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Medicina 2019, 55(6), 311; https://doi.org/10.3390/medicina55060311
Prediction of the Lethal Outcome of Acute Recurrent Cerebral Ischemic Hemispheric Stroke
Department of Nervous Disease Zaporizhzhia State Medical University, 69035 Zaporizhzhia, Ukraine
Author to whom correspondence should be addressed.
Received: 26 April 2019 / Accepted: 20 June 2019 / Published: 25 June 2019
Background and objectives. Stroke-induced mortality is the third most common cause of death in developed countries. Intense interest has focused on the recurrent ischemic stroke, which rate makes up 30% during first 5 years after first-ever stroke. This work aims to develop criteria for the prediction of acute recurrent cerebral ischemic hemispheric stroke (RCIHS) outcome on the basis of comprehensive baseline clinical, laboratory, and neuroimaging examinations. Materials and Methods. One hundred thirty-six patients (71 males and 65 females, median age 74 (65; 78)) with acute RCIHS were enrolled in the study. All patients underwent a detailed clinical and neurological examination using National Institutes of Health Stroke Scale (NIHSS), computed tomography of the brain, hematological, and biochemical investigations. In order to detect the dependent and independent risk factors of the lethal outcome of the acute period of RCIHS, univariable and multivariable regression analysis were conducted. A receiver operating characteristic (ROC) analysis with the calculation of sensitivity and specificity was performed to determine the prediction variables. Results. Twenty-five patients died. The independent predictors of the lethal outcome of acute RCIHS were: Baseline NIHSS score (OR 95% CІ 1.33 (1.08–1.64), p = 0.0003), septum pellucidum displacement (OR 95% CI 1.53 (1.17–2.00), p = 0.0021), glucose serum level (OR 95% CI 1.28 (1.09–1.50), p = 0.0022), neutrophil-to-lymphocyte ratio (OR 95% CI 1.11 (1.00–1.21), p = 0.0303). The mathematical model, which included these variables was developed and it could determine the prognosis of lethal outcome of the acute RCIHS with an accuracy of 86.8% (AUC = 0.88 ± 0.04 (0.88–0.93), p < 0.0001).
Keywords:recurrent ischemic stroke; outcome; prognosis; NLR; glycemia; septum pellucidum; National Institutes of Health Stroke Scale (NIHSS)
Although stroke incidence, prevalence, mortality, and disability adjusted-life-year rates have declined over the last 20 years, the overall burden of stroke is still taking a lead position . The incidence of stroke recurrence is high despite developments in primary and secondary preventive treatment. The first five-year cumulative incidence of stroke recurrence varies between 16% and 30% in Western countries . Early recurrent stroke is relatively rare, but far more severe than first-ever stroke, is associated with longer duration of hospitalization and increased neurological disability, which makes this problem extremely relevant in medical, social, and economic aspects [3,4]. The importance of an early and reliable prognosis for recovery in patients with acute stroke is undisputed and crucial for both the treatment neurologist to optimize treatment and rehabilitation options as well as for the patient’s family [5,6].
Various prognostic indices derived from clinical features or patient characteristics and ancillary tests have been used to predict survival, discharge disposition, length of hospital stay, functional and vital outcomes. Multiple studies have proven that one of the factors, most widely accepted as prognostically helpful with I level of evidence, is baseline neurological status measured by the NIHSS [7,8,9,10,11]. Numerous studies identified a strong association between increasing age and unfavorable stroke outcome, which is independent of stroke severity, characteristics, or complication [12,13]. It was underlined that hyperglycemia on admission is associated with a worsened clinical outcome. Thus, according to Christensen H. and Boysen G. (2002), the increase in blood glucose was associated with stroke severity and short-term mortality, but not the outcome at three months . Certain information has also accumulated about influence of computed tomography (CT) findings, time to treatment and recanalization, current smoking, atrial fibrillation (AF), statin intake before stroke, and proinflammatory activation on the course and outcome of ischemic stroke (IS) [15,16,17,18].
There is lack of researchers dedicated to the short-term prognosis of recurrent IS outcome described in the literature, so this justifies the necessity of our investigation, which aims to develop criteria for predicting the lethal outcome of the acute period of recurrent cerebral ischemic hemispheric stroke (RCIHS) based on a comprehensive clinical and paraclinical investigations.
2. Materials and Methods
This prospective, cohort, and comparative hospital-based study was approved by the ethics committee of the Zaporizhzhia state medical university (code №7 form 27 October 2016) and was performed in accordance with the Declaration of Helsinki.
Inform consent was obtained during admission of the patient to the hospital. If patient was able to give informed consent, it was written by patient; if patient was not able to write, then oral informed consent in the presence of an independent witness was given by patient. If the patient was unable to give informed consent because of physical limitation (aphasia or consciousness disorder) it was obtained from an available legal guardian (written form) or, if there was no available legal guardian, then the patient was enrolled in the study if consent was signed by next of kin. Patient/person who signed the inform consent had the opportunity to revoke the informed consent at any time during investigation.
One hundred thirty-six patients (71 males and 65 females, median age 74 (65; 78)) with acute RCIHS were enrolled in the study. The patients’ inclusion to research was performed according to the following criteria: Men and women aged from 45 to 85 years, verified IS in the past, clinical and neuroimaging confirmations of acute RCIHS (a focal neurological deficit of sudden onset that persisted beyond 24 h as well as CT imaging indicating the presence of infarction in the area perfused by the middle cerebral artery (MCA)), atherothrombotic or cardioembolic subtypes of IS according to the Trial of Org 10172 in Acute Stroke Treatment (TOAST classification), first 24 h from RCIHS onset and signed informed consent of the patient‘s participation in the study.
The exclusion criteria were: Multiple ischemic strokes, hemorrhagic transformation of ischemic lesion, combined cerebral stroke, baseline NIHSS score ≥ 20, admission mRS score ≥ 3 (after first-ever stroke), presence of oncological and/or decompensated somatic pathology, anamnestic data of alcohol abuse, craniocerebral trauma, psychopathological syndrome.
