Vagus nerve stimulation for medically refractory absence epilepsy

A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patie...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Seizure (London, England) Ročník 22; číslo 4; s. 267 - 270
Hlavní autoři: Arya, Ravindra, Greiner, Hansel M., Lewis, Amanda, Mangano, Francesco T., Gonsalves, Cornelia, Holland, Katherine D., Glauser, Tracy A.
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Elsevier Ltd 01.05.2013
Témata:
ISSN:1059-1311, 1532-2688, 1532-2688
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patient population. Patients were identified by a chart review of all VNS recipients between January 1, 2006 and December 31, 2011. The diagnosis of CAE and JAE was based on conventional criteria. Details of demography, epilepsy phenomenology, management and outcomes were extracted. The outcome measures included reduction in daily seizure frequency measured as a percentage of pre-VNS seizure frequency and classified on International League Against Epilepsy (ILAE) outcome scale. Nine patients (7 CAE, 2 JAE) with a mean age of seizure onset of 5.4 years (±3.9) were identified. Mean duration of epilepsy prior to VNS implant was found to be 3.9 years (±1.4). These patients had failed a median of 5 anti-epileptic drugs before being referred for consideration of surgical treatment. After a mean follow-up of 33.9 months (±25.5, minimum 4 months), 1 patient attained complete seizure freedom (ILAE class 1), 6 had ILAE class 4 and 2 had ILAE class 5 outcomes, respectively. Mean reduction in daily seizure frequency was found to be 53.5±60.3% (1-sided p-value for paired t-test=0.04), with a 50% responder rate of 55.6%. VNS may be considered as a therapeutic option in patients with medically refractory absence epilepsy.
AbstractList A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patient population. Patients were identified by a chart review of all VNS recipients between January 1, 2006 and December 31, 2011. The diagnosis of CAE and JAE was based on conventional criteria. Details of demography, epilepsy phenomenology, management and outcomes were extracted. The outcome measures included reduction in daily seizure frequency measured as a percentage of pre-VNS seizure frequency and classified on International League Against Epilepsy (ILAE) outcome scale. Nine patients (7 CAE, 2 JAE) with a mean age of seizure onset of 5.4 years (±3.9) were identified. Mean duration of epilepsy prior to VNS implant was found to be 3.9 years (±1.4). These patients had failed a median of 5 anti-epileptic drugs before being referred for consideration of surgical treatment. After a mean follow-up of 33.9 months (±25.5, minimum 4 months), 1 patient attained complete seizure freedom (ILAE class 1), 6 had ILAE class 4 and 2 had ILAE class 5 outcomes, respectively. Mean reduction in daily seizure frequency was found to be 53.5±60.3% (1-sided p-value for paired t-test=0.04), with a 50% responder rate of 55.6%. VNS may be considered as a therapeutic option in patients with medically refractory absence epilepsy.
Abstract Purpose A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patient population. Methods Patients were identified by a chart review of all VNS recipients between January 1, 2006 and December 31, 2011. The diagnosis of CAE and JAE was based on conventional criteria. Details of demography, epilepsy phenomenology, management and outcomes were extracted. The outcome measures included reduction in daily seizure frequency measured as a percentage of pre-VNS seizure frequency and classified on International League Against Epilepsy (ILAE) outcome scale. Results Nine patients (7 CAE, 2 JAE) with a mean age of seizure onset of 5.4 years (±3.9) were identified. Mean duration of epilepsy prior to VNS implant was found to be 3.9 years (±1.4). These patients had failed a median of 5 anti-epileptic drugs before being referred for consideration of surgical treatment. After a mean follow-up of 33.9 months (±25.5, minimum 4 months), 1 patient attained complete seizure freedom (ILAE class 1), 6 had ILAE class 4 and 2 had ILAE class 5 outcomes, respectively. Mean reduction in daily seizure frequency was found to be 53.5 ± 60.3% (1-sided p -value for paired t -test = 0.04), with a 50% responder rate of 55.6%. Conclusion VNS may be considered as a therapeutic option in patients with medically refractory absence epilepsy.
