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2l January2006
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This is an Open Accessarticledistributedunder the terms of the CreativeCommonsAttribution License(http://creativecommons.orgllicenses/b),/2.O),
w h i c hp e r m i t su n r e str icte u
d se ,d istr ib u tio na, n d r e p r o d u ctioni n anymedi um,provi dedthe ori gi nalw ork i s properl yci ted-
Abstract
Background: The reliabilityand measurementerror of severalimpairmentmeasuresusedduring
the clinical examination of patients with patellofemoralpain syndrome (PFPS)has not been
established.
The purpose was to determine the inter-tester reliabilityand measurementerror of
measuresof imoairmentsassociatedwith PFPSin Datientswith PFPS.
Methods: A singlegroup repeated measuresdesignwas used.Two pairs of physicaltherapists
participatedin data collection.Examinerswere blindedto each others' measurements.
Resufts: Thirty patients(age29 +l- 8; 17 female)with PFPSparticipatedin this study. Inter-tester
reliabilitycoefficientswere substantialfor measuresof hamstrings,quadriceps,plantarflexors,and
ITB/TFL complex length, hip abductors strength, and foot pronation (lCCs from .85 to .97);
moderate for measuresof Q-angle,tibialtorsion, hip external rotation strength,lateralretinacular
tightness,and quality of movement during a step down task (lCCs lrom .67 to .79); and poor for
femoral anteversion(lCC of .45). Standarderror of measurement(SEM)for measuresof muscle
length ranged from 1.6 degrees to 4.3 degrees.SEM for Q-angle, tibial torsion, and femoral
anteversionwere 2.4 degrees,2.9 degrees,and 4.5 degreesrespectively.SEM for foot pronation
was I mm. SEMfor measuresof musclestrengthwas | .8 Kg for abductionand 2.4 Kg lor external
rotation.
Conclusion: Severalof the impairmentsassociatedwith PFPShad sufficientreliabilityand low
measurementerror. Further investigationis neededto test if these impairment measurementsare
relatedto physicalfunction and whether or not they are usefulfor decision-making.
Background
Patellofemoral pain syndrome (PFPS) is a common knee
problem among young active individuals [1-31. The
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2e.| (8.4)
2 (7%)
r6(s3%)
7 (23%)
s (17%)
t7 (se%)
r7r(i l. r )
7e( r8 . 6)
.26(.0s)
3.e(r. e)
67.3( | 7 .3)
* Numericpainratingscaleranges
from 0 (No Pain)to l0 (Worst
lmaginable
Pain)points.
8xActivityof dailylivingscaleranges
from 0 to 100points.One
hundred
indicates
absence
of symptoms
limitations.
andfunctional
procedures to ensure standardization. ltach examiner was
provided with the Manual of Standard Operating Procedures oIthe study, which contained detailed explanations
about the performance of each test.
'Iwo pairs of physical therapists (1 pair from each site)
with different levelsof experienceparticipated in data collection. One pair of testers had 3 and 5 years of clinical
practice (pair 1); whereas the other pair had 2 and 10
years of clinical experience(pair 2). During each data collection session,the subject remained inside an examina
tion room. 'Io ensure that the examiners remained
blinded to each other's assessments,the two examiners
entered the examination room independently, performed
and recorded the measurements, and then left the room.
The results were not shared with the other examiner. 'l'he
ffreasurements were always performed in the same order.
Order of testing was based on patient positioning in the
following order: supine, prone, side-lying, and standing
positions. This was done to avoid excessivechanging o[
positions, ensure that the examiners were performing all
testsunder the same conditions, and ensure that any order
effect would be the same for each examiner. Each examiner in the pair alternated serving as the initial exarniner.
Meosures
Each participant completed a demographic questionnaire
and self-reported measures of pain and function prior to
the physical examination. Subjects' age, gender, height,
weight, prior history of knee problems, mechanism of
injury, current episode duration, and symptom location
were recorded.
