Background Cognitive domain deficits can occur after aneurysmal subarachnoid haemorrhage (aSAH) though few studies systemically evaluate its impact on 1-year outcomes.
Objective We aimed to evaluate the pattern and functional outcome impact of cognitive domain deficits in aSAH patients at 1 year.
Methods We carried out a prospective observational study in Hong Kong, during which, 168 aSAH patients (aged 21–75 years and had been admitted within 96 h of ictus) were recruited over a 26-month period. The cognitive function was assessed by a domain-specific neuropsychological assessment battery at 1 year after ictus. The current study is registered at ClinicalTrials.gov of the US National Institutes of Health (NCT01038193).
Results Prevalence of individual domain deficits varied between 7% to 15%, and 13% had two or more domain deficits. After adjusting for abbreviated National Institute of Health Stroke Scale and Geriatric Depressive Scale scores, unfavourable outcome (Modified Rankin Scale 3–5) and dependent instrumental activity of daily living (Lawton Instrumental Activity of Daily Living<15) were significantly associated with two or more domain deficits and number of cognitive domain deficits at 1 year. Two or more domain deficits was independently associated with age (OR, 1.1; 95% CI 1.1 to 1.2; p<0.001) and delayed cerebral infarction (OR, 6.1; 95% CI 1.1 to 33.5; p=0.036), after adjustment for years of school education.
Interpretation In patients with aSAH, cognitive domain deficits worsened functional outcomes at 1 year. Delayed cerebral infarction was an independent risk factor for two or more domain deficits at 1 year.
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Although aneurysmal subarachnoid haemorrhage (aSAH) accounts for only 3% of strokes, its profound consequences and unique window for intervention have justified its classification as a separate entity.1 Estimated independence varied between 36% and 60% only after aSAH.2 ,3 Previous studies have suggested that 27–44% of patients who returned to the community exhibited cognitive dysfunction.4–6 In a systemic review of aSAH cognitive dysfunction, the main cognitive domain impairments reported included memory, executive function and language, the prevalence of which ranged from 0% to 76% among different studies, although few studies explored the correlations between domain-specific cognitive deficits and disability.3 Previous reports confirmed that cognitive deficits were associated with functional outcome at 3 months after aSAH.7 ,8 However, they were not adjusted for motor function. There was also suggestion that cognitive dysfunction might further improve even after 9 months.9 It would be of interest to understand the pattern and impact of chronic cognitive dysfunction on functional outcomes.
There is another important reason to understand impact of cognitive impairment after aSAH. Currently employed neurological outcome measures may not be disease-sensitive enough to detect aSAH-related brain injuries, and this lack of sensitivity may account for negative results in aSAH neuroprotection trials. Cognitive impairment was thought to be a potential candidate to target in future clinical trials. Thus, there is an urgent need to better understand cognitive impairment after aSAH.
We therefore aimed to (a) describe the cognitive domain deficit pattern at 1 year; (b) evaluate the impact of cognitive domain deficits on functional outcomes at 1 year.
This prospective observational four-center study was carried out in Hong Kong. It is registered at ClinicalTrials.gov of the US National Institutes of Health (NCT01038193) and has been approved by hospital ethics committees. This study conforms to the Declaration of Helsinki, and written informed consent was obtained from all of the participants or their next of kin.
The patient inclusion criteria were: (1) spontaneous SAH with angiography-confirmed aetiology of intracranial aneurysms; (2) hospital admission within 96 h after ictus; (3) between 21 and 75 years of age; (4) a speaker of Chinese (Cantonese); and (5) informed consent from the patients or their next of kin. The patient exclusion criteria were: (a) a history of previous cerebrovascular or neurological disease other than unruptured intracranial aneurysm; or (b) a history of neurosurgical operation before ictus.
Delayed cerebral infarction due to the delayed cerebral ischaemia (DCI) is defined as a new cerebral infarction identified on CT scans after the exclusion of early (including procedure-related) infarctions.10 Early infarction is defined as hypodensity apparent on the post-treatment CT scans at around 12–24 h after aneurysm treatment. All of the recruited patients had delayed CT scans of their brains at 2–3 weeks after presentation available for assessment. The diagnosis of cerebral infarction due to DCI was made by site investigators and confirmed by a local neuroradiologist.
Assessments were conducted 1 year after ictus by one of the two research assistants (psychology graduates) trained by a post-doctoral research psychologist.
Neuropsychological tests for cognitive domains
The battery of cognitive assessments had previously been applied in our local Chinese population.11 The choice of the battery of cognitive assessments is based on: (a) Previous cognitive studies in local Chinese patients and standard cognitive tests validated in the Cantonese-speaking population; (b) A balanced battery covering verbal and visuospatial memory, attention and working memory, executive functions, psychomotor speed, and language.
