TY - JOUR
T1 - Arthroplasty registries at a glance
T2 - an initiative of the International Society of Arthroplasty Registries (ISAR) to facilitate access, understanding, and reporting of registry data from an international perspective
AU - Lübbeke, Anne
AU - Hoogervorst, Lotje A
AU - Marang-van de Mheen, Perla J
AU - Prentice, Heather A
AU - Rolfson, Ola
AU - Nelissen, Rob G H H
AU - Steinbrück, Arnd
AU - McGauran, Gearoid
AU - Barea, Christophe
AU - Erikson, Kajsa
AU - Porter, Martyn
AU - ISAR Group
AU - Overgaard, Søren
AU - Pedersen, Alma B
PY - 2025/1/24
Y1 - 2025/1/24
N2 - BACKGROUND AND PURPOSE: The amount of information publicly available from arthroplasty registries is large but could be used more effectively. This project aims to improve the knowledge concerning existing registries to facilitate access, transparency, harmonization, and reporting.METHODS: Within the International Society of Arthroplasty Registries (ISAR) we aimed at developing, testing, adopting, and making publicly available a short, standardized registry description with items considered relevant for stakeholders using a cross-sectional study survey. Items were chosen based on a literature review and expert advice, selected by 9 ISAR working group members, tested iteratively in 3 registries, and commented upon by 4 external experts. All 29 ISAR member registries as of July 2023 were invited to participate in the project.RESULTS: Included items covered general descriptive information regarding registries, information related to governance, outcomes, data quality, data access, and registry production. The template was adopted, completed, and made publicly available by 25 of the 29 registries. Of those, 2/3 were national registries. 23 captured both hip and knee arthroplasties and 10 captured shoulder arthroplasties. Most registries had public reporting of data quality, methods, and results. Data was accessible in all but 2 registries, mainly as aggregated data. Important items relevant to registry quality for researchers to consistently indicate in scientific papers include scope, inclusion criteria, outcomes definitions, coverage/completeness, and validation processes.CONCLUSION: This ISAR initiative implemented a short, standardized description to facilitate appropriate use of orthopedic registry data worldwide relevant for a diverse group of stakeholders including researchers, industry, public health and regulatory agencies.
AB - BACKGROUND AND PURPOSE: The amount of information publicly available from arthroplasty registries is large but could be used more effectively. This project aims to improve the knowledge concerning existing registries to facilitate access, transparency, harmonization, and reporting.METHODS: Within the International Society of Arthroplasty Registries (ISAR) we aimed at developing, testing, adopting, and making publicly available a short, standardized registry description with items considered relevant for stakeholders using a cross-sectional study survey. Items were chosen based on a literature review and expert advice, selected by 9 ISAR working group members, tested iteratively in 3 registries, and commented upon by 4 external experts. All 29 ISAR member registries as of July 2023 were invited to participate in the project.RESULTS: Included items covered general descriptive information regarding registries, information related to governance, outcomes, data quality, data access, and registry production. The template was adopted, completed, and made publicly available by 25 of the 29 registries. Of those, 2/3 were national registries. 23 captured both hip and knee arthroplasties and 10 captured shoulder arthroplasties. Most registries had public reporting of data quality, methods, and results. Data was accessible in all but 2 registries, mainly as aggregated data. Important items relevant to registry quality for researchers to consistently indicate in scientific papers include scope, inclusion criteria, outcomes definitions, coverage/completeness, and validation processes.CONCLUSION: This ISAR initiative implemented a short, standardized description to facilitate appropriate use of orthopedic registry data worldwide relevant for a diverse group of stakeholders including researchers, industry, public health and regulatory agencies.
KW - Registries/standards
KW - Humans
KW - Cross-Sectional Studies
KW - Societies, Medical
UR - http://www.scopus.com/inward/record.url?scp=85217024840&partnerID=8YFLogxK
U2 - 10.2340/17453674.2024.42706
DO - 10.2340/17453674.2024.42706
M3 - Journal article
C2 - 39881617
SN - 1745-3674
VL - 96
SP - 116
EP - 126
JO - Acta orthopaedica
JF - Acta orthopaedica
ER -