2王玲,陈安,陈中.药品不良反应监测的智能数据分析方法及应用[J].中国药事,2007,21(7):476-477. 被引量:9
  • 3US FDA. Ensuring the Safety of Marketed Medical De- vices-CDRH's Medical Device Postmarket Safety Program, January 18 [Z]. 2006.
  • 4国家食品药品监督管理局,卫生部.关于印发《医疗器械不良事件监测和再评价管理办法》(试行)的通知[Z].国食药监械[2008]766号,2008.
  • 5FDA: Medical Device Reporting (MDR) [EB/OL]. (2014- 04-16). [2014 -06 -20].http ://www.fda.gov/MedicalDevices/ Safety/ReportaProblern/defauh.htm.
  • 6FDA. MAUDE Information Available to the Public [EB/OL]. ( 2014-03 -24).[2014-06-20].http://www.fda.gov/downloads/ Training/CDRHLearn/UCM234355.pdf.
  • 7FDA. Manufacturer and User Facility Device Experience Database - ( M AU DE ) [E B/OL]. (2014-03 - 12 ). [2014 -06- 20].http ://www:fda.gov/MedicalDevices/DeviceRegulationand Guidance/PostmarketRequirements/ReportingAdverseEvent s/ucm127891.htm.
  • 8FDA. MAUDE - Manufacturer and User Facility Device Experience (Simple Search) [EB/OL]. (2014 -05 -31 ). [2014-06-20]. http ://www.accessdata.fda.gov/scripts/cdrh/ cfdocs/cfMAUDE/TextSearch.cfm.
  • 9FDA. MAUDE-Manufacturer and User Facility Device Experience (Advanced Search) [EB/OL]. (2014-05 -31 ). [2014-06-20]. http ://www.accessdata.fda.gov/scripts/cdrh/ cfdocs/cfMAUDE/Search.cfm.
  • 10FDA. Mandatory Reporting Requirements: Manufacturers, Importers and Device User Facilities [EB/OL]. (2014-06- 13). [2014 -06 -20]. http ://www.fda.gov/MedicalDevices/ DeviceRegulationandGuidance/PostmarketRequirements/Re portingAdverseEvents/ucm2005737.htm.

共引文献108

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部