Prospective cohort study.
To study upper extremity musculoskeletal pain during and after rehabilitation in wheelchair-using subjects with a spinal cord injury (SCI) and its relation with lesion characteristics, muscle strength and functional outcome.
Eight rehabilitation centers with an SCI unit in the Netherlands.
Using a questionnaire, number, frequency and seriousness of musculoskeletal pain complaints of the upper extremity were measured. A pain score for the wrist, elbow and shoulder joints was calculated by multiplying the seriousness by the frequency of pain complaints. An overall score was obtained by adding the scores of the three joints of both upper extremities. Muscle strength was determined by manual muscle testing. The motor score of the functional independence measure provided a functional outcome. All outcomes were obtained at four test occasions during and 1 year after rehabilitation.
Upper extremity pain and shoulder pain decreased over time (30%) during the latter part of in-patient rehabilitation (P<0.001). Subjects with tetraplegia (TP) showed more musculoskeletal pain than subjects with paraplegia (PP) (P<0.001). Upper extremity pain and shoulder pain were significantly inversely related to functional outcome (P<0.001). Muscle strength was significantly inversely related to shoulder pain (P<0.001). Musculoskeletal pain at the beginning of rehabilitation and BMI were strong predictors for pain 1 year after in-patient rehabilitation (P<0.001).
Subjects with TP are at a higher risk for upper extremity musculoskeletal pain and for shoulder pain than subjects with PP. Higher muscle strength and higher functional outcome are related to fewer upper extremity complaints.
Based on epidemiological studies, it seems evident that manual wheelchair propulsion and wheelchair-related daily life activities cause a heavy load on the upper extremities, especially for persons with cervical spinal cord injury (SCI).1, 2 Other suggested risk factors for the development of shoulder pain are the duration of injury, age (ie older people have a higher risk than younger people), higher body mass index (BMI)3, 4, 5 and wheelchair propulsion style.6 However, research has been limited in terms of methodology and power. Most of the previous studies were cross-sectional and/or retrospective studies and focused on subjects who had a longer duration of the injury. Some of the studies collected data on pain by questionnaires,7, 8 while other studies performed an additional physical examination.2, 3, 5 Only few studies looked at complaints that originated during the in-patient rehabilitation.9, 10, 11 Musculoskeletal complaints during in-patient rehabilitation can be crucial to the progress and the duration of the rehabilitation.9 Further, there is not much evidence-based information about the relationship between upper extremity complaints and the functionality of subjects with an SCI.
In the current study, the course of upper extremity musculoskeletal pain over time is described and analyzed in association with the course of muscle strength and functional outcome during and 1 year after rehabilitation. Musculoskeletal pain and functionality are expected to be related since persons with a better physical condition have fewer complaints or less intensive pain.12
Knowledge about the course and prognostic determinants of upper extremity complaints is of importance not only to predict the condition of the persons with SCI at the end of the rehabilitation period, but also for treatment and prevention of pain. Timing of more- or less-straining training periods could be beneficial to the occurrence and course of pain complaints.13
The aim of this study was to investigate the course of upper extremity musculoskeletal pain and its relationship with lesion characteristics, muscle strength and functional outcome of subjects with an SCI, with special attention to the shoulder joint. Furthermore, the most important predictors for upper extremity musculoskeletal pain 1 year after the rehabilitation were investigated. It is expected that subjects with tetraplegia (TP) have more upper extremity musculoskeletal pain and that subjects with higher muscle strength and higher functional outcome develop fewer complaints.
The present study was part of the Dutch research program ‘Physical Strain, Work Capacity and Mechanisms of Restoration of Mobility in the Rehabilitation of Persons with Spinal Cord Injuries’. Persons with an acute SCI were followed during their in-patient rehabilitation and until 1 year after discharge. Subjects were measured four times: at the start of active rehabilitation, defined as being able to sit in a wheelchair for 3–4 h (t1), 3 months after t1 (t2), at the time of discharge from in-patient rehabilitation (t3) and a year after discharge (t4). In eight Dutch rehabilitation centers, specialized in the rehabilitation of persons with SCI, a trained local research assistant conducted the measurements, according to a standardized protocol.
