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Although 40 assessment tools are described in the literature, very few of them have been correctly validated. The Standardized Index of Shoulder Function (FI2S) encompasses pain, mobility, strength and function. The aim of this work is to describe the FI2S and to study its construct validity, reliability and responsiveness to change. Fifty-nine patients with non-surgical (rotator cuff lesions, frozen shoulders, osteoarthritis) or post-surgical (acromioplasty, repairs of rotator cuff tears, arthroplasty) shoulder disorders were included. The FI2S was compared with the Disabilities of the Arm, Shoulder and Hand questionnaire (DASH), with the Constant-Murley Score (CMS), and with a visual analogue scale for pain. Inter-test reliability and inter-rater reliability are excellent, with intra-class correlation coefficient of 0.93 (0.88-0.96) and 0.94 (0.90-0.96), respectively. Under a convergent hypothesis, the Spearman's correlation coefficients with the CMS and DASH score are 0.91 (p < 0.0001) and -0.64 (p < 0.0001), respectively. Correlations between the FI2S and the CMS are excellent for mobility and strength, but moderate for pain and functional capacities. Under a divergent hypothesis, no correlation is observed between the FI2S total score and age. Responsiveness to change is excellent. The FI2S appears to be a proper assessment tool for pain, mobility, strength and function in shoulder disorders, easy to administer and of good metric value.
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ORIGINAL REPORT
J Rehabil Med 2010; 42: 967–972
J Rehabil Med 42
© 2010 The Authors. doi: 10.2340/16501977-0627
Journal Compilation © 2010 Foundation of Rehabilitation Information. ISSN 1650-1977
Objective: Although 40 assessment tools are described in the
literature, very few of them have been correctly validated.
The Standardized Index of Shoulder Function (FI2S) en-
compasses pain, mobility, strength and function. The aim of
this work is to describe the FI2S and to study its construct
validity, reliability and responsiveness to change.
Patients: Fifty-nine patients with non-surgical (rotator cuff
lesions, frozen shoulders, osteoarthritis) or post-surgical
(acromioplasty, repairs of rotator cuff tears, arthroplasty)
shoulder disorders were included.
Methods: The FI2S was compared with the Disabilities of the
Arm, Shoulder and Hand questionnaire (DASH), with the
Constant-Murley Score (CMS), and with a visual analogue
scale for pain.
Results: Inter-test reliability and inter-rater reliability are ex-
cellent, with intra-class correlation coefcient of 0.93 (0.88–
0.96) and 0.94 (0.90–0.96), respectively. Under a convergent
hypothesis, the Spearman’s correlation coefcients with
the CMS and DASH score are 0.91 (p < 0.0001) and –0.64
(p < 0.0001), respectively. Correlations between the FI2S
and the CMS are excellent for mobility and strength, but
moderate for pain and functional capacities. Under a diver-
gent hypothesis, no correlation is observed between the FI2S
total score and age. Responsiveness to change is excellent.
Conclusion: The FI2S appears to be a proper assessment tool
for pain, mobility, strength and function in shoulder disor-
ders, easy to administer and of good metric value.
Key words: shoulder; assessment; heterogeneous score; valida-
tion.
J Rehabil Med 2010; 42: 967–972
Correspondence address: Arnaud Dupeyron, Département de
Médecine Physique & Réhabilitation, CHU de Nîmes, Place
du Pr Robert Debré, FR-30 029 Nîmes, cedex 09, France. E-
mail: arnaud.dupeyron@chu-nimes.fr
Submitted January 3, 2010; accepted August 31, 2010
INTRODUCTION
    
it with another one, particularly in different study designs, we
need accurate, reliable and widely used tools to assess pain, mo-
tor function and impact on physical and participatory activities.
This is especially true for shoulder disorders (1). For shoulder
pathologies, more than 40 assessment tools are available (2).
-
stability, osteoarthritis) (3, 4). Others, such as the Disabilities
of the Arm, Shoulder and Hand (DASH) questionnaire score,
measure the general function of the upper arm (5), regardless
of the original pathological cause. Out of 43 evaluation tools,
only 9 have undergone a correct validation process for reliability
-
gies (Western Ontario Shoulder Instability index (WOSI)
or Shoulder Instability Questionnaire (SIQ) for instability,
Western Ontario Osteoarthritis of the Shoulder (WOOS) for
osteoarthritis, Oxford Shoulder Questionnaire (OSQ) for sur-
   



designed for all shoulder pathologies in general is lacking.
In order to completely describe “shoulder outcomes”, clini-
cians usually take into account self-reported pain (7), range of
motion (ROM), strength and function. Some argue that physical
impairments such as strength or mobility, are not closely related

indexes, such as self-administered questionnaires, based either on
functional abilities or quality of life, are limited by the lack of an
objective evaluation of mobility and strength. In this context, the
Standardized Index of Shoulder Function (FI2S) was designed to
measure both objective and subjective data. In order to be widely
and easily accessible, it needs acceptable psychometric properties,
especially reproducibility, construct validity, and a good sensibil-
ity to responsiveness to change (10). Therefore, the objective of
this study is: (i) to describe this new shoulder assessment tool;
(ii) to test its reliability and responsiveness; and (iii) to compare
it with other tools to partly assess concurrent validity.
Standardized Index of Shoulder Function description
In order to build the most pertinent assessment tool for shoulder
disorders, a panel of clinical and surgical shoulder experts was
selected based on their clinical expertise, critical literature and
review of existing scales.


Arnaud Dupeyron, MD, PhD1,5, Anthony Gelis, MD1,5, Philippe Sablayrolles, MD2, Philippe-Jean
Bousquet, MD, PhD3, Marc Julia, MD2, Christian Herisson, MD2,5, Jacques Pélissier, MD1,5
and Philippe Codine, MD4
From the 1Département de Médecine Physique & Réadaptation, Centre Hospitalier Universitaire de Nîmes, Nîmes,
2Service Central de Rééducation, Centre Hospitalo-Universitaire Lapeyronie, Montpellier, 3BESPIM, Centre Hospitalier
Universitaire de Nîmes, Nîmes, 4Clinique La Pinede Centre Médical sur route de Peyrestortes, St Esteve and
5Movement to Health, Montpellier-1 University, EuroMov, Montpellier, France
968 A. Dupeyron et al.
The following criteria were distributed to the panel of
experts:
 
