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Potts, Matthew B.

https://orcid.org/0000-0002-0534-5097

Mayo Clinic

Northwestern University

Citations 3

Long-Term Clinical and Angiographic Outcomes Following Pipeline Embolization Device Treatment of Complex Internal Carotid Artery Aneurysms: Five-Year Results of the Pipeline for Uncoilable or Failed Aneurysms Trial
Becske, Tibor , Brinjikji, Waleed , Potts, Matthew B. , Kallmes, David F. , Shapiro, Maksim , Moran, Christopher J. , McDougall, Cameron G. , Szikora, István , Woo, Henry H. , Siddiqui, Adnan H. , Albuquerque, Felipe C. , Saatçi, Işıl , Cekirge, Saruhan H., Berez, Aaron L., Cher, Daniel , Berentei, Zsolt, Nelson, Peter K. , Levy, Elad I. , Lanzino, Giuseppe , Lopes, Demetrius K. , Fiorella, David , Marosföi, Miklós , Siddiqui, Adnan H , Szikora, Istvan

Neurosurgery | February 5, 2017 | Volume: 80 | Issue: 1 | Pages: 40-48

10.1093/neuros/nyw014 Get It

Abstract BACKGROUND: Early and mid-term safety and efficacy of aneurysm treatment with the Pipeline Embolization Device (PED) has been well demonstrated in prior studies. OBJECTIVE: To present 5-yr follow-up for patients treated in the Pipeline for Uncoilable or Failed Aneurysms clinical trial. METHODS: In our prospective, multicenter trial, 109 complex internal carotid artery (ICA) aneurysms in 107 subjects were treated with the PED. Patients were followed per a standardized protocol at 180 d and 1, 3, and 5 yr. Aneurysm occlusion, in-stent stenosis, modified Rankin Scale scores, and complications were recorded. RESULTS: The primary endpoint of complete aneurysm occlusion at 180 d (73.6%) was previously reported. Aneurysm occlusion for those patients with angiographic follow-up progressively increased over time to 86.8% (79/91), 93.4% (71/76), and 95.2% (60/63) at 1, 3, and 5 yr, respectively. Six aneurysms (5.7%) were retreated. New serious device-related events at 1, 3, and 5 yr were noted in 1% (1/96), 3.5% (3/85), and 0% (0/81) of subjects. There were 4 (3.7%) reported deaths in our trial. Seventy-eight (96.3%) of 81 patients with 5-yr clinical follow-up had modified Rankin Scale scores ≤2. No delayed neurological deaths or hemorrhagic or ischemic cerebrovascular events were reported beyond 6 mo. No recanalization of a previously occluded aneurysm was observed. CONCLUSION: Our 5-yr findings demonstrate that PED is a safe and effective treatment for large and giant wide-necked aneurysms of the intracranial ICA, with high rates of complete occlusion and low rates of delayed adverse events.
Pipeline for uncoilable or failed aneurysms: 3-year follow-up results
Becske, Tibor , Potts, Matthew B. , Shapiro, Maksim , Kallmes, David F. , Brinjikji, Waleed , Saatçi, Işıl , McDougall, Cameron G. , Szikora, István , Moran, Christopher J. , Woo, Henry H. , Berez, Aaron L., Cher, Daniel , Siddiqui, Adnan H. , Albuquerque, Felipe C. , Berentei, Zsolt, Marosföi, Miklós , Cekirge, Saruhan H., Nelson, Peter K. , Lanzino, Giuseppe , Lopes, Demetrius K. , Levy, Elad I. , Fiorella, David , Siddiqui, Adnan H , Szikora, Istvan

Journal of Neurosurgery | October 14, 2016 | Volume: 127 | Issue: 1 | Pages: 81-88

10.3171/2015.6.jns15311 Get It

OBJECTIVEThe long-term effectiveness of endovascular treatment of large and giant wide-neck aneurysms using traditional endovascular techniques has been disappointing, with high recanalization and re-treatment rates. Flow diversion with the Pipeline Embolization Device (PED) has been recently used as a stand-alone therapy for complex aneurysms, showing significant improvement in effectiveness while demonstrating a similar safety profile to stent-supported coil treatment. However, relatively little is known about its long-term safety and effectiveness. Here the authors report on the 3-year safety and effectiveness of flow diversion with the PED in a prospective cohort of patients with large and giant internal carotid artery aneurysms enrolled in the Pipeline for Uncoilable or Failed Aneurysms (PUFS) trial.METHODSThe PUFS trial is a prospective study of 107 patients with 109 aneurysms treated with the PED. Primary effectiveness and safety end points were demonstrated based on independently monitored 180-day clinical and angiographic data. Patients were enrolled in a long-term follow-up protocol including 1-, 3-, and 5-year clinical and imaging follow-up. In this paper, the authors report the midstudy (3-year) effectiveness and safety data.RESULTSAt 3 years posttreatment, 74 subjects with 76 aneurysms underwent catheter angiography as required per protocol. Overall, complete angiographic aneurysm occlusion was observed in 71 of these 76 aneurysms (93.4% cure rate). Five aneurysms were re-treated, using either coils or additional PEDs, for failure to occlude, and 3 of these 5 were cured by the 3-year follow-up. Angiographic cure with one or two treatments of Pipeline embolization alone was therefore achieved in 92.1%. No recanalization of a previously completely occluded aneurysm was noted on the 3-year angiograms. There were 3 (2.6%) delayed device- or aneurysm-related serious adverse events, none of which led to permanent neurological sequelae. No major or minor late-onset hemorrhagic or ischemic cerebrovascular events or neurological deaths were observed in the 6-month through 3-year posttreatment period. Among 103 surviving patients, 85 underwent functional outcome assessment in which modified Rankin Scale scores of 0–1 were demonstrated in 80 subjects.CONCLUSIONSPipeline embolization is safe and effective in the treatment of complex large and giant aneurysms of the intracranial internal carotid artery. Unlike more traditional endovascular treatments, flow diversion results in progressive vascular remodeling that leads to complete aneurysm obliteration over longer-term follow-up without delayed aneurysm recanalization and/or growth.Clinical trial registration no.: NCT00777088 (clinicaltrials.gov)
O-036 pufs safety and effectiveness outcomes by aneurysm shape
Becske, Tibor , Potts, Matthew B. , Brinjikji, Waleed , Kallmes, David F. , Shapiro, Maksim , Nelson, Peter K.

Oral abstracts | June 8, 2016 | Volume: No volume available | Issue: No issue available | Pages: A19-A20

10.1136/neurintsurg-2015-011917.36 Get It