SYSTEMATIC REVIEW article

Front. Neurol., 22 June 2021

Sec. Stroke

Volume 12 - 2021 | https://doi.org/10.3389/fneur.2021.687134

Comparison of Risk Factors, Safety, and Efficacy Outcomes of Mechanical Thrombectomy in Posterior vs. Anterior Circulation Large Vessel Occlusion

  • 1. Department of Neurology & Stroke, Eberhard-Karls University, Tübingen, Germany

  • 2. Hertie Institute for Clinical Brain Research, Eberhard-Karls University, Tübingen, Germany

  • 3. Department of Neuroradiology, Eberhard-Karls University, Tübingen, Germany

Abstract

Background and Purpose: It is believed that stroke occurring due to posterior circulation large vessel occlusion (PCLVO) and that occurring due to anterior circulation large vessel occlusion (ACLVO) differ in terms of their pathophysiology and the outcome of their acute management in relation to endovascular mechanical thrombectomy (MT). Limited sample size and few randomized controlled trials (RCTs) with respect to PCLVO make the safety and efficacy of MT, which has been confirmed in ACLVO, difficult to assess in the posterior circulation. We therefore conducted a meta-analysis to study to which extent MT in PCLVO differs from ACLVO.

Materials and Methods: We searched the databases PubMed, Cochrane, and EMBASE for studies published between 2010 and January 2021, with information on risk factors, safety, and efficacy outcomes of MT in PCLVO vs. ACLVO and conducted a systematic review and meta-analysis; we compared baseline characteristics, reperfusion treatment profiles [including rates of intravenous thrombolysis (IVT) and onset-to-IVT and onset-to-groin puncture times], recanalization success [Thrombolysis In Cerebral Infarction scale (TICI) 2b/3], symptomatic intracranial hemorrhage (sICH), and favorable functional outcome [modified Rankin Score (mRS) 0–2] and mortality at 90 days.

Results: Sixteen studies with MT PCLVO (1,172 patients) and ACLVO (7,726 patients) were obtained from the search. The pooled estimates showed higher baseline National Institutes of Health Stroke Scale (NIHSS) score (SMD 0.32, 95% CI 0.15–0.48) in the PCLVO group. PCLVO patients received less often IVT (OR 0.65, 95% CI 0.53–0.79). Onset-to-IVT time (SMD 0.86, 95% CI 0.45–1.26) and onset-to-groin puncture time (SMD 0.59, 95% CI 0.33–0.85) were longer in the PCLVO group. The likelihood of obtaining successful recanalization and favorable functional outcome at 90 days was comparable between the two groups. PCLVO was, however, associated with less sICH (OR 0.56, 95% CI 0.37–0.85) but higher mortality (OR 1.92, 95% CI 1.46–2.53).

Conclusions: This meta-analysis indicates that MT in PCLVO may be comparably efficient in obtaining successful recanalization and 90 day favorable functional outcome just as in ACLVO. Less sICH in MT-treated PCLVO patients might be the result of the lower IVT rate in this group. Higher baseline NIHSS and longer onset-to-IVT and onset-to-groin puncture times may have contributed to a higher 90 day mortality in PCLVO patients.

Introduction

Intravenous thrombolysis (IVT) has become the mainstay of acute intervention in ischemic stroke presenting within 4.5 h of symptom onset when other contraindications have been excluded (1). However, IVT has been shown to be less effective in proximal large vessel occlusion (LVO), mainly in the terminal internal carotid artery, proximal middle cerebral artery, and basilar artery, than in more distal occlusion (2). Therefore, clinical worsening is to be expected in many cases of LVO unless endovascular mechanical thrombectomy (MT) is initiated (2).

The second-generation MT devices that were introduced in the last decade have shown superiority to first-generation MT devices and, hence, have been widely used in MT since then (35). Consequently, it could be argued that most studies on MT conducted before the surge of second-generation MT devices could have been compromised by the inferiority of first-generation MT devices. Nowadays, MT in LVO may be conducted up to 24 h without waiting for IVT outcome (68).

To date, many randomized controlled trials (RCTs) have reported the safety and efficacy of MT in acute ischemic stroke due to anterior circulation LVO (ACLVO). However, there is lack of substantial data on the safety and efficacy of MT in posterior circulation LVO (PCLVO) (5, 6, 9).

Posterior circulation stroke is defined as the development of ischemic lesions occurring in the vascular territories supplied by branches of the vertebrobasilar arterial system (10). It occurs in about 20–25% of all ischemic strokes (11, 12), and neurological deficits caused by PCLVO have been described as catastrophic with severe disability and death occurring in about 68% of patients (13, 14). The rarity of PCLVO poses the challenge of obtaining a significant sample size for conducting observational and controlled trials in comparison to anterior circulation stroke.

MT in ACLVO has been accepted in most clinical settings as the best way for obtaining recanalization, and therefore, the randomization of patients with PCLVO into groups including no-MT is considered mostly unethical. Among the very few RCTs that focused on posterior circulation stroke, the Basilar Artery Occlusion Endovascular Intervention vs. Standard medical Treatment (BEST) RCT was terminated due to loss of equipoise, which resulted from a high crossover rate and was topped by a small sample size. This trial, however, reported no difference in favorable outcomes of MT patients and those receiving only standard medical treatment including IVT (15). On the other hand, a larger non-randomized cohort study, the Endovascular Treatment for Acute Basilar Artery Occlusion (BASILAR) study, reported that MT within 24 h of estimated occlusion time in basilar artery occlusion patients is associated with better functional outcomes and reduced mortality (16). Data on the safety and efficacy of MT in PCLVO from the randomized controlled Basilar Artery International Cooperation Study (BASICS) and Basilar Artery Occlusion Chines Endovascular Trial (BAOCHE) trials are pending (17, 18). Available data show a strong probability of differences in MT in PCLVO and ACLVO, which may contribute to their safety and efficacy outcomes (19, 20). An improved functional outcome and reduced mortality in moderate-to-severe ACLVO stroke patients have been shown to be dependent on a small infarct core, moderate-to-good collateral circulation, and rapid MT (21). Some PCLVO studies have associated MT with a poor outcome despite having a high recanalization rate, and this has raised interest in possible predicting factors of outcome in PCLVO such as initial stroke symptom severity, collateral status, age, infarct volume, stroke etiology, respiratory insufficiency, and other comorbidities (2226). Bad outcome could also be a consequence of a delayed treatment since symptoms of posterior circulation stroke are known to be often fluctuating with about 55–63% cases of prodromal transient ischemic attack in spite of a persistent vessel occlusion (14).