    -
tomical restrictions at the same time;
           -
ments;
      
age and sex groups; and
  
inherent clinical relevance.
In consequence, the FI2S items were selected and divided
into 4 subgroups: pain, function, mobility and strength, as
summarized in Appendix I. The total score is 100:
 pain is attributed 28 points with a qualitative and quantitative
evaluation (1, 7, 11) at night, at rest and during activity and
also with analgesic drug administration;
 active mobility is attributed 24 points. ROM is measured with
a goniometer (°) and thumb-C7 distance is also measured
(cm);
 function (or limitation of activities) is attributed 30 points.
The selected items correspond to different kinds of activi-
ties, such as activities of daily living (dressing, catching an
object, open a door, etc.) that can be easily performed during
clinical examination;
 strength assessment is essential since it has been demon-
strated that it is directly related to quality of life (12, 13)
and is attributed 18 points.
According to the Constant method of strenght assess-
ment (14), the patient holds the handle of a spring
balance in his or her hand, with the palm of the hand
         -
ion in the sagittal plane. The patient resists the force
applied by the examiner and is asked to maintain this posi-
tion for 5 s. Three tests are performed and the average (kg)
is noted. The strength value has to be adjusted for gender
and age as it has been addressed in the CMS (15, 16). This
adjustment has been determined using strength measured
with an electronic Kinedyne-type dynamometer (Kinetec®,
Tournes, France) in 86 control subjects with no upper arm

in subjects under the age of 50 years, and according to the
linear decrease in isometric strength with age (17), only 3
age groups were retained: under 50 years, between 50 and
60 years, and over of 60 years; in order to reach the score of
18 attributed to strength, and according to these normal val-
    
used to calculate the value of the subgroup strength from
strength measured with the balance spring (see Appendix I).

Copenhagen City Heart Study (17). The total score in the
control sample was always 100, except for one person who
achieved a total score of 93/100. Thus, the mean score for the
86 control subjects was 99.9.
Finally, the FI2S was in French, and translation was based
on the guidelines of translation/back-translation in order to
        
French one (18).
Standardized Index of Shoulder Function comparison
To address the second objective of this study, the FI2S was com-
pared with the Constant-Murley score (CMS) and the DASH
questionnaire, which are widely used in shoulder disease. The
CMS has the advantage of including pain, function, motion and
strength for shoulder assessment (19). It has been demonstrated

probably because shoulder pain is assessed by only a single
visual analogue scale, function is evaluated by global discom-
fort in daily life activities, range of motion is partially assessed
by functional tests and shoulder strength assessment requires
the use of a weighting table. The DASH is a 30-item, validated,
self-report questionnaire designed to measure physical function
and symptoms in people with any of several musculoskeletal
disorders of the upper limb. Whereas this questionnaire is not

wish to monitor arm pain and function in individual patients
has been widely demonstrated (21).

  
with one of the following shoulder pathologies were recruited: rotator
cuff lesions with or without rupture, frozen shoulder, or osteoarthritis.
       
shoulder arthroplasty were also included. Other pathologies, such as
shoulder pain caused by cancer, fracture, rheumatoid arthritis, septic ar-
thritis, or shoulder instability, as well as acute painful shoulder caused


complete the questionnaires, or who did not give their consent, were
also excluded. The local ethics committee authorized this study and a
signed consent form was obtained from all recruited patients.
Reliability was assessed by practitioners specialized in physical
       
tested by administering the FI2S index at D0 (day 0) and D1 (day 1)
by the same examiner, assuming that results observed at D1 were not
  -
ability was evaluated by administering the FI2S twice to two examiners

    
carried out at the time of inclusion and the second an hour later. The
patients were asked not to report previous examinations and results
to the examiners, and examiners were blinded to the results of other
examinations. Reliability was tested by the intra-class correlation coef-

    
Table I. Strength in the control group, according to age and gender
(n= 86)
Age (years) n (F/M)
Strength (kg)
Female (n = 47) Male (n = 39)
Right arm Left arm Right arm Left arm
20–29 11/9 5.99 5.48 11.50 10.60
30–39 9/7 6.50 5.90 9.55 9.30
40–49 10/8 5.55 5.53 11.75 11.19
50–59 9/8 5.43 5.18 8.72 8.42
> 60 8/7 3.48 3.26 7.85 7.15
F: female; M: male.
J Rehabil Med 42
969
Standardized Index of Shoulder Function
regression tested for a linear relation between the means of the two
measurements and the difference between the two measurements.
Construct validity of the FI2S was assessed by correlating the overall
score with scores on variables supposedly assessing similar dimensions
or concepts (10). We hypothesized that the FI2S score would have: (i)
strong to moderate associations with the CSM and DASH scores, both in
general and for sub-domains; (ii) weaker associations with pain at rest,

       

Responsiveness was evaluated by calculating the effect size and the
standardized response mean (SRM). Since this analysis was not the
main target of the present study, the responsiveness was studied only

All analyses were performed under SAS v8.1 (SAS Institute, Cary,
NC, USA). The alpha level was set at 5%.

Population
Fifty-nine shoulders corresponding to 59 patients (24 (41%)
were men whose mean age and standard deviation (SD) at
evaluation was 60.3 years (SD 10.6)) were evaluated (Table
II). The majority of the patients were right-handed (55 (93%)).
The shoulder disorder was located on the right side in 34 (58%)
cases, and corresponded to the dominant side in 32 (54%) cases
(31 right-handed and 1 left-handed). Symptom duration lasted
a median of 24 months (8–60). For 27 (46%) of the patients,
there was no surgery: 16 rotator cuff lesions including 8 with
ruptures, 8 frozen shoulders, and 3 cases of osteoarthritis.
Thirty-two patients underwent surgery: 9 for acromioplasty, 18
repairs of rotator cuff ruptures, and 5 for arthroplasty. The mean
age at surgery was 59.9 (SD 11.7) years; the median evaluation
for patients after the surgery was 1.5 months (0.9–1.8) after the
surgery. Discharge occurred from 18 to 61 days after inclusion

as well as the FI2S, CMS and DASH scores at inclusion are
summarized in Table II. At discharge, the mean CMS was 57.54
(SD 19.05) and the mean FI2S was 68.71 (SD 17.71).
Reproducibility
Intra-rater reliability.     

excellent, and over 90% (ICC = 0.94 (0.90–0.96)). The mean
difference between the two measurements was 1.4 (SD –5.5),
and not statistically different (p = 0.06). Results for mobility,
function, and strength are excellent and good for pain (Table
III). All but one point (2%) out of 59 were observed within

analysis for the intra-rater comparison, thus indicating a very
good reliability between the two examinations (Fig. 1A).
                
