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British Journal of Neurosurgery, June 2014; 28(3): 374–377

© 2014 The Neurosurgical Foundation


ISSN: 0268-8697 print / ISSN 1360-046X online
DOI: 10.3109/02688697.2013.841854

ORIGINAL ARTICLE

Comparison of therapeutic effects between selective


amygdalohippocampectomy and anterior temporal lobectomy
for the treatment of temporal lobe epilepsy: A meta-analysis
Yongqin Kuang1, Tao Yang1,2, Jianwen Gu1, Bin Kong1,2 & Lin Cheng1
1Department of Neurosurgery, Chengdu Military General Hospital, Chengdu, P. R. China, and 2Third Military Medical University,

Chongqing, P. R. China

medicine. However, more than 20% of the epilepsy patients


Abstract
with intractable drug resistance ultimately develop differ-
Background. Temporal lobe epilepsy (TLE) is a recurrent
ent levels of neurological dysfunction and psychological
chronic nervous system disease. The conventional treatment
changes.2 For such patients, surgical treatment is particu-
is medicine. So far, anterior temporal lobectomy (ATL) and
larly important as it can not only control epileptic fit, but
selective amygdalohippocampectomy (SAH) are becoming the
also facilitate the effectiveness of drugs in order to bring
two main approaches. Methods.To compare the therapeutic
down the morbidity and mortality.3–5
effects between SAH and ATL in the treatment of temporal
Patients have to undergo rigorous preoperative evalua-
lobe epilepsy, we conducted a meta-analysis of published
tion and diagnosis before the surgical treatment of epilepsy
randomized controlled trials. The review applied the search
to ascertain operation indication and surgical technique and
strategy developed by the Cochrane Epilepsy Group and the
locate epileptic foci. So far, anterior temporal lobectomy
Rev. Man 5.0 software to analyze. We also drew the forest plots
(ATL)6 and selective amygdalohippocampectomy (SAH)7
with Risk Ratio (RR) as effect size. Six studies were eligible,
have been the two main approaches to treat TLE and ATL
with a total of 626 patients (337 patients with SAH and 289
has been the most widely applied standard resection for
patients with ATL). Results. There was no statistical significance
TLE with over 70% patients being cured postoperatively.8,9
of postoperative seizure control rate after 1 year, as well as
ATL can ensure a wide operative field and reduce stress on
the increase rate and decrease rate of verbal memory function
the surgeon. Nevertheless, ATL often damages the anterior
between SAH and ATL. There is no statistical difference of
bundle fibers of the optic radiation and the language areas
therapeutic effects between SAH and ATL in the treatment
located at the temporal tip and temporal base.10–12
of temporal lobe epilepsy. Conclusion. It is advised that
SAH was first described by Niemeyer in 1895 when
clinically, physicians should choose the appropriate approach
he applied a transcortical approach via middle temporal
according to operation indications to improve the results of
gyrus.13 In 1985, Yasargil et al. reported that they con-
postoperative recovery.
ducted SAH by a trans-sylvian approach.14 Recently, a
Keywords: anterior temporal lobectomy; meta-analysis; selective transcortical approach via superior temporal sulcus and
amygdalohippocampectomy; temporal lobe epilepsy a subtemporal approach have been widely applied.15–17
During SAH, only mesial temporal structures (hippocam-
pus, parahippocampal gyrus and amygdalas) are resected
with lateral temporal cortex preserved so as to conserve
Introduction
functional temporal lobe as much as possible and minimize
Temporal lobe epilepsy (TLE) is a recurrent chronic ner- the occurrence of complications such as aphasia caused
vous system disease, originating from the epilepsy foci by the damaged cortex associated with verbal function in
localized in basolateral temporal lobe including fusiform lateral temporal lobe.
gyrus, parahippocampal gyrus, hippocampus and amygda- To investigate the usefulness of the two types of surgical
las.1 The feature of TLE is simple partial seizure, generally techniques and provide reliable foundation for their clinical
manifesting itself as partial seizure, secondary generalized application, we compared the efficacy of SAH versus ATL for
seizure or mixed seizure. The conventional treatment is the treatment of TLE with meta-analysis.

Kuang Yongqin and Yang Tao should be regarded as co-first authors.


Correspondence: Jianwen Gu, Department of Neurosurgery, Chengdu Military General Hospital, Chengdu 610083, P. R. China. Tel: ⫹ 86-28-86570361.
E-mail: gujianwengjwgu@hotmail.com.
Received for publication 8 April 2013; accepted 31 August 2013

374
Comparison of therapeutic effects of TLE 375

Table I. The principal characteristics of eligible studies.


