Literature DB >> 28862519

Novel insights into symptomatology of moyamoya disease in pediatric patients: survey of symptoms suggestive of orthostatic intolerance.

Haruto Uchino1, Ken Kazumata1, Masaki Ito1, Naoki Nakayama1, Kiyohiro Houkin1.   

Abstract

OBJECTIVE A specific population of young patients with moyamoya disease (MMD) persistently experience physical symptoms not attributable to focal ischemia. These symptoms, highly suggestive of orthostatic intolerance (also termed "orthostatic dysregulation"), were investigated and reported as potential determinants of quality of life in young MMD patients. METHODS Forty-six patients (6-30 years of age) were selected from a group of 122 patients who were diagnosed with MMD before 18 years of age. The authors administered a structured questionnaire consisting of 11 items based on screening checklists published in the Japanese clinical guidelines for juvenile orthostatic dysregulation in young patients. The results were tabulated, and correlations with clinical data were explored. RESULTS Thirty-seven (80%) patients (mean age 15.9 years) responded to the questionnaire. Frequent headache, vertigo/dizziness on standing, fatigue, difficulty with getting out of bed, and motion sickness were the top 5 symptoms, resulting in 57% of patients being unable to attend school. Forty-three percent of the patients demonstrated multiple symptoms suggestive of orthostatic intolerance, even as long as 5 years after revascularization surgery. The number of symptoms was inversely associated with the number of years after surgery (p = 0.028). The number of symptoms was not associated with a history of surgery, clinical presentations, vascular involvement, cerebral perfusion, brain lesions, or history of transient ischemic attacks. CONCLUSIONS The present study provided novel insight into the symptomatology of young patients with MMD. Failure to notice nonfocal physical symptoms can significantly impair quality of life in young patients with MMD even years after successful revascularization surgery. These symptoms may serve as independent clinical markers used to assess disease outcome, although the underlying mechanisms of this disease are, as of yet, unclear.

Entities:  

Keywords:  MMD = moyamoya disease; TIA = transient ischemic attack; hemodynamic compromise; juvenile; moyamoya; orthostatic intolerance; quality of life; vascular disorders

Mesh:

Year:  2017        PMID: 28862519     DOI: 10.3171/2017.5.PEDS17198

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


  3 in total

1.  Clinical presentation of Moyamoya angiopathy in Europeans: experiences from Germany with 200 patients.

Authors:  Markus Kraemer; Jan Claudius Schwitalla; Frank Diesner; Orhan Aktas; Hans-Peter Hartung; Peter Berlit
Journal:  J Neurol       Date:  2019-03-13       Impact factor: 4.849

Review 2.  Neurological vertigo in the emergency room in pediatric and adult age: systematic literature review and proposal for a diagnostic algorithm.

Authors:  Noemi Pellegrino; Vincenzo Di Stefano; Eleonora Rotondo; Alessandro Graziosi; Marianna Gabriella Rispoli; Angelo Torrente; Antonino Lupica; Filippo Brighina; Umberto Raucci; Pasquale Parisi
Journal:  Ital J Pediatr       Date:  2022-07-27       Impact factor: 3.288

3.  Assessment of Single-Barrel Superficial Temporal Artery-Middle Cerebral Artery Bypass in Treatment for Adult Patients with Ischemic-Type Moyamoya Disease.

Authors:  Xiaoyang Tao; Yin Liu; Jun Chen; Li Xu; Zhijie Zhou; Haiyan Lei; Yiming Yin
Journal:  Med Sci Monit       Date:  2018-10-19
  3 in total

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