You are on page 1of 4

Seizure 18 (2009) 193–196

Contents lists available at ScienceDirect

Seizure
journal homepage: www.elsevier.com/locate/yseiz

Seizure recurrence following epilepsy surgery: Is post-operative EEG helpful?


Georges A. Ghacibeh a,b,*, Jeffrey D. Smith b, Steven N. Roper c, Robin Gilmore b, Stephan Eisenschenk b
a
Northeast Regional Epilepsy Group, Hackensack University Medical Center, Comprehensive Epilepsy Center, 20 Prospect Avenue, Suite 800, Hackensack, NJ 07601, USA
b
University of Florida, Department of Neurology, P.O. Box 100236, Gainesville, FL 32610, USA
c
University of Florida, Department of Neurosurgery, P.O. Box 100265, Gainesville, Florida 32610, USA

A R T I C L E I N F O A B S T R A C T

Article history: Objectives: We examined whether the relationship between interictal epileptiform discharges (IED) on
Received 8 August 2008 post-operative EEG and seizure recurrence after epilepsy surgery was different in patients with neocortical
Accepted 12 September 2008 and mesiotemporal resections.
Methods: We reviewed the records of 93 consecutive patients who underwent epilepsy surgery at our
Keywords: center and who had adequate post-operative follow-up and a post-operative EEG to determine the type of
Epilepsy surgery surgery, the recurrence of seizures and the presence of IED on post-operative EEG.
EEG
Results: Chi-square test revealed that for the entire group, there was a significant relationship between
Interictal epileptiform discharges
the presence of IED and seizure recurrence. However, this relationship was significant in neocortical
Seizure recurrence
surgery but not in mesiotemporal surgery. Time distribution of seizure recurrence revealed that in more
than half the cases, seizures recurred with the first 3 months. Time distribution was not influenced by the
presence of IED.
Conclusions: This study revealed that IED on early post-operative EEG correlate with seizure recurrence in
neocortical but not mesiotemporal surgeries and may be used to guide patient counseling in this group of
patients.
ß 2008 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

1. Introduction Intraoperative factors, such as electrocorticography (ECoG),13 and


completeness of resection,9,14 are also controversial.
Patients undergoing surgery for the treatment of medically Post-operatively, early seizure recurrence after surgery has
intractable epilepsy have variable rates of seizure remission. reliably predicted a poor outcome,4,15,16 worse with generalized
Counseling patients regarding surgical outcome is challenging, seizures.10 Seizure freedom in the first post-operative year is
given the impact recurrent seizures can have on quality of life, associated with good long term outcome.5,11 The presence of
vocation, driving, family planning, and discontinuation of anti- interictal epileptiform discharges on the post-operative EEG has
epileptic drugs.1–3 The prediction of post-surgical outcome remains also been studied, with conflicting results. Some studies showed a
uncertain, but several factors have fairly reliable predictive value. strong predictive value4,5,10,11,13,14,17,18 and others showed no
Preoperative predictors for post-operative seizure remission predictive value.5,14,17,19,20 Conflicting results are likely due to a
include electrographic, structural and historical factors, such as number of factors. For example, there is no standard time to
unilateral interictal epileptiform discharges (IED),4–7 MRI abnorm- perform a post-operative EEG, and centers that do perform them
alities4,8 including hippocampal sclerosis5,6 and tumors,9 febrile routinely, set their own protocols. Furthermore, the studied
convulsions in childhood6 and complex partial seizures without populations vary considerably among studies with the majority
secondary generalization.10 Other preoperative factors, such as age of of series focusing on anterior temporal lobectomy (ATL). Some
onset, duration of epilepsy, and etiology remain controversial.5,8,11,12 studies compared ATL to extratemporal resection,11,14,17 reveal-
ing better predictive value in the ATL patients. Other studies have
found a positive predictive value in neocortical parietal21 and
frontal22 resections.
In this study, we compared the predictive value of IED identified
* Corresponding author at: Northeast Regional Epilepsy Group, Hackensack
University Medical Center, Comprehensive Epilepsy Center, 20 Prospect Avenue,
on a 3-month post-operative EEG for seizure recurrence in patients
Suite 800, Hackensack, NJ 07601, USA. Tel.: +1 201 996 3205; fax: +1 201 343 6689. with mesiotemporal lobe epilepsy (MTLE) and patients with
E-mail address: gghacibeh@gmail.com (G.A. Ghacibeh). neocortical epilepsy who underwent surgical resection.

