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Ann Rehabil Med > Volume 42(3); 2018 > Article
Choi, Han, Jung, Kim, Eom, and Bae: Evaluation of Ataxia in Mild Ischemic Stroke Patients Using the Scale for the Assessment and Rating of Ataxia (SARA)



To demonstrate the utility of Scale for the Assessment and Rating of Ataxia (SARA) for evaluation of posterior circulation-related features in patients with mild stroke.


Forty-five subjects, diagnosed with acute infarction in the cerebellum, basis pontis, thalamus, corona radiata, posterior limb of internal capsule, and their National Institutes of Health Stroke Scale (NIHSS) scores ≤5 were enrolled. SARA scores were graded by the cut-off value of severity in dependency of activities of daily living (ADL). SARA, Berg Balance Scale (BBS), Timed Up-and-Go (TUG), and Trunk Control Test (TCT) were correlated in regression analysis with the modified Rankin Scale (mRS) at discharge. Correlation between SARA and other tools was analyzed. Patients were divided based on mRS at admission (group A, mRS 0–2; group B, mRS 3–5). Scores between the two groups were compared.


Among the subjects, 48.9% (22/45) scored above 5.5 on SARA, and even 11.1% (5/45) scored higher than 14.25, which is the cut-off value of ‘severe dependency’ in ADL. SARA showed significant value for prediction of mRS at discharge. SARA was correlated with BBS (r=-0.946, p<0.001), TUG (r=-0.584, p<0.001), and TCT (r=-0.799, p<0.001). The SARA, BBS, TUG, and TCT scores between were lower in group B than in group A patients. SARA as well as BBS, TUG, and TCT reflect the functional severity of all patients.


SARA is a complementary tool for evaluation of the severity of ataxia in mild stroke patients with features of posterior circulation.


Ataxia is a neurological dysfunction of motor coordination, which affects the fundamental activities such as gaze, speech, gait, and balance [1]. It induces disorders of limb movement such as dyssynergia, dysmetria, kinetic or postural tremor and dysdiadochokinesia. Ataxia also affects trunk control resulting in balance or gait dysfunction [2]. These manifestations of ataxia interrupt physical performances and often contribute to poor functional outcome despite relatively well preserved muscle strength [3].
Although ataxia is caused mostly by cerebellar lesions, lesion in the basis pontis, corona radiata, thalamus, posterior limb of internal capsule also cause ataxia with ipsilateral pyramidal signs, and most of these regions are associated with posterior circulation [4,5]. This clinical syndrome is known as ataxic hemiparesis (AH), which was first defined by Fisher and Cole [4] and later modified by Fisher [5]. AH was initially described as a lacunar syndrome correlating with lacunar infarctions, which resulted from the occlusion of small penetrating arteries. However, recent studies demonstrated that cardioembolic and large-artery atherosclerosis as well as lacunar infarctions cause AH [6]. Therefore, AH is not a rare clinical manifestation among ischemic stroke patients.
The National Institutes of Health Stroke Scale (NIHSS) provides a quantitative measure of key symptoms in stroke patients and consists of 15 subscales: level of consciousness, questions, commands, visual fields, facial palsy, left/right arm/leg strength, ataxia, sensation, language, dysarthria and extinction/inattention. It is most widely used as a standard neurologic examination for the assessment of acute stroke patients, and its reliability, validity and predictive value is established [7,8]. However, NIHSS has limited application for features of posterior circulation stroke such as cranial nerve signs or ataxia because it mostly focuses on features of anterior circulation stroke [9,10]. NIHSS contains only one item assessing limb ataxia, and none related to trunk function.
Impaired trunk control is common in stroke patients even if limb ataxia is not manifested explicitly. Ataxia affects trunk control resulting in balance or gait dysfunction, increased risk of fall, and decline in independence of activities of daily living (ADL). Studies reported that the balance status is related to hospitalization period [11]. Trunk control in early stages of stroke is a predictor of comprehensive ADL function at 6 months [12]. Standing balance is correlated with change in functional state over the course of acute rehabilitation [13]. Sitting balance also shows strong correlation with ADL function [14]. Therefore, appropriate trunk control is fundamental to motor function and ADL. Apparently, detailed assessment of not only muscle strength but also trunk and limb control is essential for comprehensive evaluation of stroke patients.
Among the scales for ataxia, the International Cooperative Ataxia Rating Scale (ICARS) [15] is widely used as a tool to evaluate the severity and treatment efficacy. Consisting of 19 sub-items divided into 4 subscales, various ataxic symptoms can be assessed comprehensively with ICARS [1]. However, its clinical utility is questionable because of the prolonged duration to complete the test.
Schmitz-Hubsch et al. [16] devised a new scale known as the Scale for the Assessment and Rating of Ataxia (SARA) in 2006 to assess cerebellar ataxia. SARA is semiquantitative and is a 40-point scale consisting of 8 items: gait, stance, sitting, speech disturbance, finger chase, nose-finger test, fast alternating hand movements, and heel-shin slide. SARA has fewer scoring items than ICARS, and is therefore, faster than ICARS. SARA is more efficient than ICARS for the assessment of ataxia of trunk because it has 3 items related to trunk control (gait, stance, and sitting). SARA is characterized by high interrater reliability, test-retest reliability and internal consistency in the spinocerebellar atrophy patient group [16]. Further, Kim et al. [17,18] presented that SARA was useful as a functional measure in stroke patients due to high intra-rater and inter-rater reliability. However, subjects in these studies included patients with both ischemic and hemorrhagic stroke characterized by lesions of either anterior or posterior circulation and at varying severities of stroke. Their functional severity was not considered except for muscle strength measured using the Medical Research Council (MRC) scale [17,18].
Therefore, we focused on subjects diagnosed with mild stroke including NIHSS scores ranging from 0 to 5, and ischemic lesions of cerebellum and AH region. The specific definition of ‘mild’ has not been agreed upon universally, and there is variability in the interpretation and implementation [19]. In this study, we used the definition of ‘mild’ as NIHSS 0–5, referring to the previous studies of Spokoyny et al. [19] and Logallo et al. [20]. We investigated the need and utility of SARA for assessment of posterior circulation symptoms related to motor control function, which can be overlooked during assessment only based on NIHSS.



