-
A new method for predicting functional recoveryof stroke
patients with hemiplegia: logarithmicmodellingTetsuo Koyama, Kenji
Matsumoto, Taiji Okuno Department of Rehabilitation Medicine,
Nishinomiya KyoritsuRehabilitation Hospital and Department of
Physical and Rehabilitation Medicine, Hyogo College of Medicine
andKazuhisa Domen Department of Physical and Rehabilitation
Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo,Japan
Received 25th August 2004; returned for revisions 14th December
2004; revised manuscript accepted 3rd January 2005.
Objective: To examine the validity and applicability of
logarithmic modelling forpredicting functional recovery of stroke
patients with hemiplegia.
Design: Longitudinal postal survey.Subjects: Stroke patients
with hemiplegia staying in a long-term rehabilitation facility,who
had been referred from acute medical service 30/60 days after
onset.Methods: Functional Independence Measure (FIM) scores were
periodicallyassessed during hospitalization. For each individual, a
logarithmic formula that was
scaled by an interval increase in FIM scores during the initial
2/6 weeks was used forpredicting functional recovery.
Results: For the study, we recruited 18 patients who showed a
wide variety ofdisability levels on admission (FIM scores 25/107).
For each patient, the predictedFIM scores derived from the
logarithmic formula matched the actual change in FIM
scores. The changes predicted the recovery of motor rather than
cognitive functions.
Regression analysis showed a close fit between logarithmic
modelling and actual
FIM scores (across-subject R2/0.945).Conclusions: Provided with
two initial time-point samplings, logarithmic modellingallows
accurate prediction of functional recovery for individuals. Because
the
modelling is mathematically simple, it can be widely applied in
daily clinical practice.
Introduction
In the rehabilitative treatment of stroke patientswith
hemiplegia, prediction of functional recoveryis crucial. Accurate
prediction facilitates properdefinition of goals of intervention
for individualpatients, thus improving the quality and efficiencyof
rehabilitation service.1 For providers of services
and for those paying for it, accurate predictionenables
effective use of resources by allowing betterestimation of such
factors as length of hospitaliza-tion.2 Thus, for both individual
patients and healthcare administrators, accurate prediction of
func-tional recovery would provide crucially
importantinformation.
For predicting functional recovery, variousmathematical
modelling and other methods havebeen employed.312 Multivariable
linear regressionmodelling has proved the most popular.12,13
This type of linear modelling has been usefulfor predicting
outcome at a specific time-point
Address for correspondence: Tetsuo Koyama, Department
ofRehabilitation Medicine, Nishinomiya Kyoritsu
RehabilitationHospital, Jurinji-Minamimachi 2-13, Nishinomiya,
Hyogo,Japan 662-0002. e-mail: [email protected]
Clinical Rehabilitation 2005; 19: 779/789
# 2005 Edward Arnold (Publishers) Ltd
10.1191/0269215505cr876oa
-
(e.g., six months after stroke). Stroke patientstypically,
however, show nonlinear recovery pat-terns.14,15 In most stroke
cases, patients show rapidrecovery during the initial few months,
after whichthe pace of recovery to six months from onsetslows
towards the final outcome.16 Consequently,linear modelling is not
up to the task of accuratelypredicting the prospective outcome. To
simulatethe nonlinear aspects of functional recovery, neu-ral
network modelling,17 logistic modelling,18,19
and other types of nonlinear modelling have beenproposed.
Although more successfully predictive,these modelling methods are
not widely appliedbecause of their mathematical complexity.
Thus,for general clinical applicability, there has been aneed for a
simpler means of accurately predictingthe progress of recovery.
To explore more simple modelling methods, weinvestigated
mathematical powers, logarithms,double-logarithms, and other simple
mathematicalfunctions. Of those, we focused on natural loga-rithmic
functions (ln) because they displayed threeadvantages for modelling
functional recovery.First, the progress curves (Figure 1)
resembledactual recovery patterns: if the recovery target isset at
180 days from onset and assigned a value of100%, approximately 70%
of recovery is registeredat 90 days and subsequent progress occurs
at areduced rate.1,16,20 Similarly, a logarithmic func-tion fitted
the recovery patterns of upper limbfunction of stroke patients.21
Second, based onscores sampled on two days separated by aninterval,
using simple mathematical procedures(Figure 1), the modelling
formula can easily be
Figure 1 Model formula and predictive curve. (A) shows a generic
structure; (B) shows mathematical procedures to tailor thegeneric
structure to fit individual degree of recovery. For this, actual
FIM scores recorded at two time points (Day A and Day B)are
required. DFIM indicates change in FIM scores between Day A and Day
B. Constant in (A) is countervailed in this procedure.(C) shows the
final form of the model formula. Predicted value for Day X can be
calculated with this form. FIM, FunctionalIndependence Measure; ln,
natural logarithm.
