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(Stroke. 1999;30:963-968.)
© 1999 American Heart Association, Inc.
Original Contributions |
From the Bioengineering Unit, University of Strathclyde, Glasgow, Scotland.
Correspondence to Dr Malcolm H. Granat, PhD, Bioengineering Unit, University of Strathclyde, 106 Rottenrow, Glasgow G4 0NW, Scotland, UK. E-mail m.h.granat{at}strath.ac.uk
| Abstract |
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MethodsA prospective, randomized controlled study was used to determine the efficacy of electrical stimulation in preventing shoulder subluxation in patients after cerebrovascular accidents. Forty patients were selected and randomly assigned to a control or treatment group. They had their first assessment within 48 hours of their stroke, and those in the treatment group were immediately put on a regimen of electrical stimulation for 4 weeks. All patients were assessed at 4 weeks after stroke and then again at 12 weeks after stroke. Assessments were made of shoulder subluxation, pain, and motor control.
ResultsThe treatment group had significantly less subluxation and pain after the treatment period, but at the end of the follow-up period there were no significant differences between the 2 groups.
ConclusionsElectrical stimulation can prevent shoulder subluxation, but this effect was not maintained after the withdrawal of treatment.
Key Words: electric stimulation randomized controlled trials rehabilitation shoulder stroke
| Introduction |
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Traditionally, slings have been applied to prevent or reduce shoulder subluxation after stroke. The most effective slings have the drawback of holding the limb in a poor position that is likely to cause soft tissue contracture and have a disadvantageous effect on symmetry, balance, and body image.6 7 8 9
In view of the shortcomings associated with the use of slings, alternative approaches to deal with this problem have been sought. Two studies10 11 have investigated the application of electrical stimulation to the supraspinatus and posterior deltoid muscles.
Faghri et al11 recruited 26 patients on average 17 days after stroke and allocated them randomly to experimental and control groups. Subjects in the experimental group demonstrated a mean subluxation of 6 mm on initial x-ray, and the control group showed a mean subluxation of 4 mm. The experimental group received a program of electrical stimulation for 6 weeks, followed by a nontreatment period of 6 weeks. Baker and Parker10 used a similar method in their study of 63 subjects, with the main difference being that all subjects had a chronic subluxation of at least 5 mm compared with the unaffected arm. Both studies demonstrated a beneficial effect on subluxation over the treatment period, with that Faghri et al11 showing improvement in other parameters, such as pain, range of motion, and arm function. However, both studies showed deterioration following withdrawal of electrical stimulation, although not back to pretreatment levels.
These studies recruited subjects with preexisting shoulder subluxation, and the treatment did not resolve this problem. Patient outcome may be enhanced if shoulder subluxation can be prevented, thus potentially avoiding the associated complications.
The purpose of this study was to evaluate the effectiveness of using electrical stimulation immediately after stroke to prevent glenohumeral subluxation and prevent possible associated problems of shoulder pain and impaired motor function.
| Subjects and Methods |
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2 on the Manual
Muscle Test12 ; (3) adequate communication ability to cope
with a verbal rating score for pain; (4) no cardiac pacemaker or metal
in situ; (5) no women of childbearing age (because of x-rays); and
(6) recruitment and all initial measurements must have been completed
and treatment commenced within 48 hours of admission to the Acute
Stroke Unit. Forty subjects were recruited and randomized into
treatment and control groups before initial assessments.
A total of 40 subjects were recruited, and all completed the study
(Table 1
). Eighteen men and 22 women were
recruited; 9 had a right-sided hemiparesis and 31 a left-sided
hemiparesis. This imbalance was a result of the recruitment criterion
requiring sufficient communication ability to cope with a verbal rating
score for pain, which excluded many subjects with right-sided
hemiparesis. The age range was from 45 to 84 years. The mean age for
the treatment group was 71 years and that for the control group 73
years. Two subjects were unable to complete all measurements because
they were unable to travel to the radiography
department for final x-rays; all the other measures, however, were
completed on these subjects. The classification of strokes, made
according to the Oxford classification system,12 is shown
in Table 1
.