Due to the conflicting nature of available studies, we conducted a systematic review and meta-analysis on studies published from 2010 to January 2021 with data comparing MT in PCLVO vs. ACLVO in order to assess the differences of risk factors, as well as safety and efficacy outcomes between both circulations.

Materials and Methods

This study was conducted in accordance with the guidelines of the Preferred Reporting Item for Systematic Reviews and Meta-Analysis (PRISMA) (27).

Data Source and Searching

We conducted a database search in PubMed, Cochrane library, and EMBASE before January 23, 2021, for literature from 2010 to 2021 using the following medical search heading (MeSH) and keywords: “acute stroke,” “mechanical thrombectomy,” “endovascular treatment,” “posterior circulation,” “vertebrobasilar occlusion,” “anterior circulation,” and “large vessel occlusion” (see Supplementary Methods). The PubMed search strategy was adapted for use in Cochrane library and EMBASE search databases. No restrictions were made in relation to literature type and text availability. Literature was however screened for study suitability based on title and abstract. Only subject-relevant studies were therefore assessed for eligibility.

Study Selection and Data Extraction

Studies were included if they met the following criteria: (1) retrospective or prospective observational studies with a combined sample size for PCLVO and ACLVO of at least 40, (2) comparison of baseline characteristics and at least two reperfusion treatment profile parameters (i.e., rate of IVT, onset-to-IVT time, onset-to-groin puncture time, onset-to-recanalization time, and number of passages) in PCLVO and ACLVO as main and/or subgroup analysis, and (3) outcome defined by at least two of the following: Thrombolysis In Cerebral Infarction scale (TICI) 2b/3 (28), symptomatic intracranial hemorrhage (sICH), modified Rankin Scale score (mRS) 0–2 at 90 days, and mortality at 90 days. Exclusion criteria included the following: (1) non-English literature, (2) no MT conducted, (3) duplicate literature, (4) insufficient data for comparison purposes, and (5) same datasets used by multiple studies. Duplicates were identified and eliminated using EndNote X9 citation manager software (Clarivate, Philadelphia, PA, USA).

Data extracted from the included studies were patient age, sex, comorbidities/cardiovascular risk factors, stroke etiology, baseline NIHSS, site of LVO, reperfusion treatment profile (rate of IVT, onset-to-IVT time, onset-to-groin puncture time, onset-to-recanalization time, and number of passages), TICI 2b/3, sICH, 90 day mRS 0–2 and mortality.

Quality Assessment

Quality assessment by means of Risk of Bias Assessment tool for Non-randomized Studies (RoBANS) was performed to assess the methodological quality of all included studies under which studies were rated as having either a high, a low, or an uncertain risk of bias (29).

Data search, eligibility assessment, selection, and extraction as well as quality assessment were conducted and crosschecked by two independent investigators and contentions were resolved through a consensus between the two. Publication bias was assessed by means of a funnel plot asymmetry.

Statistical Analysis

Statistical analyses were performed using Review Manager (RevMan) [Computer program], version 5.4.1 (30). We used the Mantel–Haenszel statistical method and a random or fixed effects analysis model for studies with moderate/high and low heterogeneity, respectively, to estimate the pooled effect size. Cochrane I2 statistics was used to assess heterogeneity. We defined high heterogeneity as I2 > 75%, moderate heterogeneity as 25% < I2 <75%, and low heterogeneity as I2 <25% (31). PCLVO and ACLVO were the comparison groups, and the corresponding meta-analysis was performed for each outcome of interest.

Sensitivity analysis was performed for baseline characteristics and recanalization treatment profiles in which retrospective studies were excluded due to higher risk of selection bias (29). We furthermore conducted subgroup analyses in which we excluded studies with <20 patients with PCLVO due to a possible risk of lack of representation of PCLVO with low sample sizes in the real world and studies that primarily recruited patients who received MT until 2012, with the presumption that results could have been compromised by the use of first-generation MT devices (32).

Odds ratios (ORs) and standardized mean difference (SMD) were calculated with 95% confidence intervals (CIs) and p < 0.05 was considered significant. For continuous data, the corresponding estimated mean and estimated standard deviation were calculated (33).

Results

Search Results and Study Characteristics

The database search yielded 6,777 citations of literature published between January 1, 2010 and January 23, 2021. A total of 535 duplicate studies were excluded. A total of 6,242 studies were screened, out of which 6,189 were eliminated on the basis of subject and study irrelevance. The remaining 53 studies were individually assessed for eligibility by means of full-text review with 37 studies being excluded due to lack of sufficient data. Sixteen eligible studies that met the study inclusion criteria were therefore included in our meta-analysis (Figure 1). Data from 11 studies (26, 3443) were acquired from multiple centers and data from 5 studies (4448) were acquired from single centers. Among these studies, 6 were retrospective (35, 39, 4447) and 10 were prospective studies (26, 34, 3638, 4043, 48). This study comprised a total of 8,898 patients with 1,172 belonging to PCLVO and 7,726 belonging to ACLVO.

Figure 1

Risk of Bias Assessment

Data on risk of bias are shown in Supplementary Figure 1; generally, there was a high risk of bias with respect to patient selection, confounding variables, and outcome reporting and a lower risk of incomplete data across all studies.

The funnel plots showed no asymmetry with respect to sICH, indicating a low probability of publication bias across the included studies for sICH. Asymmetry was, however, observed for recanalization success, favorable functional outcome, and mortality (Supplementary Figure 2).

Baseline Characteristics

Results of age, sex, baseline NIHSS, and site of LVO for the included studies are reported in Table 1. PCLVO patients were younger than ACLVO [SMD = −0.31 (95% CI 0.59–0.03), p = 0.03] (I2 = 92%, p < 0.00001) (Figure 2). Further results showed less females in the PCLVO group [OR = 0.54 (95% CI 0.39–0.73), p < 0.0001] (I2 = 59%, p = 0.008) (Figure 3).

