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AJNR: American Journal of Neuroradiology logoLink to AJNR: American Journal of Neuroradiology
. 2017 May;38(5):991–998. doi: 10.3174/ajnr.A5105

Risk of Thrombus Fragmentation during Endovascular Stroke Treatment

J Kaesmacher a, T Boeckh-Behrens a, S Simon b, C Maegerlein a, JF Kleine a, C Zimmer a, L Schirmer b, H Poppert b, T Huber a,
PMCID: PMC7960366  PMID: 28279987

The authors evaluated the potential relationship between thrombus histology and clot stability in 85 patients with anterior circulation stroke treated with thrombectomy. The number and location of emboli after retrieving the primary thrombus, the number of maneuvers, and TICI scores were evaluated. H&E and neutrophil elastase staining of retrieved clots was performed. An inverse correlation between maneuvers required for thrombus retrieval and the number of distal and intermediate emboli was observed. Younger patients were at higher risk for periprocedural thrombus fragmentation. Bridging thrombolysis tended to be associated with fewer maneuvers but more emboli. They conclude that younger age, easy-to-retrieve thrombi, and bridging thrombolysis may be risk factors for periprocedural thrombus fragmentation. Higher neutrophil levels in the thrombus tissue were related to an increased risk of periprocedural thrombus fragmentation.

Abstract

BACKGROUND AND PURPOSE:

Periprocedural thrombus fragmentation is a relevant risk in endovascular stroke treatment. Because factors influencing its occurrence are largely unknown, this study addresses a potential relationship between thrombus histology and clot stability.

MATERIALS AND METHODS:

Eighty-five patients with anterior circulation stroke treated with thrombectomy were included in this retrospective study. The number and location of emboli after retrieving the primary thrombus, the number of maneuvers, and TICI scores were evaluated. H&E and neutrophil elastase staining of retrieved clots was performed, and semiquantitative measurements of thrombus components were correlated with procedural parameters.

RESULTS:

An inverse correlation between maneuvers required for thrombus retrieval and the number of distal and intermediate emboli was observed (Spearman r, −0.23; P = .032). Younger patients were at higher risk for periprocedural thrombus fragmentation (Spearman r, −0.23; P = .032). Bridging thrombolysis tended to be associated with fewer maneuvers (2 vs 3, P = .054) but more emboli (1 vs 0, P = .067). While no consistent correlation between procedural parameters and red/white blood cells and fibrin-/platelet fractions could be found, higher amounts of neutrophil elastase–positive cells within the thrombus were independently associated with the occurrence of multiple emboli (adjusted OR, 4.6; 95% CI, 1.1–19.7; P = .041) and lower rates of complete recanalization (adjusted OR, 0.3; 95% CI, 0.1–0.9; P = .050).

CONCLUSIONS:

Younger age, easy-to-retrieve thrombi, and bridging thrombolysis may be risk factors for periprocedural thrombus fragmentation. Findings from standard histologic stains did not provide insight into thrombectomy-relevant thrombus stability. However, higher neutrophil levels in the thrombus tissue were related to an increased risk of periprocedural thrombus fragmentation. This observation aligns with the proposed thrombolytic capacity of neutrophil elastase and points to its potential clinical relevance in the context of stroke thrombectomy.


Mechanical thrombectomy (MT) of large-vessel occlusion has evolved as a safe and effective procedure that plays an indispensable role in modern therapeutic management of acute ischemic stroke.15 In recent randomized trials, high rates of successful recanalization (range, 59%–88%) were considered a key element in achieving excellent rates of good functional outcome (range, 33%–71%).6 However, not all successfully treated patients showed complete (TICI 3) recanalization; this outcome potentially limits therapeutic benefit.

In general, all endovascular MT techniques are accompanied by the risk of periprocedural thrombus fragmentation (PTF) and subsequent downstream embolism,79 preventing complete recanalization. Because the neurologic outcome of patients with complete (TICI 3) recanalization is significantly better compared with patients with “almost complete” (TICI 2b)10 or incomplete recanalization (TICI 1–2a),11 understanding the factors contributing to PTF may prove beneficial in achieving maximal therapeutic benefit. Previous reports demonstrated that thrombus stability12 may influence the incidence of PTF, and analyses of cellular thrombus composition have revealed a possible association between thrombus histology and thrombus etiology13,14 as well as clinical outcome.15,16 Discrepant results in previous studies17 might be primarily explained by low patient numbers and the risk of clot fragmentation. The latter may bias the representative character of the analyzed fragment.