We considered definition “recurrent cerebral ischemic hemispheric stroke” as any recurrent ischemic stroke occurring 24 h after the stroke onset in a different vascular region and any recurrent stroke occurring in the same region 21 days after the first-ever stroke. Affected hemispheres were defined as left and right hemisphere. Ipsilateral stroke was considered as RCIHS in the same vascular region, contralateral RCIHS–in the opposite vascular region regarding first stroke focus.
Lethal outcome (LO) of RCIHS was defined as stroke-induced mortality during the acute period of disease (during first 21 days of stroke).
All patients who survived after 21 days from stroke onset had a non-lethal outcome (NLO).
Neurological examination, neuroimaging, and laboratory investigations were performed at admission. The assessment of stroke severity was administered by an appropriately trained neurologist using the NIHSS. Brain CT was performed to evaluate the RCIHS localization, the infarct volume (IV), the presence of mass effect on the midline structures, the size and localization of the post-stroke cyst (a sign of a previously, first-ever IS). Infarct volume was calculated during CT examination by using the following formula: IV = (a × b × c × π)/6, where a, b, and c are the larger perpendicular diameters of the zone of hypodensity (cm). All CT evaluations were performed by the same neuroradiologist, who was blinded to the clinical results.
Upon admission, fasting blood samples were collected from the cubital vein to assess the levels of absolute white blood cells (WBC) and their subpopulations (absolute neutrophils count (ANC), absolute lymphocyte count (ALC), absolute monocyte count, (AMC)), glucose levels, prothrombin index, fibrinogen values in plasma, and the neutrophil-to-lymphocytic ratio (NLR).
2.2. Statistical Analyses
Statistical processing of the obtained results was performed using the software Statistica 13.0 (Software Inc., serial number JPZ804I382130ARCN10-J). Values were expressed as median and 25th–75th percentiles because of abnormally distributed variables (according to the Shapiro–Wilk criterion). The presence of intergroup differences in quantitative parameters was determined using the Mann–Whitney criterion. To assess the correlations between qualitative indicators Pearson χ2 criterion was used. In order to detect the dependent and independent risk factors of the LO of acute RCIHS, univariable and multivariable regression analysis were conducted. The predictive value of the indicators was evaluated using ROC analysis with the calculation of sensitivity and specificity. Area under curve (AUC) was calculated with 95% confidence interval (CI) for these variables and compared with each other. Probability (p) values of less than 0.05 were considered statistically significant.
3.1. Baseline Data of Participants in Comparison with the Stroke Outcome
Baseline characteristics of participants are summarized in Table 1. The study included 136 patients with RCIHS, among them 111 patients were survived (62 males and 49 females, median age 72.0 (64.0; 77.0) and 25 patients (9 males and 16 females, median age 76.0 (74.0; 78.0) died within first 21 days of disease. Patients from both groups did not differ in gender structure (62 (55.86%) males and 49 (44.14%) females with NLO versus 9 (36.00%) and 16 (64.00%) respectively with LO (χ² = 3.22, p = 0.2679). No differences were observed in affected hemisphere (65 (58.56%) patients with NLO had RCIHS in the left hemisphere versus 10 (40.00%) patients with LO, χ² = 2.84, p = 0.9188). Patients with LO had tendency to more frequent right hemisphere stroke localization (15 (60.00%) versus 46 (41.44%), χ² = 2.84, p = 0.0919). Cardioembolic subtype of RCIHS, diabetes mellitus, and AF were diagnosed among 15 (60.00%), 8 (32.00%), and 15 (60.00%) patients with LO respectively; overall, there was no significant intergroup difference in the parameters of stroke localization, lateralization, stroke subtypes, and co-morbidity pathology. Patients who had LO were elder than patients with NLO (76 (74; 78) versus 72.0 (64.0; 77.0), p = 0.0073. The median of the time interval between first-ever stroke and recurrent one among patients with LO was 12 (6; 12) months, that was significantly different from patients with NLO, who had RCIHS in 21 (11; 36) months (p = 0.0034).
Clinical and paraclinical characteristics of the general cohort patients as well as results of comparative analysis of neurological, neuroimaging, biochemical, and hematological parameters in comparison with the RCIHS outcome are presented in Table 2.
As shown in the Table 2, patients with LO upon admission, had significant intergroup difference in the following variables: NIHSS score (14.0 (12.0; 16.0) points versus 12.0 (10.0; 13.0) points, p = 0.0003) infarct volume (64,4 (31.9; 78.5) mL versus 32.4 (17.9; 56.9) mL, p = 0.0118), septum pellucidum displacement (6.0 (3.5; 9.5) mm versus 2.5 (2.0; 4.0) mm, p = 0.0009), glucose serum level (7.8 (6.7; 9.6) mmol/L versus 5.9 (5.0; 7.2) mmol/L p = 0.0024), WBC (9.3 (7.3; 12.0) G/L versus 7.6 (6.3; 9.4) G/L, p = 0.0132), ANC (7.5 (6.2; 10.8) G/L versus 5.6 (4.3; 7.6) G/l, p = 0.0013), NLR (8.2 (5.0; 12.9) versus 4.5 (2.8; 7.0), p = 0.0041).
3.2. Univariable and Multivariable Logistic Regression Analysis and Prediction Model Development
All patients had complete data. The strategy of logistic regression analysis was presented as follows: At the first stage, using a simple (univariable) logistic regression analysis, among all studied indicators, the potential predictors of the lethal outcome of the acute RCHIS (OR 95% CI, p ˂ 0.05) were identified; at the second stage, the previously obtained predictors were step by step included in the multivariable logistic regression model and among all obtained models, one was chosen, which was distinguished by the greatest accuracy in the classification of observations.
The results of the univariable and multivariable logistic regression analysis are summarized in the Table 3.
