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.
Aperçu de l'étude
Statut
Description détaillée
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 .
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
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Bruxelles, Belgique, 1000
- CHU Saint-Pierre
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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description of traumatic injuries
Délai: 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
Délai: 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
Délai: Baseline
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Immediately after the accident or delayed visit.
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Baseline
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Accident mechanism
Délai: 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
Délai: 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
Délai: 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
Délai: 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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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Treatment
Délai: 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
Délai: Up to 24 hours
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radiography, scanner,
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Up to 24 hours
|
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orientation
Délai: 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
Délai: 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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Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- Trottinette19-20
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Délai de partage IPD
Critères d'accès au partage IPD
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- ANALYTIC_CODE
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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