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Comparison of Three Instruments for Activity Disability in Acute Ischemic Stroke Survivors

Published online by Cambridge University Press:  14 July 2020

Qian Wu
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China College of Medicine, Tongji University, Shanghai, People’s Republic of China
Aijie Tang
Affiliation:
College of Medicine, Tongji University, Shanghai, People’s Republic of China
Shuzhen Niu
Affiliation:
College of Medicine, Tongji University, Shanghai, People’s Republic of China
Aiping Jin
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China
Xiaoqing Liu
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China
Li Zeng
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China College of Medicine, Tongji University, Shanghai, People’s Republic of China
Jinxia Jiang
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China College of Medicine, Tongji University, Shanghai, People’s Republic of China
Jennifer Kue
Affiliation:
College of Nursing, The Ohio State University, Columbus, OH, USA
Yan Shi*
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China College of Medicine, Tongji University, Shanghai, People’s Republic of China
Xiaoping Zhu*
Affiliation:
Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China
*
Correspondence to: Xiaoping Zhu, RN, Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China; Yan Shi, RN, PhD, Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China. Email: [email protected] Phone: 18917683111
Correspondence to: Xiaoping Zhu, RN, Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China; Yan Shi, RN, PhD, Shanghai Tenth People’s Hospital Affiliated to Tongji University, Shanghai, People’s Republic of China. Email: [email protected] Phone: 18917683111
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Abstract:

Background:

Disabilities in physical activity and functional independence affect the early rehabilitation of stroke survivors. Moreover, a good instrument for assessing activity disability allows accurate assessment of physical disability and assists in prognosis determination.

Objective:

To compare three assessment tools for physical activity in acute-phase stroke survivors.

Methods:

We conducted this prospective observational study at an affiliated hospital of a Medical University in Shanghai, China, from June 2018 to November 2019. We administered three instruments to all patients during post-stroke days 5–7, including the Modified Barthel Index (MBI), Instrumental Activities of Daily Living (IADL), and modified Rankin scale (mRs). We analyzed correlations among the aforementioned scales and the National Institutes of Health Stroke Scale (NIHSS) using Spearman’s rank-order correlations test. Univariate analyses were performed using the Mann–Whitney U test. We used a binary logistic regression model to assess the association between the NIHSS (30 days) and patient-related variables. Finally, we used receiver operating characteristic (ROC) curves to assess the predictive value of the multivariate regression models.

Results:

There was a high correlation among the three instruments; furthermore, the MBI had a higher correlation with the NIHSS (days 5–7). The NIHSS (day 30) was correlated with thrombolysis. ROC analysis revealed that the mRs-measured disability level had the highest predictive value of short-term stroke severity (30 days).

Conclusion:

The MBI was the best scale for measuring disability in physical activity, whereas the mRs showed better accuracy in short-term prediction of stroke severity.

Résumé :

RÉSUMÉ :

Comparaison entre trois outils d’évaluation de l’invalidité dans le cas de patients ayant survécu à un AVC ischémique aigu.

Contexte :

Des limitations fonctionnelles en matière d’activité physique et d’autonomie vont affecter les premières étapes de la réadaptation des survivants à un AVC. Par ailleurs, on sait qu’un bon outil d’évaluation de ces limitations permettra de les évaluer adéquatement et d’établir un pronostic.

Objectif :

Comparer trois outils d’évaluation des limitations fonctionnelles liées à l’activité physique dans le cas de survivants à un AVC.

Méthodes:

De juin 2018 à novembre 2019, nous avons effectué une étude prospective d’observation au sein d’un établissement hospitalier affilié à une école de médecine de Shanghai. Entre les cinquièmes et septièmes jours consécutifs à un AVC, tous nos patients ont été évalués au moyen des trois outils suivants : l’indice modifié de Barthel (IMB), l’échelle de Lawton ciblant les activités instrumentales de la vie quotidienne et la Modified Rankin Scale (MRS). Au moyen du test de Spearman, nous avons ensuite analysé les corrélations se dessinant entre ces trois outils et les résultats obtenus avec un autre outil, la National Institutes of Health Stroke Scale (NIHSS). Nos analyses univariées ont été par ailleurs effectuées à l’aide du test de Wilcoxon-Mann-Whitney. Nous avons également recouru à un modèle de régression logistique binaire afin d’évaluer l’association existant entre le NIHSS (30 jours) et des variables liées aux patients. Finalement, nous avons fait appel à la fonction d’efficacité du récepteur (ou courbe ROC) pour évaluer la valeur prédictive de nos modèles de régression multivariés.

Résultats :

Une forte corrélation entre nos trois outils a émergé. De plus, il est apparu que c’est le IMB qui a montré la plus forte corrélation avec la NIHSS (jours 5, 6 et 7). La NIHSS (jour 30) a été également corrélée avec un traitement thrombolytique. Nos analyses au moyen de la fonction d’efficacité du récepteur ont révélé que le niveau de limitations fonctionnelles mesuré par la MRS avait la valeur prédictive la plus élevée pour le degré de sévérité des AVC à court terme (jour 30).

