Introduction
More than 10% of endovascular stroke treatments (EVTs) for acute ischaemic stroke are associated with perioperative complications.1 They include distal embolisation to a new territory (4%–6%), de novo stenosis of target vessels (3.4%), vessel perforation (0.6%–4.9%), dissection (0.6%–3.9%), groin haematoma (2%–10%) and vasospasm (3.9%–23%).2–4 Iatrogenic vasospasm is a common complication that occurs due to the vessel wall irritation during probing or thrombectomy manoeuvres. Extracranial vasospasms of target vessel arteries occur when placing guiding catheters and intracranial vasospasms occur during stent retriever or contact aspiration instrumentation. On angiography, vasospasm can be perceived as a concentric contraction of the arterial vessel wall.5
Vasospasm is more likely to occur in younger patients with stroke as well as in EVT with multiple thrombectomy attempts.6 While vasospasm during EVT is generally considered as non-serious and a transient complication by many authors,7 others discuss vasospasm as a potential cause for extended infarction after EVT, difficulties in further EVT manoeuvres with ‘snagging’ of stent retrievers or stroke recurrence.8 The clinical relevance of vasospasm as a complication during EVT remains uncertain as well as geographical differences in incidence rates or related clinical sequelae. A higher prevalence of coronary vasospasm is demonstrated in Asian populations compared with the Western world.9 While racial differences in vasomotor reactivity after acute myocardial infarction are being discussed for several years10 and genetic determinants of vasospasm after subarachnoid haemorrhage have been defined,11 regional differences have not been investigated for cerebral vasospasm during EVT yet.
Intra-arterial application of vasodilators, such as calcium channel blockers (CCBs), can resolve vasospasm in most cases.12 CCBs can be added to catheter flushes to prevent vasospasm during EVT or they can be given intra-arterially via the intermediate or guide catheter after detection of vasospasm. Withdrawal of the catheter from the affected vessel and waiting is another strategy to manage vasospasm. As there are no guidelines available to guide management for vasospasm during EVT, we aimed to define the current treatment practice for vasospasm during EVT among neurointerventionalists (NIs).
Methods
This was an international, anonymous online survey conducted from 4 April 2023 to 15 May 2023. In total, 18 questions were developed to evaluate treatment strategies of vasospasm during EVT by NIs with a survey duration of approximately 5 min. Angiographic images of three patients with vasospasm in different territories (extracranial internal carotid artery, proximal middle cerebral artery M1 segment, distal medium-vessel segment) were shown and respondents asked to answer whether they would treat with intra-arterial vasodilator or not. The complete survey questions are listed in the online supplemental material. Analysis and reporting followed the recommendations of the Consensus-Based Checklist for Reporting of Survey Studies.13
The survey was distributed at a neurointerventional conference (World Live Neurovascular Conference 2023), via electronic communication of the German Society for Neuroradiology (distributed to 1450 members) and the European Society of Minimally Invasive Neurological Therapy (distributed to 3438 members, email opened by 33%, link opened by 5.4%), and via invitation by coauthors to their global colleagues. Internet protocol addresses were anonymously saved by the survey’s online platform to prevent duplicate response bias. Data are available on reasonable request to the corresponding author.
Statistical analysis
Data are shown as number of events and percentage (n, %). After testing for normal distribution with the Shapiro-Wilk test, further analysis was conducted with the Mann-Whitney U test or χ2 test to compare groups, as appropriate. All tests were performed on the basis of a two-sided level of p<0.05 considered statistically significant. P values were corrected for a false discovery rate of 0.05 (Benjamini-Hochberg adjusted p values). Statistical analyses were performed by using SPSS Statistics (V.29.0; IBM, Armonk, New York, USA).