Number
Study Year Journal Start (Year) End (Year) ATL SAH
Arruda 199618 Ann Neurol NA NA 37 37
Clusmann 200219 J Neurosurg 1989 1997 98 138
Morino 200620 Epilepsy and Behavior 1999 2003 17 32
Paglioli 200621 J Neurosurg 1992 2002 80 81
Sagher 201222 Neurosurg Focus 2001 2007 51 45
Tahir 201223 Epilepsy Research 2006 2008 6 4
and Treatment
NA: not available.

Materials and methods Statistical analysis


Meta-analysis was conducted by Review Manager 5.0. Stan-
Literature search strategy
dardized mean difference with 95% confidence interval was
Published studies in SAH versus ATL for the treatment of
used for continuous data and relative risk ratio (RR) with
TLE were collected using PubMed, MEDLINE, EMBASE,
95% confidence interval was used for dichotomous data. A
Cochrane Controlled Trials Register and recursive literature
probability of P ⬍ 0.05 was considered significant. Statistical
searching up to October 2012 and Google scholar was used
heterogeneity was assessed before pooled analysis. A fixed
to search relevant studies. Key words of search were Tempo-
effect was applied for calculations in the absence of evidence
ral Lobe Epilepsy AND Anterior Temporal Lobectomy AND
of heterogeneity; otherwise, a random effects model was
Selective Amygdalohippocampectomy.
applied.
Study selection
Inclusion criteria: 1) The studies were original research Results
articles. 2) Experiment design was a randomized clinical
trial. 3) The studies had time limit on research duration
Description of studies
The initial search yielded 86 studies related to SAH versus
or publication. 4) The studies had explicit indication on
ATL as the treatment intervention for TLE, of which 25 were
sample size. 5) Patients were diagnosed with TLE. 6) Treat-
reviews or commentary literatures, 30 not randomized
ment intervention was SAH or ATL. 7) Outcome measures
controlled trials and 27 other types of literatures. Of these,
were seizure control rate, memory and IQ. 8) The method
four articles of randomized clinical trials met inclusion
of collecting materials was scientific. 9) The method of data
criteria. The second search yielded two articles. Finally, by
analysis was correct.
October 2012, we included six eligible studies of randomized
Exclusion criteria: 1) The studies did not provide the
clinical trials.18–23
source and exact number of case and control patients and the
studies were non-medical clinical research, animal experi-
ments and non-primary literature. 2) There were no clear Principal characteristics of studies
diagnostic criteria for the cases. 3) Patients had other types The principal characteristics (author, publishing year,
of epilepsy. 4) Treatment intervention was non-surgical such journal and the number of patients) are reported in
as medicine. 5) The studies were not randomized controlled Table I. These studies were published from 1989 to 2008. A
trials. 6) The method of data analysis was incorrect or not total of 626 patients are included (337 SAH and 289 ATL).
provided. 7) The studies were reviews. 8) The studies were dupli- Demographic data involving patients’ gender, age of onset
cate publications. 9) The studies were retrospective analysis. and mean duration are listed in Table II.

Quality assessment and data extraction Seizure control rate after 1 year
Two independent reviewers performed quality assessment All the six studies18–23 involved seizure control rate after
with respect to 1) general data: the first author, publishing 1 year. No evidence of statistical heterogeneity was found and
year, source and publishing date, 2) protocol of each study, therefore, we used a fixed effect model. The pooled estimate
3) sample size, features and therapeutic outcomes of each of combined RR (95% CI) was 1.01 (0.94, 1.09), suggesting no
study and 4) conclusions. statistical significance (Z ⫽ 0.24, P ⫽ 0.81). It is evident that

Table II. The demographic data.


Age Gender Age of onset Duration (Year)
Study ATL SAH ATL SAH ATL SAH ATL SAH
Arruda 199618 32.5 31.6 33/4 1/36 NA NA 20.8 18.1
Clusmann 200219 29.7* NA NA NA NA 17.9*
Morino 200620 32.2 37.5 9/8 13/19 12.0 11.9 NA NA
Paglioli 200621 31.9 30.7 43/37 45/36 NA NA 22.8 25.1
Sagher 201222 36.0 38.3 26/25 20/25 15.0 17.1 21.0 21.2
Tahir 201223 22.0* NA NA NA NA NA NA
*Combined average number of the two groups.
376 Y. Kuang et al.