This study is a retrospective review of the medical records of stroke patients who were admitted to the Inje University Busan Paik Hospital and consulted for rehabilitation during the period October 2015 to April 2016. We sorted ischemic stroke patients with lesions of the cerebellum and AH region (basis pontis, corona radiata, thalamus, and posterior limb of internal capsule) confirmed via neuro-imaging (computed tomography and magnetic resonance imaging). In that group, we selected patients whose NIHSS score ranged from 0 to 5, and who were evaluated with Berg Balance Scale (BBS), Timed Up-and-Go (TUG) test, Trunk Control Test (TCT), modified Rankin Scale (mRS) and SARA. SARA, BBS, TUG, and TCT were tested immediately after the release from absolute bed rest (within 5 days from admission), and mRS was scored serially from admission to discharge. A total of 45 subjects finally met the inclusion and exclusion criteria. Inclusion criteria were (1) first onset of ischemic stroke and (2) age above 20 years. Exclusion criteria were (1) history of previous brain disease; (2) neurologic impairment, not resulting from brain lesion; (3) severe motor weakness, inability to resist against gravity; (4) severe cognitive impairment, Mini-Mental State Examination (MMSE) <26; (5) severe orthopedic problems; (6) history of visual or vestibular disease; and (7) medically instability.


We reviewed the subjects’ clinical and demographic information such as age, gender, site of lesion, stroke subtype by Trial of ORG 10172 in Acute Stroke Treatment (TOAST) classification, history of smoking and underlying diseases. Subsequently, the diversity of subjects’ SARA scores were graded by the cut-off value of severity in dependency of ADL proposed in the study of Kim et al. [18]: (1) minimal <5.5, (2) moderate 5.5–10.0, (3) maximal 10.0–14.25, (4) severe 14.25–23, and (5) total >23.
SARA’s predictive value of functional outcome was investigated by analyzing mRS at discharge with SARA, and compared with BBS, TUG, and TCT. We correlated SARA scores with BBS, TUG, and TCT scores to determine whether or not SARA reflected the motor control and balance state adequately. To ascertain whether SARA reflected the functional severity of mild stroke patients, subjects were divided into two groups according to their mRS at admission including (1) group A (mRS 0–2), favorable outcome group and (2) group B (mRS 3–5), poor outcome group [21]. SARA, BBS, TUG, and TCT scores of each group were compared.
We used descriptive statistics to analyze the subjects’ clinical and demographic information. Continuous variables were expressed as mean±standard deviation or median. Categorical variables were expressed as number of patients or ratio (%). The Kolmogorov-Smirnov test was used to investigate the normality of the distribution of the continuous variables. Stepwise multiple linear regression analysis was conducted to investigate the prognostic value of SARA with the mRS at discharge. A p-value <0.05 was used as the probability criterion for entry into the regression model and p-value >0.1 excluded from the model. Relationships between SARA and BBS, TUG, TCT were compared using Pearson correlation analysis. To investigate the differences between groups A and B, we used Student t-test for SARA and Mann-Whitney test for BBS, TUG, and TCT. The Mann-Whitney test for MMSE was carried out to determine any significant differences between the two groups. All the statistical analyses were performed using SPSS for Windows version 20.0 (IBM, Armonk, NY, USA), and a p-value less than 0.05 was considered statistically significant. Floor or ceiling effects were considered if more than 15% of the subjects had minimal or maximal scores [22].


