Association of intravenous thrombolysis and pre-interventional reperfusion: a post hoc analysis of the SWIFT DIRECT trial.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 30 08 2022
accepted: 13 10 2022
medline: 6 11 2023
pubmed: 18 11 2022
entrez: 17 11 2022
Statut: ppublish

Résumé

A potential benefit of intravenous thrombolysis (IVT) before mechanical thrombectomy (MT) is pre-interventional reperfusion. Currently, there are few data on the occurrence of pre-interventional reperfusion in patients randomized to IVT or no IVT before MT. SWIFT DIRECT (Solitaire With the Intention For Thrombectomy Plus Intravenous t-PA vs DIRECT Solitaire Stent-retriever Thrombectomy in Acute Anterior Circulation Stroke) was a randomized controlled trial including acute ischemic stroke IVT eligible patients being directly admitted to a comprehensive stroke center, with allocation to IVT with MT versus MT alone. The primary endpoint of this analysis was the occurrence of pre-interventional reperfusion, defined as a pre-interventional expanded Thrombolysis in Cerebral Infarction score of ≥2a. The effect of IVT and potential treatment effect heterogeneity were analyzed using logistic regression analyses. Of 396 patients, pre-interventional reperfusion occurred in 20 (10.0%) patients randomized to IVT with MT, and in 7 (3.6%) patients randomized to MT alone. Receiving IVT favored the occurrence of pre-interventional reperfusion (adjusted OR 2.91, 95% CI 1.23 to 6.87). There was no IVT treatment effect heterogeneity on the occurrence of pre-interventional reperfusion with different strata of Randomization-to-Groin-Puncture time (p for interaction=0.33), although the effect tended to be stronger in patients with a Randomization-to-Groin-Puncture time >28 min (adjusted OR 4.65, 95% CI 1.16 to 18.68). There were no significant differences in rates of functional outcomes between patients with and without pre-interventional reperfusion. Even for patients with proximal large vessel occlusions and direct access to MT, IVT resulted in an absolute increase of 6% in rates of pre-interventional reperfusion. The influence of time strata on the occurrence of pre-interventional reperfusion should be studied further in an individual patient data meta-analysis of comparable trials. clinicaltrials.gov NCT03192332.

Sections du résumé

BACKGROUND BACKGROUND
A potential benefit of intravenous thrombolysis (IVT) before mechanical thrombectomy (MT) is pre-interventional reperfusion. Currently, there are few data on the occurrence of pre-interventional reperfusion in patients randomized to IVT or no IVT before MT.
METHODS METHODS
SWIFT DIRECT (Solitaire With the Intention For Thrombectomy Plus Intravenous t-PA vs DIRECT Solitaire Stent-retriever Thrombectomy in Acute Anterior Circulation Stroke) was a randomized controlled trial including acute ischemic stroke IVT eligible patients being directly admitted to a comprehensive stroke center, with allocation to IVT with MT versus MT alone. The primary endpoint of this analysis was the occurrence of pre-interventional reperfusion, defined as a pre-interventional expanded Thrombolysis in Cerebral Infarction score of ≥2a. The effect of IVT and potential treatment effect heterogeneity were analyzed using logistic regression analyses.
RESULTS RESULTS
Of 396 patients, pre-interventional reperfusion occurred in 20 (10.0%) patients randomized to IVT with MT, and in 7 (3.6%) patients randomized to MT alone. Receiving IVT favored the occurrence of pre-interventional reperfusion (adjusted OR 2.91, 95% CI 1.23 to 6.87). There was no IVT treatment effect heterogeneity on the occurrence of pre-interventional reperfusion with different strata of Randomization-to-Groin-Puncture time (p for interaction=0.33), although the effect tended to be stronger in patients with a Randomization-to-Groin-Puncture time >28 min (adjusted OR 4.65, 95% CI 1.16 to 18.68). There were no significant differences in rates of functional outcomes between patients with and without pre-interventional reperfusion.
CONCLUSION CONCLUSIONS
Even for patients with proximal large vessel occlusions and direct access to MT, IVT resulted in an absolute increase of 6% in rates of pre-interventional reperfusion. The influence of time strata on the occurrence of pre-interventional reperfusion should be studied further in an individual patient data meta-analysis of comparable trials.
TRIAL REGISTRATION NUMBER BACKGROUND
clinicaltrials.gov NCT03192332.