780 T Koyama et al.
-
scaled to fit each individuals magnitude of recov-ery. Third,
owing to mathematical specificity oflogarithms, the model formula
can easily becalculated (e.g., ln(90)/ln(30)/ln(90/30)/ln(3),see
Figure 1B). To evaluate the practical usefulnessof logarithmic
modelling we carried out a long-itudinal study.
Methods
PatientsStroke patients with hemiplegia who were ad-
mitted to our long-term rehabilitation hospitalduring August
2003 to April 2004 were recruitedinto the study. Criteria for
inclusion were:no past history of hemiplegia; capable of
indepen-dent ADL (activities of daily life) before
stroke;wheelchair required for locomotion at admission.As a result
of Japanese health insurance proce-dures, patients were referred
from local communityacute medical services, typically 30/60 days
afterthe stroke occurred, and received inpatient care inour
long-term rehabilitation hospital for 30/180days. During the prior
period of acute medicalhospitalization they received physical
therapy.During long-term rehabilitation hospitalizationthey
received physical therapy, occupational ther-apy and speech therapy
for a joint total of 120 minevery day. To minimize the influence of
variabilityof therapeutic regimen, we also limited recruitmentto
patients who received treatment from the samerehabilitation team
directed by a single physiatrist(first author of this article). The
protocol wasreviewed and approved by our hospitals ethicalcommittee
and informed consent was obtainedfrom all patients.
Assessment of functional recoveryTo assess functional recovery,
we employed the
Functional Independence Measure (FIM), whichhas been widely used
in rehabilitation medicine.22
The FIM is derived from scoring 18 items accord-ing to a
seven-point scale (1/totally dependent,7/completely independent) to
assess functionalindependence in ADL. These 18 items arecategorized
as self-care (6 items), sphinctercontrol (2 items), transfers (3
items), locomotion(2 items), communication (2 items), and
socialcognition (3 items). The first four categories
involve motor functions (FIM-motor) and othertwo concern
cognitive functions (FIM-cognition).The total scores score for all
18 items (FIM-total) is commonly used to assess
functionalindependence in rehabilitation medicine (totallydependent
in ADL/18, completely independentin ADL/126).
Using FIM scores, nursing staff assessed thefunctional recovery
of patients in terms of ADL.Evaluations were typically recorded a
few daysafter admission, again at two to six weeks afteradmission,
and then once a month during hospi-talization. In our study, to
assure reliability of theevaluations, FIM scores were reviewed at
weeklyconferences.
Modelling and evaluationA generic structure of modelling was
given in a
simple natural logarithmic formula (independentvariable/days
from onset) (Figure 1A). To tailorthe generic structure to fit each
individuals degreeof functional recovery, we performed
calculationson the total FIM scores at the first two
time-pointsafter admission. For each patient, the increase intotal
FIM scores between these two time-points(DFIM) was used as the
basis for scaling a co-efficient (b) in the generic structure
(Figure 1B).The introduction of this countervailed the constantin
the generic structure. Thus, using the scores atthe initial two
sampling points, a generic struc-ture could be tailored to forecast
each patientsfunctional recovery (model formula shown inFigure
1C).
To assess the fit of the time-course of themodel, FIM scores
(FIM-total, FIM-motor andFIM-cognition) were, on an individual
basis,longitudinally plotted with predicted values foreach patient
derived from the model formula. Toassess the general applicability
of logarithmicmodelling, using data from all patients, a
conven-tional linear regression analysis was performed tocompare
the total FIM scores that were actuallyobtained and the predicted
values that werederived from the model formula. For this
analysis,we excluded the scores obtained at the firsttwo sampling
points (indicated by arrowheadsin Figures 2 and 3) to determine the
particular bcoefficients.