Subjects were asked to enter the program if they had an acute SCI, were between 18 and 65 years of age and were classified as A, B, C or D on the American Spinal Injury Association (ASIA) Impairment Scale.14 Exclusion criteria were progressive diseases, psychiatric problems and insufficient knowledge of the Dutch language. Subjects who were able to walk were excluded from this study, but a small group of subjects with a high lesion level who eventually are using a power wheelchair were included.
For some subjects, the length of stay in in-patient rehabilitation was no longer than 3 months; in these cases, their second measurement was performed at the time of discharge. Data of those subjects were considered as measurements at t3, meaning that of those subjects no data were available at t2.
After they had been given information about the testing procedures, the subjects gave their written, informed consent. All tests and protocols were approved by the Medical Ethics Committee of Rehabilitation Centre Hoensbroek, The Netherlands.
Lesion and personal characteristics
At each test occasion, the lesion characteristics (level and completeness) were assessed by a physician according to the International Standards for Neurological Classification of Spinal Cord Injury.14 Also the BMI was determined (body mass/height2).
At the four test occasions (t1–t4), the participants were asked in a separate standardized questionnaire if they experienced pain on the joints or muscles of the upper extremity joints, that is, the wrist, elbow and shoulder of both arms. Musculoskeletal pain in each joint was scored as 0 when no pain was present or as 1 when pain was present. Subjects were also asked about the seriousness of pain complaints and about the frequency of pain occurrence. The seriousness was measured subjectively on a Likert scale of 1–5 ranging from very mild to very severe. Frequency was scored as 1 if pain occurred once a week or less, as 2 if pain occurred two or three times a week and as 3 when pain occurred more than 3 times a week.
An overall upper extremity pain score was obtained by multiplying the pain score of each joint by the seriousness and by the frequency of complaints. The scores of the three joints of both upper extremities were added together to obtain an upper extremity pain score, ranging from 0 to 90. The pain score was also analyzed for the shoulder joints separately (score ranging from 0 to 30).
Another section of the survey asked for other (among others neurogenic) pain complaints with specific note about other pain complaints than musculoskeletal pain.
Manual muscle strength
To assess the strength of six muscle groups of the upper extremities, standardized manual muscle tests (MMT) were performed for the wrist extensors, elbow flexors and extensors, shoulder internal and external rotators, and shoulder abductors. The MMT for each muscle group was performed in a standardized position.15 Muscle force was measured subjectively by the research assistant on a scale of 0–5 as follows: (0) no muscle contraction, (1) palpable or visible muscle contraction, (2) active movement through full range of motion (ROM) with gravity eliminated, (3) active movement through full ROM against gravity, (4) active movement through full ROM against resistance, (5) normal muscular strength. The muscle group scores of the right and left upper extremities were added together to obtain an overall MMT score, ranging from 0 to 60.
Functional independence measure motor score
The motor score of the functional independence measure (FIM)16 was used to measure the level of independence in activities of daily living. The Dutch version of the FIM was used for this study.17 The items were scored on a seven-point scale (1 (completely dependent)−7 (independent)) and the 13 items were added together to obtain an overall FIM motor score, ranging from 13 to 91.
Only those subjects who took part in more than one test occasion were included in the analyses. Furthermore, subjects who were community walkers (persons who walk indoors and outdoors possibly with aid and use a wheelchair only for long distances outdoors) at the last test occasion were removed from the database to prevent a positive selection.
To determine whether pain in the upper extremities increased or decreased during and after rehabilitation, the multilevel modeling program MlwiN18, 19 was used. In the longitudinal data set of this study, the hierarchy in the data is the repeated measurement ‘test occasion (t1–t4)’ (level 1), which is grouped within the individual participants (level 2), who are grouped in the rehabilitation centers (level 3). Overall pain in the upper extremity (ranging from 0 to 90) and shoulder pain (from 0 to 30) were the outcome variables of this multilevel regression analysis. Since pain was not normally distributed, this count variable was analyzed with a Poisson model. Time was modeled with three categorical dummy variables, with t1 as the reference to t2, t3 and t4, for example, the regression coefficient of t1–t4 indicated the difference in pain score between t1 and t4. A priori, time was also modeled with t3 as the reference to t1, t2 and t4, to examine when significant changes over the time occurred.