A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patient population.PURPOSEA proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap for the treatment of such patients, this series is reported to generate estimate for efficacy of vagus nerve stimulation (VNS) in this patient population.Patients were identified by a chart review of all VNS recipients between January 1, 2006 and December 31, 2011. The diagnosis of CAE and JAE was based on conventional criteria. Details of demography, epilepsy phenomenology, management and outcomes were extracted. The outcome measures included reduction in daily seizure frequency measured as a percentage of pre-VNS seizure frequency and classified on International League Against Epilepsy (ILAE) outcome scale.METHODSPatients were identified by a chart review of all VNS recipients between January 1, 2006 and December 31, 2011. The diagnosis of CAE and JAE was based on conventional criteria. Details of demography, epilepsy phenomenology, management and outcomes were extracted. The outcome measures included reduction in daily seizure frequency measured as a percentage of pre-VNS seizure frequency and classified on International League Against Epilepsy (ILAE) outcome scale.Nine patients (7 CAE, 2 JAE) with a mean age of seizure onset of 5.4 years (±3.9) were identified. Mean duration of epilepsy prior to VNS implant was found to be 3.9 years (±1.4). These patients had failed a median of 5 anti-epileptic drugs before being referred for consideration of surgical treatment. After a mean follow-up of 33.9 months (±25.5, minimum 4 months), 1 patient attained complete seizure freedom (ILAE class 1), 6 had ILAE class 4 and 2 had ILAE class 5 outcomes, respectively. Mean reduction in daily seizure frequency was found to be 53.5±60.3% (1-sided p-value for paired t-test=0.04), with a 50% responder rate of 55.6%.RESULTSNine patients (7 CAE, 2 JAE) with a mean age of seizure onset of 5.4 years (±3.9) were identified. Mean duration of epilepsy prior to VNS implant was found to be 3.9 years (±1.4). These patients had failed a median of 5 anti-epileptic drugs before being referred for consideration of surgical treatment. After a mean follow-up of 33.9 months (±25.5, minimum 4 months), 1 patient attained complete seizure freedom (ILAE class 1), 6 had ILAE class 4 and 2 had ILAE class 5 outcomes, respectively. Mean reduction in daily seizure frequency was found to be 53.5±60.3% (1-sided p-value for paired t-test=0.04), with a 50% responder rate of 55.6%.VNS may be considered as a therapeutic option in patients with medically refractory absence epilepsy.CONCLUSIONVNS may be considered as a therapeutic option in patients with medically refractory absence epilepsy.
Author Gonsalves, Cornelia
Mangano, Francesco T.
Greiner, Hansel M.
Glauser, Tracy A.
Arya, Ravindra
Lewis, Amanda
Holland, Katherine D.
Author_xml – sequence: 1
  givenname: Ravindra
  surname: Arya
  fullname: Arya, Ravindra
  email: ravindra.arya4@gmail.com, Ravindra.Arya@cchmc.org
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 2
  givenname: Hansel M.
  surname: Greiner
  fullname: Greiner, Hansel M.
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 3
  givenname: Amanda
  surname: Lewis
  fullname: Lewis, Amanda
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 4
  givenname: Francesco T.
  surname: Mangano
  fullname: Mangano, Francesco T.
  organization: Division of Pediatric Neurosurgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 5
  givenname: Cornelia
  surname: Gonsalves
  fullname: Gonsalves, Cornelia
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 6
  givenname: Katherine D.
  surname: Holland
  fullname: Holland, Katherine D.
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
– sequence: 7
  givenname: Tracy A.
  surname: Glauser
  fullname: Glauser, Tracy A.
