NCT07746674尚未招募不适用
Central Line-Associated Bloodstream Infection (CLABSI) Quality Improvement Project
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Total number of central line days without a documented indication
研究概览
简要总结
This study evaluates a daily electronic health record (EHR) alert designed to reduce unnecessary central venous catheter (CVC) use among hospitalized adults. The alert identifies patients with an active CVC and no documented indication, prompting the first-contact provider to document line necessity. The study compares alert and a secure chat intervention to usual care, with the goal of reducing unnecessary line days and related CLABSI risk.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Not hospice patient class
- •Active central line for at least 24 hours
排除标准
- •No active central line
- •Central line present for less than 24 hours
研究组 & 干预措施
Usual Care
Adult inpatients meeting eligibility criteria.
Secure Chat + Alert Cohort
Adult inpatients meeting eligibility criteria whose provider receives a daily EHR OPA alert and additional secure chat communication.
结局指标
主要结局
Total number of central line days without a documented indication
时间窗: Up to Month 3
次要结局
- Number of femoral central lines in place for more than 2 days(Up to Month 3)
- Number of non-tunneled hemodialysis catheters without an active hemodialysis or continuous renal replacement therapy order(Up to Month 3)
研究者
研究点 (1)
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