While the main cellular components of a thrombus are known to be fibrin-/platelet accumulations (F/P) as well as red (RBC) and white blood cells (WBC),15,17 a higher fraction of RBC has been associated with increased rates of successful endovascular recanalization as noninvasively measured by whole-thrombus density (CT)13,18 and corresponding blooming artifacts (MR imaging).16,1821 Besides common thrombus characteristics obtained from H&E staining, new evidence has emerged that the degree of inflammatory cell invasion, particularly by neutrophils, may alter the stability and degradation of a thrombus.22,23 This finding is of particular interest because neutrophils exhibit fibrinolytic activity, which may weaken clot stability.24 Nevertheless, the impact of inflammatory cells on the mechanical properties of a thrombus remains uncertain, especially in the context of stroke thrombectomy. Potential knowledge of the clot composition before MT may be a further valuable tool to aid in the selection of the most appropriate devices and techniques to avoid PTF.

To this end, this is the first study investigating the dependency of procedural thrombectomy characteristics on anatomic and immune-histochemical thrombus histology, to our knowledge.

Materials and Methods

Subjects and Outcome

All consecutive patients presenting with a stroke due to large-vessel occlusion in the anterior circulation between July 2010 and September 2012 at a tertiary care center were included in this retrospective single-center study. Parts of this cohort and histologic analyses have been previously published.14,15 All patients underwent MT at the Department of Neuroradiology, and thrombus material was preserved. All patients in whom no thrombus material could be retrieved were excluded. Under this premise, 85 patients (45 women; median age, 73 years) formed the final study cohort. This study was approved by the local ethics committee at the Klinikum rechts der Isar of the Technical University of Munich, Germany, in accordance with the ethical standards of the 1964 Declaration of Helsinki and its later amendments.25 Clinical outcomes were measured as NIHSS at the day of discharge. Substantial neurologic improvement was defined as either NIHSS at day of discharge ≤1 or the difference between NIHSS on admission and NIHSS at the day discharge ≥8.26 This definition was based on previous studies that have shown this criterion to be a sensitive outcome measure.26

Image Analysis

The primary occlusion site (POS) was defined as the location and extent of the initial thrombus as evaluated on a synopsis of admission CT/CTA and initial DSA. After recanalization of the POS, any vessel occlusions distal from the POS were considered emboli due to PTF. This simplified definition is based on previous findings, which have shown that >90% of intracranial vessel occlusions are caused by a single thrombus.27 Hence, most vessel occlusions after POS recanalization are due to PTF. Emboli following PTF were further categorized into proximal, intermediate, and distal, according to their localization in lateral and corresponding anteroposterior DSA projections (On-line Fig 1). Emboli involving the M1 or M2 segment were always defined as proximal emboli, whereas those located distal to the pericallosal artery (on lateral projections) were considered distal emboli (see examples of emboli in Figs 1 and 2). The remaining vessel occlusions were assigned to the group of intermediate emboli. A schematic classification of emboli locations in cases of initial MCA or carotid-T occlusions is presented in On-line Fig 1. The success of POS recanalization (TICI-POS) as well as after additional rescue maneuvers (TICI-FINAL) was rated according to the original TICI scale, with TICI 2b defined as reperfusion of more than two-thirds of the initial occluded territory.25 Note that TICI-POS and TICI-FINAL may be the same (ie, if no additional maneuvers were performed). All images were evaluated in consensus by 2 experienced neuroradiologists.

Fig 1.

Fig 1.

DSA images in a lateral projection in a case of initial carotid-T occlusion (A). Dynamic images (delay = 1 second) after successful POS recanalization resulting in 1 proximal (filled arrow) and 1 intermediate embolus (open arrow) due to PTF (B–D).

Fig 2.

Fig 2.

DSA images in a lateral projection in a case of initial M1 occlusion (A). Dynamic images (delay = 1 second) after successful recanalization of the POS, resulting in 1 intermediate (open arrow) and 2 distal emboli (filled arrows) due to PTF (B–D).

