Evidence map›Paper›PMID 41093368›Full record

ArticleStroke and vascular neurology2026

Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study.

Cheng Chen, Gan Gao, Desheng Li, Hui Wang, Minjie Wang, Jingjie Li, Simeng Liu, Zhangwei Zeng, Shuainan Ning, Ronghui Gu and 3 more

Abstract read
In one paragraph

Article in Stroke and vascular neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Cheng Chen *Medical School of Chinese PLA, Beijing, Beijing, China.
Gan Gao *Medical School of Chinese PLA, Beijing, Beijing, China.
Desheng Li *Department of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China.
Hui WangDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-1152-5860
Minjie WangMedical School of Chinese PLA, Beijing, Beijing, China.
Jingjie LiMedical School of Chinese PLA, Beijing, Beijing, China.
Simeng LiuMedical School of Chinese PLA, Beijing, Beijing, China.
Zhangwei ZengMedical School of Chinese PLA, Beijing, Beijing, China.
Shuainan NingMedical School of Chinese PLA, Beijing, Beijing, China.
Ronghui GuDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China.
Songtao PeiDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China.
Cong HanDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China duanlian307@sina.com hc82225@126.com.
Lian DuanDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, China duanlian307@sina.com hc82225@126.com.ORCID http://orcid.org/0000-0001-7210-056X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPaediatric hemorrhagic moyamoya disease (hMMD) is rare, with unclear clinical features and long-term outcomes owing to limited data. We comprehensively evaluated the clinical characteristics, prognosis and optimal treatment strategies for pediatric hMMD.

methodsWe screened paediatric patients with hMMD hospitalised between November 2003 and December 2024. Clinical features, treatments and long-term outcomes were retrospectively analysed. Multivariate logistic regression was used to evaluate risk factors for rebleeding and poor prognosis.

resultsDuring the first decade, hemorrhagic events were rare. However, in the second decade, females experienced hemorrhage at age 13-15 years and males at 10-12 years. Over 1103 patient-years, 96 hemorrhagic events occurred. Before encephaloduroarteriosynangiosis (EDAS), seven rehemorrhage instances occurred among 94 patients over 93.2 patient-years of observation. A modified Rankin Scale score ≥3 on admission independently predicted rehemorrhage (p=0.040; OR 5.280; 95% CI 1.083 to 25.739), while early EDAS (within 3 months of the first hemorrhage) significantly reduced this risk (p=0.043; OR 0.107; 95% CI 0.012 to 0.933). EDAS patients had lower rehemorrhage rates compared with their natural history. Anterior choroidal artery dilation and early-onset and delayed-onset posterior cerebral artery involvement increased postoperative complication risk. Early EDAS reduced postoperative complications (p=0.028; OR 0.219; 95% CI 0.057 to 0.845).

conclusionAlthough rare, paediatric hMMD carries a high rebleeding rate. The second decade of life may represent the peak period for bleeding in paediatric patients with MMD, necessitating close monitoring. Early EDAS reduces rebleeding and postoperative complications in hMMD. Compared with the natural course, EDAS safely reduces paediatric rehemorrhage.

Indexed as

Cerebral RevascularizationIntracranial HemorrhagesMoyamoya DiseaseAdolescentAge FactorsChildFemaleFollow-Up StudiesHumansMaleRecurrenceRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsTreatment OutcomeCerebrovascular DisordersHemorrhagePediatricsStroke

Identifiers

PMID41093368
PMCPMC13540288

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.