Table 1

Posterior circulationAnterior circulation
PublicationNAge, yearsFemale sexBaseline NIHSSOccluded vesselNAge, yearsFemale sexBaseline NIHSSOccluded vessel
Mourand et al. (44)1521 (3–38)14 BA, 1 VA2517 (9–23)16 MCA, 9 ICA
Abilleira et al. (34)6564 ± 142116 (8–27)47168 ± 1322118 (14–21)
Lefevre et al. (45)2625 BA, 1 PCA3620 ICA, 16 MCA
Fockaert et al. (35)1556 (22–86)233 (7–42)15 PCA6564 (22–86)4315 (6–42)47 MCA, 18 ICA
Serles et al. (36)4372 (63–77)1919 (13–30)40 BA, 3 VA25870 (60–77)13317 (13–20)189 MCA, 65 ICA, 1 ACA
Alonso De Lecinana et al. (26)5264 (50–74)1711 (6–23)52 VBA42770 (60–77)21418 (14–21)284 MCA, 100 ICA, 43 tandem occlusion
Hu et al. (46)2466 (32–85)1114 (2–34)24 VBA13766 (22–87)5910 (3–26)94 MCA, 42 ICA, 1 ACA
Khoury et al. (37)55 VBA3529 MCA, 6 ICA
Singh et al. (38)2556 ± 9919 ± 925 BA11258 ± 134116 ± 1361 MCA, 51 ICA
Alawieh et al. (47)5627 ± 48817 ± 1138067 ± 1519215 ± 7
Meinel et al. (39)16570 (59–80)6918 (8–30)*1,57473 (61–82)81017 (12–20)**
Weber et al. (40)13965 ± 1612 (6–21)96169 ± 1415 (12–19)
Wollenweber et al. (41)303250 BA, 69 PCA, 59 VA2,2651,890 MCA, 666 ICA, 86 ACA
Uno et al. (48)5073 (65–79)1725 (13–32)29577 (69–84)15118 (13–22)
Renieri et al. (43)4438 BA, 4 VA, 2 PCA9053 MCA, 37 ICA
Huo et al. (42)14564 ± 133720 (11–26)59664 ± 1421616 (12–21)

Baseline characteristics reported in included studies.

*

n = 155,

**

n = 1,558; – = not available, ACA, anterior cerebral artery; BA, basilar artery; ICA, internal carotid artery; MCA, middle cerebral artery; N, number of patients; n, reference number of patients; NIHSS, National Institutes of Health Stroke Scale score; PCA, posterior cerebral artery; VA, vertebral artery; VBA, vertebrobasilar arteries.

Figure 2

Figure 3

Hypertension seemed to be the predominant comorbidity in both PCLCO (56.0%) and ACLVO (62.6%) (Supplementary Table 1). Although the pooled results showed hypertension to be comparable in both circulations, there seemed to be a tendency of fewer cases of hypertension as a comorbidity in PCLVO [OR = 0.76 (95% CI 0.54–1.09), p = 0.14] (I2 = 76%, p < 0.0001) (Supplementary Figure 3). In addition, atrial fibrillation [OR = 0.62 (95% CI 0.50–0.77), p < 0.00001] (I2 = 0%, p = 0.71) and hyperlipidemia [OR = 0.73 (95% CI 0.61–0.89), p = 0.001] (I2 = 9%, p = 0.36) were less likely comorbidities of PCLVO, with smoking being a more likely comorbidity of PCLVO [OR = 1.22 (95% CI 1.01–1.48), p = 0.004] (I2 = 0%, p = 0.47) (Supplementary Figures 4–6, respectively). Diabetes mellitus [OR = 0.98 (95% CI 0.72–1.34), p = 0.91] (I2 = 51%, p = 0.04), coronary artery disease [OR = 0.64 (95% CI 0.36–1.27), p = 0.22] (I2 = 62%, p = 0.02), and previous stroke/TIA [OR = 1.21 (95% CI 0.96–1.53), p = 0.11] (I2 = 17%, p = 0.30) were, however, comparable between both groups (Supplementary Figures 7–9, respectively).

The average baseline NIHSS was higher in PCLVO [SMD = 0.32 (95% CI 0.15–0.48), p = 0.0001] (I2 = 75%, p < 0.00001) (Figure 4). In ACLVO, middle cerebral artery occlusion was the most prevalent site of LVO (31.0%) followed by internal carotid artery (13.1%). Basilar artery occlusion was the predominant lesion location in the PCLVO (33.5%) followed by posterior cerebral artery (7.4%).

Figure 4

Large artery atherosclerosis was a more likely stroke etiology in PCLVO [OR = 1.55 (95% CI 1.26–1.91), p < 0.0001] (I2 = 0%, p = 0.76) in comparison to ACLVO (Supplementary Figure 10). On the other hand, cardiac embolism was a less likely stroke etiology in PCLVO [OR = 0.63 (95% CI 0.52–0.75), p < 0.0001] (I2 = 0%, p = 0.67) in comparison to ACLVO (Supplementary Figure 11). Results obtained from sensitivity analyses conducted for the baseline characteristics age, sex, admission NIHSS, stroke etiology, and all comorbidities except “prior stroke or transient ischemic attack” had no influence on their respective results (Supplementary Figures 3–8, 10–14). However, sensitivity analysis showed “prior stroke or transient ischemic attack” being more likely in PCLVO [OR = 1.39 (95% CI 1.06–1.82), p = 0.02] (I2 = 0%, p = 0.51) (Supplementary Figure 9).

Recanalization Treatment Profiles

Studies that reported number of IVT showed moderate heterogeneity (I2 = 27%, p < 0.0001). The pooled results indicated a lower frequency of IVT in PCLVO patients [OR = 0.65 (95% CI 0.53–0.79), p < 0.0001] (Figure 5).

Figure 5

With a high heterogeneity across the studies reporting onset to IVT (I2 = 79%, p = 0.008), the pooled estimates showed a longer onset to IVT in PCLVO [SMD = 0.86 (95% CI 0.45–1.26), p < 0.0001] (Figure 6). Further analyses also showed a longer onset-to-groin puncture time in PCLVO [SMD = 0.59 (95% CI 0.33–0.85), p < 0.00001] (I2 = 86%, p < 0.00001) (Figure 7). Results from onset-to-recanalization time in PCLVO, however, did not show any difference compared to ACLVO [SMD = 0.29 (95% CI −0.04–0.60), p = 0.08] (I2 = 90%, p < 0.00001) (Supplementary Figure 15). Pooled results for the number of passages did not reveal a difference between PCLVO and ACLVO [SMD = 0.21 (95% CI −0.05–0.46), p = 0.11] (I2 = 79%, p = 0.0008) (Supplementary Figure 16).

