Does prior administration of rtPA influence acute ischemic stroke clot composition? Findings from the analysis of clots retrieved with mechanical thrombectomy from the RESTORE registry.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 22 05 2021
accepted: 15 08 2021
revised: 29 06 2021
pubmed: 21 8 2021
medline: 25 3 2022
entrez: 20 8 2021
Statut: ppublish

Résumé

There is still much debate whether bridging-therapy [intravenous thrombolysis (IVT) prior to mechanical thrombectomy (MT)] might be beneficial compared to MT alone. We investigated the effect of IVT on size and histological composition of the clots retrieved from patients undergoing bridging-therapy or MT alone. We collected mechanically extracted thrombi from 1000 acute ischemic stroke (AIS) patients included in RESTORE registry. Patients were grouped according to the administration (or not) of IVT before thrombectomy. Gross photos of each clot were taken and Extracted Clot Area (ECA) was measured using ImageJ software. Martius Scarlett Blue stain was used to characterize the main histological clot components [red blood cells (RBCs), fibrin (FIB), platelets/other (PTL)] and Orbit Image Analysis was used for quantification. Additionally, we calculated the area of each main component by multiplying the component percent by ECA. Chi-squared and Kruskal-Wallis tests were used for statistical analysis. 451 patients (45%) were treated with bridging-therapy while 549 (55%) underwent MT alone. When considering only percent histological composition, we did not find any difference in RBC% (P = 0.895), FIB% (P = 0.458) and PTL% (P = 0.905). However, bridging-therapy clots were significantly smaller than MT-alone clots [32.7 (14.8-64.9) versus 36.8 (20.1-79.8) mm Our results suggest that previous IVT administration significantly reduces thrombus size, proportionally releasing all the main histological components.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
There is still much debate whether bridging-therapy [intravenous thrombolysis (IVT) prior to mechanical thrombectomy (MT)] might be beneficial compared to MT alone. We investigated the effect of IVT on size and histological composition of the clots retrieved from patients undergoing bridging-therapy or MT alone.
METHODS METHODS
We collected mechanically extracted thrombi from 1000 acute ischemic stroke (AIS) patients included in RESTORE registry. Patients were grouped according to the administration (or not) of IVT before thrombectomy. Gross photos of each clot were taken and Extracted Clot Area (ECA) was measured using ImageJ software. Martius Scarlett Blue stain was used to characterize the main histological clot components [red blood cells (RBCs), fibrin (FIB), platelets/other (PTL)] and Orbit Image Analysis was used for quantification. Additionally, we calculated the area of each main component by multiplying the component percent by ECA. Chi-squared and Kruskal-Wallis tests were used for statistical analysis.
RESULTS RESULTS
451 patients (45%) were treated with bridging-therapy while 549 (55%) underwent MT alone. When considering only percent histological composition, we did not find any difference in RBC% (P = 0.895), FIB% (P = 0.458) and PTL% (P = 0.905). However, bridging-therapy clots were significantly smaller than MT-alone clots [32.7 (14.8-64.9) versus 36.8 (20.1-79.8) mm
CONCLUSIONS CONCLUSIONS
Our results suggest that previous IVT administration significantly reduces thrombus size, proportionally releasing all the main histological components.

Identifiants

pubmed: 34415423
doi: 10.1007/s00415-021-10758-5
pii: 10.1007/s00415-021-10758-5
pmc: PMC8940807
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1913-1920

Subventions

Organisme : Science Foundation Ireland
ID : 13/RC/2073_2
Pays : Ireland

Informations de copyright

© 2021. The Author(s).

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Auteurs

Rosanna Rossi (R)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Sara Molina (S)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Oana Madalina Mereuta (OM)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Andrew Douglas (A)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Seán Fitzgerald (S)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.

Ciara Tierney (C)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Abhay Pandit (A)

CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland.

Paul Brennan (P)

Department of Radiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.

Sarah Power (S)

Department of Radiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.

Alan O'Hare (A)

Department of Radiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.

Michael Gilvarry (M)

Cerenovus, Galway, Ireland.

Ray McCarthy (R)

Cerenovus, Galway, Ireland.

Georgios Magoufis (G)

Metropolitan Hospital, Stroke Unit, Piraeus, Greece.

Georgios Tsivgoulis (G)

Second Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Athens, Greece.

András Nagy (A)

Department of Neurointerventions, National Institute of Clinical Neurosciences, Budapest, Hungary.

Ágnes Vadász (Á)

Department of Neurointerventions, National Institute of Clinical Neurosciences, Budapest, Hungary.

Katarina Jood (K)

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Petra Redfors (P)

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Annika Nordanstig (A)

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Erik Ceder (E)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Dennis Dunker (D)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Jeanette Carlqvist (J)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Klearchos Psychogios (K)

Metropolitan Hospital, Stroke Unit, Piraeus, Greece.

István Szikora (I)

Department of Neurointerventions, National Institute of Clinical Neurosciences, Budapest, Hungary.

Turgut Tatlisumak (T)

Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

Alexandros Rentzos (A)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

John Thornton (J)

Department of Radiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.

Karen M Doyle (KM)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland Galway, University Road, Galway, Ireland. karen.doyle@nuigalway.ie.
CÚRAM-SFI Research Centre in Medical Devices, National University of Ireland Galway, Galway, Ireland. karen.doyle@nuigalway.ie.

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