Flow Diverting Stents in Cerebral Small Caliber Vessels for Aneurysm Treatment

Purpose The off-label use of flow diverting stents (FDS) for treating cerebral aneurysms in small distal vessels is increasing in clinical practice with encouraging results; however, data directly addressing the parent vessel size are still scarce. Our aim was to evaluate the safety and efficacy of...

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Veröffentlicht in:Clinical neuroradiology (Munich) 2023-03, Vol.33 (1), p.99-105
Hauptverfasser: Hohenstatt, Sophia, Vinci, Sergio L, Vollherbst, Dominik F, Tessitore, Agostino, Schmitt, Niclas, Pitrone, Antonio, Caragliano, Antonio A
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container_end_page 105
container_issue 1
container_start_page 99
container_title Clinical neuroradiology (Munich)
container_volume 33
creator Hohenstatt, Sophia
Vinci, Sergio L
Vollherbst, Dominik F
Tessitore, Agostino
Schmitt, Niclas
Pitrone, Antonio
Caragliano, Antonio A
description Purpose The off-label use of flow diverting stents (FDS) for treating cerebral aneurysms in small distal vessels is increasing in clinical practice with encouraging results; however, data directly addressing the parent vessel size are still scarce. Our aim was to evaluate the safety and efficacy of FDS placement in anterior and posterior circulation aneurysms with parent arteries [less than or equal to]â¯2â¯mm in a real-world representative setting. Methods We retrospectively reviewed patients treated with FDS at the three participating university hospitals between 2009 and 2021. The inclusion criteria were the placement of at least one FDS in a parent vessel with a maximum diameter of 2â¯mm or less. The primary clinical safety endpoint was the absence of death, major or minor symptomatic stroke, transient ischemic attack and procedure-related intracranial hemorrhage. Clinical outcome was assessed using the modified Rankin Scale (mRS) score at the follow-up visit at 1 year. The primary efficacy endpoint was defined as complete and near-complete occlusion at the 1âyear follow-up. Results We identified 55 patients harboring 56 aneurysms. The primary clinical safety endpoint was obtained in 93% of cases. The hemorrhagic and thromboembolic complication rates were 4% and 9%, respectively. No patient died or had a relevant discrepancy (>â¯1 point) at the pre-mRS and post-mRS. The primary efficacy endpoint was reached in 80% of cases. Conclusion The use of FDS in vessels
doi_str_mv 10.1007/s00062-022-01187-6
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Our aim was to evaluate the safety and efficacy of FDS placement in anterior and posterior circulation aneurysms with parent arteries [less than or equal to]â¯2â¯mm in a real-world representative setting. Methods We retrospectively reviewed patients treated with FDS at the three participating university hospitals between 2009 and 2021. The inclusion criteria were the placement of at least one FDS in a parent vessel with a maximum diameter of 2â¯mm or less. The primary clinical safety endpoint was the absence of death, major or minor symptomatic stroke, transient ischemic attack and procedure-related intracranial hemorrhage. Clinical outcome was assessed using the modified Rankin Scale (mRS) score at the follow-up visit at 1 year. The primary efficacy endpoint was defined as complete and near-complete occlusion at the 1âyear follow-up. Results We identified 55 patients harboring 56 aneurysms. The primary clinical safety endpoint was obtained in 93% of cases. The hemorrhagic and thromboembolic complication rates were 4% and 9%, respectively. No patient died or had a relevant discrepancy (&gt;â¯1 point) at the pre-mRS and post-mRS. The primary efficacy endpoint was reached in 80% of cases. Conclusion The use of FDS in vessels &lt;â¯2â¯mm is technically feasible with good aneurysm occlusion rates and an acceptable safety profile. Nevertheless, it is essential to be aware of the of the main complications associated when operating in small diameter vessels.</description><identifier>ISSN: 1869-1439</identifier><identifier>EISSN: 1869-1447</identifier><identifier>DOI: 10.1007/s00062-022-01187-6</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Aneurysms ; Care and treatment ; Chief financial officers ; Clopidogrel ; Stent (Surgery) ; Stroke (Disease) ; Tirofiban</subject><ispartof>Clinical neuroradiology (Munich), 2023-03, Vol.33 (1), p.99-105</ispartof><rights>COPYRIGHT 2023 Springer</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1446-a4e10babe0ee2f22dffeb54a694af2f871f617e1c3b70cff1e7164bf65a4c04d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Hohenstatt, Sophia</creatorcontrib><creatorcontrib>Vinci, Sergio L</creatorcontrib><creatorcontrib>Vollherbst, Dominik F</creatorcontrib><creatorcontrib>Tessitore, Agostino</creatorcontrib><creatorcontrib>Schmitt, Niclas</creatorcontrib><creatorcontrib>Pitrone, Antonio</creatorcontrib><creatorcontrib>Caragliano, Antonio A</creatorcontrib><title>Flow Diverting Stents in Cerebral Small Caliber Vessels for Aneurysm Treatment</title><title>Clinical neuroradiology (Munich)</title><description>Purpose The off-label use of flow diverting stents (FDS) for treating cerebral aneurysms in small distal vessels is increasing in clinical practice with encouraging results; however, data directly addressing the parent vessel size are still scarce. Our aim was to evaluate the safety and efficacy of FDS placement in anterior and posterior circulation aneurysms with parent arteries [less than or equal to]â¯2â¯mm in a real-world representative setting. Methods We retrospectively reviewed patients treated with FDS at the three participating university hospitals between 2009 and 2021. The inclusion criteria were the placement of at least one FDS in a parent vessel with a maximum diameter of 2â¯mm or less. The primary clinical safety endpoint was the absence of death, major or minor symptomatic stroke, transient ischemic attack and procedure-related intracranial hemorrhage. Clinical outcome was assessed using the modified Rankin Scale (mRS) score at the follow-up visit at 1 year. The primary efficacy endpoint was defined as complete and near-complete occlusion at the 1âyear follow-up. Results We identified 55 patients harboring 56 aneurysms. The primary clinical safety endpoint was obtained in 93% of cases. The hemorrhagic and thromboembolic complication rates were 4% and 9%, respectively. No patient died or had a relevant discrepancy (&gt;â¯1 point) at the pre-mRS and post-mRS. The primary efficacy endpoint was reached in 80% of cases. Conclusion The use of FDS in vessels &lt;â¯2â¯mm is technically feasible with good aneurysm occlusion rates and an acceptable safety profile. 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subjects Aneurysms
Care and treatment
Chief financial officers
Clopidogrel
Stent (Surgery)
Stroke (Disease)
Tirofiban
title Flow Diverting Stents in Cerebral Small Caliber Vessels for Aneurysm Treatment
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