To investigate changes in upper extremity pain over time, only the time dummies were included in the basic model.
To investigate the effect of lesion characteristics, lesion level (paraplegia (PP)=1; TP=0) and completeness (incomplete=0; complete=1) were added to the basic model and a backward regression technique was used (model 2). Personal characteristics (age, gender, BMI) were added to the final model 2 to investigate their effect on the relation between pain complaints and lesion level or completeness. Variables that changed the regression coefficients of lesion level or completeness by at least 10% were identified as confounders and were corrected for in the final analysis. Interaction terms between lesion level and time were also added to check for possible effect modifications (P<0.05). To investigate the effect of muscle strength and motor FIM on pain, these variables were added separately to model 2. These parameters were not put together in the same model since they could have an effect on each other.
To find out which parameters were the most important predictors for pain, a prediction model was set up with upper extremity pain or shoulder pain at t4 as the outcome variable. Lesion characteristics, personal characteristics, muscle strength and functional outcome at t1 were used in separate analyses to predict the pain at t4. Pain at t1 was a variable that was always added first to the model to account for pain complaints at t4. First, the independent variables were included separately, and if they showed a P-value below 0.1 the variables were added to the Poisson model. Second, a backward elimination technique was used until only significant determinants remained (P<0.05).
A total of 169 subjects participated in this study. The t1 measurement was performed by 169 subjects. At t2–t4, the number of participants was 133, 161 and 116, respectively (Table 1).
The neurological level of the (incomplete) injuries ranged from C2 to S5 (Figure 1). Of the 169 subjects, 20 subjects eventually used a power wheelchair next to their manual wheelchair, whereas seven subjects used only a power wheelchair.
The mean number of days (SD) between t1 and t3 was 230 (136) for all subjects, 179 (90) days for those with PP and 309 (157) days for those with TP.
For the parameters muscle strength and motor FIM, the number of subjects who took part in the measurements was smaller and varied over time and over tests. The FIM was scored for almost all subjects while about 20 subjects did not perform the MMTs. The mean values (SD) of the manual muscle score for the time intervals t1–t4 were, respectively, 49.4 (15.1), 50.8 (14.1), 52.9 (12.6) and 55.1 (10.4), and the mean values (SD) for the FIM motor score were 39.0 (19.0), 51.0 (22.5), 61.0 (21.8) and 63.4 (21.2).
Musculoskeletal pain was reported most frequently for the left and right shoulder (Table 2). In addition, subjects with TP reported more complaints in the hand, wrist and elbow when compared to subjects with PP. Pain in all joints was experienced as mild to moderate and occurred three or more times a week. The seriousness and the frequency of the shoulder pain complaints seemed to decrease over time.
Course of upper extremity musculoskeletal pain over time and the relationship with lesion level, muscle strength and functional outcome
The basic model, to describe the course of upper extremity musculoskeletal pain, showed a significant reduction in upper extremity complaints (P<0.001) between t2 and t3 of 30% (Figure 2). There were no significant changes between t1 and t2 or t3 and t4.
For subjects with TP, the risk of upper extremity complaints was a factor 2.8 higher than for subjects with PP (P<0.001) (Figure 2). The interaction terms between time and lesion level showed that subjects with TP showed a stronger decrease in upper extremity musculoskeletal pain than subjects with PP over time intervals t1–t3 and t1–t4.
None of the personal characteristics were found to be a confounder for the relationship between pain complaints and lesion level over time.
When the parameter ‘functional outcome’ was added to the model including the time dummies and lesion level, the FIM score was a significant explanatory variable for upper extremity musculoskeletal pain. A 10-point increase of the FIM motor score between subjects and within subjects over a period of time is associated with an 11% decrease in upper extremity pain (P<0.001).
Muscle strength was not found to be an explanatory variable of upper extremity musculoskeletal pain.
The basic model, to describe the course of shoulder pain, showed that there was a significant increase in total shoulder pain for the time between t1 and t2 (P=0.018) and a significant decrease between t2 and t3 (P<0.001).
Lesion level had a significant effect on shoulder complaints (P<0.001) and the personal characteristics had no confounding effect. The risk of shoulder complaints was a factor 2.2 higher for subjects with TP than for subjects with PP. In this model, the increase in shoulder pain between t1 and t2 was not significant anymore.