  organization: Comprehensive Epilepsy Center, Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23391567$$D View this record in MEDLINE/PubMed
BookMark eNqNkktv1TAQhS1URB_wE0BZskkY24mTCEFVVUCRKrHgsbWcyQT54htf7KRS-uvrcC8sKlVlZcs658jznTllR6MfibGXHAoOXL3ZFJHs7RyoEMBlAbwAaJ6wE15JkQvVNEfpDlWbc8n5MTuNcQMAbcnlM3YspGx5peoTdvHD_JxjNlK4oSxOdjs7M1k_ZoMP2ZZ6i8a5JQs0BIOTD0tmukgjUkY762gXl-fs6WBcpBeH84x9__jh2-VVfv3l0-fLi-scq6ae8qHGErBD0SEIgEoZgdBi1_alBNOpFrksy7JWdd-B7Ac1mL41Td9ieqFSyTP2ep-7C_73THHSWxuRnDMj-TlqLoXipZAASfrqIJ27NIPeBbs1YdF_x06Cai_A4GNMw_2TcNArXr3RB7x6xauB64Q3-d7e86Gd_vCagrHuUff53k0J042loCPalWVvA-Gke28fTXh_LwGdHdeOftFCcePnMKYONNdRaNBf1wVY--eJSiq_SgHvHg74jw_cAfv6w9w
CitedBy_id crossref_primary_10_1016_j_seizure_2024_01_019
crossref_primary_10_1016_j_yebeh_2013_05_021
crossref_primary_10_1016_j_arcped_2016_08_005
crossref_primary_10_3390_ijms25010091
crossref_primary_10_1227_NEU_0000000000001165
crossref_primary_10_4103_0028_3886_302476
crossref_primary_10_1016_j_ejpn_2015_07_008
crossref_primary_10_1016_j_pediatrneurol_2016_02_016
crossref_primary_10_1007_s00405_021_06943_x
crossref_primary_10_1016_j_neurol_2024_01_002
crossref_primary_10_1016_j_neurol_2023_11_010
crossref_primary_10_1016_j_yebeh_2018_06_032
crossref_primary_10_1016_j_eplepsyres_2014_06_020
crossref_primary_10_1007_s12098_020_03423_8
crossref_primary_10_1016_j_eplepsyres_2013_06_004
crossref_primary_10_1177_0883073818766599
crossref_primary_10_1177_15357597211065587
crossref_primary_10_1111_cns_13209
crossref_primary_10_1080_17512433_2021_1959317
crossref_primary_10_1016_j_pediatrneurol_2013_10_009
crossref_primary_10_3390_pediatric13040078
crossref_primary_10_1007_s00381_015_3004_z
crossref_primary_10_1111_epi_12762
crossref_primary_10_1212_WNL_0000000000012030
crossref_primary_10_1016_j_seizure_2023_09_019
crossref_primary_10_1016_j_neuroscience_2017_05_038
crossref_primary_10_1016_j_pediatrneurol_2023_07_019
crossref_primary_10_1111_aor_12945
crossref_primary_10_1007_s11940_014_0290_9
Cites_doi 10.1056/NEJMoa0902014
10.1016/j.seizure.2003.09.002
10.1016/0887-8994(91)90004-5
10.1007/BF00313944
10.1212/WNL.35.4.579
10.1212/WNL.13.11.959
10.1016/j.pediatrneurol.2012.02.004
10.1016/j.seizure.2009.05.009
10.1212/WNL.0b013e3181eb58b4
10.1111/j.1528-1157.1989.tb05316.x
10.1111/j.1528-1167.2009.02397.x
10.1212/WNL.52.7.1510
10.1016/S1474-4422(02)00220-X
10.1212/WNL.47.3.802
10.1016/j.nurt.2009.01.010
10.1111/j.1600-0404.2007.00848.x
10.1001/jama.1965.03090160005001
10.1046/j.1528-1157.2001.4220282.x
10.1016/S0022-3476(05)81922-5
10.1111/j.1528-1167.2006.00377.x
ContentType Journal Article
Copyright 2013 British Epilepsy Association
British Epilepsy Association
Copyright © 2013 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
Copyright_xml – notice: 2013 British Epilepsy Association
– notice: British Epilepsy Association
– notice: Copyright © 2013 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
DBID 6I.
AAFTH
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1016/j.seizure.2013.01.008
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE

MEDLINE - Academic


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1532-2688
EndPage 270
ExternalDocumentID 23391567
10_1016_j_seizure_2013_01_008
S1059131113000095
1_s2_0_S1059131113000095
Genre Journal Article
GrantInformation_xml – fundername: NCATS NIH HHS
  grantid: UL1 TR000077
GroupedDBID ---
--K
--M
-RU
.1-
.FO
.~1
0R~
123
1B1
1P~
1RT
1~.
1~5
4.4
457
4G.
53G
5VS
7-5
71M
8P~
9JM
9JO
AADFP
AAEDT
AAEDW
AAGJA
AAGUQ
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAQXK
AATTM
AAWTL
AAXKI
AAXLA
AAXUO
AAYWO
ABBQC
ABCQJ
ABFNM
ABIVO
ABJNI
ABMAC
ABMZM
ABOYX
ABTEW
ABWVN
ABXDB
ACDAQ
ACGFS
ACIEU
ACLOT
ACRLP
ACRPL
ACVFH
ACXNI
ADBBV
ADCNI
ADEZE
ADMUD
ADNMO
ADVLN
AEBSH
AEIPS
AEKER
AEUPX
AEVXI
AEXQZ
AFJKZ
AFPUW
AFRHN
AFTJW
AFXIZ
AGHFR
AGQPQ
AGUBO
AGWIK
AGYEJ
AHHHB
AIEXJ
AIGII
AIIUN
AIKHN
AITUG
AJRQY
AJUYK
AKBMS
AKRLJ
AKRWK
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
ANKPU
ANZVX
ASPBG
AVWKF
AXJTR
AZFZN
BAWUL
BKOJK
BLXMC
BNPGV
CAG
COF
CS3
DIK
E3Z
EBS
EFJIC
EFKBS
EFLBG
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
G-2
G-Q
GBLVA
HDW
HMK
HMO
HVGLF
HZ~
IHE
IXB
J1W
KOM
LX8
M29
M41
MO0
MOBAO
N9A
O-L
O9-
OAUVE
OK1
OKEIE
OP~
OZT
P-8
P-9
P2P
PC.