A. Verbal memory domain
Hong Kong List Learning Test (HKLLT).12 The HKLLT was developed based on the California Verbal Learning Test, which has been used in vascular cognitive impairment studies. It is a verbal learning and memory test that consists of two 16-word lists with three learning trials with immediate recall, 10-min delayed recall, and 30-min delayed recall and recognition for each list. The HKLLT has been validated in both normal and pathological local populations.12
B. Visuospatial skill and memory domain
The Rey Osterrieth Complex Figure13 is a commonly used test for assessing visuospatial construction skills and visuospatial memory.
C. Attention and working memory domain
Verbal and visual digit span forward and backward from the Chinese Wechsler Memory Scale Third Edition14 for the examination of simple attention and working memory. Verbal and visual spans have been used as donor scales for composite psychometric measures.
D. Executive function and psychomotor speed domain
Symbol-Digit Modalities Test.15 This brief, easy-to-administer, timed coding test is a variant of the Digit-Symbol Coding Task in the Wechsler Adult Intelligence Scale-Third edition. Timed coding tasks have been used in studies that involve subjects with suspected vascular cognitive impairment.16
Color Trails Test (CTT). This test originated from the Trail Making Test (TMT), which is used for the timed assessment of psychomotor speed and executive functions. Using coloured numbers instead of the English alphabet, the CTT is considered to be an acceptable cultural substitute for the original TMT with similar psychometric properties.17
Animal Fluency. This test requires subjects to generate as many animal names as possible in 1 min. It is a simple timed test that sensitively measures speed and activation, as well as such executive processes as clustering, set-shifting, and retrieval.12 ,18
E. Language domain
Modified Boston Naming Test (mBNT).19 The Boston Naming Test is the most frequently used confrontation naming test for assessing language. Here, we have used a validated modified version that contains 15 stimuli appropriate for use in Chinese cultures.19
Cognitive domain scores were computed by averaging the z scores of the respective test measures derived from the established age-matched and education-matched norms. A cognitive domain deficit was defined through a cognitive domain z score <−1.65 (below the fifth percentile). We employed the presence of two or more cognitive domain deficits rather than any cognitive domain deficits as the definition of cognitive impairment as in neuropsychological outcome study of the International Subarachnoid Aneurysm Trial.20
Modified Rankin Scale
The Modified Rankin Scale (mRS) is a valid and clinically relevant instrument that is used to assess recovery (death, disability, and dependence) after stroke and is a commonly used outcome measure in SAH studies.21–24 The mRS ranges from 0 (no symptoms) to 6 (death). Unfavourable outcome in survivors is defined as mRS 3–5.
Chinese Lawton IADL Scale
The Lawton IADL Scale is an appropriate instrument for assessing independent living skills. Items that are assessed include the ability to use the telephone, go shopping, prepare food, do the housekeeping and laundry, secure transportation, be responsible for medications and handle finances.25 The Chinese version was previously validated and used.26
Geriatric Depressive Scale
Poststroke depressive symptoms were assessed by the validated Chinese version of the 15-item version of the Geriatric Depressive Scale (GDS).27 ,28 This scale had been validated to have satisfactory accuracy in detecting poststroke depression in the Chinese population.29
Abbreviated National Institute of Health Stroke Scale
We assessed the motor outcome using Abbreviated National Institute of Health Stroke Scale (aNIHSS) that was previously applied in aSAH clinical trials.30 ,31 The aNIHSS is a measure of the level of facial and limb movement and strength and is composed of the facial palsy section (one score from 0 to 3) and the motor section (four separate scores for each limb, from 0 to 4). The aNIHSS ranges from 0 (normal) to 19 (no movement).
The statistical analyses were generated using SPSS for Windows V.15.0 (SPSS Inc., Chicago, Illinois, USA) and MedCalc V.126.96.36.199. Categorical data are given as numbers (percentages) unless otherwise specified; numerical data are given as medians and IQR. A difference with a p value of less than 0.05 was regarded as statistically significant.
Binary logistic regression analyses were performed to evaluate the predictors of functional outcomes and two or more domain deficits using the enter method, with the F probability of entry set at 0.05 and that of removal set at 0.10. All analyses passed the goodness of fit tests, which included Omnibus tests of model coefficients and the Hosmer and Lemeshow tests. The ORs with 95% CIs and the percentage accuracy of classifications (with cut value of 0.500) were calculated. Cox and Snell R2 and Nagelkerke R2 values provided an indication of the degree of variation in the dependent variable explained by the model (from a minimum value of 0 to a maximum value of approximately 1).
The reproducibility of assessments was not assessed because it was not the focus of this study and would have been impractical considering the study's design (possible rehearsal effect and additional inconvenience to patients and their families).