Figure 6

Figure 7

Sensitivity analyses performed for rates of IVT, onset-to-IVT time, onset-to-groin puncture time, and number of passages had no influence on their respective results (Supplementary Figures 16–19). However, sensitivity analysis showed PCLVO to be associated with a longer onset-to-recanalization time [SMD = 0.43 (95% CI 0.10–0.77), p = 0.01] (I2 = 89%, p < 0.00001) (Supplementary Figure 15).

Outcomes of Study

Results of TICI 2b/3, sICH, mRS 0-2 at 90 days, and mortality for the included studies are reported in Table 2.

Table 2

Posterior circulationAnterior circulation
PublicationNSuccessful recanalizationsICHmRS 0–2 at 90 daysMortalityNSuccessful recanalizationsICHmRS 0–2 at 90 daysMortality
Mourand et al. (44)15115*7251598
Abilleira et al. (34)6548525224713482520797
Lefevre et al. (45)262314362311
Fockaert et al. (35)1515276547214
Serles et al. (36)43350102582071824
Alonso De Lecinana et al. (26)5239121174273592323748
Hu et al. (46)241914137110128
Khoury et al. (37)51435197
Singh et al. (38)252121121047
Alawieh et al. (47)5654324163803512016468
Meinel et al. (39)165149855**55**1,5741,299‡‡98‡‡‡604§§344§§
Weber et al. (40)13996#035***31***961719§29281§§§203§§§
Wollenweber et al. (41)303246100##82##2,2651,857732570
Uno et al. (48)5050027###4###29525038†††105††22††
Renieri et al. (43)44339065
Huo et al. (42)1451194495965204498

Outcomes reported in included studies.

*

n = 14,

**

n = 152,

***

n = 92,

#

n = 134,

##

n = 265,

###

n = 42,

n = 22,

‡‡

n = 1571,

‡‡‡

n = 1,562,

§

n = 964,

§§

n = 1,409,

§§§

n = 660,

n = 1,997,

†‡

n = 213,

ࠠ

n = 290; – = not available, sICH, symptomatic intracranial hemorrhage; mRS, modified ranking score; N, number of patients; n, reference number of patients.

Successful Recanalization

Studies that reported successful recanalization (i.e., TICI 2b/3) showed moderate heterogeneity (I2 = 50%, p = 0.01). The pooled estimates showed no difference in outcomes in both PCLVO and ACLVO [OR = 1.07 (95% CI 0.81–1.42), p = 0.44]. In a subgroup analysis in which three studies were excluded on the basis of <20 PCLVO patients and patient recruitment primarily until 2012, the remaining studies showed similar results [OR = 1.03 (95% CI 0.76–1.41), p = 0.83] (I2 = 55%, p = 0.01) (Figure 8).

Figure 8

Symptomatic Intracerebral Hemorrhage

Studies that reported sICH showed moderate heterogeneity (I2 = 42%, p = 0.08). Our results indicated a lower likelihood of sICH in PCLVO [OR = 0.56 (95% CI 0.37–0.85), p = 0.006]. In our subgroup analysis (exclusion of two studies based on <20 PCLVO patients and patient recruitment primarily until 2012), the studies showed a rather reduced heterogeneity (I2 = 19%, p = 0.28). The pooled estimates once again indicated a lower likelihood of sICH in PCLVO compared to ACLVO [OR = 0.44 (95% CI 0.27–0.71), p = 0.0008] (Figure 9).

Figure 9

Favorable Functional Outcome at 90 Days

Studies that reported favorable functional outcome, defined by mRS ≤ 2 at 90 days, showed a moderate heterogeneity (I2 = 41%, p = 0.08) with comparable likelihood of favorable functional outcome in both PCLVO and ACLVO [OR = 0.92 (95% CI 0.73–1.16), p = 0.48]. The subgroup analysis (after exclusion of three studies based on <20 PCLVO patients and patient recruitment primarily until 2012) showed similar findings (I2 = 55%, p = 0.04) [OR = 0.97 (95% CI 0.73–1.27), p = 0.80] (Figure 10).

Figure 10

Mortality

Studies reporting mortality showed a moderate heterogeneity (I2 = 57%, p = 0.004). MT in PCLVO was associated with a higher likelihood of mortality as compared to ACLVO [OR = 1.92 (95% CI 1.46–2.53), p < 0.00001]. The subgroup analysis (after exclusion of four studies due to <20 PCLVO patients and patient recruitment primarily until 2012) likewise showed a higher likelihood of mortality in PCLVO patients [OR = 1.82 (95% CI 1.33–2.48), p = 0.0002] (I2 = 65%, p = 0.003) (Figure 11).

Figure 11

Discussion

To the best of our knowledge, until the conduction of this meta-analysis, there had been two prior meta-analyses comparing MT in anterior and posterior circulation stroke with both studies, however, focusing on MT safety and efficacy outcomes (19, 20). This study, conducted independently from previous studies, included more recent literature on MT in PCLVO and ACLVO and, in a detailed meta-analysis, further sought to compare demographics and baseline characteristics, risk factors, as well as recanalization treatment profiles between the two brain circulations. Hence, this study presents at the time of publication the most current data on MT in PCLVO vs. ACLVO.

Results on etiology of LVO in our meta-analysis show large artery atherosclerosis (36.7% and 23.1%) and cardiac embolism (34.8 and 47.0%) to be the most common causes of PCLVO and ACLVO, respectively (Supplementary Table 2), with large artery atherosclerosis and cardiac embolism being an equally likely etiology in PCLVO. This was consistent with reports from previous literature that reported 26–36% for large artery atherosclerosis and 30–35% for cardiac embolism in PCLVO, although this was based only on basilar artery occlusion (14). The difference in stroke etiologies for the other classification groups such as other determined LVO etiologies (dissection, thrombophilia, paraneoplastic, etc.) and unknown causes, might, however, be inconclusive due to a possible lack of standardized classification of etiology across studies (49).

It is thought that NIHSS gives more weight to neurological deficits in anterior circulation stroke due to factors such as aphasia, facial palsy, and hemiparesis as opposed to limb ataxia, oculomotor disorders, and hemianopia in posterior circulation stroke. However, depending on the level of occlusion, some cases of PCLVO are accompanied by hemiparesis, facial palsy, and dysarthria. It could therefore be argued that a substantial overlap in clinical characteristics exists in both anterior and posterior circulation strokes (14, 50). Contrary to the presumption that NIHSS gives more weight to neurological deficits in anterior circulation strokes, our study detected a higher admission NIHSS in PCLVO than in ACLVO (Figure 4). This could be due to more PCLVO patients with reduced consciousness on admission although we do not have data to support this presumption.

