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1994 An Examination of Cyriax - S Passive Motion Tests With Patients Having Osteoarthritis of The Knee
1994 An Examination of Cyriax - S Passive Motion Tests With Patients Having Osteoarthritis of The Knee
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Research Repofl
Karen W Hayes
Cheryl Petersen
Judlth Falconer
697 / 9
KW Hayes, PhD, PT,is Assistant Professor of Physical Therapy, Northwestern University Medical
School. Address correspondence to Dr Hayes at Programs in Physical Therapy, Northwestern University Medical School, 345 E Superior St, Room 1323, Chicago, IL 60611 (USA).
This article was submitted April 22, 1993, and was accepted January 6, 1994.
10 / 698
Passive Range of
Motion
Wlnful
Sequence of pain
and resirtsnee
Amount ofmotion
End-feel
I
Win
Wln
with
resismee
A m m e n t with
active m d o n
t e t rnults
alter
resismee
Something (bone.
unilape) being
p~nchcd
Not active
Less achve
Same u,
AROM
Ca ulw
possure
~ d i , of
~ ~ , ~E x m d c u l a r
Full sapsular problem ligamenl
a
Icsion (adherent
pan ofulnvlc
musle. swelling.
(directionof
bUrSiU6)
limilationa
rrls1ca D pan
involved)
Inerlslrucbre
Internal
derangement(fmgmenrol
bone a d l a g e ; direction of
limitations relate lo location
of b l a k )
Capvlw
Spaam
Tissue
I
Acute
a ~ u b
Nmal
hthe
logical if
dy
or
where not
acute
ConMtile
8rnbI-e
Springy
blT
Nonnal
demge
,,,
Bonc~bone
Normal
hb
Empty
Implant
diaeaae;
bundtia.
innammation
crpocted
hikqhyte.
Neumpahc
mdunited lrafrure,
vthmpPthY
myasitis oaaifima
Figure. Schematic diagram of the passive motion testing component of the selective
tension .ystem of sofr tissue diagnosis proposed by Cyriax.2(AROM=active range of
motion.)
Method
Subjects for the study were 79 patients with OA of the knee who had
consented to be screened for a study
of the effectiveness of ultrasound on
chronic soft tissue tightness.4 Their
OA was diagnosed by radiography or
clinical examination by physicians.
Among the important criteria for a
clinical diagnosis of OA are the presence of osteophytes, morning stiffness
for less than 30 minutes, crepitus,
Procedure
SD
Age (Y)
Duration of knee stiffness (mo)
68.5
13.3
83.6
122.4
Range
28.0-95.0
1.0-612.0
Knee pain
5.6
3.1
0.0-10.0
Weight (kg)
81.1
18.6
49.8-124.9
Height (cm)
166.6
9.9
149.9-1 93.0
Examiners
Four examiners participated in the
study. The examiners had practiced
physical therapy for 4 to 18 years. All
examiners were familiar with the
evaluation techniques from their professional and postprofessional education, and they met with each other
and the principal investigator (KWH)
to review the measurement techniques, specific study procedures, and
grading prior to their participation in
the study. Each examiner performed
all measures on the same set of patients at baseline, after treatment, and
after 2 months without active inter-
Description
Capsular
Tissue approximation
Springy block
Bony
Spasm
Empty
Pain occurs before the end of motion and patient asks for the
motion to stop; examiner feels no resistance
Painlresistance sequence
1
No pain
12 / 700
Passive ROM of the knee was measured with a large universal goniometer with the subjects in the supine
position with the hip flexed to 90
degrees. According to Cyriax, in OA
extension loss is 6% to 11% of flexion
loss.1@56)In our study, therefore, a
capsular pattern was defined as extension loss (with full extension defined
as 0")eing
5 11% of the flexion loss
(with full flexion defined as 150" to
accommodate the maximum flexion
ROM of all subjects and to avoid
negative loss values). Extension
losses greater than 11% of flexion
loss were defined as representing a
noncapsular pattern. End-feel was
assessed at each end of passive ROM
using overpressure and assigned to
one of six categories. The pain/
resistance sequence was also assessed at each end of passive ROM
and graded on a four-point scale.
These scales are shown in Table 2.
The pain/resistance sequence scale
was used in three ways. When it was
studied as an indicator of OA, subjects
with no pain and subjects with pain
after resistance were combined into
one category, and subjects who had
pain with resistance and pain before
resistance were combined into one
category. When the pain/resistance
scale was used as a variable for examining the pain relationships, it was
considered a four-point scale as described. When the pain/resistance
scale was used for analysis of the
concept of chronicity, subjects without
pain on end-feel testing were
dropped from the analysis. Pain in OA
does not correlate with stage of disease activity.5 Patients with early disease may be pain-free, as may patients
with very advanced diseze,5 The
inclusion of a "no pain" category
would abrogate the ordinal nature of
the scale as a measure of chronicity.
