Early Postmarket Results After Treatment of Intracranial Aneurysms With the Pipeline Embolization Device

Author:

Kan Peter12,Siddiqui Adnan H.132,Veznedaroglu Erol4,Liebman Kenneth M.4,Binning Mandy J.4,Dumont Travis M.12,Ogilvy Christopher S.125,Gaughen John R.6,Mocco J7,Velat Gregory J.8,Ringer Andrew J.9,Welch Babu G.10,Horowitz Michael B.11,Snyder Kenneth V.132,Hopkins L. Nelson13212,Levy Elad I.132

Affiliation:

1. Department of Neurosurgery and Toshiba Stroke and Vascular Research Center and School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, New York

2. Department of Neurosurgery, Gates Vascular Institute, Kaleida Health, Buffalo, New York

3. Department of Radiology, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, New York

4. Department of Neurosciences, Stroke and Cerebrovascular Center of New Jersey, Capital Health, Trenton, New Jersey

5. Neurovascular Service, Massachusetts General Hospital, Boston, Massachusetts

6. University of South Florida, Department of Neurosurgery, Tampa, Florida

7. Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee

8. Department of Neurosurgery, University of Florida, Gainesville, Florida

9. Mayfield Clinic, Department of Neurosurgery, University of Cincinnati, Cincinnati, Ohio

10. Departments of Neurosurgery and Neuroradiology, University of Texas Southwestern, Dallas, Texas

11. Department of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania

12. Jacobs Institute, Buffalo, New York

Abstract

ABSTRACT BACKGROUND: The Pipeline embolization device (PED) is the latest technology available for intracranial aneurysm treatment. OBJECTIVE: To report early postmarket results with the PED. METHODS: This study was a prospective registry of patients treated with PEDs at 7 American neurosurgical centers subsequent to Food and Drug Administration approval of this device. Data collected included clinical presentation, aneurysm characteristics, treatment details, and periprocedural events. Follow-up data included degree of aneurysm occlusion and delayed (> 30 days after the procedure) complications. RESULTS: Sixty-two PED procedures were performed to treat 58 aneurysms in 56 patients. Thirty-seven of the aneurysms (64%) treated were located from the cavernous to the superior hypophyseal artery segment of the internal carotid artery; 22% were distal to that segment, and 14% were in the vertebrobasilar system. A total of 123 PEDs were deployed with an average of 2 implanted per aneurysm treated. Six devices were incompletely deployed; in these cases, rescue balloon angioplasty was required. Six periprocedural (during the procedure/within 30 days after the procedure) thromboembolic events occurred, of which 5 were in patients with vertebrobasilar aneurysms. There were 4 fatal postprocedural hemorrhages (from 2 giant basilar trunk and 2 large ophthalmic artery aneurysms). The major complication rate (permanent disability/death resulting from perioperative/delayed complication) was 8.5%. Among 19 patients with 3-month follow-up angiography, 68% (13 patients) had complete aneurysm occlusion. Two patients presented with delayed flow-limiting in-stent stenosis that was successfully treated with angioplasty. CONCLUSION: Unlike conventional coil embolization, aneurysm occlusion with PED is not immediate. Early complications include both thromboembolic and hemorrhagic events and appear to be significantly more frequent in association with treatment of vertebrobasilar aneurysms.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

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