1059-1311/$ – see front matter ß 2008 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
doi:10.1016/j.seizure.2008.09.003
194 G.A. Ghacibeh et al. / Seizure 18 (2009) 193–196

2. Methods Table 1
Patient characteristics

2.1. Subjects Surgery type Total Side IED Seizure recurrence

Right Left
All patients who underwent surgery for the treatment of
medically intractable epilepsy at the University of Florida between Mesiotemporal 69 37 32 15 22
Neocortical—All 24 16 8 14 13
January 1997 and December 2002 were identified. The electronic
Frontal 14 10 4 8 7
medical records were reviewed including operative reports, clinic Temporal 9 6 3 5 5
notes and EEG reports. Parietal 1 0 1 1 1

IED: Interictal epileptiform discharges on the post-operative EEG.


2.2. Data collection

All surgeries were performed by the same neurosurgeon with relationship in the mesiotemporal group (P = 0.446), but a
subspecialty training in epilepsy surgery. Operative reports were significant relationship is the neocortical group (P = 0.005), with
reviewed to define the type of surgery. No patient was excluded an odds ratio of 14.7 (95% CI: 1.97; 109.2).
based on the type of resection or underlying pathology. Resections Ongoing treatment with AEDs was also analyzed. Seventeen
were classified as mesiotemporal if the surgery was a standard patients had their AEDs discontinued at some point during follow-
ATL,23 and neocortical for all other types of resections. Clinic notes up, and four of them (24%) had seizure-recurrence, all with ATL
were reviewed up to the last available to determine the recurrence surgeries. There was no significant relationship between the
of seizures. If seizures recurred, seizure type, date of recurrence presence or absence of IED and discontinuation of medications.
and anti-epileptic drug status were determined. Only focal motor, Two (17%) of the 12 patients who had IED and who remained
complex partial (CPS) and generalized seizures (GTC) were seizure-free, had all AEDs discontinued by the last follow-up, and
considered seizure recurrences. Patients who had persistence or 11 (24%) of the 46 patients with no IED and who remained seizure-
recurrence solely of auras were considered seizure-free. For free had all AEDs discontinued by the last follow-up. Furthermore,
patients to be included in the analysis, a post-operative follow- analysis was performed on the 17 patients who were taken off their
up of at least 2 years was required. Finally, post-operative EEG AEDs, to assess the predictive value of IED for seizure recurrence in
reports were reviewed to assess for the presence of IED. Patients this group of patients (Fig. 2). Of the 3 patients who had IED, 1
who did not have a post-operative EEG were excluded from the (33%) had recurrent seizures and of the 14 patients without IED, 3
analysis. All EEGs were routine 30-min scalp studies performed (21%) had recurrent seizures. The relationship was not statistically
using a 21-channel digital recording. If more than one outpatient significant (P = 0.6), however, the sample size is too small to draw
EEG study was performed after surgery, the one recorded closest any conclusions.
to 3 months after surgery was used. All EEGs were reviewed The time distribution of seizure recurrence was also analyzed.
and interpreted by experienced electroencephalographers. Epi- The time to first seizure (TFS) was calculated for each patient as the
leptiform abnormalities were defined as sharp waves, spikes or period in months between surgery and the first seizure. For the
electrographic seizures. entire sample, TFS was: mean = 9.1  2.2; median = 2; for the ATL
group: mean = 11.4  3.2; median = 2; and for the neocortical group:
2.3. Data analysis mean = 5.4  2; median = 1. Group comparison using a log rank test
revealed no significant difference (P = 0.09). In addition, the TFS of
The association between the presence of IED on post-operative patients with IED (mean: 6.7  2.3; median: 2) was not significantly
EEG and seizure recurrence was evaluated for the entire group of different (P = 0.182) from those without IED (mean: 11.5  3.6;
patients, and in the two subgroups, mesiotemporal and neocortical median: 2).
resection. In addition, the relationship between the presence of IED Time distribution analysis revealed that 57% of patients with
and discontinuation of anti-epileptic drugs was also analyzed. post-operative seizures experienced recurrence prior to the post-
Statistical comparison was made using x2 or Fischer Exact test, as operative EEG. Therefore, a second analysis was performed on
appropriate. Statistical significance was set at a P value of less than patients who had their first seizure more than 3 months after
0.05.