Univariable logistic regression analysis revealed that age of patients (OR 95% CI 1.09 (1.03–1.16), p = 0.0059), baseline NIHSS score (OR 95% CІ 1.37 (1.17–1.63), p = 0.0003), infarct volume (OR 95% CI 1.01 (1.00–1.02), p = 0.0181), septum pellucidum displacement (OR 95% CI 1.67 (1.31–2.15), p = 0.0001), epiphysis displacement (OR 95% CI 1.55 (1.20–2.00), p = 0.0008), glucose serum level (OR 95% CI 1.21 (1.06–1.38), p = 0.0057), ANC (OR 95% CI 1.11 (1.00–1.23), p = 0.0473), ALC (OR 95% CI 0.92 (0.86–0.96), p = 0.0042), and NLR (OR 95% CI 1.09 (1.09–1.17), p = 0.0019) were the main variables, associated with the lethal RCIHS outcome.
To find out independent risk factors, which are associated with lethal RCIHS outcome, the multivariable logistic regression analysis was performed.
It was found, that the baseline NIHSS score (OR 95% CІ 1.33 (1.08–1.64), p = 0.0003), septum pellucidum displacement (OR 1.53 95% CI 1.17–2.00, p = 0.0021), glucose serum level (OR 95% CI 1.28 (1.09–1.50), p = 0.0022), and NLR (OR 95% CI 1.11 (1.00–1.21), p = 0.0303) were independent risk factors which influenced on the stroke outcome.
Independent variables have been integrated into a prediction model of the following form: β = 0.29 × P1 + 0.42 × Р2 + 0.25 × Р3 + 0.10 × P4-8.37, where P1—baseline NIHSS score, Р2—septum pellucidum displacement, P3—baseline glucose serum level, P4—NLR.
Based on ROC-analysis, it was found that β > −1.18 is the integral predictor of LO of the acute RCIHS (AUC = 0.88 ± 0.04 (0.88–0.93), p < 0.0001) with high sensitivity (80.0%) and specificity (86.5%) (Figure 1).
The prediction accuracy of the developed mathematical model was 86.8%.
In this study, the predictors of LO and NLO were analyzed comprehensively and formed the prognostic model, which included baseline clinical, laboratory, and neuroimaging parameters.
The median of the time interval between first-ever stroke and recurrent one among patients with LO was 12.0 (6.0; 12.0) months, that was significantly different from patients with NLO, who had RCIHS in 21.0 (11.0; 36.0) months (p = 0.0034). This result is similar to data from many population-based studies dedicated to risk of recurrent stroke after a first-ever stroke and proved the hypothesis that the most “critical period” for recurrent stroke event with lethal outcome ranged from 30 days to 12 months [19,20,21,22].
Ischemic stroke patients with history of AF have repeatedly been shown to have higher baseline stroke severity, leading to greater disability and mortality compared to those without a history of AF We found out the tendency to higher fatality in patients with AF (60,00% vs. 39.64%). This result coincides with the opinion of Arboix A. et al. (2000) that AF was a clinical predictor of in-hospital mortality in IS patients . The same assumption about higher risk of early death in acute ischemic stroke patients with AF was described by Saxena R et al. .
Based on our investigation, it was found that age of patient negatively affected the outcome of RCIHS. Our results are in agreement with the data from many studies, which proved that age is a significant risk factor of poor stroke outcome. Fonarow G. et al. (2010) reported that the mean age of ≥74 years was found to be important determining factor related to stroke recurrence , which was in accordance with data from our study. It was shown, that elderly patients have worse stroke outcomes and they have lower ability for recovering [26,27,28,29]. This result may be due to the fact that neuronal plasticity of the brain declines with ageing in contrast with increasing comorbidity and medical complications; particularly, older patients are more likely to have preexisting diseases and disabilities which may hinder their recovery.
We confirmed the hypothesis about the influence of ischemic stroke volume on the stroke outcome, which was in accordance with the results of many studies [30,31,32,33,34]. Some scientists have proven that the prediction of clinical outcomes after ischemic stroke can be improved by using imaging parameters, such as the location and volume of the ischemic lesion. Gerhard Vogt et al. (2012) in a statistical regression model included the initial lesion size, which was a strong and independent predictor of stroke outcome.
We also considered the influence of the volume of post-stroke cyst on the RCIHS outcome; however, it was not proven in our study.
It was marked that severe middle cerebral artery stroke, accompanied by malignant edema, leads to midline brain shift, which is the common cause of high mortality . Based on both univariable and multivariable logistic regression analysis, we found that middle cerebral displacement, particularly displacement of septum pellucidum and epiphysis dislocation, were independent risk factors, associated with LO. This result is fully in line with W. T. Kimberly et al. (2018), who verified the association between midline shift and worse stroke outcome .
The baseline NIHSS score on admission is considered as the most important predictor of acute ischemic stroke outcome [37,38,39,40]. Our investigation also revealed that the severity of neurological deficits on admission assessed by NIHSS was an independent predictor of LO (OR 95% CІ 1.33 (1.08–1.64), p = 0.0003). Previously, Natalia S. Rost et al. (2016) reported that the NIHSS score appears to be a far more significant predictor than comorbidity score, which was thought to be an important outcome contributor .
High blood glucose levels in acute stroke patients is known to be related to initial neurological severity and poor outcome during the three months after stroke onset. Several studies reported that hyperglycemia after stroke is independently associated with poor functional outcome [41,42]. This study suggests that hyperglycemia has been significantly proven to be associated with LO. Our results are also similar to GLIAS (GLycemia in Acute Stroke) multicenter study where a high predictive value of an initial glucose serum levels in patients with IS was described . Obtained findings are also in line with the Sung J. et al. (2017) study where serum glucose concentration during hospitalization of a patient with IS are considered highly informative indicator for the determination of stroke outcome .
We established that ANC in patients with LO was significantly higher than in patients with NLO and was a significant predictor of the stroke outcome. This result is consistent with Fang Y.-N. et al. (2017) who found out that higher neutrophil count was significantly predictive for in-hospital mortality in patients after non-atrial fibrillation-caused ischemic stroke (OR 95% CI 0.081 (0.057–0.104), p ≤ 0.0001) .
