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Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish

BACKGROUND AND PURPOSE: The Banff Patellofemoral Instability Instrument (BPII) 2.0 is a patient-reported outcome measure (PROM) designed specifically for patellofemoral instability. We translated and adapted the BPII 2.0 into Swedish and assessed its psychometric properties. PATIENTS AND METHODS: Th...

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Autores principales: VON HEIDEKEN, Johan, IVERSEN, Maura D, HELLSTEN, Anna, ASKENBERGER, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical Journals Sweden, on behalf of the Nordic Orthopedic Federation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617520/
https://www.ncbi.nlm.nih.gov/pubmed/37905565
http://dx.doi.org/10.2340/17453674.2023.21194
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author VON HEIDEKEN, Johan
IVERSEN, Maura D
HELLSTEN, Anna
ASKENBERGER, Marie
author_facet VON HEIDEKEN, Johan
IVERSEN, Maura D
HELLSTEN, Anna
ASKENBERGER, Marie
author_sort VON HEIDEKEN, Johan
collection PubMed
description BACKGROUND AND PURPOSE: The Banff Patellofemoral Instability Instrument (BPII) 2.0 is a patient-reported outcome measure (PROM) designed specifically for patellofemoral instability. We translated and adapted the BPII 2.0 into Swedish and assessed its psychometric properties. PATIENTS AND METHODS: The BPII 2.0 was forward- and back-translated. Children aged 10–16 years with patellar dislocation and instability or recurrent dislocation were recruited. Children completed the Swedish BPII 2.0 and KOOS-Child during their initial visit (t(0)) and 1 week later (t(1)). Internal consistency and test–retest reliability were evaluated using intraclass correlation coefficients (ICCs) for the BPII 2.0 and KOOS-Child scores comparison. Pearson correlation coefficients examined concurrent validity of the Swedish BPII 2.0 subscales with KOOS-Child subscales. RESULTS: 64 children (46 females), mean age 13.8 (10.0–16.3) years, participated. Time after patellar dislocation or surgery was 3–24 months. 55 patients (86%) returned the second BPII 2.0 and KOOS-Child after an average of 9 (5–22) days. There were no ceiling or floor effects for the total score of the new Swedish BPII 2.0 or for its subscales. BPII 2.0 demonstrated excellent internal consistency at t(0) (ICC 0.96, 95% confidence interval [CI] 0.95–0.97) and at t(1) (ICC 0.97, CI 0.95–0.98), as well as excellent test–retest reliability (ICC 0.97, CI 0.96–0.98). Concurrent validity of the BPII 2.0 subscales with KOOS-Child subscales was moderate to strong (rho 0.40–0.88). CONCLUSION: The Swedish BPII 2.0 showed excellent internal consistency as well as excellent test–retest reliability and is a reliable and valid questionnaire.
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spelling pubmed-106175202023-11-01 Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish VON HEIDEKEN, Johan IVERSEN, Maura D HELLSTEN, Anna ASKENBERGER, Marie Acta Orthop Article BACKGROUND AND PURPOSE: The Banff Patellofemoral Instability Instrument (BPII) 2.0 is a patient-reported outcome measure (PROM) designed specifically for patellofemoral instability. We translated and adapted the BPII 2.0 into Swedish and assessed its psychometric properties. PATIENTS AND METHODS: The BPII 2.0 was forward- and back-translated. Children aged 10–16 years with patellar dislocation and instability or recurrent dislocation were recruited. Children completed the Swedish BPII 2.0 and KOOS-Child during their initial visit (t(0)) and 1 week later (t(1)). Internal consistency and test–retest reliability were evaluated using intraclass correlation coefficients (ICCs) for the BPII 2.0 and KOOS-Child scores comparison. Pearson correlation coefficients examined concurrent validity of the Swedish BPII 2.0 subscales with KOOS-Child subscales. RESULTS: 64 children (46 females), mean age 13.8 (10.0–16.3) years, participated. Time after patellar dislocation or surgery was 3–24 months. 55 patients (86%) returned the second BPII 2.0 and KOOS-Child after an average of 9 (5–22) days. There were no ceiling or floor effects for the total score of the new Swedish BPII 2.0 or for its subscales. BPII 2.0 demonstrated excellent internal consistency at t(0) (ICC 0.96, 95% confidence interval [CI] 0.95–0.97) and at t(1) (ICC 0.97, CI 0.95–0.98), as well as excellent test–retest reliability (ICC 0.97, CI 0.96–0.98). Concurrent validity of the BPII 2.0 subscales with KOOS-Child subscales was moderate to strong (rho 0.40–0.88). CONCLUSION: The Swedish BPII 2.0 showed excellent internal consistency as well as excellent test–retest reliability and is a reliable and valid questionnaire. Medical Journals Sweden, on behalf of the Nordic Orthopedic Federation 2023-10-31 /pmc/articles/PMC10617520/ /pubmed/37905565 http://dx.doi.org/10.2340/17453674.2023.21194 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for non-commercial purposes, provided proper attribution to the original work.
spellingShingle Article
VON HEIDEKEN, Johan
IVERSEN, Maura D
HELLSTEN, Anna
ASKENBERGER, Marie
Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title_full Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title_fullStr Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title_full_unstemmed Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title_short Adaptation of the Banff Patellofemoral Instability Instrument (BPII) 2.0 into Swedish
title_sort adaptation of the banff patellofemoral instability instrument (bpii) 2.0 into swedish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617520/
https://www.ncbi.nlm.nih.gov/pubmed/37905565
http://dx.doi.org/10.2340/17453674.2023.21194
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