The separate analyses of muscle strength and functional outcome showed that both the MMT score (P<0.001) and FIM motor score (P<0.001) were explanatory variables of shoulder pain complaints. A 10-point increase of the FIM motor score led to 14% less shoulder pain and a 10-point increase of the MMT score led to 12% less shoulder pain (Figure 3).
The interaction terms between time and lesion showed again that subjects with TP showed a stronger decrease in shoulder pain than subjects with PP over the time intervals t1–t3 and t1–t4.
When the significant univariate variables were combined in a model together with upper extremity musculoskeletal pain at t1, the BMI and the FIM motor score at t1 were significant (Table 3) predictors for upper extremity pain at t4. A 10-point higher FIM score at t1 was associated with a 10% increased risk on developing upper extremity musculoskeletal pain at t4 (P<0.001).
For shoulder pain, age, BMI, completeness of the lesion and FIM motor score at t1 were significant predictors when corrected for shoulder pain at t1. Except for the completeness of the lesion (78%), the effect on pain was small (<10%). Older persons with a higher BMI, a higher FIM motor score and an incomplete lesion were at a higher risk for developing shoulder pain.
Pain is defined as an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage.20 Not only is pain related to the physical state, but also to the psychological state of the persons. Since pain is a subjective score, and not a physical outcome measurement, it is a difficult variable to work with.
The musculoskeletal pain survey we used in this study was not validated or used in previous studies. As in several other studies. the survey was solely used to ask whether subjects experienced pain. Next to musculoskeletal pain, in a separate section subjects were asked for neurogenic pain at or under the lesion (tight band feeling, phantom pain and dull pain). In this study, it was tried to distinguish musculoskeletal pain from neurogenic pain. It is not always possible to distinguish clearly between these two types of pain and therefore part of the scored musculoskeletal pain could be related to neurogenic pain.
In a large-scale research like the current project, it is impossible to perform physical and technical (MRI) exams at all test occasions. However, for a better analysis of the problem, these exams might be necessary. Therefore, further research would benefit from surveys combined with physical and technical exams.
It has since long been acknowledged that the shoulder joint is especially at risk for overuse injuries due to its complex functional anatomy and its limited muscle mass. The arm is very mobile via the connection to the scapula and its joint structure (a small saucer within a large cup). This mobility goes at the expense of the stability of the joint21 and makes it especially vulnerable for the development of instability complaints.22 In the current study, we looked at the development of musculoskeletal pain during and after the rehabilitation process and found that pain complaints develop very quickly, which leads to the conclusion that pain was not simply due to overuse. Musculoskeletal pain could also have developed due to adaptation, in which case pain will probably develop in the long run due to overuse. In this study, the shoulder pain score significantly increased during the first 3 months of active rehabilitation and decreased after that period. Since subjects with SCI in rehabilitation had become dependent on the use of their upper extremities, which are often not well trained in early rehabilitation, training of new skills might have led to stressed muscles and pain. During rehabilitation, when subjects get more experience with arm exercise and had had muscle strength training, pain could diminish. This study showed that the upper extremity musculoskeletal pain score decreased most between t2 and t3. It might have been possible that increased independence, more frequent performance of ADL tasks in a less adjusted environment after rehabilitation and less specific muscle training would have led to an increase in pain after the rehabilitation. However, after discharge of in-patient rehabilitation, the musculoskeletal pain complaints did not increase but stabilized.
Lesion level was highly correlated to upper extremity and shoulder pain. This finding was not supported by Dalyan et al8 and Subbarao et al,23 but consistent with Sie et al2 and Turner et al.24 Owing to partial muscle paralysis of thoracohumeral muscles and shoulder muscle imbalance, individuals with high-level SCI are at higher risk of developing musculoskeletal pain.1, 25 It is suggested that muscle paralysis will influence the remaining upper extremity muscles, which have to stabilize the joints and have to produce the necessary external force to perform the task. The subjects with TP also need more external stabilization to maintain trunk balance to perform the task. On the condition that most subjects with a C6 or C7 lesion performed ADL independently, the extra muscle force needed for stabilization could have been responsible for the higher incidence of overload injuries for subjects with higher level lesions. It is possible that shoulder instability, which can arise after muscle paralysis, leads to shoulder complaints, but instability might contribute to the (earlier) onset of complaints due to overuse in subjects with high SCI lesions.
