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Address for correspondence: Natasha A. Lannin, Lecturer, Rehabilitation Studies Unit, University of Sydney, PO Box 6,
Ryde NSW 1680, Australia, E-mail: nlannin@mail.usyd.edu.au
BRAIN IMPAIRMENT
VOLUME
237
Selection Criteria
We included English language studies of the effects
of upper limb rehabilitation that fulfilled the following criteria:
Methods
Search Strategy
Search strategies developed by the Cochrane
Injuries Group were used. The literature search
was limited to published studies, available in fulltext in English. The following electronic databases
were searched by one person on August 2 2008:
the Cochrane Central Register of Controlled
Trials (CENTRAL); The Cochrane Database of
Systematic Reviews (Issue 3, 2008), the Database
of Effectiveness Reviews (DARE), MEDLINE
(1956 to August 2008), EMBASE (1974 to
August 2008), CINAHL (1983 to August 2008),
the Physiotherapy Evidence Database (PEDro),
Occupational Therapy Systematic Evaluation of
Effectiveness database (OTseeker); and Google
Scholar. Reference lists of retrieved studies and
review articles were also hand searched to identify
additional studies. Unpublished, nonpeer-reviewed
sources such as theses were not included.
Keywords were mapped to MeSH/subject
headings and included: brain injury, craniocerebral trauma, head injury, hemiplegia, hemiparesis,
upper extremity, arm, rehabilitation, therapy, exercise therapy, physical therapy, physiotherapy and
occupational therapy (full search strategy available upon request). Selection of articles was based
on the title and abstract content.
238
Study designs. Studies which generated systematic reviews or randomised controlled trials
(RCTs) (i.e., Level Ia & Ib evidence of the
Oxford Centre for Evidence-based Medicine
levels of evidence (Phillips, Ball, Sackett,
Badenoch, Straus, & Haynes, 2000).
Interventions. Studies concerning any intervention aimed at improving motor function of a
hemiparetic/hemiplegic arm in adults after
TBI. The range of interventions includes exercise therapies such as physiotherapy, occupational therapy, neurodevelopmental therapy and
motor retraining strategies; sensorimotor strategies; biofeedback and/or electrical stimulation;
peripheral splinting and casting; imagery; and
surgery to improve upper limb function or correct deformity. Focal or generalised pharmacotherapy interventions (e.g. botulinum
toxin-A) were excluded.
Participants. Studies that explicitly involved
humans in which 50% or more of the sample
were adults who had experienced a TBI, or
studies where the data pertaining to adults who
had experienced a TBI were able to be separated from the remaining data.
Outcome measures. Outcomes which measure
changes in participants Impairments, Activity
Limitations and Participation Restrictions
(WHO, 2001).
Organisation of Evidence
Data extraction. Data extracted from eligible
studies included authors and date of study, study
Not stated
Not stated
(1970s
onwards)
Not stated
Unclear
72
19662004
1
26
19802005
2
Watson, 2001
Total number of
studies included
in the review
Objective of review
Review
Results
TABLE 1
Characteristics of Published Systematic Reviews (n = 3) Included in the Current Review
36
Range of years of
studies included
in review
1,180
239
240
Passive stretching 1
hour per day
Sham stimulation,
8 hours/day while
in coma for up to
14 days; sham
machine had no
discernable
difference from the
genuine stimulation
machine
Electrical
stimulation of the
median nerve of
the dominant hand
(intermittent pulse
at 40 hz, 1520
mA); 8 hours/day
while in coma for
up to 14 days
Meal preparation
tasks, completed as
part of a group
session, for 30
mins x 3 times
weekly for 6 weeks
(9 hours total)
Moseley
et al.,
2008
Peri
et al.,
2001
Neistadt,
1994
45 TBI (41 closed,
1 open), 3 anoxia;
Mean age 33.2 years
(SD 9.1);
Mean time post-injury
7.9 years (SD 6.6)
10 TBI (7 post-MVA, 2
falls, 1 struck by a
beam);
Mean age of 40 (range
19 66);
ES was started a mean
of 62 hours postinjury
(range 48 72 hours).
