Literature DB >> 34800279

Endovascular Treatment in Acute Ischemic Stroke with Large Vessel Occlusion According to Different Stroke Subtypes: Data from ANGEL-ACT Registry.

Xiaochuan Huo1, Dapeng Sun1, Baixue Jia1, Xu Tong1, Anxin Wang2, Ning Ma1, Feng Gao1, Dapeng Mo1, Gaoting Ma1, Sheyar Amin3, Zeguang Ren4, Zhongrong Miao5.   

Abstract

INTRODUCTION: Endovascular treatment's (EVT) safety and efficacy have been proven in treating acute ischemic stroke (AIS) due to large vessel occlusion (LVO). However, limited data exist in different stroke subtypes. We aimed to investigate the differences in efficacy and safety of EVT for acute LVO according to different stroke subtypes.
METHODS: A total of 1635 AIS patients with LVO undergoing EVT from a prospective cohort of the Endovascular Treatment Key Technique and Emergency Work Flow Improvement of Acute Ischemic Stroke (ANGEL-ACT) registry were classified into three types according to the Trial of ORG 10172 in Acute Stroke Treatment (TOAST) criteria. We compared the primary outcome: 90-day modified Rankin Scale (mRS) score, the secondary outcomes: 90-day mRS (0-1, 0-2, and 0-3), successful recanalization (mTICI 2b/3), and complete recanalization (mTICI 3), and the safety outcomes: death within 90 days, parenchymal hemorrhage (PH), and symptomatic intracranial hemorrhage (SICH) among the three subtypes of stroke patients. Then, multivariable logistic regression models adjusting for potential baseline-confounding variables to determine the associations between stroke subtypes and safety and efficacy endpoints were performed. Finally, we performed subgroup analyses to explore discrepancies in the relationships.
RESULTS: EVT of cardioembolic LVO (CE-LVO) had a higher rate of mTICI 3 (71.7% vs. 65.9% and 63.2%; P = 0.024) and a higher rate of PH (13.8% vs. 5.4% and 6.7%; P < 0.001) when compared to other stroke subtypes. Even multivariable analysis demonstrated that CE-LVO was associated with mTICI 3 [adjusted odds ratio (OR), 1.50 (95% CI 1.04-2.17)] and PH [adjusted OR, 1.97 (95% CI 1.09-3.55)]. However, the 90-day mRS distribution and 90-day mRS (0-1, 0-2, and 0-3) did not differ among the stroke subtypes, and nor did the SICH (P > 0.05).
CONCLUSIONS: Functional outcomes were similar among different stroke subtypes. Despite a higher rate of complete recanalization, there is an increased risk of parenchymal hemorrhage in CE-LVO. TRIAL REGISTRATION: Clinical trial registration number: NCT03370939.
© 2021. The Author(s).

Entities:  

Keywords:  Efficacy; Endovascular treatment; Outcomes; Safety; TOAST classification

Year:  2021        PMID: 34800279      PMCID: PMC8857367          DOI: 10.1007/s40120-021-00301-z

Source DB:  PubMed          Journal:  Neurol Ther        ISSN: 2193-6536


Key Summary Points

Introduction

Endovascular treatment (EVT) has become the standard management for acute ischemic stroke caused by large vessel occlusions (LVO) [1]. However, different stroke subtypes have different risk factors, clinical features, and prognoses [Stroke. 2020 ">2-6]. Determining the stroke subtypes is crucial to optimizing and improving the safety and efficacy of EVT. Due to the ease of use and the reliability in the clinic, the Trial of ORG 10172 in Acute Stroke Treatment (TOAST) classification has been widely used to classify the ischemic stroke subtype [5, 7]. Many researchers have undertaken a range of studies to evaluate the clinical features and prognosis of acute ischemic stroke (AIS) patients undergoing EVT based upon the TOAST classification [2–4, 8, 9]. However, those studies were mainly in the western population, and there is still a lack of data from Asian populations, and the proportions of stroke etiologic subtypes are different among different ethnicities and countries [10, 11] Therefore, in this large registry study of an Asian population, mainly Chinese, we evaluate the safety and efficacy of EVT in different stroke subtypes to provide further information to supplement the global data.

