Seizure | 2019

Peri-ictal magnetic resonance imaging in status epilepticus: Temporal relationship and prognostic value in 60 patients

 
 
 
 
 

Abstract


PURPOSE\nMagnetic resonance imaging (MRI) changes associated with status epilepticus (SE) have been described in recent studies. Our aim was to evaluate the diagnosis and prognosis of the peri-ictal MRI changes detected in SE patients.\n\n\nMETHOD\nAll adults diagnosed with SE and examined by MRI within 240\u202fh after SE onset were enrolled (2011-2017). Demographic, clinical and electroencephalography data, and functional status at admission and discharge were collected. MRI findings were recorded and relationships between clinical and MRI data, and between these data and functional outcome were analyzed.\n\n\nRESULTS\nSixty patients included, 50% women, mean age 57.5 years. Median duration of SE was 51.46\u202fh and median time from SE onset to MRI was 86.5\u202fh. Of the total, 41.7% had a restricted diffusion pattern on diffusion-weighted imaging (DWI) and 63.3% had hyperintensities suggestive of edema on T2-weighted (T2WI)/FLAIR sequences. The factors independently associated with T2WI hyperintensities were the presence of acute cerebral lesions (p\u202f=\u202f0.023), baseline STESS (p\u202f=\u202f0.007), and MRI performed within 84\u202fh (p\u202f=\u202f0.007). Variables independently associated with diffusion restriction were a potentially fatal cause (p\u202f=\u202f0.020), SE duration >24\u202fh (p\u202f=\u202f0.022), and MRI performed within the first 84\u202fh (p\u202f=\u202f0.045). In patients undergoing MRI within 84\u202fh, the DWI and T2WI abnormalities were both highly associated with an unfavorable outcome.\n\n\nCONCLUSIONS\nCharacteristic signal changes on DWI and T2WI sequences were seen in approximately half our SE patients undergoing early (<84\u202fh) brain MRI studies, and were independently related to the patients functional status at discharge.

Volume 71
Pages 289-294
DOI 10.1016/j.seizure.2019.08.013
Language English
Journal Seizure

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