Conclusion :

L’IMB est donc apparu comme le meilleur outil pour évaluer les limitations fonctionnelles en matière d’activité physique tandis que la MRS a montré la meilleure précision quand il s’agit de prédire à court terme le niveau de sévérité des AVC.

Type
Original Article
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press on behalf of The Canadian Journal of Neurological Sciences Inc.

Introduction

In recent years, there has been an increase in the prevalence of stroke in China. A nationwide population-based survey reported that stroke is becoming a major cause of adult disability and premature death in China.Reference Wang, Jiang and Sun1 Specifically, there has been a steady increase in ischemic stroke (IS) cases, which accounted for 87.5% of all stroke cases from 2013 to 2015.Reference Tian, Yang, Dong, Li and Fan2 Early disability severity is an important predictor of functional outcome and the effectiveness of stroke treatment.Reference Banks and Marotta3 Moreover, functional independence of stroke survivors ultimately affects their early rehabilitation, the ability to fully integrate into social life, and the resource cost.Reference Dewilde, Annemans and Peeters4,Reference Gialanella, Santoro and Ferlucci5

Previous studies have suggested that patients admitted to an acute stroke unit are inactive and physically limited during the first 2 weeks after stroke.Reference Bernhardt6 Early evaluation of disability allows to prompt intervention and therapy, which provide a basis for early recovery planning and lead to better outcomes ultimately. Moreover, assessing the activities of daily living could assist nurses and caregivers to deliver proper care, health services, and living assistance. Ovbiagele et al.Reference Ovbiagele and Saver7 reported that the assessment of disability or dependence in activities of daily living could strongly predict long-term disability in patients with stroke, especially those who had ischemic stroke onset within 1 week. Given the availability of data in the hospital and the lack of long-term evaluation due to loss to follow-up, 1 week is considered as the best and most practical time point for measuring the direct effect of thrombolysis.Reference Cappellari, Moretto and Bovi8

Several instruments are available for assessing physical disability and dependency in patients with stroke. Among these instruments, the Modified Barthel Index (MBI),Reference Collin, Wade, Davies and Horne9 modified Rankin scale (mRs),Reference Bamford, Sandercock, Warlow and Slattery10 and instrumental activities of daily living (IADL)Reference Gladman11 are the most widely and frequently used in clinical practice and trials. Each instrument has its advantages and disadvantages. For example, the MBI assesses patients’ basic activities; however, it lacks information on the IADL. Compared with the MBI, the mRs is considered as a global but more subjective scale. The IADL is related to cognitive changes, because it not only measures the ability of patients to live independently and take care of themselves, but also assesses cognitive, intellectual, and social skills by evaluating their ability to use the phone, manage finance, and take transportation.Reference Zucchella, Federico and Martini12 It is not usually or conveniently used among acute stroke survivors for completing the test content, which is difficult. Most previous studies assessed disability in stroke survivors during the rehabilitation and recovery period.Reference Burns, White and Magwood13 For example, a previous qualitative review recommended the MBI and mRs as prognostic assessment tools for long-term outcomes after stroke.Reference Huybrechts and Jaime Caro14 Cioncoloni et al.Reference Cioncoloni, Piu, Tassi, Acampa and Mazzocchio15 reported that mRs had better sensitivity in determining functional recovery at 6 months after stroke onset. However, few studies used those three instruments simultaneously on the assessment of physical activity in acute stroke survivors. Moreover, it remains unclear that which tool is more sensitive and more suitable to be used as a reference tool for acute stroke survivors.

In this study, we compared MBI, IADL, and mRs in stroke survivors in an acute care unit before post-stroke day 30. In the first stage, we administered four instruments for all patients during post-stroke days 5–7, including mRs, MBI, IADL, and NIHSS assessments. In the second stage, we evaluated the NIHSS scores on the 30th day after post-stroke. We aimed to describe the distribution of the scores of the three instruments and factors affecting the recovery of prognosis on the 30th day after stroke by using NIHSS. Moreover, we aimed to compare the three instruments and determine the best and most sensitive measures for determining physical disability.

Patients and Methods

Patients

We conducted this prospective observational study at Shanghai Tenth People’s Hospital Affiliated to Tongji University from June 2018 to November 2019. The inclusion criteria were a diagnosis of acute ischemic stroke and an age of >18 years. We excluded patients with dementia; no significant functional improvement after 48 hours of treatment; psychiatric history; and severe complications, including heart, renal, and hepatic failure, as well as patients that were isolated due to infectious diseases.

Measures

Sociodemographic Questionnaire

This questionnaire items included age, education, marital status, body mass index (BMI), hospitalization cost, length of hospital stay, career, and habits (sedentary lifestyle, smoking, and drinking habits).

