Literature DB >> 29856299

Encephaloduroarteriosynangiosis for pediatric moyamoya disease: long-term follow-up of 100 cases at a single center.

Yong Zhang1,2, Xiang-Yang Bao2, Lian Duan1,2, Wei-Zhong Yang2, De-Sheng Li2, Zheng-Shan Zhang2, Cong Han2, Feng Zhao2, Qian Zhang2, Qian-Nan Wang2.   

Abstract

OBJECTIVE The object of this study was to summarize the long-term effect of encephaloduroarteriosynangiosis (EDAS) for the treatment of pediatric moyamoya disease (MMD) and to investigate factors influencing the clinical outcomes of EDAS. METHODS Clinical features, angiographic findings, and clinical outcomes were analyzed among MMD patients younger than 18 years who had been treated with EDAS between 2002 and 2007 at the authors' institution. The Kaplan-Meier method was used to estimate stroke risk after EDAS. Predictors of neurological outcome were assessed. RESULTS One hundred fifteen patients were identified. The mean age at symptom onset was 7.3 ± 4.0 years. The incidence of familial MMD was 11.3%. The female/male ratio was 1:1.16. A total of 232 EDAS procedures were performed, and the incidence of postoperative complications was 3%. Postoperative digital subtraction angiography was performed in 54% of the patients, and about 80% of the hemispheres showed good or excellent results. Neovascularization showed significant correlations with delay time (from symptom onset to first operation), Suzuki stage, and preoperative stroke (all p < 0.05). Clinical follow-up was available in 100 patients with a mean follow-up of 124.4 ± 10.5 months. Ten-year cumulative survival was 96.5% after surgery, and the risk of stroke was 0.33%/person-year. An independent life with no significant disability was reported by 92% of the patients. A good outcome correlated with a low Suzuki stage (p = 0.001). Older children and those without preoperative stroke had better clinical outcomes (p < 0.05). CONCLUSIONS On the basis of long-term follow-up data, the authors concluded that EDAS is a safe and effective treatment for pediatric MMD, can reduce the risk of subsequent neurological events, and can improve quality of life. The risk of ischemia-related complications was higher in younger patients, and older children showed better outcomes. Compensation was greater with more prominent cerebral ischemia. The long-term clinical outcome largely depended on the presence and extent of preoperative stroke.

Entities:  

Keywords:  CBF = cerebral blood flow; EDAS = encephaloduroarteriosynangiosis; MCA = middle cerebral artery; MMD = moyamoya disease; MRA = MR angiography; PCA = posterior cerebral artery; STA = superficial temporal artery; TIA = transient ischemic attack; encephaloduroarteriosynangiosis; long-term outcome; mRS = modified Rankin Scale; moyamoya disease; pediatric; vascular disorders

Mesh:

Year:  2018        PMID: 29856299     DOI: 10.3171/2018.2.PEDS17591

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  6 in total

1.  Clinical outcomes after revascularization for pediatric moyamoya disease and syndrome: A single-center series.

Authors:  Ramin A Morshed; Adib A Abla; Daniel Murph; Jasmin M Dao; Ethan A Winkler; Jan-Karl Burkhardt; Kathleen Colao; Steven W Hetts; Heather J Fullerton; Michael T Lawton; Nalin Gupta; Christine K Fox
Journal:  J Clin Neurosci       Date:  2020-08-19       Impact factor: 1.961

2.  Endothelial Progenitor Cells Induce Angiogenesis: a Potential Mechanism Underlying Neovascularization in Encephaloduroarteriosynangiosis.

Authors:  Qian-Nan Wang; Zheng-Xing Zou; Xiao-Peng Wang; Qian Zhang; Ya-Qun Zhao; Lian Duan; Xiang-Yang Bao
Journal:  Transl Stroke Res       Date:  2020-07-06       Impact factor: 6.829

3.  Seizure outcome in moyamoya after indirect revascularization in pediatric patients: Retrospective study and literature review.

Authors:  Abdullah Alramadan; Anwar Ul Haq; Sarah Basindwah; Essam Alshail
Journal:  Surg Neurol Int       Date:  2021-02-23

4.  Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort.

Authors:  Chiara Po'; Margherita Nosadini; Marialuisa Zedde; Rosario Pascarella; Giuseppe Mirone; Domenico Cicala; Anna Rosati; Alessandra Cosi; Irene Toldo; Raffaella Colombatti; Paola Martelli; Alessandro Iodice; Patrizia Accorsi; Lucio Giordano; Salvatore Savasta; Thomas Foiadelli; Giuseppina Sanfilippo; Elvis Lafe; Federico Zappoli Thyrion; Gabriele Polonara; Serena Campa; Federico Raviglione; Barbara Scelsa; Stefania Maria Bova; Filippo Greco; Duccio Maria Cordelli; Luigi Cirillo; Francesco Toni; Valentina Baro; Francesco Causin; Anna Chiara Frigo; Agnese Suppiej; Laura Sainati; Danila Azzolina; Manuela Agostini; Elisabetta Cesaroni; Luigi De Carlo; Gabriella Di Rosa; Giacomo Esposito; Luisa Grazian; Giovanna Morini; Francesco Nicita; Francesca Felicia Operto; Dario Pruna; Paola Ragazzi; Massimo Rollo; Alberto Spalice; Pasquale Striano; Aldo Skabar; Luigi Alberto Lanterna; Andrea Carai; Carlo Efisio Marras; Renzo Manara; Stefano Sartori
Journal:  Front Pediatr       Date:  2022-05-06       Impact factor: 3.418

5.  Recognition of the Effect of Indirect Revascularization for Moyamoya Disease: The Balance Between the Stage Progression and Neoangiogenesis.

Authors:  Xiang-Yang Bao; Qian-Nan Wang; Xiao-Peng Wang; Ri-Miao Yang; Zheng-Xing Zou; Qian Zhang; De-Sheng Li; Lian Duan
Journal:  Front Neurol       Date:  2022-05-06       Impact factor: 4.003

6.  The Potential Mechanism Behind Native and Therapeutic Collaterals in Moyamoya.

Authors:  Xiang-Yang Bao; Yan-Na Fan; Qian-Nan Wang; Xiao-Peng Wang; Ri-Miao Yang; Zheng-Xing Zou; Qian Zhang; De-Sheng Li; Lian Duan; Xin-Guang Yu
Journal:  Front Neurol       Date:  2022-04-26       Impact factor: 4.003

  6 in total

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