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(Stroke. 2001;32:973.)
© 2001 American Heart Association, Inc.
Original Contributions |
From the Department of Rehabilitation Medicine, Center for Rehabilitation Medicine, Emory University School of Medicine, Atlanta, Ga.
| Abstract |
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MethodsTwenty-six poststroke patients were followed up prospectively in a rehabilitation day-treatment program. The mEFAP, Berg Balance Test (BBT), and 7-item mobility subsection of the Functional Independence Measure + Functional Assessment Measure (FAMm) were completed at admission and discharge.
ResultsmEFAP interrater reliability (intraclass coefficient [ICC] 0.999) and test-retest reliability (ICC 0.998) were high. The BBT demonstrated high interrater (ICC 0.992) but poor test-retest (ICC 0.605) reliability. Initial and final scores comparing the mEFAP with the BBT (r=-0.735, r=-0.703) and the mEFAP with the FAMm (r=0.685, r=-0.775) were strongly correlated. Improvement on the mEFAP correlated with improved BBT performance (r=-0.524). There was no correlation between overall change observed on the FAMm and change on the mEFAP (r=-0.145). Total mEFAP and all mEFAP subtask scores improved over time (P<0.0001).
ConclusionsThe mEFAP is a reliable gait-assessment tool for patients with stroke and is sensitive to change in ambulation speed.
Key Words: gait movement disorders rehabilitation stroke outcome
| Introduction |
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The Functional Ambulation Profile (FAP) is a timed walking test that was specifically designed to track the progress of patients with neurological impairments throughout their participation in a comprehensive outpatient rehabilitation program.9 In its most recent form, this test (the Emory Functional Ambulation Profile, or EFAP) requires an individual to negotiate 5 common environmental challenges, and it incorporates the use of orthotics or assistive devices (AD).5 9 Wolf et al5 demonstrated that the EFAP had high interrater reliability, construct validity, and concurrent validity in a group of 28 chronic poststroke patients.
The present study extends the assessment of the EFAP by incorporating the important component of manual assistance. The main objective of this study was to determine whether a modified version of the EFAP, which we call the mEFAP, is sensitive to changes that occur in the gait of poststroke patients during outpatient rehabilitation. We also established its interrater and test-retest reliability. The concurrent validity of the mEFAP was assessed by establishing a correlation between the mEFAP and 2 other measures that are often used in the assessment of ambulation for poststroke patients in our clinic: the mobility subsection of the Functional Independence Measure + Functional Assessment Measure (FIM+FAM) and the Berg Balance Test (BBT).
| Materials and Methods |
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The majority of subjects had right-sided brain lesions (n=18, 70%). Left-sided and bilateral lesions were equally represented (n=4, 15% for each group). There were more subjects with cortically based lesions (n=11, 42%) than with subcortical (n=9, 35%), brain stem (n=3,11%), mixed cortical-subcortical (n=2, 8%), or mixed subcorticalbrain stem (n=1, 4%) lesions. Ischemic strokes (n=20, 77%) predominated in this subject pool.
Measurements and Instrumentation
The mEFAP comprises 5 individually timed tasks
performed over different environmental terrains. The subtasks include
(1) a 5-meter walk on a hard floor; (2) a 5-meter walk on a carpeted
surface; (3) rising from a chair, a 3-meter walk, and return to a
seated position (the "timed up-and-go" test); (4) traversing a
standardized obstacle course; and (5) ascending and descending 5
stairs. The mEFAP is performed with or without the use of an orthotic
device or an AD. Manual assistance (MA) is provided as necessary. The
subject can use rails when climbing the stairs. The 5 timed subscores
are added to derive a total score. The level of MA is recorded
separately from the timed data, in accordance with an ordinal scale
(Table 1
) adapted from the FIM and the
FIM+FAM.10 11 The
use of any orthotic device or AD is also recorded separately. The
ADs are ranked in order of the perceived severity of the gait-related
dysfunction that mandates their use. For example, use of a straight
cane is considered to reflect less underlying dysfunction than use of a
narrow-based quad cane. The ordering of the ADs is shown in
Table 1
.