Clinical Characteristics

We assessed the following clinical characteristics: infarct site, stroke severity, thrombolysis process, sleep situation as assessed by the Pittsburgh sleep quality index (PSQI), history of chronic disease (hypertension, coronary heart disease, atrial fibrillation, diabetes, and hyperlipidemia), and history of TIA. We obtained patients’ clinical characteristics from the medical records. Based on the neuroimaging and clinical characteristics, experienced stroke neurologists made a definitive diagnosis of ischemic stroke. Moreover, neurologists and radiologists confirmed the stroke type and localization using head magnetic resonance imaging and/or computed tomography.

Physical Disability Assessment

In this study, we used the mRs, MBI, and IADL to assess physical disability.

The Modified Barthel Index (MBI)

The MBI is a 10-item scale used to investigate the patient’s capacity in activities of daily living (feeding, bowel control, bladder control, personal hygiene, transfer, dressing, ambulation, bathing, and stair climbing).Reference Cioncoloni, Piu, Tassi, Acampa and Mazzocchio15 The 10 subscale scores add up to a maximum possible score of 100 (independent) and minimum possible score of 0 (completely dependent). Moreover, a score of 0–40, 41–60, and 61–95 points indicates severe, moderate, and mild functional impairment. The Chinese version of the MBI has been reported to have good validity and reliability among patients with stroke.Reference Leung, Chan and Shah16

Modified Rankin Scale (mRs)

The mRs is a 6-point scale: a 0 score indicates no symptoms at all; a 1 score indicates no significant disability despite symptoms and able to perform all usual duties; a 2 score indicates slight disability, and inability to perform all previous activities, but able to look after their own affairs without assistance; a 3 score indicates moderate disability, requiring some help but able to walk without assistance; a 4 score indicates moderately severe disability, and unable to walk and attend to their own bodily needs without assistance; and a 5 score indicates severe disability, bedridden, incontinent, and requiring constant nursing care and attention.Reference Haan, Limburg, Bossuyt, Meulen and Aaronson17 This scale has poor sensitivity to change; however, it has relatively good psychometric properties, especially with respect to inter-rater reliability.Reference Fearon, Mcarthur, Garrity, Graham and Quinn18

Instrumental Activities of Daily Living (IADL)

The IADL scale is an 8-item care worker-rated instrument that assesses the ability to use a telephone, shop, prepare food, housekeep, do laundry, use transportation modes, responsibly take medications, and handle finances. The total score ranges from 0 (the lowest function) to 8 (the highest function). In the IADL, disability is defined as presenting impairment in one or two of the eight IADL scale items.Reference Yang, Xu, Yang, Jiang and Dong19 The IADL scores are correlated with tasks that require sufficient capacity to make good decisions and those that require significant interaction with the environment.Reference Millán-Calenti, Tubío and Pita-Fernández20

The National Institute of Health Stroke Scale (NIHSS)

The NIHSS is a 15-item neurologic examination stroke scale that assesses consciousness, ocular movement, vision, coordination, speech and language, sensory function, upper and lower limb strength, facial muscle function, and visual hemi-neglect.Reference Lyden, Lu and Jackson21 It reflects both the degree of neurological damage and the mobility of the patient. A higher score indicates greater stroke severity. The cutoff of NIHSS categories is 0–5 for mild stroke, 6–14 for moderate stroke, 15–24 for severe stroke, and >24 indicates a very severe stroke.Reference Martin, Alastair, Jesse and Terrence22 NIHSS >5 includes all non-mild stroke categories. It is a well-validated assessment tool that is commonly used in acute-clinical stroke practice up to 3 months after stroke; moreover, it has shown good agreement with other outcome measures.Reference Alvarez-Sabín, Molina, Montaner, Arenillas and Quintana23 Notably, the baseline scores have strong predictive validity that patient with a baseline score of <5 is considered to satisfy the discharge criteria. In this study, we considered an NIHSS score of <5 as a good outcome.Reference Martin, Alastair, Jesse and Terrence22

Sleep Assessment

The Pittsburgh Sleep Quality Index (PSQI)

The PSQI was proposed by Buyess et al.Reference Buysse, Iii and Monk24 in 1989 and consists of 24 items. All items are divided into seven dimensions: subjective sleep quality, time to sleep, sleep time, sleep efficiency, sleep disorders, hypnotic drugs, and daytime function. Higher PSQI scores indicate more severe insomnia. Because it is easy to use and has good reliability and validity, it has become a commonly used scale for clinical assessment in psychiatry.Reference Zheng, Li and Wang25

Procedure

Three nurses were trained to use the three instruments, simultaneously; their consistency was assessed on 20 patients prior to study onset. We collected information on the sociodemographic and clinical characteristics from the medical records. The trained nurses conducted assessments for physical disability and the sleep situation. When a patient could not complete an interview, we used a proxy, for example, the nurse-in-charge or caregiver. We assessed the NIHSS scoreReference Kwah and Diong26 at 5–7 post-stroke days and at 30 post-stroke days. This open descriptive study received approval from the Shanghai Tenth People’s Hospital Ethics Committee (SHSY-IEC-KY-4.0/17-47/01).

