Concurrent criterion-related validity and reliability of a clinical device used to assess lateral patellar displacement

Susumu Ota, Samuel R. Ward, Yu Jen Chen, Yi-Ju Tsai, Christopher M. Powers

研究成果: Article

17 引文 (Scopus)

摘要

Study Design: Repeated-measures, within-subject design. Objective: To assess the concurrent criterion-related validity and reliability of a clinical device to quantify lateral patellar displacement. Background: Excessive lateral displacement of the patella is an impairment that is widely associated with patellofemoral pain and/or pathology. Currently, no valid or reliable clinical method to assess lateral patellar displacement has been described in the literature. Methods and Measures: A total of 26 individuals (14 asymptomatic and 12 symptomatic; mean ± SD age, 27 ± 4 years) participated in the validity portion of this study, while an additional 10 asymptomatic volunteers (mean ± SD age, 28 ± 5 years) participated in the reliability portion. Lateral displacement of the patella was assessed using a custom-designed patellofemoral arthrometer (PFA) and was compared to actual position of the patella as determined by magnetic resonance imaging (MRI). Both PFA and MRI measurements of lateral patellar displacement were made with the knee extended and the quadriceps contracted. The intraclass correlation coefficient (ICC) was used to assess the level of agreement between the PFA and MRI measurements, as well as the intrarater and interrater reliability of the PFA measurements. Results: The ICC assessing the level of agreement between the MRI and PFA measures of lateral patellar displacement was good (0.86). Excellent intratester (ICC, 0.96 and 0.97) and intertester reliability (ICC, 0.92) were demonstrated. Conclusion: Our results suggest that reasonable estimations of lateral patellar displacement can be obtained using the PFA.

原文English
頁(從 - 到)645-652
頁數8
期刊Journal of Orthopaedic and Sports Physical Therapy
36
發行號9
DOIs
出版狀態Published - 2006 九月 1

指紋

Reproducibility of Results
Patella
Magnetic Resonance Imaging
Equipment and Supplies
Volunteers
Knee
Pathology
Pain

All Science Journal Classification (ASJC) codes

  • Physical Therapy, Sports Therapy and Rehabilitation

引用此文

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title = "Concurrent criterion-related validity and reliability of a clinical device used to assess lateral patellar displacement",
abstract = "Study Design: Repeated-measures, within-subject design. Objective: To assess the concurrent criterion-related validity and reliability of a clinical device to quantify lateral patellar displacement. Background: Excessive lateral displacement of the patella is an impairment that is widely associated with patellofemoral pain and/or pathology. Currently, no valid or reliable clinical method to assess lateral patellar displacement has been described in the literature. Methods and Measures: A total of 26 individuals (14 asymptomatic and 12 symptomatic; mean ± SD age, 27 ± 4 years) participated in the validity portion of this study, while an additional 10 asymptomatic volunteers (mean ± SD age, 28 ± 5 years) participated in the reliability portion. Lateral displacement of the patella was assessed using a custom-designed patellofemoral arthrometer (PFA) and was compared to actual position of the patella as determined by magnetic resonance imaging (MRI). Both PFA and MRI measurements of lateral patellar displacement were made with the knee extended and the quadriceps contracted. The intraclass correlation coefficient (ICC) was used to assess the level of agreement between the PFA and MRI measurements, as well as the intrarater and interrater reliability of the PFA measurements. Results: The ICC assessing the level of agreement between the MRI and PFA measures of lateral patellar displacement was good (0.86). Excellent intratester (ICC, 0.96 and 0.97) and intertester reliability (ICC, 0.92) were demonstrated. Conclusion: Our results suggest that reasonable estimations of lateral patellar displacement can be obtained using the PFA.",
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Concurrent criterion-related validity and reliability of a clinical device used to assess lateral patellar displacement. / Ota, Susumu; Ward, Samuel R.; Chen, Yu Jen; Tsai, Yi-Ju; Powers, Christopher M.

於: Journal of Orthopaedic and Sports Physical Therapy, 卷 36, 編號 9, 01.09.2006, p. 645-652.

研究成果: Article

TY - JOUR

T1 - Concurrent criterion-related validity and reliability of a clinical device used to assess lateral patellar displacement

AU - Ota, Susumu

AU - Ward, Samuel R.

AU - Chen, Yu Jen

AU - Tsai, Yi-Ju

AU - Powers, Christopher M.

PY - 2006/9/1

Y1 - 2006/9/1

N2 - Study Design: Repeated-measures, within-subject design. Objective: To assess the concurrent criterion-related validity and reliability of a clinical device to quantify lateral patellar displacement. Background: Excessive lateral displacement of the patella is an impairment that is widely associated with patellofemoral pain and/or pathology. Currently, no valid or reliable clinical method to assess lateral patellar displacement has been described in the literature. Methods and Measures: A total of 26 individuals (14 asymptomatic and 12 symptomatic; mean ± SD age, 27 ± 4 years) participated in the validity portion of this study, while an additional 10 asymptomatic volunteers (mean ± SD age, 28 ± 5 years) participated in the reliability portion. Lateral displacement of the patella was assessed using a custom-designed patellofemoral arthrometer (PFA) and was compared to actual position of the patella as determined by magnetic resonance imaging (MRI). Both PFA and MRI measurements of lateral patellar displacement were made with the knee extended and the quadriceps contracted. The intraclass correlation coefficient (ICC) was used to assess the level of agreement between the PFA and MRI measurements, as well as the intrarater and interrater reliability of the PFA measurements. Results: The ICC assessing the level of agreement between the MRI and PFA measures of lateral patellar displacement was good (0.86). Excellent intratester (ICC, 0.96 and 0.97) and intertester reliability (ICC, 0.92) were demonstrated. Conclusion: Our results suggest that reasonable estimations of lateral patellar displacement can be obtained using the PFA.

AB - Study Design: Repeated-measures, within-subject design. Objective: To assess the concurrent criterion-related validity and reliability of a clinical device to quantify lateral patellar displacement. Background: Excessive lateral displacement of the patella is an impairment that is widely associated with patellofemoral pain and/or pathology. Currently, no valid or reliable clinical method to assess lateral patellar displacement has been described in the literature. Methods and Measures: A total of 26 individuals (14 asymptomatic and 12 symptomatic; mean ± SD age, 27 ± 4 years) participated in the validity portion of this study, while an additional 10 asymptomatic volunteers (mean ± SD age, 28 ± 5 years) participated in the reliability portion. Lateral displacement of the patella was assessed using a custom-designed patellofemoral arthrometer (PFA) and was compared to actual position of the patella as determined by magnetic resonance imaging (MRI). Both PFA and MRI measurements of lateral patellar displacement were made with the knee extended and the quadriceps contracted. The intraclass correlation coefficient (ICC) was used to assess the level of agreement between the PFA and MRI measurements, as well as the intrarater and interrater reliability of the PFA measurements. Results: The ICC assessing the level of agreement between the MRI and PFA measures of lateral patellar displacement was good (0.86). Excellent intratester (ICC, 0.96 and 0.97) and intertester reliability (ICC, 0.92) were demonstrated. Conclusion: Our results suggest that reasonable estimations of lateral patellar displacement can be obtained using the PFA.

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