Pain intensity was measured using an 11-point numeric
pain rating scale ranging from 0 (No Pain) to 10 (Worst
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Figure I
lllustration of the techniques used to measure impairments associated with PFPS
(A) Hamstringslength - straight leg raise test
(B) Tightnessof the lateralretinacularstructures- patellartilt test
(C) Q-angle
(D) Tibial torsion - angleformed between inter-epicondilarand intermalleolarlines
(E) Quadricepsmusclelength- quadricepsfemoris muscleangle
(F) Femoralanteversion- Craig'stest
(G) Plantarflexors length
(H) Hip external rotation strength
(l) Hip abductionstrength
0) ITB/TFLcomplex length-Ober's test
(K) Foot pronation - naviculardrop test
(L) Quality of movement - example of lateral step down test trial using arm strategy
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the hip and knee to maintain stability. The gravity goniometer was zeroed on a horizontal surface prior to the
measurement and was placed over the distal portion of
the ITB/TFL complex (Figure 1). The test leg was flexed to
a right angle at the knee and grasped just below the knee
with the examiner's distal hand. The examiner moved the
subiect's thigh first in flexion, then through abduction
combined with extension until the hip was positioned in
mid-range abduction with neutral flexion/extension.
From this position the thigh was allowed to drop toward
the table until the point where the limb stopped moving
toward the table. At that point the measurement was
taken. The result was recorded as a continuous variable.
Negative values representmore tightness whereas positive
values (below horizontal) represent less tightness. 'fhe
averagemeasurement of two trials with 5-second pause
between trials was recorded.
Foot pronation was measured by the navicular drop test
114,47];. Navicular drop test measures the difference
between height of the navicular at subtalar joint neutral
position and that of the relaxed stance position 114,47|1.
The sublect stood on a high hard surface with his feet
shoulder width apart. 'fhe examiner stayed behind the
subject with the eyesleveled at subject'sfeet.The examiner
marked the subject's navicular tuberosity with a demographic pencil, which was wiped out after the measurement.'l'he examiner put the subject in the subtalar ioint
neutral position. [Ising an index card placed perpendicular to the table, the examiner recorded the distance from
the navicular to the floor (Figure 1). The subject was then
instructed to relax from the subtalar neutral position and
the measurement was repeated.'l'hen,with a metric ruler,
the distance between the two dots, in the index card
(which represents the difference in the position of the
navicular tubercle with respect to the floor between the
subtalar neutral and relaxed standing positions) was
recorded in millimeters. Creater distances between the
dots indicate greater pronation.
Quality of movement during the lateral step down test
was assessedusing a scale designed for this purpose.'I'he
subject was asked to stand in single lirnb support with the
hands on the waist, the knee straight and the foot positioned close to the edge of a 20 cm high step. 'I'he contralateral leg was positioned over the floor adjacent to the
step and was maintained with the knee in extension.The
subjectthen bent the tested knee until the contralateralleg
gently contacted the floor and then re-extended the knee
to the start position. This maneuver was repeated for 5
repetitions. The examiner faced the subject and scored the
test based on 5 criteria: 1) Arm strategy.Ifsubject used an
arm strategy in an attempt to recover balance, 1 point was
added (Figure l);2) Trunk movement. If the trunk leaned
to any side, I point was added; 3) Pelvis plane. If pelvis
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The sample size was calculated a priori using SamplePower'" (Chicago, Illinois) statistical software based on
the calculation of Cohen Kappa coefficientson a dichotomous variable (i.e. tight or not tight during the patellar tilt
test). To ensure sufficient statistical power to achieve a
lower bound ofthe 95%oconfidence interval for Kappa of
0 . 3 0 , a s s u m i n g K a p p a w o u l d b e e q u a l t o 0 . 6 0 , a sa m p l e
size of 30 subjects was needed [aBl. This sample size
would also be adequate to calculate ICC coefficients on
the continuous variables, given that we had 2 testersper
subject, hoping for an ICC of .85, and having determined
that reliability of .60 or higher would be acceptable[53].
Results
All the continuous variables were found to approximate a
normal distribution (Kolrnogorov Smirnov Z tests p >
.10). Resultsof the reliability analysis are in Table 2. I'able
2 shows the means and standard deviations of the 4 testers
on the continuous variables, the percentage of findings
and percentage of agreement for categorical or ordinal
variables, the reliability model used during the analysis,
the reliability coefficient with the 95o/oCl, and the standard error of measurement for continuous variables.'I'able
3 shows the reliability coefficient values for the overall
sample and for each of the two pairs of testers.
Table 2: Means and standard deviations ofthe 4 testers ofthe continuous variables, percentage offindings for categorical or ordinal
variables, the reliability model used during the analysis, the reliability coefficient, the percentage of agreement for Kappa calculation,
the 95% Cl, and the standard error of measurement for continuous variables.