Statistical Analysis

We analyzed all data using the Statistical Package for Social Sciences version 21.0 software package (IBM Inc., Armonk, NY). For descriptive statistics, we used frequency and proportion for categorical variables and mean ± standard deviation (SD) and number (percentage) for continuous variables.

We assessed the relationship among the MBI, IADL, and mRs scores in the acute stroke survivors. We used boxplots to present the distribution of MBI and IADL scores within each mRs grade. We used cross tabulation in Pearson’s chi-squared test to determine the overlap of samples at each level of the three scales and Spearman’s rank-order correlations test to analyze the correlations among the MBI, mRs, IADL, and the NIHSS (5–7 days) scores.

We used the Mann–Whitney U test for univariate analysis. We used a binary logistic regression model to assess the association between the NIHSS (30 days) scores and patient-related variables, including demographic and clinical characteristics. The NIHSS scores were dichotomized and coded as ≤5 (good outcome) and >5 (bad outcome). The categorical variables were MBI (cutoff values: 40 and 60), IADL (cutoff values: 0 and 1), mRs (cutoff value: 2), and the NIHSS scores. We performed a multivariate analysis using variables with a p-value of <0.05 in the univariate analysis. Receiver operating characteristic (ROC) curves were used to assess the predictive value of the multivariate regression models. ROC analysis was conducted to examine the best assessment tool to predict the presence of NIHSS >5 on 5–7 days after stroke onset. We used the area under the curve (AUC) to assess the fit of the models. The results were interpreted as follows: 0.7–0.9 as moderate accuracy and 0.5–0.7 as low accuracy. We considered variables with a p-value of <0.05 as significant for all analyses.

Results

Patient Characteristics

We enrolled 136 acute stroke survivors. Table 1 summarizes the demographic and clinical characteristics.

Table 1: Demographic and clinical characteristics of the participants

PSQI = Pittsburgh sleep quality index; IADL = instrumental activities of daily living; mRs = modified rankin scale; MBI = modified barthel index; BMI = body mass index; NIHSS = national institute of health stroke scale.

Distribution of the MBI and IADL Scores Related to the mRs Grades

We determined the frequency distribution of the MBI and IADL scores within each mRs grade. There was a significant difference (P < 0.001) in the distribution of the MBI and IADL median scores within the mRs grades (Kruskal–Wallis: 109.549 and 54.547 for MBI and IADL, respectively) (Figure 1).

Figure 1: (A) Distribution of the MBI scores within the mRs grades. The frequency distribution of the MBI scores within each mRs grade at 5–7 days is shown. The figure presents boxplots of the MBI score within each mRS grade at 5–7 days post-stroke. There is no overlap in the median frequency distribution at 5–7 days. There are significant differences between grade 5 and the remaining grades. (B) Distribution of the IADL scores within the mRs grades. The frequency distribution of the IADL scores within each mRs level at 5–7 days is shown. The figure shows the boxplots of the IADL score within each mRS grade at 5–7 days post-stroke. There is no overlap in the median frequency distribution at 5–7 days. There are significant differences between grade 5 and the remaining grades.

Table 2 presents the number of patients overlapping at each level of the three scales. We observed that when the mRs score was <2, the MBI score was >60. With an increase in the mRs score, there was an increase in MBI scores that were <60. When the mRs score was equal to 5, all the MBI scores were <60. The distribution of the IADL scores within the mRs grades overlapped when the mRs score was <3 points and >4 points. Given the meticulous classification of the IADL and its different emphasis compared with the mRs, the intersection of the intermediate scores is more complicated compared with that of MBI.

Table 2: Overlapping of samples at each level of the three scales

MBI = modified barthel index.

Note: 0 = 61–99 scores; 1 = 41–60 scores; 2 = 0–40 scores in the MBI.

Correlation among the Three Scales

Spearman’s correlation analysis revealed correlations among the three scales (P < 0.001); specifically, the IADL, mRs, and MBI were negatively correlated (r < 0), while the IADL and mRs were positively correlated (r > 0). Moreover, there was a high correlation between the mRs and MBI (r = −0.870) and a moderate correlation of the IADL and mRs with MBI (r = 0.559 and −0.587, respectively) (Table 3).

Table 3: The correlation between the three scales

IADL = instrumental activities of daily living; mRs = modified rankin scale; MBI = modified barthel index.

Correlation between Each of the Three Scales and the NIHSS (5–7 Days)

Spearman correlation analysis revealed correlations between each of the three scales and the NIHSS (days 5–7) (P < 0.001). Specifically, there was a negative correlation of the NIHSS (days 5–7) with the MBI (r < 0) and a positive correlation of the NIHSS (admission) with the IADL and mRs (r > 0). There was a high correlation of the MBI and mRs with NIHSS (days 5–7) (r = −0.823 and 0.769, respectively) and a moderate correlation of the IADL with NIHSS (days 5–7) (r = 0.569) (Table 4).

Table 4: The correlation between the three scales and the NIHSS (admission)

IADL = instrumental activities of daily living; mRs = modified rankin scale; MBI = modified barthel index.