3. Results

A total of 186 patients were identified. Of those, 90 had no post-


operative EEGs and 3 had insufficient clinic follow-up after their
surgery. Data on the remaining 93 patients were analyzed
(Table 1). EEGs were performed on average 106  22 days after
surgery. Patients were followed in clinic on average 40  20 months,
with a range of 24–99 months after surgery.
Patients who had only recurrent auras were grouped with
patients who remained seizure-free and compared to patients who
had seizure recurrence. For the entire sample, of the 29 (31%)
patients with IED, 17 (59%) had seizures and 12 (41%) remained
seizure-free. In contrast, of the 64 (69%) patients who had no IED,
18 (28%) had seizures and 46 (72%) remained seizure-free. Chi- Fig. 1. Relationship between the presence of interictal epileptiform discharges on
square analysis revealed a significant relationship (P = 0.005) the post-operative EEG and seizure recurrence in the mesiotemporal and
neocortical surgery groups. The bars represent the number of patients with and
between the presence of IED and seizure recurrence, with an odds without IED. The black sections of the bars represent the proportion of patients with
ratio of 3.62 (95% CI: 1.445; 9.068). When the two surgery-type seizure recurrence and the grey sections represent the proportion of patients who
groups were analyzed separately (Fig. 1), there was no significant remained seizure-free.
G.A. Ghacibeh et al. / Seizure 18 (2009) 193–196 195

a stronger predictive value for temporal versus extratemporal


patients.11,14,17
Inconsistencies between various studies may be related to
several factors. The timing of the EEG at 3 months after surgery
was chosen randomly at our center. Other studies reported different
timing of the EEG, including 6 months and 24 months.14,24 This
may have an impact on the occurrence of IED. Interictal epilepti-
form activity has been reported on EEGs performed early after brain
surgery without associated seizures.25 Therefore, it is conceivable
that EEGs performed earlier after surgery might potentially have a
higher chance of showing spikes and sharp waves due to the surgical
intervention itself, rather than the persistence of epileptogenic
cortex. Furthermore, if patients are followed longer, the classifica-
tion of outcome may change, as patients may remain seizure-free
Fig. 2. Relationship between the presence of interictal epileptiform discharges on
for a period of time after surgery, with later recurrence of seizures.
the post-operative EEG and seizure recurrence after discontinuation of all anti-
epileptic drugs. The bars represent the number of patients with and without IED.
Most studies tend to set their minimum follow-up time at 2 years
The black sections of the bars represent the proportion of patients with seizure after surgery, however, some series had shorter follow-up.14,17
recurrence and the grey sections represent the proportion of patients who remained Finally, the main outcome measure analyzed is another important
seizure-free. confounding factor. In this study, we investigated the presence or
absence of post-operative seizures, and did not assess or classify
surgery, excluding all patients who had seizures prior to their post- outcome.2 This is a significant difference between our studies and
operative EEG from the analysis (Fig. 3). For the entire group, of the others that focused on the relationship between IED and outcome.
19 patients with IED, 7 (37%) had seizure recurrence and 12 (63%) Some patients may have seizures after their surgery and still qualify
remained seizure-free. In contrast, of the 54 patients without IED, 8 for a fair outcome if they show significant improvement in seizure
(15%) had seizures and 46 (85%) remained seizure-free. The control. Furthermore, in our study, about half the patients were
relationship between seizure recurrence and presence of IED was excluded from the analysis because they did not have a post-