Demographic characteristics of the subjects are summarized in Table 1. The mean age was 63.96±11.57 years, and the participants included 25 males and 20 females. The mean±standard deviation of subjects’ duration from onset to admission was 1.64±2.72 days, and that of hospitalization period was 10.36±4.46 days. Among the subjects, 48.9% (22/45) scored SARA above 5.5, and even 11.1% (5/45) scored above 14.25 which is the cut-off value of ‘severe dependency’ in ADL (Fig. 1).
The stepwise multiple linear regression analysis showed that SARA and TCT scores were significant predictors of mRS at discharge in patients with mild ischemic stroke (Table 2). Other variables (BBS and TUG) were originally included in analysis but not presented because of insignificant relationships with mRS at discharge after controlling for the variables. The largest variance inflation factor was 1.194, indicating lack of multi-collinearity among variables. Residual error showed normal distribution. In predicting mRS at discharge, the regression coefficient of SARA was 0.223, which was statistically significant (p<0.001). The SARA score was the strongest predictive variable among the four functional outcome measures (standardized β coefficient : SARA=0.873, TCT=0.345). The coefficient of determination was 61.5%.
The SARA score showed strong negative correlation with BBS in mild ischemic stroke patients (r=-0.946, p<0.001) (Fig. 2A). It also indicated that SARA showed strong negative correlation with TCT (r=-0.799, p<0.001) (Fig. 2C). However, the ceiling effect should be considered for accurate interpretation because 85.7% of subjects obtained complete scores on TCT. The SARA score showed positive correlation with TUG (r=-0.584, p<0.001) (Fig. 2B). The subjects were assigned to groups A and B based on the mRS at admission (group A, mRS 0–2; group B, mRS 3–5). Group A included 26 subjects and group B included 19 subjects. The group B showed weaker results in all assessments compared with group A. Significant differences were found in SARA as well as BBS, TUG and TCT scores between groups A and B (Table 3). No significant difference in cognitive function (Mann-Whitney test of MMSE, p=0.677) existed between the two groups. Other complications that affected the functional status were not detected.