Univariate and Multivariate Analysis of the NIHSS Scores (Day 30)

Table 5 presents the results of univariate and multivariate analyses of the NIHSS scores (day 30). Thrombolysis (P < 0.001) and time from onset to admission (P = 0.016) showed statistically significant associations with the NIHSS score (day 30). Binary logistic regression analysis revealed the significant association between thrombolysis and the NIHSS score (day 30) after adjusting for the variable time from onset to admission. Concomitantly, thrombolysis was an independent protective factor of NIHSS (day 30) (OR = 0.057, 95% CI = 0.042–0.585, P = 0.006).

Table 5: Univariate and multivariate analysis of factors associated with the NIHSS (day 30)

BMI = body mass index; TIA = transient ischemic attack; PSQI = Pittsburgh sleep quality index.

* Mann–Whitney U test.

Statistically significant (P < 0.05).

Odds ratio indicated that patients with functional recovery (NIHSS < 5) were 0.057 times more likely to be functionally impaired (NIHSS > 5) at 30 days compared to patients who did not undergo thrombolysis.

Receiver Operator Curves of the Predictive Ability of the MBI, IADL, and mRs Compared to that of the NIHSS (Day 30)

ROC curves showed the predictive power of the multivariable model for the three scales (Figure 2). Figure 2 demonstrates that the MBI score (cutoff value: 60), IADL score (cutoff value: 1), and mRs scores (cutoff value: 2) had the best sensitivity, which indicates that these scales had the best prognosis for acute stroke. The area under the ROC curve for the model for the mRs score (cutoff value: 2), MBI scores (cutoff value: 60), and IADL score (cutoff value: 1) was 0.831 (95% CI: 0.761–0.901), 0.749 (95% CI: 0.664–0.835), and 0.698 (95% CI: 0.608–0.789).

Figure 2: The area under the ROC curve shows an improved predictive value (0.698–0.831) for total prognosis after inclusion of the MBI score (cutoff value: 60), IADL score (cutoff value: 1), and mRs score (cutoff value: 2).

Figure 3 shows the predictive power of the NIHSS (day 30) in the multivariable model. The area under the ROC curve for the model for the NIHSS (day 30) was 0.659 (95% CI: 0.563–0.755). The regression analysis model that included thrombolysis and time from onset to admission as the independent variables showed low sensitivity for explaining stroke prognosis.

Figure 3: The area under the ROC curve of the multivariable model for the NIHSS (day 30) is 0.659 (95% CI: 0.563–0.755) with the inclusion of thrombolysis and time from onset to admission as independent variables.

Figure 4 presents the predictive power of the multivariable model for the MBI (cutoff value: 60 and cutoff value: 40, respectively). The area under the ROC curve for the model for the MBI (cutoff value: 40) and MBI (cutoff value: 60) was 0.706 (95% CI: 0.613–0.798) and 0.749 (95% CI: 0.664–0.835), respectively. Both regression analysis models with the inclusion of thrombolysis and time from onset to admission as independent variables showed moderate sensitivity for explaining acute stroke prognosis.

Figure 4: The area under the ROC curve of the multivariable model for the MBI (cutoff value: 40) is 0.706 (95% CI: 0.613–0.798) with the inclusion of thrombolysis, time from onset to admission, and the MBI score (cut off value: 40) as independent variables. The area under the ROC curve of the multivariable model for the MBI (cutoff value: 60) is 0.749 (95% CI: 0.664–0.835) with the inclusion of thrombolysis, time from onset to admission, and MBI (cutoff value: 60) as independent variables.

Figure 5 presents the predictive power of the multivariable model for the IADL (using cutoff values of 0 or 1). The area under the ROC curve for two different models of the IADL (cutoff value: 0) and IADL (cutoff value: 1) was 0.665 (95% CI: 0.570–0.760) and 0.698 (95% CI: 0.608–0.789). Both regression analysis models, with the inclusion of thrombolysis and time from onset to admission as independent variables, showed low sensitivity for explaining acute stroke prognosis.

Figure 5: The area under the ROC curve of the multivariable model for the IADL (cutoff value: 0) is 0.665 (95% CI: 0.570–0.760) with the inclusion of thrombolysis, time from onset to admission, and the IADL (cutoff value: 0) as independent variables. The area under the ROC curve of the multivariable model for the IADL (cutoff value: 1) is 0.698 (95% CI: 0.608–0.789) with the inclusion of thrombolysis, time from onset to admission, and IADL (cutoff value: 1) as independent variables.

