Outcomes and User Acceptance of the IntelliVue Alarm Advisor Software (Europe)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,487
- 试验地点
- 1
- 主要终点
- Clinical Alarms
研究概览
简要总结
This Clinical Study will be conducted as a comparative study focusing on usability and efficiency by comparing alarm burden pre- and post-implementation of an "Alarm Advisor software".
详细描述
In a first phase of data collection (pre-implementation) all alarms of an intensive care unit population are recorded.
In an interim period an Alarm Advisor software will be introduced to the unit.
In a second phase (post-implementation) the same set of alarm data will be recorded.
The "Alarm Advisor" Software can identify alarms based on criteria set by the medical staff and provide hints to reduce alarms and alarm nuisance (e.g. by proposing adjustments of alarm limits).
The effect of reduction of recurring nuisance alarms through the implementation of the Alarm Advisor shall be evaluated.
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
- •Patients admitted to the intensive care unit during the study period
排除标准
- 未提供
结局指标
主要结局
Clinical Alarms
时间窗: six to eight months
Number of Different Alarms on Intensive Care
次要结局
未报告次要终点