Logarithmic modelling in hemiplegic stroke 781
-
Figure 2 Time-course of actually obtained and predicted FIM
scores for patients with left hemisphere lesions (cases
1/10).Closed circles show actually obtained FIM-total scores,
closed triangles show actually obtained FIM-motor scores,
closedsquares show actually obtained FIM-cognition scores and open
circles show predictive values derived from the model
formula(Figure 1). Arrowheads indicate initial two sampling
time-points for data to tailor the model formula for each
individual.FIM, Functional Independence Measure.
782 T Koyama et al.
-
Results
PatientsWe collected and manipulated data for 18
patients (12 male, 6 female; 10 left, 8 right,
hemisphere lesion; age 33/78 (median 67.5) yearsold). For both
motor and cognitive functions,these patients showed widely varying
levelsof disability on admission (Table 1, Figures 2and 3). Total
FIM scores ranged from 25 to 107
Figure 3 Time-course of actually obtained and predicted FIM
scores for patients with right hemisphere lesions (cases
11/18).Closed circles show actually obtained FIM-total scores,
closed triangles show actually obtained FIM-motor scores,
closedsquares show actually obtained FIM-cognition scores and open
circles show predictive values derived from the model
formula(Figure 1). Arrowheads indicate initial two sampling
time-points for data to tailor the model formula for each
individual.FIM, Functional Independence Measure.
Logarithmic modelling in hemiplegic stroke 783
-
(median, 63.5), motor FIM scores ranged from 14to 74 (median,
36), and cognition FIM scoresranged from 6 to 35 (median, 25).
Initial FIMscores were sampled at from 32 to 77 days (median50)
after occurrence of stroke and the second set
of FIM scores were sampled at from 46 to 104 days(median 72)
after occurrence (indicated by arrow-heads in Figures 2 and 3). The
interval betweenthese two time-points ranged from 13 to 44
days(median 32).
Table 1 Patients profiles
Case Age Gender Hemisphere Lesion Cause of stroke Ope.
Intervention Comorbidity
No. 1 82 M Left Corona radiata Infarct (/) OT, PT CADNo. 2 63 F
Left Putamen Hemorrhage (/) OT, PT, ST HTNo. 3 53 M Left Corona
radiata Infarct (/) OT, PT, ST HTNo. 4 33 F Left Putamen Hemorrhage
(/) OT, PT, ST HT, HLNo. 5 62 M Left Putamen Hemorrhage (/) OT, PT,
ST (/)No. 6 73 F Left Putamen Infarct (/) OT, PT, ST DM, HTNo. 7 78
F Left Corona radiata Infarct (/) OT, PT (/)No. 8 74 F Left MCA
Infarct (/) OT, PT, ST Af, CAD, HTNo. 9 74 M Left Putamen
Hemorrhage (/) OT, PT, ST HCCNo. 10 65 M Left Prefrontal cortex
Hemorrhage (/) OT, PT (/)No. 11 74 M Right Prefrontal cortex
Hemorrhage (/) OT, PT, ST (/)No. 12 50 M Right Corona radiata
Infarct (/) OT, PT DM, HTNo. 13 73 M Right Corona radiata Infarct
(/) OT, PT DM, HTNo. 14 70 F Right MCA Infarct (/) OT, PT (/)No. 15
70 M Right MCA Infarct (/) OT, PT CAD, DMNo. 16 54 M Right Thalamus
Hemorrhage (/) OT, PT, ST HTNo. 17 65 M Right MCA Infarct (/) OT,
PT HTNo. 18 54 M Right Putamen Hemorrhage (/) OT, PT HT
CAD, coronary artery disease; DM, diabetes mellitus; HCC,
hepatic cell carcinoma (post operation); HL, hyperlipidaemia;
HT,hypertension; MCA, middle cerebral artery; Ope., operation
(open-skull) during acute medical hospitalization; OT,
occupationaltherapy; PT, physical therapy; ST, speech therapy.
Figure 4 Scatterplots showing the relationships between actually
obtained FIM-total scores and predicted values derivedfrom the
model formula (see Figures 2 and 3). Data from the two initial
sampling time-points for each patient (indicated byarrowheads in
Figures 2 and 3) were excluded from the scatterplots. FIM,
Functional Independence Measure.
