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Grant: Project Grant

Ottawa Hospital Research Institute

$397,800.00

Validation of the Canadian Prehospital Syncope Risk Score

FY 2020-21

Summary
Background: Syncope is defined as a sudden, brief loss of consciousness (LOC) followed by a rapid complete recovery. It accounts for 160,000 emergency department (ED) visits each year in Canada. Despite this, few people are hospitalized (~15%) and even fewer will die (~1%). Two-thirds of patients with syncope arrive to the ED by calling 911. There are many causes of syncope. Identifying patients at low risk for bad outcome would allow paramedics to safely determine which patients need care in the ED from those who can remain home. We recently developed the Canadian Prehospital Syncope Risk Score (CPSRS) which accurately identified patients at low risk for 30-day serious outcomes. Objective: The goal of this study is to validate the accuracy of the CPSRS in the prehospital setting to predict the risk of 30-day serious outcome for patients with syncope. Methods: We will enrol patients with syncope from five paramedic services across Canada (British Columbia - Vancouver and Kelowna areas only, London-Middlesex, York Region, Frontenac, and Ottawa). We will exclude patients <18 years old, LOC >5 minutes, changes in mental status from baseline, alcohol or drug intoxication, or language barrier. Paramedics will fill out a study data collection form with the CPSRS items and additional data should the tool need refinement. The data will be entered into a secure database and will assess patient outcomes (death and potentially life-threatening medical conditions) at 30 days. We will examine model accuracy using standard prediction measures and look to improve model accuracy if needed. We expect to enrol 4875 patients over a 1-year recruitment period based on annual call volumes. Expected Outcomes: Once validated, the tool could reduce the number of patients transported to hospital by identifying those at low risk. This would improve patient-oriented care, while at the same time saving valuable paramedic and ED resources.
Program
Project Grant
Location
Ontario, Canada
Recipient Type
Other
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
434502
Name
Thiruganasambandamoorthy Venkatesh
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Health Services and Policy Research
Theme2
Clinical
Prcname2
Health Services Evaluation &amp; Interventions Research
Projecttitle
Validation of the Canadian Prehospital Syncope Risk Score
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$397,800
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Crowding; Diversion; Emergency Department; Emergency Medicine Services; Prehospital; Risk-Stratification; Syncope
Abstract
Background: Syncope is defined as a sudden, brief loss of consciousness (LOC) followed by a rapid complete recovery. It accounts for 160,000 emergency department (ED) visits each year in Canada. Despite this, few people are hospitalized (~15%) and even fewer will die (~1%). Two-thirds of patients with syncope arrive to the ED by calling 911. There are many causes of syncope. Identifying patients at low risk for bad outcome would allow paramedics to safely determine which patients need care in the ED from those who can remain home. We recently developed the Canadian Prehospital Syncope Risk Score (CPSRS) which accurately identified patients at low risk for 30-day serious outcomes. Objective: The goal of this study is to validate the accuracy of the CPSRS in the prehospital setting to predict the risk of 30-day serious outcome for patients with syncope. Methods: We will enrol patients with syncope from five paramedic services across Canada (British Columbia - Vancouver and Kelowna areas only, London-Middlesex, York Region, Frontenac, and Ottawa). We will exclude patients <18 years old, LOC >5 minutes, changes in mental status from baseline, alcohol or drug intoxication, or language barrier. Paramedics will fill out a study data collection form with the CPSRS items and additional data should the tool need refinement. The data will be entered into a secure database and will assess patient outcomes (death and potentially life-threatening medical conditions) at 30 days. We will examine model accuracy using standard prediction measures and look to improve model accuracy if needed. We expect to enrol 4875 patients over a 1-year recruitment period based on annual call volumes. Expected Outcomes: Once validated, the tool could reduce the number of patients transported to hospital by identifying those at low risk. This would improve patient-oriented care, while at the same time saving valuable paramedic and ED resources.
Competitiondate
202010
Approvedterm2
1 yr 9 mths
Pinamesdelim
Thiruganasambandamoorthy, Venkatesh
Approvedterm
1 an 9 mois
Cihrcontribution2
~ $397,800~ $0~