A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

First clinical multicenter experience with the new Pipeline Vantage flow diverter




TekijätVollherbst Dominik F, Cekirge H Saruhan, Saatci Isil, Baltacioglu Feyyaz, Onal Baran, Koc Osman, Rautio Riitta, Sinisalo Matias, Tomasello Alejandro, Vega Pedro, Martinez-Galdamez Mario, Lynch Jeremy, Pereira Vitor Mendes, Bendszus Martin, Möhlenbruch Markus A

KustantajaBMJ Publishing Group

Julkaisuvuosi2023

JournalJournal of NeuroInterventional Surgery

Tietokannassa oleva lehden nimiJOURNAL OF NEUROINTERVENTIONAL SURGERY

Lehden akronyymiJ NEUROINTERV SURG

Vuosikerta15

Aloitussivu63

Lopetussivu69

Sivujen määrä7

ISSN1759-8478

eISSN1759-8486

DOIhttps://doi.org/10.1136/neurintsurg-2021-018480

Verkko-osoitehttp://dx.doi.org/10.1136/neurintsurg-2021-018480


Tiivistelmä

Background: Flow diversion is an innovative and increasingly used technique for the treatment of intracranial aneurysms. New flow diverters (FDs) are being introduced to improve the safety and efficacy of this treatment. The aim of this study was to assess the safety, feasibility, and efficacy of the new Pipeline Vantage (PV) FD.

Methods: Patients with intracranial aneurysms treated with the PV at 10 international neurovascular centers were retrospectively analyzed. Patient and aneurysm characteristics, procedural parameters, complications, and the grade of occlusion were assessed.

Results: 60 patients with 70 aneurysms (5.0% with acute hemorrhage, 90.0% located in the anterior circulation) were included. 82 PVs were implanted in 61 treatment sessions. The PV could be successfully implanted in all treatments. Additional coiling was performed in 18.6%, and in-stent balloon angioplasty (to enhance the vessel wall apposition) in 24.6%. Periprocedural technical complications occurred in 24.6% of the treatments, were predominantly FD deployment problems, and were all asymptomatic. The overall symptomatic complication rate was 8.2% and the neurological symptomatic complication rate was 3.3%. Only one symptomatic complication was device-related (perforator artery infarctions leading to stroke). After a mean follow-up of 7.1 months, the rate of complete aneurysm occlusion was 77.9%. One patient (1.7%) died due to aneurysmal subarachnoid hemorrhage which occurred before treatment, unrelated to the procedure.

Conclusions: The new PV FD is safe and feasible for the treatment of intracranial aneurysms. The short-term occlusion rates are promising but need further assessment in prospective long-term follow-up studies.



Last updated on 2024-26-11 at 14:12