医学
外围设备
干预(咨询)
设定值
指令
重症监护医学
外科
内科学
护理部
计算机科学
控制工程
工程类
程序设计语言
作者
James H. Black,D. Buckley,Martha J. Velezis,Jens Eldrup-Jørgensen,Nina D. Serratore,Jorge Gutiérrez,Eleni Whatley,Rebecca A. Marmor,Daniel J. Bertges,James E. Tcheng,Sara Royce,Misti Malone,Andrew Farb,Eric A. Secemsky,Sahil A. Parikh,Joshua A. Smale,Michael R. Jaff,Roseann White,Rebecca W. Wilgus,Mitchell W. Krucoff
标识
DOI:10.1016/j.jvs.2023.07.050
摘要
Registry Assessment of Peripheral Interventional Devices (RAPID) initiated the Pathways Program to provide a transparent, collaborative forum in which to pursue insights into multiple unresolved questions on benefit-risk of paclitaxel-coated devices, including understanding the basis of the mortality signal, without a demonstrable potential biological mechanism, and whether the late mortality signal could be artifact intrinsic to multiple independent prospective randomized data sources that did not prespecify death as a long-term end point. In response to the directive, the LEAN-Case Report Form working group focused on enhancements to the RAPID Phase I Minimum Core Data set through the addition of key clinical modifiers that would be more strongly linked to longer-term mortality outcomes after peripheral arterial disease intervention in the drug-eluting device era, with the goal to have future mortality signals more accurately examined.
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