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Canadian Sudden Cardiac Arrest Network (C-SCAN)

U

Unity Health Toronto

Status

Completed

Conditions

Sudden Cardiac Arrest
Sudden Cardiac Death

Treatments

Other: There is no intervention in this study.

Study type

Observational

Funder types

Other

Identifiers

NCT03642587
CSCAN version 2

Details and patient eligibility

About

The overall aim of the project is to develop a national registry to accurately measure the burden of Sudden Cardiac Arrest (SCA) among the general Canadian population. This project will create a common platform to link existing sources of information (EMS, Coroner and Administrative Databases) in order to fully understand the causes and outcomes of SCA. This comprehensive, unique registry will inform the progress and effectiveness of all CANet SCA programs aimed at reducing SCA. Understanding the antecedents, causes and outcomes of SCA will allow for new initiatives/investigations to reduce SCA, by using targeted interventions both effectively and efficiently.

Full description

SCA is defined as an abrupt collapse with documented loss of vital signs,in a seemingly healthy individual and attributable to a cardiac cause. Estimates of SCA incidence vary widely from 53 to 153 per 100,000 persons/year. Most published studies use public reporting, death certificates or autopsy based registries to identify and classify SCA cases, but limited sources often result in missed cases. Prospective registries monitoring SCAs over time in large populations provide the most accurate estimation of incidence rates.

An ongoing challenge in developing effective strategies to decrease SCA are the varying definitions used to define SCA. Many published studies identify SCA as OHCA of "no obvious cause" (assumed to be a cardiac arrest due to an underlying primary cardiac cause); however, the two are not synonymous. Verifying that a particular OHCA is due to cardiac disease requires careful establishment, using data from multiple sources and case-by-case adjudication, which is difficult and not routinely performed. Accurate identification of true SCAs is crucial if we plan to implement interventions aimed to prevent them.

The Canadian Resuscitation Outcomes Consortium (CanROC) investigators are proposing to leverage experience gained from developing a sophisticated registry of all emergency medical service (EMS)-attended OHCA patients in Ontario and British Columbia (Resuscitation Outcomes Consortium - ROC 2005-2015). This registry has since been spread across Canada to include nine other provinces covering >15 million people in urban and rural communities. The proposed C-SCAN Registry will leverage and expand upon the CanROC infrastructure by augmenting its dataset to include detailed information both preceding and following the SCA event. Using this information to identify high-risk patients, we aim to implement targeted initiatives to decrease the incidence of SCA in Canada.

Objectives:

  1. To accurately identify and classify all possible SCA cases within the study area using new and existing data sources.
  2. To accurately measure the incidence and causes of SCA by age and sex.
  3. To measure the triggers and warning signs of SCA cases in relation to age, sex and etiology for the purposes of prediction and prevention.
  4. To confirm if the preliminary/pilot observations seen in southern Ontario are mirrored in other Canadian communities, both urban and rural, and in communities that are culturally and ethnically different from those in urban Toronto.

Enrollment

82,054 patients

Sex

All

Ages

2 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All out of hospital cardiac arrest cases of "no obvious cause"
  • Age between 2 and 85 years
  • Attended to by paramedics, and survived or died.

Exclusion criteria

  • Patients under the age of 2 years old or older than the age of 85 years old
  • Do not resuscitate orders
  • Cardiac arrests with obvious causes such as trauma, anaphylaxis, sudden upper airway occlusion, asthma, confirmed drug overdoses, homicides and suicides.

Trial design

82,054 participants in 1 patient group

Study Population
Description:
People between the ages of 2 and 85 years old with out of hospital cardiac arrest of no obvious cause who are attended to by paramedics who survive or die
Treatment:
Other: There is no intervention in this study.

Trial contacts and locations

6

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Central trial contact

Katie Allan, PhD

Data sourced from clinicaltrials.gov

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