Endovascular Procedure

Patients underwent angiography if groin puncture could be performed within 6 hours after symptom onset, clinical presentation was severe (NIHSS ≥4), and no early infarct signs involving more than one-third of the MCA territory were present on cranial CT on admission. IV rtPA was administered as “bridging therapy” in the absence of contraindication (n = 58, 68.2%). All stent-retriever passages were counted, and the number of maneuvers was registered after POS recanalization and at the end of the procedure. All procedures were performed by using a distal access catheter (MCA/anterior cerebral artery [ACA]) or proximal flow arrest by balloon occlusion (carotid-T) and one of the following stent retrievers (maneuvers with the respective device): Solitaire (n = 45; Covidien, Irvine, California), pREset 4–20 (n = 58; Phenox, Bochum, Germany), Trevo (n = 29; Stryker, Kalamazoo, Michigan), Revive (n = 2; Codman Neurovascular, Raynham, Massachusetts), Pulse (n = 4; Penumbra, Almeda, California), and Separator 3D (n = 6, Penumbra). Aspiration techniques, applied as stand-alone approach, were not performed in this study.

Thrombus Histology

After clot retrieval, thrombus material was fixed in phosphate-buffered 4% formalin. H&E staining and subsequent quantitative analysis of WBC, RBC, and F/P content were performed as described previously.14,15 To assess the prevalence of neutrophils within the thrombus, we stained the samples immunohistochemically by using an anti-neutrophil elastase monoclonal mouse antibody (clone NP57, M0752; Dako Denmark, Glostrup, Denmark). The number of neutrophil elastase (NE)-positive cells was semiquantitatively evaluated by 2 independent raters (NE index) who were blinded to the clinical data. Discrepancies were rated in consensus in a separate session. Evaluation was performed by using a 5-step grading scale: 0 (none), 1 (scattered), 2 (intermediate), 3 (clustered), 4 (high, >50% of all cells) (Fig 3).

Fig 3.

Fig 3.

Histologic specimens of 2 different clots with H&E staining (magnification ×30) (A and E), segmentation of RBC (red), F/P (purple), WBC (blue), and staining artifacts (brown) for composite quantification (B and F). H&E staining (magnification ×200) (C and G) and NE staining (magnification ×200) (D and H) with accumulation of NE-positive cells marked (asterisks). Clot composition is the following: upper row: 30% RBC, 51% F/P, 19% WBC; NE index 1; lower row: 7% RBC, 84% F/P, 9% WBC, NE index 4.

Statistical Analysis and Illustrations

The Shapiro-Wilk test was applied to analyze data for normal distribution. Because all variables, except NIHSS on admission (P = .322 in Shapiro-Wilk test), were non-normally distributed, bivariate correlation analysis with the 2-sided Spearman correlation was performed. Frequency counts and median/mean comparison were evaluated by using standard statistical measures (Fisher exact test, Mann-Whitney U test). For median values, the interquartile range (IQR) is shown; for mean values, the SD is shown. Because PTF was shown to be a multifactorial process (eg, age, MCA/ACA versus ICA occlusion, bridging therapy; see “Results”), we adjusted the analysis of histologic clot characteristics for these potential confounders by using a multivariate logistic regression. For statistical analysis, SPSS statistics, release 23.0 (IBM, Armonk, New York), was used. Illustrations were prepared by using Adobe Photoshop CS4 (Adobe Systems, Mountain View, California).

Results

Study Population and Outcomes

Inclusion criteria were met by 85 patients (mean age, 70.2 ± 14.6 years; 45 women) (Table). Approximately one-third (n = 26, 30.6%) of patients presented with a carotid-T occlusion, while the rest had isolated occlusions of the MCA/ACA (n = 57, 67.1%, and n = 2, 2.3%, respectively). The median NIHSS score at presentation was 15 (IQR, 10.5–18) and improved to 5.5 (IQR, 2–14) by the day of discharge. The median symptom-onset-to-treatment-time of 225 minutes (IQR, 165–278.75 minutes) could be sufficiently determined for 72 patients. Following recanalization of the POS, 36 patients (42.2%) showed no peripheral emboli, corresponding to an instant TICI 3 recanalization. Rescue therapy, namely retrieving downstream thrombi due to PTF, was successful in 27 cases. A median of 1 (IQR, 1–3.5) additional stent-retriever maneuver was required to perform the rescue therapy. The final rate of successful recanalization was 91.7%.

