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Authors
Åkerstedt, Josefin
Buwaider, Ali
El-Hajj, Victor Gabriel
Wänman, Johan
Frisk, Henrik
Blixt, Simon
MacDowall, Anna
Edström, Erik
Elmi-Terander, Adrian
Charalampidis, Anastasios
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Funding
Funding for this research was provided by:
Region Stockholm
Karolinska Institute
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Article History
Received: 13 May 2024
Accepted: 15 February 2025
First Online: 21 February 2025
Declarations
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: As in the majority of the Swedish quality registries, patient participation in the Swedish Fracture Registry is made using the opt-out method. This means that patients automatically consent to the registration and use of surgical information and can delete their collected information by contacting the registry. Answering the patient-reported outcome questionnaire is voluntary. Thus consent from each human participant was provided. Swedish Ethical review Board Dnr: 2020–00193 and 2021–04773.
: Not required.
: The authors declare no competing interests.
