Overview of the 2011 Food and Drug Administration Circulatory System Devices Panel of the Medical Devices Advisory Committee Meeting on the CardioMEMS Champion Heart Failure Monitoring System

被引:39
作者
Loh, Joshua P. [1 ]
Barbash, Israel M. [1 ]
Waksman, Ron [1 ]
机构
[1] MedStar Washington Hosp Ctr, Washington, DC 20010 USA
关键词
Food and Drug Administration; heart failure; pulmonary artery pressure monitoring;
D O I
10.1016/j.jacc.2012.08.1035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The CardioMEMS Champion Heart Failure Monitoring System (CardioMEMS, Atlanta, Georgia) is a permanently implantable pressure measurement system designed to wirelessly measure and monitor pulmonary artery (PA) pressure and heart rate in heart failure (HF) patients to guide ambulatory HF management and to reduce HF hospital stays. On December 8, 2011, the Food and Drug Administration (FDA) Circulatory System Device Panel reviewed the CardioMEMS Champion HF Monitoring System premarket approval (PMA) application. The majority of Panel members agreed that that the discussed monitoring system is safe for use in the indicated patient population. However, new information reported by the FDA with regard to preferential support in management of patients in the treatment group raised concerns among the Panel members with regard to potential bias in analyzing the efficacy of the device itself. Additionally, Panel members raised concerns with regard to the efficacy of the device in certain patient subpopulations. Hence, most Panel members decided that there was not reasonable assurance that the discussed monitoring system is effective. This summary aims to describe the discussions and recommendations made during this meeting. (J Am Coll Cardiol 2013;61:1571-6) (c) 2013 by the American College of Cardiology Foundation
引用
收藏
页码:1571 / 1576
页数:6
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