Patient characteristics, clot histology, and procedural parameters

No. or Median with Interquartile Range
Patients (No.) 85
Male/female (No.) 40/45 (47%/53%)
Age (median) (yr) 73 (65–80)
POS (No.)
    ICA/carotid-T 26 (30.6%)
    ACA 2 (2.3%)
    MCA 57 (67.1%)
IV rtPA bridging therapy (No.) 58 (68%)
Maneuvers (No.) 2 (1–4)
Procedure time for POS recanalization (min) 37 (21–64)
TICI after POS recanalization (No.)
    1 1 (1%)
    2a 27 (32%)
    2b 21 (25%)
    3 36 (42%)
Occlusions due to PTF (n = 101)
    Proximal 26 (26%)
    Intermediate 50 (50%)
    Distal 25 (25%)
Clot histology (fraction in %)
    RBC 37 (27–48)
    F/P 57 (47–67)
    WBC 5 (4–7)

When a single device type was used, distribution of final reperfusion success and the number of emboli did not differ among different stent-retriever types (P = .442 for final reperfusion success and P = .931 for the number of all emboli; On-line Fig 2). Use of multiple device types during a solitary thrombectomy was associated with lower rates of successful recanalization (P = .042). Occurrence of proximal and intermediate emboli after recanalization of the POS was associated with poorer neurologic outcome (NIHSS-proximal emboli: Spearman r, 0.279; P = .013; NIHSS-intermediate emboli: Spearman r, 0.223; P = .049), whereas patients showing a substantial neurologic improvement had fewer proximal (P = .029) and intermediate emboli (P = .018).

Physical Clot Properties

A consistent, inverse trend could be observed between the ease of the procedure and the risk of PTF: An easier procedure, namely requiring fewer stent-retriever maneuvers and less time to POS recanalization, was associated with a higher risk of distal and intermediate embolization (On-line Table). We also noted an age dependency of emboli occurrence because younger patients were at higher risk for PTF, resulting in higher numbers of intermediate and overall thrombus fragments distal to the POS. No correlation could be found between the time from symptom onset to groin puncture and the risk of embolization or maneuvers required. Administration of preinterventional IV rtPA tended to be associated with fewer endovascular maneuvers (2 versus 3, P = .054), shorter time to POS recanalization (30 minutes versus 47 minutes, P = .051), but a higher sum of overall emboli (1 versus 0, P = .067). In carotid-T occlusions as opposed to isolated MCA/ACA occlusions, more device passages were required to retrieve the primary thrombus (3 versus 2, P = .006), resulting in longer times for POS recanalization (66 versus 33 minutes, P < .001). However, no difference could be found regarding the location or number of occurring emboli (all P > .5).

Thrombus Histology

The mean fraction of RBC, F/P, and WBC was 42% (IQR, 22%–57%), 49% (IQR, 36%–69%), and 7% (IQR, 5%–11%), respectively. The median NE index, as determined for 42 patients, was 2 (IQR, 1–3). Clot histology characteristics did not differ between patients receiving bridging therapy and patients who did not (all, P > .3). Except for a higher NE index in carotid-T thrombi (median 2; IQR, 2–3.5, versus 2; IQR, 1–2; P = .008), no difference in histologic clot characteristics could be found when comparing MCA and carotid-T occlusions (all, P > .3). We could not observe a correlation between the time from symptom onset to recanalization or age and fraction of RBC, F/P, and WBC (all, P > .5). No consistent association between procedural parameters and RBC, F/P, or WBC content within the clot could be found (all, P > .1; On-line Table). This was also true when restricting analysis to different stent-retriever types (all, P > .2). However, the fraction of RBC (median RBC fraction, 50% [IQR, 28%–59%], versus 39% [IQR, 21%–57%]; P = .183) and the degree of neutrophil invasion (median NE index, 2 [IQR, 2–3] versus 2 [IQR, 1–3]; P = .192) tended to be higher in patients with multiple embolizations. The effect of neutrophil invasion on the occurrence of multiple emboli remained statistically tangible (without case restriction) when adjusting for age, site of occlusion (carotid-T versus MCA/ACA), and bridging therapy in a multivariate logistic regression model with multiple (>1) emboli defined as dependent variables (adjusted OR, 4.6; 95% CI, 1.1–19.7 for every NE index grade increase; P = .041; pseudo-R2 = 0.568). In contrast, the fraction of RBC was not a significant factor associated with the occurrence of multiple emboli by using the same logistic regression model (OR, 1.0; 95% CI, 0.9–1.0; P = .390). Pursuant to the first finding, the median NE index was lower in successfully recanalized patients (2 versus 3; P = .033, On-line Fig 3). Furthermore, the NE index was an independent predictor of unsuccessful recanalization (TICI-FINAL < 2b, [see above for the logistic regression used]; adjusted OR, 0.3; 95% CI, 0.1–0.9; P = .050; pseudo-R2 = 0.322).

