The aim of the study is to look retrospectively at all children who presented with high-energy trauma at the Amsterdam UMC in the past five years, how this research was conducted and what findings were noted. In addition, we want to draw up a…
ID
Source
Brief title
Condition
- Fractures
Synonym
Research involving
Sponsors and support
Intervention
- Other intervention
N.a.
Outcome measures
Primary outcome
<p>Data will be collected about the patient (age, gender, comorbidity, medication use), the injury (nature, ER procedures, any interventions), the findings during the primary/secondary survey, the findings during the tertiary survey and how this was recorded in the status and by whom it was carried out. The purpose of the study is solely descriptive.</p>
Secondary outcome
<p>/</p>
Background summary
The care of children in the trauma room in connection with high-energy trauma is an intensive, multidisciplinary and busy setting. Small or less noticeable lesions may be missed. Therefore, after a primary and secondary survey (carried out in the emergency room), a tertiary survey must take place within 24 hours. There is only limited literature regarding the structure and findings during the tertiary survey in children.
Study objective
The aim of the study is to look retrospectively at all children who presented with high-energy trauma at the Amsterdam UMC in the past five years, how this research was conducted and what findings were noted. In addition, we want to draw up a framework based on this data that can provide various centers with a handle for carrying out a tertiary survey in children.
Study design
This is a retrospective study during 01-01-2020 -01-01-2025.
Intervention
There is no intervention, this only concerns retrospective file research.
Study burden and risks
No additional risks
Listed location countries
Age
Inclusion criteria
Children (patients < 18 years) who presented to the trauma room at the Amsterdam UMC with a high-energy trauma during 01/01/2020 to 01/01/2025 and were subsequently admitted and a primary, secondary and tertiary survey took place.
Exclusion criteria
Death < 24 hours
Design
Recruitment
Medical products/devices used
IPD sharing statement
Plan description
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| Research portal | NL-009299 |