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-33<br />
EXTRINSIC AND INTRINSIC VARIATION IN KINEMATIC DATA FROM THE<br />
GAIT OF HEALTHY ADULT SUBJECTS<br />
Eve Linda, McNee Anne, Shortland Adam<br />
One Small Step Gait Laboratory, Guy’s Hospital, London, UK<br />
Summary/Conclusions<br />
3D kinematic data from 10 healthy adult subjects were collected from 3 sessions within a<br />
week. In one session, marker placement was gui<strong>de</strong>d by in<strong>de</strong>lible pen marks ma<strong>de</strong> on the<br />
subjects in a data collection 2 days previously. Using this experimental <strong>de</strong>sign, we were able to<br />
distinguish variation due to marker placement and that due to the intrinsic variation of human<br />
walking. We found that, un<strong>de</strong>r near i<strong>de</strong>al circumstances, marker placement accounted for only<br />
a small amount of inter-sessional variation, with the greater proportion due to intrinsic<br />
differences in the gait patterns of the study subjects.<br />
Introduction<br />
3D gait analysis is used clinically to assist treatment planning and assess outcome following<br />
intervention. The ability to report changes in gait with confi<strong>de</strong>nce is reliant on repeatable data<br />
collection. The validity of gait analysis has been questioned (1,2) with variation in the data<br />
collected, in the interpretation of the results and in the subsequent recommendations. Previous<br />
studies have reported better repeatability in kinematic data recor<strong>de</strong>d on the same day than from<br />
sessions recor<strong>de</strong>d on different days, with the greater variability attributed to marker placement<br />
(3,4,5,6). In this study, we wished to quantify the variation in kinematic data due to marker<br />
placement and the intrinsic inter-sessional variability of normal walking.<br />
Statement of clinical significance<br />
Our results suggest when a single therapist applies retroreflective markers on subjects of<br />
mo<strong>de</strong>rate body-mass in<strong>de</strong>x, the portion of the inter-sessional standard error due to marker<br />
misplacement is less than 0.3 <strong>de</strong>grees for a set of commonly used kinematic variables. Most of<br />
the inter-sessional variation observed in pathological groups is likely to be due to intrinsic<br />
variation in human walking.<br />
Methods<br />
3D gait data was collected from 10 adult volunteers (mean age 31.4 years, mean BMI 22.65),<br />
with no history of musculo-skeletal abnormality, using Vicon 612 motion analysis system. A<br />
lower limb marker set was applied (modified Helen Hayes), by the same experienced therapist<br />
to each subject, on 3 separate occasions within a week. On one of the occasions, in<strong>de</strong>lible ink<br />
was used to mark the skin over the anatomical locations prior to application of the marker set.<br />
These pen marks were then used to gui<strong>de</strong> the marker placement for the subsequent data<br />
collection session 2 days later. One other data collection session was conducted two days<br />
before or after the marked sessions (randomised). The ink marks ma<strong>de</strong> on the skin were not<br />
visible during this session. In each session, data were collected during five walking trials with<br />
the subjects walking at their own self selected speed. Data were processed using the plug-ingait<br />
mo<strong>de</strong>l (Vicon Workstation) at which time thigh rotation was adjusted to correct the knee<br />
varus curve in swing (7). The intra- and inter- sessional standard errors (SEs) were calculated<br />
(6) for each of 9 commonly-used kinematic variables and for a combination of all these<br />
variables (Table 1). The average SE over the gait cycle was calculated for those trials<br />
belonging to a single session (intra-sessional), for those trials in marked and unmarked sessions<br />
(inter-sessional, including marker error), and for those belonging to the two marked sessions<br />
(inter-sessional, excluding marker error). Data were analysed using a two factor ANOVA<br />
(subjects, source of error). Post-hoc paired t-tests were conducted to establish if there were<br />
significant differences in the size of the error sources.<br />
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