Discussion

PTF during MT in acute stroke is common and was observed in more than half of the patients. This study shows 3 major findings: 1) In vivo clots differ regarding their MT-relevant mechanical properties, 2) common histologic clot characteristics do not consistently correlate with the mechanical clot properties, and 3) neutrophil invasion of the clot is linked to PTF and might serve as a novel surrogate for clot stability.

Our results show that easily retractable clots are generally prone to small/intermediate fragment dissociation, while those retracted with considerable effort are usually more stable and less susceptible to PTF. During endovascular stroke treatment, the use of stent retrievers and aspiration devices has a risk of thrombus fragmentation, which can lead to an “embolic shower.”28,29 Smaller fragments (<200 μm) constitute, by far, the highest percentage of occurring emboli.28 They usually dissolve due to spontaneous thrombolysis or revascularization as achieved by embolus extravasation.30 However, those emboli are usually undetected by conventional DSA, and their true clinical impact remains unclear.31 Larger emboli (>200 μm) cause clinically relevant cerebral occlusion32 and lead to angiographically defined incomplete recanalization (TICI < 3). We have found those emboli to be clinically important because intermediate and proximal emboli were associated with lower NIHSS scores at discharge. Occurrence and “rescue” removal of those emboli are of important clinical relevance because patients with complete recanalization have fewer neurologic deficits.10

The beneficial effects of preinterventional systemic rtPA administration concur with our assessment; this finding suggests a facilitating effect of bridging therapy.3335 Patients receiving rtPA needed fewer maneuvers and had shorter procedure times. However, the presumed bridging therapy–related thrombus softening came with the risk of PTF, which has been reported previously.36

Thrombus characteristics have been shown to predict technical outcome in endovascular stroke therapy. Particularly, thrombi with higher Hounsfield units are associated with higher rates of successful recanalization.19,21 Given prior histologic analyses, it seems reasonable to assume that those thrombi are RBC rich and have low F/P content.18 In the present study, thrombi prone to dissociate into multiple emboli tended to have a higher RBC fraction. However, this association was inconsistent and statistically irrelevant when correcting for possible confounders. Our data regarding the true success rate of thrombectomy are particularly limited because we only analyzed cases in which thrombus material could be retrieved (usually TICI > 1–2a). Hence, the true impact of RBC on the capability of retrieving the clot and POS recanalization cannot finally be assessed in the presented cohort.

To the best of our knowledge, this is the first study that establishes a possible link between procedurally relevant thrombus stability and the content of neutrophils. Neutrophils invade newly formed thrombi through recruitment due to adherent activated platelets.37 Adhesion triggers activation of neutrophils and subsequent release of neutrophil elastase.38 Initially, proinflammatory mediators promote fibrin cross-linking and the formation of neutrophil extracellular traps, which promote a procoagulatory state.39 However, activated neutrophils in the later phase also seem to restrict growth and promote thrombus degradation by NE-dependent fibrinolysis (“cell-dependent thrombolysis”).22 Komorowicz et al24 could indeed show that NE triggers the release of thrombus fragments in the soluble phase when incubated under shear stress conditions. Beyond altering the stability properties of thrombi, experimental data further suggest that NE seems to be involved in inflammatory reperfusion damage,40 and a recent study proposed an association between the presence of CD4+ T-cells and CD68+-monocytes/macrophages within the thrombus and stroke severity.41 However, the true impact of “thromboinflammation” has yet to be evaluated in further studies.42 In this context, the presented data underscore the need for considering and correcting for potential effects of inflammatory cells on thrombus stability, when evaluating its effect on clinical outcome in patients with stroke who were endovascularly treated.