Q38
R2-
ROL
RPZ
SAE
SCC
SDF
SDG
SEL
SES
SEW
SSB
SSH
SSN
SSY
SSZ
T5K
TR2
WUQ
Z5R
~G-
~HD
0SF
6I.
AACTN
AAFTH
ABVKL
AFCTW
AFKWA
AJOXV
AMFUW
NCXOZ
RIG
AADPK
AAIAV
ABLVK
ABYKQ
AFYLN
AJBFU
LCYCR
9DU
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-c587t-f7c40cbc2bc020056a2c09cb9d430ab69c13444767db03df6fad9a8d9c67de463
ISICitedReferencesCount 33
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000318057000003&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1059-1311
1532-2688
IngestDate Sun Nov 09 10:12:29 EST 2025
Thu Apr 03 06:59:10 EDT 2025
Sat Nov 29 07:07:52 EST 2025
Tue Nov 18 22:16:46 EST 2025
Fri Feb 23 02:28:33 EST 2024
Sun Feb 23 10:18:46 EST 2025
Tue Oct 14 19:28:39 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Medically refractory epilepsy
Absence seizures
Juvenile absence epilepsy
Vagus nerve stimulation
Childhood absence epilepsy
Language English
License http://www.elsevier.com/open-access/userlicense/1.0
Copyright © 2013 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c587t-f7c40cbc2bc020056a2c09cb9d430ab69c13444767db03df6fad9a8d9c67de463
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.clinicalkey.com/#!/content/1-s2.0-S1059131113000095
PMID 23391567
PQID 1326142300
PQPubID 23479
PageCount 4
ParticipantIDs proquest_miscellaneous_1326142300
pubmed_primary_23391567
crossref_primary_10_1016_j_seizure_2013_01_008
crossref_citationtrail_10_1016_j_seizure_2013_01_008
elsevier_sciencedirect_doi_10_1016_j_seizure_2013_01_008
elsevier_clinicalkeyesjournals_1_s2_0_S1059131113000095
elsevier_clinicalkey_doi_10_1016_j_seizure_2013_01_008
PublicationCentury 2000
PublicationDate 2013-05-01
PublicationDateYYYYMMDD 2013-05-01
PublicationDate_xml – month: 05
  year: 2013
  text: 2013-05-01
  day: 01
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Seizure (London, England)
PublicationTitleAlternate Seizure
PublicationYear 2013
Publisher Elsevier Ltd
Publisher_xml – name: Elsevier Ltd
References Nei, O’Connor, Liporace, Sperling (bib0050) 2006; 47
Shahar, Brand (bib0030) 1992; 121
Perry, Bailey, Kotecha, Malik, Hernandez (bib0025) 2012; 46
Ben-Menachem (bib0070) 2002; 1
Bouma, Westendorp, van Dijk, Peters, Brouwer (bib0005) 1996; 47
Shields, Lake, Chugani (bib0035) 1985; 35
Wieser, Blume, Fish, Goldensohn, Hufnagel, King (bib0060) 2001; 42
Mullen, Suls, De Jonghe, Berkovic, Scheffer (bib0090) 2010; 75
Livingston, Torres, Pauli, Rider (bib0105) 1965; 194
Akman, Montenegro, Jacob, Eck, Chiriboga, Gilliam (bib0085) 2009; 18
Hirsch, Thomas, Panayiotopoulos (bib0020) 2008
Milby, Halpern, Baltuch (bib0065) 2009; 6
Kwan, Arzimanoglou, Berg, Brodie, Allen Hauser, Mathern (bib0015) 2010; 51
Wolf, Inoue (bib0110) 1984; 231
Hedstrom, Olsson (bib0095) 1991; 7
(bib0055) 1989; 30
Glauser, Cnaan, Shinnar, Hirtz, Dlugos, Masur (bib0010) 2010; 362
Holmes, Silbergeld, Drouhard, Wilensky, Ojemann (bib0045) 2004; 13
Kostov, Larsson, Roste (bib0040) 2007; 187
Labar, Murphy, Tecoma (bib0075) 1999; 52
Spuck, Tronnier, Orosz, Schonweiler, Sepehrnia, Nowak (bib0080) 2010; 67
Currier, Kooi, Saidman (bib0100) 1963; 13
Ben-Menachem (10.1016/j.seizure.2013.01.008_bib0070) 2002; 1
Perry (10.1016/j.seizure.2013.01.008_bib0025) 2012; 46
Wieser (10.1016/j.seizure.2013.01.008_bib0060) 2001; 42
Akman (10.1016/j.seizure.2013.01.008_bib0085) 2009; 18
Shahar (10.1016/j.seizure.2013.01.008_bib0030) 1992; 121
Hirsch (10.1016/j.seizure.2013.01.008_bib0020) 2008
Currier (10.1016/j.seizure.2013.01.008_bib0100) 1963; 13
Milby (10.1016/j.seizure.2013.01.008_bib0065) 2009; 6
Kostov (10.1016/j.seizure.2013.01.008_bib0040) 2007; 187
Livingston (10.1016/j.seizure.2013.01.008_bib0105) 1965; 194
Shields (10.1016/j.seizure.2013.01.008_bib0035) 1985; 35