Discussion

We aimed to compare three assessment tools of physical disability at two time points in the acute post-stroke stage (within 30 days after stroke) among first-stroke survivors. We observed a high correlation among the three assessment tools (P < 0.05). Although they all measured physical disability, they placed emphasis on different activity aspects. The MBI and mRs measure the degree of assistance required from other people to perform basic activities of daily living, while the IADL places emphasis on assistance required from devices. This could have contributed to the significant differences (P < 0.001) in the distribution of the MBI and IADL scores within the mRs grades (Figures 1 and 2). Our study is consistent with a previous work,Reference Cioncoloni, Piu, Tassi, Acampa and Mazzocchio15 which shows that the MBI score distribution within mRS grades overlapped at 10 days. Kwon et al. assessed the frequency distribution of MBI scores within mRs grades and showed that the highest MBI scores (95–100, indicating excellent to complete recovery) corresponded to mRs grades 0, 1, 2, and 4.Reference Kwon, Hartzema, Duncan and Minlai27 The MBI is used to assess activity function; however, its efficiency is compromised when administered too early (within 5 days post-stroke).Reference Quinn, Langhorne and Stott28

The American Heart Association/American Stroke Association recommends early assessment of patients with acute ischemic stroke,Reference Winstein, Stein and Arena29 which could be facilitated by accurate assessment tools, which help to screen patients with the ability to perform activities and evaluate the effectiveness of rehabilitation treatment. The NIHSS is an important scale that reflects stroke-induced global neurological and motor impairment. Compared with the other two scales, we found that the MBI had the highest correlation (r = −0.823, P < 0.001) with the NIHSS. A previous study reported that the MBI is more reliable for disability assessment than the mRs.Reference Alvarez-Sabín, Molina, Montaner, Arenillas and Quintana23 The inter-rater reliability and internal consistency of the MBI can be assessed, while the internal item consistency of the mRs cannot be evaluated, because it is one-dimensional. Compared to the mRs, the MBI is considered less subjective since it allows for objective and specific evaluation, while the mRs obscurely describes the activity levels. As a disability measure, the mRs subsumes some items in the IADL and MBI (e.g., walking, dressing, bathing) and emphasizes compromised motor function. However, the mRs is more sensitive than the MBI in the measurement of stroke disability.Reference Balu30

It is recognized that activity ability could predict long-term outcomes and independence in the subsequent recovery period in patients with stroke. Univariate and multivariate analyses showed that thrombolysis (95% CI: 0.042–0.585; P = 0.006) was independently associated with the NIHSS (day 30). A previous study reported an association of thrombolysis with post-stroke outcome.Reference Saňák, Herzig and Zapletalová31 Moreover, we compared the sensitivity and specificity of the three assessment tools in predicting stroke severity at the end of the acute stage. The multivariate analysis model with the mRs (cutoff value: 2) had the highest AUC (Figure 3), indicating that it could better predict functional recovery after acute stroke. Consistent with our findings, Dewilde et al.Reference Dewilde, Annemans and Peeters4 reported that prognostic outcomes were associated with increasing levels of the mRs: in the first few months after a stroke, higher mRs scores were associated with higher disability levels and a higher cost of rehabilitation in the first month after the stroke. Moreover, the predictive validity of the mRs is indicated by the association between short-term and long-term post-stroke care needs.Reference Mayo, Wood-Dauphinee and Cote32 With respect to the IADL and MBI, different cutoff values showed different ROC curves and AUCs. Specifically, the AUCs of the MBI (cutoff value: 60) and the MBI (cutoff value: 40) were 0.794 (95% CI: 0.664–0.835) and 0.706 (95% CI: 0.613–0.798), respectively. On the other hand, the AUCs of the IADL (cutoff value: 0) and the IADL (cutoff value: 1) were 0.665 (95% CI: 0.570–0.760) and 0.698 (95% CI: 0.608–0.789), respectively. Therefore, when using the MBI or IADL to predict the short-term stroke severity, moderate scores of the MBI (cutoff value: 60) and IADL (cutoff value: 1) could be employed as predictive factors.

Limitations

Our study has several limitations. First, we enrolled first ischemic stroke survivors during the acute stage (30 days after stroke). The main short-term outcome was the NIHSS score at day 30; however, other studies could employ mortality and assess readmission rates with larger samples. Additionally, in this study, we only assessed physical disability at a single time point rather than multiple time points throughout the 30 days. Finally, we did not assess and account for the relevant biochemical markers.

Conclusions and Policy Implications in Practice

In summary, compared with the other two instruments, we found that the BI was the best scale for reflecting disability in physical activity in acute stroke survivors; moreover, it was highly correlated with the NIHSS. This indicates that the MBI could assist nurses and caregivers to accurately assess physical disability and functional independence, which providing information for the degree of assistant and early as well as making a personal early rehabilitation plan in the acute stage. Furthermore, we found that the mRs showed better accuracy in the prediction of short-term stroke severity, which is consistent with previous findings regarding its utility for long-term outcomes. The level of mRs could guide doctors and nurses to make a proper decision for the follow-up plan. The findings are relevant to stroke care and might be meaningful for the rational utilization of medical resources.

Acknowledgments

This research was funded by the National Natural Science Foundation of China (71704135).

Conflict of Interest

None.

Statement of Authorship

QW, YS, and XPZ were responsible for the study’s concept and design. AIT and SZN did the statistical analysis and data collection. QW wrote the paper. SZN, APJ, XQL, and LZ contributed to the analysis and interpretation of the data. JXJ and JK were responsible for subsequent drafts and revision.