Our meta-analysis showed that fewer PCLVO patients are likely to receive IVT in comparison to ACLVO (Figure 5). Previous literature have reported prodromal symptoms in up to 60% cases of PCLVO, which, in most cases, is a reason for misdiagnosis and wrong specialty consultation (17, 51). As a result, PCLVO patients may not succeed presenting within the widely accepted 4.5-h time window to receive IVT (52).

Furthermore, the delay in neurological intervention in patients with posterior circulation stroke was reflected in the longer onset-to-IVT and onset-to-groin puncture times in PCLVO (Figures 6, 7). This association is supported by previous studies (53). In spite of the longer onset-to-IVT and onset-to-groin puncture times in PCLVO, a favorable 90 day functional outcome in PCLVO is, however, equally possible just as in ACLVO (Figure 10). This could support the hypothesis that salvageable brain tissue in posterior circulation stroke persists for a longer time as compared to anterior circulation stroke possibly due to a better collateralization in the brainstem (54). Shorter onset-to-IVT and onset-to-groin puncture times could therefore influence a better functional MT outcome in PCLVO. Although onset-to-recanalization time and number of passages were comparable between PCLVO and ACLVO, they tended to be increased in PCLVO patients (Supplementary Figures 7, 8). MT in PCLVO was, however, shown to be associated with longer onset-to-recanalization times in the sensitivity analysis, which was not surprising due to the known delays in hospital admission and intervention of PCLVO patients (14, 53).

In our study, we found lower likelihood of sICH in PCLVO (Figure 9). Previous literature has attributed the scarcity of sICH in posterior circulation stroke to relatively smaller infarct volumes and the anatomically smaller nature of vessels that supply the brainstem and cerebellum (55, 56). However, this could also be attributed to the lower number of PCLVO patients who receive IVT (Figure 5). Several other studies have shown IVT in posterior circulation stroke to be associated with lower occurrence of sICH than IVT in anterior circulation stroke (57, 58). Similar results have been demonstrated by a more recent meta-analysis that indicated a lower likelihood of sICH after IVT in posterior circulation stroke (59). On the other hand, a randomized clinical trial that enrolled 656 patients showed no significant difference in sICH in IVT and non-IVT patients although this study included patients with either ACLVO or PCLVO (60). This raises the question as to whether sICH after MT in PCLVO could therefore be independent of IVT administration. In the anterior circulation, however, MT in addition to IVT has been identified as a significant independent predictor of ICH (56, 61).

Studies by previous meta-analyses showed no statistical difference between PCLVO and ACLVO in both recanalization success and 90 day functional outcome (19, 20). A comparable likelihood of obtaining successful recanalization (Figure 8) and 90 day favorable functional outcome (Figure 10) was also found in our meta-analysis that included more recent studies. A successful recanalization could therefore influence a good functional outcome irrespective of the circulation involved. Although this study makes a comparison between MT in PCLVO vs. ACLVO, we believe that RCTs are warranted to study if MT in PCLVO is generally efficient.

The incidence of higher mortality in PCLVO has been discussed in numerous previous studies (19, 20). Our study likewise provided data to support the claim that MT in PCLVO is associated with a higher mortality as compared to ACLVO (Figure 11). Although it is believed that younger patients tend to have a better stroke outcome in comparison to older patients (55, 56), this study shows that PCLVO patients are younger but yet are still associated with a higher mortality than ACLVO patients.

Futile recanalization, a phenomenon defined as poor functional outcome with mRS 4–6, despite successful recanalization by MT, have been reported in individual studies as being significantly higher in PCLVO than ACLVO [OR = 2.15 (95% CI 1.27–3.63)] (39).

Due to the higher probability of futile recanalization, physicians may be more conservative and may not attempt MT in older PCLVO patients, hence creating a selection bias with higher numbers of younger patients being considered for MT. It is, however, worth mentioning that this study does not include data on futile recanalization and physicians' patient management.

The higher rate of mortality in PCLVO compared to ACLVO could be partly due to the relatively higher NIHSS on admission and, hence, stroke severity in posterior circulation stroke (Figure 4). This is in line with previous suggestions that stroke severity on admission is an important predictor of stroke outcome, especially in the posterior circulation, and that higher baseline NIHSS in PCLVO is associated with a poor outcome (24, 62).

In addition, stroke due to basilar artery occlusion has been described as severe in relation to other occlusion sites in PCLVO (63). We reported basilar artery occlusion as the most frequent site of PCLVO (33.5%) (Table 1), which may also have contributed to the higher mortality. This study therefore suggests onset-to-IVT and onset-to-groin puncture times, NIHSS, and basilar artery occlusion as factors that could influence outcome in PCLVO. As a reason for high mortality in PCLVO, we propose a subtle progressive-over-time damage or a non-life supporting damage in the posterior circulation, possibly due to the gravity and irreversible nature of the damage to support life despite neurorehabilitation. Such damages have been described as a comatose state or locked-in syndrome, dysphagia, tracheostomy, hypostatic pneumonia, and complications as a result of being long-term bedridden (42). However, this hypothesis cannot be supported by the present study and we therefore encourage further studies to detect causes of higher mortality of MT in PCLVO.

Limitations

Although we implemented measures to limit setbacks in this study, we were nonetheless posed with a couple of challenges. Firstly, such a meta-analysis with several studies over such long duration faces the problem of high heterogeneity with respect to stroke management across studies. Secondly, although efforts were made to exclude the possible effects of the use of first-generation MT devices, there was no 100% guarantee that all remaining studies included in our subgroup analyses exclusively used second-generation MT devices. Thirdly, there was a huge disparity in number of PCLVO and ACLVO patients. Finally, the lack of RCT in both groups introduces selection bias.

Conclusion

Although MT in PCLVO differs characteristically and also in terms of outcome from ACLVO, our meta-analysis indicates that MT in PCLVO may be equally efficient just as in ACLVO in achieving successful recanalization and a favorable 90 day functional outcome. Although MT in PCLVO is associated with lower likelihood of sICH, possibly due to fewer PCLVO patients receiving IVT because of late recognition and presentation, PCLVO is associated with a higher occurrence of mortality. This higher mortality could be explained through the high baseline NIHSS, longer onset-to-IVT and onset-to-groin puncture times, and basilar artery occlusion being the most predominant site of PCLVO.

