- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02307123
One-year Outcome After Prehospital Intubation
Study Overview
Status
Intervention / Treatment
Detailed Description
The aim of helicopter emergency medical services (HEMS) is to supplement ground EMS units in the care of prehospital patients. The need for advanced airway management in critical out-of-hospital patients can be considered as one indicator of the severity of the patient's condition.
A recent European initiative suggested advanced airway management to be included in the top five research priorities for physician-provided prehospital care.To our knowledge, no previous studies describe the long-term outcome of critical prehospital patients treated by an EMS physician.
The primary aim of this study was to describe the long-term outcome of critically ill or severely injured patients not in cardiac arrest treated by an EMS physician. Our secondary aims were to determine the indications and causes for EMS physician performed prehospital endotracheal intubation.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All non-cardiac arrest patients.
Exclusion Criteria:
- Patients with a known need for personal assistance in activities of daily life prior to the incident leading to prehospital intubation (outcome evaluation).
- Patients intubated by EMS before HEMS arrival.
- Death on scene or during transportation.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
HEMS treated patients
Patients whose airways were secured by the HEMS physician.
|
HEMS physician prehospital intubation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Mortality
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Glasgow Outcome Score (GOS)
Time Frame: 1 year
|
GOS 1 = Death GOS 2 = Poor neurological outcome GOS 3 = Good neurological outcome Modified from the original 5 - step classification.
|
1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Arvi Yli-Hankala, Professor, Tampere University Hospital
- Principal Investigator: Toni VS Pakkanen, MD, Tampere University Hospital
- Study Chair: Ilkka Virkkunen, MD, PhD, Tampere University Hospital
- Study Chair: Tom Silfvast, MD, PhD, Helsinki University Central Hospital
- Study Chair: Tarja Randell, MD, PhD, Helsinki University Central Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
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