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Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.

Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.

期刊: Frontiers in neurology 日期: 2026-01-01 PMID: 42656445 DOI: 10.3389/fneur.2026.1896356 浏览: 8
作者: Shen H, Qian Y, Hu J, Gao T, Sheng M, Qian X, Chen J, Ding Y, Jiang X, Dong S
H, S., Y, Q., J, H., T, G., M, S., X, Q., J, C., Y, D., X, J., & S, D. (2026). Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.. Frontiers in neurology. https://doi.org/10.3389/fneur.2026.1896356
H S, Y Q, J H, T G, M S, X Q, et al. Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.. Frontiers in neurology. 2026; doi: 10.3389/fneur.2026.1896356
H S, Y Q, J H, et al. Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.[J]. Frontiers in neurology. 2026. DOI: 10.3389/fneur.2026.1896356.
@article{h2026,
  author = {Shen H and Qian Y and Hu J and Gao T and Sheng M and Qian X and Chen J and Ding Y and Jiang X and Dong S},
  title = {Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.},
  journal = {Frontiers in neurology},
  year = {2026},
  doi = {10.3389/fneur.2026.1896356},
  note = {PMID: 42656445},
}
TY  - JOUR
AU  - Shen H
AU  - Qian Y
AU  - Hu J
AU  - Gao T
AU  - Sheng M
AU  - Qian X
AU  - Chen J
AU  - Ding Y
AU  - Jiang X
AU  - Dong S
TI  - Adjunctive middle meningeal artery embolization with low-viscosity liquid embolic agents for acute epidural hematoma: technical considerations and a case series.
T2  - Frontiers in neurology
PY  - 2026
DO  - 10.3389/fneur.2026.1896356
AN  - PMID:42656445
ER  - 

摘要

OBJECTIVE: To assess the feasibility, safety, and short-term outcomes of adjunctive middle meningeal artery (MMA) embolization using low-viscosity liquid embolic agents (1:1 diluted Onyx/DMSO and 1:9 diluted Glubran 2/Ethiodized Poppyseed Oil Injection) for acute epidural hematoma (AEDH). METHODS: We retrospectively reviewed 9 consecutive AEDH patients evaluated for MMA embolization at our institution. Eight underwent embolization, and one was converted to immediate craniotomy after pre-procedural cranial CT showed rapid hematoma expansion. In the embolization subgroup, low-viscosity agents included 1:1 diluted Onyx with dimethyl sulfoxide (DMSO) (n = 6) and 1:9 diluted Glubran 2/ethiodized oil (n = 2). Primary observations included technical success, radiographic evolution, clinical outcomes, and periprocedural complications. RESULTS: Technical success was achieved in all embolized cases (8/8). Across the eight embolized cases, low-viscosity agents reached distal dural branches without relevant proximal reflux, and no catheter adherence or catheter entrapment was observed. No procedure-related complications occurred. Follow-up imaging showed stable or resolving hematomas in all embolized patients, and none required rescue surgery for post-embolization expansion. Median discharge GCS was 15, and no new neurologic deficits were observed. In the non-embolized conversion case, immediate pre-procedural CT showed interval progression, and prompt craniotomy was performed. CONCLUSION: In selected AEDH patients, adjunctive MMA embolization with low-viscosity liquid embolic agents (1:1 diluted Onyx/DMSO and 1:9 diluted Glubran 2/ethiodized oil) was technically feasible with a favorable short-term safety profile and may help control bleeding and reduce the risk of hematoma expansion while balancing distal penetration and catheter control. This strategy may provide a minimally invasive treatment option for high-risk AEDH, but multicenter studies with larger retrospective case series are needed for confirmation.

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