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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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