REmote MOnitoring of paTiEnts witH pacEmaker or implAntable cardioverteR defibrillaTor
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 800
- 试验地点
- 1
- 主要终点
- The composite of all-cause mortality, heart failure events
研究概览
简要总结
However, the current guidelines recommend the use of remote monitoring (RM) in patients with cardiac implantable electronic devices (CIED) to reduce inappropriate shocks or early detection of atrial fibrillation, data is incomprehensive on the effectiveness of decreasing heart failure events or mortality in patients with heart failure and reduced ejection fraction (HFrEF). The only randomized trial, which proved the efficacy of RM on mortality was the IN-TIME trial, which used a strict protocol for detection and intervention of the heart failure events.
The primary aim of this study is to optimize the use of remote monitoring system in HFrEF patients already implanted an implantable cardiac defibrillator (ICD) or a cardiac resynchronization therapy (CRT). By creating a high-quality system with structured safety-net, which is able to use the data of remote monitoring messages and alerts of our patients, we can improve their outcome. The primary endpoint is the non-fatal heart failure event or all-cause mortality. Secondary outcomes include all-cause mortality, cardiovascular mortality, heart failure hospitalization, cardiovascular hospitalization, unscheduled visits, af burden, stroke, inappropriate shocks, quality of life, NYHA functional class.
By using artificial intelligence-based methods, the optimal cut-off values of the previously, empirically used alert parameters will be validated or challenged. Additionally, cost-effectiveness to reduce the hospitalizations will be calculated.
Due to this remote monitoring structured safety-net, these patients with severe heart failure can be treated more efficiently, safely and cost-effectively.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 100 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •CRT-P/CRT-D patients with a feasible device for home monitoring
- •ICD (VVI/VDD/DDD) patients with a feasible device for home monitoring
- •Transmission performance >80% in the first 2 weeks with new device
- •Informed consent
排除标准
- •Life expectancy<1 year
- •Unable to transmit data
- •Patient is unable to visit the physician/clinic in 12 hours when it is indicated by the alerts
- •Expected non-compliance
- •Known drug, alcohol abuse
- •Participation in other study or HM system concept
结局指标
主要结局
The composite of all-cause mortality, heart failure events
时间窗: 12 months
次要结局
- cardiovascular hospitalization(12 months)
- cardiovascular mortality(12 months)
- unscheduled visits(12 months)