Participants
Diagnosis, age, length
of time post-injury
45
10
26
Total
n
JTHFT Subtests
Simulated page
turning and picking up
small object; Line
Bisection Test;
Parquetry Block Test,
RKE-R and WAIS-R
Measured at baseline
and after 6 weeks
Torque-controlled
passive elbow
extension; Maximum
seated forward reach;
TEMPA
Outcome Measures
Mean ROM
1 day post-cast removal: 11(95% CI 0 to 21)
4 weeks post-cast removal: 2(95% CI 13 to 17)
Maximum reach
Post-cast removal: 0cm (95% CI 18 to 47)
4 weeks post-cast removal: 11cm (95% CI 34 to 52)
TEMPA (hand function)
Post-cast removal: 1(95% CI 5 to 2)
4 weeks post-cast removal: 0(95% CI 7 to 6)
Note: * Change scores were used in the calculation of 95% confidence intervals around mean treatment difference.
Standard deviations were not reported in the original publication, precluding calculation of 95% confidence intervals around mean treatment difference.
ROM: range of elbow extension movement; TEMPA: Test valuant la Performance des Membres Suprieurs des Personnes ges; JTHFT: Jebsen-Taylor Hand Function Test; RKE-R:
Rabideau Kitence Evaluation Revised; WAIS-R: Weschler Adult Intelligence Scale Revised; GCS: Glasgow Coma Scale; GOS: Glasgow Outcome Scale; FIM/FAM: Functional
Independence Measure/Functional Assessment Measure
Parquetry block
puzzle assembly
group, for 30 mins
x 3 times weekly
for 6 weeks (9
hours total)
Control Intervention
Therapy
Intervention
Study
TABLE 2
Summary of Included Randomised Controlled Trials (n = 3): Participants, Interventions, Outcome Measures and Main Results
Y
Y
N
Y
Y
Y
Y
Y
Y
Y
Y
N
N
N
N
N
N
N
Y
Y
Y
Y
Y
N
N
Y
N
Marshall et al., 2007
van Dijk et al., 2005
Watson, 2001
Note: Explanation of score items: The QUOROM Statement checklist items are: (1) title identifies the report as a meta-analysis [or systematic review] of RCTs; (2) abstract uses a structured format;
(3) abstract objective states the clinical question explicitly; (4) abstract outlines the data sources; (5) abstract outlines the review methods; (6) abstract identifies the characteristics of the RCTs
included and excluded; qualitative and quantitative findings and subgroup analyses; (6) abstract conclusion includes the main results; (7) introduction states the explicit clinical problem,
biological rationale for the intervention, and rationale for review; (8) methods outlines the information sources, in detail and any restrictions; (9) methods states the inclusion and exclusion
criteria; (10) methods outlines the criteria and process used for assessment of study validity; (11) methods outlines the process or processes used for data abstraction; (12) methods outlines
how study characteristics were assessed; (13) methods outlines the procedure for quantitative data synthesis; (14) results provide a meta-analysis profile summarising trial flow; (15)
results present descriptive data for each trial; (16) results present quantitative data synthesis where appropriate; (17) Discussion summarises key findings; discuss clinical inferences
based on internal and external validity; interpret the results in light of the totality of available evidence; describe potential biases in the review process; and suggest a future research
agenda. N = absent, or not clearly present; Y= present.
N
Y
N
N
N
N
Y
Y
N
N
N
N
Y
Y
N
Y
Y
N
Y
Y
Y
Y
Y
N
12
5
4
3
2
1
Review
TABLE 3
Assessment of Included Reviews using the QUOROM Statement Checklist
13
14
15
16
17
241
TABLE 4
Methodological Quality of Included Randomised Controlled Trials (n = 3)
Study
Moseley et al., 2008
Neistadt, 1994
Peri et al., 2001
1#
Y#
N#
Y#
Y
Y
Y
Y
N
N
Y
Y
Y
N
N
Y
Y
Y
Y
Y
N
Y
10
11
TOTAL
Y
N
N
Y
Y
Y
Y
Y
Y
8
5
7
Note: Explanation of score items: The PEDro scale criteria are: (1) specification of eligibility criteria (# Not included in the
PEDro score); (2) random allocation; (3) concealed allocation; (4) prognostic similarity at baseline; (5) subject blinding; (6) therapist blinding; (7) assessor blinding; (8) > 85% follow-up of at least one key outcome; (9) intention-to-treat
analysis; (10) between group statistical comparison for at least one key outcome; and (11) point estimates of variability provided for at least one key outcome. Only items 211 are summed to provide total score. N = absent or not
clearly present, Y = present.