The term, ‘mild’ ischemic stroke suggests possible favorable outcomes. However, several previous studies demonstrated otherwise. Schlegel et al. [23] reported that not all (81%) of mild stroke patients were discharged home, which suggests that 19% of mild stroke patients required long-term medical support such as rehabilitation or nursing facilities after acute period. Another study showed that a third of all mild stroke patients were not functionally independent after 90 days from the onset [19]. This mismatch was attributed to other symptoms not focused by NIHSS. Even patients scoring zero on NIHSS often presented with other stroke symptoms, especially trunk ataxia (45%) [24]. In this study, SARA played an adjunct role in differentiating the presence of ataxic symptoms and grades. Subjects in this study had homogeneous scores of NIHSS (0–5) and all were graded as mild stroke. However, their SARA scores were distributed across a wide range (Fig. 1). Mild ischemic stroke patients should evaluated with SARA as well as NIHSS and an individualized treatment plan should be developed.
Especially in patients carrying a posterior circulation lesion, the initial NIHSS score is often lower. In a recent cohort study, 76% of patients with posterior circulation stroke presented with baseline NIHSS scores ≤5 [25]. Again, lower NIHSS scores are often interpreted as assurance of a favorable outcome. However, in one retrospective study, death or disability occurred in 15% of patients with posterior circulation stroke with NIHSS scores ≤4 at 3-month follow-up as a direct consequence of their stroke [26]. In subjects enrolled in this study, who had mild ataxic hemiparesis, 48.9% of subjects (22/45) scored above the cut-off value suggesting ‘moderate dependent’ and 11.1% (5/45) showed that they needed maximal assistance in ADL. It is clear that NIHSS cannot be used as an independent and comprehensive evaluation tool for posterior circulation stroke. Other tools such as SARA are required for concurrent evaluation and reliable prediction with NIHSS.
BBS, TUG, and TCT are typical tools for assessment of overall motor control function, and they include items for evaluation of trunk control as well. Since these tools do not entail additional cost or equipment, and are rapid and easy to use, they are widely used in the clinical setting. BBS is a simple clinical tool for assessing static and dynamic balance in sitting or standing positions. Validity, reliability and sensitivity of BBS are well established in stroke patients. BBS consists of 14 subscales with a total score of 56, and a higher score suggests better functional state [27,28]. If the patient can walk, TUG test is reliable and applicable for the measurement of functional mobility based on the time taken by a patient to rise from a chair, walk 3 m, turn around and back to the chair and sit down [29-31]. TCT is not only reliable and valid, but also sensitive for the assessment of the progression of stroke. It consist of 4 items of functional movement (rolling to weak side, rolling to strong side, balance in sitting position, and sitting up from lying down) [32-34]. Based on the certainty and universality of these tools in assessing the overall limb and trunk motor function, we analyzed their correlation with SARA to determine the value of SARA in motor functional assessment of patients with mild ataxic hemiparetic stroke.
In regression analysis, SARA showed statistically significant results for prediction of mRS at discharge. Compared with BBS, TUG and TCT, SARA showed the highest standardized β coefficient (=0.873), which suggests that SARA has the strongest predictive value for functional prognosis. There are many factors for predicting the stroke patient’s functional outcome, and the strongest and most consistent predictor is the functional ability at admission. [35]. In a patient with mild stroke manifesting impaired limb or trunk control associated with ataxia, SARA is a sound tool for the prediction of functional outcome at discharge.
SARA showed a strong correlation with BBS and significant correlation with TUG and TCT (p<0.001) in mild stroke patients. However, most of the subjects scored complete TCT scores, and the result showed a ceiling effect. TCT comprises items of movement with relatively low level of functional activity compared with BBS or TUG, which contributed to the emergence of ceiling effect in mild (NIHSS 0–5) stroke patients. In the comparison between group A with group B, SARA as well as BBS, TUG and TCT showed statistical significance in functional severity.
Until now, few studies investigated the utility of SARA in assessing posterior circulation in patients with mild (low NIHSS) stroke. Kim et al. [18] reported the benefit of SARA in that it corresponded with the gait status and ADL dependency. However, no criteria were available to determine the severity excluding MRC or criteria for stroke lesions. Accordingly, this study represents an advance over previous studies.
The study limitation relates to the small sample size of subjects and non-standardized hospital period for follow-up of mRS. Several patients were excluded during screening due to failure to undergo SARA, BBS, TUT, TCT, and mRS testing. As a retrospective study, the hospitalized period and test duration were not controlled. As the study of Jorgensen et al. [36] which showed that 95% of 239,886 patients diagnosed with stroke attained optimal neurological recovery in 3 months, scores of long-term follow-up are needed. Furthermore, most of the subjects were not transferred to rehabilitation units so that their medical records did not sufficiently cover the data related to functional ability such as Modified Barthel Index (MBI) or Functional Independence Measure (FIM). To investigate the predictive value of functional outcome using SARA, only mRS was included in this study. Further, the correlation between SARA and TCT showed a ceiling effect suggesting that the result was of limited value. A prospective study design with sufficient sample size and controlled follow-up period is needed. Functional outcome assessment with more detailed and universal tools used in rehabilitation, such as MBI or FIM, is also needed.
Considering limited resources and patients’ clinical frustration, efficient selection of measurement tools is essential. Carefully selected tools of assessment facilitate the most appropriate and critical evaluation rapidly and cost-effectively, eliminating redundancy. SARA is a more efficient and complementary evaluation tool compared with other conventional tools such as BBS, TUG, and TCT for the assessment of mild stroke patients manifesting symptoms of posterior circulation.
In conclusion, SARA represents a useful tool for evaluation of severity of deficit and prediction of functional outcome in patients with mild ischemic stroke characterized by symptoms of posterior circulation. SARA is recommended as an adjunct to NIHSS in the initial evaluation of patients with mild ischemic stroke.