References

Wang, W, Jiang, B, Sun, H, et al. Prevalence, incidence, and mortality of stroke in China. Circulation. 2017;135(8):759.CrossRefGoogle ScholarPubMed
Tian, D, Yang, Q, Dong, Q, Li, N, Fan, D. Trends in stroke subtypes and vascular risk factors in a stroke center in China over 10 years. Sci Rep. 2018;8(1):5037.CrossRefGoogle Scholar
Banks, JL, Marotta, CA. Outcomes validity and reliability of the modified Rankin scale: implications for stroke clinical trials: a literature review and synthesis. Stroke. 2007;38(3):1091–6.CrossRefGoogle ScholarPubMed
Dewilde, S, Annemans, L, Peeters, A, et al. Modified Rankin scale as a determinant of direct medical costs after stroke. Int J Stroke. 2017;12:392400.CrossRefGoogle ScholarPubMed
Gialanella, B, Santoro, R, Ferlucci, C. Predicting outcome after stroke: the role of basic activities of daily living. Eur J Phys Rehabil Med. 2013;49(5):629–37.Google ScholarPubMed
Bernhardt, J. Inactive and alone: physical activity within the first 14 days of acute stroke unit care. Stroke. 2004;35(4):1005–9.CrossRefGoogle ScholarPubMed
Ovbiagele, B, Saver, JL. Day-90 acute ischemic stroke outcomes can be derived from early functional activity level. Cerebrovasc Dis. 2010;29(1):50–6.CrossRefGoogle ScholarPubMed
Cappellari, M, Moretto, G, Bovi, P. Day-7 modified Rankin scale score as the best measure of the thrombolysis direct effect on stroke? J Thromb Thrombolys. 2012;36(3):314–5.CrossRefGoogle Scholar
Collin, C, Wade, DT, Davies, S, Horne, V. The Barthel ADL Index: a reliability study. Int Disabil Stud. 1988;10(2):61–3.CrossRefGoogle ScholarPubMed
Bamford, JM, Sandercock, PA, Warlow, CP, Slattery, J. Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 1989;20(6):828.CrossRefGoogle ScholarPubMed
Gladman, JRF. Measurement of instrumental activities of daily living in stroke. Stroke. 1995;26(11):2197.Google ScholarPubMed
Zucchella, C, Federico, A, Martini, A, et al. Neuropsychological testing. Pract Neurol. 2018;18(3):227–37.CrossRefGoogle ScholarPubMed
Burns, SP, White, BM, Magwood, G, et al. Racial and ethnic disparities in stroke outcomes: a scoping review of post-stroke disability assessment tools. Disabil Rehabil. 2019;41(15):1835–45.CrossRefGoogle ScholarPubMed
Huybrechts, KF, Jaime Caro, J. The Barthel Index and modified Rankin scale as prognostic tools for long-term outcomes after stroke: a qualitative review of the literature. Curr Med Res Opin. 2007;23(7):1627–36.CrossRefGoogle ScholarPubMed
Cioncoloni, D, Piu, P, Tassi, R, Acampa, M, Mazzocchio, R. Relationship between the modified Rankin scale and the Barthel Index in the process of functional recovery after stroke. Neurorehabilitation. 2012;30(4):315–22.CrossRefGoogle ScholarPubMed
Leung, SOC, Chan, CCH, Shah, S. Development of a Chinese version of the modified Barthel Index validity and reliability. Clin Rehabil. 2007;21(10):912–22.CrossRefGoogle ScholarPubMed
Haan, RD, Limburg, M, Bossuyt, P, Meulen, JVD, Aaronson, N. The clinical meaning of Rankin ‘handicap’ grades after stroke. Stroke. 1995;26(11):2027–30.CrossRefGoogle ScholarPubMed
Fearon, P, Mcarthur, KS, Garrity, K, Graham, LJ, Quinn, TJ. Prestroke modified Rankin stroke scale has moderate interobserver reliability and validity in an acute stroke setting. Stroke. 2012;43(12):3184–8.CrossRefGoogle Scholar
Yang, M, Xu, H, Yang, L, Jiang, J, Dong, B. Metabolic syndrome and disability in Chinese nonagenarians and centenarians. Aging Clin Exp Res. 2018;30(8):943–9.CrossRefGoogle ScholarPubMed
Millán-Calenti, JC, Tubío, J, Pita-Fernández, S, et al. Prevalence of functional disability in activities of daily living (ADL), instrumental activities of daily living (IADL) and associated factors, as predictors of morbidity and mortality. Arch Gerontol Geriatr. 50(3):306–10.CrossRefGoogle Scholar
Lyden, P, Lu, M, Jackson, C, et al. Underlying structure of the National Institutes of Health Stroke Scale: results of a factor analysis. Stroke. 1999;30(11):2347–54.CrossRefGoogle ScholarPubMed
Martin, TR, Alastair, W, Jesse, D, Terrence, JQ. Functional assessment for acute stroke trials: properties, analysis, and application. Front Neurol. 2018;9:191.Google Scholar
Alvarez-Sabín, J, Molina, CA, Montaner, J, Arenillas, JF, Quintana, M. Effects of admission hyperglycemia on stroke outcome in reperfused tissue plasminogen activator-treated patients. Stroke. 2003;34(5):1235–41.CrossRefGoogle ScholarPubMed
Buysse, DJ, Iii, C F R, Monk, T H, et al. The Pittsburgh sleep quality index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989;28(2):193213.CrossRefGoogle ScholarPubMed
Zheng, B, Li, M, Wang, KL, et al. Analysis of the reliability and validity of the Chinese version of Pittsburgh sleep quality index among medical college students. Beijing Da Xue Bao Yi Xue Ban. 2016;48(3):424–8.Google ScholarPubMed
Kwah, LK, Diong, J. National Institutes of Health Stroke Scale (NIHSS). J Physiother. 2014;60(1):61.CrossRefGoogle Scholar
Kwon, S, Hartzema, AG, Duncan, PW, Minlai, S. Disability measures in stroke relationship among the Barthel Index, the functional independence measure, and the modified Rankin scale. Stroke. 2004;35(4):918–23.CrossRefGoogle ScholarPubMed
Quinn, TJ, Langhorne, P, Stott, DJ. Barthel Index for stroke trials: development, properties, and application. Stroke. 2011;42(4):1146–51.CrossRefGoogle ScholarPubMed
Winstein, CJ, Stein, J, Arena, R, et al. Guidelines for adult stroke rehabilitation and recovery: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2016;47(6):e98we169.CrossRefGoogle ScholarPubMed
Balu, S. Differences in psychometric properties, cut-off scores, and outcomes between the Barthel Index and modified Rankin scale in pharmacotherapy-based stroke trials: a systematic literature review. Curr Med Res Opin. 2009;25(6):1329–41.CrossRefGoogle Scholar
Saňák, D, Herzig, R, Zapletalová, J, et al. Predictors of good clinical outcome in acute stroke patients treated with intravenous thrombolysis. Acta Neurol Scand. 2011;123(5):339–44.CrossRefGoogle ScholarPubMed
Mayo, NE, Wood-Dauphinee, S, Cote, R, et al. There’s no place like home : an evaluation of early supported discharge for stroke. Stroke. May 2000;31(5):1016–23.CrossRefGoogle ScholarPubMed
Figure 0

