Evidence map›Paper›PMID 40664428›Full record

ArticleJournal of neurointerventional surgery2026

Electrical impedance spectroscopy signatures of red blood cells and platelets in acute ischemic stroke clots in the Clotbase International Registry: Significance for etiology and first pass effect.

Cansu Sahin, Alice Giraud, Nazan Güner Sak, Wenyi Liu, Pierluca Messina, Franz Bozsak, Jean Darcourt, Federico Sacchetti, Anne-Christine Januel, Guillaume Bellanger and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of neurointerventional surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Cansu SahinCÚRAM Research Ireland Centre for Medical Devices, University of Galway, Galway, County Galway, Ireland.ORCID http://orcid.org/0000-0001-5201-6619
Alice GiraudSensome SAS, Massy, France.
Nazan Güner SakCÚRAM Research Ireland Centre for Medical Devices, University of Galway, Galway, County Galway, Ireland.
Wenyi LiuDepartment of Physiology, University of Galway, Galway, County Galway, Ireland.ORCID http://orcid.org/0009-0003-1808-4708
Pierluca MessinaSensome SAS, Massy, France.ORCID http://orcid.org/0000-0003-0624-9926
Franz BozsakSensome SAS, Massy, France.
Jean DarcourtDepartment of Diagnostic and Therapeutic Neuroradiology, CHU de Toulouse Pôle neurosciences, Toulouse, France.
Federico SacchettiNeuroradiology, CHU Toulouse, Toulouse, Occitanie, France.
Anne-Christine JanuelNeuroradiology, University Hospital of Purpan, Toulouse, France.
Guillaume BellangerToulouse 2 University, Toulouse, Occitanie, France.
Jorge PagolaParis-Saclay University Faculty of Medicine, Le Kremlin-Bicetre, France.
Jesus JuegaDepartment of Neurology, Hospital Germans Trias i Pujol, Badalona, Spain.ORCID http://orcid.org/0000-0003-1309-0730
Hirotoshi ImamuraStroke Unit, Neurology, Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0001-8923-7861
Tsuyoshi OhtaMedicina, Universitat Autònoma de Barcelona, Barcelona, Spain.
Laurent SpelleParis-Saclay University Faculty of Medicine, Le Kremlin-Bicetre, France.ORCID http://orcid.org/0000-0002-6748-8528
Vanessa ChalumeauDepartment of Physiology, University of Galway, Galway, Ireland.
Uros MircicStroke Unit, Neurology, Hospital Vall d'Hebron, Barcelona, Spain.
Predrag D StanarcevicStroke Unit, Neurology, Hospital Vall d'Hebron, Barcelona, Spain.
Ivan VukasinovicDepartment of Diagnostic and Therapeutic Neuroradiology, University Hospital of Toulouse, Toulouse, France.
Marc RiboStroke Unit, Neurology, Hospital Vall d'Hebron, Barcelona, Spain.ORCID http://orcid.org/0000-0001-9242-043X
Nobuyuki SakaiNeurosurgery, Kobe City Medical Center General Hospital, Kobe-city, Hyogo, Japan.ORCID http://orcid.org/0000-0002-3289-1210
Christophe CognardDiagnostic and Therapeutic Neuroradiology, Hôpital Purpan, Toulouse, France.ORCID http://orcid.org/0000-0003-4287-2627
Karen DoyleCÚRAM Research Ireland Centre for Medical Devices, University of Galway, Galway, County Galway, Ireland karen.doyle@universityofgalway.ie.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClot composition plays a key role in the pathophysiology of Acute Ischemic Stroke (AIS) and impacts the effectiveness of treatments such as thrombolysis and mechanical thrombectomy (MT). Developing an electrochemical impedance spectroscopy (EIS) based device to identify clot characteristics could improve stroke treatment outcomes. This study aims to estimate the red blood cell (RBC) and platelet content in extracted AIS clots and explore EIS's relevance to clinically important parameters, including stroke etiology and First Pass Effect (FPE).

methodsA total of 508 clots from 426 MT patients at five stroke centers in France, Japan, Serbia, and Spain (February 2021-2024) were analyzed in the Clotbase International Registry. EIS was performed on retrieved clots, followed by Martius Scarlet Blue staining and CD42b immunohistochemistry. EIS based models to quantify RBCs and platelets were designed using a development dataset (n=309), validated on a blinded dataset (n=199), and combined in a full dataset (n=508). Components (median interquartile range (IQR)) were quantified, correlating RBC and platelet percentages with impedance and clinical parameters.

resultsCorrelations between content as determined by EIS and histology were validated in a blind dataset for RBCs (r=0.7, P<0.0001) and platelets (r=0.5, P<0.0001). Similar correlations were observed in the full dataset. Large-artery atherosclerosis clots had significantly higher RBC (46.0% (25.7-67.7)) and lower platelet content (31.7% (22.4-42.7)) compared with cardioembolic (RBCs: 34.9% (14.0-56.2); platelets: 36.5% (26.7-51.0)) and cryptogenic (RBCs: 31.5% (17.4-63.6); platelets: 37.8% (28.4-50.8)). FPE was associated with significantly higher RBC (40.0% (25.6-55.4) vs non-FPE: 31.2% (6.6-50.2)) and lower platelet content (42.0% (32.0-54.0) vs non-FPE: 47.7% (30.6-65.0)), confirmed by histology.

conclusionEIS of RBCs and platelets provide an accurate assessment of clot composition, correlating strongly with histology. EIS holds the potential to deliver clinically relevant information on clot characteristics at the point of care.

Indexed as

Blood PlateletsDielectric SpectroscopyErythrocytesIschemic StrokeAgedAged, 80 and overFemaleHumansMaleMiddle AgedRegistriesThrombectomyStrokeThrombectomy

Identifiers

PMID40664428
PMCPMC13217077

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.