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首页> 外文会议>ASME international design engineering technical conferences and computers and information in engineering conference 2015 >A DETAILED FIVE-YEAR REVIEW OF MEDICAL DEVICE ADDITIVE MANUFACTURING RESEARCH AND ITS POTENTIAL FOR TRANSLATION TO CLINICAL PRACTICE
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A DETAILED FIVE-YEAR REVIEW OF MEDICAL DEVICE ADDITIVE MANUFACTURING RESEARCH AND ITS POTENTIAL FOR TRANSLATION TO CLINICAL PRACTICE

机译：五年来医疗器械添加制造研究的详尽回顾及其对翻译成临床实践的潜力

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摘要

This paper provides a systematic review of over 350 publications that document specific medical device examples in which the design and manufacturing relied on additive manufacturing processes (more popularly referred to as "3d Printing"). Existing reviews on 3d printing for medical device design focus on the range of clinical applications and potential uses for this technology. However, existing work tends to omit key medical device development and regulatory requirements pertaining to the use of 3d printing for technology translation. These omissions often present a skewed view of each device s potential for rapid translation to commercialization and common clinical practice. To fill gaps in existing literature, this review includes medical device journal articles and identifies each article's country of origin, the product development stage in which 3d printing was used, and the device's specific type and classification under the U.S. Food and Drug Administration. The findings from this systematic review provide a detailed international snapshot of current additive manufacturing research and its near term potential for changing clinical practice.
机译：本文提供了超过350种出版物的系统综述，这些出版物记录了特定的医疗设备示例，在这些示例中，设计和制造均依赖于增材制造过程（更普遍地称为“ 3d打印”）。关于医疗设备设计的3D打印的现有评论集中于该技术的临床应用范围和潜在用途。但是，现有的工作往往会忽略与使用3d打印进行技术翻译有关的关键医疗设备开发和法规要求。这些遗漏通常代表了每种设备快速转化为商业化和常见临床实践的潜力。为了填补现有文献中的空白，本次审查包括医疗器械期刊文章，并确定每篇文章的原产国，使用3d打印的产品开发阶段以及美国食品和药物管理局规定的器械的特定类型和分类。这篇系统综述的发现为当前增材制造研究及其改变临床实践的近期潜力提供了详细的国际概况。

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