Mullen (10.1016/j.seizure.2013.01.008_bib0090) 2010; 75
Nei (10.1016/j.seizure.2013.01.008_bib0050) 2006; 47
Hedstrom (10.1016/j.seizure.2013.01.008_bib0095) 1991; 7
Glauser (10.1016/j.seizure.2013.01.008_bib0010) 2010; 362
Wolf (10.1016/j.seizure.2013.01.008_bib0110) 1984; 231
Kwan (10.1016/j.seizure.2013.01.008_bib0015) 2010; 51
Spuck (10.1016/j.seizure.2013.01.008_bib0080) 2010; 67
Bouma (10.1016/j.seizure.2013.01.008_bib0005) 1996; 47
(10.1016/j.seizure.2013.01.008_bib0055) 1989; 30
Holmes (10.1016/j.seizure.2013.01.008_bib0045) 2004; 13
Labar (10.1016/j.seizure.2013.01.008_bib0075) 1999; 52
References_xml – volume: 13
  start-page: 340
  year: 2004
  end-page: 345
  ident: bib0045
  article-title: Effect of vagus nerve stimulation on adults with pharmacoresistant generalized epilepsy syndromes
  publication-title: Seizure
– volume: 362
  start-page: 790
  year: 2010
  end-page: 799
  ident: bib0010
  article-title: Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy
  publication-title: New England Journal of Medicine
– volume: 187
  start-page: 55
  year: 2007
  end-page: 58
  ident: bib0040
  article-title: Is vagus nerve stimulation a treatment option for patients with drug-resistant idiopathic generalized epilepsy?
  publication-title: Acta Neurologica Scandinavica
– start-page: 2397
  year: 2008
  end-page: 2412
  ident: bib0020
  article-title: Childhood and juvenile absence epilepsies
  publication-title: Epilepsy: a comprehensive textbook
– volume: 231
  start-page: 225
  year: 1984
  end-page: 229
  ident: bib0110
  article-title: Therapeutic response of absence seizures in patients of an epilepsy clinic for adolescents and adults
  publication-title: Journal of Neurology
– volume: 42
  start-page: 282
  year: 2001
  end-page: 286
  ident: bib0060
  article-title: ILAE commission report. Proposal for a new classification of outcome with respect to epileptic seizures following epilepsy surgery
  publication-title: Epilepsia
– volume: 46
  start-page: 243
  year: 2012
  end-page: 245
  ident: bib0025
  article-title: Amantadine for the treatment of refractory absence seizures in children
  publication-title: Pediatric Neurology
– volume: 52
  start-page: 1510
  year: 1999
  end-page: 1512
  ident: bib0075
  article-title: Vagus nerve stimulation for medication-resistant generalized epilepsy, E04 VNS Study Group
  publication-title: Neurology
– volume: 75
  start-page: 432
  year: 2010
  end-page: 440
  ident: bib0090
  article-title: Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency
  publication-title: Neurology
– volume: 6
  start-page: 228
  year: 2009
  end-page: 237
  ident: bib0065
  article-title: Vagus nerve stimulation in the treatment of refractory epilepsy
  publication-title: Neurotherapeutics
– volume: 194
  start-page: 227
  year: 1965
  end-page: 232
  ident: bib0105
  article-title: Petit mal epilepsy, results of a prolonged follow-up study of 117 patients
  publication-title: JAMA
– volume: 13
  start-page: 959
  year: 1963
  end-page: 967
  ident: bib0100
  article-title: Prognosis of “Pure” petit mal; a follow-up study
  publication-title: Neurology
– volume: 47
  start-page: 802
  year: 1996
  end-page: 808
  ident: bib0005
  article-title: The outcome of absence epilepsy: a meta-analysis
  publication-title: Neurology
– volume: 121
  start-page: 819
  year: 1992
  end-page: 821
  ident: bib0030
  article-title: Effect of add-on amantadine therapy for refractory absence epilepsy
  publication-title: Journal of Pediatrics
– volume: 1
  start-page: 477
  year: 2002
  end-page: 482
  ident: bib0070
  article-title: Vagus-nerve stimulation for the treatment of epilepsy
