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ON-SCENE Initiation of Extracorporeal CardioPulmonary Resuscitation During Refractory Out-of-Hospital Cardiac Arrest

Recruiting
Conditions
Cardiac Arrest
ECPR
10019280
10014623
Registration Number
NL-OMON52845
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
390
Inclusion Criteria

- Age between 18 and 50 years
- Witnessed arrest (last seen well <5 min), OR signs of life (gasping, movement)
- Initial rhyme is VT/VF OR Suspected of having a pulmonary embolism
- Refractory cardiac arrest lasting longer than 20 minutes and shorter than 45
min

Exclusion Criteria

- CO2 et<1.2 kPa (10 mmHg) during CPR
- No clear echographic visualisation of either the femoral artery or the
femoral vein.
- Expected time from collapse to arrival at an ECPR center with a direct
available ECPR team is less than 30 min.
- Patients from a dispatch region which is not ready to deploy HEMS on a
routine basis for OHCA patients with the age between 18 and 50 years.

The following patients will be withdrawed after initial inclusion as soon as
the following information becomes available:
- Known malignancy
- Known intracranial haemorrhage/ischemia <6 weeks
- Care dependent for daily activities before arrest
- Patients with a *do not resuscitate* order, which was not known at time of
the arrest.
- Refusal of defferred consent by the next of kin or by the patient himself to
use the data.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Hospital survival and costs/QALY (EQ-D5), favourable neurological outcome (CPC<br /><br>1-2) at 6 and 12 months after cardiac arrest.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>To study the health care costs per OCHA patient (iPCQ, iMCQ), costs per Quality<br /><br>Adjusted Life Year (QALY), Quality of life 6 and 12 months after OHCA and total<br /><br>costs per life gained in the intervention group and in the control group</p><br>
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