During the 26-month period, 168 aSAH patients, aged 21–75 years and admitted within 96 h of ictus, were recruited and consented to participate during the acute admission. The current cohort was an extension of our previous report cohort of 3-month outcome.8 Eighteen patients died before 1 year follow-up, 30 patients could not cooperate for assessments, and 120 patients completed the assessments at 1 year. The profiles of the recruited patients are shown in table 1. Compared to the patients who completed the assessments, the patients who were not assessed (due to death or not follow commands) were more likely to be of less years of formal education, poor admission World Federation of Neurosurgical Societies grade and have DCI.
Cognitive domain deficits
The prevalence of cognitive deficits in the five tested domains ranged from 7% to 15% (table 2). The highest prevalence was in visuospatial memory and skill, and the lowest prevalence was in verbal memory as well as attention and working memory. No adverse events were reported in relation to the assessments.
At 1 year, unfavourable outcome (mRS 3–5) was independently associated with number of cognitive domain deficits (OR, 2.3; 95% CI 1.4 to 3.8; p=0.002), aNIHSS score (OR, 2.1; 95% CI 1.1 to 4.0; p=0.021), and GDS score (OR, 1.24; 95% CI 1.1 to 1.3; p<0.001), which correctly classified 87.5% of cases. Unfavourable outcome (mRS 3–5) was also significantly associated with the presence of two or more domain deficits (OR, 8.8; 95% CI 1.9 to 39.4; p=0.005), after adjustments of aNIHSS and GDS scores.
At 1 year, dependent instrumental activity of daily living (IADL<15) was independently associated with number of cognitive domain deficits (OR, 1.8; 95% CI 1.1 to 2.9; p=0.015), aNIHSS score (OR, 1.9; 95% CI 1.0 to 3.5; p=0.038), and GDS score (OR, 1.2; 95% CI 1.1 to 1.2; p<0.001), which correctly classified 89.2% of cases. Dependency (IADL<15) was also significantly associated with the presence of two or more domain deficits (OR, 4.4; 95% CI 1.1 to 17.8; p=0.038), after adjustments of aNIHSS and GDS scores.
The presence of two or more domain deficits was independently associated with age (OR, 1.1; 95% CI 1.1 to 1.2; p<0.001) and delayed cerebral infarction (OR, 6.1; 95% CI 1.1 to 33.5; p=0.036), after adjustment for years of school education. Admission World Federation of Neurosurgical Societies Grade and mode of aneurysm treatment was not significantly associated with the presence of two or more domain deficits. The presence of any domain deficit was independently associated with age (OR, 1.06; 95% CI 1.01 to 1.12; p=0.023), after adjustment for years of school education. Aneurysm location was not a significant risk factor for cognitive impairment. The binary logistic regression model as a whole explained between 17% (Cox and Snell R2) and 32% (Nagelkerke R2) of variance in the presence of cognitive impairment and correctly classified 89.2% of cases.
We identified cognitive domain deficits in 7 to 15 percent of patients 1 year after an aSAH and 13% had two or more domain deficits. The commonest deficit (15%) was in visuospatial memory and skill, which was essential for recording information about one's environment and its spatial orientation, might impact on fall risk, and was related to activity of daily living (Barthel Index) at 3 months.3 ,7 ,32 Depending on the timing of assessments and definition, prevalence of visuospatial memory and skill domain deficits ranged from 14% to 49% in the literature.3 We reported a low (7%) verbal memory domain deficit at 1 year as compared to 14% to 61% in the literature.3 Verbal memory is key to language understanding and communication. The verbal memory finding should be further assessed with future hippocampal volume studies. In contrast to executive function and psychomotor speed domain deficit, attention and working memory domain deficits were less common (7%) than previously reported due to the more stringent criteria than reported cut-off scores in the tests employed (verbal and visual digit span forward and backward from the Chinese Wechsler Memory Scale).4 Our executive function and psychomotor speed domain and attention and working memory domain are considered by some authors as a broader category of executive function or cognitive ‘control’ (planning and organisation).
Upon systemic review of clinical prediction models for aSAH, it was noted that neither Glasgow Outcome Scale nor mRS were developed for use in SAH33 and their lack of sensitivity might explain the failure to show a benefit from the treatment of angiographic vasospasm and other interventions.34 Cognitive outcome measures, in conjunction with other outcome scales, would improve outcome assessments in SAH trials.
