TY - JOUR
T1 - Prognostic value of the second ictal intracranial pattern for the outcome of epilepsy surgery
AU - Jiménez-Jiménez, Diego
AU - Martín-López, David
AU - Masood, Mojtaba A.
AU - Selway, Richard P.
AU - Valentín, Antonio
AU - Alarcón, Gonzalo
N1 - Publisher Copyright:
© 2015 International Federation of Clinical Neurophysiology.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Objective: To investigate the prognostic value of the second ictal pattern (SIP) that follows the first ictal pattern (FIP) seen at seizure onset in order to predict seizure control after epilepsy surgery. Methods: SIPs were analysed in 344 electro-clinical and subclinical seizures recorded with intracranial electrodes in 63 patients. SIPs were classified as (a) electrodecremental event (EDE); (b) fast activity (FA); (c) runs of spikes; (d) spike-wave activity; (e) sharp waves; (f) alpha activity; (g) delta activity and (h) theta activity. Engel surgical outcome scale was used. Results: The mean follow-up period was 42.1 months (SD = 30.1). EDE was the most common SIP seen (41%), followed by FA (19%), spike-wave activity (18%), alpha activity (8%), sharp-wave activity (8%), delta activity (3%), runs of spikes (2%) and theta activity (2%). EDE as SIP was associated with favourable outcome when compared with FA (p = 0.0044) whereas FA was associated with poor outcome when compared with any other pattern (p = 0.0389). FA as SIP tends to occur after EDE (75%) whereas EDE tends to evolve from a FIP containing FA (77%). SIP extent was focal in 46% of patients, lobar in 24%, multilobar in 14% and bilateral in 16%. There is a gradual decrease in the proportion of Engel grade I with the extent of SIP. Focal and delayed (in temporal lobe epilepsy) SIPs appear to be associated with better outcome. Conclusions: As SIP, EDE was associated with favourable surgical outcome whereas FA was associated with poor outcome, probably because outcome is dominated by FIP. Significance: EDE as SIP should not discourage surgery. However, FA as SIP should be contemplated with caution. SIP focality and latency can have prognostic value in epilepsy surgery.
AB - Objective: To investigate the prognostic value of the second ictal pattern (SIP) that follows the first ictal pattern (FIP) seen at seizure onset in order to predict seizure control after epilepsy surgery. Methods: SIPs were analysed in 344 electro-clinical and subclinical seizures recorded with intracranial electrodes in 63 patients. SIPs were classified as (a) electrodecremental event (EDE); (b) fast activity (FA); (c) runs of spikes; (d) spike-wave activity; (e) sharp waves; (f) alpha activity; (g) delta activity and (h) theta activity. Engel surgical outcome scale was used. Results: The mean follow-up period was 42.1 months (SD = 30.1). EDE was the most common SIP seen (41%), followed by FA (19%), spike-wave activity (18%), alpha activity (8%), sharp-wave activity (8%), delta activity (3%), runs of spikes (2%) and theta activity (2%). EDE as SIP was associated with favourable outcome when compared with FA (p = 0.0044) whereas FA was associated with poor outcome when compared with any other pattern (p = 0.0389). FA as SIP tends to occur after EDE (75%) whereas EDE tends to evolve from a FIP containing FA (77%). SIP extent was focal in 46% of patients, lobar in 24%, multilobar in 14% and bilateral in 16%. There is a gradual decrease in the proportion of Engel grade I with the extent of SIP. Focal and delayed (in temporal lobe epilepsy) SIPs appear to be associated with better outcome. Conclusions: As SIP, EDE was associated with favourable surgical outcome whereas FA was associated with poor outcome, probably because outcome is dominated by FIP. Significance: EDE as SIP should not discourage surgery. However, FA as SIP should be contemplated with caution. SIP focality and latency can have prognostic value in epilepsy surgery.
KW - Epilepsy
KW - Epilepsy surgery
KW - Intracranial EEG
KW - Invasive recordings
KW - Second ictal pattern
KW - Surgical outcome
UR - http://www.scopus.com/inward/record.url?scp=84938634390&partnerID=8YFLogxK
U2 - 10.1016/j.clinph.2015.07.001
DO - 10.1016/j.clinph.2015.07.001
M3 - Artículo
C2 - 26253031
AN - SCOPUS:84938634390
SN - 1388-2457
VL - 127
SP - 230
EP - 237
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
IS - 1
ER -