proportional bias. Differences between measurements were
stable, even with extreme values. The absence of bias was
      
the mean measurements and the difference between the two
measurements (slope = 0.02, p = 0.66).
Inter-rater reliability. 
inter-rater comparison. The ICC was set at 0.93 (0.88–0.96)
and results for each sub-score were good (Table III). The mean
difference between the two measurements was 0.02 (SD 6.2),
p = 0.87). All but one point


graphically observed and differences were stable, including
       
(slope = 0.04, p = 0.42).
Construct validity


(p  
Table III. Overall and sub-score reproducibility (interclass correlation
coefcient) and condence intervals

First examiner
At day 0 and 1
First and second examiner
At day 0
 0.84 (0.74–0.90) 0.81 (0.71–0.89)
Mobility 0.92 (0.87–0.95) 0.87 (0.79–0.92)
Function 0.90 (0.85–0.94) 0.82 (0.72–0.89)
Strength 0.93 (0.86–0.96) 0.80 (0.65–0.89)
Overall 0.94 (0.90–0.96) 0.93 (0.88–0.96)
Table II. Description of the studied population at inclusion (n = 59)
Whole group
Non-surgery Surgery
Osteoarthritis Rotator cuff
Adhesive
capsulitis Arthroplasty Acromioplasty Rotator cuff
Total, n59 3 16 8 5 9 18
Women, n35 2 7 6 2 5 13
Men, n24 1 9 2 3 4 5
Age, years, mean (SD) 60.3 (10.6) 62.3 (8.1) 60.8 (8.5) 57.4 (14.2) 64.2 (1) 58.6 (12.1) 59.4 (10.5)
Disease duration, months, mean (SD) 41.8 (48.9) 132 (95.2) 48.6 (51.9) 15.6 (18.2) 40.8 (13.7) 19.6 (17.8) 43.7 (48.2)
 22.4 (24.3) 37 (32.1) 37.4 (28.7) 34 (22.4) 5 (6.2) 10.3 (15.8) 12.2 (15.3)
 49.1 (24.7) 40.7 (16.2) 54.6 (28.8) 58.4 (27.6) 41.6 (19.6) 43.2 (18) 46.6 (25.2)
FI2S, mean (SD) 55.5 (15.9) 42 (8.8) 62.7 (17.5) 44.9 (12.7) 53.9 (12.4) 60.1 (16.2) 54.3(14.7)
CMS, mean (SD) 43.2 (15.0) 27,8 (6.5) 52,2 (15) 31,1 (9.5) 44.2 (8.4) 46.2 (13.4) 41.3 (15.1)
DASH, mean (SD) 47.8 (20.7) 50.1 (17.9) 49.3 (25.5) 59.1 (13.1) 39 (14.2) 39.4 (19.2) 47.6 (20.8)
SD: standard deviation; DASH: Disabilities of the Arm, Shoulder and Hand questionnaire; CMS: Constant-Murley Score; FI2S: Standardized Index
of Shoulder Function.
J Rehabil Med 42
970 A. Dupeyron et al.

which is excellent for mobility and strength, but moderate for pain
and function. For pain, the overall FI2S score is fairly correlated
 p
and rho = –0.42, p = 0.001) and/or at rest (rho = –0.40, p = 0.002
and rho = –0.37, p = 0.004, respectively). The DASH score is
moderately correlated with the total FI2S score (rho = –0.53,
p  p    

scores (rho = –0.50, pp
correlation was observed between the FI2S total score and age
(rho = 0.14, p = 0.28 and rho = 0.10, p = 0.43, respectively).
Responsiveness to change
Responsiveness to change was calculated by comparing FI2S
at inclusion and at discharge (mean 8 weeks (SD 1.2)) in a
subgroup of 25 patients. In this subgroup there were 12 women
(48%), with a mean age of 58.6 (SD 9.5) years. The mean
symptom duration was 49.3 (SD 53.0) months. Ten (40%)

with a mean change of 20.5 and an initial standard deviation
of 13.6). The SRM was 1.26 (with a 20.5 change (SD 16.2)
in the FI2S total score), and could be considered a “wide”
change in score.
DISCUSSION
-
der disorders, the FI2S appears to be a relevant, reproducible
assessment tool with a good responsiveness to change. The
intra and inter-rater reliability were very good with both ICCs
over 90% (0.94 (0.90–0.96) and 0.93 (0.88–0.96), respec-
tively), and with nearly all the patients falling within the 95%

This study has some limitations. First, the FI2S was designed
-
der. The FI2S has not been tested for neurological shoulders,
arthritis or infections not included in this study. Secondly, as
concerns acceptability, it has been argued that the FI2S was
easy to use both in clinical practice or clinical trials. However,
the time needed to administer the FI2S has not been studied.
The CMS is widely used, but failed to demonstrate any
metric properties and became a gold standard with use.
Furthermore, the weight of some items or the measurement
method has been criticized (22). These drawbacks limit its use
in clinical research. Another example, the American Shoul-
       
metric qualities (23), but whereas pain and function are well
described, objective measurements, such as range of motion
or strength, are lacking (24). Subjective indices, although easy
 
to analyse; many studies have shown a frequent lack of cor-
relation between the self-reported disability and functional
performances (13, 25, 26).
The FI2S was issued following analysis by a group of experts
with the standardization of 4 assessment scales commonly used
in shoulder disorders, thus enhancing its content relevance.
The differences and similarities based on the convergence
and divergence hypothesis were examined. The FI2S had a
good convergent validity with CMS, moderate with DASH
and poor with pain. This can be explained by the content of
Fig. 1. 
Index of Shoulder Function.
(A)
(B)
-
20
-
15
-
10
-
5
0
5
1
0
1
5
2
0
Means of the two measurements
2
0
6
0
8
0
Differences between the two measurements
-
20
-
15
-
10
-
5
0
5
1
0
1
5
2
0
2
0
4
0
6
0
8 10
Means of the two measurements
Differences between the two measurements
Spearman correlation coefcients between Standardized Index of
Shoulder Function and Constant-Murley Score components and overall
estimation at different times

Day 0
First
examiner
Day 0
Second
examiner
Day 1
First
examiner
 0.55* 0.58* 0.65*
Mobility 0.90* 0.91* 0.89*
Function 0.66* 0.67* 0.74*
Strength 0.92* 0.90* 0.94*
Overall 0.91* 0.93* 0.92*