again significant (P = 0.041). However, when analysis was per- operative EEG. Therefore, this study was not designed to examine
formed on each surgery-type separately, there was no significant the outcome of epilepsy surgery.
relationship between seizure recurrence and IED for either group. In general, the occurrence of IED on EEG correlates strongly
with the diagnosis of epilepsy. This has been established in
4. Discussion multiple studies in which EEGs performed on subjects who never
had seizures rarely showed IED.26–29 However, the reverse is not
The results of this study indicate that interictal epileptiform true. The absence of IED on a single EEG does not correlate as
activity identified on outpatient EEG performed 3 months after strongly with the absence of seizures. In fact, IED are present in as
surgery for epilepsy is associated with a higher risk of seizure few as 29% of epilepsy patients on a single routine EEG, but
recurrence, however, this relationship was present only for increase substantially with repeated EEGs.30,31 Therefore, longer
neocortical surgery, and not for mesiotemporal surgery. Our duration EEGs or repeated EEGs performed at different time-
results are in agreement with previous studies that revealed the intervals after surgery might have increased the chance of
lack of predictive value of IED on post-operative EEG in ATL capturing IED, especially if periods of sleep are included.
patients5,19,20 and in agreement with prior studies that found a Ongoing treatment with AEDs represents another confounding
positive predictive value of post-operative EEG in extratemporal variable. Patients with IED on their post-operative EEG are
epilepsy.21,22 However, other studies revealed results that were probably less likely to be taken off their AEDs. It is possible that
inconsistent with our findings, including a strong predictive value in some patients, seizure freedom is achieved due to the combined
for post-operative EEG in temporal lobectomy patients14,17 and benefit of surgery and the protective action of AEDs. Therefore,
patients who have IED and are seizure-free may very well have
recurrent seizures if they are taken off their AEDs. Analysis of the
relationship between IED and seizure-recurrence after withdrawal
of AEDs is therefore important in order to determine with certainty
whether IED indicates the presence of residual epileptogenic
cortex after surgery. In our study, the presence of IED on post-
operative EEG did not predict seizure-recurrence after disconti-
nuation of AEDs. However, the sample size (17 patients) was too
small to draw any definite conclusions. This kind of study requires
a more rigorous prospective design with longer follow-up periods.
Analysis of the time-distribution of seizure recurrence revealed
that in more that half the patients, seizures recurred within the
first 3 months. This is consistent with previous observations,
indicating that early recurrence of seizures often predicts poor
outcome.4,15,16 Therefore, we performed a separate analysis on
Fig. 3. Relationship between the presence of interictal epileptiform discharges on patients who had seizure recurrence more than 3-months after
the post-operative EEG and seizure recurrence in the mesiotemporal and surgery and found a significant relationship between IED and
neocortical surgery groups, excluding patients who had seizure recurrence prior seizure recurrence. Subgroup analysis did not reveal a statistical
to 3 months after surgery. The bars represent the number of patients with and
without IED. The black sections of the bars represent the proportion of patients with
significance for either group. This is likely related to the sample
seizure recurrence and the grey sections represent the proportion of patients who size and the small number of patients with seizure recurrence,
remained seizure-free. especially in the neocortical group.
196 G.A. Ghacibeh et al. / Seizure 18 (2009) 193–196