According to our data, the median NLR among patients with LO was almost two times higher than in patients with NLO (8.2 (5.0; 12.9) vs. 4.5 (2.8; 7.0), p = 0.0041). Based on univariable (NLR (OR 1.09 95% CI 1.09–1.17, p = 0.0019)) and multivariable (NLR (OR 95% CI 1.11 (1.00–1.21), p = 0.0303) analysis, the NLR appears to play a significant role in mortality after a recurrent stroke and was marked as independent predictor of LO. Our finding supports the results of Celikbilek A. et al., where proinflammatory activation and its influence on the stroke outcome have been described, particularly that NLR was significantly correlated with unfavorable clinical outcome in patients after IS. It has been highlighted that NLR is a simple, inexpensive, and readily available marker for prognosis in acute IS . Tokgoz S. et al. (2014) demonstrated that NLR at the time of admission could be a predictor of short-term mortality regardless of infarct volume in IS patients . Chamorro A. and Hallenbeck J. (2006) described participation of the inflammatory response in all pathophysiological processes of acute IS and clarified that ischemic brain could induce the release of proinflammatory cytokines and recruitment of immune cells, which represent an important mechanism of secondary progression of brain lesion .
In numerous studies was described that dementia negatively affects both survival and functional outcomes after stroke [47,48]. However, in present investigation we did not study the cognitive status of the patient, but we are hypothesized the negative influence of cognitive impairments on outcome of RCHIS. In the previous works it was found out that recurrent stroke is accompanied by more frequent and severe cognitive impairments which associated with higher disability [49,50]. We completely support the idea of A. Subic. et al.  and Henon H. et al.  that suggested that dementia could be associated with more severe global vascular disease, and a higher risk of complications, or could be a worsening factor when an intercurrent disease occurs, either because of a limited ability to respond to illness or because less invasive treatments are prescribed to demented patients. According to Béjot Y. et al. , dementia after stroke was not independently associated with an increased risk of death at one year. It could be explained by a shorter time window to evaluate survival compared with that used in previous studies that addressed this topic. We suggest that detailed neuropsychological assessment of stroke patients could be the crucial in order to estimate the prognosis and program for secondary prevention as well as to find the optimal treatments and for stroke patients when they are not considered as candidates for crucial intervention or thrombolysis.
We would like to emphasize that psychosocial characteristics of stroke patients may also be important predictors of mortality, especially among elder patients, who have RCHIS more often than young patients. It was estimated a higher risk of mortality in people suffering from post-stroke depression (PSD), considering depressive symptoms occurring in the early stage after the acute event. Subjects with early PSD had a risk of death about 1.5 higher as compared with non-depressed individuals, considering both short- and long-term mortality [54,55,56]. Taking into account the strong association between depressive disorders and stroke mortality, we assume that PSD requires periodic clinical attention in the long term that should focus on patients at highest risk so that, earlier identification of post-stroke depression could lead to better treatment, recovery, and reduction of the expense of patient care.
During making a prognosis of stroke outcome it is important to consider the comorbidity pathology, particularly, heart dysfunction, cardiac remodeling, and atrial fibrillation which may all affect the stroke outcome [57,58].
It was reported that hyperthermia appears to correlate with poor outcome in stroke patients. Fever leads to cerebral edema, potentially reducing cerebral perfusion pressure, and enlargers the volume of ischemic injury. Weimar at al. presented data that fever of more than 38 °C within three days after stroke was one of the most important predictors for functional dependence or death [59,60].
Taking into account all mentioned above, in order to make a reliable prognosis of the RCHIS outcome, it is important to include in predictive models the wide spectrum of variables such as age, time-interval between first-ever stroke and the recurrent one, level of neurological deficiency, neuroimaging and laboratory data, comorbidity pathology, cognitive impairments and depressive disorders. Based on our findings and statistical analysis, we have developed the prediction mathematical model, which contains variable parameters and may be implemented in the routine clinical work of Stroke Unit to obtained high sensitivity (80.0%) and specificity (86.5%) prognosis of RCIHS outcome upon admission.
Initial level of neurological deficiency, baseline glucose serum level, NLR, and septum pellucidum displacement are independent variables and have the most significant influence on the lethal outcome of the acute recurrent cerebral ischemic hemispheric stroke. The developed model can be applied in clinical practice to make an individual approach for the patient’s treatment as well as enlarge the variety of prescribed drugs or crucial intervention with involvement of other specialists in order to improve the care of patients.
Conceptualization, O.K., A.K. and L.N.; Data curation, L.N.; Formal analysis, A.K. and L.N.; Funding acquisition, A.K. and L.N.; Investigation, L.N.; Methodology, O.K., A.K. and L.N.; Project administration, O.K.; Resources, L.N.; Software, L.N.; Supervision, O.K.; Writing—original draft, LN.; Writing—review & editing, O.K., A.K. and L.N.
This study is part of Ph.D. thesis of Liubov Novikova. This work has no external funding
Conflicts of Interest
The authors declare no conflict of interest.
