Balzer2015 PDF
Balzer2015 PDF
Balzer2015 PDF
1 Pediatric Rehab Research Group, Rehabilitation Center for Children and Adolescents, University Children’s Hospital Zurich, Affoltern am Albis; 2 Regional Group
Zurich Foundation Cerebral Palsy (RGZ), Zurich, Switzerland. 3 Rehabilitation Sciences, School of Health Sciences, Queen Margaret University, Edinburgh, UK.
Correspondence to Julia Balzer, Pediatric Rehab Research Group, Rehabilitation Center for Children and Adolescents, University Children’s Hospital Zurich, M€uhlebergstrasse 104, CH-8910
Affoltern am Albis, Switzerland. E-mail: Julia.Balzer@kispi.uzh.ch
PUBLICATION DATA AIM Assessing impaired selective voluntary movement control in children with cerebral palsy
Accepted for publication 14th April 2015. (CP) has gained increasing interest. We investigated construct validity and intra- and
Published online 20th May 2015. interrater reliability of the Selective Control Assessment of the Lower Extremity (SCALE).
METHOD Thirty-nine children (21 males, 18 females) with spastic CP, mean age 12 years 6
ABBREVIATIONS months [range 6y 11mo–19y 9mo], Gross Motor Function Classification System (GMFCS)
FMA Fugl-Meyer Assessment levels I to IV, participated. Differences in SCALE scores were determined on joint levels and
ICC Intraclass correlation coefficient between patients categorized according to their limb distribution and GMFCS levels. SCALE
IQR Interquartile range scores were correlated with the Fugl-Meyer Assessment, Manual Muscle Test, and Modified
MAS Modified Ashworth Scale Ashworth Scale. To determine reliability, the SCALE was applied once and recorded on
MDC Minimal detectable change video.
MMT Manual Muscle Test RESULTS SCALE scores differed significantly between the less and more affected leg
SCALE Selective Control Assessment (p<0.001) and between most leg joints. Total SCALE scores differed significantly between
of the Lower Extremity GMFCS levels I and II. Correlations with Fugl-Meyer Assessment, Manual Muscle Test, and
SVMC Selective voluntary motor con- Modified Ashworth Scale were 0.88, 0.88, and –0.55 respectively. Intraclass correlation
trol coefficients were all above 0.9, with the minimal detectable change below 2 points.
INTERPRETATION The SCALE appears to be a valid and reliable tool to assess selective
voluntary movement control of the legs in children with spastic CP.
With an incidence of 2 to 3 per 1000 in Europe, cerebral the past decades, recent studies have indicated the impor-
palsy (CP) is the most common motor disorder in child- tance of SVMC in relation to motor performance.5–7 The
hood.1 Depending on the severity and location of the results of several studies suggest that a loss of SVMC inter-
congenital brain lesion, the appearance of positive and neg- feres much more with motor performance, such as walking,
ative motor signs are heterogeneous.2 Positive motor signs than, for instance, hypertonia and contractures.5–7 Further-
are associated with an involuntarily increased frequency or more, impaired selective activation can initiate and worsen
magnitude of muscle activity (i.e. hypertonia), whereas neg- a vicious cycle of limited active movement, joint contrac-
ative signs are characterized by insufficient muscle activity tures, hampered motor function, and diminished activity,
(i.e. muscle weakness) and their control (i.e. selective volun- thereby causing pain and appearance of secondary deformi-
tary motor control [SVMC]).2 Impaired SVMC has been ties in children with CP.8 Although the clinical importance
defined as the inability ‘to isolate the activation of muscles of physiological muscle activation is obvious, routinely
in a selected pattern in response to demands of a voluntary assessing selectivity is rare in the clinical environment,
movement or posture’.2 It is one of the most common which, in turn, hampers evaluation of therapy-induced
motor impairments of the lower extremity in children with changes in SVMC.9
spastic CP.2,3 As impaired SVMC can be caused by a reduc- This lack of clinical assessment might be explained by
tion of corticospinal drive as well as by increased input of the fact that testing SVMC is challenged by the coexis-
descending subcortical pathways, consensus about its exact tence of other motor signs. For instance, besides impaired
pathophysiological nature is still lacking.2–4 Although in SVMC, increased muscle tone or a lack of muscle strength,
comparison to other motor signs (e.g. hypertonia, muscle range of motion, sensory awareness, or stability in other
strength) improving SVMC has received little attention in joints can also result in limitations of movement quality.8
(b) SCALE and limb involvement (c) SCALE and GMFCS levels
p<0.001 p=0.002 20 Overall differences p<0.001
10
18
8 16
14
6 12
10
4 8
6
4
p=0.007
2
2
0 0
Spastic Spastic Spastic Spastic GMFCS I GMFCS II GMFCS III GMFCS IV
unilateral unilateral bilateral bilateral (n=23) (n=5) (n=8) (n=3)
l. a. leg m. a. leg l. a. leg m. a. leg
Figure 1: Discriminant validity for children with spastic cerebral palsy. (a) SCALE and joint pairs: SCALE joint scores between more and less involved
limb and on adjacent pairs of joints: Friedman test and post hoc Wilcoxon signed rank test (post hoc tests: p values below 0.01 are considered signifi-
cant). (b) SCALE and limb distribution: total SCALE scores of less affected (l.a.) versus more affected (m.a.) leg in children with spastic unilateral and
bilateral limb involvement: Wilcoxon signed rank test. (c) SCALE and GMFCS levels: significant differences between all GMFCS levels (Kruskal–Wallis
test) and between GMFCS I versus II (post hoc Mann–Whitney U test: p values below 0.025 are considered significant). SCALE, Selective Control
Assessment of the Lower Extremity; STJ, subtalar joint; GMFCS, Gross Motor Function Classification System.