V a r i a b l e( n = 3 0 )
Mean(S D ) or
% of findings
Model used
95%C I
SEM
(.82;.e6)
(.57;.86)
(.46r.8s)
(.4s;.8s)
(.80;.96)
(.l0; .70)
(.83;.96)
(.7t; .94)
( . s 6 .; el )
(.68r.93)
(.e3;.e8)
(.84:.e7)
(.58;.76)
4.3
c al c ul ati on
Hamstringslength(degrees)
Lateralretinacularlength(tight, normal)
Q - a n g l e( d e g r e e s )
Tibial torsion (degrees)
Quadricepslength(degrees)
Femoralanteversion(degrees)
Gastrocnemiuslength(degrees)
Soleuslength(degrees)
Hip external rotation strength (Kg)
Hip abductionstrength(Kg)
ITB/TFLcomplex length(degrees)
Foot pronation (mm)
Quality of movement
( f r o m 0 t o I = g o o d; fr o m 2 to 3 = m e d iu m ;,
r7.r(s.2)
t2.e(4.6)
rs . (r
s r.r)
s.e(2.7)
"n 6 "6 o "9
= poor)
33%good
50%medi um
l 7% poor
K appa
rcc (2,r)
rcc (2,r)
rcc (2,2)
rcc (2,r)
rcc (2,2)
rcc (2,2)
rcc (2,2)
rcc (2,2)
rcc (2,2)
rcc (2,r)
K appa
.92
7 t ( e 3 %)
.70
.70
.91
.45
.92
.85
.79
.85
.97
.93
.67(8o%)
2.4
2.9
3.8
4.s
1.6
2.2
L .4
1.8
2.1
0.7
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Table 3: Comparison of reliability coefficient for the overall sample and for each of the pairs of testers.
Variable
Hamstringslength(degrees)
Lateralretinacularlength (tight, normal)
Q-angle(degrees)
Tibial torsion (degrees)
Quadricepslength(degrees)
Femoralanteversion(degrees)
Gastrocnemiuslength (degrees)
Soleuslength(degrees)
Hip external rotation strength (Kg)
Hip abductionstrength(Kg)
ITB/TFLcomplex length(degrees)
Foot pronation (mm)
Q u a l i t yo f m o v e m en t
( f r o m 0 t o I = g o o d :fr o m 2 to 3 = m e d iu m ;4 a n da b o ve= poor)
Discussion
Shrout has suggesteda classification of reliability coefficients in which values lessthan 0.10 are considered virtually none agreement;.1 1 to .40 indicate slight agreement;
.41 to .60 indicate fair agreement;values between .61 and
.80 indicate moderate; and values greater than .Bl indicate substantial agreement [501. I]ased on this classification the inter-testerreliability coefficientswere substantial
for measuresof hamstrings length, quadriceps length, gastrocnemius length, soleus length, I'l'B/'lTl. complex
length, hip abductors strength, and foot pronation. Moderatevalues of reliability were observed for measuresof Qangle, tibial torsion, hip external rotation strength, lateral
retinacular tightness, and test of quality of movement.
Measurement of femoral anteversion resulted in fair reliability.
'l'o n-rakevalid interpretation of measurerrrents,the measLlrements must first dernonstrate reasonable reliability.
lnterpretatior.rof the confidence intervals around the values with substantial agreement (above .80) leads to the
estimation that the inter-tester reliability of these meas,
ures falls anlnvhere between .68 and .98. Therefore, considering the worst case(lower bound of the 95% CI of hip
abduction strength of .68), the reliability o[ these measures are still satisfactory for clinical use. Measures with a
moderate level of reliability had their confidence intervals
ranging from .45 and .91, with the lower bound of these
intervals ranging from .45 to .58, which warrants some
caution when interpreting the findings of Q-angle, tibial
torsion, hip external rotation strength, tightness oflateral
retinacular structures, and quality of movement. Regarding the interpretation of femoral anteversion, both the
reliability coefficient value and the confidence intervals
suggestthat interpretation of this test's finding may not be
consistent.
Reliability coefficient
Overallsample
(n = 30)
.92
.71
.70
.70
.91
.45
.92
-db
.79
.oJ
.97
.93
.67
P ai r I (n =
.88
t.0
.56
.60
.90
. 31
.78
.85
.71
.86
.90
.89
.6 L
?O\
P ai r2(n = l 0)
.98
.55
.77
.83
.93
.oa
.97
.92
.97
. 59
.99
.7 )
.ot
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Competing interests
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