Our study has several limitations beyond the common ones of a retrospective study design. Due to our inclusion criteria, the cohort exhibits a selection bias for successfully recanalized patients because histologic analysis was feasible only in cases in which the thrombus could be retrieved. Thus, results regarding the effects of histologic parameters on the true success rates of MT should be interpreted cautiously. Second, assessing the rate and location of emboli by using midprocedural DSA is a simplification and might not be as sensitive as susceptibility-weighted imaging for thrombus detection.43 However, it is the only feasible method of PTF detection during the procedure and has the advantage of assessing the hemodynamic relevance of emboli due to PTF. Third, this technique is not capable of differentiating peri- and preprocedural thrombus fragmentation (distal to the POS). However, because previous studies have found a low frequency of preprocedural fragmentation (<10%),27,43 the rate of false-positive classification is expected to be rather low. Fourth, the grading of the NE of the clot is based on a semiquantitative scale and was performed visually. Subjective analysis may, in the future, be overcome by ensuring comparable staining intensity and following threshold-based software quantification (comparable with the algorithm used for the analysis of H&E staining). Fifth, because we analyzed the thrombus retrieved from the POS, the histologic characteristics of the fragments causing distal emboli remain uncertain and might differ from the clot composition of the retrieved thrombus. One may speculate that dissolvable tissue islands or additional apposition thrombi might accumulate at the clot margins. These areas may be more prone to fragmenting during endovascular manipulation than the main thrombus and might show a different histology. Finally, because different stent retrievers were used, recanalization success and subsequent risk of PTF might be influenced by the choice of the device.

Conclusions

Younger age, easy-to-retrieve thrombi, and bridging thrombolysis are factors that may have a higher risk of PTF. Conventional histologic characteristics (RBC, WBC, F/P) do not seem to influence MT-relevant thrombus stability. However, higher amounts of clot-infiltrating neutrophils were related to an increased risk of PTF. This observation aligns well with the proposed thrombolytic capacity of neutrophilic enzymes and may implicate them as a novel marker for clot stability, which should be addressed in future clot studies.

Supplementary Material

16-00889.pdf
16-00889.pdf (565.3KB, pdf)

ABBREVIATIONS:

ACA

anterior cerebral artery

F/P

fibrin-/platelet accumulations

IQR

interquartile range

MT

mechanical thrombectomy

NE

neutrophil elastase

POS

primary occlusion site

PTF

periprocedural thrombus fragmentation

RBC

red blood cells

WBC

white blood cells

Footnotes

Disclosures: Claus Zimmer—UNRELATED: Board Membership: Philips Healthcare and Bayer Schering Pharma, Comments: scientific advisory boards*; Payment for Lectures including Service on Speakers Bureaus: Bayer Schering Pharma and Philips Healthcare, Comments: speaker honoraria; Other: Biogen Idec, Quintiles, MSD Sharp & Dome, Boehringer Ingelheim, Inventive Health Clinical UK Ltd, advanceCOR, BrainsGate, Pfizer, Bayer Schering Pharma, Novartis, Roche, Servier, Penumbra, WCT GmbH, Syngis, SSS International Clinical Research, PPD Germany GmbH, Worldwide Clinical Trials Ltd, phenox, Covidien, Actelion, Medivation, Medtronic, Harrison Clinical Research, Concentric, pharmtrace, Reverse Medical Corp, Premier Research Germany Ltd, Surpass Medical Ltd, and GlaxoSmithKline, Comments: research support and investigator fees for clinical studies.* Lucas Schirmer—UNRELATED: Patents (Planned, Pending, or Issued): WO2015166057A1; Comments: I filed a patent for the detection of antibodies against KIR4.1 in a subpopulation of patients with MS; the patent has been published, however, payments have not been made yet; Travel/Accommodations/Meeting Expenses Unrelated to Activities Listed: Genzyme, Comments: travel support. Holger Poppert—UNRELATED: Consultancy: Bayer HealthCare, Daiichi Sankyo Pharmaceuticals; Grants/Grants Pending: Deutsche Stiftung Neurologie*; Payment for Lectures including Service on Speakers Bureaus: Bayer HealthCare, Daiichi Sankyo Pharmaceuticals, Boehringer Ingelheim, Bristol-Myers Squibb, Pfizer, DEGUM, RG Gesellschaft für Information und Organisation, Medkom Akademie, CVA-Cardio Vascular Academy gemeinnützige GmbH. Thomas Huber—UNRELATED: Consultancy: Brainlab, Feldkirchen, Germany, Comments: consultancy for atlas-based segmentation techniques. *Money paid to the institution.

Paper previously presented at: World Stroke Congress, October 26–29, 2016; Hyderabad, India.

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