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An Educational Program to Improve Cardiac Arrest Diagnostic Accuracy of Ambulance Telecommunicators

O

Ottawa Hospital Research Institute

Status

Active, not recruiting

Conditions

Cardiac Arrest, Sudden
Heart Arrest
Cardiopulmonary Arrest
Cardiac Arrest
Heart Arrest, Out-Of-Hospital
Death, Sudden, Cardiac

Treatments

Other: Educational Intervention

Study type

Observational

Funder types

Other

Identifiers

NCT03894059
CRRF 1298

Details and patient eligibility

About

Cardiac arrest is the number one cause of death in Canada. It is often the first symptom of cardiac disease for the victims. Eighty-five percent of victims collapse in their own home. Fifty percent collapse in the presence of a family member. Bystander cardiopulmonary resuscitation (CPR) can improve the chance to survive a cardiac arrest by three to four times, but needs to be started quickly. In most communities, less than 30% of victims receive CPR before the ambulance arrives. Currently, only 8% of cardiac arrest victims can leave the hospital alive.

Many things have been tried to improve the number of times people do CPR. So far, the only thing that really increased the number of times that someone did CPR is when 9-1-1 attendants started to give CPR instructions to callers over the phone. The only problem is that about 25% of cardiac arrest victims gasp for air in the first few minutes. This can fool the 9-1-1 callers and attendants into thinking that the victim is still alive.

The investigators have looked at all the studies on how to help 9-1-1 attendants to recognize abnormal breathing over the phone. The investigators have also learned what should be taught after finishing a large survey with 9-1-1 attendants from across Canada. This survey was done with the help of psychologists and other education experts. It measured the impact of attitudes, social pressures, and 9-1-1 attendants' perceived control over their ability to recognize abnormal breathing and cardiac arrest. Then the investigators developed a teaching tool which helped Ottawa 9-1-1 attendants recognize abnormal breathing. When they could do that, they could also recognize more cardiac arrest.

The main goal of this project is to use the tool developed in Ottawa in more centres to help 9-1-1 attendants save the lives of even more cardiac arrest victims across Canada.

Enrollment

12,224 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

We will enroll ALL patients with prehospital cardiac arrest (absence of a detectable pulse, unresponsiveness, and apnea):

  • That are of presumed cardiac origin;
  • That occur in the catchment area of our participating sites; and
  • For which resuscitation is attempted by a bystander and/or the emergency responders.

Exclusion criteria

  • Cardiac arrest witnessed by paramedics after their arrival (no opportunity for bystander intervention);
  • Patients younger than 16 years of age (cardiac arrest usually respiratory and rare in this population);
  • Patients who are "obviously dead";
  • Trauma victims, including hanging and burns; or
  • Patients with cardiac arrest clearly of other non-cardiac origin including drug overdose, carbon monoxide poisoning, drowning, exsanguination, electrocution, asphyxia, hypoxia related to respiratory disease, cerebrovascular accident and documented terminal illness.

Trial design

12,224 participants in 2 patient groups

Retrospective
Description:
Consecutive cases of out-of-hospital cardiac arrest occurring at participating sites, meeting the study eligibility criteria over a 12-month period preceding the implementation of the educational intervention for ambulance telecommunicators.
Prospective
Description:
Consecutive cases of out-of-hospital cardiac arrest occurring at participating sites, meeting the study eligibility criteria over a 12-month period following the implementation of the educational intervention for ambulance telecommunicators.
Treatment:
Other: Educational Intervention

Trial contacts and locations

1

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Central trial contact

Manya Charette, MSc; Christian Vaillancourt, MD, MSc

Data sourced from clinicaltrials.gov

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