Pain intensity was measured by asking
subjects to mark a VAS6 representing
their pain intensity on the previous
day. Chronicity was measured by
SD
Range
Extensior~
Baselinea
9.77
Posttre,atmentb
7.05
Follow-upb
7.46
Flexion
Baselinea
120.56
Posttreatmentb
124.25
Follow-upb
122.35
Data Analysis
One-way chi-square analyses were
used to test the first set of hypotheses
pertaining to the proportion of subjects with capsular patterns (H:l),
capsular end-feels for both extension
and flexion (H:2), and painless endfeels o r pain after resistance (H:3) at
baseline. The hypotheses that the
passive ROM of subjects with tissue
approximation end-feels would be
larger than the passive ROM of subjects with spasm o r capsular end-feels
@:4) and that the pain intensity of
subjects with spasm o r empty endfeels would be greater than the pain
intensity of subjects with other end-
Results
The descriptive statistics for passive
extension and flexion ROM are displayed in Table 3. At baseline, only 8
subjects displayed a capsular pattern
and 71 subjects displayed a noncapsular pattern. The frequencies of capsular and noncapsular patterns were
significantly different (X'= 50.24,
P<.001), but the hypothesis that a
significant proportion of subjects
would have a capsular pattern (H:l)
was not supported because the results
were in the wrong direction.
The number of subjects demonstrating each type of end-feel is shown in
Table 4. The differences in number of
subjects with each type of end-feel
were significant at baseline for both
extension (X"193.43, P<.001) and
flexion (X'=80.31, P<.001). Most of
the subjects had a capsular end-feel
for extension, accounting for 82.0% of
the chi-square value. In flexion, most
Capsular
Tissue
Approximation
Springy
Block
Bony
Spasm
Empty
Extension
Baselinea
59
Posttreatmentb
56
Follow-upb
45
0
10
Flexion
Baselinea
17
40
Posttreatmentb
11
38
Follow-upb
11
28
before or after resistance. The hypothesis that most subjects would have no
pain or pain after resistance (H:3) was
not supported for either extension or
flexion. There was no statistical difference in the number of subjects in the
two categories for extension
(X'=2.32). The number of subjects in
each of the combined categories of
paidresistance sequence differed
from a uniform distribution (50% of
the subjects in each of the two cells)
for flexion (X'=5.23, PC.05), but the
majority of the subjects were in the
Table 5. Number of Subjects With Each Extension and Flexion Sequence of Pain
and Resistance
No Pain
Pain After
Resistance
Pain With
Resistance
Pain Before
Resistance
Baselinea
Posttreatmentb
[I
28
7dl
1
[29
18
edl
1
62
48
Follow-UP"
24
11
42
62
Extension
Flexion
Baselinea
[I 7C
sdl
[29
11
Posttreatmentb
22
17
48
Follow-upb
17
17
41
14 / 702
dl
SS
MS
Examiner 1
Between people
21
1264.91
60.23
Within people
22
229.00
10.41
Between measures
Residual
Total
11.OO
11.OO
21
218 00
10.38
1493.91
34.74
43
5.79
<.01
1.06
NSa
14.62
< .01
ICCb(3,1)=.71
Examiner 2
Between people
369.43
61.57
Within people
29.50
4.21
Between measures
0.07
0.07
Residual
29.43
4.90
13
398.93
30 69
Total
0.01
NS
ICC(3,1)=.85
Examiner 3
Between people
17
1996.25
117.43
Within people
18
156.50
8.69
8.03
8.03
17
148.47
8.73
2152.75
61.51
Between measures
Residual
Total
35
13.51
0.92
< .01
NS
ICC(3,1)=.86
"NS=not significant.
b~~~=intraclass
correlation coeficient
Discussion
Pattern of Restriction, End-feel,
and Pain/Resistance Sequence
as Indicators of Osteoarthritis
Pattern of restriction.A capsular
pattern is supposed to indicate involvement of the entire capsule and is
expected in OA.l(p406j There was a
scarcity of patients with OA who had
a capsular pattern. Perhaps the majority of these patients had not yet developed the capsular pattern. If the capsular pattern did not develop until
very late in the disease, then the system would not be of much assistance
in diagnosing OA. Cyriax stated, however, that the capsular pattern would
exist regardless of whether the patient
is early or late in the course of the
disease. He claimed that only the
end-feel, not the pattern of restriction,
would change with an advancing
condition.I(p53)
loss of e x t e n ~ i o n . ~
Patients
~ J ~ would
be inclined to retain more extension
ROM by using their knees in their
daily activities.
