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Outcomes of Bypass Surgery in Adult Moyamoya Disease by Onset Type
DC Field | Value | Language |
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dc.contributor.author | Lim, YC | - |
dc.contributor.author | Lee, E | - |
dc.contributor.author | Song, J | - |
dc.date.accessioned | 2024-07-10T03:11:22Z | - |
dc.date.available | 2024-07-10T03:11:22Z | - |
dc.date.issued | 2024 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/32658 | - |
dc.description.abstract | Importance: Moyamoya disease (MMD) is a rare chronic cerebrovascular disease, and the outcomes of bypass management in adult patients remain controversial. Objective: To categorize adult MMD based on asymptomatic, ischemic, and hemorrhagic onset and compare the outcomes (death, hemorrhagic stroke [HS], and ischemic stroke [IS]) of bypass surgery (direct or indirect) with those of conservative management. Design, Setting, and Participants: This retrospective, nationwide, population-based longitudinal cohort study used Korean National Health Insurance Research data to identify adults (aged ≥15 years) with MMD who were diagnosed between January 1, 2008, and December 31, 2020, and followed up until December 31, 2021 (median follow-up, 5.74 [IQR, 2.95-9.42] years). A total of 19700 participants (3194 with hemorrhagic, 517 with ischemic, and 15989 with asymptomatic MMD) were included. Data were analyzed from January 2 to April 1, 2023. Exposures: Bypass surgery and conservative management. Main Outcomes and Measures: Death constituted the primary outcome; secondary outcomes consisted of HS or IS. Kaplan-Meier survival curve and Cox proportional hazards regression analysis were applied. The propensity score-matching and stratified analyses were performed to control covariate effects. Results: A total of 19700 patients (mean [SD] age, 45.43 [14.98] years; 12766 [64.8%] female) were included. Compared with conservative management, bypass was associated with a reduced risk of death (adjusted hazard ratio [AHR], 0.50 [95% CI, 0.41-0.61]; P <.001) and HS (AHR, 0.36 [0.30-0.40]; P <.001) in hemorrhagic MMD; reduced risk of IS (AHR, 0.55 [95% CI, 0.37-0.81]; P =.002) in ischemic MMD; and reduced risk of death (AHR, 0.74 [95% CI, 0.66-0.84]; P <.001) in asymptomatic MMD. However, bypass was associated with an increased risk of HS (AHR, 1.76 [95% CI, 1.56-2.00]; P <.001) in asymptomatic MMD. Both direct and indirect bypass demonstrated similar effects in hemorrhagic and asymptomatic MMD, except only direct bypass was associated with a reduced risk of IS (AHR, 0.52 [95% CI, 0.33- 0.83]; P =.01) in ischemic MMD. After stratification, bypass was associated with a reduced risk of death in patients younger than 55 years with ischemic (AHR, 0.34 [95% CI, 0.13- 0.88]; P =.03) and asymptomatic (AHR, 0.69 [95% CI, 0.60-0.79]; P <.001) MMD, but an increased risk of HS in patients 55 years or older with ischemic MMD (AHR, 2.13 [95% CI, 1.1-4.16]; P =.03). Conclusions and Relevance: The findings of this cohort study of bypass outcomes for patients with MMD emphasize the importance of tailoring management strategies in adult patients based on onset types. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Cerebral Revascularization | - |
dc.subject.MESH | Conservative Treatment | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Ischemic Stroke | - |
dc.subject.MESH | Longitudinal Studies | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Moyamoya Disease | - |
dc.subject.MESH | Republic of Korea | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Young Adult | - |
dc.title | Outcomes of Bypass Surgery in Adult Moyamoya Disease by Onset Type | - |
dc.type | Article | - |
dc.identifier.pmid | 38842810 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11157360 | - |
dc.contributor.affiliatedAuthor | Lim, YC | - |
dc.contributor.affiliatedAuthor | Song, J | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1001/jamanetworkopen.2024.15102 | - |
dc.citation.title | JAMA network open | - |
dc.citation.volume | 7 | - |
dc.citation.number | 6 | - |
dc.citation.date | 2024 | - |
dc.citation.startPage | e2415102 | - |
dc.citation.endPage | e2415102 | - |
dc.identifier.bibliographicCitation | JAMA network open, 7(6). : e2415102-e2415102, 2024 | - |
dc.identifier.eissn | 2574-3805 | - |
dc.relation.journalid | J025743805 | - |
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