Implementation of Canadian Syncope Risk Score Based Practice Recommendations for Emergency Department Syncope Management - a Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 900
- 试验地点
- 1
- 主要终点
- Feasibility of implementing the practice recommendations.
研究概览
简要总结
Syncope is a common reason for emergency department (ED) presentation. While often benign, some patients have serious and life-threatening underlying causes, both cardiac and non-cardiac, which may or may not be apparent at the time of the initial ED assessment. Identifying which patients will benefit from further investigation, ongoing monitoring and/or hospital admission is essential to reduce both adverse outcomes and the high costs. Our group has spent over a decade developing the evidence base for a risk stratification tool directed at optimizing the accuracy of ED decisions: the Canadian Syncope Risk Score (CSRS). This tool is now ready for the final phase of its introduction into clinical practice, namely a robust, multicentre implementation trial of the CSRS based practice recommendations to demonstrate its real-world effectiveness. Prior to the launch of the large-scale implementation trial, a pilot study to assess primarily the feasibility and secondarily the effectiveness is needed.
详细描述
ED crowding limits the ability of the emergency providers to provide quality care, is a growing crisis in North America and Europe, and leads to unsafe and rushed disposition decisions which compromise patient care. On the other hand, hospital admission is expensive, and an increasing awareness of nosocomial morbidity and the harms of unnecessary testing and hospitalization exert countervailing pressure on low-yield admissions from the ED. Therefore, improved accuracy in ED disposition decision-making is more important than ever, and syncope typifies a common, high stakes condition in which improvements in efficiency are badly needed.
Identifying which patients will benefit from further cardiac rhythm monitoring and/or hospital admission is essential to reduce both adverse outcomes and high costs. A comprehensive literature review of risk-tools and international guidelines concede that previously published tools lack or have failed external validation, are excessively complex, include as outcomes obvious conditions readily identified during the index ED evaluation, or lacked power and specificity. These tools also do not offer specific clinical actions and are not supported by the guidelines. The CSRS addresses each of the above weaknesses and coupled with outpatient live cardiac monitoring is an innovative and standardized approach to ED syncope management to expedite ED care, improve patient safety and reduce healthcare costs. The investigators have identified the barriers and facilitators to effectively adapt knowledge into local contexts as per the Knowledge to Action cycle, and have selected implementation strategies accordingly. The proposed pilot study is a right step before widescale implementation.
The primary objective of this pilot study is to assess the feasibility of implementing the practice recommendations. The secondary objectives are to assess the effectiveness and safety of the intervention, implementation of the CSRS-based practice recommendations. Specific objectives include:
Feasibility objectives:
Primary: to assess the reach of the intervention Secondary: to assess the adoption, adherence, and sustainability of the intervention; to assess the acceptability, the feasibility of use and the complexity of the intervention; and to assess the satisfaction to the dose (i.e., exposure) of the intervention received including support and resources.
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
- •adult (aged > 18 years) patients who present within 24 hours of syncope
排除标准
- •non-syncope (prolonged LOC >5 minutes, change in the mental status from baseline, patients with witnessed obvious seizure, or head trauma preceding the LOC),
- •those unable to provide proper details - e.g., intoxication, and those with significant trauma requiring admission as per international consensus.
- •patients who had a serious underlying condition identified during the index ED evaluation
- •hospitalization for a reason other than syncope work-up (i.e. unable to cope at home).
结局指标
主要结局
Feasibility of implementing the practice recommendations.
时间窗: The intervention period of 6 months
To assess the reach of the intervention. We will adopt a pragmatic application of the RE-AIM (Reach Effectiveness Adoption Implementation Maintenance) framework to evaluate the pilot study outcomes. The primary feasibility outcome is the Reach or penetration, the proportion of eligible patients who had the intervention applied.
Rate of hospitalization
时间窗: At time of ED disposition, an average timeframe is 6 hours
To assess the impact on hospitalizations.
次要结局
- Rate of consultation(at 6 hours from time of ED disposition)
- Mortality(within 30-days and 1-year of the index ED visit)
- Rate of adoption(The intervention period of 6 months)
- Number of return ED visits(within 30-days and 1-year)
- Rate of adherence(The intervention period of 6 months)
- Rate of acceptability(The intervention period of 6 months)
- ED disposition time(At time of ED disposition, an average timeframe is 6 hours)
- Degree of satisfaction of the use of CSRS practice recommendation(The intervention period of 6 months)
研究者
Venkatesh Thiruganasambandamoorthy
Principal Investigator
Ottawa Hospital Research Institute