Methods

Study Population

The present study enrolled 1793 consecutive patients with AIS caused by acute large vessel occlusion undergoing EVT in 111 hospitals in China between November 2017 and March 2019. The inclusion and exclusion criteria followed the previous study [12]. Patients who underwent EVT were included in the study. The exclusion criteria were as follows: (1) patients without an EVT record; (2) patients without a TOAST assessment; (3) patients with small-artery occlusion lacunar (SAA). The study protocol was approved by the Ethics Committees of Beijing Tiantan Hospital and the ethics committees of all participating centers. The number of the approval: KY2017-048–01. The study procedures were in accordance with the 1964 Helsinki declaration and its later amendments. Subjects or their legally authorized representatives provided written informed consent.

Data Collection and Outcomes Measurement

Information on demographics, risk factors, medical history, National Institutes of Health Stroke Scale (NIHSS) score on admission, location of infarct cerebral tissue (anterior/posterior circulation), procedural characteristics (general anesthesia, GPIIb/IIIa receptor inhibitor, stent retriever, intra-arterial thrombolysis, balloon angioplasty, and stenting), number of mechanical thrombectomies, and the time points of working flow were prospectively collected. Baseline computed tomography (CT)/magnetic resonance (MR), CTA/MRA, DSA images during EVT, and follow-up head CT or MRI were evaluated by an imaging core laboratory blinded to clinical data and outcomes. All imaging was independently assessed by two neuroradiologists, with a third available for adjudication when needed. Alberta Stroke Program Early CT Score (ASPECTS) for anterior circulation strokes and posterior circulation Alberta Stroke Program Early CT Score for posterior circulation strokes were assessed on baseline CT [13, 14]. Final modified thrombolysis in cerebral ischemia score (mTICI) were assessed on the DSA [15]. We considered functional outcome at the 90-day (90-day mRS) primary endpoint. Meanwhile, we considered mRS 0–1, mRS 0–2, and mRS 0–3, successful recanalization (mTICI 2b/3), and complete recanalization (mTICI 3) as the secondary outcomes. Any symptomatic ICH (SICH) per Heidelberg Bleeding Classification within 24 h post-EVT [16], and parenchymal hemorrhage (PH) according to ECASS II Classification [17], and death within 90 days were considered safety endpoints.

Classification of the Stroke Subtypes

We categorized the stroke subtypes according to the TOAST classification [18]. Based on imaging and angiographic findings, we classified the stroke subtypes into large artery atherosclerosis (LAA), CE cardioembolism, and SUE/SOE stroke of unknown etiology/stroke of other determined etiology. We determined the classification through reconstructed images acquired from preprocedural CT angiography (CTA) or MR angiography (MRA), confirmed by intraprocedural digital subtraction angiography (DSA). We defined LAA as the presence of a lesion with significant stenosis (> 50%) or occlusion of the involved artery due to atherosclerosis during the EVT procedure. A history of intermittent claudication, transient ischemic attack in the same vascular territory, a carotid bruit, or diminished pulses help to support the clinical diagnosis. We defined CE as the arterial occlusions caused by embolus arising from the cardiac as either a high- or medium-risk. Potential large-artery atherosclerotic sources of thrombosis or embolism should be eliminated. In SUE, the stroke etiology could not be determined even after extensive evaluation was performed. Patients with two or more potential causes of stroke, which lead to physicians being unable to make final diagnoses, were also included in this group. Meanwhile, patients with rare causes of stroke, such as nonatherosclerotic vasculopathy, hypercoagulable states, or hematologic disorders, were categorized as SOE. These diagnoses had to be confirmed by diagnostic studies such as angiography or blood tests. In addition, cardiac sources of embolism and large-artery atherosclerosis had to be excluded by other studies [18].

Statistical Analysis

We used proportions for categorical variables, and median with interquartile range (IQR) for the continuous variables. We compared the baseline characteristics among groups using the Pearson χ2 test or the Kruskal–Wallis test. Variables with P < 0.05 in the univariable analysis were selected as the confounders into the multivariable logistic regression model. Then, we performed logistic regression to calculate the odds ratios (OR) or common OR with 95% confidence intervals (CI). We performed further subgroup analysis to discriminate the relationship between stroke subtypes and efficacy and safety outcomes in a different stratification. Significance level was set to P = 0.05 (2-sided). We used SAS software v.9.4 (SAS Institute, Cary, NC, USA) to conduct the statistical analyses.