784 T Koyama et al.
-
Assessment of model fitFor each individual, the pattern of
increase in
the predicted values that were derived from themodel formula was
very similar to the total FIMscores that were actually obtained: so
close in fact,that the correspondence in some cases (3, 6, 8,
10,14, 15 and 16) was almost identical (Figures 3 and4). Actual
total FIM scores comprised two maincomponents: measures of motor
and cognitiveability. Close observation of the time-courses ofthese
subcomponents showed that the main con-tribution to the growth
patterns of total FIMscores was mainly from the motor
subcomponents.In sharp contrast, changes in cognitive
subcompo-nents were, in most cases, minimal (Figures 3 and4). This
finding indicates that the model formulasimulates the recovery
pattern of motor ratherthan cognitive components.
For cases 1, 4 and 12, the predicted valuesexceeded the actually
obtained total FIM scores.Dissociation between actual and predicted
valuestended to be greater towards the high end (/120)of the total
FIM range. The predicted values forcase 11 also exceeded the actual
FIM scores. Thiscase was exceptional, being the only patient
whoscored large changes in FIM-cognition soon afteradmission.
Nonetheless, even in this case, thegrowth pattern of FIM-motor
scores was compar-able to other cases and similar to
logarithmiccurve.
Model fit was then assessed using group data.Regression analysis
comparing actual data andpredicted values revealed that the model
formulaaccurately predicted actually obtained FIM-totalscores
(Figure 4; R2/0.945).
Discussion
A logarithmic function was applied to simulate thetime-course of
functional recovery of stroke pa-tients with hemiplegia. Based on
this, we developeda new model formula that, using FIM
resultssampled from two points in time during recovery,could be
applied accurately to predict the patternof functional recovery in
individual recovery.Among patients with a wide variety of motor
andcognitive disability, the model formula accuratelypredicted
actual functional recovery during hospi-
talization. Thus, the new model formula based onlogarithmic
function could be a powerful tool forpredicting functional recovery
of stroke patientswith hemiplegia.
Modelling using raw FIM-total scoresFIM assessment was
originally based on an
ordinal rather than an interval scale. Subsequently,Rasch
analysis has provided a model for convert-ing the ordinal scale of
raw FIM-total scores intoan interval scale.23 Although after Rasch
conver-sion the data showed shows a logistic curve, rawFIM-total
scores tend to show an almost linearrelationship with converted
values within therange from 25 to 120. Within this range,
rawFIM-total scores have been widely employed asinterval values in
many previous studies.24,25
Accordingly, to keep our model simple, we emp-loyed raw FIM
scores as the basis for mathema-tical modelling.
Validity of logarithmic modelling using twotime-point
samplings
During actual treatment, naturally each patientand those giving
them care are intensely interestedin the particular prospects of
functional recovery.Few studies, however, have focused on
individualtime-course and degree of functional recovery.1 Inthis
study, for each patient, we longitudinallysampled FIM scores at 4/7
time-points duringhospitalization. Observation of this data
indicatedthat recovery patterns assessed by FIM scorescould be
modeled as logarithmic function. More-over, using data for
individual patients that weresampled at two time-points during
recovery, the
Clinical messages
/ Logarithmic modelling accurately predictsfunctional recovery
of stroke patients withhemiplegia.
/ Provided with two initial time-point sam-plings, logarithmic
modelling can be tai-lored to forecast each patients
functionalrecovery.
/ The modelling is mathematically simpleenough to be adopted in
daily clinicalpractice.
Logarithmic modelling in hemiplegic stroke 785
-
model accurately predicted the actual results laterobtained for
the individuals. We know of no otherprediction modelling studies
that provide useful,simple, individual-based mathematical
modelling.
When forecasting the functional recovery of anindividual stroke
patient, a single physiatrist oftentakes many clinical parameters
into consideration.These include: initial motor and cognitive
impair-ment levels,26,27 initial day of rehabilitation,28
recovery rate,29 site and size of lesion,30,31 age,32
psychological status,33 unilateral spatial neglect,34
co-morbidities35 and other factors.36 Most of theseprevious
prediction studies have attempted tointegrate multiple factors into
the model. Ourstudy, however, uses only FIM scores sampled
ondifferent days with an interval of 2/6 weeksbetween them. The
results show that, processedthrough our logarithmic equation, these
dataenable powerful and accurate forecasting of func-tional
recovery. Since initial patterns of recoverycould be affected by
any of the multiple factorsmentioned above, the FIM scores of
individualpatients are likely to be influenced by some or allof
these factors.