|
The BBT is a 14-item assessment tool initially developed to help identify geriatric subjects at risk for falls.6 8 12 13 More recently, the BBT scores of poststroke patients have been shown to be strongly associated with performance indices on other validated measures of motor function and functional ambulation.5 13 Strong interrater reliability (intraclass coefficient [ICC] 0.98), test-retest reliability (ICC=0.97), and responsiveness to change have been observed when the BBT has been administered to poststroke subjects.14 15 The 14 items on the BBT are ordered according to increasing difficulty. Performance on each item is ranked on an ordinal scale from 0 to 4 (0 reflecting the need for assistance to even minimally perform the requirements of the task and 4 reflecting independence in maximal performance of the task), with a maximal total score of 56 points. A score of less than 45 predicts the need for an AD or supervision during ambulation.13
The FIM+FAM is the primary outcome measure presently
used in our RDP. The FIM+FAM, an expanded version of the FIM, has
increased sensitivity to functional changes that are observed in
patients with traumatic brain injury in the subacute and chronic
stages of
recovery.10 11
The FIM+FAM consists of 30 items that are each scored on an ordinal
scale from 1 to 7 (1 reflecting complete dependence and 7 affirming
total independence). The majority of the 12 FAM items address cognitive
and psychological functioning; however, 2 of the FAM items assess
mobility. The 7-item mobility subsection of the FIM+FAM (the FAMm)
includes assessments of transfers, walking and/or wheelchair
locomotion, stair climbing, and community mobility. When administered
as a series of clinical vignettes, a group of trained raters
demonstrated agreement of 86% to 92% (
=0.85) on FAM items and 89%
(
=0.87) on the FIM
items.16 Specific testing of
the FIM+FAM in a poststroke population has not been reported. The
maximal FIM+FAM score is 210. The maximal FAMm subscore is 49. Only the
FAMm data from the FIM+FAM were assessed in the present
study.
Procedure
All testing took place in the same setting. The mEFAP
and the BBT were administered and graded by members of the study team.
Subjects underwent initial testing within 2 days of enrollment in and
discharge from the RDP. The mEFAP and the BBT were administered in
random order during the same physical therapy session. Reliability
assessments occurred during the initial testing sessions. Interrater
reliability was assessed via simultaneous ratings of
subject performance on 27% (n=7) of the initial
administrations of the mEFAP. Interrater reliability for the BBT was
assessed for 23% (n=6) of the subjects in the same fashion.
Test-retest reliability was addressed by repeat testing during the same
session with either the mEFAP or the BBT in 19% (n=5) and 15% (n=4)
of the subjects, respectively. Adequate rest periods were provided
between the test administrations. The FAMm was scored by the subjects
assigned physical therapist (who was a member of the study team) and by
the subjects occupational therapist (who was not part of the team).
The FAMm scores obtained closest to the time of admission and discharge
were included in the analyses. Each subject used the orthotic
device or AD that was most recently recommended by the subjects
treating physical therapist or physiatrist.
Treatment
There was no controlled intervention. Each subject
received pregait and gait-related therapy at the discretion of the
treating physical therapist. Because the therapy time fluctuated daily,
the total therapy time was divided by the duration of a typical session
(45 minutes) to derive the number of sessions completed by each
subject. The mean number of 45-minute sessions attended was 16.03±4.68
(range 8 to 25.88).
Statistical Analyses
SAS 6.12 statistical software (SAS Institute Inc) was
used for all analyses. The mean, median, SD, and range were
determined for age, days since stroke onset, test scores, and number of
sessions attended. Gender was evaluated by frequency of occurrence. All
measured variables were analyzed to determine the
possibility of nonrandom effects on the outcome data by
t test, ANOVA, or correlations
as appropriate. Interrater and test-retest reliability were assessed
for the mEFAP and the BBT with the ICC. The mean and SD of the
interrater and test-retest differences were calculated. With the
exception of reliability testing, all analyses were conducted
with the measurements obtained only by the primary observer. Continuous
data were tested for normality with the Shapiro-Wilkes assessment.
Because of a lack of normality in some of the timed mEFAP data,
nonparametric statistics (eg, Spearman correlation
coefficient, Wilcoxon rank sum, Friedman test, or
Kruskal-Wallis test) were used for the remainder of the
analyses. No attempt was made to normalize the data before the
final analysis. Only the timed mEFAP data were used for the
correlational analyses with the BBT and the FAMm.
Nonparametric statistics were used to analyze the
relationship between the use of ADs (eg, Kruskal-Wallis test and
Wilcoxon 2-sample test) and the amount of required MA (eg,
Spearman correlation coefficient and Wilcoxon rank sum) to the
initial, final, and change scores on the 3 outcome measures. An
-level of P<0.05 was
selected as the minimum criterion for statistical significance on all
tests.