Identifiants

pubmed: 36396433
pii: jnis-2022-019585
doi: 10.1136/jnis-2022-019585
pmc: PMC10646907
doi:

Substances chimiques

Fibrinolytic Agents 0

Banques de données

ClinicalTrials.gov
['NCT03192332']

Types de publication

Meta-Analysis Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e232-e239

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: GM reports consulting fees from Stryker Neurovascular, and paid lectures for Medtronic and Microvention Europe. ON reports funding from a Stryker research grant, and payment or honoraria for Phenox lecture and Stryker lecture. MR reports consulting fees from Medtronic, Stryker, Cerenovus, Philips, and Apta Targets; payment or honoraria from Ischemia View; participates on a data safety monitoring board or advisory board of Sensome; and has stock or stock options in Anaconda Biomed, CVAid, and Methinks. DSL reports consulting fees from Cerenovus, Genentech, Medtronic, Stryker, and Rapid Medical as imaging core laboratory. JG reports a Swiss National Funds grant for MRI in stroke. UF reports financial support for the present study from Medtronic; research grants from Medtronic BEYOND SWIFT registry, the Swiss National Science Foundation, and the Swiss Heart Foundation; consulting fees from Medtronic, Stryker, and CSL Behring (fees paid to institution); has membership of a data safety monitoring board for the IN EXTREMIS trial and the TITAN trial; was on the advisory board for Portola (Alexion; fees paid to institution); is an editor at the Journal of Neurointerventional Surgery; and is Vice President of the Swiss Neurological Society. JK reports financial support from Medtronic for the BEYOND SWIFT registry (fees paid to institution), and research grants from the Swiss National Science Foundation supporting the TECNO trial (fees paid to institution), Swiss Academy of Medical Sciences supporting MRI research (fees paid to institution), and Swiss Heart Foundation supporting cardiac MRI in the etiological work-up of stroke patients (fees paid to institution).

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Auteurs

Adnan Mujanovic (A)

University Institute of Diagnostic and Interventional Neuroradiology, University Hospital Bern Inselspital, University of Bern, Bern, Switzerland.

Omer Eker (O)

Department of Neuroradiology, Hospices Civils de Lyon, Bron, France.

Gaultier Marnat (G)

Interventional and Diagnostic Neuroradiology, University Hospital Centre Bordeaux, Bordeaux, France.

Daniel Strbian (D)

Department of Neurology, HUS Helsinki University Hospital, Helsinki, Finland.

Petra Ijäs (P)

Department of Neurology, HUS Helsinki University Hospital, Helsinki, Finland.

Cécile Préterre (C)

Stroke Unit, University Hospital Centre Nantes, Nantes, France.

Aude Triquenot (A)

Department of Neurology, University Hospital Centre Rouen, Rouen, France.

Jean François Albucher (JF)

Neurology, University Hospital Centre Toulouse, Toulouse, France.

Maxime Gauberti (M)

Department of Neuroradiology, University Hospital Centre Caen, Caen, France.

David Weisenburger-Lile (D)

Department of Stroke and Diagnostic and Interventional Neuroradiology, Hospital Foch, Suresnes, France.

Marielle Ernst (M)

Department of Diagnostic and Interventional Neuroradiology, University Medical Center Göttingen, Gottingen, Germany.

Omid Nikoubashman (O)

Neuroradiology, University Hospital Aachen, Aachen, Germany.

Anastasios Mpotsaris (A)

Department of Neuroradiology, München Klinik Harlaching, Munchen, Germany.

Benjamin Gory (B)

Department of Diagnostic and Interventional Neuroradiology, University Hospital Centre Nancy, Nancy, France.

Vi Tuan Hua (V)

Department of Neurology, University Hospital Centre Reims, Reims, France.

Marc Ribo (M)

Stroke Unit, Neurology, Hospital Vall d'Hebron, Barcelona, Spain.

David S Liebeskind (DS)

Department of Neurology, University of California Los Angeles, Los Angeles, California, USA.

Tomas Dobrocky (T)

University Institute of Diagnostic and Interventional Neuroradiology, University Hospital Bern Inselspital, University of Bern, Bern, Switzerland.

Thomas R Meinel (TR)

Department of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.

Lukas Buetikofer (L)

CTU Bern, University of Bern, Bern, Switzerland.

Jan Gralla (J)

University Institute of Diagnostic and Interventional Neuroradiology, University Hospital Bern Inselspital, University of Bern, Bern, Switzerland.

Urs Fischer (U)

Department of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.
Department of Neurology, University Hospital Basel, Basel, Switzerland.

Johannes Kaesmacher (J)

University Institute of Diagnostic and Interventional Neuroradiology, University Hospital Bern Inselspital, University of Bern, Bern, Switzerland johannes.kaesmacher@insel.ch.

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