Literature DB >> 22957756

Long-term follow-up of surgically treated juvenile patients with Moyamoya disease.

Maki Mukawa1, Tadashi Nariai, Yoshiharu Matsushima, Yoji Tanaka, Motoki Inaji, Taketoshi Maehara, Masaru Aoyagi, Kikuo Ohno.   

Abstract

OBJECT: Surgical revascularization is considered an effective treatment for juvenile patients with moyamoya disease (MMD). Yet the long-term outcome in surgically treated patients still needs to be clarified. More than 30 years have passed since the authors' department started intensively treating pediatric patients with MMD using indirect anastomosis techniques. In this study the authors surveyed the current status of these patients.
METHODS: Activities of daily living (ADLs) were surveyed and present clinical status was assessed based on the modified Rankin scale (mRS). Cerebrovascular events subsequent to surgical treatment were also recorded.
RESULTS: Since 1979, 208 patients younger than 19 years of age with MMD were surgically treated and followed up for > 3 years. Data were available on 172 patients (83%), who had been followed up for a mean of 14.3 years (range 3-32 years). Activity of daily living outcomes were as follows: 138 patients (80.2%) had mRS scores of 0-2, 29 (16.9%) a score of 3, 1 (0.6%) a score of 4, 1 (0.6%) a score of 5, and 3 (1.7%) a score of 6. Cerebrovascular events occurred 8 or more years after surgery in 6 patients (3.4%), that is, 6 hemorrhages and 3 infarctions. The cumulative risk of late-onset stroke at 10, 20, and 30 years after surgical intervention was 0.8%, 6.3%, and 10.0%, respectively.
CONCLUSIONS: This long-term survey demonstrated that most surgically treated pediatric patients with MMD maintain good ADL outcomes. However, a significant number of new cerebrovascular events occurred more than 10 years after the initial surgery. Additional follow-up will help to identify which events may occur during the adult years of patients treated as children.

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Year:  2012        PMID: 22957756     DOI: 10.3171/2012.8.PEDS11539

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


  5 in total

Review 1.  Recent advances in moyamoya disease: pathophysiology and treatment.

Authors:  Annick Kronenburg; Kees P J Braun; Albert van der Zwan; Catharina J M Klijn
Journal:  Curr Neurol Neurosci Rep       Date:  2014-01       Impact factor: 5.081

2.  Long-term Outcome of Motor Function in a Child with Moyamoya Disease: A Case Report.

Authors:  Ki Seok Nam
Journal:  J Phys Ther Sci       Date:  2014-01-08

Review 3.  Late Cerebrovascular Events and Social Outcome after Adolescence: Long-term Outcome of Pediatric Moyamoya Disease.

Authors:  Takeshi Funaki; Jun C Takahashi; Susumu Miyamoto
Journal:  Neurol Med Chir (Tokyo)       Date:  2018-05-21       Impact factor: 1.742

4.  Clinical Features, Surgical Treatment, and Long-Term Outcome of a Multicenter Cohort of Pediatric Moyamoya.

Authors:  Jun Zheng; Le-Bao Yu; Ke-Fang Dai; Yan Zhang; Rong Wang; Dong Zhang
Journal:  Front Neurol       Date:  2019-01-22       Impact factor: 4.003

5.  Predictors of clinical or cerebral lesion progression in adult moyamoya angiopathy.

Authors:  Dominique Hervé; Nathanaelle Ibos-Augé; Lionel Calvière; Christina Rogan; Marc Antoine Labeyrie; Jean Pierre Guichard; Ophélia Godin; Manoelle Kossorotoff; Marie Odile Habert; Elisabeth Tournier Lasserve; Sylvie Chevret; Hugues Chabriat
Journal:  Neurology       Date:  2019-06-25       Impact factor: 9.910

  5 in total

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