Simplicity of logarithmic modellingWith the goal of developing a
new forecasting
technique to predict functional recovery, we testedseveral
mathematical functions in our preliminaryanalyses. Taking a lead
from a previous study thatemployed logarithmic transformations of
FIM-total scores to model functional outcome,12 wetested, among
other manipulations, various dou-ble-logarithmic functions. In
fact, in some cases,preliminary models using double-logarithmic
func-tions did fit actual data slightly better than themodel
formula that we are presenting here. Evenso, we preferred not to
employ double-logarithmicmodelling because of its complexity.
Focusing on logarithmic modelling, we at-tempted to adjust the
clause for days from onsetto improve the model fit. We attempted
adjustmentbased on the clinical observation that the start
offunctional recovery varies from case to casedepending on site,
size, and age of lesion. Ourpreliminary analyses, however, revealed
that thecontribution of such adjustments was minimal.Thus, to keep
things simple, we applied logarithmicmodelling without any
adjustments (Figure 1).
The model formula is simple and structurallyflexible (Figure
1C). For consistency, in this study,we used data from the first and
second FIMsamplings after admission. Any pair of periodicsamplings,
however, are suitable for defining thecoefficient (b) of the model
formula. The flexibilityof the model formula enables easy
re-estimation ifpredictive and actual values deviate. This
simpli-city and flexibility means that the model formula issuitable
for wide clinical application.
Possible limitations of logarithmic modellingIn this study, we
customized the individuals
model formula by using scores from two FIMsamples: based on
results of assessment done withan intervening period of from 13 to
44 days, datafrom this sampling pair were collected at between32
and 104 days after the occurrence of stroke. Themodel was effective
within these sampling para-meters. Further studies are needed to
find out thelimits of applicability to FIM data collected atearlier
or later phases of affliction.37 It is promisingthat case 15
(Figure 3), using data collectedrelatively soon (33 days) after
stroke occurrenceand with a short sampling interval (13
days),provided accurate prediction. This modellingmight be useful
even at earlier stages of illnessand during shorter periods of
hospitalization.
Close observation of the time-course dataplotted for each
individual revealed that factorsfor change in the predictive model
were the motorcomponents rather than cognitive components.Thus the
model may not be applicable for patientswhose clinical
manifestations are mainly cognitiverather than motor (e.g.,
patients with subara-chnoid haemorrhage).38,39 Time-course
plottingalso revealed a tendency for predicted values toexceed the
actual data towards the high end of theFIM-total range. In view of
the linearity of rawFIM-scores (as discussed above) this might
implythat the model formula is best utilized whenpredictive values
range from 25 to 120.
Applicability of logarithmic modellingOur study samples yielded
data on patients who
varied widely in age, lesion characteristics, andlevels of motor
and cognitive disabilities. Theresults that we obtained indicate
that the logarith-mic model formula (Figure 1C) could be
effectivelyapplied for various types of hemiplegic stroke
786 T Koyama et al.
-
patients. Our new model is valuable for itssimplicity and
applicability on an individual basis.Using FIM scores that were
sampled at twodifferent time-points, using a regular pocket
calcu-lator (without a log function) and a logarithmlook-up table
(see Appendix), within minutes it ispossible to come up with a
prediction for eachindividuals functional status for a particular
day.Thus, the model formula, based on simple loga-rithmic function,
could be adopted in everydayclinical practice for predicting the
functionalrecovery of stroke patients with hemiplegia.
References
1 Tilling K, Sterne JA, Rudd AG, Glass TA, WitykRJ, Wolfe CD. A
new method for predictingrecovery after stroke. Stroke 2001; 32:
2867/73.
2 Dam M, Tonin P, Casson S et al . The effects oflong-term
rehabilitation therapy on poststrokehemiplegic patients. Stroke
1993; 24: 1186/91.
3 Allen CM. Predicting the outcome of acute stroke: aprognostic
score. J Neurol Neurosurg Psychiatry1984; 47: 475/80.
