1st Joint ESMAC-GCMAS Meeting - Análise de Marcha
1st Joint ESMAC-GCMAS Meeting - Análise de Marcha
1st Joint ESMAC-GCMAS Meeting - Análise de Marcha
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O-32<br />
QUANTIFICATION OF KINEMATIC MEASUREMENT<br />
VARIABILITY IN GAIT ANALYSIS<br />
McGinley, Jennifer, Dr 1 , Baker, Richard, Dr 1,2,3,4 , Wolfe, Rory, Dr<br />
1 Gait CCRE, Murdoch Childrens Research Institute, Melbourne, Australia<br />
2 Royal Children’s Hospital, Melbourne, Australia. 3 The University of Melbourne, Melbourne,<br />
Australia, 4 La Trobe University, Melbourne, Australia,<br />
5 Monash University, Melbourne, Australia<br />
Summary/conclusions<br />
A method is proposed to i<strong>de</strong>ntify the components of variability of gait analysis kinematic<br />
measures. This quantifies the repeatability of data from individual assessors and will permit<br />
i<strong>de</strong>ntification of systematic differences between multiple assessors. Results <strong>de</strong>monstrate that<br />
individual assessors differ in error magnitu<strong>de</strong> across gait parameters. Such specific information<br />
may direct clinical training and quality assurance programs.<br />
Introduction<br />
Repeated three-dimensional gait analysis (3DGA) of a single subject is known to exhibit<br />
inconsistency. This can be attributed to the inherent variability of walking and errors associated<br />
with the measurement process. Inconsistent marker placement has been i<strong>de</strong>ntified as a key<br />
factor contributing to data variability across repeat sessions [1]. This variability is increased<br />
when different assessors perform the measures. Despite many reports of the reliability of<br />
3DGA, there are limited methods available to clinical laboratories to quantify the sources of<br />
variability within kinematic data. Further, few studies (most usefully Schwartz et al.[2]) have<br />
quantifed this error in a manner that is readily accessible to gait laboratory clinical practice,<br />
i<strong>de</strong>ntifying variation attributable to the differences between trials within a single session (intertrial),<br />
between sessions measured by a single assessor (inter-session), and between data<br />
measured by different assessors (inter-assessor). The purpose of this study was to use the<br />
statistical analysis approach of variance components estimation to evaluate the variability of<br />
kinematic gait measures of a single unimpaired adult by six assessors from three Gait<br />
Laboratories.<br />
Statement of clinical significance<br />
Three-dimensional kinematic gait measurements are routinely used within clinical gait analysis<br />
to evaluate the effect of interventions on individuals. Detailed un<strong>de</strong>rstanding of the error<br />
associated with these measures may assist clinical <strong>de</strong>cision-making and provi<strong>de</strong> direction to<br />
staff training and quality assurance activities within gait laboratories.<br />
Methods<br />
A single adult subject (22 years, height 165cm, weight 76kg) atten<strong>de</strong>d three Gait Laboratories<br />
for 3DGA. At each laboratory, marker placement was in<strong>de</strong>pen<strong>de</strong>ntly conducted by two staff<br />
members. Assessor experience ranged from novice (< 30 3DGA’s) to expert (>500 3DGA’s).<br />
Each assessor repeated the analysis on two occasions within the same day. For each gait<br />
session, six left and six right gait trials were captured, in a manner consistent with typical<br />
laboratory procedures. Necessary anthropometric measures obtained at the first test session<br />
were used in the subsequent session. A conventional biomechanical mo<strong>de</strong>l (Plug-in-gait) was<br />
used to calculate lower extremity joint kinematics. Components of variability due to session<br />
and trial were estimated separately for each combination of staff member, kinematic variable<br />
and percentage of the gait cycle. A multi-level mixed-effects linear regression mo<strong>de</strong>l was fitted<br />
with a fixed effect for si<strong>de</strong> (right or left) and a random effect for session [3]. Variability due to<br />
session was estimated by the standard <strong>de</strong>viation of the session random effect and variability<br />
due to trial estimated by the standard <strong>de</strong>viation of the mo<strong>de</strong>l’s residual error term. Maximum<br />
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