Circulation Improving Resuscitation Care (CIRC)
Status: | Completed |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 7/26/2018 |
Start Date: | January 2008 |
End Date: | December 2013 |
A Randomized Controlled Study Comparing Autopulse To Manual CPR In A CPR-First Protocol For Out-Of-Hospital Cardiac Arrest
During resuscitation of out of hospital cardiac arrest patients the use of a mechanical chest
compression device Autopulse will improve survival compared to manual compressions.
compression device Autopulse will improve survival compared to manual compressions.
Sudden out-of-hospital cardiac arrest (OOH-CA) remains a significant cause of death, in spite
of recent declines in overall mortality from cardiovascular disease. Several studies document
sub optimal quality of manual chest compressions and this may influence outcome. However,
studies comparing manual and mechanical chest compressions have resulted in conflicted
results. The investigators think this may be based on methodology and design issues of the
trials as much as not focusing on training and experience in operating a mechanical device
clinically. Therefore the investigators will focus on these issues and implement three phases
in the study (In field training, Run In phase, and Study phase). The investigators will also
focus on early use of mechanical CPR after arrival at patient side and randomization at
arrival. In order to achieve this the investigators will follow the Norwegian CPR Guidelines
with 3 min CPR before defibrillation and the 3 min algorithm. Quality of CPR will be
monitored.
of recent declines in overall mortality from cardiovascular disease. Several studies document
sub optimal quality of manual chest compressions and this may influence outcome. However,
studies comparing manual and mechanical chest compressions have resulted in conflicted
results. The investigators think this may be based on methodology and design issues of the
trials as much as not focusing on training and experience in operating a mechanical device
clinically. Therefore the investigators will focus on these issues and implement three phases
in the study (In field training, Run In phase, and Study phase). The investigators will also
focus on early use of mechanical CPR after arrival at patient side and randomization at
arrival. In order to achieve this the investigators will follow the Norwegian CPR Guidelines
with 3 min CPR before defibrillation and the 3 min algorithm. Quality of CPR will be
monitored.
Inclusion Criteria:
- Patents aged 18 years (or local age of consent) or more who suffer non-traumatic
arrest of presumed cardiac etiology in an out-of-hospital setting and who do not meet
any of the exclusion criteria below.
Exclusion Criteria:
- Traumatic arrest (blunt, penetrating, burns)
- Arrest due to exsanguinations, strangulation, smoke inhalation, drug overdose,
electrocution, hanging, drowning.
- Known or clinically apparent pregnancy
- Do Not Attempt to Resuscitate (DNAR) orders
- Apparent patient weight more than 225 kg (500 lbs)
- Wards of the state
- Prisoner
- CPR device other than AutoPulse
- Patients who are reached after 16 minutes after the time of emergency call (911). This
exclusion is determined at the time of CRF abstraction, not during treatment of the
patient.
- If patient is unaccompanied, or accompanied by a person or persons unfamiliar
with their his-tory, determination of these exclusion criteria will, perforce, be
left to the best estimation of the rescue personnel. At no time, should an
attempt to determine these criteria be allowed to delay the administration of
life-saving treatment.
- These criteria will be determined in the best estimation of the rescue
personnel, or if the AutoPulse signals that the patient is outside the
parameters for AutoPulse deployment.
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