Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study
Background Paediatric 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.Methods We screened paediatric pati...
| Published in: | Stroke and Vascular Neurology |
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| Main Authors: | , , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
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BMJ Publishing Group
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| Online Access: | https://svn.bmj.com/content/early/2025/10/14/svn-2025-004515.full |
| _version_ | 1848757017151275008 |
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| author | Hui Wang Cheng Chen Lian Duan Minjie Wang Jingjie Li Cong Han Gan Gao Desheng Li Simeng Liu Zhangwei Zeng Shuainan Ning Ronghui Gu Songtao Pei |
| author_facet | Hui Wang Cheng Chen Lian Duan Minjie Wang Jingjie Li Cong Han Gan Gao Desheng Li Simeng Liu Zhangwei Zeng Shuainan Ning Ronghui Gu Songtao Pei |
| author_sort | Hui Wang |
| collection | DOAJ |
| container_title | Stroke and Vascular Neurology |
| description | Background Paediatric 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.Methods We 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.Results During 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).Conclusion Although 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. |
| format | Article |
| id | doaj-art-c63d64aafc384ee8b9b3910fd7e6f60e |
| institution | Directory of Open Access Journals |
| issn | 2059-8696 |
| language | English |
| publisher | BMJ Publishing Group |
| record_format | Article |
| spelling | doaj-art-c63d64aafc384ee8b9b3910fd7e6f60e2025-10-16T05:55:11ZengBMJ Publishing GroupStroke and Vascular Neurology2059-869610.1136/svn-2025-004515Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up studyHui Wang0Cheng Chen1Lian Duan2Minjie Wang3Jingjie Li4Cong Han5Gan Gao6Desheng Li7Simeng Liu8Zhangwei Zeng9Shuainan Ning10Ronghui Gu11Songtao Pei12Department of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaMedical School of Chinese PLA, Beijing, Beijing, ChinaDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaDepartment of Neurosurgery, the First Medical Center of Chinese PLA General Hospital, Beijing, ChinaBackground Paediatric 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.Methods We 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.Results During 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).Conclusion Although 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.https://svn.bmj.com/content/early/2025/10/14/svn-2025-004515.full |
| spellingShingle | Hui Wang Cheng Chen Lian Duan Minjie Wang Jingjie Li Cong Han Gan Gao Desheng Li Simeng Liu Zhangwei Zeng Shuainan Ning Ronghui Gu Songtao Pei Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title | Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title_full | Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title_fullStr | Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title_full_unstemmed | Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title_short | Clinical features, treatment and long-term outcomes of hemorrhagic moyamoya disease in children: an extensive follow-up study |
| title_sort | clinical features treatment and long term outcomes of hemorrhagic moyamoya disease in children an extensive follow up study |
| url | https://svn.bmj.com/content/early/2025/10/14/svn-2025-004515.full |
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