  publication-title: Lancet Neurology
– volume: 47
  start-page: 115
  year: 2006
  end-page: 122
  ident: bib0050
  article-title: Refractory generalized seizures: response to corpus callosotomy and vagal nerve stimulation
  publication-title: Epilepsia
– volume: 67
  start-page: 489
  year: 2010
  end-page: 494
  ident: bib0080
  article-title: Operative and technical complications of vagus nerve stimulator implantation
  publication-title: Neurosurgery
– volume: 18
  start-page: 524
  year: 2009
  end-page: 529
  ident: bib0085
  article-title: Seizure frequency in children with epilepsy: factors influencing accuracy and parental awareness
  publication-title: Seizure
– volume: 30
  start-page: 389
  year: 1989
  end-page: 399
  ident: bib0055
  article-title: Proposal for revised classification of epilepsies and epileptic, syndromes. Commission on Classification and Terminology of the International League Against Epilepsy
  publication-title: Epilepsia
– volume: 35
  start-page: 579
  year: 1985
  end-page: 581
  ident: bib0035
  article-title: Amantadine in the treatment of refractory epilepsy in childhood: an open trial in 10 patients
  publication-title: Neurology
– volume: 51
  start-page: 1069
  year: 2010
  end-page: 1077
  ident: bib0015
  article-title: Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies
  publication-title: Epilepsia
– volume: 7
  start-page: 100
  year: 1991
  end-page: 104
  ident: bib0095
  article-title: Epidemiology of absence epilepsy: EEG findings and their predictive value
  publication-title: Pediatric Neurology
– volume: 362
  start-page: 790
  year: 2010
  ident: 10.1016/j.seizure.2013.01.008_bib0010
  article-title: Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy
  publication-title: New England Journal of Medicine
  doi: 10.1056/NEJMoa0902014
– volume: 13
  start-page: 340
  year: 2004
  ident: 10.1016/j.seizure.2013.01.008_bib0045
  article-title: Effect of vagus nerve stimulation on adults with pharmacoresistant generalized epilepsy syndromes
  publication-title: Seizure
  doi: 10.1016/j.seizure.2003.09.002
– volume: 7
  start-page: 100
  year: 1991
  ident: 10.1016/j.seizure.2013.01.008_bib0095
  article-title: Epidemiology of absence epilepsy: EEG findings and their predictive value
  publication-title: Pediatric Neurology
  doi: 10.1016/0887-8994(91)90004-5
– volume: 231
  start-page: 225
  year: 1984
  ident: 10.1016/j.seizure.2013.01.008_bib0110
  article-title: Therapeutic response of absence seizures in patients of an epilepsy clinic for adolescents and adults
  publication-title: Journal of Neurology
  doi: 10.1007/BF00313944
– start-page: 2397
  year: 2008
  ident: 10.1016/j.seizure.2013.01.008_bib0020
  article-title: Childhood and juvenile absence epilepsies
– volume: 35
  start-page: 579
  year: 1985
  ident: 10.1016/j.seizure.2013.01.008_bib0035
  article-title: Amantadine in the treatment of refractory epilepsy in childhood: an open trial in 10 patients
  publication-title: Neurology
  doi: 10.1212/WNL.35.4.579
– volume: 13
  start-page: 959
  year: 1963
  ident: 10.1016/j.seizure.2013.01.008_bib0100
  article-title: Prognosis of “Pure” petit mal; a follow-up study
  publication-title: Neurology
  doi: 10.1212/WNL.13.11.959
– volume: 46
  start-page: 243
  year: 2012
  ident: 10.1016/j.seizure.2013.01.008_bib0025
  article-title: Amantadine for the treatment of refractory absence seizures in children
  publication-title: Pediatric Neurology
  doi: 10.1016/j.pediatrneurol.2012.02.004
– volume: 18
  start-page: 524
  year: 2009
  ident: 10.1016/j.seizure.2013.01.008_bib0085
  article-title: Seizure frequency in children with epilepsy: factors influencing accuracy and parental awareness