- Feigin, V.L.; Roth, G.A.; Naghavi, M.; Parmar, P.; Krishnamurthi, R.; Chugh, S.; Mensah, G.A.; Norrving, B.; Shiue, I.; Ng, M.; et al. Global burden of stroke and risk factors in 188 countries, during 1990–2013: A systematic analysis for the global burden of disease study 2013. Lancet Neurol. 2016, 15, 913–924. [Google Scholar] [CrossRef]
- Kocaman, G.; Duru, H.; Kocer, A.; Asil, T. Recurrent ischemic stroke characteristics and assessment of sufficiency of secondary stroke prevention. Noro Psikiyatri Arsivi 2015, 52, 139–144. [Google Scholar] [CrossRef] [PubMed]
- Maier, I.L.; Bauerle, M.; Kermer, P.; Helms, H.-J.; Buettner, T. Risk prediction of very early recurrence, death and progression after acute ischaemic stroke. Eur. J. Neurol. 2012, 20, 599–604. [Google Scholar] [CrossRef] [PubMed]
- Chin, Y.Y.; Sakinah, H.; Aryati, A.; Hass, B.M. Prevalence, risk factors and secondary prevention of Stroke recurrence in eight countries from south, east and southeast asia: A scoping review. Med. J. Malays. 2018, 73, 90–99. [Google Scholar]
- Wouters, A.; Nysten, C.; Thijs, V.; & Lemmens, R. Prediction of outcome in patients with acute ischemic stroke based on initial severity and improvement in the first 24 h. Front. Neurol. 2018, 9, 1–6. [Google Scholar] [CrossRef] [PubMed]
- Sablot, D.; Belahsen, F.; Vuillier, F.; Cassarini, J.F.; Decavel, P.; Tatu, L.; Moulin, T.; Medeiros de Bustos, E. Predicting acute ischaemic stroke outcome using clinical and temporal thresholds. ISRN Neurol. 2011, 2011, 354642. [Google Scholar] [CrossRef]
- Hand, P.; Wardlaw, J.; Lindley, R.; Keir, S. Prediction of outcome after stroke. Lancet 2001, 358, 1552–1553. [Google Scholar] [CrossRef]
- Gajurel, B.P.; Dhungana, K.; Parajuli, P.; Karn, R.; Rajbhandari, R.; Kafle, D.; Oli, K.K. The national institute of health stroke scale score and outcome in acute ischemic stroke. J. Inst. Med. 2014, 36, 9–13. [Google Scholar]
- Tian, H.; Parsons, M.W.; Levi, C.R.; Lin, L.; Aviv, R.I.; Spratt, N.J.; Bivard, A. Influence of occlusion site and baseline ischemic core on outcome in ischemic stroke patients. Neurology 2019, 92, e2626–e2643. [Google Scholar] [CrossRef]
- German Stroke Study Collaboration. Predicting outcome after acute ischemic stroke: An external validation of prognostic models. Neurology 2004, 62, 581–585. [Google Scholar] [CrossRef]
- Fonarow, G.C.; Saver, J.L.; Smith, E.E.; Broderick, J.P.; Kleindorfer, D.O.; Sacco, R.L.; Pan, W.; Olson, D.M.; Hernandez, A.F.; Peterson, E.D.; et al. Relationship of national institutes of health stroke scale to 30-day mortality in medicare beneficiaries with acute ischemic stroke. J. Am. Heart Assoc. 2012, 1, 42–50. [Google Scholar] [CrossRef] [PubMed]
- Knoflach, M.; Matosevic, B.; Rücker, M.; Furtner, M.; Mair, A.; Wille, G.; Zangerle, A.; Werner, P.; Ferrari, J.; Schmidauer, C.; et al. Austrian stroke unit registry collaborators. functional recovery after ischemic stroke—A matter of age: Data from the austrian stroke unit registry. Neurology 2012, 78, 279–285. [Google Scholar] [CrossRef] [PubMed]
- Black-Schaffer, R.M.; Winston, C. Age and functional outcome after stroke. Top. Stroke Rehabil. 2004, 11, 23–32. [Google Scholar] [CrossRef] [PubMed]
- Capes, S.E.; Hunt, D.; Malmberg, K.; Pathak, P.; Gerstein, H.C. Stress hyperglycemia and prognosis of stroke in nondiabetic and diabetic patients: A systematic overview. Stroke 2001, 32, 2426–2432. [Google Scholar] [CrossRef] [PubMed]
- Reid, J.M.; Gubitz, G.J.; Dai, D.; Kydd, D.; Eskes, G.; Reidy, Y.; Christian, C.; Counsell, C.E.; Dennis, M.; Phillips, S.J. Predicting functional outcome after stroke by modelling baseline clinical and CT variables. J. Age Ageing 2010, 39, 360–366. [Google Scholar] [CrossRef] [PubMed]
- Zhang, J.; Ren, Q.; Song, Y.; He, M.; Zeng, Y.; Liu, Z.; Xu, J. Prognostic role of neutrophil–lymphocyte ratio in patients with acute ischemic stroke. Medicine 2017, 96, e8624. [Google Scholar] [CrossRef]
- Nardi, K.; Milia, P.; Eusebi, P.; Paciaroni, M.; Caso, V.; Agnelli, G. Predictive value of admission glucose serum levelon short-term mortality in acute cerebral ischemia. J. Diabetes Complic. 2012, 26, 70–76. [Google Scholar] [CrossRef]
- Lee, S.-J.; Hong, J.M.; Lee, S.E.; Kang, D.R.; Ovbiagele, B.; Demchuk, A.M.; Lee, J.S. Association of fibrinogen level with early neurological deterioration among acute ischemic stroke patients with diabetes. BMC Neurol. 2017, 17, 101. [Google Scholar] [CrossRef]
- Lovett, J.K.; Coull, A.J.; Rothwell, P.M. Early risk of recurrence by subtype of ischemic stroke in population-based incidence studies. Neurology 2004, 62, 569–573. [Google Scholar] [CrossRef]
- Hankey, G.J.; Jamrozik, K.; Broadhurst, R.J.; Forbes, S.; Burvill, P.W.; Anderson, C.S. Five-year survival after first-ever stroke and related prognostic factors in the Perth community stroke study. Stroke 2000, 31, 2080–2086. [Google Scholar] [CrossRef]
- Hardie, K.; Hankey, G.J.; Jamrozik, K.; Broadhurst, R.J.; Anderson, C.S. Ten-year risk of first recurrent stroke and disability after first-ever stroke in the perth community stroke study. Stroke 2004, 35, 731–735. [Google Scholar] [CrossRef] [PubMed]
