Flow diversion treatment of complex bifurcation aneurysms beyond the circle of Willis: complications, aneurysm sac occlusion, reabsorption, recurrence, and jailed branch modification at follow-up.

ACoA = anterior communicating artery DSA = digital subtraction angiography DWI = diffusion-weighted imaging FD = flow diverter FRED = flow redirection endoluminal device MCA = middle cerebral artery PED = Pipeline embolization device PerA = pericallosal artery SAH = subarachnoid hemorrhage TOF = time-of-flight WEB = Woven EndoBridge endovascular treatment flow diverter interventional neurosurgery intracranial aneurysm mRS = modified Rankin Scale magnetic resonance imaging recurrence vascular disorders

Journal

Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357

Informations de publication

Date de publication:
01 12 2019
Historique:
received: 13 03 2018
accepted: 19 07 2018
pubmed: 24 12 2018
medline: 19 2 2020
entrez: 23 12 2018
Statut: epublish

Résumé

The purpose of this study is to present the authors' medium-term results, with special emphasis on complications, occlusion rate of the aneurysm sac (digital subtraction angiography [DSA] and MRI), and the fate of cortical branches and perforating arteries covered ("jailed") by the flow diverter (FD) stent. Between January 2010 and September 2017, 29 patients (14 female) with 30 aneurysms were treated with an FD stent. Twenty-one aneurysms were at the middle cerebral artery bifurcation, 8 were in the anterior communicating artery region, and 1 was a pericallosal artery bifurcation. Thirty-five cortical branches were covered. A single FD stent was used in all patients. Symptomatic and asymptomatic periprocedural and delayed complications were reported. DSA and MRI controls were analyzed to evaluate modification of the aneurysm sac and jailed branches. Permanent morbidity was 3.4% (1/29), due to a jailed branch occlusion, with a modified Rankin Scale (mRS) score of 2 at the last follow-up. Mortality and permanent complication with poor prognosis (mRS score > 2) rates were 0%. The mean follow-up time for DSA and MRI (mean ± SD) was 21 ± 14.5 months (range 3-66 months) and 19 ± 16 months (range 3-41 months), respectively. The mean time to aneurysm sac occlusion (available for 24 patients), including stable remodeling, was 11.8 ± 6 months (median 13, range 3-27 months). The overall occlusion rate was 82.1% (23/28), and it was 91.7% (22/24) in the group of patients with at least 2 DSA control sequences. One recanalization occurred at 41 months posttreatment. At the time of publication, at the latest follow-up, 7 (20%) of 35 covered branches were occluded, 18 (51.4%) showed a decreased caliber, and the remaining 10 (28.5%) were unchanged. MRI T2-weighted sequences showed complete sac reabsorption in 7/29 aneurysms (24.1%), and the remaining lesions were either smaller (55.2%) or unchanged (17.2%). MRI revealed asymptomatic and symptomatic ischemic events in perforator territories in 7/28 (25%) and 4/28 (14.3%) patients, respectively, which were reversible within 24 hours. Flow diversion of bifurcation aneurysms is feasible, with low rates of permanent morbidity and mortality and high occlusion rates; however, recurrence may occur. Caliber reduction and asymptomatic occlusion of covered cortical branches as well as silent perforator stroke are common. Ischemic complications may occur with no identified predictable factors. MRI controls should be required in all patients to evaluate silent ischemic lesions and aneurysm sac reabsorption over time.

Identifiants

pubmed: 30579280
doi: 10.3171/2018.7.JNS18654
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1751-1762

Auteurs

Caterina Michelozzi (C)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Jean Darcourt (J)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Adrien Guenego (A)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Anne-Christine Januel (AC)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Philippe Tall (P)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Matthias Gawlitza (M)

2Service de Neuroradiologie, CHU Reims, France.

Fabrice Bonneville (F)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

Christophe Cognard (C)

1Service de Neuroradiologie, Hôpital Pierre-Paul Riquet, CHU de Toulouse; and.

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