Impact on Adverse Events (AE) Occurrence of Two Types of Experience Feedback on AE Analysed During Local Morbidity Mortality Reviews (MMR), (by Multi Professional Simulation Education Versus Simple Diffusion of MMR Decisions)
试验速览
- 阶段
- 不适用
- 入组人数
- 144,000
- 试验地点
- 1
- 主要终点
- Occurence of adverse events related to medical care
研究概览
简要总结
After implementing a French version of a trigger tool validated for computerized detection of adverse events in patient's medical record, the study will be performed in three parallel randomized arms of three identical departments (each steaming from 6 types of medical, surgical or obstetrical departments with a total of 18 departments involved). This three arms will be: no intervention, education of department's staff by multi professional in situ simulation (adapted to the discovered adverse events), or simple but large diffusion of results and decisions of Morbidity Mortality Reviews.
The interventions will be performed during a two-years period.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •patients aged > 18 years old
- •patients hospitalized in the involved departments during the two-years intervention's period
排除标准
- •patient aged < 18 years old
- •no other exclusion criteria
结局指标
主要结局
Occurence of adverse events related to medical care
时间窗: During patient hospitalization, up to 2 years
Occurrence of any adverse effects detected by the trigger tool. Trigger tool is used to detect more patient's adverse events that voluntary medical report
次要结局
- Contributive factors identification(During patient hospitalization, up to 2 years)
- Severity of adverse events related to medical care(During patient hospitalization, up to 2 years)