Statements

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author contributions

JM and SP conceived and designed the study, undertook data extraction, analyzed the data, and drafted the manuscript. KP and JT independently rechecked all extracted data and analysis. AG-E, YW, KF, and AM helped with data analysis. UZ helped interpret the data. SP had full access to all the data in the study and had final responsibility for the decision to submit for publication. All authors reviewed and edited the manuscript and approved the final version of the manuscript.

Funding

We acknowledge support by Open Access Publishing Fund of University of Tübingen.

Conflict of interest

UZ received research grants from BMS, European Research Council, German Federal Ministry of Education and Research, German Research Foundation, Janssen Pharmaceuticals, and Takeda, and personal consulting fees from Bayer, CorTec, and Pfizer. SP received research grants from BMS/Pfizer, Daiichi Sankyo, European Union, German Federal Joint Committee Innovation Fund, and German Federal Ministry of Education and Research, and speakers' honoraria/consulting fees from AstraZeneca, Bayer, Boehringer-Ingelheim, BMS/Pfizer, Daiichi Sankyo, Portola, and Werfen. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fneur.2021.687134/full#supplementary-material

References

  • 1.

    HackeWKasteMBluhmkiEBrozmanMDavalosAGuidettiDet al. Thrombolysis with alteplase 3 to 4.5 hours after acute ischemic stroke. N Engl J Med. (2008) 359:131729. 10.1056/NEJMoa0804656

  • 2.

    BhatiaRHillMDShobhaNMenonBBalSKocharPet al. Low rates of acute recanalization with intravenous recombinant tissue plasminogen activator in ischemic stroke: real-world experience and a call for action. Stroke. (2010) 41:22548. 10.1161/STROKEAHA.110.592535

  • 3.

    NogueiraRGLutsepHLGuptaRJovinTGAlbersGWWalkerGAet al. Trevo versus Merci retrievers for thrombectomy revascularisation of large vessel occlusions in acute ischaemic stroke (TREVO 2): a randomised trial. Lancet. (2012) 380:123140. 10.1016/S0140-6736(12)61299-9

  • 4.

    SaverJLJahanRLevyEIJovinTGBaxterBNogueiraRGet al. Solitaire flow restoration device versus the Merci Retriever in patients with acute ischaemic stroke (SWIFT): a randomised, parallel-group, non-inferiority trial. Lancet. (2012) 380:12419. 10.1016/S0140-6736(12)61384-1

  • 5.

    GoyalMMenonBKVan ZwamWHDippelDWMitchellPJDemchukAMet al. Endovascular thrombectomy after large-vessel ischaemic stroke: a meta-analysis of individual patient data from five randomised trials. Lancet. (2016) 387:172331. 10.1016/S0140-6736(16)00163-X

  • 6.

    NogueiraRGJadhavAPHaussenDCBonafeABudzikRFBhuvaPet al. Thrombectomy 6 to 24 hours after stroke with a mismatch between deficit and infarct. N Engl J Med. (2018) 378:1121. 10.1056/NEJMoa1706442

  • 7.

    PowersWJRabinsteinAAAckersonTAdeoyeOMBambakidisNCBeckerKet al. Guidelines for the early management of patients with acute ischemic stroke: 2019 update to the 2018 guidelines for the early management of acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. (2019) 50:e344418. 10.1161/STR.0000000000000211

  • 8.

    TurcGBhogalPFischerUKhatriPLobotesisKMazighiMet al. European Stroke Organisation (ESO) - European Society for Minimally Invasive Neurological Therapy (ESMINT) guidelines on mechanical thrombectomy in acute ischaemic stroke endorsed by stroke alliance for Europe (SAFE). Eur Stroke J. (2019) 4:612. 10.1177/2396987319832140

  • 9.

    YangPZhangYZhangLZhangYTreurnietKMChenWet al. Endovascular thrombectomy with or without intravenous alteplase in acute stroke. N Engl J Med. (2020) 382:198193. 10.1056/NEJMoa2001123

  • 10.

    NouhARemkeJRulandS. Ischemic posterior circulation stroke: a review of anatomy, clinical presentations, diagnosis, and current management. Front Neurol. (2014) 5:30. 10.3389/fneur.2014.00030

  • 11.

    TaoWDLiuMFisherMWangDRLiJFurieKLet al. Posterior versus anterior circulation infarction: how different are the neurological deficits?Stroke. (2012) 43:20605. 10.1161/STROKEAHA.112.652420

  • 12.

    MerwickAWerringD. Posterior circulation ischaemic stroke. BMJ. (2014) 348:g3175. 10.1136/bmj.g3175

  • 13.

    SchonewilleWJWijmanCAMichelPRueckertCMWeimarCMattleHPet al. Treatment and outcomes of acute basilar artery occlusion in the Basilar Artery International Cooperation Study (BASICS): a prospective registry study. Lancet Neurol. (2009) 8:72430. 10.1016/S1474-4422(09)70173-5

  • 14.

    MattleHPArnoldMLindsbergPJSchonewilleWJSchrothG. Basilar artery occlusion. Lancet Neurol. (2011) 10:100214. 10.1016/S1474-4422(11)70229-0

  • 15.

    LiuXDaiQYeRZiWLiuYWangHet al. Endovascular treatment versus standard medical treatment for vertebrobasilar artery occlusion (BEST): an open-label, randomised controlled trial. Lancet Neurol. (2020) 19:11522. 10.1016/S1474-4422(19)30395-3

  • 16.

    ZiWQiuZWuDLiFLiuHLiuWet al. Assessment of endovascular treatment for acute basilar artery occlusion via a nationwide prospective registry. JAMA Neurol. (2020) 77:56173. 10.1001/jamaneurol.2020.0156

  • 17.

    Van Der HoevenEJSchonewilleWJVosJAAlgraAAudebertHJBergeEet al. The Basilar Artery International Cooperation Study (BASICS): study protocol for a randomised controlled trial. Trials. (2013) 14:200. 10.1186/1745-6215-14-200

  • 18.

    JiXJovinTG. Basilar Artery Occlusion Chinese Endovascular (BAOCHE) Trial. ClinicalTrials.gov. Available online at: https://clinicaltrials.gov/ct2/show/NCT02737189 (accessed January 20, 2021).

  • 19.

    WangFWangJHeQWangLCaoYZhangHet al. Mechanical thrombectomy for posterior circulation occlusion: a comparison of outcomes with the anterior circulation occlusion - a meta-analysis. J Atheroscler Thromb. (2020) 27:132539. 10.5551/jat.54221

  • 20.

