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SW-RCT Implementation of Canadian Syncope Risk Score Based Practice Recommendations

Syncope

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 high costs. The research team 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. These recommendations, if applied, could lead to reduction in hospitalization with only 6% of high-risk patients requiring hospitalization, shorter ED lengths of stay for the 76% of ED syncope patients who are at low risk for 30-day serious outcomes, and more standardized disposition decisions, specifically discharge of 18% of medium-risk patients after appropriate discussion. Hence, the investigators hypothesize that an important reduction in hospitalization and ED disposition time can be achieved by implementing the CSRS-based recommendations with potential improvements in patient safety. The overall objective of this study is to evaluate the effectiveness of the knowledge translation (KT) of the CSRS-based practice recommendations in multiple Canadian EDs using a stepped wedge cluster randomized trial (SW-CRT) on health care efficiency and patient safety.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Physicians:

Inclusion criteria:

* ED physicians involved in ED syncope care
* Non-ED physicians involved in ED syncope care
* Physician's delegates involved in ED syncope care

Exclusion criteria:

* ED physicians not involved in ED syncope care
* Non-ED physicians not involved in ED syncope care
* Physician's delegates not involved in ED syncope care

Patients:

Inclusion criteria:

* Patients who are adults (aged \> 18 years)
* Patients who present to the ED within 24 hours of syncope.

Exclusion criteria:

* Patients who do not fulfill the definition of syncope, namely those with a prolonged loss of consciousness (i.e., \> 5 minutes), Glasgow Coma Scale \< 15 in patients without dementia (or a change in the mental status from baseline in those with dementia);
* Patients with witnessed obvious seizure, or head trauma preceding the loss of consciousness; and those who are unable to provide proper details (e.g., alcohol intoxication or other substance use).
* Patients who had a serious underlying for the syncope identified during the index ED evaluation and those who were consulted to an inpatient service or hospitalized for reasons other than syncope workup (e.g., social reasons such as inability to cope at home, pain due to the fall, significant trauma).

Study Location

University Health Network
University Health Network
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Konika Nirmalanathan

Hôpital de L'Enfant-Jésus
Hôpital de L'Enfant-Jésus
Québec, Quebec
Canada

Contact Study Team

Primary Contact

Alexandra Nadeau

Thunder Bay Regional Health Sicences Centre
Thunder Bay Regional Health Sicences Centre
Thunder Bay, Ontario
Canada

Contact Study Team

Backup Contact

Amanda Bakke

Primary Contact

Rabail Siddiqui

Royal Victoria Hospital & Montreal General Hospital
Royal Victoria Hospital & Montreal General Hospital
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

David Iannuzz

St. Boniface Hospital
St. Boniface Hospital
Winnipeg, Manitoba
Canada

Contact Study Team

Primary Contact

Mona Hegdekar

Winchester District Memorial Hospital
Winchester District Memorial Hospital
Winchester, Ontario
Canada

Contact Study Team

Primary Contact

Mohamed Gazarin

Health Sicence North
Health Sicence North
Sudbury, Ontario
Canada

Contact Study Team

Primary Contact

Danielle Waltenbury

[email protected]
Jewish General Hospital
Jewish General Hospital
Montréal, Quebec
Canada

Contact Study Team

Primary Contact

Xiaoqing Xue

Study Sponsored By
Ottawa Hospital Research Institute
Participants Required
More Information
Study ID: NCT04972071