*p
J Rehabil Med 42
971
Standardized Index of Shoulder Function
the pain subgroup in the FI2S, which takes into account pain
intensity and its variation during the day, the consumption of

at a certain given point. The correlation with the DASH is
average, which is not surprising because the DASH focuses on
pain and shoulder stiffness (beyond the shoulder on the whole
upper arm mobility) in addition to function. The correlation
between this functional subgroup of the CMS and the FI2S is
also average, which can be related to different abilities of the
shoulder at different times after lesions or surgeries. In the
FI2S, strength is tested in a more comfortable position and the
measure is less disturbed by pain. The importance of strength
in the total score has been lowered in relation to its importance
in the CMS, where a higher value can distort the total score
when rest and function recovery are reached, corresponding
to treatment objectives.
The FI2S has excellent psychometric properties: inter-test
and inter-examiner reproducibility, correlation with the CMS,
both qualities that make it a good tool to assess shoulder disor-
ders and evaluate treatment results. For orthopaedic research,
the good responsiveness of the FI2S will make it an essential
tool in clinical trials for calculating sample size and power
estimates. The equal importance given to the subscales make it

than the CMS; more focus on pain and function, less on range
of motion and strength makes it different from the CMS. Yet
function (described through 5 activities) and pain (analysed
through intensity, duration and analgesic consumption) are
  
where the aim is not to achieve a range of motion or acquire
   
and quality of life.
The FI2S was tested for main shoulder pathologies, in re-
habilitation settings as well as post-surgical settings, but not
for shoulder stability; it therefore cannot be used in that case.
         
more adapted to a rehabilitation context without losing its
value in post-operative follow-up. The major interest of this
heterogeneous scale is to obtain an overall value from objective
and subjective data that can be used in comparative studies.
Using some items independently can certainly be relevant for
the follow-up of an isolated patient, but may lead to a loss of
reproducibility, since the reproducibility of the total score does
not necessarily correspond to that of each subgroup. Therefore,
as suggested by Angst et al. (27), who compared metric prop-
erties and especially responsiveness to change of 6 shoulder
evaluation scales, do we need to choose the most adapted tool
for the objective of the assessment? For an overall, simple and


In conclusion, the FI2S is a heterogeneous index for assess-
ing pain, mobility, strength and function, and gives greater im-
portance to pain and function than the CMS; for these reasons


at rest and during activity, it has a good constructed validity.
Its inter-test and inter-rater reproducibility is also good, much
like its responsiveness to change. It appears to be an easy to
administer, simple assessment tool with good metric value for
shoulder disorders.




1.
randomized controlled trials of interventions for painful shoulder:

316: 354–360.
Fayad F, Mace Y, Lefevre-Colau MM. Shoulder disability ques-2.
               
48: 298–306.
3.
quality of life measurement tool for osteoarthritis of the shoulder:
the Western Ontario Osteoarthritis of the Shoulder (WOOS) index.
Osteoarthritis Cartilage 2001; 9: 771–778.
        4.
         
1–16.
5.
extremity outcome measure: the DASH (disabilities of the arm,
     

 6.
Revel M. Measurement of shoulder disability in the athlete: a

  7.
of diagnostic tests for the assessment of shoulder pain due to
soft tissue disorders: a systematic review. Health Technol Assess
2003; 7: 1–166.
    8.
  -
tional performance of the upper extremity and neck (FIT-HaNSA)

2007; 8: 42.
9.
pain and motion indicators recorded on a movement diagram of

10.
and rehabilitation: how are psychometric properties determined?

11.
Systematic review of prognostic cohort studies on shoulder dis-

-12.
der strength measurement for the Constant score with a spring

  13.
The impact of rotator cuff pathology on isometric and isokinetic
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2004; 13: 593–598.
-14.
stone; 1969, p. 28–29.
      15.

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16.

-17.
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  18.
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
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        20.

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 21.
        
responsiveness of the Disabilities of the Arm, Shoulder and Hand
outcome measure in different regions of the upper extremity.
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       22.

 23.
Hawkins RJ. Reliability, validity, and responsiveness of the Ameri-
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patients with shoulder instability, rotator cuff disease, and gleno-

       24.
        
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    -25.
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activity in rheumatoid arthritis patients with shoulder problems.
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    26.
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
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  -
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Standardized Index of Shoulder Function (FI2S)
Standardized Index of Shoulder Function
 Analgesics drug
consumption
Daily
0
Irregular
3.5
Never
7
Total pain
/28
 Unbearable
0

3.5
None
7
 Unbearable
0

3.5
Normal
7
Night-time pain Sleep is very disturbed
0
Sleep is moderately disturbed
3.5
Normal
7
Range of
motion

0–60 1
61–80 2
81–100 3
101–120 4
121–140 5
141–160 6
Abduction
0–60 1
61–80 2
81–100 3
101–120 4
121–140 5
141–160 6

(at abduction 90°)
0–30 1
31–45 2
46–60 4
61–90 6
Thumb/C7
Distance (cm)
> 60 0
41–60 2
21–40 4
 
Total ROM
/24
Function Ask the patient to perform every activity:
6 points if performed without any compensation

0 pt if impossible
Total
function
/30
To comb hair back from the forehead
To pull on or off a sweater
To catch an object at eye-level
To open a door
To pull up pants or skirt
Strength
F = kg × p



