Prospective study on embolization of intracranial aneurysms with the pipeline device: the PREMIER study 1 year results
AuthorsHanel, Ricardo A.
Puri, Ajit S.
UMass Chan AffiliationsNew England Center for Stroke Research, Department of Radiology
Document TypeJournal Article
Analytical, Diagnostic and Therapeutic Techniques and Equipment
Health Services Administration
MetadataShow full item record
AbstractBACKGROUND: Preliminary clinical studies on the safety and efficacy of the pipeline embolization device (PED) for the treatment of small/medium aneurysms have demonstrated high occlusion rates with low complications. OBJECTIVE: To evaluate the safety and effectiveness of the PED for treatment of wide necked small and medium intracranial aneurysms. METHODS: PREMIER is a prospective, multicenter, single arm trial. Patients were treated with the PED for unruptured wide necked aneurysms, measuring < /=12 mm along the internal carotid artery or vertebral artery, between July 2014 and November 2015. At 1 year post-procedure, the primary effectiveness endpoint was complete occlusion (Raymond grade 1) without major parent vessel stenosis ( < /=50%) or retreatment, and the primary safety endpoint was major stroke in the territory supplied by the treated artery or neurologic death. RESULTS: A total of 141 patients were treated with PEDs (mean age 54.6+/-11.3 years, 87.9% (124/141) women). Mean aneurysm size was 5.0+/-1.92 mm, and 84.4% (119/141) measured < 7 mm. PED placement was successful in 99.3% (140/141) of patients. Mean number of PEDs implanted per patient was 1.1+/-0.26; a single PED was used in 92.9% (131/141) of patients. At 1 year, 97.9% (138/141) of patients underwent follow-up angiography with 76.8% (106/138) of patients having met the study's primary effectiveness endpoint. The combined major morbidity and mortality rate was 2.1% (3/140). CONCLUSIONS: Treatment of wide necked small/medium aneurysms with the PED results in high rates of complete occlusion without significant parent vessel stenosis and low rates of permanent neurologic complications. TRIAL REGISTRATION: NCT02186561.
J Neurointerv Surg. 2019 Jul 15. pii: neurintsurg-2019-015091. doi: 10.1136/neurintsurg-2019-015091. [Epub ahead of print] Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/48376
Full author list omitted for brevity. For the full list of authors, see article.