- Eriksson, S.-E.; Olsson, J.-E. Survival and recurrent strokes in patients with different subtypes of stroke: A fourteen-year follow-up study. Cerebrovasc. Dis. 2001, 12, 171–180. [Google Scholar] [CrossRef] [PubMed]
- Arboix, A.; García-Eroles, L.; Massons, J.B.; Oliveres, M.; Pujades, R.; Targa, C. Atrial fibrillation and stroke: Clinical presentation of cardioembolic versus atherothrombotic infarction. Int. J. Cardiol. 2000, 73, 33–42. [Google Scholar] [CrossRef]
- Saxena, R.; Lewis, S.; Berge, E.; Sandercock, P.A.; Koudstaal, P.J. Risk of early death and recurrent stroke and effect of heparin in 3169 patients with acute ischemic stroke and atrial fibrillation in the international stroke trial. Stroke 2001, 32, 2333–2337. [Google Scholar] [CrossRef] [PubMed]
- Fonarow, G.C.; Reeves, M.J.; Zhao, X.; Olson, D.M.; Smith, E.E.; Saver, J.L.; Schwamm, L.H. Get with the guidelines-stroke steering committee and investigators. Age-related differences in characteristics, performance measures, treatment trends, and outcomes in patients with ischemic stroke. Circulation 2010, 121, 879–891. [Google Scholar] [CrossRef] [PubMed]
- Everink, I.H.; van Haastregt, J.C.; van Hoof, S.J.; Schols, J.M.; Kempen, G.I. Factors influencing home discharge after inpatient rehabilitation of older patients: A systematic review. BMC Geriatr. 2016, 16, 5. [Google Scholar] [CrossRef] [PubMed]
- Mutai, H.; Furukawa, T.; Araki, K.; Misawa, K.; Hanihara, T. Factors associated with functional recovery and home discharge in stroke patients admitted to a convalescent rehabilitation ward. Geriatr. Gerontol. Int. 2012, 12, 215–222. [Google Scholar] [CrossRef]
- Ng, Y.S.; Stein, J.; Ning, M.; Black-Schaffer, R.M. Comparison of clinical characteristics and functional outcomes of ischemic stroke in different vascular territories. Stroke 2007, 38, 2309–2314. [Google Scholar] [CrossRef]
- Ostwald, S.K.; Swank, P.R.; Khan, M.M. Predictors of functional independence and stress level of stroke survivors at discharge from inpatient rehabilitation. J. Cardiovasc. Nurs. 2008, 23, 371–377. [Google Scholar] [CrossRef]
- Albers, G.W.; Thijs, V.N.; Wechsler, L.; Kemp, S.; Schlaug, G.; Skalabrin, E.; Bammer, R.; Kakuda, W.; Lansberg, M.G.; Shuaib, A.; et al. Magnetic resonance imaging profiles predict clinical response to early reperfusion: The diffusion and perfusion imaging evaluation for understanding stroke evolution (DEFUSE) study. Ann. Neurol. 2006, 60, 508. [Google Scholar] [CrossRef]
- Yoo, A.J.; Verduzco, L.A.; Schaefer, P.W.; Hirsch, J.A.; Rabinov, J.D.; González, R.G. MRI-based selection for intra-arterial stroke therapy: Value of pretreatment diffusion-weighted imaging lesion volume in selecting patients with acute stroke who will benefit from early recanalization. Stroke 2009, 40, 2046–2054. [Google Scholar] [CrossRef] [PubMed]
- Lansberg, M.G.; Straka, M.; Kemp, S.; Mlynash, M.; Wechsler, L.R.; Jovin, T.G.; Wilder, M.J.; Lutsep, H.L.; Czartoski, T.J.; Bernstein, R.A.; et al. MRI profile and response to endovascular reperfusion after stroke (DEFUSE 2): A prospective cohort study. Lancet Neurol. 2012, 11, 860–867. [Google Scholar] [CrossRef]
- Schiemanck, S.K.; Kwakkel, G.; Post, M.W.; Prevo, A.J. Predictive value of ischemic lesion volume assessed with magnetic resonance imaging for neurological deficits and functional outcome poststroke: A critical review of the literature. Neurorehabil. Neural Repair 2006, 20, 492–502. [Google Scholar] [CrossRef] [PubMed]
- Vogt, G.; Laage, R.; Shuaib, A.; Schneider, A. VISTA Collaboration. Initial lesion volume is an independent predictor of clinical stroke outcome at day 90: An analysis of the virtual international stroke trials archive (VISTA) database. Stroke 2012, 43, 1266–1272. [Google Scholar] [CrossRef] [PubMed]
- Wijdicks, E.F.M.; Diringer, M.N. Middle cerebral artery territory infarction and early brain swelling: Progression and effect of age on outcome. Mayo Clin. Proc. 1998, 73, 829–836. [Google Scholar] [CrossRef]
- Kimberly, W.T.; Dutra, B.G.; Boers, A.M.M.; Alves, H.C.B.R.; Berkhemer, O.A.; Van den Berg, L. Association of reperfusion with brain edema in patients with acute ischemic stroke. JAMA Neurol. 2018, 453, E1–E9. [Google Scholar] [CrossRef] [PubMed]
- Ji, R.; Du, W.; Shen, H.; Pan, Y.; Wang, P.; Liu, G.; Wang, Y.; Li, H.; Zhao, X.; Wang, Y. Web-based tool for dynamic functional outcome after acute ischemic stroke and comparison with existing models. BMC Neurol. 2014, 14, 214. [Google Scholar] [CrossRef]
- Sato, S.; Toyoda, K.; Uehara, T.; Toratani, N.; Yokota, C.; Moriwaki, H.; Naritomi, H.; Minematsu, K. Baseline NIH stroke scale score predicting outcome in anterior and posterior circulation strokes. Neurology 2008, 70, 2371–2377. [Google Scholar] [CrossRef]
- Schlegel, D.; Kolb, S.J.; Luciano, J.M.; Tovar, J.M.; Cucchiara, B.L.; Liebeskind, D.S.; Kasner, S.E. Utility of the NIH stroke scale as a predictor of hospital disposition. Stroke 2003, 34, 134–137. [Google Scholar] [CrossRef]
