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This randomized trial investigated whether middle meningeal artery embolization added to standard surgical or nonsurgical treatment reduced treatment failure in 310 patients with symptomatic chronic subdural hematoma. Participants were assigned to embolization plus standard treatment (n=149) or standard treatment alone (n=161); the primary efficacy endpoint was a composite of residual or recurrent hematoma greater than 10 mm, reoperation or surgical rescue, or major disabling stroke, myocardial infarction, or neurological death within 180 days. In the primary efficacy analysis, treatment failure occurred in 19 of 120 patients (16%) receiving embolization compared with 47 of 129 (36%) receiving standard treatment alone, corresponding to an odds ratio of 0.36 (95% CI, 0.20–0.66; P=0.001) and an absolute difference of 20 percentage points. The primary safety endpoint of major disabling stroke or death within 30 days occurred in 4 of 144 patients (3%) in the embolization group and 5 of 166 (3%) in the control group. By 180 days, deaths had occurred in 12 patients (8%) receiving embolization and 9 (5%) receiving standard treatment; neurological deaths occurred in 1 patient (1%) and 3 patients (2%), respectively. These findings suggest that adjunctive embolization reduces treatment failure without a detected increase in the prespecified 30-day safety endpoint, although longer-term safety requires continued evaluation.

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This randomized trial investigated whether middle meningeal artery embolization added to standard surgical or nonsurgical treatment reduced treatment failure in 310 patients with symptomatic chronic subdural hematoma. Participants were assigned to embolization plus standard treatment (n=149) or standard treatment alone (n=161); the primary efficacy endpoint was a composite of residual or recurrent hematoma greater than 10 mm, reoperation or surgical rescue, or major disabling stroke, myocardial infarction, or neurological death within 180 days. In the primary efficacy analysis, treatment failure occurred in 19 of 120 patients (16%) receiving embolization compared with 47 of 129 (36%) receiving standard treatment alone, corresponding to an odds ratio of 0.36 (95% CI, 0.20–0.66; P=0.001) and an absolute difference of 20 percentage points. The primary safety endpoint of major disabling stroke or death within 30 days occurred in 4 of 144 patients (3%) in the embolization group and 5 of 166 (3%) in the control group. By 180 days, deaths had occurred in 12 patients (8%) receiving embolization and 9 (5%) receiving standard treatment; neurological deaths occurred in 1 patient (1%) and 3 patients (2%), respectively. These findings suggest that adjunctive embolization reduces treatment failure without a detected increase in the prespecified 30-day safety endpoint, although longer-term safety requires continued evaluation.
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