Table 1: Demographic and clinical characteristics of the participants

Figure 1

Figure 1: (A) Distribution of the MBI scores within the mRs grades. The frequency distribution of the MBI scores within each mRs grade at 5–7 days is shown. The figure presents boxplots of the MBI score within each mRS grade at 5–7 days post-stroke. There is no overlap in the median frequency distribution at 5–7 days. There are significant differences between grade 5 and the remaining grades. (B) Distribution of the IADL scores within the mRs grades. The frequency distribution of the IADL scores within each mRs level at 5–7 days is shown. The figure shows the boxplots of the IADL score within each mRS grade at 5–7 days post-stroke. There is no overlap in the median frequency distribution at 5–7 days. There are significant differences between grade 5 and the remaining grades.

Figure 2

Table 2: Overlapping of samples at each level of the three scales

Figure 3

Table 3: The correlation between the three scales

Figure 4

Table 4: The correlation between the three scales and the NIHSS (admission)

Figure 5

Table 5: Univariate and multivariate analysis of factors associated with the NIHSS (day 30)

Figure 6

Figure 2: The area under the ROC curve shows an improved predictive value (0.698–0.831) for total prognosis after inclusion of the MBI score (cutoff value: 60), IADL score (cutoff value: 1), and mRs score (cutoff value: 2).

Figure 7

Figure 3: The area under the ROC curve of the multivariable model for the NIHSS (day 30) is 0.659 (95% CI: 0.563–0.755) with the inclusion of thrombolysis and time from onset to admission as independent variables.

Figure 8

Figure 4: The area under the ROC curve of the multivariable model for the MBI (cutoff value: 40) is 0.706 (95% CI: 0.613–0.798) with the inclusion of thrombolysis, time from onset to admission, and the MBI score (cut off value: 40) as independent variables. The area under the ROC curve of the multivariable model for the MBI (cutoff value: 60) is 0.749 (95% CI: 0.664–0.835) with the inclusion of thrombolysis, time from onset to admission, and MBI (cutoff value: 60) as independent variables.

Figure 9

Figure 5: The area under the ROC curve of the multivariable model for the IADL (cutoff value: 0) is 0.665 (95% CI: 0.570–0.760) with the inclusion of thrombolysis, time from onset to admission, and the IADL (cutoff value: 0) as independent variables. The area under the ROC curve of the multivariable model for the IADL (cutoff value: 1) is 0.698 (95% CI: 0.608–0.789) with the inclusion of thrombolysis, time from onset to admission, and IADL (cutoff value: 1) as independent variables.