Musculoskeletal pain in SCI is experienced during daily life activities and especially weight-bearing tasks such as transfers and weight relief lifts.3, 23 For these tasks, balance is very important and the net moments and compression forces around the shoulder are high.26, 27 It is common that more than 25% of the body weight is transferred through the humerus to the thorax during the performance of these tasks. Reduction of the subacromial space and impingement of the supraspinatus muscle are possible explanations for the development of pain. However, in this study, all subjects with an acute SCI were included, including seven subjects with a high cervical lesion who had to use a power wheelchair for mobility. Although a small minority group in this study, overload injuries due to manual wheelchair use will not apply to these subjects.
How damage to the joints and the muscles develops is unfortunately unknown, which makes the evaluation of the load on the upper extremity during various ADL one of the utmost importance. More specifically, there is a need for a combined biomechanical epidemiological study, where the dose–response relationship between everyday mechanical load and pain can be studied.
We found that both muscle strength and functional outcome were inversely related to shoulder pain. Subjects with higher maximal muscle forces may perform the ADL tasks at a lower relative force compared to subjects with lower muscle strength. Therefore, these subjects had a lower risk for stress on the muscles. As previously described, higher forces and, as a consequence, higher compression forces in the joint (van Drongelen et al, submitted to Clin Biomech) increase the risk on impingement, joint damage and muscle damage. It has been shown13 that a specific exercise protocol of stretching and strengthening shoulder muscles can lead to a decrease in upper extremity pain. Curtis et al13 found an effect of a 6-month exercise protocol, where the intensity of the experienced pain was decreased. The effect was almost twice as high for subjects with PP than for subjects with TP, reflecting the interaction between functional status and lesion level.
MMT is a fairly crude way to measure muscle strength.28, 29, 30 However, to include a large number of subjects, the MMT data were used instead of the strength data measured with a hand-held dynamometer because the latter were only collected when the MMT score was 4 or 5. In our study, not only the strength of the muscles, which provide the score for the lesion level was measured but the strength of the shoulder internal and external rotators, and shoulder abductors as well. Lesion level will have an influence on the MMT score, but will not necessarily dictate the MMT score since there is variation in the paralysis due to variation in the segment innervation and variation in the completeness of the lesion. From the results, it might be concluded that higher muscle strength would lead to less pain and that exercise could reduce pain complaints.
The FIM motor score can be seen as an indicator of the number of ADL tasks subjects can perform independently. Neurological level of injury will have an effect on the FIM score but will not determine this score, because coordination, skill level, physical capacity and attitude will have an effect on the FIM score as well. Since the FIM motor score is positively correlated to the muscle score,31, 32 it was no surprise that both parameters were explanatory variables for shoulder pain. We expected that subjects with a higher FIM score developed fewer complaints because they have a better physical capacity. However, it was also possible that these subjects with a higher FIM score perform too many ADL and develop complaints as a consequence of overuse, while, on the other hand, subjects with a low FIM score perform fewer tasks and are therefore less susceptible to overuse pain complaints.
In this study, the possibility of having musculoskeletal pain 1 year after the rehabilitation was found to be much higher when pain was already present at an earlier time (t1). Silfverskiold10 reported that 33% of subjects with TP who had pain after 6 months still had shoulder pain after 18 months. Therefore, early onset of shoulder pain within 6 months has a high predictive value for pain after 18 months.
Further, BMI, FIM motor score and completeness of the lesion were consistent predictors of musculoskeletal pain in the upper extremity and shoulder. It is not surprising that BMI was found to be a significant variable in the prognostic model, since BMI is obviously related to the amount of physical strain experienced. Heavier persons, due to more body fat or more muscle mass, have a higher mass to transfer and experience a higher drag force during wheelchair propulsion.
It is difficult to relate a higher FIM motor score at the beginning of the rehabilitation to more upper extremity musculoskeletal pain after the rehabilitation, but it is possible that due to their good functionality these persons started performing all sorts of tasks too early while they are generally not aware of the increased risk for upper extremity complaints. They probably have enough strength but they have no experience and are not trained for specific arm function.