The comparison of mesiotemporal to neocortical resection is 12. McIntosh AM, Wilson SJ, Berkovic SF. Seizure outcome after temporal lobect-
omy: current research practice and findings. Epilepsia 2001;42:1288–307.
important, since several reports indicated a significant difference 13. Tuunainen A, Nousiainen U, Mervaala E, Pilke A, Vapalahti M, Leinonen E, et al.
in terms of surgical outcome between the two groups. Mesio- Postoperative EEG and electrocorticography: relation to clinical outcome in
temporal epilepsy and neocortical epilepsy with a focal MRI lesion patients with temporal lobe surgery. Epilepsia 1994;35:1165–73.
14. Godoy J, Luders H, Dinner DS, Morris HH, Wyllie E, Murphy D. Significance of
are usually considered good predictors of favorable surgical sharp waves in routine EEGs after epilepsy surgery. Epilepsia 1992;33:285–8.
outcomes.32–34 Several series indicate that neocortical resections 15. Malla BR, O’Brien TJ, Cascino GD, So EL, Radhakrishnan K, Silbert P, et al. Acute
are generally less successful than temporal resections, with seizure postoperative seizures following anterior temporal lobectomy for intractable
partial epilepsy. J Neurosurg 1998;89:177–82.
freedom achieved in 55–70% of temporal resections and 30–50% of
16. Radhakrishnan K, So EL, Silbert PL, Cascino GD, Marsh WR, Cha R, et al.
neocortical resections.35–38 This led to a recent decrease in the Prognostic implications of seizure recurrence in the first year after anterior
enthusiasm to perform surgical resections on patients with non- temporal lobectomy. Epilepsia 2003;44:77–80.
17. Patrick S, Berg A, Spencer SS. EEG and seizure outcome after epilepsy surgery.
lesional neocortical epilepsy.36,39–42 The difference in outcome
Epilepsia 1995;36:236–40.
may be related to a fundamental difference in the surgery itself and 18. Van Buren JM, Marsan CA, Mutsuga N. Temporal-lobe seizures with additional
in the pathophysiology of the type of epilepsy—the mechanism of foci treated by resection. J Neurosurg 1975;43:596–607.
seizure evolution in the hippocampus is different from that of the 19. Groppel G, Aull-Watschinger S, Baumgartner C. Temporal evolution and prog-
nostic significance of postoperative spikes after selective amygdala-hippocam-
neocortex. The key to successful epilepsy surgery is complete pectomy. J Clin Neurophysiol 2003;20:258–63.
resection of the epileptogenic zone. This requires an accurate 20. Mintzer S, Nasreddine W, Passaro E, Beydoun A. Predictive value of early EEG
localization of the epileptic focus, which can be difficult in after epilepsy surgery. J Clin Neurophysiol 2005;22:410–4.
21. Boesebeck F, Schulz R, May T, Ebner A. Lateralizing semiology predicts the
neocortical epilepsy, especially in the absence of an MRI lesion. seizure outcome after epilepsy surgery in the posterior cortex. Brain
Therefore, the relationship between seizure freedom and the 2002;125:2320–31.
completeness of the surgical resection may be stronger in 22. Janszky J, Jokeit H, Schulz R, Hoppe M, Ebner A. EEG predicts surgical outcome in
lesional frontal lobe epilepsy. Neurology 2000;54:1470–6.
neocortical than mesiotemporal epilepsy, however, this relation- 23. Fried I, Spencer D. Temporal lobectomy: surgical aspects. In: Wyllie E, editor.
ship needs to be studied systematically. Furthermore, the question The treatment of epilepsy: principles and practice. 2nd ed. Baltimore: Williams
of whether the persistence of residual epileptogenic cortex is more & Willkins; 1996. p. 1050–9.
24. Hildebrandt M, Schulz R, Hoppe M, May T, Ebner A. Postoperative routine EEG
likely to produce IED in neocortical versus mesiotemporal
correlates with long-term seizure outcome after epilepsy surgery. Seizure
surgeries also needs to be answered. 2005;14:446–51.
Our study demonstrates that persistence of IED on an EEG 25. Cabral RJ, Scott DF. EEG features associated with the occurrence of epilepsy
after surgery for intracranial aneurysm and acoustic neuroma. J Neurol Neuro-
obtained 3 months after surgery is associated with a higher risk
surg Psychiatry 1977;40:97–9.
of seizure recurrence and the absence of IED predicts a better 26. Bridgers SL. Epileptiform abnormalities discovered on electroencephalographic
chance for seizure freedom in patients with neocortical but not screening of psychiatric inpatients. Arch Neurol 1987;44:312–6.
mesiotemporal epilepsy. Our results therefore indicate that the 27. Goodin DS, Aminoff MJ. Does the interictal EEG have a role in the diagnosis of
epilepsy? Lancet 1984;1:837–9.
routine performance of EEGs in the early post-operative period is a 28. Gregory RP, Oates T, Merry RT. Electroencephalogram epileptiform abnormal-
useful prognostic tool in selected patients. However, the most ities in candidates for aircrew training. Electroencephalogr Clin Neurophysiol