Results

Baseline Characteristics

We enrolled 1793 AIS patients who underwent EVT. Of these, 158 patients were eliminated based on the exclusion criteria (Fig. 1). The baseline characteristics, procedure characteristics, and outcomes of the enrolled patients are presented in Table 1. LAA-LVO was the most prevalent etiology (n = 861) group, followed by CE-LVO (n = 573) and SUE/SOE-LVO (n = 201). Patients with CE-LVO were older, more likely to be female, and had higher NIHSS scores on admission than those in the LAA-LVO and SUE/SOE-LVO groups (Table 1). Patients with LAA-LVO had higher comorbidities, such as current smoking habits, hypertension, diabetes mellitus, hyperlipidemia, and prior stroke compared with patients with CE-LVO and SUE/SOE-LVO. Atrial fibrillation was highest in the CE-LVO group, and systolic blood pressure (SBP) on admission was highest in the LAA-LVO group. We identified higher anticoagulants in the CE-LVO group than the other two groups, but we noted higher use of antiplatelet agents in the SUE/SOE-LVO group. CE-LVO was more frequently found in the anterior circulation, while LAA-LVO and SUE/SOE-LVO were more frequent in the posterior circulation.
Fig. 1

Flow chart of patient selection. EVT endovascular treatment, SAA small-artery occlusion lacunar, LAA large-artery atherosclerosis, CE cardioembolism, SUE/SOE stroke of unknown etiology/stroke of other determined etiology, LVO large vessel occlusion