- Rost, N.S.; Bottle, A.; Lee, J.M.; Randall, M.; Middleton, S.; Shaw, L.; Thijs, V.; Rinkel, G.J.; Hemmen, T.M. Global Comparators Stroke GOAL Collaborators. Stroke severity is a crucial predictor of outcome: An international prospective validation study. J. Am. Heart Assoc. 2016, 5, e002433. [Google Scholar] [CrossRef]
- Fuentes, B.; Castillo, J.; San Jose, B.; Leira, R.; Serena, J.; Vivancos, J. The prognostic value of capillary glucose levels in acute stroke: The glycemia in acute stroke (GLIAS) study. Stroke 2008, 40, 562–568. [Google Scholar] [CrossRef] [PubMed]
- Sung, J.Y.; Chen, C.I.; Hsieh, Y.C.; Chen, Y.R.; Wu, H.C.; Chan, L.; Hu, C.J.; Hu, H.H.; Chiou, H.Y.; Chi, N.F. Comparison of admission random glucose, fasting glucose, and glycated hemoglobin in predicting the neurological outcome of acute ischemic stroke: A retrospective study. Peer J. 2017, 5, e2948. [Google Scholar] [CrossRef] [PubMed]
- Fang, Y.N.; Tong, M.S.; Sung, P.H.; Chen, Y.L.; Chen, C.H.; Tsai, N.W.; Huang, C.J.; Chang, Y.T.; Chen, S.F.; Chang, W.N.; et al. Higher neutrophil counts and neutrophil-to-lymphocyte ratio predict prognostic outcomes in patients after non-atrial fibrillation-caused ischemic stroke. Biomed. J. 2017, 40, 154–162. [Google Scholar] [CrossRef] [PubMed]
- Celikbilek, A.; Ismailogullari, S.; Zararsiz, G. Neutrophil to lymphocyte ratio predicts poor prognosis in ischemic cerebrovascular disease. J. Clin. Lab. Anal. 2014, 28, 27–31. [Google Scholar] [CrossRef] [PubMed]
- Tokgoz, S.; Keskin, S.; Kayrak, M.; Seyithanoglu, A.; Ogmegul, A. Is neutrophil/lymphocyte ratio predict to short-term mortality in acute cerebral infarct independently from infarct volume? J. Stroke Cerebrovasc. Dis. 2014, 23, 2163–2168. [Google Scholar] [CrossRef]
- Chamorro, A.; Hallenbeck, J. The harms and benefits of inflammatory and immune responses in vascular disease. J. Stroke 2006, 37, 291–293. [Google Scholar] [CrossRef]
- Saposnik, G.; Kapral, M.K.; Cote, R.; Rochon, P.A.; Wang, J.; Raptis, S.; Mamdani, M.; Black, S.E. Is pre-existing dementia an independent predictor of outcome after stroke? A propensity score-matched analysis. J. Neurol. 2012, 259, 2366–2375. [Google Scholar] [CrossRef]
- Mellon, L.; Brewer, L.; Hall, P.; Horgan, F.; Williams, D.; Hickey, A. Cognitive impairment six months after ischaemic stroke: A profile from the ASPIRE-S study. BMC Neurol. 2015, 15, 1–9. [Google Scholar] [CrossRef]
- Pendlebury, S.T.; Rothwell, P.M. Prevalence, incidence, and factors associated with pre-stroke and post-stroke dementia: A systematic review and meta-analysis. Lancet Neurol. 2009, 8, 1006–1018. [Google Scholar] [CrossRef]
- Henon, H.; Pasquier, F.; Leys, D. Poststroke dementia. Cerebrovasc. Dis. 2006, 22, 61–70. [Google Scholar] [CrossRef]
- Subic, A.; Cermakova, P.; Norrving, B.; Winblad, B.; von Euler, M.; Kramberger, M.G.; Eriksdotter, M.; Garcia-Ptacek, S. Management of acute ischaemic stroke in patients with dementia. J. Int. Med. 2017, 281, 348–364. [Google Scholar] [CrossRef] [PubMed]
- Henon, H.; Durieu, I.; Lebert, F.; Pasquier, F.; Leys, D. Influence of prestroke dementia on early and delayed mortality in stroke patients. J. Neurol. 2003, 250, 10–16. [Google Scholar] [CrossRef] [PubMed]
- Béjot, Y.; Jacquin, A.; Rouaud, O.; Durier, J.; Aboa-Eboulé, C.; Hervieu, M.; Giroud, M. One-year survival of demented stroke patients: Data from the dijon stroke registry, France (1985–2008). Eur. J. Neurol. 2011, 19, 712–717. [Google Scholar] [CrossRef] [PubMed]
- Bartoli, F.; Di Brita, C.; Crocamo, C.; Clerici, M.; Carrà, G. Early post-stroke depression and mortality: meta-analysis and meta-regression. Front. Psychiatr. 2018, 9, 1–7. [Google Scholar] [CrossRef] [PubMed]
- Horackova, K.; Kopecek, M.; Machů, V.; Kagstrom, A.; Aarsland, D.; Motlova, L.B.; Cermakova, P. Prevalence of late-life depression and gap in mental health service use across European regions. Eur. Psychiatr. 2019, 57, 19–25. [Google Scholar] [CrossRef] [PubMed]
- Jørgensen, T.S.; Wium-Andersen, I.K.; Wium-Andersen, M.K.; Jørgensen, M.B.; Prescott, E.; Maartensson, S.; Kragh-Andersen, P.; Osler, M. Incidence of depression after stroke, and associated risk factors and mortality outcomes, in a large cohort of Danish patients. JAMA Psychiatr. 2016, 73, 1032–1040. [Google Scholar] [CrossRef] [PubMed]
- Corso, G.; Bottacchi, E.; Tosi, P.; Caligiana, L.; Lia, C.; Veronese Morosini, M.; Dalmasso, P. Outcome predictors in first-ever ischemic stroke patients: A population-based study. Int. Sch. Res. Not. 2014, 2014, 1–8. [Google Scholar] [CrossRef] [PubMed]
- Cuadrado-Godia, E.; Ois, A.; Roquer, J. Heart failure in acute ischemic stroke. Curr. Cardiol. Rev. 2010, 6, 202–213. [Google Scholar] [CrossRef] [PubMed]
- Greer, D.M.; Funk, S.E.; Reaven, N.L.; Ouzounelli, M.; Uman, G.C. Impact of fever on outcome in patients with stroke and neurologic injury: A comprehensive meta-analysis. Stroke 2008, 39, 3029–3035. [Google Scholar] [CrossRef]
- Weimar, C.; Ziegler, A.; König, I.R.; Diener, H.-C. Predicting functional outcome and survival after acute ischemic stroke. J. Neurol. 2002, 249, 888–895. [Google Scholar] [CrossRef]
Figure 1. ROC-curve of predictive model.