There were no preexisting data from interventional studies
to predict the magnitude of an effect size. Power analysis was
based on the range of subject performance data from a
reliability and validity study of the EFAP (the predecessor to the
mEFAP) in which poststroke subjects and age-matched healthy controls
were tested with the EFAP one
time.5 Review of those data
indicated that a sample size of 25 subjects would be required in the
present study to detect a change in initial-to-final mEFAP scores
of at least 40% to yield a statistical power of 0.9. Post hoc
analysis was performed to assess mEFAP effect size and power.
The power analysis was done with nonparametric
adjustments. With an SD of change on the mEFAP (n=26,
=0.05), there
was a power of 0.9 to detect a change of 24 seconds (61.29±37.35
seconds change observed in the present study). For all
correlational analyses, there was a power of 0.9 to detect a
correlation of 0.59.
| Results |
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Reliability
Interrater reliability and test-retest reliability
(Table 3
) were high for the total (summed) mEFAP and all
mEFAP subtasks (all ICCs
0.985). For the BBT, interrater reliability
was high, but test-retest reliability was less favorable. The mean and
SDs of the interrater and test-retest differences are presented
in
Table 3
.
|
Sensitivity to Change
Table 4
shows data for the mEFAP final-minus-initial
scores, along with the results of nonparametric
(Wilcoxon) analyses. All subjects showed a significant
decrease in the time taken to complete the total mEFAP
(Wilcoxon signed rank,
P<0.0001). A slight increase
in time to completion was seen in 1 subject on the mEFAP floor subtask
(0.97 seconds), 1 subject on the carpet subtask (0.93 seconds), 1
subject on the up-and-go subtask (1.3 seconds), and 2 subjects on the
stairs (2.88 and 10.35 seconds). When initial mEFAP scores were
compared with final mEFAP scores (Spearman correlation coefficient,
r=0.885,
P<0.0001) and absolute mEFAP
change (r=0.688,
P<0.0001), more substantial
improvements were generally seen in subjects who were slower at initial
testing
(Figure
).
Analysis of the contribution of the individual mEFAP subtasks
to the overall total mEFAP change by nonparametric
repeated-measures ANOVA revealed substantial
subject-by-time-interaction (Friedman test,
P<0.993); that is, the pattern
of performance across the mEFAP subtasks over time differed
both within and between subjects. As a group, the subjects were
35%
faster on each of the 5 subtasks on final testing
|
|
Wilcoxon signed rank comparison of initial and final
scores on the BBT and on the FAMm revealed significant improvement in
subject performances on each measure during treatment
(Table 4
), with each improving a mean of 9.65 points. No
subject showed a maximum score (ie, 56) at initial BBT testing, but 5
(19%) subjects did after treatment. Most subjects demonstrated
significant improvement on the FAMm over time. However, no subjects
achieved the maximal FAMm score (ie, 49) during either the initial or
the final testing session.
Concurrent Validity: Comparison of
Measures
Spearman correlation coefficients were calculated for
comparison of subject performance on the mEFAP with
performance on the BBT
(Table 5
). The inverse relationship seen between the mEFAP
and the BBT scores reflects the improvement in performance over
time as a lower value on the mEFAP and a higher value on the BBT. A
significant correlation
(r=-0.735,
P<0.0001) was detected between
initial mEFAP and initial BBT group scores. Final scores on the mEFAP
and the BBT were also highly correlated
(r=-0.703,
P<0.0001). A weaker but
statistically significant association was observed between the absolute
change in the group scores seen over time on the total mEFAP and the
BBT (r=-0.524,
P<0.006). Change on the BBT
was correlated with change on 3 of the 5 mEFAP subtasks (carpet,
r=-0.519; get-up-and-go,
r=-0.449; and obstacles,
r=-0.522). Visual
analysis of the change scores revealed 2 consistent
outliers, both of whom appeared to have had more substantial changes on
the BBT than the mEFAP. No unique features were identified that would
justify removal of these subjects from post hoc
analysis.
|
Nonparametric testing indicated a significant
correlation between the mEFAP and FAMm scores before
(r=-0.685,
P<0.0001) and after
(r=-0.775,
P<0.0001) rehabilitation
(Table 5
). The magnitude of absolute change on the FAMm did
not correlate with the amount of overall change in total mEFAP
scores (r=-0.145,
P<0.479). Change on the mEFAP
carpet subtask correlated marginally
(r=-0.407,
P<0.039) with change on the
FAMm.