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The overall study design is given in Table 2
. All assessments were made, before any
therapy was given, by an assessor blinded to the protocol. Initial
assessments were carried out within 48 hours of admission. Subjects in
the treatment group received a program of electrical stimulation over
the next 4 weeks (treatment period) in addition to conventional
physiotherapy and occupational therapy. Subjects in the control group
received their conventional physiotherapy and occupational therapy only
during this period (treatment period). A second set of measurements
were made at the end of this 4-week period. Both treatment and control
groups continued with conventional physiotherapy and occupational
therapy for the next 8 weeks (follow-up period). Final measurements
were made 3 months after stroke. Over the follow-up period, no
electrical stimulation was applied. The period from first to final
assessment is referred to as the "total study period."
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Subjects received electrical stimulation 4 times each day, with a
minimum of 2 hours between sessions. The length of each session was
increased gradually, starting at 30 minutes in week 1, 45 minutes in
weeks 2 and 3, and 60 minutes in week 4. Two electrodes were positioned
on the supraspinous fossa and the posterior aspect of the upper arm to
stimulate the supraspinatus and posterior deltoid muscles. This
position was checked in a pilot study before beginning the project
to ensure that the movement obtained produced good correction of
subluxation (Figure 1
). The stimulation
consisted of asymmetrical biphasic pulses with a pulse width of 300
µs applied at a frequency of 30 Hz. The duty cycle was 15 seconds on,
which incorporated a ramp up time of 3 seconds and a ramp down time of
3 seconds and 15 seconds off.
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Outcome Measures
Measurements were made of shoulder subluxation (radiological),
pain, arm girth and motor control.
Shoulder subluxation was assessed by a single AP radiograph taken of
the affected shoulder. Two methods were used for evaluating the X-rays.
One method was a categorization of subluxation 1 to 414
(Figure 2
). In the second method, the
displacement was quantified. This involved using a line bisecting the
glenoid fossa, then measuring the distance from the line to the most
superior aspect of the head of the humerus (Figure 3
).
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Pain was assessed by measuring the pain-free range of passive lateral rotation (PLRL) using a clinical goniometer, where a loss of range indicated an increase in pain.15 Subjects were also asked to grade the pain they perceived on a verbal rating scale (0=none, 1=slight, 2=moderate, 3=severe, and 4=very severe).14
Motor function was assessed by the upper arm section of the Motor Assessment Scale.16 This tests the subjects' ability to perform motor tasks of increasing difficulty on a scale of 0 to 6 (0=poor function, 6=good function).
Measurement of upper arm girth was made to monitor changes in muscle bulk. This was measured with a tape measure wrapped around the upper arm from the axillary fold. The distance from the acromial process to the tape was recorded to aid accuracy of repeat measurement.
The main hypotheses of this study were that (1) electrical stimulation applied immediately after stroke could prevent the development of shoulder subluxation and (2) a program of electrical stimulation would have a beneficial effect in preventing pain, motor impairment, and muscle atrophy.
To test these hypotheses, the change for all outcome measures over both the treatment period and the control period for each subject was calculated. The Mann-Whitney U test was used to test for significant differences of these changes between the control and treatment groups over the treatment period, the follow-up period, and the total study period.
| Results |
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The control group demonstrated greater subluxation than the treatment
group over the treatment period, with a mean subluxation grade score of
0.80 compared with 0.30 in the treatment group (P=0.067;
Mann-Whitney U test) (Figure 4
). The results of the humeral
displacement measure followed the same pattern as the subluxation
grading, with a mean change of 0.63 cm in the control group compared
with 0.22 cm in the treatment group (P=0.06; Mann-Whitney
U test) At the end of the follow-up period, subluxation
grade score for both groups was the same (0.63). The change in
subluxation grading in the treatment group over the follow-up period
was significantly greater than that in the control group
(P=0.019; Mann-Whitney U test). The mean change
in the vertical displacement measure over the follow-up period for the
control group was -0.05 cm (indicating improvement) in the control
group and 0.3 cm (indicating further subluxation) in the treatment
group (P=0.22; Mann-Whitney U test).
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Over the total study period, there was no significant difference between the groups in either the subluxation grading or the humeral displacement measure, with the mean subluxation grade for both groups 0.63 at final assessment (P=0.955; Mann-Whitney U test). The mean change in the vertical displacement measure over the total study period was 0.62 cm in the control group and 0.52 cm in the treatment group (P=0.748; Mann-Whitney U test).