    ZhaoWMaPZhaoWYangBZhangYSongJet al. The safety and efficacy of mechanical thrombectomy in posterior vs. anterior emergent large vessel occlusion: a systematic review and meta-analysis. J Stroke Cerebrovasc Dis. (2020) 29:104545. 10.1016/j.jstrokecerebrovasdis.2019.104545

  • 21.

    GoyalMDemchukAMMenonBKEesaMRempelJLThorntonJet al. Randomized assessment of rapid endovascular treatment of ischemic stroke. N Engl J Med. (2015) 372:101930. 10.1056/NEJMoa1414905

  • 22.

    NagelSHerwehCKohrmannMHuttnerHBPoliSHartmannMet al. MRI in patients with acute basilar artery occlusion - DWI lesion scoring is an independent predictor of outcome. Int J Stroke. (2012) 7:2828. 10.1111/j.1747-4949.2011.00705.x

  • 23.

    SingerOCBerkefeldJNolteCHBohnerGHaringHPTrenklerJet al. Mechanical recanalization in basilar artery occlusion: the ENDOSTROKE study. Ann Neurol. (2015) 77:41524. 10.1002/ana.24336

  • 24.

    GoryBEldesoukyISivan-HoffmannRRabilloudMOngERivaRet al. Outcomes of stent retriever thrombectomy in basilar artery occlusion: an observational study and systematic review. J Neurol Neurosurg Psychiatr. (2016) 87:5205. 10.1136/jnnp-2014-310250

  • 25.

    MokinMSonigASivakanthanSRenZElijovichLArthurAet al. Clinical and procedural predictors of outcomes from the endovascular treatment of posterior circulation strokes. Stroke. (2016) 47:7828. 10.1161/STROKEAHA.115.011598

  • 26.

    Alonso De LecinanaMKawiorskiMMXimenez-CarrilloACruz-CulebrasAGarcia-PastorAMartinez-SanchezPet al. Mechanical thrombectomy for basilar artery thrombosis: a comparison of outcomes with anterior circulation occlusions. J Neurointerv Surg. (2017) 9:11738. 10.1136/neurintsurg-2016-012797

  • 27.

    MoherDLiberatiATetzlaffJAltmanDGGroupP. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. (2009) 6:e1000097. 10.1371/journal.pmed.1000097

  • 28.

    HigashidaRTFurlanAJRobertsHTomsickTConnorsBBarrJet al. Trial design and reporting standards for intra-arterial cerebral thrombolysis for acute ischemic stroke. Stroke. (2003) 34:e10937. 10.1161/01

  • 29.

    KimSYParkJELeeYJSeoHJSheenSSHahnSet al. Testing a tool for assessing the risk of bias for nonrandomized studies showed moderate reliability and promising validity. J Clin Epidemiol. (2013) 66:40814. 10.1016/j.jclinepi.2012.09.016

  • 30.

    The Cochrane Collaboration. London (2020).

  • 31.

    HigginsJPThompsonSGDeeksJJAltmanDG. Measuring inconsistency in meta-analyses. BMJ. (2003) 327:55760. 10.1136/bmj.327.7414.557

  • 32.

    SpiottaAMChaudryMIHuiFKTurnerRDKelloggRTTurkAS. Evolution of thrombectomy approaches and devices for acute stroke: a technical review. J Neurointerv Surg. (2015) 7:27. 10.1136/neurintsurg-2013-011022

  • 33.

    McgrathSZhaoXSteeleRThombsBDBenedettiACollaborationDESD. Estimating the sample mean and standard deviation from commonly reported quantiles in meta-analysis. Stat Methods Med Res. (2020) 29:252037. 10.1177/0962280219889080

  • 34.

    AbilleiraSCardonaPRiboMMillanMObachVRoquerJet al. Outcomes of a contemporary cohort of 536 consecutive patients with acute ischemic stroke treated with endovascular therapy. Stroke. (2014) 45:104652. 10.1161/STROKEAHA.113.003489

  • 35.

    FockaertNConinckxMHeyeSDefreyneLBrisboisDGoffettePet al. Mechanical endovascular thrombectomy for acute ischemic stroke: a retrospective multicenter study in Belgium. Acta Neurol Belg. (2016) 116:714. 10.1007/s13760-015-0552-7

  • 36.

    SerlesWGattringerTMutzenbachSSeyfangLTrenklerJKiller-OberpfalzerMet al. Endovascular stroke therapy in Austria: a nationwide 1-year experience. Eur J Neurol. (2016) 23:90611. 10.1111/ene.12958

  • 37.

    KhouryNNDarsautTEGhostineJDeschaintreYDaneaultNDurocherAet al. Endovascular thrombectomy and medical therapy versus medical therapy alone in acute stroke: a randomized care trial. J Neuroradiol. (2017) 44:198202. 10.1016/j.neurad.2017.01.126

  • 38.

    SinghRKChafaleVALallaRSPanchalKCKarapurkarAPKhadilkarSVet al. Acute ischemic stroke treatment using mechanical thrombectomy: a study of 137 patients. Ann Indian Acad Neurol. (2017) 20:2116. 10.4103/aian.AIAN_158_17

  • 39.

    MeinelTRKaesmacherJChaloulos-IakovidisPPanosLMordasiniPMosimannPJet al. Mechanical thrombectomy for basilar artery occlusion: efficacy, outcomes, and futile recanalization in comparison with the anterior circulation. J Neurointerv Surg. (2019) 11:117480. 10.1136/neurintsurg-2018-014516

  • 40.

    WeberRMinnerupJNordmeyerHEydingJKrogiasCHadisuryaJet al. Thrombectomy in posterior circulation stroke: differences in procedures and outcome compared to anterior circulation stroke in the prospective multicentre REVASK registry. Eur J Neurol. (2019) 26:299305. 10.1111/ene.13809

  • 41.

    WollenweberFATiedtSAlegianiAAlberBBangardCBerrouschotJet al. Functional outcome following stroke thrombectomy in clinical practice. Stroke. (2019) 50:25006. 10.1161/STROKEAHA.119.026005

  • 42.

    HuoXRaynaldGaoFMaNMoDSunXet al. Characteristic and prognosis of acute large vessel occlusion in anterior and posterior circulation after endovascular treatment: the ANGEL registry real world experience. J Thromb Thrombolysis. (2020) 49:52732. 10.1007/s11239-020-02054-2

  • 43.

