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A DELPHI consensus statement on antiplatelet management for intracranial stenting due to underlying atherosclerosis
Mayank Goyal1, Kirill Orlov2, Mary E Jensen3
1Departments of Radiology and Clinical Neurosciences, Foothills Medical Centre, University of Calgary, 1403 29th St. NW, Calgary, AB, T2N2T9, Canada. mgoyal@ucalgary.ca.
Insights
Experts reached consensus on post-procedure antiplatelet therapy for intracranial stenting in atherosclerosis, favoring aspirin and a P2Y12 inhibitor. However, pre- and intra-procedure management lacked agreement, highlighting the need for further research on optimal antiplatelet regimens.
Area of Science:
- Neurology
- Interventional Neuroradiology
- Cardiology
Background:
- Intracranial stenting for atherosclerosis lacks consensus on antiplatelet management.
- Endovascular treatment (EVT) for intracranial atherosclerosis presents unique challenges for antiplatelet strategies.
Purpose of the Study:
- To achieve expert consensus on antiplatelet management for intracranial stenting in atherosclerosis during EVT.
- To identify areas of agreement and disagreement among neurointerventionalists regarding antiplatelet regimens.
Main Methods:
- Modified DELPHI approach utilized with an international expert panel (19 neurointerventionalists).
- Anonymized online questionnaires with iterative feedback loops were employed over 5 survey rounds.
- Consensus defined as ≥70% agreement for binary questions and ≥50% for multi-option questions.
Main Results:
- Experts acknowledged insufficient data for evidence-based recommendations in many aspects.
- A standardized regimen was preferred irrespective of imaging or reperfusion quality.
- Consensus was achieved on postprocedural therapy (aspirin plus P2Y12 inhibitor), but not on pre- and intraprocedural timing or agents.
Conclusions:
- Limited data exists for antiplatelet management in intracranial stenting for atherosclerosis.
- Postprocedural antiplatelet management achieved expert consensus, but pre- and intraprocedural strategies did not.
- Prospective studies are necessary to optimize antiplatelet regimens for these procedures.
Purpose:
There is little data and lack of consensus regarding antiplatelet management for intracranial stenting due to underlying intracranial atherosclerosis in the setting of endovascular treatment (EVT). In this DELPHI study, we aimed to assess whether consensus on antiplatelet management in this situation among experienced experts can be achieved, and what this consensus would be.
Methods:
We used a modified DELPHI approach to address unanswered questions in antiplatelet management for intracranial stenting due to underlying atherosclerosis in the setting of EVT. An expert-panel (19 neurointerventionalists from 8 countries) answered structured, anonymized on-line questionnaires with iterative feedback-loops. Panel-consensus was defined as agreement ≥ 70% for binary closed-ended questions/≥ 50% for closed-ended questions with > 2 response options.
Results:
Panel members answered a total of 5 survey rounds. They acknowledged that there is insufficient data for evidence-based recommendations in many aspects of antiplatelet management for intracranial stenting due to underlying atherosclerosis in the setting of EVT. They believed that antiplatelet management should follow a standardized regimen, irrespective of imaging findings and reperfusion quality. There was no consensus on the timing of antiplatelet-therapy initiation. Aspirin was the preferred antiplatelet agent for the peri-procedural period, and oral Aspirin in combination with a P2Y12 inhibitor was the favored postprocedural regimen.
Conclusion:
Data on antiplatelet management for intracranial stenting due to underlying atherosclerosis in the setting of EVT are limited. Panel-members in this study achieved consensus on postprocedural antiplatelet management but did not agree upon a preprocedural and intraprocedural antiplatelet regimen. Further prospective studies to optimize antiplatelet regimens are needed.
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