Abstracts

STEREOTACTIC LASER AMYGDALO-HIPPOCAMPOTOMY FOR MESIAL TEMPORAL LOBE EPILEPSY:
COLLECTIVE EXPERIENCE FROM SEVEN SINGLE-CENTER, PROSPECTIVE, INVESTIGATOR-INITIATED STUDIES
OBJECTIVES

Abstract number : 2.339
Submission category : 9. Surgery
Year : 2014
Submission ID : 1868421
Source : www.aesnet.org
Presentation date : 12/6/2014 12:00:00 AM
Published date : Sep 29, 2014, 05:33 AM

Authors :
Robert Gross, Jon Willie, Sandra Helmers, Kimford Meador, Suzette Laroche, R. Edward Faught, Evan Gedzelman, Ashwini Sharan, Michael Sperling, Richard Marsh, Gregory Cascino, Gregory Worrell, Jerry Shih, R. Wharen, William Tatum, Gautam Popli, A. Laxton,

Rationale: To evaluate effectiveness, safety, and related findings following stereotactic laser amygdalohippocampotomy (SLAH), a minimally invasive option to open anterior temporal lobectomy and selective amygdalohippocampectomy for mesial temporal lobe epilepsy (MTLE). Methods: Data from 7 centers enrolling 66 adult subjects with medically resistant MTLE that underwent SLAH (Visualase, Houston, TX) at least 6 mo prior was collected via validated case report forms (CRFs); 44 subjects reached 12 mo follow-up. Only subjects with completed data are reported: 11 and 6 subjects had incomplete data at 6 and 12 mo follow-up, respectively, due to late patient visits or the site not collecting 6 mo data. Each center had IRB approval for its respective single-center, investigator-initiated study. Screening and follow-up visits were arranged per protocol at a given center, with some variation per center. Demographic, medical history, and medical/surgical care data were also gathered, along with seizure outcome. Results: For the subjects with data available, age was 43±14 (range 19-75). 66% were female. Mesial temporal sclerosis (MTS) was reported in 70%. Duration of epilepsy was 25±18 years (range 2-68, n=43), and subjects had taken a median of 6 anti-epileptic drugs (range 2-11, n=43) prior to SLAH. The most common pre-ablation seizure type was complex partial, with some exhibiting simple partial and secondarily generalized seizures as well. At 6-mo follow-up of all available subjects since the beginning of SLAH being performed (8/2011), 53% of subjects (n=55) were Engel I (free of disabling seizures). At one-year follow-up, analysis of all available reported adult data showed 55% subjects achieving Engel I status (n=38); 7 had non-disabling simple partial seizures (Engel Ib) with 1 occurring only within the first month post-ablation. Seizure-free rates were 61% in subjects with MTS and 53% in those without at 6 mo, but this was not statistically significant (p=0.28, two-tailed Fisher's exact test). Two hemorrhages occurred: 1 subdural hematoma with no transient or permanent neurological deficit; 1 temporal lobe hematoma with visual field deficit that recovered. Overall there were 4 visual field deficit & transient subjective diplopia (1); transient confusion/difficulty with expression (3), anxiety (5) and other psychological problems of uncertain relation to ablation, superficial skin erythema, and headache (8 episodes in 7 subjects), among other reported events of uncertain relation to ablation. Steroids were given post-operative period ranging from 4 to 15 days at most centers. Median length of stay was 1 day. Anti-epileptic medications were kept constant throughout the one-year course by most centers, and altered based upon high blood levels or seizure activity. Conclusions: SLAH achieved Engel 1 outcome in the majority of subjects at 6- and 12-month follow-up, with acceptable saftey. Further prospective study, with greater numbers of subjects, will help elucidate and/or strengthen these findings.
Surgery