No potential conflict of interest relevant to this article was reported.

Fig. 1.
Scale for the Assessment and Rating of Ataxia (SARA) score graded by the cut-off value of severity in dependency of activities of daily living (ADL). SARA was assessed immediately after the patients’ release from absolute bed rest (within 5 days from admission). Values are presented as mean±standard deviation, ratio (%), and number of patients.
Fig. 2.
Pearson correlation analysis between the SARA total scores and BBS (A), TUG (B), and TCT (C). Measuring tools were assessed immediately after the patients’ release from absolute bed rest (within 5 days from admission). SARA, Scale for the Assessment and Rating of Ataxia; BBS, Berg Balance Scale; TUG, Timed Up-andGo; TCT, Trunk Control Test. ***p<0.001.
Table 1.
Patient demographics (n=45)
Characteristic Value
 Male 25 (55.6)
 Female 20 (44.4)
Age (yr) 63.96±11.57
BMI (kg/m2) 24.9±2.88
Duration from onset to admission (day) 1.64±2.72
Hospitalization period (day) 10.36±4.46
Side of lesion
 Right 19 (42.2)
 Left 23 (51.1)
 Both 3 (6.7)
Location of lesion at MRI
 Cerebellum 13 (28.9)
 Basis pontis 12 (26.7)
 Corona radiata 9 (20.0)
 Thalamus 6 (13.3)
 Posterior limb of internal capsule 5 (11.1)
TOAST classification
 Large artery atherosclerosis 4 (8.9)
 Cardioembolism 6 (13.3)
 Small artery occlusion 25 (55.6)
 Other etiology 0 (0)
 Undetermined 10 (22.2)
 Yes 14 (31.1)
 No 31 (68.9)
Cardiovascular disease
 Yes 3 (6.7)
 No 42 (93.3)
Left ventricular hypertrophy
 Yes 10 (22.2)
 No 35 (77.8)
 Yes 32 (71.1)
 No 13 (28.9)
Diabetes mellitus
 Yes 14 (31.1)
 No 31 (68.9)
Atrial fibrillation
 Yes 4 (8.9)
 No 41 (91.1)
 Admission 2.18±1.70
 Discharge 1.52±1.57
 Admission 1.91±1.26
 Discharge 1.10±0.88

Values are presented as number (%) or mean±standard deviation.

BMI, body mass index; MRI, magnetic resonance imaging; TOAST, Trial of ORG 10172 in Acute Stroke Treatment; NIHSS, National Institutes of Health Stroke Scale; mRS, modified Rankin scale.

Table 2.
Stepwise multiple linear regression analysis of variables predicting functional outcomes related to ‘mRS at discharge’ in patients diagnosed with mild ischemic stroke with acute ataxia
Unstandardized coefficient
Standardized coefficient
t p-value F-value Adjusted R²
B SE β
SARA 0.223 0.030 0.873 7.399 <0.001 27.376*** 0.615
TCT 0.064 0.022 0.345 2.927 0.006

Variables are based on their order of listing in stepwise multiple linear regression analysis. Measuring tools were assessed immediately after patients’ release from absolute bed rest (within 5 days from admission).

mRS, modified Rankin scale; SE, standard error; SARA, Scale for the Assessment and Rating of Ataxia; TCT, Trunk Control Test.

*** p<0.001.

Table 3.
Comparison of SARA, BBS, and TCT between groups A and B
Group A (n=26) Group B (n=19) p-value
SARA 4.81±3.64 10.16±7.36 0.007**
BBS 45.73±10.14 33.53±15.17 0.000***
TUG 12.31±4.49 15.67±4.56 0.026*
TCT 99.04±4.90 92.11±16.34 0.031*

Values are presented as mean±standard deviation.

Measuring tools were assessed immediately after the patients’ release from absolute bed rest (within 5 days from admission). Groups were divided according to the mRS score at the date of admission (group A, mRS 0–2; group B, mRS 3–5).

SARA, Scale for the Assessment and Rating of Ataxia; BBS, Berg Balance Scale; TUG, Timed Up-and-Go; TCT, Trunk Control Test.

* p<0.05,

** p<0.01,

*** p<0.001.


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