# The effect of antiseizure medication on mortality in spontaneous aneurysmal subarachnoid hemorrhage

**Authors:** John Harold Kanter, Adam C. Glaser, Pablo Martinez-Camblor, Jakob V.E. Gerstl, Anna B. Lebouille-Veldman, Harshit Arora, Lauren Buhl, Myles D. Boone, Christopher S. Ogilvy

PMC · DOI: 10.2478/jccm-2025-0014 · The Journal of Critical Care Medicine · 2025-04-30

## TL;DR

This study found that early use of antiseizure medication in patients with aneurysmal subarachnoid hemorrhage is linked to lower early mortality, despite increasing seizure risk.

## Contribution

The study provides new evidence that early ASM reduces 7-day mortality in aSAH patients, challenging current guidelines limited to high-risk cases.

## Key findings

- Early ASM was associated with a 74% lower risk of death within 7 days (aOR: 0.26).
- Patients receiving early ASM were 7.6 times more likely to experience a seizure.
- Early ASM reduced the composite outcome of death or seizure within 7 days.

## Abstract

Spontaneous aneurysmal subarachnoid hemorrhage (aSAH) is a major cause of morbidity and mortality in the United States. The efficacy of early antiseizure medication (ASM) is debated. Recent literature reports seizure rates ranging from 7.8% to 15.2% following spontaneous aSAH. Current guidelines recommend use of early ASM in patients with “high-risk features,” but whether early ASM use decreases the rate of death associated with aSAH remains unclear. This study assessed whether early administration of early ASM impacts mortality rates after spontaneous aSAH.

We conducted a retrospective cohort study using a publicly available dataset from the Massachusetts Institute of Technology, Medical Information Mart for Intensive Care-III (MIMIC) database of all patients over the age of 18 with spontaneous aSAH resulting in an intensive care unit (ICU) admission to a major United States trauma center from 2001 to 2012. The primary exposure was receiving early ASM and primary outcome of death within 7 days. Different regression models were created to explore the association between early ASM administration within 24 hours of admission and a composite outcome of seizure and/or death within 7 days of admission. Secondary outcomes included 30-day and one-year mortality.

Of 253 patients with spontaneous aSAH, 148 received early ASM within 24 hours. Patients who did receive early ASM were less likely to die within 7 days of admission (adjusted odd ratio, [aOR]: 0.26 95% CI 0.10 to 0.68; P=0.006) but were more likely to have a seizure (aOR: 7.63 95% CI 2.07 to 28.17; P=0.002).

Early ASM administration was associated with lower rates of death and composite death/seizure within 7 days of admission among patients who presented to an ICU with spontaneous aSAH. These findings suggest broader use of early ASM in patients who present with spontaneous aSAH may improve early mortality.

## Full-text entities

- **Diseases:** ICH (MESH:D002543), trauma (MESH:D014947), neurologic injury (MESH:D020196), cortical infarction (MESH:D007238), depression (MESH:D003866), death (MESH:D003643), anterior circulation aneurysms (MESH:D020520), hydrocephalus (MESH:D006849), Stroke (MESH:D020521), TBI (MESH:D000070642), aneurysm (MESH:D000783), Seizure (MESH:D012640), cognitive disability (MESH:D003072), epileptiform discharges (MESH:D019522), NCSE (MESH:D013226), HH (MESH:C535287), middle cerebral artery (MCA) aneurysm (MESH:D002532), ASM (MESH:D000069279), SAH (MESH:D013345), hemorrhage (MESH:D006470), DCI (MESH:D002545)
- **Chemicals:** oxcarbazepine (MESH:D000078330), propofol (MESH:D015742), Tegretol (MESH:D002220), benzodiazepines (MESH:D001569), Lamictal (MESH:D000077213), phenobarbital (MESH:D010634), Keppra (MESH:D000077287), fosphenytoin (MESH:C043114), ASM (-), Depakene (MESH:D014635), Vimpat (MESH:D000078334), phenytoin (MESH:D010672), Lyrica (MESH:D000069583)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12080531/full.md

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Source: https://tomesphere.com/paper/PMC12080531