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. Author manuscript; available in PMC: 2016 May 17.
Published in final edited form as: Epilepsia. 2014 Nov 10;55(12):2059–2068. doi: 10.1111/epi.12852

Table 1. List of diagnostic categories and their frequencies as definitive SE etiology.

Underlying etiology after complete workup (n = 212) n %
Total, n = 212
ASD-related (nonadherence, recent change or low levels) 34 16.04
Brain tumor without acute change
 (no change or increase in tumor load)
28 13.21
Acute hemorrhagic cerebrovascular event 21 9.91
Known epilepsy (non structural) without provocative
 factors (breakthrough seizures)
16 7.55
Remote ischemic cerebrovascular event 14 6.6
Unclassifieda 13 6.13
CNS infection (meningitis or encephalitis) 12 5.66
Unknown origin 11 5.19
Toxic-metabolic 10 4.72
Systemic infection/sepsis 10 4.72
Remote hemorrhagic cerebrovascular event 8 3.77
Acute TBI 7 3.3
Acute ischemic cerebrovascular event 5 2.36
Remote TBI 6 2.83
Alcohol related (withdrawal or intoxication) 6 2.83
Brain tumor with acute change
 (bleeding, recent biopsy/surgery or
 rapid increase in edema)
5 2.36
Benzodiazepine withdrawal 4 1.89
Neurodegenerative disease 2 0.94
Other drugs known to reduce seizure threshold 0 0

ASD, antiseizure drug; CNS, central nervous system; TBI, traumatic brain injury.

a

Unclassified includes: three multiple sclerosis, two confirmed and one possible posterior reversible encephalopathy syndrome (PRES), two tumoral meningitis, one NMDA encephalitis, one neurosarcoidosis, one eclampsia, one arteriovenous malformation without bleeding, and one case of microangiopathic hemolytic anemia.