Table 1

Baseline characteristics and outcome of different stroke subtypes

VariablesTotal (n = 1635)LAA-LVO (n = 861)CE-LVO (n = 573)SUE/SOE-LVO (n = 201)P
Baseline clinical parameters
 Age, median(IQR)65 (55–73)64 (55–71)69 (62–77)59 (48–67) < 0.001
 Male, n (%)1097 (67.1)682 (79.2)277 (48.3)138 (68.7) < 0.001
Premorbid mRSa, n (%)0.481
 mRS 01414 (86.5)737 (85.6)498 (86.9)179 (89.5)
 mRS 1193 (11.8)109 (12.7)64 (11.2)20 (10.0)
 mRS 227 (1.7)15 (1.7)11 (1.9)1 (0.5)
 Current smoking, n (%)550 (33.6)377 (43.8)97 (16.9)76 (37.8) < 0.001
SBP, median(IQR)145 (130–160)149 (134–165)145 (130–160)140 (127–158) < 0.001
Admission NIHSSb, median (IQR)16 (11–21)15 (11–21)17 (13–21)14 (11–20) < 0.001
ASPECTSc, median (IQR)9 (7–10)8 (7–10)10 (7–10)10 (8–10) < 0.001
Comorbidities
 Hypertension, n (%)930 (56.9)530 (61.6)313 (54.6)87 (43.3) < 0.001
 Diabetes mellitus, n (%)283 (17.3)169 (19.6)88 (15.4)26 (12.9)0.024
 Hyperlipidemia, n (%)148 (9.1)91 (10.6)47 (8.2)10 (5.0)0.031
 Atrial fibrillation, n (%)500 (30.6)63 (7.3)418 (73.0)19 (9.5) < 0.001
 Prior stroke, n (%)360 (22.0)196 (22.8)122 (21.3)42 (20.9)0.740
Pretreatment
Prior use of antiplatelet agents, n (%)270 (16.5)147 (17.1)78 (13.6)45 (22.4)0.013
Prior use of anticoagulants, n (%)66 (4.0)10 (1.2)51 (8.9)5 (2.5) < 0.001
Bridging IVT, n (%)474 (29.0)243 (28.2)169 (29.5)62 (30.9)0.722
Procedural parameters
Occlusion location, n (%) < 0.001
 Anterior circulation1273 (77.9)620 (72.0)503 (87.8)150 (74.6)
 Posterior circulation362 (22.1)241 (28.0)70 (12.2)51 (25.4)
 General anesthesia, n (%)651 (39.8)364 (42.3)212 (37.0)75 (37.3)0.100
 GP IIb/IIIa receptor inhibitor, n (%)858 (52.5)586 (68.1)204 (35.6)68 (33.8) < 0.001
 Stent retriever as first-line, n (%)1092 (66.8)534 (62.0)411 (71.7)147 (73.1) < 0.001
 Direct aspiration as first-line, n (%)100 (6.1)39 (4.5)50 (8.7)11 (5.5)0.005
 Direct aspiration + stent retriever as first-line168 (10.3)74 (8.6)80 (14.0)14 (7.0)0.001
 IAT, n (%)136 (8.3)75 (8.7)31 (5.4)30 (14.9) < 0.001
 Rescue balloon/stenting angioplasty, n (%)234 (14.3)191 (22.2)18 (3.1)25 (12.4) < 0.001
 MT times, median (IQR)1 (1–2)1 (1–2)2 (1–3)1 (1–2) < 0.001
 FPR, n (%)803 (49.1)424 (49.3)278 (48.5)101 (50.3)0.909
 Intraprocedural embolization, n (%)80 (4.9)29 (3.4)43 (7.5)8 (4.0)0.002
Time-metric parameters
 OTDd, median (IQR), min150 (63–287)164.5 (68–305)135 (60–260)160 (66–275)0.030
 DTPe, median (IQR), min120 (80–178)127 (89–190)115 (75–161)115.5 (78–170) < 0.001
 Procedure durationf, median (IQR), min85 (53–128)88 (53–130)80 (50–118)90 (57.5–144.5)0.018
Primary outcome
 90-day mRS, median (IQR)3 (0–5)3 (0–4)3 (0–5)2 (0–4)0.002
Secondary outcomes
 90-day mRS 0–1g, n (%)688 (42.6)388 (45.4)204 (36.2)96 (49.0) < 0.001
 90-day mRS 0–2g, n (%)753 (46.7)419 (49.1)232 (41.1)102 (52.0)0.004
 90-day mRS 0–3g, n (%)919 (56.9)499 (58.4)296 (52.5)124 (63.3)0.014
mTICI, n (%)0.006
 mTICI 0–1106 (6.5)58 (6.7)31 (5.4)17 (8.5)
 mTICI 2a68 (4.2)27 (3.1)32 (5.6)9 (4.5)
 mTICI 2b356 (21.8)209 (24.3)99 (17.3)48 (23.9)
 mTICI 31105 (67.6)567 (65.9)411 (71.7)127 (63.2)
 Successful recanalization, n (%)1461 (89.4)776 (90.1)510 (89.0)175 (87.1)0.423
 Complete recanalization, n (%)1105 (67.6)567 (65.9)411 (71.7)127 (63.2)0.024
Safety outcomes
 Death within 90 days, n (%)211 (13.1)97 (11.4)85 (15.1)29 (14.8)0.095

 PHh

n (%)

135 (8.5)45 (5.4)77 (13.8)13 (6.7) < 0.001
 SICHh, n (%)102 (6.5)40 (4.8)52 (9.5)10 (5.2)0.002
 SAHI, n (%)2 (0.1)1 (0.1)1 (0.2)00.845
 IVHI, n (%)7 (0.4)3 (0.4)3 (0.5)1 (0.5)0.654

LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, SD standard deviation, SBP systolic blood pressure, IQR interquartile range, NIHSS National Institutes of Health Stroke Scale score, ASPECTS Alberta Stroke Program Early CT score, OTD onset-to-door, DTP door-to-puncture, PTR puncture-to-recanalization, IVT intravenous thrombolysis, IAT intraarterial thrombolysis, MT menchanial thrombectomy, FPR first pass recanalization, SICH symptomatic intracranial hemorrhage, PH parenchymal hemorrhage, mRS modified Rankin score, IVH intraventricular hemorrhage, OTD onset to door, DTP door to puncture

