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首页> 外文期刊>The International journal of oral & maxillofacial implants >Cleaning, Disinfection, and Sterilization Protocols Employed for Customized Implant Abutments:An International Survey of 100 Universities Worldwide
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Cleaning, Disinfection, and Sterilization Protocols Employed for Customized Implant Abutments:An International Survey of 100 Universities Worldwide

机译:用于定制植入基台的清洁,消毒和灭菌协议:全球100名大学的国际调查

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Purpose: American and European standards recommend sterilization of customized abutments before connecting them to implants, as customized abutments are considered semi-critical medical devices. Since standardized procedures could not be identified in the literature on implantology, this survey evaluated the protocols employed at different universities worldwide to clean, disinfect, and/or sterilize customized abutments before their connection to bone-level implants. Materials and Methods: The survey took place between October 2015 and January 2016. A single question acquiring information on how customized abutments were treated prior to connection to the implants was sent by email to researchers affiliated at 100 universities worldwide. To avoid any bias, the survey was kept rigorously anonymous. A total of 100 universities from Europe (56), USA and Canada (25), Latin America (9), South Africa (1), Asia (6), and Australia and New Zealand (3) were invited to participate in the survey. Results: Altogether, 85 universities responded to the survey question, and 22 (25.9%) declared that no cleaning protocols were adopted. More than half of the respondents (n = 49, 57.6%) performed only one of the three procedures required by the standards (cleaning, disinfection, or sterilization). Twelve respondents (14.1%) adopted two procedures, and only two universities performed all three required procedures (2.4%). Conclusion: This survey indicated substantial heterogeneity in treating customized abutments before connecting them to implants. This study demonstrated that the majority of the universities applied either cleaning, disinfection, or sterilization which may not meet the prevailing standards.
机译:目的:美国和欧洲标准建议在将定制基台的灭菌灭菌之前,因为定制基台被视为半关键医疗器械。由于无法在植入类学的文献中识别出标准化程序,因此本次调查评估了全球不同大学采用的议定书,以清洁,消毒和/或在与骨级植入物联系之前进行定制的基台。材料和方法:调查发生于2015年10月至2016年1月。通过电子邮件向植入物在全球100名大学附属的研究人员发送有关如何处理定制基台的单一问题。为了避免任何偏见,调查严格匿名。来自欧洲(56),美国和加拿大的100所大学(25),拉丁美洲(9),南非(1),亚洲(6)和澳大利亚和新西兰(3)被邀请参加调查。结果:共有85所大学应对调查问题,22名(25.9%)宣布未采用清洁议定书。超过一半的受访者(n = 49,57.6%)只执行标准要求的三个程序中的一个(清洁,消毒或灭菌)。十二名受访者(14.1%)通过了两次程序,只有两个大学进行所有三个所需程序(2.4%)。结论:本调查显示在将它们连接到植入之前处理定制基台的大量异质性。本研究表明,大多数大学应用了可能不符合现行标准的清洁,消毒或灭菌。

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