obtain the total strength score.
Total
strength
/18
p 50–60 years old > 60 years old
Men 2 2.5 3
Women 3 4 5
Total
/100
J Rehabil Med 42
... Further, they require a higher level of function even at the lowest level of performance. On the other hand, tests in open kinetic chain 4,5,[16][17][18] better represent activities of daily living of the arms. However, these performance tests 4,5,[16][17][18] have limitations, such as required equipment, long test duration, 4 lack of adjustment for patient height and external load, 5 and limited assessment of endurance. ...
... On the other hand, tests in open kinetic chain 4,5,[16][17][18] better represent activities of daily living of the arms. However, these performance tests 4,5,[16][17][18] have limitations, such as required equipment, long test duration, 4 lack of adjustment for patient height and external load, 5 and limited assessment of endurance. [16][17][18] Moreover, symptoms and effort are typically not a part of prior performance tests. ...
... However, these performance tests 4,5,[16][17][18] have limitations, such as required equipment, long test duration, 4 lack of adjustment for patient height and external load, 5 and limited assessment of endurance. [16][17][18] Moreover, symptoms and effort are typically not a part of prior performance tests. 19, 20 We developed a shoulder performance test, the Shoulder Performance Activity Test (SPAT), to improve the assessment of shoulder functional limitations by having patients perform 3 tasks that require repetitive arm movements in multiple positions that simulate elements of daily arm functional activity, and do not include equipment to apply external loads. ...
Article
Objective: The purpose of this study was to assess feasibility, reliability, and validity of a new performance-based test, the Shoulder Performance Activity Test (SPAT). Methods: People with shoulder pain (n = 93) and without shoulder pain (n = 43) were included. The SPAT consists of overhead reach, hand behind head, and hand behind back tasks, each performed with 20 repetitions and rated by time, pain, and effort. The SPAT scores were summed for time, pain, and effort, and a total score across the 3 tasks. Feasibility was assessed by the percentage of SPAT task completion, test–retest reliability by intraclass correlation coefficient, standard error measurement, minimal detectable change, and known-groups construct validity by comparing between groups (shoulder pain and no pain) and between shoulders in those with pain. Results: All participants performed the 3 SPAT tasks. The ICC was 0.74 to 0.91, and the minimal detectable change was 3.1 to 4.7 for task scores and 10.0 points for the total score. Individuals with pain presented higher tasks and total scores compared with those without pain. The moderate/severe pain group had higher scores than the low pain and no shoulder pain groups, and the low pain group had higher scores than the no pain group. Scores were higher in the involved shoulder compared with the uninvolved shoulder. Conclusion: The SPAT is a feasible and reliable performance-based test for use in patients with shoulder pain and can differentiate between individuals with and without pain, among different levels of pain, and between involved and uninvolved shoulders. Impact: The SPAT provides a standardized method for clinicians to assess shoulder functional performance tasks, which can enable a comprehensive assessment of shoulder disability and clinical decision making. The error metrics can be used to determine meaningful changes in performance.
... One of the important considerations is to have specific criteria for clinical decision making for return to activity (RTA). A combination of patients' subjective pain scales, impairment measures, strength and power tests, and upper extremity functional performance tests (UEFPT) have been traditionally used as outcome measures to document patients' progression and criteria for RTA (Cools et al., 2020;Dupeyron et al., 2010;Franchignoni et al., 2014;Kumta et al., 2012;MacDermid et al., 2007;Olds et al., 2019;Pinheiro et al., 2020). Patient-reported outcomes (PRO) are another way to measure the patient's progression and readiness for discharge from rehabilitation and return to activity (Liebs et al., 2019;Mardani-Kivi et al., 2016;Marzetti et al., 2014). ...
... Currently there are limited studies using UEFPTs as criteria for patients being discharged from treatments (Olds et al., 2019;Pontillo et al., 2020) seeking to return to levels of activity above simply activities of daily living. Furthermore, studies examining the relationship between PRO and UEFTPs have been limited to UEFPT that largely consisted of activities of daily living (Dupeyron et al., 2010;Kumta et al., 2012;Mac-Dermid et al., 2007;van de Water et al., 2016) and not the more rigorous UEFPTs. Therefore, the aim of the study was to assess the relationship between the SSASPT and the Quick-DASH in patients being discharged from physical therapy after shoulder injury or surgery. ...
... Interestingly, when Kumta et al. (2012) considered the three tasks comprising (FIT-HaNSA) separately, a much weaker correlation (r = − 0.49) was revealed between the most challenging task and DASH scores. Using the Standardized Index of Shoulder Function (SISF), an assessment that combines objective and subjective items, Dupeyron et al. (2010) reported moderate (rho = − 0.53 to − 0.60) associations with DASH scores. ...
Article
Background Research examining the relationship between patient reported outcomes (PRO) and upper extremity functional performance tests (UEFPT) in patients with shoulder pathology are limited. Objective To assess the relationship between the seated single arm shot put test (SSASPT) and the PRO Quick-Disabilities of Arm, Shoulder, and Hand (DASH) in patients being discharged from physical therapy after shoulder injury or surgery. Methods Six physical therapists who regularly use the SSASPT and DASH from six different clinical sites provided SSASPT scores and completed Quick-DASH forms on 75 patients being discharged from rehabilitation following shoulder injury or surgery. Patients were grouped according to whether the involved shoulder was the dominant (n = 43) or nondominant (n = 32) limb. Three separate simple linear regression models, whole cohort and two patient groups, were created to determine the magnitude of the relationships (standardized betas) and change (betas) between DASH scores and the SSASPT limb symmetry index (LSI). Results Neither whole cohort nor two groups exhibited statistically significant (P > .05) relationships between LSI and Quick-DASH scores based upon the standardized betas (−0.197–.038). Additionally, neither the standardized betas (z = 1.49, P = .135) nor betas (z = 1.28, P = .200) were statistically different between the two groups. Conclusions The current study revealed no association between SSASPT and the Quick-DASH at discharge from physical therapy following shoulder injury or surgery. Consequently, it may be important to perform a battery of tests that include both subjective PRO and objective UEFPT tests to obtain a comprehensive perspective of the patient's functional and perceived status.
... 4,5 FS is the condition that has been restricted to clinical and functional aspects, such assessments do not allow considering all the implications that the disease can cause to the patient's life. 6 The Disabilities of the Arm, Shoulder, and Hand Questionnaire (DASH) is a regional questionnaire consisting of 30 questions, rather specific to evaluate the functional capacity of the affected upper limb, also being self-administered. 7 Frozen shoulder is subdivided into primary and secondary, primary also called idiopathic, and occurs without any specific trauma. ...
Article
Full-text available