242
Contraindications
Exclusion criteria reported in the studies were
considered potential clinical contraindications to
the upper limb rehabilitation interventions. Only
one study (Peri et al., 2001) reported exclusion
criteria relating to the study intervention (electrical stimulation). These included: participants with
implanted pacemakers or defibrillators, spinal
cord injury, or who were pregnant, to avoid possible negative interactions with the electrical stimulation. Careful review of the inclusion criteria of
the casting trial (Moseley et al., 2008, p. 407) suggests that orthopaedic or other injuries which
would preclude serial casting of the elbow, and
active heterotopic bone growth were contraindications to upper limb serial casting.
Therapy Protocol
Trials were not homogenous, therefore therapy
protocols will be discussed separately. The casting
protocol described by Moseley and colleagues
(2008) applied long arm synthetic casts for two
weeks to the elbow in a stretched position of
Discussion
This systematic literature review of upper limb
rehabilitation for adults after brain injury found
little evidence to inform clinical decision-making.
Only three randomised controlled trials were
located and appraised. While a greater number of
clinical trials were located which included participants who had experienced a TBI, the proportion of
participants was commonly less than 50% (it was
not possible to discern the TBI-only data from the
results of located studies which was disappointing).
Included RCTs all studied different interventions. Heterogeneity of the included studies,
including study design, time postinjury and outcomes, prevented pooling of the data across the
trials. Ultimately, included trials reported mixed
findings on upper limb outcomes, with clinically
significant findings being reported for range of
movement following upper limb casting (Moseley
et al., 2008) and statistically significant findings
reported for fine motor coordination after functional training in meal preparation tasks (Neistadt,
1994). Remaining outcomes were not significant.
The use of less than optimal methods for measuring these outcomes, however, may have contributed to these results. Since function and
quality of life are what matter to our patients, outcome measures at the level of activities are understandably important. However, generic measures
of basic activities of daily living (e.g., FIM + FAM
as used in the trial by Peri et al., 2001) are likely
to suffer from both ceiling and floor effects,
decreasing the potential to show a difference
between groups in outcome and significantly
reducing the power of the study. Consequently,
researchers must consider recovery beyond ADL
where the clinical rationale for treatment is to
improve functional movement and, ultimately,
participation. Measures that assess a higher level
of activity may be more sensitive to differences
between groups.
Three previous systematic reviews were
appraised, which included studies of the effectiveness of upper limb rehabilitation after brain injury
(Marshall et al., 2007; van Dijk et al., 2005;
Watson, 2001). The review by Watson (2001)
reported on research studies (including n-of-1
designs) that evaluated the outcomes of physiotherapy for adults with TBI. Each study was categorised under one of nine types of intervention,
three addressing functional upper limb rehabilitation (Underlying approaches to therapy,
Functional skills training and Casting, splinting
and associated therapies). The review did not
report the number of studies located or reviewed.
Watson (2001) did not include the trial by Neistadt
(1994) that had been published at the time.
Although not stated, it is possible that the trial by
Neistadt (1994) was excluded because the upper
limb motor training intervention was described as
an occupational therapy, and not a physiotherapy,
intervention. No explanation for the reasons for
non-inclusion of the Neistadt trial, in addition to
the low QUOROM rating, contribute to the low
methodological quality of Watsons (2001) review.
A second systematic review of 26 randomised
controlled trials evaluated the effect of augmented
feedback on motor function, and was published by
van Dijk and colleagues (2005). Unlike the
reviews by Watson (2001) and Marshall and colleagues (2007), van Dijk and colleagues included
a range of rehabilitation populations and was not
limited to TBI. The varied diagnoses and populations included by van Dijk and colleagues (2005)
resulted in one study only in common with the
present review the RCT by Peri and colleagues
243
244
entry into the database. There are, however, limitations to this review. We only included studies
published in English and thus acknowledge a language bias, and review conclusions have been
based on only three RCTs. Having only three
RCTs included in this review, and with those trials
having mixed findings on functional outcomes
(less than 50% of studies reporting significant
findings), it is not possible to draw conclusions
about the effectiveness of upper limb rehabilitation for adults after traumatic brain injury.
