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The Norwegian national trauma registry: development process and essential data insights
Kjetil Gorseth Ringdal1,2,3, Kjetil Tengesdal Holm4, Olav Røise5,6,7
1Norwegian Trauma Registry, Norwegian National Centre on Trauma, Division of Emergencies and Critical Care, Oslo University Hospital, P.O. Box 4950, Nydalen, Oslo, 0424, Norway. kjetil.ringdal@siv.no.
The Norwegian Trauma Registry successfully collects data on over 78,000 trauma patients, revealing insights into injury patterns and long-term patient outcomes, including mental health and return to work.
Area of Science:
- Trauma care and epidemiology
- Public health surveillance
- Health services research
Background:
- Optimizing trauma systems requires understanding epidemiology, demographics, injury characteristics, and outcomes.
- The Norwegian Trauma Registry (NTR) was established to monitor and improve the Norwegian Trauma System.
- NTR was officially recognized as a national register in 2013, facilitating population-based data collection.
Purpose of the Study:
- To outline the establishment of the population-based national trauma registry.
- To provide an overview of selected data collected by the NTR.
- To assess patient-reported outcomes and return to work/education.
Main Methods:
- Data collected from trauma centres, acute care hospitals, and prehospital services in Norway.
- Local NTR databases linked to a central database, with data entry and validation by certified registrars.
- Descriptive statistics used for trauma patients registered between 2015-2023; Patient-Reported Outcome Measures (PROMs) from 2022 assessed.
Main Results:
- 78,275 trauma patients recorded from 2015-2023, with increasing annual inclusion.
- Median age 41 years, 66.5% male; highest injury rate in 15-24 year olds.
- 21.3% had NISS ≥ 16, 13.4% had ISS ≥ 16; 47.2% reported anxiety/depression at 12 months post-injury.
Conclusions:
- The NTR has been successfully implemented across all Norwegian trauma hospitals.
- Comprehensive data collection supports trauma care improvements and research.
- Registry data highlights significant long-term impacts on patient mental health and return to work/education.
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