Frozen shoulder (FS) is a disease caused by an inflammatory condition that causes severe pain and decreased range of motion by loss of glenohumeral mobility. Frozen Shoulder restricts daily life’s functional aspect, increasing morbidity. Hypertension and diabetes mellitus are risk factors that make an FS poor prognosis during treatment because of the diabetes glycation process and hypertension-enhanced vascularization. Prolotherapy injects an irritant solution into the tendon, joints, ligaments, and joint spaces to release growth factors and collagen deposition, reducing pain, restoring joint stability, and increasing the quality of life. We report 3 cases of patients with confirmed FS. Patient A with no comorbidity, patient B with diabetes mellitus, and patient C with hypertension, with all patient’s chief complaints of shoulder pain and limited ROM, and symptoms affected the general quality of daily life. This patient was provided injection with Prolotherapy treatment combined with physical therapy intervention. Patient A had significantly improved ROM to maximum after 6 weeks with relieved pain and improved shoulder function. Patients B and C showed increased ROM, still tiny, decreased pain, and improved shoulder function. In conclusion, prolotherapy demonstrated a beneficial effect in a patient with FS with comorbidities, although not to the maximum extent in patients without comorbidity.
... En relación con la validez de criterio, al no existir una escala que cumpla de manera convincente con las características de estándar de referencia, se hace complejo obtener la más alta calificación en esta propiedad. Encontramos en esta revisión que se han utilizado frecuentemente las escalas CMS, WORC, ASES, SPADI como criterio de referencia, (28,29,33,34,42) las cuales no cumplen en su totalidad con esta característica. Finalmente, en relación a la validez de constructo hay dificultad por una parte, en el planteamiento de una hipótesis, y por otra cuando es planteada la hipótesis, por lo cual muchos estudios no son capaces de lograr que el 75 % de los resultados estén de acuerdo con ella. ...
Article
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Resumen Introducción: El hombro es una de las articulaciones con mayor movilidad del cuerpo humano, lo que incrementa su probabilidad de lesión. Se torna complejo reconocer cuál es la condición de salud real de un individuo asociada a un trastorno de hombro. Por ello, en las últimas tres décadas ha aumentado el interés de investigadores y clínicos por la generación y desarrollo de instrumentos que permitan evaluar y cuantificar la percepción de los usuarios con trastornos de hombro en relación a su funcionamiento. Objetivos: Identificar las escalas que evalúan funcionamiento del hombro y describir su consistencia interna, confiabilidad, validez de criterio, constructo y contenido. Métodos: Se revisaron 9 bases de datos, con fecha de cierre 31 enero de 2020. Se incluyeron artículos originales sin distinción de sexo, límite de edad, ni año. Se evaluó la calidad metodológica de la consistencia interna, confiabilidad, validez de contenido, constructo y criterio mediante el uso de la lista de verificación COSMIN. Análisis y síntesis de la información: Se obtuvieron 15 771 artículos, de los que se seleccionaron finalmente 56, que hacían referencia a 36 escalas, y estaban asociados a la evaluación de 7819 sujetos. Se identificaron 40 dominios diferentes y un rango de 3 a 33 ítems. Se evaluaron 117 propiedades de medición, de las cuales sólo 19,7 % obtuvieron excelente o buena calidad metodológica. Las escalas con resultados favorables en la evaluación de sus propiedades psicométricas fueron WORC, Short-WORC, SPADI, ASES, SPWC, SDQ y SACS. Conclusiones: Existen múltiples escalas para la evaluación del funcionamiento del hombro, y al mismo tiempo revela la heterogeneidad que hay en la generación de ellas. Aunque hay instrumentos que presentan buenas propiedades de medición y son recomendables para investigadores y clínicos, su uso depende de la población en estudio. Este artículo espera ser una guía para la evaluación del funcionamiento del hombro.
... Perhaps a shift toward an assessment of functional ability, as opposed to measures of physical impairments may help circumvent some of the pitfalls of the VE. Several standardized physical performance measures already exist for assessing the functional ability of patients with several operative and non-operative shoulder conditions [20,21]. As these measures focus more on the ability to perform basic or more advanced activities of daily living they seem more suited for administration by way of a VE, and may, therefore, help to more clearly establish the need for interventions such as physical therapy or subacromial injection. ...
Article
Full-text available
Background The delivery of orthopaedic care via telemedicine services has the potential to promote accessibility and decrease medical care expenses, while facilitating the control of infectious disease spreading. The purpose of this study was to assess agreement regarding diagnosis, recommended course of management and the perceived need for additional diagnostic testing between a video examination (VE) and a face to face (FTF) assessment of patients with shoulder disorders. Methods Forty-seven (18 females) patients presenting to a shoulder surgery clinic were assessed consecutively by VE and a FTF examination. All assessments were conducted by a shoulder specialist. Agreement regarding the established diagnosis, the recommended course of management and the need for additional diagnostic tests was assessed using percent agreement and kappa (95% CI) coefficient. Differences in the content, duration and satisfaction between the two examination modes were also assessed. Results Percent agreement and kappa (95% CI) coefficient for agreement regarding diagnosis were 85.1% and 0.82 (0.69–0.94), respectively. Percent agreement and kappa (95% CI) coefficient regarding the recommended course of management and the need for additional diagnostic testing were 61.7% and 0.43 (0.22–0.63), and 74.5% and 0.49 (0.25–0.74), respectively. The VE resulted in collection of less physical examination information, took longer to complete and was associated with less satisfaction by both patient and examiner. Conclusions Video examination of patients with shoulder disorders may present a valid alternative to FTF examination. Nevertheless, the content of the video-based physical examination may need to be modified to facilitate a clearer detection of indications for specific interventions or diagnostic tests.
Article
Objective: The purpose of this study was to determine the feasibility, reliability, validity, and responsiveness of the Timed Functional Arm and Shoulder Test (TFAST) in patients with shoulder problems. Methods: This study was a repeated-measures clinical measurement observational cohort study. A total of 104 individuals who were symptomatic participated in this study. The TFAST was collected as part of a patient's outpatient physical therapy care at 6 different sites. The test and data collection were performed at 3 time points: baseline (initial evaluation), follow-up at the patient's first return visit within 7 days of evaluation, and discharge at the patient's final visit for care. Results: All participants were able to perform the TFAST at baseline, with 1 exception, and 67 participants completed data collection at all 3 time points. There were no adverse effects in any participant related to performing the TFAST. Intrarater intersession reliability, reported as ICC(2,1), was 0.91 (95% CI = 0.79-0.95). The mean difference in TFAST scores for the affected arm was 23.2 repetitions (77.4 at baseline to 100.6 at discharge). The Cohen d effect size was 1.02, and the standardized response mean was 0.95. The minimal clinically important difference was determined to be 21 repetitions. Conclusion: The TFAST seems to be feasible and appropriate for use in a wider population than other existing shoulder performance measures. The TFAST has demonstrated adequate reliability, validity, and responsiveness in patients with shoulder problems. Clinicians may consider using the TFAST to objectively assess patient performance. Impact: The TFAST may be used to expand measurement of objective shoulder performance in a wide population of patients with shoulder problems. This test may provide information beyond patient self-report and contribute to clinical decision making.