The same might be true for the predictor variable completeness of the lesion for shoulder pain. Persons with a complete lesion may perform fewer tasks and have a lower risk on developing pain, while persons with an incomplete lesion are less needy and use less assistive devices with the risk on overload.
The occurrence of upper extremity musculoskeletal pain during in-patient rehabilitation decreased over time. In the studied SCI population using wheelchairs as their primary means of mobility, the reduction in pain complaints was 30% between t2 and t3. There was a significant relationship between upper extremity and shoulder pain and lesion level. Subjects with TP were at a higher risk for pain than subjects with PP.
Muscle strength and functional outcome were identifiers for shoulder pain. Higher scores on these tests resulted in 10–15% fewer shoulder pain complaints.
Early onset of upper extremity pain seemed to be the most important predictor of pain at a later time. Thus, in the beginning of the in-patient rehabilitation, one should be very careful to prevent overload (by performing heavy ADL like transfers). The rehabilitation should focus on a balanced training of the upper extremity to make up for the arrears in strength of the upper extremity. Further, overweight should be prevented and one should strive for optimal wheelchair qualities.
Curtis KA, Drysdale GA, Lanza RD, Kolber M, Vitolo RS, West R . Shoulder pain in wheelchair users with tetraplegia and paraplegia. Arch Phys Med Rehabil 1999; 80: 453–457.
Sie IH, Waters RL, Adkins RH, Gellman H . Upper extremity pain in the postrehabilitation spinal cord injured patient. Arch Phys Med Rehabil 1992; 73: 44–48.
Pentland WE, Twomey LT . Upper limb function in persons with long term paraplegia and implications for independence: Part I. Paraplegia 1994; 32: 211–218.
Lal S . Premature degenerative shoulder changes in spinal cord injury patients. Spinal Cord 1998; 36: 186–189.
Boninger ML, Towers JD, Cooper RA, Dicianno BE, Munin MC . Shoulder imaging abnormalities in individuals with paraplegia. J Rehabil Res Dev 2001; 38: 401–408.
Boninger ML, Souza AL, Cooper RA, Fitzgerald SG, Koontz AM, Fay BT . Propulsion patterns and pushrim biomechanics in manual wheelchair propulsion. Arch Phys Med Rehabil 2002; 83: 718–723.
Samuelsson KA, Tropp H, Gerdle B . Shoulder pain and its consequences in paraplegic spinal cord-injured, wheelchair users. Spinal Cord 2004; 42: 41–46.
Dalyan M, Cardenas DD, Gerard B . Upper extremity pain after spinal cord injury. Spinal Cord 1999; 37: 191–195.
Hara Y . Dorsal wrist joint pain in tetraplegic patients during and after rehabilitation. J Rehabil Med 2003; 35: 57–61.
Silfverskiold J, Waters RL . Shoulder pain and functional disability in spinal cord injury patients. Clin Orthop 1991; 272: 141–145.
Siddall PJ, Taylor DA, McClelland JM, Rutkowski SB, Cousins MJ . Pain report and the relationship of pain to physical factors in the first 6 months following spinal cord injury. Pain 1999; 81: 187–197.
Fullerton HD, Borckardt JJ, Alfano AP . Shoulder pain: a comparison of wheelchair athletes and nonathletic wheelchair users. Med Sci Sports Exerc 2003; 35: 1958–1961.
Curtis KA et al. Effect of a standard exercise protocol on shoulder pain in long-term wheelchair users. Spinal Cord 1999; 37: 421–429.
Marino RJ et al. International Standards for Neurological Classification of Spinal Cord Injury. American Spinal Injury Association: Chicago, IL 2000.
Kendall FP, Kendall Mc Creary E . Spieren. 3rd edn Bohn Stafleu Van Loghum: Houten 2000.
Hamilton BB, Granger CV, Sherwin FS, Zeilizny M, Tashman JS . Uniform national data system for medical rehabilitation. In: Fuhrer MJ (ed). Rehabilitation Outcomes: Analysis and Measurement. Paul H Brookes Publication: Baltimore, MD 1987 pp 137–147.
