Influence of the Education in Layperson in Out of Hospital Resuscitation

Sponsor
University of Zurich (Other)
Overall Status
Completed
CT.gov ID
NCT02473679
Collaborator
(none)
1,662
1
162
10.3

Study Details

Study Description

Brief Summary

Cardiac arrest occurs frequently and the outcome after out-of-hospital resuscitation is often fatal. Disturbing is that more than half of the surviving patients suffer from permanent impairment of cognitive functions, such attention, memory and executive functioning. With all the efforts to achieve a high quality initial resuscitation management the time delay between cardiac arrest and the beginning the initial resuscitation maneuver is the main reason for the still poor outcome. To shorten this fatal time delay, current efforts of national and supranational health authorities aime at the non-medically trained lay person, who should carry out basic life support directly on the scene supported by the use of public available semi-automatic defibrillators (AED).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    It is a combined retrospective and prospective observational single center study. Data of all Out of Hospital patients suffered a cardiac arrest in Zurich city will be collected according to the Utstein criteria. The aim of this study is to investigate the impact of trained police forces in the resuscitation outcome.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1662 participants
    Observational Model:
    Cohort
    Official Title:
    Influence of the Education in Layperson Resuscitation and Preparation the Patrol Car of the City Police With Automatic External Defibrillators and Automated Ventilation Equipment on Out of Hospital Resuscitation Outcome
    Study Start Date :
    Jan 1, 2003
    Actual Primary Completion Date :
    Jul 1, 2016
    Actual Study Completion Date :
    Jul 1, 2016

    Outcome Measures

    Primary Outcome Measures

    1. Time line for restoration the circulation [participants will be followed from origin of the event up to 12 month or death]

      Timeline for restoration the circulation after layperson started the reanimation

    Secondary Outcome Measures

    1. Time interval to first shock , [participants will be followed from origin of the event up to 12 month or death]

      Time interval from the emergency call to first shock for ventricular fibrillation

    2. Neurologic outcome [participants will be followed from origin of the event for duration of hospital stay, follow up after 12 month or death]

      Data will be collected according to Utstein criteria

    3. Time interval removal from ICU as well as discharged from hospital [participants will be followed from origin of the event up to 12 month or death]

      Time interval up to the removal from ICU as well as duration of hospital stay

    4. Definitive survival rate [participants will be followed from origin of the event up to 12 month or death]

      Survival rate of participants resuscitated by layperson after cardiac arrest

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All Out of hospital patients suffering cardiac arrest in Zurich City, resuscitated by lay persons, city police and or trained emergency medical services
    Exclusion Criteria:
    • individuals with cardiac arrest occurring in the presence of EMS

    • individuals in whom there were apparent toxic, traumatic or suicidal etiologies for unconsciousness

    • drowned individuals and individuals with terminal illness

    • documented negation of data collection

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital Zurich Zurich Switzerland 8091

    Sponsors and Collaborators

    • University of Zurich

    Investigators

    • Principal Investigator: Donat R Spahn, Prof, IFA, University Hospital Zurich

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Zurich
    ClinicalTrials.gov Identifier:
    NCT02473679
    Other Study ID Numbers:
    • KEK2014 - 0665
    First Posted:
    Jun 16, 2015
    Last Update Posted:
    Nov 2, 2016
    Last Verified:
    Nov 1, 2016
    Keywords provided by University of Zurich
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 2, 2016