relevant clinical question is the ability to predict the risk of seizure 1993;86:75–7.
29. Zivin L, Marsan CA. Incidence and prognostic significance of ‘‘epileptiform’’
recurrence after discontinuation of AEDs. Therefore, further activity in the eeg of non-epileptic subjects. Brain 1968;91:751–78.
research should examine the predictive value of post-operative 30. Salinsky M, Kanter R, Dasheiff RM. Effectiveness of multiple EEGs in supporting
EEGs performed at different time intervals after surgery, especially the diagnosis of epilepsy: an operational curve. Epilepsia 1987;28:331–4.
31. Marsan CA, Zivin LS. Factors related to the occurrence of typical paroxysmal
in the subgroup of patients who discontinue AEDs. abnormalities in the EEG records of epileptic patients. Epilepsia 1970;11:361–
81.
References 32. Cascino GD. Surgical treatment for extratemporal epilepsy. Curr Treat Options
Neurol 2004;6:257–62.
1. Schachter SC. Quality of life for patients with epilepsy is determined by more 33. Engel J, Cascino GD, Shields W. Surgically remediable syndromes. In: Engel J,
than seizure control: the role of psychosocial factors. Expert Rev Neurother Pedley T, editors. Epilepsy: a comprehensive textbook. Philadelphia: Lippincott-
2006;6:111–8. Raven; 1997. p. 1687.
2. Engel J. Classification of outcome. J Epilepsy 1990;3(Suppl.):219–26. 34. Williamson P, Jobst B. Selection of candidates for extratemporal resection. In:
3. Elwes RD, Dunn G, Binnie CD, Polkey CE. Outcome following resective surgery Wyllie E, editor. The treatment of epilepsy principles and practice, 3rd ed.,
for temporal lobe epilepsy: a prospective follow up study of 102 consecutive Philadelphia: Lippincott-Raven; 2001. p. 1095.
cases. J Neurol Neurosurg Psychiatry 1991;54:949–52. 35. Tonini C, Beghi E, Berg AT, Bogliun G, Giordano L, Newton RW, et al. Predictors
4. Armon C, Radtke RA, Friedman AH, Dawson DV. Predictors of outcome of of epilepsy surgery outcome: a meta-analysis. Epilepsy Res 2004;62:75–87.
epilepsy surgery: multivariate analysis with validation. Epilepsia 1996;37: 36. Zentner J, Hufnagel A, Ostertun B, Wolf HK, Behrens E, Campos M, et al. Surgical
814–21. treatment of extratemporal epilepsy: clinical, radiologic, and histopathologic
5. Radhakrishnan K, So EL, Silbert PL, Jack Jr CR, Cascino GD, Sharbrough FW, et al. findings in 60 patients. Epilepsia 1996;37:1072–80.
Predictors of outcome of anterior temporal lobectomy for intractable epilepsy: 37. Haglund MM, Ojemann GA. Extratemporal resective surgery for epilepsy.
a multivariate study. Neurology 1998;51:465–71. Neurosurg Clin N Am 1993;4:283–92.
6. Salanova V, Andermann F, Rasmussen T, Olivier A, Quesney L. The running down 38. Talairach J, Bancaud J, Bonis A, Szikla G, Trottier S, Vignal J, et al. Surgical
phenomenon in temporal lobe epilepsy. Brain 1996;119(Pt 3):989–96. therapy for frontal epilepsies. Adv Neurol 1992;57:707–32.
7. Rougier A, Dartigues JF, Commenges D, Claverie B, Loiseau P, Cohadon F. A 39. Quesney L, Risinger M, Shewmon D. Extracranial EEG evaluation. In: Engel J,
longitudinal assessment of seizure outcome and overall benefit from 100 editor. Surgical treatment of the epilepsies. 2nd ed. New York: Raven Press;
cortectomies for epilepsy. J Neurol Neurosurg Psychiatry 1992;55:762–7. 1993. p. 173.
8. Jutila L, Immonen A, Mervaala E, Partanen J, Partanen K, Puranen M, et al. Long 40. Rasmussen T. Cortical resection in the treatment of focal epilepsy. In: Pupura D,
term outcome of temporal lobe epilepsy surgery: analyses of 140 consecutive Penry R, Walter R, editors. Neurosurgical management of the epilepsies. New
patients. J Neurol Neurosurg Psychiatry 2002;73:486–94. York: Raven Press; 1975. p. 139.
9. Kirkpatrick PJ, Honavar M, Janota I, Polkey CE. Control of temporal lobe epilepsy 41. Williamson P, Van Ness P, Weiser H. Surgically remediable extratemporal
following en bloc resection of low-grade tumors. J Neurosurg 1993;78:19–25. syndromes. In: Engel J, editor. Surgical treatment of the epilepsies. New York:
10. Velasco AL, Boleaga B, Brito F, Jimenez F, Gordillo JL, Velasco F, et al. Absolute Raven Press; 1993. p. 35.
and relative predictor values of some non-invasive and invasive studies for the 42. Engel J, Wiebe S, French J, Sperling M, Williamson P, Spencer D, et al. Practice
outcome of anterior temporal lobectomy. Arch Med Res 2000;31:62–74. parameter: temporal lobe and localized neocortical resections for epilepsy.
11. Cascino GD, Kelly PJ, Sharbrough FW, Hulihan JF, Hirschorn KA, Trenerry MR. Report of the quality standards subcommittee of the American academy of
Long-term follow-up of stereotactic lesionectomy in partial epilepsy: predic- neurology, in association with the American epilepsy society and the American
tive factors and electroencephalographic results. Epilepsia 1992;33:639–44. association of neurological surgeons. Epilepsia 2003;44:741–51.

You might also like