The scarcity of high-level research evidence is
neither unexpected nor surprising. RCTs that evaluate upper limb rehabilitation with the TBI population pose unique challenges. Trials need to cope
with variability in functional levels of people
with TBI, and accommodate different levels of
outcome (for example, impairments such as range
of movement versus hand function). The complex
range of pathologies, variable levels of motor
function, and typically small populations compared to stroke, make the conduct of RCTs particularly challenging (Maas, Marmarou, Murray,
Teasdale, & Steyerbergm, 2007). Operationalisation and description of interventions is also difficult because each participants rehabilitation
frequently needs to be individualised. Nonetheless, adequate description is important, so that
replication is possible in future trials.
Despite difficulties in conducting RCTs with a
TBI population, there remains a need for highlevel evidence about the effectiveness of upper
limb rehabilitation after TBI. Research is needed
to determine with confidence not only whether
specific interventions are helpful but also what
intensity is required to effect change, and how feasible it is to deliver interventions to samples of
people with TBI. Similar questions have been
raised, and are being addressed in stroke rehabilitation. For example, systematic reviews involving
people with stroke indicate that the following
interventions may improve motor recovery: use of
mental practice or imagery (Braun et al., 2006),
electrical stimulation alone, or combined with
biofeedback (de Kroon, Ijzerman, Chae,
Lankhorst, & Zilvold, 2005); restraining the noninvolved arm (Hakkennes & Keating, 2005); and
engaging people in repetitive, novel tasks assisted
by robotics (Barreca, Wolf, Fasoli & Bohannon,
2003; de Kroon et al., 2005; Prange, Jannick,
Groothuis-Oudshoom, Hermens, & Ijzerman,
2006). Researchers and clinicians can use this
existing research to guide their selection of upper
limb treatment techniques in future TBI research
and practice. Ultimately, however, research still
needs to be conducted with a TBI population.
Reviewers Conclusions
There is still insufficient evidence to either support or refute the effectiveness of any one specific
rehabilitation intervention to improve upper limb
motor function in adults following TBI. There is a
need for studies which investigate the effect of
motor training interventions on upper limb outcomes in a TBI-only population. Adequately powered RCTs are needed such as that reported by
Moseley and colleagues (2008) but that also
use consistent therapy protocols and outcome
measures. Such trials should include a no-therapy
condition or group (i.e., a true control group) so
that interventions not involving motor training do
not confound results. Future trials also need an
adequate sample size to avoid type-II errors, that
is, where small numbers do not detect a positive
treatment effect when this exists (Domholdt,
2000). In the present review, caution is needed
when interpreting results that were not statistically
significant, which was the case for some outcomes
in each of the three trials (see Table 1). These nonsignificant results may be due to a lack of adequate power rather than lack of significant effect.
It is difficult to determine if this was the case in
the included trials as power calculations were not
reported for two of the trials (Neistadt, 1994; Peri
et al., 2001). In the casting trial (Moseley et al.,
2008), the outcome of interest (upper limb function) was a secondary outcome, and so again, findings must be interpreted with caution. Finally,
while there is a need for further research, it is
important to make the distinction between a lack
of evidence, versus evidence of lack of effect.
There is still a lack of robust evidence due to the
limited number of studies to guide clinicians with
regard to upper limb motor rehabilitation for
adults with TBI.
References
Barreca, S., Wolf, S., Fasoli, S., & Bohannon, R. (2003).
Treatment interventions for the paretic upper limb
of stroke survivors: A critical review. Neurorehabilitation and Neural Repair, 17(4), 220226.
Bateman, A., Culpan, J. & Pickering, A.D. (2001) The
effect of aerobic training on rehabilitation outcomes
after recent severe brain injury: A randomized controlled evaluation. Archives of Physical Medicine
and Rehabilitation, 82, 174182.
Braun, S.M., Beurskens, A.J., Borm, P.J., Schack, T., &
Wade, D.T. (2006). The effects of mental practice in
stroke rehabilitation: A systematic review. Archives
of Physical Medicine and Rehabilitation, 87(6),
842852.
de Kroon, J., Ijzerman, M., Chae, J., Lankhorst, G., &
Zilvold, G. (2005). Relation between stimulation
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