Ackerman, Ilana N. http://orcid.org/0000-0002-6028-1612
Cashman, Kara
Lorimer, Michelle
Heath, Emma
Harris, Ian A.
Funding for this research was provided by:
State Government of Victoria (Victorian Health and Medical Research Fellowship)
Article History
Received: 12 October 2023
Accepted: 12 March 2024
First Online: 21 March 2024
Declarations
:
: Ethics approval for this analysis was obtained from the Monash University Human Research Ethics Committee (#17924) and the University of South Australia Human Research Ethics Committee (#201433). All patients undergoing primary and revision hip replacement surgery in Australia provide consent for routine Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) data collection on an opt-out basis. For PROMs data collection, an opt-in patient consent process was used by the AOANJRR and an opt-out patient consent process was used by the Arthroplasty Clinical Outcomes Registry National (ACORN).
: Not applicable.
: INA is Deputy Chair of the Australian Orthopaedic Association National Joint Replacement Registry Patient-Reported Outcome Measures Research Advisory Group; IAH is Chair of the Arthroplasty Clinical Outcomes Registry National (ACORN) Steering Committee.