A weak correlation was observed between the BBT and the FAMm initial test scores (r=0.494, P<0.010). Final scores on the BBT and the FAMm were highly correlated (r=0.852, P<0.0001). No correlation was found between the absolute change in scores on the BBT and the FAMm over time (r=0.244, P<0.231).
Orthotic Device and AD Usage
Only 1 subject had a change in the use of an orthotic
device (discontinued use of an ankle-foot orthotic). No subject
required a transition to a more supportive AD (eg, from a straight cane
to a narrow-based quad cane) during the study. Five subjects (19%) had
an improvement (ie, required a less elaborate AD) of 1 rank, 5 (19%)
changed by 2 ranks, and 16 (62%) had no change in the use of an AD. AD
usage had no significant effect on the initial, final, or change scores
on the mEFAP (Kruskal-Wallis test,
P<0.311), the FAMm
(Kruskal-Wallis test,
P<0.461), or the BBT
(Kruskal-Wallis test,
P<0.420). The absolute change
scores on the outcome measures in the 16 subjects who improved by 2 or
more AD ranks were not different from the remaining 10 subjects
(Wilcoxon 2-sample test,
P<0.133 for mEFAP,
P<0.413 for BBT, and
P<0.233 for
FAMm).
Manual Assistance
Two (8%) of the subjects had no improvement in the
maximal amount of MA required during mEFAP testing. In contrast, 17
(65%) of the subjects improved (ie, required less MA) by 1 level and 7
(27%) improved by 2 or more levels. Spearman correlational
analysis revealed a correlation between change in the level of
MA and change in the mEFAP floor
(r=0.528,
P<0.006) and carpet
(r=0.533,
P<0.005) subtasks but not with
the other subtasks or with the total mEFAP change
(r=0.343,
P<0.086). A significant
(r=-0.553,
P<0.003) correlation was
detected between change in MA and change in FAMm but not between change
in MA and change in the BBT
(r=-0.348,
P<0.08). Subjects who
demonstrated the most dramatic decreases in required MA (ie,
improvement of 2 or more levels) had higher final BBT
(P<0.020) and FAMm
(P<0.015) scores and a greater
amount of positive change on the both the BBT
(P<0.019) and the FAMm
(P<0.008, Wilcoxon
rank sum). An improvement of 2 or more levels in MA was not associated
with higher mEFAP change scores (Wilcoxon,
P<0.908).
Subject Variables
Gender did not significantly influence
performance on the mEFAP, BBT, or FAM (Wilcoxon
2-sample test, P<0.05).
Subject age was correlated with final scores on the BBT
(r=-0.580,
P<0.002), FAMm change scores
(r=0.576,
P<0.002), FAMm final scores
(r=-0.494,
P<0.010), and change in MA
required (r=-0.565,
P<0.003) by
nonparametric analysis. No correlation was found
between subject age and mEFAP scores
(P>0.05). Visual
analysis of the data (scattergrams) revealed a tendency toward
better functional performance on these measures in younger
subjects. Differences in the number of days between stroke onset and
initial testing were not associated with differential
performance on any of the initial, final, or change measures by
Spearman correlations
(P>0.05).
Number of Sessions
There was no significant relationship between the
number of sessions attended and change in performance on the
FAMm (r=-0.174,
P<0.395), the BBT
(r=-0.159,
P<0.437), or the mEFAP
(r=0.048,
P<0.815). Grouping of the
mEFAP scores according to the number of completed sessions (ie,
Wilcoxon signed ranking of <14 and
14 sessions and <18 and
18 sessions) did not reveal any statistically significant effect of
session number on mEFAP change scores
(P<0.813 and
P<0.306).
| Discussion |
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Normality
In spite of the continuous nature of the timed mEFAP
data, a lack of normality was found in the distribution of many of the
mEFAP scores. Skewness of the data appeared to account for the lack of
normality in all instances. Given the range in the severity of
impairments and gait dysfunction in this subject pool, it is not
surprising that we found striking differences in the distribution of
performance on the 5 subtasks and differences in the magnitude
of change in gait speed among the subjects.
Reliability
Interrater and test-retest reliabilities for the timed
portion of the mEFAP were high and were consistent with
previous findings for similarly constructed
scales.4 5 7
The relatively poor test-retest reliability of the BBT seen in the
present study has not been reported previously. Berg et
al14 found a considerably
higher test-retest reliability (ICC 0.97) for 6 poststroke subjects
when measured by the same observer twice, 1 week apart. In the
present study, a practice effect may have been responsible for some
of the improvements that were seen on intrasession repeat testing.