SS
MS
Between people
21
28219.73
1343.80
52.51
Within people
22
563.00
25.59
29.45
29.45
21
533.55
25.41
43
28782.73
669.37
Source of Variation
Exam~ner1
Between measures
Residual
Total
1.16
NSa
98.66
<.01
ICCb(3,1)=.96
Examiner 2
Between people
4735.43
789.24
Within people
56.00
8.00
23.14
23.14
Between measures
Residual
Total
32.86
5.48
13
4791.43
368.57
4.23
NS
ICC(3,1)=.99
Examiner 3
Between people
17
14440.25
Within people
18
468.50
26.03
66.69
66.69
17
401.81
23.64
Between measures
Residual
849.43
32.63
2.82
<.01
NS
Total
"NS=not significant.
h ~ ~ ~ = i n t r a c lcorrelation
ass
coefficient.
16 / 704
is nonredundant, contributing a
unique bit of information beyond
pain averaged over daily activity.
The correlation between pain/resistance sequence and the number of
months of stiffness was extremely low,
suggesting that the paidresistance
sequence is not a measure of chronicity. Even when corrected for unreliability, assuming that the number of
months of stiffness was measured
without error, the correlation coefficients were still low (rho=.O7 for
extension and -.02 for flexion). If the
paidresistance sequence represented
the concept of chronicity, then pain
after resistance would represent a
chronic state; pain with resistance
would indicate a subacute state, and
pain before resistance would indicate
an acute state. The low corrected
correlation coefficients suggest that
this pattern is not present in these
data.
Reliability
The reliability estimates for measurements of extension and flexion ROM
do not differ markedly from those of
other reliability studies of goniometric
measurements of knee ROM in which
intrarater reliability values of .85 to
.98 for extension and .95 to .99 for
flexion were found.22-24 AS in these
previous studies, reliability was better
for flexion than for extension. The
lower reliability for knee extension
could reflect the dficulty therapists
have aligning the goniometer in extension and the inability of a goniometer to account for the rotation of the
tibia that occurs as the knee comThis lower reliabilpletes e~tension.~5
ity may also be a result of the smaller
variability in knee extension ROM
among subjects compared with the
variability of knee flexion.
The reliability estimates of end-feel
and paidresistance sequence assessments may have been low because
there was limited variability in the
group on both variables. Consequently, chance agreement would be
high, decreasing the kappa coeffi~ i e n tKappa
. ~ ~ changes with the probabilities of each of the possible categories and is best when the
probabilities are approximately equal.
The maximum possible kappa coefficient can be calculated for a given set
of marginal probabilities.13 Given the
distributions in this study, the maximum kappa coefficient would be .78
for extension end-feel, .78 for flexion
end-feel, .75 for paidresistance sequence in extension, and .88 for paid
resistance in flexion. For both variables, the reliability estimates are
considerably below these values. The
reliability of the paidresistance sequence assessments may be low because the time interval between the
onset of pain and the onset of resistance may be too short to determine
clinically through manual palpation.
The low reliability estimates could
represent actual patient change over
the 2-month period; however, there
were no statistical differences in
grades between measurements, and
passive ROM reliability estimates were
acceptable or nearly acceptable over
The results of this study provide evidence of the need to question and
further examine selective tension
testing as a diagnostic system. Testretest reliability estimates were acceptable for passive ROM measurements but not for end-feel and paid
resistance sequence classification.
Very few subject. exhibited a capsular
pattern by Cyriax's quantitative definition. A proportional definition of a
capsular pattern should be abandoned, but the concept of a pattern of
ROM loss may be useful. When corrected for unreliability, paidresistance
sequence is an indicator of pain intensity but not chronicity. Poor reliability estimates limit our ability to
interpret additional findings. For example, more subjects retained tissue
approximation end-feels than predicted; fewer subjects had painless
end-feels o r pain after resistance during end-feel testing than predicted,
and end-feel was related to joint motion but not to pain intensity. More
investigation of selective tension testing is needed to improve the reliability and examine other facets of validity, particularly the use of the system
to guide treatment decisions.
Acknowledgments
29 Potter NA, Rothstein JM. Intenester reliability for selected clinical tests of the sacroiliac
joint. Phys Ther 1985;65:1671-1675.
30 Patla CE, Paris SV. Reliability of interpretation of the Paris classification of normal end
feel for elbow flexion and extension. Journal
of Manual and Manipulative the rap.^. 1993;l:
60-66.
Invited Commentary
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