Article
Objectives: To identify, critically appraise, and synthesize the reported psychometric properties of shoulder performance-based functional tests in patients with shoulder diseases. Data Sources: MEDLINE, Embase, Scopus, and Cumulative Index to Nursing and Allied Health databases from inception until March 2019 were searched. Study Selection: Randomized/prospective studies of patients with shoulder diseases that reported on the psychometric properties (reliability, validity, responsiveness) of performance-based functional tests (Standardized Index of Shoulder Function [FI2S], Functional Impairment Test–Hand and Neck/Shoulder/Arm, Closed Kinetic Chain Upper Extremity Stability Test, Timed Functional Arm and Shoulder Test, Shoulder Function Index [SFInX], and hand to neck, scapula, and opposite scapula). Data Extraction: We used the Consensus-Based Standards for the Selection of Health Measurement Instruments 2018 guideline for systematic reviews. We performed a qualitative synthesis in which the results were summarized based on reported measurement properties and study quality. Data Synthesis: Eight eligible studies were included with 28 measures (16 reliability; 10 validity; 2 responsiveness). Performance-based functional tests reliability (test-retest, intra- and interrater) measures indicated excellent reliability properties. Intraclass correlation coefficient (ICC) was ≥0.83 and standard error of the mean (SEM) ranged from 0.03-13.3 points. Validity (construct/convergent/concurrent) measures displayed correlations of −0.76 to 0.91 between performance-based functional tests and other patient-reported outcomes (Disabilities of the Arm, Shoulder, and Hand, Constant, Shoulder Pain and Disability Index). Two studies assessed the responsiveness measures performance-based functional tests. Effect sizes of 0.44 and 1.50 and minimal clinically important differences of 10.3 using the anchor-based approach were reported. Conclusions: The FI2S and the SFInX are reliable, valid, and responsive in patients with shoulder-related diseases.
Article
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Background: While interscalenic nerve block (INB) is still considered the 'gold standard' for shoulder arthroscopy, its postoperative analgesic effectiveness has recently been called into question. Meanwhile, in light of its high-quality postoperative pain relief, a renewed interest has emerged in suprascapular nerve block (SNB). The first aim of our study was to compare the postoperative analgesia effects of these two types of block at 2, 4 and 6 hours after surgery. We also assessed shoulder functional recovery over a six-month follow-up period. Methods: All patients requiring arthroscopic shoulder surgery for rotator cuff repair during the study period were enrolled. INB or SNB was performed under ultrasound guidance. The patients underwent general anaesthesia. Numerical rate scores (NRS) at rest and in motion at 2, 4 and 6 postoperative hours were recorded. Results: Over two years, 280 patients were screened. Of these, 136 were excluded. Pain scores after surgery were lower at 2 hours in INB at rest (0.70±1.50 versus 2.1±2.2; p<0.0067) and after movement (1.0 ± 2.2 versus 2.5 ± 2.3; p=0.01). A significant difference in terms of arm extrarotation degrees at week 6 and month 2 (p <0.01) in SNB was found. Conclusions: INB showed better analgesic efficacy in the immediate postoperative period. Both types of block showed similar results in terms of functional recovery over the six-month follow-up. SNB without motor block seems matched better with ambulatory surgery and with an early rehabilitation program.
Article
Study design: Survey. Introduction: Rotator cuff syndrome (RCS) is one of the most common musculoskeletal disorders reported in workers. The functional incapacity related to RCS may vary according to the sociodemographic context and to the medical management. Purpose of the study: The purpose of this is to analyze the RCS-related functional incapacity assessed by the Disabilities of the Arm, Shoulder and Hand (DASH) questionnaires in workers according to their sociodemographic characteristics and the use of care. Methods: A cross-sectional study was carried out on a French sample of workers diagnosed with RCS. The DASH and DASH-work scores were studied according to the sociodemographic factors, musculoskeletal symptoms, and RCS medical management during the preceding 12 months. Results: Two hundred seven workers who suffered from RCS filled out the questionnaire of which 80% were still working. The DASH score was significantly higher in women (24.0 vs 17.4; P < .01; effect size (d) = 0.39), in patients over the age of 50 years (23.6 vs 11.3; P < .005) and in case of another upper limb musculoskeletal disorder (P < .0001; d ≥ 0.4). The DASH and DASH-work scores were significantly higher in case of use of care for RCS (P < .005; d > 0.6). Discussion: The demographic factors and the RCS medical management influenced the overall incapacity assessed by the DASH questionnaire. Work incapacity was more especially related to the use of care for RCS. Conclusion: The sociodemographic and medical parameters added to other established predictors could help guide clinicians in managing their patients.
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To evaluate the evidence for the effectiveness and cost-effectiveness of the newer diagnostic imaging tests as an addition to clinical examination and patient history for the diagnosis of soft tissue shoulder disorders. Literature was identified from several sources including general medical databases. Studies were identified that evaluated clinical examination, ultrasound, magnetic resonance imaging (MRI), or magnetic resonance arthrography (MRA) in patients suspected of having soft tissue shoulder disorders. Outcomes assessed were clinical impingement syndrome or rotator cuff tear (full, partial or any). Only cohort studies were included. The methodological quality of included test accuracy studies was assessed using a formal quality assessment tool for diagnostic studies and the extraction of study findings was conducted in duplicate using a pre-designed and piloted data extraction form to avoid any errors. For each test, sensitivity, specificity and positive and negative likelihood ratios with 95% confidence intervals were calculated for each study. Where possible pooled estimates of sensitivity, specificity and likelihood ratios were calculated using random effects methods. Potential sources of heterogeneity were investigated by conducting subgroup analyses. In the included studies, the prevalence of rotator cuff disorders was generally high, partial verification of patients was common and in many cases patients who were selected retrospectively because they had undergone the reference test. Sample sizes were generally very small. Reference tests were often inappropriate with many studies using arthrography alone, despite problems with its sensitivity. For clinical assessment, 10 cohort studies were found that examined either the accuracy of individual tests or clinical examination as a whole: individual tests were either good at ruling out rotator cuff tears when negative (high sensitivity) or at ruling in such disorders when positive (high specificity), but small sample sizes meant that there was no conclusive evidence. Ultrasound was investigated in 38 cohort studies and found to be most accurate when used for the detection of full-thickness tears; sensitivity was lower for detection of partial-thickness tears. For MRI, 29 cohort studies were included. For full-thickness tears, overall pooled sensitivities and specificities were fairly high and the studies were not statistically heterogeneous; however for the detection of partial-thickness rotator cuff tears, the pooled sensitivity estimate was much lower. The results from six MRA studies suggested that it may be very accurate for detection of full-thickness rotator cuff tears, although its performance for the detection of partial-thickness tears was less consistent. Direct evidence for the performance of one test compared with another is very limited. The results suggest that clinical examination by specialists can rule out the presence of a rotator cuff tear, and that either MRI or ultrasound could equally be used for detection of full-thickness rotator cuff tears, although ultrasound may be better at picking up partial tears. Ultrasound also may be more cost-effective in a specialist hospital setting for identification of full-thickness tears. Further research suggestions include the need for large, well-designed, prospective studies of the diagnosis of shoulder pain, in particular a follow-up study of patients with shoulder pain in primary care and a prospective cohort study of clinical examination, ultrasound and MRI, alone and/or in combination.