a1 missing data

b 7 missing data

c12 missing data

d36 missing data

e125 missing data

f1 missing data

g21 missing data

h55 missing data

I40 missing data

Flow chart of patient selection. EVT endovascular treatment, SAA small-artery occlusion lacunar, LAA large-artery atherosclerosis, CE cardioembolism, SUE/SOE stroke of unknown etiology/stroke of other determined etiology, LVO large vessel occlusion Baseline characteristics and outcome of different stroke subtypes PHh n (%) LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, SD standard deviation, SBP systolic blood pressure, IQR interquartile range, NIHSS National Institutes of Health Stroke Scale score, ASPECTS Alberta Stroke Program Early CT score, OTD onset-to-door, DTP door-to-puncture, PTR puncture-to-recanalization, IVT intravenous thrombolysis, IAT intraarterial thrombolysis, MT menchanial thrombectomy, FPR first pass recanalization, SICH symptomatic intracranial hemorrhage, PH parenchymal hemorrhage, mRS modified Rankin score, IVH intraventricular hemorrhage, OTD onset to door, DTP door to puncture a1 missing data b 7 missing data c12 missing data d36 missing data e125 missing data f1 missing data g21 missing data h55 missing data I40 missing data EVT of CE-LVO had a higher rate of complete recanalization (71.7% vs. 65.9% and 63.2%; P = 0.024) compared to LAA-LVO and SUE/SOE-LVO. Moreover, we observed higher PH (13.8% vs. 5.4% and 6.7%; P < 0.001) and SICH (9.5% vs. 4.8% and 5.2%; P = 0.002) rate in the CE-LVO group compared to LAA-LVO and SUE/SOE-LVO. However, no significant difference regarding the incidence of subarachnoid hemorrhage (SAH) and intraventricular hemorrhage among groups (P > 0.05). We also identified lower mRS 0–1, 0–2, and 0–3 at 90 days in the CE-LVO group than with the other two groups (P < 0.05 for all) (Fig. 2). Stent retriever as first-line, direct aspiration as first-line and direct aspiration + stent retriever as first-line were higher in this group (P < 0.001). We also noted that CE-LVO required more retrieval attempts than the other two-stroke subtypes (2 vs. 1 and 1; P < 0.001). However, we observed a higher rate of used GP IIb/IIIa receptor inhibitors in LAA-LVO (68.1% vs. 35.6% and 33.8%; P < 0.001). Time from onset to door was longer in patients with LAA-LVO than CE-LVO and SUE/SOE-LVO (164.5 vs. 135 and 160 min; P = 0.03), as was the time from door to puncture (127 vs. 115 and 115 min; P < 0.001). However, the time from puncture to recanalization was longer in SUE/SOE-LVO than LAA-LVO and CE-LVO (90 vs. 88 and 80 min; P = 0.018).
Fig. 2

Shift on 90-day mRS score stratified by TOAST classification. LAA large-artery atherosclerosis, CE cardioembolism, SUE/SOE stroke of unknown etiology/stroke of other determined etiology, LVO large vessel occlusion, mRS modified Rankin Scale

Shift on 90-day mRS score stratified by TOAST classification. LAA large-artery atherosclerosis, CE cardioembolism, SUE/SOE stroke of unknown etiology/stroke of other determined etiology, LVO large vessel occlusion, mRS modified Rankin Scale CE-LVO was associated with complete recanalization after adjustment for potential confounders compared with LAA-LVO [adjusted OR, 1.50 (95% CI 1.04–2.17), P = 0.031]. Consistently, CE-LVO was also associated with parenchymal hemorrhage when compared to LAA-LVO [adjusted OR, 1.97 (95% CI 1.09–3.55), P = 0.025]. However, we did not observe any association between stroke subtypes and 90-day mRS and mRS0-1, mRS0-2, and mRS0-3 even after adjustment for potential confounders (P > 0.05 for all). Subgroup analyses showed no significant association between stroke subtypes and 90-day mRS score and SICH when we stratified the age, gender, NIHSS score on admission, the use of anesthesia, the involved circulation system, time workflow, and successful recanalization status (P > 0.05 for all) (Tables 2, 3, 4).
Table 2

Adjusted OR/HR of safety and efficacy outcome according to different stroke subtypes