There was no difference in the changes in the motor scores between the
groups over any intervention period (Figure 5
).
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Both the treatment and control groups demonstrated a loss of
passive range of lateral rotation over the first intervention period,
but a greater reduction was seen in the control group
(P=0.172). The overall change over the total study period
showed no difference between the groups (P=0.881; Figure 6
).
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Both groups demonstrated an increase in pain as measured by the
verbal rating scale (Table 3
). No
significant difference was found between the groups over any period in
this pain measure.
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Both groups demonstrated a loss of arm girth over the treatment period
(Table 4
), with a trend toward greater
loss seen in the control group (P=0.071). Further loss of
girth was shown over the follow-up period, but there was no significant
difference between the groups. The change in the upper arm girth over
the study period showed no significant difference between the
groups.
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A correlation was found between the change in subluxation grading and the actual motor score at the end of the treatment and follow-up periods for the total study group (Spearman correlation coeffecients of 0.67 [P=0.00] and 0.69 [P=0.00], respectively), the control group (correlation coeffecients of 0.76 [P=0.00] and 0.67 [P=0.00], respectively), and the treatment group (correlation coeffecients of 0.27 [P=0.25] and 0.74 [P=0.00], respectively).
| Discussion |
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The explanation for this could be that in the control group, all the
subjects who subluxed did so in the initial period, and as motor status
improved (Figure 4
) some improvement in alignment was observed
over the follow-up period. In the treatment group, however, subluxation
that would have occurred over the initial treatment period was
prevented by electrical stimulation, but this potential to sublux was
realized after withdrawal of treatment.
The relationship between motor recovery, subluxation, and the effect of electrical stimulation is reinforced by correlation of motor scores and subluxation measures. When the groups were analyzed separately, a strong correlation was found between the motor scores (at the end of the treatment period) and the subluxation grading over the initial treatment period. This was not seen in the treatment group over this period, which supports the proposition that the electrical stimulation was having an effect.
Over the follow-up period the correlation became weaker in the control group but much stronger in the treatment group. The stimulation protocol in the current study differed from previous work, and treatment was applied for a shorter time (4 weeks compared with 6 weeks). More importantly, the current study recruited subjects much sooner than the previous work, ie, prior to the development of subluxation. Faghri et al11 demonstrated that shoulder subluxation could be reduced by the use of electrical stimulation. However, this study showed that it is possible to prevent or limit shoulder subluxation immediately after a stroke.
No difference was seen between the groups in motor recovery. It was not anticipated that the application of electrical stimulation would directly improve motor recovery, except as a secondary consequence of preventing subluxation and pain. The fact that no difference was seen between the groups in motor function demonstrates that the groups were well balanced for motor status and confirms that any differences found in the other parameters were not as a result of varying degrees of recovery between the groups.
No correlation was found between pain and subluxation in this study, which supports the assertions of previous authors.7 9 However, as subjects were followed-up only for a 3-month period after stroke, development of pain due to chronic stretching of soft tissues in the longer term cannot be precluded.
No subject who scored a grade of
2 on the Motor Assessment Scale
developed subluxation. This may provide useful information on which
patients are likely to benefit from treatment and when treatment can be
withdrawn without risk of subluxation.
Concerns that subjects would find the treatment uncomfortable or inconvenient were unfounded. All subjects reported that the sensation of the muscle contraction and resultant movement of the limb were encouraging. This was particularly true when sensory inattention was present.
The study size was relatively small; however, a treatment effect was demonstrated. This study did not consider measures of disability, concentrating instead on impairment measures. It would be of interest to investigate the functional benefit of the prevention of subluxation.
Because the beneficial effect seen over the treatment period was not
maintained after withdrawal of treatment, further studies are necessary
to investigate the use of electrical stimulation over a longer period.
The results of this study suggest that such a study should recruit
subjects scoring
2 on the Motor Assessment Scale and that attainment
of this score would be a good indication of when treatment could be
discontinued.
| Acknowledgments |
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Received September 29, 1998; revision received February 18, 1999; accepted February 18, 1999.
| References |
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