    RenieriLSaiaVPereiraVMPracucciGLimbucciNNappiniSet al. Mechanical thrombectomy in patients with proximal occlusions and low NIHSS: results from a large prospective registry. J Stroke Cerebrovasc Dis. (2020) 29:105091. 10.1016/j.jstrokecerebrovasdis.2020.105091

  • 44.

    MourandIBrunelHCostalatVRiquelmeCLobotesisKMilhaudDet al. Mechanical thrombectomy in acute ischemic stroke: catch device. Am J Neuroradiol. (2011) 32:13815. 10.3174/ajnr.A2563

  • 45.

    LefevrePHLainayCThouantPChaventAKazemiARicolfiF. Solitaire FR as a first-line device in acute intracerebral occlusion: a single-centre retrospective analysis. J Neuroradiol. (2014) 41:806. 10.1016/j.neurad.2013.10.002

  • 46.

    HuSYYiHJLeeDHHongJTSungJHLeeSW. Effectiveness and safety of mechanical thrombectomy with stent retrievers in basilar artery occlusion: comparison with anterior circulation occlusions. J Korean Neurosurg Soc. (2017) 60:63543. 10.3340/jkns.2017.0404.008

  • 47.

    AlawiehAVargasJTurnerRDTurkASChaudryMILenaJet al. Equivalent favorable outcomes possible after thrombectomy for posterior circulation large vessel occlusion compared with the anterior circulation: the MUSC experience. J Neurointerv Surg. (2018) 10:73540. 10.1136/neurintsurg-2017-013420

  • 48.

    UnoJKamedaKOtsujiRRenNNagaokaSMaedaKet al. Mechanical thrombectomy for basilar artery occlusion compared with anterior circulation stroke. World Neurosurg. (2020) 134:e46975. 10.1016/j.wneu.2019.10.097

  • 49.

    AdamsHPJrBendixenBHKappelleLJBillerJLoveBBet al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in acute stroke treatment. Stroke. (1993) 24:3541. 10.1161/01.STR.24.1.35

  • 50.

    KasnerSE. Clinical interpretation and use of stroke scales. Lancet Neurol. (2006) 5:60312. 10.1016/S1474-4422(06)70495-1

  • 51.

    BairdTAMuirKWBoneI. Basilar artery occlusion. Neurocrit Care. (2004) 1:31929. 10.1385/NCC:1:3:319

  • 52.

    WardlawJMMurrayVBergeEDel ZoppoGJ. Thrombolysis for acute ischaemic stroke. Cochrane Database Syst Rev. (2014) 2014:CD000213. 10.1002/14651858.CD000213.pub3

  • 53.

    SarrajAMedrekSAlbrightKMartin-SchildSBibarsWVahidyFet al. Posterior circulation stroke is associated with prolonged door-to-needle time. Int J Stroke. (2015) 10:6728. 10.1111/j.1747-4949.2012.00952.x

  • 54.

    LindsbergPJPekkolaJStrbianDSairanenTMattleHPSchrothG. Time window for recanalization in basilar artery occlusion: speculative synthesis. Neurology. (2015) 85:180615. 10.1212/WNL.0000000000002129

  • 55.

    LindgrenANorrvingBRudlingOJohanssonBB. Comparison of clinical and neuroradiological findings in first-ever stroke. A population-based study. Stroke. (1994) 25:13717. 10.1161/01.STR.25.7.1371

  • 56.

    DornakTKralMHazlingerMHerzigRVeverkaTBurvalSet al. Posterior vs. anterior circulation infarction: demography, outcomes, and frequency of hemorrhage after thrombolysis. Int J Stroke. (2015) 10:12248. 10.1111/ijs.12626

  • 57.

    SarikayaHArnoldMEngelterSTLyrerPAMattleHPGeorgiadisDet al. Outcomes of intravenous thrombolysis in posterior versus anterior circulation stroke. Stroke. (2011) 42:2498502. 10.1161/STROKEAHA.110.607614

  • 58.

    KeselmanBGdovinovaZJatuzisDMeloTPEVilionskisACavalloRet al. Safety and outcomes of intravenous thrombolysis in posterior versus anterior circulation stroke: results from the safe implementation of treatments in stroke registry and meta-analysis. Stroke. (2020) 51:87682. 10.1161/STROKEAHA.119.027071

  • 59.

    LeeSHHanJHJungIJungJM. Do thrombolysis outcomes differ between anterior circulation stroke and posterior circulation stroke? A systematic review and meta-analysis. Int J Stroke. (2020) 15:84957. 10.1177/1747493020909634

  • 60.

    BroderickJPPaleschYYDemchukAMYeattsSDKhatriPHillMDet al. Endovascular therapy after intravenous t-PA versus t-PA alone for stroke. N Engl J Med. (2013) 368:893903. 10.1056/NEJMoa1214300

  • 61.

    NogueiraRG. Systemic thrombolysis randomization in endovascular stroke therapy (SHRINE) collaboration. In: International Stroke Conference 2021 (2021).

  • 62.

    SzmyginMSojkaMPyraKTarkowskiPLuchowskiPWojczalJet al. Mechanical thrombectomy for acute ischemic stroke in the posterior circulation: assessment of efficacy and outcome and identification of prognostic factors. Acta Radiol. (2020) 10.1177/0284185120962735

  • 63.

    DemelSLBroderickJP. Basilar occlusion syndromes: an update. Neurohospitalist. (2015) 5:14250. 10.1177/1941874415583847

Summary

Keywords

acute ischemic stroke, mechanical thrombectomy, endovascular stroke treatment, endovascular thrombectomy, posterior circulation, anterior circulation, large vessel occlusion

Citation

Mbroh J, Poli K, Tünnerhoff J, Gomez-Exposito A, Wang Y, Bender B, Hempel J-M, Hennersdorf F, Feil K, Mengel A, Ziemann U and Poli S (2021) Comparison of Risk Factors, Safety, and Efficacy Outcomes of Mechanical Thrombectomy in Posterior vs. Anterior Circulation Large Vessel Occlusion. Front. Neurol. 12:687134. doi: 10.3389/fneur.2021.687134

Received

29 March 2021

Accepted

14 May 2021

Published

22 June 2021

Volume

12 - 2021

Edited by

Simon Nagel, Heidelberg University Hospital, Germany

Reviewed by

Dennis John Cordato, University of New South Wales, Australia; Georgios Tsivgoulis, National and Kapodistrian University of Athens, Greece

Updates

Copyright

*Correspondence: Sven Poli

This article was submitted to Stroke, a section of the journal Frontiers in Neurology

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics