Trottinettes Urgences 2019-2020
Risk Assessment, Consequences and Epidemiology of Electric Scooter Accidents Admitted to Emergency Departments.
The purpose of the study was to evaluate the risk, consequences and epidemiology of electric scooter accidents admitted to the emergency room at St. Pierre University Hospital.
This prospective observational study aims to include any patient admitted to the Adult Emergency Department of St.Pierre University Hospital Brussels following an accident related to the use of an electric scooter in order to describe and understand the epidemiology, complications and treatment of injuries associated with this means of transport.
It is intended to include all accidents occurring in the emergency room during the period from 01/06/2019 to 30/06/2020.
Studie Overzicht
Toestand
Gedetailleerde beschrijving
All patients over the age of 16 years with traumatic injuries due to an accident related to the use of an electric scooter were included in the study.
Upon admission to the Emergency Department, patients over 16 years of age who accepted were included in the study. The objectives of the study were firstly to describe the context and incidence of scooter accidents, and secondly to understand the epidemiology, complications and treatment of injuries associated with this means of transport and finally, to estimate the economic impact assessed by the number of days of post-traumatic work disability, the need for access to more specialised and therefore more expensive care (operating theatre interventions, scanner-type radiological examinations or hospitalisation in intensive care units).
The data analyzed were based on :
1) the time and day of the accident, 2) the time of presentation at the hospital (same day or after the accident), 3) the mechanism of the accident, whether there were one or two people on the scooter, 4) the use or non-use of the protective helmet, 5) the influence of alcohol ; 6) the mode of arrival at the emergency room (type of ambulance or by one's own means); 7) the injury assessment, paraclinical examinations; 8) treatments; 9) hospitalization or not; 10) temporary work interruptions .
Studietype
Inschrijving (Werkelijk)
Contacten en locaties
Studie Locaties
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-
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Bruxelles, België, 1000
- CHU Saint-Pierre
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-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Beschrijving
Inclusion criteria:
- All patients with traumatic lesion following electric sccoter accident
- Be able to agree to participate in the study
Exclusion Criteria:
- < 16 years
- Unconscious
- Being unable to agree to participate in the study
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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description of traumatic injuries
Tijdsspanne: during the first 24 hours.
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description of traumatic injuries based on the medical record.
Categorised by severity and by anatomical localisation.
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during the first 24 hours.
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Arrival mode
Tijdsspanne: Up to one year
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By ambulance or by own means
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Up to one year
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Timing of arrival
Tijdsspanne: Baseline
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Immediately after the accident or delayed visit.
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Baseline
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Accident mechanism
Tijdsspanne: Baseline
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Other party ( Pedestrians hit by the scooter, accident with another) involved or not ( Loss of balance,2 drivers on the e-scooter,
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Baseline
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alcohol
Tijdsspanne: baseline up to 24 hours
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Did the driver report to being under the influence of alcohol or not
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baseline up to 24 hours
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Hour of admission
Tijdsspanne: Baseline up to 24 hours
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Admission between 7am-6pm; 6pm-11pm or 11pm-7am
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Baseline up to 24 hours
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Ownership
Tijdsspanne: Baseline up to 24 hours
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E-scooter owned or rented by the patient
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Baseline up to 24 hours
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Treatment
Tijdsspanne: Up to 24 hours
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Emergency department or operative room
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Up to 24 hours
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Paraclinical examination
Tijdsspanne: Up to 24 hours
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radiography, scanner,
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Up to 24 hours
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orientation
Tijdsspanne: Up to 24 hours
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Intensive care unit, normal hospitalisation, discharge home
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Up to 24 hours
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Cost of the treatment
Tijdsspanne: Through study completion, an average of 1 year
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Ambulance, hospitalisation, treatment in the ED or operative room , temporary incapacity for work.
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Through study completion, an average of 1 year
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publicaties en nuttige links
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- Trottinette19-20
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
IPD-tijdsbestek voor delen
IPD-toegangscriteria voor delen
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- ANALYTIC_CODE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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