Indeed, all 4 of the subjects who were tested by the BBT twice during
the first session had higher scores on the second administration
(within that session) of the test. It is difficult to draw firm
conclusions regarding the test-retest reliability of the BBT in this
population because of the small sample size.
Sensitivity to Change
A few subjects demonstrated no change, or a decrement
in performance, on 1 of the 3 final measures. A poorer
performance on only 1 of the measures likely reflects both the
differences in content of the 3 tools and the intersubject differences
in impairments, disabilities, and comorbidities. Differences in the
magnitude of an individual subjects change scores between the mEFAP
and the BBT, or the mEFAP and the FAMm, support the task-specific
nature of the mEFAP. Additionally, subjects demonstrated substantial
variability in the magnitude of change on the mEFAP subtasks compared
with change on the summed mEFAP, which indicates that the individual
subtasks may each offer unique information and argues against the
inclination to remove any of the tasks because they may appear
redundant.
Concurrent Validity: Comparison of
Measures
The strong agreement in initial-to-initial and
final-to-final comparisons between the mEFAP and BBT and between the
mEFAP and FAMm scores supports the concurrent validity of the mEFAP.
Gait-related impairments and disability, when present, often
improve during the first 3 months after
stroke.1 7 17
The overall consistency of improvement, both within and
between the tests, suggests that these changes are related to
spontaneous or therapy-enhanced functional recovery and do not
represent an artifact of repeated testing.
The significant correlation between initial, final, and change scores on the mEFAP and the BBT may be explained by an overlap in the fundamental abilities tested by these measures (particularly balance and strength). Poststroke subject performance on the BBT has shown similarly strong correlation with performance on other measures of functional ambulation (the EFAP and the Barthel Mobility Subscale), balance (the Fugl-Meyer Balance Subscale), and motor function (the Fugl-Meyer Arm and Leg Subscales).5 13 Individual differences in baseline impairments or comorbidities may contribute to differences in the magnitude of change observed between the BBT and the mEFAP scores.
The correlation between the mEFAP and FAMm initial-to-initial and final-to-final scores suggests that improvement in subject performance can be detected with either scale. Lack of correlation between mEFAP and FAMm change scores may reflect a difference in the tasks evaluated (content), the difficulty in comparing the FAMm (an ordinal scale) with the mEFAP (a continuous scale), or the heterogeneity of impairments displayed by these poststroke subjects.
ADs and MA
The inclusion of subjects who required more MA reflects
a shift in our patient population toward a higher severity of
impairments and disabilities since the original scale was developed and
supports the decision to adapt the mEFAP to account for greater MA
required by these subacute poststroke subjects. In the present
study, 12 subjects needed minimal assistance (ie, the subject required
manual support for up to 25% of the physical work) on at least 1 of
the subtasks at the time of initial testing. No subject needed greater
external support (eg, AD or MA) at the final testing session, and most
required less. Although no statistical relationship was observed
between the absolute amount of mEFAP change and changes in required
support, the possibility still exists that subjects would have been
faster or slower at final testing if they had been tested under the
same support conditions on both the initial and final measurements.
Post hoc analysis comparing subjects who improved by
2 ranks
of AD use or
2 levels of MA with those with improvement of a lesser
degree revealed no significant differences in the absolute amount of
change on the mEFAP. This negative finding suggests that the mEFAP
change scores were of sufficient magnitude not to be significantly
altered by changes in AD or MA over time. The apparent independence of
the AD and MA changes from the time changes on mEFAP supports the
separation of these entities in the reporting system of the
mEFAP.
Subject Variables
Improved functional outcome has been reported in
younger stroke patients.18
An association between younger age and improved final
performance on the BBT and FAMm, greater absolute change on the
FAMm, and greater reduction in the amount of required manual support
was observed in the present study. Why age was not an influential
factor on mEFAP performance remains unclear. Successful
completion of the BBT, the FAMm, and the mEFAP requires significant
balance, strength, and complex motor planning capabilities. Age-related
physiological changes, or the accumulation of more
significant comorbidity with advancing age, may have greater impact on
the tasks encountered on the BBT and FAMm relative to those encountered
with the mEFAP. Alternatively, age in and of itself may not be a factor
that influences performance on the specific tasks that make up
the mEFAP.
