医学
卫生技术
食品药品监督管理局
间隙
临床试验
医疗保健
叙述性评论
新兴技术
一套
内镜治疗
医学物理学
内窥镜检查
重症监护医学
医疗急救
外科
内科学
泌尿科
历史
经济
考古
纳米技术
材料科学
经济增长
作者
Megan Hennessey,Shan Xue,Rebecca Z. Strigenz,Pamela J. Bagley,Eric D. Shah
标识
DOI:10.14309/ajg.0000000000003359
摘要
ABSTRACT Medical technology in gastroenterology spans devices, point-of-care diagnostics, digital health and artificial intelligence. We conducted a narrative review of US Food and Drug Administration-reviewed medical technology on the available evidence base to support uptake in clinical practice. 713 new GI devices were FDA-approved or cleared between 2013 and 2023. The most frequent technologies had indications for use in general endoscopy (442 or 62.0% of all new technologies) with advanced endoscopy technologies being the second most common (172 or 24.1%). Ninety-nine new technologies had indications for use outside of the endoscopy suite. 99% of new technologies were FDA-cleared against existing technologies via the 510(k) pathway rather than approved on new clinical data. Among the 19 devices with clinical trial data, trials were limited in sample size and generally evaluated disease-related changes or technical success rather than patient-reported outcomes that anchor drug trials. Twelve devices (63.2%) had fsavorable, published cost-effective data. To promote evidence-based discussion and uptake of new technology, and especially disruptive or high-risk technology, we propose a practical framework informed by balancing probable efficacy and safety and considering cost-effectiveness.
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