4 Reding MJ, Potes E. Rehabilitation outcomefollowing initial
unilateral hemispheric stroke. Lifetable analysis approach. Stroke
1988; 19: 1354/58.
5 Gladman JR, Harwood DM, Barer DH. Predictingthe outcome of
acute stroke: prospective evaluationof five multivariate models and
comparison withsimple methods. J Neurol Neurosurg Psychiatry1992;
55: 347/51.
6 Falconer JA, Naughton BJ, Dunlop DD, Roth EJ,Strasser DC,
Sinacore JM. Predicting strokeinpatient rehabilitation outcome
using aclassification tree approach. Arch Phys Med Rehabil1994; 75:
619/25.
7 Gompertz P, Pound P, Ebrahim S. Predicting strokeoutcome: Guys
prognostic score in practice.J Neurol Neurosurg Psychiatry 1994;
57: 932/35.
8 Mauthe RW, Haaf DC, Hayn P, Krall JM.Predicting discharge
destination of stroke patientsusing a mathematical model based on
six items fromthe Functional Independence Measure. Arch PhysMed
Rehabil 1996; 77: 10/13.
9 Lai SM, Duncan PW, Keighley J. Prediction offunctional outcome
after stroke: comparison of theOrpington Prognostic Scale and the
NIH StrokeScale. Stroke 1998; 29: 1838/42.
10 Sanchez-Blanco I, Ochoa-Sangrador C,Lopez-Munain L,
Izquierdo-Sanchez M,Fermoso-Garcia J. Predictive model of
functional
independence in stroke patients admitted to arehabilitation
programme. Clin Rehabil 1999; 13:464/75.
11 Thommessen B, Bautz-Holter E, Laake K.Predictors of outcome
of rehabilitation of elderlystroke patients in a geriatric ward.
Clin Rehabil1999; 13: 123/28.
12 Inouye M. Predicting outcomes of patients in Japanafter first
acute stroke using a simple model. Am JPhys Med Rehabil 2001; 80:
645/49.
13 Giaquinto S, Buzzelli S, Di Francesco L et al . Onthe
prognosis of outcome after stroke. Acta NeurolScand 1999; 100:
202/208.
14 Partridge CJ, Johnston M, Edwards S. Recoveryfrom physical
disability after stroke: normalpatterns as a basis for evaluation.
Lancet 1987; 1:373/75.
15 Jorgensen HS, Nakayama H, Raaschou HO,Vive-Larsen J, Stoier
M, Olsen TS. Outcome andtime course of recovery in stroke. Part II:
Timecourse of recovery. The Copenhagen Stroke Study.Arch Phys Med
Rehabil 1995; 76: 406/12.
16 Sonoda S, Chino N, Domen K, Saitoh E. Changesin impairment
and disability from the third to thesixth month after stroke and
its relationshipevaluated by an artificial neural network. Am J
PhysMed Rehabil 1997; 76: 395/400.
17 Oczkowski WJ, Barreca S. Neural networkmodelling accurately
predicts the functionaloutcome of stroke survivors with
moderatedisabilities. Arch Phys Med Rehabil 1997; 78:340/45.
18 Stineman MG, Maislin G, Fiedler RC, Granger CV.A prediction
model for functional recovery instroke. Stroke 1997; 28:
550/56.
19 Lofgren B, Gustafson Y, Nyberg L.Cross-validation of a model
predicting dischargehome after stroke rehabilitation. Validating
strokedischarge predictors. Cerebrovasc Dis 2000; 10:118/25.
20 Calautti C, Baron JC. Functional neuroimagingstudies of motor
recovery after stroke in adults: areview. Stroke 2003; 34: 1553/66
Epub 2003 May 8.
21 Goodwin N, Sunderland A. Intensive, time-seriesmeasurement of
upper limb recovery in thesubacute phase following stroke. Clin
Rehabil 2003;17: 69/82.
22 Linacre JM, Heinemann AW, Wright BD, GrangerCV, Hamilton BB.
The structure and stability of theFunctional Independence Measure.
Arch Phys MedRehabil 1994; 75: 127/32.
23 Wright BD, Linacre JM, Smith RM, HeinemannAW, Granger CV. FIM
measurement properties andRasch model details. Scand J Rehabil Med
1997; 29:267/72.