One potentially important issue is the relationship between location of lesion and subject performance on the mEFAP. Parenthetically, we observed a trend toward poorer performance on the initial BBT in the small number of subjects with bilateral strokes, as well as lower initial FAMm scores in subjects with cortical and subcortical lesions. These data suggest that future evaluation of lesion type with a larger sample size is warranted.
Number of Sessions
In the present study, we were unable to detect an
association between the number of physical therapy sessions attended
and performance on any of the 3 outcome measures. This finding
may be due in part to nonrandom events, such as the criteria for
determining discharge and/or fiscal limitations set by external case
reviewers.
Ceiling Effects
At present, discharge criteria from the
comprehensive outpatient program are essentially set in accordance with
the functional levels that are defined by the FIM+FAM. Walking ability,
as measured on the FIM+FAM, reflects the distance achieved and the
external support requirements. There is no mechanism for tracking
objective changes specific to gait parameters, such as
velocity. Ceiling effects are of particular concern when a tool that
was designed for an acutely impaired group is subsequently adapted for
use with patients who are at a more advanced stage of recovery. The
developers of the FIM+FAM have elaborated on the problems of ceiling
effects in their review of outcome data for their subjects with chronic
traumatic brain injury.11
Although the maximal FAMm target score of 49 was never reached in the
present subject pool, the discharge criteria for the RDP actually
appear to be centered around the attainment of the level of modified
independence (ie, an item score of 6), with an effective maximal
attainable FAMm score of 42. On further analysis, 6 of the
subjects had an FAMm score
42 at discharge, again suggesting a
potential ceiling effect.
As anticipated with a continuous measure, the mEFAP did not demonstrate evidence of a ceiling effect. In contrast, 5 of the subjects in this study obtained the maximal BBT score of 56 at final testing, suggesting the presence of a ceiling effect with this measure. This finding is in contrast to the recent work of Wood-Dauphinee et al,15 who did not encounter evidence of a ceiling effect with the BBT when administered serially to poststroke individuals within the first 12 weeks after the event.
Limitations and Future Directions
The BBT and the FAMm may not have been the most
suitable criterion measures for this study. Direct comparison of the
mEFAP to a well-validated test of gait velocity (such as the timed
10-meter walk) may have strengthened the establishment of concurrent
(as well as construct) validity. Previous comparison of the EFAP, the
predecessor of the mEFAP, to the timed 10-meter walk revealed a strong
association between the measures in the performance
characteristics of both poststroke subjects and healthy
controls.5
The mEFAP is sensitive to changes in time taken to complete challenging ambulation tasks. Comparison of subject performance on the mEFAP and on measures of community and household ambulation is now needed to investigate the relationship between improved speed on the mEFAP and functional ambulation in a real-world setting. Age-matched normal values, as well as the minimal mEFAP values associated with successful household and community ambulation, can be established to focus treatment efforts, predict caregiver burden, and plan for appropriate discharge disposition.
The mEFAP provides clear and specific functional information, has no apparent ceiling effect, and looks at an activity (walking) that is often a high priority for the patient. Clinical scales that are currently in use, such as the FIM, Barthel, and Rankin scales, may not provide appropriately detailed task-specific information and may be limited by ceiling effects in the assessment of functional ambulation for individuals after stroke. Further research will be required to determine whether the mEFAP will be sufficiently sensitive and specific as an outcome measure for defined therapeutic interventions.
Ambulation status after intensive rehabilitation may greatly affect a stroke survivors sense of self, ease of community reentry, and vocational prospects. Future trials should look at the relationship between mEFAP score changes and measures of stroke-specific quality of life, such as the Stroke Impact Scale.
Future investigations should also address the possible added benefit of serial measurements with this tool during rehabilitation. Performing repeated measurements might allow treatment planning to be altered when the patient does not follow an expected course of functional recovery.
With the economic pressures that are exerted on provision of care in acute and postacute stroke rehabilitation settings, functionally based assessments (such as the FIM and the FIM+FAM) have gained widespread support for setting rehabilitation goals, documenting change, and justifying the use of resources. These measures, however, may be better at describing the patients success in mastering adaptive strategies and functional substitutions than they are at reflecting more subtle changes in the performance of specific tasks. The mEFAP can provide task-specific feedback regarding the speed of ambulation across common environmental barriers and the need for external support over the course of poststroke rehabilitation. The mEFAP is inexpensive, easily understood, and can be administered in approximately 20 minutes.
| Acknowledgments |
|---|
| Footnotes |
|---|
Received September 26, 2000; revision received December 1, 2000; accepted December 19, 2000.
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