Post MWM, Dallmeijer AJ, Angenot ELD, Van Asbeck FWA, Van der Woude LHV . Duration and functional outcome of spinal cord injury rehabilitation in the Netherlands. J Rehabil Res Dev 2005 in press.
Rasbash J et al. A User's Guide to MLwiN. Version 2.1d. University of London: London, UK 2000.
Twisk JWR . Applied Longitudinal Data Analysis for Epidemiology, A Practical Guide. Cambridge University Press: Amsterdam 2003.
IASP. Classification of Chronic Pain. 2nd edn. IASP Press: Seattle 1994.
Codman EA . The Shoulder. Thomas Todd: Boston 1934.
Myers JB, Lephart SM . Sensorimotor deficits contributing to glenohumeral instability. Clin Orthop Relat Res 2002; 400: 98–104.
Subbarao JV, Klopfstein J, Turpin R . Prevalence and impact of wrist and shoulder pain in patients with spinal cord injury. J Spinal Cord Med 1995; 18: 9–13.
Turner JA, Cardenas DD, Warms CA, McClellan CB . Chronic pain associated with spinal cord injuries: a community survey. Arch Phys Med Rehabil 2001; 82: 501–509.
Powers CM, Newsam CJ, Gronley JK, Fontaine CA, Perry J . Isometric shoulder torque in subjects with spinal cord injury. Arch Phys Med Rehabil 1994; 75: 761–765.
Van Drongelen S, Van der Woude LH, Janssen TW, Angenot EL, Chadwick EK, Veeger DH . Mechanical load on the upper extremity during wheelchair activities. Arch Phys Med Rehabil 2005; 86: 1214–1220.
Van Drongelen S, Van der Woude LH, Janssen TW, Angenot EL, Chadwick EK, Veeger DH . Glenohumeral contact forces and muscle forces evaluated in wheelchair-related activities of daily living in able-bodied subjects versus subjects with paraplegia and tetraplegia. Arch Phys Med Rehabil 2005; 86: 1434–1440.
Herbison GJ, Isaac Z, Cohen ME, Ditunno Jr JF . Strength post-spinal cord injury: myometer vs manual muscle test. Spinal Cord 1996; 34: 543–548.
Schwartz S, Cohen ME, Herbison GJ, Shah A . Relationship between two measures of upper extremity strength: manual muscle test compared to hand-held myometry. Arch Phys Med Rehabil 1992; 73: 1063–1068.
Noreau L, Vachon J . Comparison of three methods to assess muscular strength in individuals with spinal cord injury. Spinal Cord 1998; 36: 716–723.
Fujiwara T, Hara Y, Akaboshi K, Chino N . Relationship between shoulder muscle strength and functional independence measure (FIM) score among C6 tetraplegics. Spinal Cord 1999; 37: 58–61.
Beninato M, O’Kane KS, Sullivan PE . Relationship between motor FIM and muscle strength in lower cervical-level spinal cord injuries. Spinal Cord 2004; 42: 533–540.
The work of the research assistants (Annelieke Niezen, Hennie Rijken, Ferry Woldring, Karin Postma, Jos Bloemen, Linda Valent, Sacha van Langeveld and Marijke Schuitemaker) and the rehabilitation physicians is greatly acknowledged. We also thank the eight rehabilitation centers – Rehabilitation Center Amsterdam, De Hoogstraat (Utrecht), Het Roessingh (Enschede), Rijndam Revalidatiecentrum (Rotterdam), Hoensbroeck Revalidatiecentrum (Hoensbroek), Sint Maartenskliniek (Nijmegen), Beatrixoord (Haren) and Heliomare (Wijk aan Zee) – and the subjects for their participation. This study is supported by the Netherlands Organization for Health Research and Development (ZonMW), under Grants 14350003 and 14350010, and is part of the research program ‘Physical strain, work capacity and mechanisms of restoration of mobility in the rehabilitation of individuals with SCI’.
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Cite this article
van Drongelen, S., de Groot, S., Veeger, H. et al. Upper extremity musculoskeletal pain during and after rehabilitation in wheelchair-using persons with a spinal cord injury. Spinal Cord 44, 152–159 (2006). https://doi.org/10.1038/sj.sc.3101826
- upper extremity
- spinal cord injury
- prospective study
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