Fig. 1. Comparison of seizure control rate after 1 year in patients who underwent ATL or SAH.

with respect to seizure control rate after 1 year, there was no effects of surgical treatment of epilepsy. The results showed
statistical difference between ATL and SAH (see Fig. 1). that there is no statistical difference between SAH and ATL
for the treatment of TLE with regard to seizure control rate
Verbal memory gain and loss after 1 year after 1 year.
There were two studies19,21 indicating verbal memory gain Previous studies24–26 compared cognitive outcome in
after 1 year and the data were not statistically heterogeneous. patients who underwent either SAH or ATL. Some claimed
Therefore, data were pooled under a fixed effect model with that SAH offered cognitive advantages over ATL.24,25 Some
combined RR (95% CI) at 1.08 (0.68, 1.72), suggesting no did not find any significant differences between the two types
statistical significance (Z ⫽ 0.33, P ⫽ 0.74) (see Fig. 2). of surgery.26 Others, however, provided equivocal conclu-
There were two studies19,21 containing verbal memory sion.27 In this study, the results showed no statistical varia-
loss after 1 year and no evidence of statistical heterogeneity tion in the increase rate and decrease rate of verbal memory
was found. Therefore, data were pooled under a fixed effect function between patients who underwent SAH or ATL 1 year
model with combined RR (95% CI) at 1.34 (0.95, 1.90), sug- before. Instead of increase rate and decease rate, Morino
gesting no detection of statistically significant association et al. averaged the measurement of verbal and behavioral
(Z ⫽ 1.66, P ⫽ 0.10) (Fig. 3). memory function changes in the report of SAH versus ATL
for the treatment of TLE.20 Therefore, this study was excluded
from our study. Besides, Morino et al. compared the changes
Discussion
of IQ between the two groups, which is a rare measurement
After an exhaustive literature search and a second focused in other literatures.20 As a consequence, we did not conduct
search, six studies were included and underwent reading meta-analysis with respect to IQ.
in full and meta-analysis.18–23 The patients in each study Our study has several limitations which deserve notice.
had more than 1 year of follow-up. This study assessed the 1) Only six studies were included and some had small
efficacy of SAH and ATL for the treatment of TLE with three sample sizes, let alone less data with the same measure-
main outcome measures: postoperative seizure control rate ments, which might affect the pooled analysis. 2) Without
after 1 year, the increase rate and decrease rates of verbal mentioning the issues such as blinding or random alloca-
memory function. Among the three measures, seizure con- tion in the eligible studies, Jadd score could not take place.
trol rate was the important one to reflect the therapeutic 3) It is unlikely to exclude selection biases and uncertain

Fig. 2. Comparison of verbal memory gain after 1 year in patients who underwent ATL or SAH.

Fig. 3. Comparison of verbal memory loss after 1 year in patients who underwent ATL or SAH.
Comparison of therapeutic effects of TLE 377

