Klintö, Kristina http://orcid.org/0000-0002-7044-9386
Karsten, Agneta
Marcusson, Agneta
Paganini, Anna
Rizell, Sara
Cajander, Jenny
Brunnegård, Karin
Hakelius, Malin
Okhiria, Åsa
Peterson, Petra
Abdiu, Avni
Havstam, Christina
Mark, Hans
Hagberg, Emilie
Björnström, Lena
Wiedel, Anna-Paulina
Becker, Magnus
Funding for this research was provided by:
Sveriges Kommuner och Landsting (None)
Article History
Received: 3 January 2020
Accepted: 1 June 2020
First Online: 11 June 2020
Ethics approval and consent to participate
: Studies based on the Swedish CLP registry must obtain approval from an Ethics Board. Before retrieving data, approval from Region Skåne is required, which is responsible for the personal data in the registry. Ethical approval was obtained from the Regional Ethics Committee in Lund (Reference no.: 2016/1070). Personal data may be processed in a national or regional quality registry if the individual or caregivers approve. Information is given orally and in writing before registration. Verbal consent was obtained for all participants. Written consent from participants in national quality health care registries is not mandatory by Swedish law and Swedish implementation of the EU Data Protection Directive 95/46/EC.
: Not applicable.
: The authors declare that they have no competing interests.