OutcomesGroupsunadjusted OR/HR (95% CI)P valueAdjusted OR/HR (95% CI)P value
90-day mRSa, median (IQR)LAA-LVORefRef
CE-LVO1.39(1.15–1.68)0.0061.05(0.79–1.41)0.727
SUE/SOE-LVO0.99(0.75–1.30)0.9430.95(0.69–1.30)0.746
90-day mRS 0–1a, n (%)LAA-LVORefRef
CE-LVO0.68(0.55–0.85)0.0010.91(0.64–1.30)0.603
SUE/SOE-LVO1.15(0.85–1.57)0.3691.19(0.82–1.73)0.366
90-day mRS 0–2a, n (%)LAA-LVORefRef
CE-LVO0.73(0.59–0.90)0.0031.05(0.74–1.49)0.775
SUE/SOE-LVO1.13(0.83–1.54)0.4521.23(0.84–1.78)0.288
90-day mRS 0–3a, n (%)LAA-LVORefRef
CE-LVO0.79(0.63–0.97)0.0271.31(0.89–1.93)0.946
SUE/SOE-LVO1.23(0.89–1.69)0.2150.99(0.70–1.40)0.174
Successful recanalization, n (%)LAA-LVORefRef
CE-LVO2.82(1.92–4.14) < 0.0011.02(0.58–1.79)0.951
SUE/SOE-LVO1.26(0.67–2.39)0.4750.91(0.50–1.64)0.743
Complete recanalization, n (%)LAA-LVORefRef
CE-LVO1.32(1.05–1.66)0.0201.50(1.04–2.17)0.031
SUE/SOE-LVO0.89(0.65–1.23)0.4740.96(0.65–1.41)0.830
Death within 90 days, n (%)LAA-LVORefRef
CE-LVO1.39(1.01–1.89)0.0411.09(0.67–1.79)0.724
SUE/SOE-LVO1.36(0.87–2.12)0.1831.47(0.86–2.50)0.155
SICHb, n (%)LAA-LVORefRef
CE-LVO2.08(1.36–3.19)0.0011.24(0.63–2.45)0.531
SUE/SOE-LVO1.08(0.53–2.20)0.8290.87(0.38–1.98)0.741
PHc, n (%)LAA-LVORefRef
CE-LVO2.82(1.92–4.14) < 0.0011.97(1.09–3.55)0.025
SUE/SOE-LVO1.26(0.67–2.39)0.4751.04(0.51–2.13)0.919

LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, SICH symptomatic intracranial hemorrhage, PH parenchymal hemorrhage, mRS modified rankin score

a21 missing data

b55 missing data

b40 missing data

Table 3

Subgroup analysis regarding 90-day mRSa of different stroke subtypes

VariablesNumAdjusted OR and 95% CIP for interaction
LAA-LVO (reference)CE-LVOSUE/SOE-LVO
Age
 Age < 6577110.79(0.50–1.26)0.89(0.60–1.31)0.169
 Age ≥ 6584311.22(0.84–1.78)0.78(0.46–1.31)
Gender
 Male108511.04(0.72–1.50)0.94(0.65–1.36)0.430
 Female52911.02(0.63–1.65)0.91(0.50–1.65)
NIHSS
 NIHSS ≤ 1577311.06(0.67–1.65)1.00(0.64–1.59)0.532
 NIHSS > 1584110.99(0.68–1.45)0.84(0.54–1.30)
Anesthesia
 GA64010.97(0.60–1.57)0.95(0.56–1.60)0.552
 LA97411.08(0.75–1.55)0.91(0.61–1.37)
Occlusion location
 Anterior circulation125811.04(0.76–1.42)0.90(0.63–1.30)0.244
 Posterior circulation35611.27(0.55–2.94)0.76(0.39–1.51)
OTD (min)
 OTD ≤ 270119211.10(0.78–1.54)0.94(0.65–1.35)0.906
 OTD > 27042210.97(0.56–1.68)0.84(0.44–1.60)
DTP (min)
 DTP ≤ 9058010.84(0.54–1.30)0.79(0.48–1.30)0.422
 DTP > 90103411.20(0.83–1.74)1.19(0.81–1.76)
Procedure duration (min)
 Procedure duration ≤ 9088410.90(0.61–1.32)0.83(0.53–1.30)0.484
 Procedure duration > 9073011.40(0.89–2.18)1.16(0.73–1.82)
Successful recanalization
 Yes144711.01(0.74–1.38)0.96(0.69–1.35)0.159
 No16712.83(1.16–6.91)1.47(0.54–4.02)

LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, NIHSS National Institutes of Health Stroke Scale score, GA general anesthesia, LA local anesthesia, OTD onset to door, DTP door to puncture

a21 missing data

Table 4

Subgroup analysis regarding SICHa of different stroke subtypes

VariablesNumAdjusted OR and 95% CIP for interaction
LAA-LVO (reference)CE-LVOSUE/SOE-LVO
Age
 Age < 6576011.16(0.39–3.42)0.45(0.15–1.34)0.586
 Age ≥ 6582011.37(0.54–3.46)1.38(0.35–5.41)
Gender
 Male106811.23(0.50–3.03)0.63(0.21–1.89)0.571
 Female51211.54(0.46–5.13)1.80(0.44–7.35)
NIHSS
 NIHSS ≤ 1576111.39(0.49–3.97)0.67(0.21–2.16)0.960
 NIHSS > 1581910.93(0.37–2.40)1.01(0.32–3.60)
Anesthesia
 GA62310.76(0.29–2.01)0.82(0.23–2.98)0.895
 LA95411.67(0.62–4.46)0.81(0.24–2.74)
Occlusion location
 Anterior circulation123510.06(0.01–3.41)1.90(0.03–105.68)0.775
 Posterior circulation34511.40(0.69–2.84)0.86(0.36–2.05)
OTD (min)
 OTD ≤ 270116111.94(0.88–4.30)1.31(0.53–3.24)0.256
 OTD > 27041910.38(0.08–1.69)0.12(0.01–1.40)
DTP (min)
 DTP ≤ 9056412.86(0.81–10.09)1.24(0.28–5.39)0.275
 DTP > 90101611.05(0.45–2.46)1.04(0.40–2.73)
Procedure duration (min)
 Procedure duration ≤ 9085811.41(0.44–4.51)1.47(0.35–6.13)0.517
 Procedure duration > 9072211.15(0.47–2.80)0.95(0.34–2.66)
Successful recanalization
 Yes141011.27(0.58–2.78)0.97(0.39–2.43)0.896
 No17010.89(0.07–10.72)0.35(0.02–7.51)

LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, NIHSS National Institutes of Health Stroke Scale score, GA general anesthesia, LA local anesthesia, OTD onset to door, DTP door to puncture, PTR puncture to recanalization

a55 data were missing

Adjusted OR/HR of safety and efficacy outcome according to different stroke subtypes LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, SICH symptomatic intracranial hemorrhage, PH parenchymal hemorrhage, mRS modified rankin score a21 missing data b55 missing data b40 missing data Subgroup analysis regarding 90-day mRSa of different stroke subtypes LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, NIHSS National Institutes of Health Stroke Scale score, GA general anesthesia, LA local anesthesia, OTD onset to door, DTP door to puncture a21 missing data Subgroup analysis regarding SICHa of different stroke subtypes LAA Large-artery atherosclerosis, CE cardioembolism, SOE stroke of other determined etiology, SUE stroke of undetermined etiology, LVO large vessel occlusion, NIHSS National Institutes of Health Stroke Scale score, GA general anesthesia, LA local anesthesia, OTD onset to door, DTP door to puncture, PTR puncture to recanalization a55 data were missing