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This paper describes the development of an evaluative outcome measure for patients with upper extremity musculoskeletal conditions. The goal is to produce a brief, self-administered measure of symptoms and functional status, with a focus on physical function, to be used by clinicians in daily practice and as a research tool. This is a joint initiative of the American Academy of Orthopedic Surgeons (AAOS), the Council of Musculoskeletal Specialty Societies (COMSS), and the Institute for Work and Health (Toronto, Ontario).Our approach is consistent with previously described strategies for scale development. In Stage 1, Item Generation, a group of methodologists and clinical experts reviewed 13 outcome measurement scales currently in use and generated a list of 821 items. In Stage 2a, Initial Item Reduction, these 821 items were reduced to 78 items using various strategies including removal of items which were generic, repetitive, not reflective of disability, or not relevant to the upper extremity or to one of the targeted concepts of symptoms and functional status. Items not highly endorsed in a survey of content experts were also eliminated. Stage 2b, Further Item Reduction, will be based on results of field testing in which patients complete the 78-item questionnaire. This field testing, which is currently underway in 20 centers in the United States, Canada, and Australia, will generate the final format and content of the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire. Future work includes plants for validity and reliability testing. © 1996 Wiley-Liss, Inc.
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Several methods have been devised to estimate shoulder function, none of which is entirely satisfactory. The method described in this article is applicable irrespective of the details of the diagnostic or radiologic abnormalities caused by disease or injury. The method records individual parameters and provides an overall clinical functional assessment. It is accurately reproducible by different observers and is sufficiently sensitive to reveal even small changes in function. The method is easy to perform and requires a minimal amount of time for evaluation of large population groups.
Article
Objectives: To identify all available shoulder disability questionnaires and to examine those that could be used for athlete. Methods: We systematically reviewed the literature in Medline using the keywords shoulder, function, scale, index, score, questionnaire, disability, quality of life, assessment, and evaluation. We searched for scales used for athletes with the keywords scale name AND (sport OR athlete). Data were completed by using the "Guide des Outils de Mesure et d'Evaluation en Médecine Physique et de Réadaptation" textbook. Analysis took into account the clinimetric quality of the instruments and the number of items specifically related to sports. Results: A total of 37 instruments have been developed to measure disease-, shoulder-specific or upper extremity specific outcome. Older instruments were developed before the advent of modern measurement methods. They usually combined objective and subjective measures. Recent instruments were designed with use of more advanced methods. Most are self-administered questionnaires. Fourteen scales included items assessing sport activity. Four of these scales have been used to assess shoulder disability in athlete. Six scales have been used to assess such disability but do not have specific items related to sports. Conclusion: There is no gold standard for assessing shoulder outcome in the general population and no validated outcome instruments specifically for athletes. We suggest the use of ASES, WOSI and WORC scales for evaluating shoulder function in the recreational athletes. The DASH scale should be evaluated in this population. The principal criterion in evaluating shoulder function in the high level athlete is a return to the same level of sport performance. Further studies are required to identify measurement tools for shoulder disability that have a high predictive value for return to sport.
Article
Objectives. – To identify all available shoulder disability questionnaires designed to measure physical functioning and to examine those with satisfactory clinimetric quality.Methods. – We used the Medline database and the “Guide des outils de mesure de l'évaluation en médecine physique et de réadaptation” textbook to search for questionnaires. Analysis took into account the development methodology, clinimetric quality of the instruments and frequency of their utilization. We classified the instruments according to the International Classification of Functioning, Disability and Health.Results. – Thirty-eight instruments have been developed to measure disease-, shoulder- or upper extremity-specific outcome. Four scales assess upper-extremity disability and 3 others shoulder disability. We found 6 scales evaluating disability and shoulder pain, 7 scales measuring the quality of life in patients with various conditions of the shoulder, 14 scales combining objective and subjective measures, 2 pain scales and 2 unclassified scales. Older instruments developed before the advent of modern measurement development methodology usually combine objective and subjective measures. Recent instruments were designed with appropriate methodology. Most are self-administered questionnaires.Conclusion. – Numerous shoulder outcome measure instruments are available. There is no “gold standard” for assessing shoulder function outcome in the general population.
Article
Article
Muscle strength is an excellent indicator of general health when based on reliable measurements. Muscle strength data for a healthy population are rare or non-existent. The aim of the present study was to measure a set of normal values for isometric and isokinetic muscle strength for all the major joint movements of the body and, from these data, to create a basis for comparison of the muscle strength of an individual with the expected value in a normal population. A randomly selected group, aged 20-80 years, from the Copenhagen City Heart Study were studied. The group was subgrouped according to age and gender. Isometric and isokinetic muscle strength was measured in each subject across the main joints in the body. A statistical model was developed that encompassed the three main muscle groups: upper limbs, trunk and lower limbs. Muscle strength in healthy men decreases in a linear fashion from the age of 25 years down to between 54% and 89% at the age of 75 years, and seems not highly dependent on any other parameter than age. For women, the muscle strength is dependent on weight and is only related to age from around 40 years of age. The decrease in muscle strength from the age around 40 to 75 years is 48-92%. For most muscle groups, men are 1.5-2 times stronger than women, with the oldest men having strength similar to that observed among the youngest women. We developed a model to compare the isometric and isokinetic muscle strength of all the major joint movements of an individual with values for a healthy man or woman at any age in the range of 20-80 years. In all age groups, women have lower muscle strength than men. Men's muscle strength declines with age, while women's muscle strength declines from the age of 41 years.
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