TY - JOUR
T1 - Middle Meningeal Artery Embolization for Nonacute Subdural Hematoma
T2 - A Meta-Analysis of Large Randomized Controlled Trials
AU - Chen, Huanwen
AU - McIntyre, Matthew K.
AU - Kan, Peter
AU - Gandhi, Dheeraj
AU - Colasurdo, Marco
N1 - Publisher Copyright:
© 2025 American Society of Neuroradiology. All rights reserved.
PY - 2025/10/1
Y1 - 2025/10/1
N2 - BACKGROUND: Middle meningeal artery embolization (MMAE) has emerged as a novel treatment for non-acute subdural hematoma (SDH), particularly for reducing the risk of SDH recurrence. Recently, 5 randomized controlled trials (RCTs) of MMAE as an adjunct to conventional management (surgical or observant) have concluded their investigation and reported their outcomes. PURPOSE: Our goal was to synthesize trial results to provide more definitive guidance on the role of MMAE in the management of non-acute SDH. DATA SOURCES: The MEDLINE database from inception up to November 23, 2024 was used. English-language clinical articles reporting large randomized controlled trials (n ¼ 100 or more) investigating the efficacy and safety of MMAE for patients with non-acute subdural hematoma were identified. STUDY SELECTION: Five trials were identified–EMBOLISE, STEM, MAGIC-MT, EMPROTECT, and MEMBRANE. DATA ANALYSIS: The primary efficacy end point was SDH treatment failure (broadly defined as SDH recurrence or requirement of surgical rescue) within 3 to 6 months. Safety end points include death and stroke. DATA SYNTHESIS: There was significant heterogeneity in terms of patient populations as well as reported outcomes. Overall, MMAE was associated with significantly lower odds of SDH treatment failure (OR 0.51 [95% CI 0.39–0.67], P, .001), with minimal inter study heterogeneity. Compared with conventional management, MMAE was not significantly associated with different odds of death (OR 1.03 [95% CI 0.36–2.99], P ¼ .95) or stroke (OR 1.10 [95% CI 0.36–3.39], P ¼ .86). LIMITATIONS: Our meta-analysis is limited by selection bias and high heterogeneity in study design and reported outcomes. CONCLUSIONS: This study provides high-level evidence that, for patients with non-acute SDH, MMAE is a safe and effective adjunct to conventional management for preventing treatment failure.
AB - BACKGROUND: Middle meningeal artery embolization (MMAE) has emerged as a novel treatment for non-acute subdural hematoma (SDH), particularly for reducing the risk of SDH recurrence. Recently, 5 randomized controlled trials (RCTs) of MMAE as an adjunct to conventional management (surgical or observant) have concluded their investigation and reported their outcomes. PURPOSE: Our goal was to synthesize trial results to provide more definitive guidance on the role of MMAE in the management of non-acute SDH. DATA SOURCES: The MEDLINE database from inception up to November 23, 2024 was used. English-language clinical articles reporting large randomized controlled trials (n ¼ 100 or more) investigating the efficacy and safety of MMAE for patients with non-acute subdural hematoma were identified. STUDY SELECTION: Five trials were identified–EMBOLISE, STEM, MAGIC-MT, EMPROTECT, and MEMBRANE. DATA ANALYSIS: The primary efficacy end point was SDH treatment failure (broadly defined as SDH recurrence or requirement of surgical rescue) within 3 to 6 months. Safety end points include death and stroke. DATA SYNTHESIS: There was significant heterogeneity in terms of patient populations as well as reported outcomes. Overall, MMAE was associated with significantly lower odds of SDH treatment failure (OR 0.51 [95% CI 0.39–0.67], P, .001), with minimal inter study heterogeneity. Compared with conventional management, MMAE was not significantly associated with different odds of death (OR 1.03 [95% CI 0.36–2.99], P ¼ .95) or stroke (OR 1.10 [95% CI 0.36–3.39], P ¼ .86). LIMITATIONS: Our meta-analysis is limited by selection bias and high heterogeneity in study design and reported outcomes. CONCLUSIONS: This study provides high-level evidence that, for patients with non-acute SDH, MMAE is a safe and effective adjunct to conventional management for preventing treatment failure.
UR - https://www.scopus.com/pages/publications/105018013678
UR - https://www.scopus.com/pages/publications/105018013678#tab=citedBy
U2 - 10.3174/ajnr.A8781
DO - 10.3174/ajnr.A8781
M3 - Article
C2 - 40204352
AN - SCOPUS:105018013678
SN - 0195-6108
VL - 46
SP - 2069
EP - 2074
JO - American Journal of Neuroradiology
JF - American Journal of Neuroradiology
IS - 10
ER -