MedPath

Quality of Cardiopulmonary Resuscitation Without and With Defibrillator Feedback

Phase 2
Completed
Conditions
Cardiac Arrest
Registration Number
NCT00138996
Lead Sponsor
University of Oslo
Brief Summary

Quality of bystander cardiopulmonary resuscitation (CPR) affect patient survival. Quality of professional CPR on patients has not been studied in detail, but it is regularly reported that the quality when tested on manikins deteriorates dramatically within months after training. Automated direct feedback on CPR quality from manikins brings quality back within a couple of minutes. Similar feedback has been incorporated into a defibrillator which also monitors quality of CPR. We hypothesise that quality of professional clinical CPR improves with such feedback

Detailed Description

Defibrillators which monitor quality of CPR via changes in thoracic impedance (for ventilation) and movement of the sternum employing an accelerometer (for chest compressions) will be employed in ambulances in Akershus county (Norway), Stockholm (Sweden) and London (UK). During phase 1 quality of CPR will be monitored without feedback from the defibrillator. During phase 2 the ambulance personnel will receive feedback via the defibrillator. During phase 3 the ambulance personnel will be retrained with particular attention to the quality problems that became apparent in phase 3.

Quality of CPR will be continuously recorded by the defibrillators and the data collected and sent via internet to Laerdal Medical. All other cardiac arrest data including survival will be recorded using standard datasets for cardiac arrest research as developed by a task force with members from the organisations in International Liaison Committee on resuscitation (Utstein guidelines). The data will be annotated and analyzed in detail by researchers at University of Oslo

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Cardiac arrest out-of-hospital
Exclusion Criteria
  • < 18 years old

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
fraction of time without CPR
chest compression depth
chest compression frequency
chest compression/decompression duty cycle
ventilation frequency
Secondary Outcome Measures
NameTimeMethod
rate of return of spontaneous circulation

Trial Locations

Locations (3)

Ulleval University Hospital

🇳🇴

Oslo, Norway

Stockholm Ambulance Service

🇸🇪

Stockholm, Sweden

London Ambulance Service

🇬🇧

London, United Kingdom

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