Table 1. Baseline characteristics of participants in comparison with the stroke outcome.
(N = 136)
((N = 111)
|(N = 25)|
|Men||71 (52.21%)||62 (55.86%)||9 (36.00%)|
|Women||65 (47.79%)||49 (44.14%)||16 (64.00%)|
|Lateralization of RCIHS||0.75||0.3878|
|Ipsilateral carotid area||61 (44.85%)||55 (49.55%)||10 (40.00%)|
|Contralateral carotid area||75 (55.15%)||56 (50.45%)||15 (60.00%)|
|Stroke classification according TOAST||3.44||0.0635|
|Atherothrombotic RCIHS||77 (56.62%)||67 (60.36%)||10(40.00%)|
|Cardioembolic RCIHS||59 (43.38%)||44 (39.64%)||15 (60.00%)|
|Left||75 (55.15%)||65 (58.56%)||10 (40.00%)|
|Right||61 (44.85%)||46 (41.44%)||15 (60.00%)|
|Diabetes mellitus||31 (22.79%)||23 (20.72%)||8 (32.00%)||1.48||0.2246|
|Atrial fibrillation||59 (43.38%)||44 (39.64%)||15 (60.00%)||3.44||0.0635|
Table 2. Clinical and paraclinical characteristics of general cohort of patients with recurrent cerebral hemispheric ischemic stroke and comparative analysis of clinical neurological, computed tomography, biochemical, and hematological parameters in comparison with the outcome of acute period of disease.
(Me (Q1; Q3)
((N = 135)
((N = 111)
((N = 25)
|NIHSS score at baseline, points||12.0 (10.0; 14.0)||12.0 (10.0; 13.0)||14.0 (12.0; 16.0)||0.0003|
|Infarct volume, mL||35.7 (22.4; 65.3)||32.4 (17.9; 56.9)||64,4 (31.9; 78.5)||0.0118|
|The volume of the post-stroke cyst, mL||9.2 (1.9; 19.8)||8.3 (2.1; 18.4)||12.9 (3.7; 56.3)||0.4224|
|Septum pellucidum displacement, mm||3.5 (2.0; 6.0)||2.5 (2.0; 4.0)||6.0 (3.5; 9.5)||0.0009|
|Epiphysis displacement, mm||3.0 (2.0; 4.0)||3.0 (3.0; 4.0)||3.5 (2.0; 4.5)||0.9798|
|Glucose serum level, mmol/L||6.13 (5.0; 7.84)||5.9 (5.0; 7.2)||7.8 (6.7; 9.6)||0.0024|
|Fibrinogen, g/L||3.5 (2.9; 4.4)||3.5 (2.9; 4.4)||3.5 (3.3; 4.2)||0.4699|
|Prothrombin index, %||90.0 (85.5; 95.0)||90.0 (86.0; 96.0)||88.0 (86.0; 94.0)||0.5392|
|Hematocrit, %||41.0 (37.5; 45.0)||41.0 (37.5; 45.0)||41.0 (38.0; 45.0)||0.8460|
|White blood cells, G/L||7.8 (6.4; 10.2)||7.6 (6.3; 9.4)||9.3 (7.3; 12.0)||0.0132|
|Absolute neutrophil count, G/L||6.1 (4.5; 8.2)||5.6 (4.3; 7.6)||7.5 (6.2; 10.8)||0.0013|
|Absolute lymphocyte count, G/L||1.3 (0.8; 1.9)||1.3 (0.9; 1.9)||0.9 (0.7; 1.6)||0.0861|
|Absolute monocyte count, G/L||0.4 (0.3; 0.6)||0.4 (0.2; 0.6)||0,4 (0.3; 0.6)||0.5534|
|Neutrophil-to-Lymphocyte Ratio||4.8 (2.9; 8.1)||4.5 (2.8; 7.0)||8.2 (5.0; 12.9)||0.0041|
Table 3. The results of logistic regression analysis.
|Variables||Univariable Logistic Regression Model||Multivariable Logistic Regression Model|
|OR (95% CI)||P||OR (95% CI)||P|
|Age, years||1.09 (1.03–1.16)||0.0059|
|NIHSS score at baseline, points||1.37 (1.17–1.63)||0.0003||1.33 (1.08–1.64)||<0.0001|
|Infarct volume, mL||1.01 (0.01–1.02)||0.0181|
|Septum pellucidum displacement, mm||1.67 (1.31–2.15)||0.0001||1.53 (1.17–2.00)||0.0021|
|Epiphysis displacement, mm||1.55 (1.20–2.00)||0.0008|
|Glucose serum level, mmol/L||1.21 (1.06–1.38)||0.0057||1.28 (1.09–1.50)||0.0022|
|Absolute neutrophils count, G/L||1.11 (1.00–1.23)||0.0473|
|Absolute lymphocyte count, G/L||0.92 (0.86–0.97)||0.0042|
|Neutrophil-to-Lymphocyte Ratio||1.09 (1.02–1.17)||0.0119||1.11 (1.00–1.21)||0.0303|
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