Discussion

In our study, the functional outcome from EVT did not differ among stroke subtypes. Different characteristics in each stroke subtype might affect the outcome of EVT. We also found an increasing risk of bleeding despite complete recanalization in a patient with the CE stroke subtype. Several factors might account for this finding, such as CE-LVO patients were older, had a higher rate of atrial fibrillation, and presented with a higher NIHSS score, which implies a larger ischemic area. Our result was not in line with the previous study, which reported that EVT showed different efficacy in different stroke subtypes [2]. Our study showed that the stroke subtype did not withhold the benefit of EVT. This result might be attributed to the higher successful recanalization rate among stroke subtypes in the present study compared with Tiedt et al. [2], although we did not assess this difference statistically. The previous study reported higher efficacy of EVT in CE-LVO, which might be attributed to several factors, including (1) thrombus composition, which may determine the success of thrombectomy [19], and (2) the complexity of the atherosclerotic lesion, which may impede technical access to the occlusion site [2, 20]. In addition, CE-LVO was presented more in their study when compared with non-CE or LAA-LVO, which may bias the actual result. However, the higher number of LAA-LVO in the current study may also contribute to a biased result. However, the significant difference between groups regarding the baseline has been adjusted in our multivariate analysis, which can reduce the probability of a biased result due to the unproportionate number of patients between groups. Different nature characteristics of the lesion among stroke subtypes need different EVT strategies. LAA-LVO are relatively more complex than CE-LVO [21, 22], as our study, and previously reported literature demonstrated that LAA-LVO often presented with a longer duration of the recanalization time than CE-LVO [23-31]. Nevertheless, the complexity of the atherosclerotic lesion did not withhold achieving successful recanalization, as rescue therapy, such as the use of GP IIb/IIIa receptor inhibitors, could be given during EVT. The efficacy of GP IIb/IIIa receptor inhibitors in AIS has been reported previously [32-34]. Consistently, we noted higher use of GP IIb/IIIa receptor inhibitors in the LAA-LVO group. Furthermore, this might also explain the higher recanalization rate in LAA-LVO in the present study. A noteworthy finding from the current study is an increased risk of bleeding despite complete recanalization in the CE-LVO group. The underlying mechanism remains unclear. However, the greater severity of strokes in CE-LVO presenting with higher NIHSS scores than other stroke subtypes may partially explain this finding. Moreover, CE-LVO is often related to a more extensive core infarct and less penumbra [35, 36]. In addition, early reperfusion might also contribute to an increase in PH in CE-LVO [37], as the onset to door and door to puncture time was shorter compared with other stroke subtypes. Although recanalization represents a powerful predictor of stroke outcomes [38], this should also warn us of the possibility of reperfusion injury, which might exacerbate the outcomes. Thus, precaution and intensive management are needed to reduce the mortality and morbidity risks. There is still an ongoing debate whether “complete” recanalization (TICI 3) or “successful” recanalization (TICI 2b/3) should be achieved. This finding also has an important message: restoring brain perfusion with recanalization does not mean that the occluded vessel should be completely recanalized. Further studies to evaluate the extent of recanalization in CE-LVO are urgently needed. Our study has several limitations. First, the retrospective nature of the present study, and the lack of a control group. A further randomized controlled trial is needed to assess any intention to treat. Second, this classification only can be applied after the complete diagnostic work-up. Therefore, the value of such a classification to assess acute stroke therapeutic options remains to be elucidated. Third, the present study lacked further angiographic assessment in different stroke subtypes, such as the collateral status and ratio of the core ischemic area to the penumbra. However, the strengths of our study included a large sample size and the use of nationwide collected data. Nevertheless, this study was limited to Chinese populations, and the stroke subtype’s proportion differs among ethnicities and countries. Therefore, this result cannot be generalized to the global population.

Conclusions

Our nationwide real-world registry data provide evidence for a higher rate of complete recanalization and increased risk of PH in CE-LVO and confirmed the stroke subtypes as a determinant of EVT safety and efficacy. Further research should focus on the extent of EVT in this stroke subtype.
Functional outcomes were similar among different stroke subtypes.
Endovascular treatment for large vessel occlusion due to cardioembolism (CE-LVO) had a higher rate of complete recanalization and parenchymal hemorrhage than other stroke subtypes.
CE-LVO patients were older, had a higher rate of atrial fibrillation, and presented with a higher National Institutes of Health Stroke Scale (NIHSS) score which implies a larger ischemic area.
  1 in total

1.  Response by Tiedt and Wollenweber to Letter Regarding Article, "Stroke Etiology Modifies the Effect of Endovascular Treatment in Acute Stroke".

Authors:  Steffen Tiedt; Frank A Wollenweber
Journal:  Stroke       Date:  2020-06-22       Impact factor: 7.914

  1 in total
  2 in total

1.  Early Stroke Prediction Methods for Prevention of Strokes.

Authors:  Mandeep Kaur; Sachin R Sakhare; Kirti Wanjale; Farzana Akter
Journal:  Behav Neurol       Date:  2022-04-11       Impact factor: 3.112

2.  Predicting futile recanalization, malignant cerebral edema, and cerebral herniation using intelligible ensemble machine learning following mechanical thrombectomy for acute ischemic stroke.

Authors:  Weixiong Zeng; Wei Li; Kaibin Huang; Zhenzhou Lin; Hui Dai; Zilong He; Renyi Liu; Zhaodong Zeng; Genggeng Qin; Weiguo Chen; Yongming Wu
Journal:  Front Neurol       Date:  2022-09-28       Impact factor: 4.086

  2 in total

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