Logarithmic modelling in hemiplegic stroke 787
-
24 Ring H, Feder M, Schwartz J, Samuels G.Functional measures of
first-stroke rehabilitationinpatients: usefulness of the
FunctionalIndependence Measure total score with a
clinicalrationale. Arch Phys Med Rehabil 1997; 78: 630/35.
25 Kwon S, Hartzema AG, Duncan PW, Min-Lai S.Disability measures
in stroke: relationship amongthe Barthel Index, the Functional
IndependenceMeasure, and the Modified Rankin Scale. Stroke2004; 35:
918/23.
26 Ween JE, Alexander MP, DEsposito M, RobertsM. Factors
predictive of stroke outcome in arehabilitation setting. Neurology
1996; 47: 388/92.
27 Zinn S, Dudley TK, Bosworth HB, Hoenig HM,Duncan PW, Horner
RD. The effect of poststrokecognitive impairment on rehabilitation
process andfunctional outcome. Arch Phys Med Rehabil 2004;85:
1084/90.
28 Novack TA, Satterfield WT, Lyons K, Kolski G,Hackmeyer L,
Connor M. Stroke onset andrehabilitation: time lag as a factor in
treatmentoutcome. Arch Phys Med Rehabil 1984; 65: 316/19.
29 Mayo NE, Korner-Bitensky NA, Becker R.Recovery time of
independent function post-stroke.Am J Phys Med Rehabil 1991; 70:
5/12.
30 Chaudhuri G, Harvey RF, Sulton LD, LambertRW. Computerized
tomography head scans aspredictors of functional outcome of stroke
patients.Arch Phys Med Rehabil 1988; 69: 496/98.
31 Saeki S, Ogata H, Hachisuka K, Okubo T,Takahashi K, Hoshuyama
T. Association betweenlocation of the lesion and discharge status
of ADL
in first stroke patients. Arch Phys Med Rehabil 1994;75:
858/60.
32 Bagg S, Pombo AP, Hopman W. Effect of age onfunctional
outcomes after stroke rehabilitation.Stroke 2002; 33: 179/85.
33 Paolucci S, Antonucci G, Pratesi L, Traballesi M,Grasso MG,
Lubich S. Poststroke depression andits role in rehabilitation of
inpatients. Arch PhysMed Rehabil 1999; 80: 985/90.
34 Katz N, Hartman-Maeir A, Ring H, Soroker N.Functional
disability and rehabilitation outcome inright hemisphere damaged
patients with andwithout unilateral spatial neglect. Arch Phys
MedRehabil 1999; 80: 379/84.
35 Pettersen R, Dahl T, Wyller TB. Predictionof long-term
functional outcome after strokerehabilitation. Clin Rehabil 2002;
16: 149/59.
36 Kwakkel G, Wagenaar RC, Kollen BJ, LankhorstGJ. Predicting
disability in stroke/a critical reviewof the literature. Age Ageing
1996; 25: 479/89.
37 Asberg KH, Nydevik I. Early prognosis of strokeoutcome by
means of Katz Index of activities ofdaily living. Scand J Rehabil
Med 1991; 23: 187/91.
38 Hellawell DJ, Taylor R, Pentland B. Persistingsymptoms and
carers views of outcome aftersubarachnoid haemorrhage. Clin Rehabil
1999; 13:333/40.
39 Svensson E, Starmark JE. Evaluation of individualand group
changes in social outcome afteraneurysmal subarachnoid haemorrhage:
a long-term follow-up study. J Rehabil Med 2002; 34:251/59.
788 T Koyama et al.
-
Appendix / A quick reference for logarithmic function
x Ln (x )
1.0 0.000
1.1 0.095
1.2 0.182
1.3 0.262
1.4 0.336
1.5 0.4051.6 0.470
1.7 0.531
1.8 0.588
1.9 0.642
2.0 0.693
2.2 0.788
2.4 0.875
2.6 0.9562.8 1.030
3.0 1.099
4.0 1.386
5.0 1.609
6.0 1.792
7.0 1.946
8.0 2.079
9.0 2.19710.0 2.303
ln, natural logarithm.
Logarithmic modelling in hemiplegic stroke 789
-
Reproduced with permission of the copyright owner. Further
reproduction prohibited without permission.