Furthermore, SCALE scores differed significantly between between adjacent or contralateral joint pairs, between more
GMFCS levels (p<0.018), and, more specifically, between versus less affected limb, or between GMFCS levels, we
GMFCS levels I and II (Fig. 1c). could partly confirm our hypotheses in line with previous
results.10
Correlations Concerning the SCALE’s ability to discriminate between
For the total SCALE score, high correlations22 between the more and less affected limb in children with hemi- and
FMA and MMT were found (Fig. 2).The magnitude of the diplegia, differences were significant for both groups, but
correlations between SCALE limb and joint scores, and for the latter subgroup the difference was below the MDC.
the clinical measures were comparable to those presented On joint level, SCALE scores of the hip joint did not
for the total scores. differ between the more and less impaired limb. This could
There was a negative moderate correlation between the be because of the limited number of participants with
SCALE and the MAS total scores. greater motor impairment at the hip (i.e. GMFCS level
IV) and the large number of children with near maximal
Reliability scores (ceiling effect, i.e. 10 participants had a maximum
With ICC values exceeding 0.9 for limb and 0.8 for joint total SCALE score for their less affected leg). SCALE
SCALE scores in children with spastic CP intra- and interr- scores at most distal joint pairs tended to be lower, with
ater reliability of the SCALE can be considered excellent. the exception for comparison between the subtalar joint
The MDC varied between 1.79 and 1.96 points (Table II). and the toes. This trend was observed previously by Fow-
ler et al.12 and Brunnstrom23 who reported that selective
DISCUSSION inversion and eversion were described as the most chal-
Construct validity, as well as intra- and interrater reliability lenging movements for children with CP, as well as adult
of the SCALE in children with spastic CP are supported stroke patients. As these movements rarely occur in isola-
by this study. Regarding the SCALE’s discriminant validity tion during daily activities (but frequently in combination
(SD)2
15 Relative reliability
ICC 0.95 0.96 0.94 0.91
10 p value <0.001 <0.001 <0.001 <0.001
95% CI 0.90–0.97 0.93–0.98 0.89–0.97 0.84–0.96
5 Absolute reliability (SCALE points)
ρ=0.88 SEM 0.71 0.64 0.69 0.68
(p<0.001) MDC95 1.96 1.79 1.92 1.88
0
0 20 40 60 80 a
Because of a failure in a video recording of the SCALE, we could
MMT total score include data from only 38 participants in the reliability analyses.
CP, cerebral palsy; ICC, intraclass correlation coefficient; CI, confi-
dence interval; SD, standard deviation; SEM, standard error of mea-
(b) 20 surement; MDC95, minimum detectable change at 95% confidence
SCALE total score
interval.
15
between SCALE and MMT were also of similar magni-
10
tude. This could indicate that a correctly applied MMT
5 ρ=–0.55 will partially reflect the ability to selectively activate a mus-
(p<0.001) cle (group).
0
0 10 20 30 40
Regarding our additional hypothesis in relation to the
MAS total score
association between SVMC and spasticity, only a moderate
negative correlation was found, with a large variation of
SCALE scores in participants with low MAS scores
(Fig. 2b). This range of SCALE scores in children with
Figure 2: Spearman’s rank correlation coefficient (q) of total Selective
low spasticity might indicate that a mild level of spasticity
Control Assessment of the Lower Extremity (SCALE) scores and common
does not necessarily affect SVMC negatively, while a more
clinical assessments for children with spastic cerebral palsy. (a) concur-
clear inverse relationship between SCALE and MAS is
rent validity: SCALE versus Fugl-Meyer Assessment (FMA) and SCALE
seen in participants with higher MAS values. However, the
versus Manual Muscle Test (MMT). (b) correlation SCALE and Modified
latter would have to be confirmed in studies including par-
Ashworth Scale (MAS).
ticipants with a larger range of MAS values than reported
in our study in which the majority were only mildly
with the movement of other foot joints in supination or affected (i.e. mostly GMFCS levels I and II). In relation to
pronation) their movement performance might be experi- the functional interdependence of SVMC with muscle
enced as unusual. Another neurophysiological explanation weakness and spasticity, a possible influence of these
might be that the cortical representation of the lower impairments on the presented correlations cannot be
extremity is largest for the big toe.24 excluded. Furthermore, like Fowler et al.,10 we found a
The SCALE’s discriminant validity was reflected in an high inverse relationship (q≤ 0.80) between the severity of
overall difference between the GMFCS levels. Neverthe- CP (GMFCS levels) and the total SCALE score.
less, because of the small sample size, we could only find Our hypothesis, regarding reliability of the SCALE, was
significant differences between GMFCS levels I and II, and confirmed. We found excellent intra- and interrater reli-
interpretation should be handled with caution. Performing ability for the SCALE, as well as clinically acceptable val-
a power analysis (80% power, two-tailed alpha 0.05) ues of absolute reliability for SCALE limb scores. As these
revealed that a sample size of 19 participants in GMFCS results are based on a second rating of video recordings,
levels II and III, and 29 participants in GMFCS levels III the ICCs might be slightly higher than when rated via a
and IV, would be required to determine statistically signifi- second assessment, where interfering factors like the partic-
cant differences between these GMFCS levels. ipant’s compliance or state of health might have altered
The strong correlation between the SCALE and FMA, testing conditions. For future studies, accuracy of the video
illustrated in Figure 2, confirms that both assessments recordings could be improved by performing an additional
measure broadly similar constructs. Correlation coefficients video recording from the sagittal plane. However, our
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