We showed that the presence of two or more cognitive domain deficits was associated with disability, as measured by mRS, and with IADL, as measured by Lawton IADL. Stroke-related brain injury often results in a combination of motor and cognitive impairments, and the presence of depression may impact on functional outcome. Although aNIHSS and GDS scores might not completely discriminate the effects or presence of any motor impairment or depression, we demonstrated that the impact of two or more cognitive domain deficits on functional outcomes was independent of aNIHSS and GDS scores. Whether cognitive rehabilitation and medical treatment such as cholinesterase inhibitors could improve cognitive function and neurological outcome should be further investigated.35
The findings of the current 1 year study cannot be directly compared with the 3 month Montreal Cognitive Assessment (MoCA) study results, as the definitions of cognitive impairment were different.8 In the 3 month MoCA study, the objective is to investigate for alternations in cut-off scores to improve sensitivity and specificity to predict functional outcome. Milder forms of cognitive impairment are less likely to be detected by the MoCA cut-off score 21/22.36 In the current 1 year outcome study, we employed average z-scores below 1.65 in two or more domains as cognitive impairment. Both studies pointed to the significance of cognitive impairment to functional and neurological outcome. Nevertheless, one must understand that cognitive impairment in relative isolation is devastating in working age people and mRS type outcome scales do not detect this important patient subgroup. Confidently identifying them with comprehensive cognitive testing, or better still, bedside or clinics screening is where further work is needed.
As in normal aging and neurodegenerative diseases, age was shown to be the consistent predictor of presence of any cognitive domain deficit at 1 year. Delayed cerebral infarction was the other important predictor of presence of two or more cognitive domain deficits, supporting the recommendation that delayed cerebral infarction be included as a therapeutic target for clinical trials targeting neuroprotection after aSAH.10 Our findings also echoed that presence of two or more domain deficits was a more sensitive cognitive outcome measure than presence of any domain deficit.20 Delayed cerebral infarction was shown to predict unfavourable outcome in terms of Extended Glasgow Outcome Scale, poor outcome in terms of mRS, and dependent activity of daily living in terms of Barthel Index at 6 months, after adjustments for other prognostic factors.37 In a recent meta-analysis, delayed cerebral infarction was predicted by haemorrhage load, clinical condition on admission, and other risk factors such as smoking.38 These data further supported the importance to target delayed cerebral infarction in future researches.
Limitations of this study
This study has several limitations. First, despite the fact that the neuropsychological battery was validated in the Chinese population with established norms, it might not be sensitive and comprehensive enough to detect all patients with cognitive impairment.39 Self-reported cognitive impairment was not assessed in the current study. Second, the functional and cognitive domain outcomes are dichotomised for analyses rather than using the weighted continuous scores. The clarity in understanding the meaning of the categories may reduce the chance of detecting statistical differences. Third, we employed self-report of IADL instead of performance-based assessment. Although self-reporting facilitated the inclusion into the current battery of assessments, reliance of self-report may be biased by depressive symptoms.40 Fourth, aNIHSS and GDS scores might not completely discriminate the effects or presence of any motor impairment or depression. Fifth, although the whole battery of assessments was not validated for aSAH patients, individual tests were validated and applicable to our local population. Sixth, early cerebral infarction and their causes were not included in the design of the current multicenter study. They should be considered in future study. Lastly, the battery of cognitive and functional assessments is tiring, although we offered a 5–10 min rest in the middle of the assessment sessions or divided the assessments between two consecutive days. Fatigue was not assessed during testing.
We were able to show that (1) Cognitive domain deficits occurred in 7% to 15% of the cohort and correlated with the disabilities and dependent instrumental activities of daily living at 1 year, independent of motor and depression scores; (2) Delayed cerebral infarction was an independent risk factor of cognitive impairment at 1 year.
Collaborators Cognitive Dysfunction after Aneurysmal Subarachnoid Hemorrhage Site Investigators: Prince of Wales Hospital: GKCW, WSP and VM; Kwong Wah Hospital: John Kwok, Kwong Yau Chan, Peter Woo, Calvin Mak and Peter Pang; Princess Margaret Hospital: Yin Chung Po, Tony Chan, Wai Kei Wong and Simon Lee; Pamela Youde Nethersole Eastern Hospital: Chi Keung Wong, Michael Lee, Rebecca Ng, Alain Wong and Vincent Pang.
Contributors GKCW, AW, and VM conceived and designed the study; Cognitive Dysfunction after Aneurysmal Subarachnoid Hemorrhage Investigators were responsible for patient recruitment; SWL and KN assessed the patients; GKCW and WSP supervised the study; GKCW drafted the manuscript; all authors critically reviewed and agreed to the final version of the manuscript.
Funding This study was supported by the Neurosurgery Research and Training Fund, the Chinese University of Hong Kong.
Competing interests None.
Ethics approval Joint NTEC-CUHK Clinical Ethics Committee.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement The data could be accessed with the corresponding authors upon agreement for collaboration.
Open Access This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
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