  publication-title: Seizure
  doi: 10.1016/j.seizure.2009.05.009
– volume: 75
  start-page: 432
  year: 2010
  ident: 10.1016/j.seizure.2013.01.008_bib0090
  article-title: Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency
  publication-title: Neurology
  doi: 10.1212/WNL.0b013e3181eb58b4
– volume: 30
  start-page: 389
  year: 1989
  ident: 10.1016/j.seizure.2013.01.008_bib0055
  article-title: Proposal for revised classification of epilepsies and epileptic, syndromes. Commission on Classification and Terminology of the International League Against Epilepsy
  publication-title: Epilepsia
  doi: 10.1111/j.1528-1157.1989.tb05316.x
– volume: 51
  start-page: 1069
  year: 2010
  ident: 10.1016/j.seizure.2013.01.008_bib0015
  article-title: Definition of drug resistant epilepsy: consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies
  publication-title: Epilepsia
  doi: 10.1111/j.1528-1167.2009.02397.x
– volume: 52
  start-page: 1510
  year: 1999
  ident: 10.1016/j.seizure.2013.01.008_bib0075
  article-title: Vagus nerve stimulation for medication-resistant generalized epilepsy, E04 VNS Study Group
  publication-title: Neurology
  doi: 10.1212/WNL.52.7.1510
– volume: 1
  start-page: 477
  year: 2002
  ident: 10.1016/j.seizure.2013.01.008_bib0070
  article-title: Vagus-nerve stimulation for the treatment of epilepsy
  publication-title: Lancet Neurology
  doi: 10.1016/S1474-4422(02)00220-X
– volume: 47
  start-page: 802
  year: 1996
  ident: 10.1016/j.seizure.2013.01.008_bib0005
  article-title: The outcome of absence epilepsy: a meta-analysis
  publication-title: Neurology
  doi: 10.1212/WNL.47.3.802
– volume: 6
  start-page: 228
  year: 2009
  ident: 10.1016/j.seizure.2013.01.008_bib0065
  article-title: Vagus nerve stimulation in the treatment of refractory epilepsy
  publication-title: Neurotherapeutics
  doi: 10.1016/j.nurt.2009.01.010
– volume: 187
  start-page: 55
  issue: Suppl.
  year: 2007
  ident: 10.1016/j.seizure.2013.01.008_bib0040
  article-title: Is vagus nerve stimulation a treatment option for patients with drug-resistant idiopathic generalized epilepsy?
  publication-title: Acta Neurologica Scandinavica
  doi: 10.1111/j.1600-0404.2007.00848.x
– volume: 194
  start-page: 227
  year: 1965
  ident: 10.1016/j.seizure.2013.01.008_bib0105
  article-title: Petit mal epilepsy, results of a prolonged follow-up study of 117 patients
  publication-title: JAMA
  doi: 10.1001/jama.1965.03090160005001
– volume: 42
  start-page: 282
  year: 2001
  ident: 10.1016/j.seizure.2013.01.008_bib0060
  article-title: ILAE commission report. Proposal for a new classification of outcome with respect to epileptic seizures following epilepsy surgery
  publication-title: Epilepsia
  doi: 10.1046/j.1528-1157.2001.4220282.x
– volume: 67
  start-page: 489
  year: 2010
  ident: 10.1016/j.seizure.2013.01.008_bib0080
  article-title: Operative and technical complications of vagus nerve stimulator implantation
  publication-title: Neurosurgery
– volume: 121
  start-page: 819
  year: 1992
  ident: 10.1016/j.seizure.2013.01.008_bib0030
  article-title: Effect of add-on amantadine therapy for refractory absence epilepsy
  publication-title: Journal of Pediatrics
  doi: 10.1016/S0022-3476(05)81922-5
– volume: 47
  start-page: 115
  year: 2006
  ident: 10.1016/j.seizure.2013.01.008_bib0050
  article-title: Refractory generalized seizures: response to corpus callosotomy and vagal nerve stimulation
  publication-title: Epilepsia
  doi: 10.1111/j.1528-1167.2006.00377.x
SSID ssj0009413
Score 2.2006838
Snippet A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In view of evidence gap...