confounding factors. 4) Due to the small total number of 10. Devinsky O, Perrine K, Llinas R, Luciano DJ, Dogali M. Anterior
temporal language areas in patients with early onset of temporal
eligible studies, we did not carry out comparative analysis
lobe epilepsy. Ann Neurol 2004;34:727–32.
on side of surgery, age and gender. 11. Krauss G, Fisher R, Plate C, et al. Cognitive effects of resecting
basal temporal language areas. Epilepsia 2005;37:476–83.
12. Lüders H, Lesser R, Hahn J, Dinner D. Basal temporal language
Conclusion area demonstrated by electrical stimulation. Neurology 1986;36:
505–10.
To sum up, there were no significant postoperative group 13. Niemeyer P. The transventricular amygdala-hippocampectomy
in temporal lobe epilepsy. In: Baldwin M, Bailey P, eds. Temporal
differences with regard to efficacy of SAH versus ATL for the
Lobe Epilepsy. Springfield, IL: Charles C Thomas, 1958:461–482.
treatment of TLE, which indicates that more high-quality 14. Yaş argil M, Teddy P, Roth P. Selective amygdalo-hippocampectomy.
randomized controlled trails are needed to provide evidence. Operative anatomy and surgical technique. Adv Techn Stand
Neurosurg 1985;12:93.
It is advised that clinically, physicians should choose the
15. Hori T, Tabuchi S, Kurosaki M, et al. Subtemporal
appropriate technique according to operation indications amygdalohippocampectomy for treating medically intractable
for postoperative improvement in recovery. temporal lobe epilepsy. Neurosurgery 1993; 33:50–7.
16. Olivier A . Temporal resections in the surgical treatment of epilepsy.
Epilepsy Res Suppl 1992;5:175–88.
17. Park T, Bourgeois BFD, Silbergeld DL, Dodson WE. Subtemporal
Declaration of interest: The authors report no declarations
transparahippocampal amygdalohippocampectomy for surgical
of interest. The authors alone are responsible for the content treatment of mesial temporal lobe epilepsy. J Neurosurg 1996;85:
and writing of the paper. 1172–6.
18. Arruda F, Cendes F, Andermann F, et al. Mesial atrophy and
This work was supported by a grant from the National
outcome after amygdalohippocampectomy or temporal lobe
Natural Science Foundation of China (No. 81071037). removal. Ann Neurol 1996;40:446–50.
19. Clusmann H, Schramm J, Kral T, et al. Prognostic factors and
outcome after different types of resection for temporal lobe
References epilepsy. J Neurosurg 2002;97:1131–41.
20. Morino M, Uda T, Naito K , et al. Comparison of neuropsychological
1. French J, Williamson P, Thadani V, et al. Characteristics of outcomes after selective amygdalohippocampectomy versus
medial temporal lobe epilepsy: I. Results of history and physical anterior temporal lobectomy. Epilepsy Behav 2006;9:95.
examination. Ann Neurol 2004;34:774–80. 21. Paglioli E, Palmini A , Portuguez M, et al. Seizure and memory
2. Flor-Henry P. Psychosis and temporal lobe epilepsy; a controlled outcome following temporal lobe surgery: selective compared with
investigation. Epilepsia 2007;10:363–95. nonselective approaches for hippocampal sclerosis. J Neurosurg
3. Engel J Jr, McDermott MP, Wiebe S, et al. Early surgical therapy 2006;104:70–8.
for drug-resistant temporal lobe epilepsy a randomized trial. 22. Sagher O, Thawani JP, Etame AB, Gomez-Hassan DM. Seizure
JAMA 2012;307:922–30. outcomes and mesial resection volumes following selective
4. Chowdhury F, Haque M, Islam M, et al. Microneurosurgical amygdalohippocampectomy and temporal lobectomy. Neurosurg
management of temporal lobe epilepsy by amygdalohip- Focus 2012;32:8.
pocampectomy (AH) plus standard anterior temporal lobectomy 23. Tahir MZ, Sobani ZA , Quadri S, et al. Establishment of a
(ATL): a report of our initial five cases in Bangladesh. Asian J comprehensive epilepsy center in Pakistan: initial experiences,
Neurosurg 2010;5:10. results, and reflections. Epilepsy Res Treat 2012;2012:547382.
5. Schramm J, Clusmann H. The surgery of epilepsy. Neurosurgery 24. Helmstaedter C, Elger C, Hufnagel A , Zentner J, Schramm J.
2008;62: SHC-463-SHC-481. Different effects of left anterior temporal lobectomy, selective
6. Mizrahi EM, Kellaway P, Grossman RG, et al. Anterior temporal amygdalohippocampectomy, and temporal cortical lesionectomy
lobectomy and medically refractory temporal lobe epilepsy of on verbal learning, memory, and recognition. J Epilepsy 1996;
childhood. Epilepsia 2007;31:302–12. 9:39–45.
7. Chowdhury F, Haque M, Chowdhury S, et al. Neurosurgical 25. Helmstaedter C, Grunwald T, Lehnertz K, Gleissner U, Elger C.
management of intractable temporal lobe epilepsy by Differential involvement of left temporolateral and temporomesial
amygdalohippocampectomy plus anterior temporal lobectomy: structures in verbal declarative learning and memory: evidence
report of initial three pediatric cases with short literature review. from temporal lobe epilepsy. Brain Cogn 1997;35:110–31.
Bangladesh J Child Health 2012;35:26–31. 26. Pauli E, Pickel S, Schulemann H, Buchfelder M, Stefan H.
8. Bonelli SB, Powell RHW, Yogarajah M, et al. Imaging memory in Neuropsychologic findings depending on the type of the resection
temporal lobe epilepsy: predicting the effects of temporal lobe in temporal lobe epilepsy. Adv Neurol 1999;81:371.
resection. Brain 2010;133:1186–99. 27. Jones-Gotman M, Zatorre R, Olivier A , et al. Learning and
9. Wiebe S, Blume WT, Girvin JP, Eliasziw M. A randomized, retention of words and designs following excision from medial
controlled trial of surgery for temporal-lobe epilepsy. N Engl J Med or lateral temporal-lobe structures. Neuropsychologia 1997;35:
2001;345:311–8. 963–73.
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