# Preliminary comparison of efficacy and safety between direct bypass surgery and endovascular recanalization therapy in adult ischemic moyamoya disease

**Authors:** Ming Yang, Xin Liu, Chaohui Liang, Lin Zhao, Pengfei Dong, Guangyu Zhang, Yan Feng, Jingchen Li, Yanan Li

PMC · DOI: 10.3389/fneur.2026.1689206 · Frontiers in Neurology · 2026-02-20

## TL;DR

This study compares two treatments for moyamoya disease and finds both are effective short-term, with endovascular therapy having fewer complications.

## Contribution

A preliminary comparison of endovascular recanalization and direct bypass surgery in adult moyamoya disease patients.

## Key findings

- Both treatments improved cerebral perfusion and neurological function similarly in the short term.
- Endovascular therapy had fewer complications and shorter hospital stays.
- Long-term outcomes and restenosis rates remain unclear and need further study.

## Abstract

To compare the efficacy of endovascular recanalization therapy and direct bypass surgery in treating adult ischemic moyamoya disease.

This retrospective study evaluated vascular wall conditions and occlusion characteristics preoperatively using high-resolution magnetic resonance imaging (HRMRI). Computed tomography angiography (CTA) and CT perfusion (CTP) were performed preoperatively, at 7 days, and 3 months postoperatively to assess vascular patency and cerebral perfusion. Modified Rankin Scale (mRS) scores were used to evaluate neurological function at corresponding time points.

A total of 67 adult patients with ischemic moyamoya disease were included, comprising 43 patients undergoing direct bypass surgery (bypass group) and 24 receiving endovascular recanalization therapy (endovascular group). Intraoperative indocyanine green angiography confirmed successful anastomosis or recanalization in all patients. Postoperative imaging showed no cerebral hemorrhage or acute infarction. Both groups demonstrated significant improvements in cerebral perfusion parameters compared to baseline (p < 0.05). The majority of patients in both groups maintained a favorable functional outcome (mRS ≤ 2) postoperatively, and no significant differences in mRS scores were found between groups at any time point (p > 0.05). Complications were fewer and hospitalization duration was shorter in the endovascular group, with lower incidence of hyperperfusion symptoms and perioperative adverse events.

In this preliminary study, endovascular recanalization therapy was feasible and demonstrated promising short-term outcomes, showing comparable improvements in cerebral perfusion and neurological function to direct bypass surgery at 3-month follow-up. However, the long-term durability, restenosis rates, and clinical implications of this finding require further investigation.

## Linked entities

- **Diseases:** moyamoya disease (MONDO:0016820)

## Full-text entities

- **Diseases:** seizures (MESH:D012640), cerebrovascular stenosis (MESH:D003251), ischemia (MESH:D007511), Stroke (MESH:D020521), intracranial hemorrhage (MESH:D020300), EDAS (MESH:D001159), hemorrhage (MESH:D006470), insomnia (MESH:D007319), vessel occlusion (MESH:C536223), ischemic (MESH:D002545), weakness (MESH:D018908), diabetes (MESH:D003920), hyperperfusion syndrome (MESH:D013577), PD (MESH:D010300), complications (MESH:D008107), headache (MESH:D006261), injury (MESH:D014947), II disease with (MESH:D004194), hyperlipidemia (MESH:D006949), cerebral hyperperfusion syndrome (MESH:D002547), cognitive decline (MESH:D003072), neurological sequelae (MESH:D009422), perforator occlusion (MESH:D057112), allergy (MESH:D004342), MMD (MESH:D009072), ischemic attacks (MESH:D002546), Infarct (MESH:D007238), numbness (MESH:D006987), cerebrovascular disorder (MESH:D002561), dizziness (MESH:D004244), artery terminus (MESH:D012078), infections (MESH:D007239), cerebral infarction (MESH:D002544), Postoperative complications (MESH:D011183), death (MESH:D003643), occlusion (MESH:D001157), hypertension (MESH:D006973), MCA stenosis (MESH:D020244), Atherosclerotic lesion (MESH:D050197), cerebral hemorrhage (MESH:D002543), thrombus (MESH:D013927), restenosis (MESH:D023903), epilepsy (MESH:D004827)
- **Chemicals:** aspirin (MESH:D001241), calcium (MESH:D002118), tirofiban (MESH:D000077466), indocyanine green (MESH:D007208), clopidogrel (MESH:D000077144), antiplatelet (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962938/full.md

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Source: https://tomesphere.com/paper/PMC12962938