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Implementation of LUCAS 2 in Helicopter Rescue in South Tyrol

I

Institute of Mountain Emergency Medicine

Status

Completed

Conditions

Cardiac Arrest

Treatments

Device: MECHANICAL CHEST COMPRESSION

Study type

Observational

Funder types

Other

Identifiers

NCT01745926
V/15/11

Details and patient eligibility

About

Cardiopulmonary resuscitation (CPR) is used to maintain adequate perfusion of vital organs in cardiac arrest patients and is fundamental for the neurological outcome and survival of these individuals. Unfortunately, the quality of CPR may be inadequate due largely to ineffective chest compressions resulting from rescuer fatigue and interruptions in compressions. The LUCAS device (Lund University Cardiopulmonary Assist System, Jolife, Lund, Sweden), introduced in 2002, is the most extensively tested and applied automated alternative to manual CPR for in-hospital care of cardiac arrest patients and during ambulance transfer; the feasibility of application of this device in helicopter emergency medical service (HEMS) operations, however, has never been addressed. The objective of this project is to equip the three active rescue helicopters in South Tyrol with the LUCAS 2 mechanical chest compression device to answer the question: What is the feasibility and efficiency of using this device for prolonged CPR in cardiac arrest patients requiring CPR during HEMS rescue operations and transport?

Full description

This is a non-controlled, observational study. Physiological endpoints: MAP (mean arterial pressure); etCO2 (end-tidal expiratory pCO2); ROSC (return of spontaneous circulation); PaO2 (arterial pO2); PaCO2 (arterial pCO2); endpoints to assess feasibility: time from arrival to start of mechanical compressions, problems during transfer into the helicopter and in-field manoeuvers, problems with application of device, problems with patient transfer to hospital premises, hands-off time, personnel requirements.

Enrollment

18 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • cardiac arrest with indication of CPR
  • informed consent for those regaining legal competence

Exclusion criteria

  • declaration of death on site
  • contraindications of using the device
  • age <18 y

Trial design

18 participants in 1 patient group

CPR
Description:
MECHANICAL CHEST COMPRESSION
Treatment:
Device: MECHANICAL CHEST COMPRESSION

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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