Abstract Purpose A proportion of patients with childhood and juvenile absence epilepsies (CAE, JAE) are likely to be classified as medically refractory. In...
SourceID proquest
pubmed
crossref
elsevier
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 267
SubjectTerms Absence seizures
Adolescent
Anticonvulsants - therapeutic use
Child
Childhood absence epilepsy
Epilepsy, Absence - drug therapy
Epilepsy, Absence - physiopathology
Epilepsy, Absence - therapy
Female
Follow-Up Studies
Humans
Juvenile absence epilepsy
Male
Medically refractory epilepsy
Neurology
Retrospective Studies
Treatment Outcome
Vagus nerve stimulation
Vagus Nerve Stimulation - methods
Young Adult
Title Vagus nerve stimulation for medically refractory absence epilepsy
URI https://www.clinicalkey.com/#!/content/1-s2.0-S1059131113000095
https://www.clinicalkey.es/playcontent/1-s2.0-S1059131113000095
https://dx.doi.org/10.1016/j.seizure.2013.01.008
https://www.ncbi.nlm.nih.gov/pubmed/23391567
https://www.proquest.com/docview/1326142300
Volume 22
WOSCitedRecordID wos000318057000003&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVESC
  databaseName: Elsevier SD Freedom Collection Journals 2021
  customDbUrl:
  eissn: 1532-2688
  dateEnd: 20210131
  omitProxy: false
  ssIdentifier: ssj0009413
  issn: 1059-1311
  databaseCode: AIEXJ
  dateStart: 19950301
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1ba9swFBZpO8Zexu7LLsWDvQV3sq1Y8mMY3bpByqDZyJuQJblkJE6w06zZ0376jiz5MprSbrAXEwyylHM-HR2dK0JvVTDUgRwarz9mPsnS0BdKD304-uB4lilghlXNJujpKZtOky-93q86F2Yzp3nOLi-T1X9lNbwDZpvU2b9gd_NReAG_genwBLbD81aM_ybOTdFVE8k4gP27cP25qnjChXXLzLcDOBiLqtXOdiDSstreegUSYlX-4ec907OfxsWwq_FH14hQbK0SKjZwxy8aUf-x0DOXUXMiTO77YHzUhgD9cK2QF6JjFxiL_FxU_cBt0w9dyuVgctS1TgSdWEBrMqvTZtoYJSNlQafzTZ2frhgOww7cSFem2n4d7ngObZ-RK5LfGiFMon5FFxO0F1UFWTFrj7omAPHMLMGswHjzjJq5hw5COkxALh6MPh1PP7eFm0lgkzTcktsssHc7J7tOv7nu_lLpMZMH6L67gHgjC5yHqKfzR-ju2IVYPEajCj9ehR-vgx8P8OM1-PFa_HgOP16Nnyfo64fjyfsT3_XZ8OWQ0bWfUUmwTGWYSmyMjLEIJU5kmigSYZHGiQwiQgiNqUpxpLI4EyoRTCUS3mgSR0_Rfr7M9XPkBSoLMiViKlRKMqwFUUxG8AGZYMki0Uekpg6Xrgi96YUy53W04XfuiMoNUTkOOBC1j46aYStbheWmAXFNel6nGMOhyAEtNw2kuwbq0u3wkge8DDnmVxDUR6wZ6bRXq5XeZtI3NTo4SHfjshO5Xl7AZHC7CuDGg3EfPbOwaQgQRqa5Q0xf_Ot_fYnutVv2FdpfFxf6NbojN-tZWRyiPTplh247_AYKe9cP
linkProvider Elsevier
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Vagus+nerve+stimulation+for+medically+refractory+absence+epilepsy&rft.jtitle=Seizure+%28London%2C+England%29&rft.au=Arya%2C+Ravindra&rft.au=Greiner%2C+Hansel+M.&rft.au=Lewis%2C+Amanda&rft.au=Mangano%2C+Francesco+T.&rft.date=2013-05-01&rft.pub=Elsevier+Ltd&rft.issn=1059-1311&rft.volume=22&rft.issue=4&rft.spage=267&rft.epage=270&rft_id=info:doi/10.1016%2Fj.seizure.2013.01.008&rft.externalDocID=S1059131113000095
thumbnail_m http://cvtisr.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F10591311%2FS1059131113X00044%2Fcov150h.gif