Tablet-based electroencephalography diagnostics for patients with epilepsy in the West African Republic of Guinea.
Africa
diagnosis
electroencephalography
epilepsy
seizure
telemedicine
Journal
European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311
Informations de publication
Date de publication:
08 2020
08 2020
Historique:
received:
29
01
2020
accepted:
24
04
2020
pubmed:
3
5
2020
medline:
22
6
2021
entrez:
3
5
2020
Statut:
ppublish
Résumé
Epilepsy is most common in lower-income settings where access to electroencephalography (EEG) is generally poor. A low-cost tablet-based EEG device may be valuable, but the quality and reproducibility of the EEG output are not established. Tablet-based EEG was deployed in a heterogeneous epilepsy cohort in the Republic of Guinea (2018-2019), consisting of a tablet wirelessly connected to a 14-electrode cap. Participants underwent EEG twice (EEG1 and EEG2), separated by a variable time interval. Recordings were scored remotely by experts in clinical neurophysiology as to data quality and clinical utility. There were 149 participants (41% female; median age 17.9 years; 66.6% ≤21 years of age; mean seizures per month 5.7 ± SD 15.5). The mean duration of EEG1 was 53 ± 12.3 min and that of EEG2 was 29.6 ± 12.8 min. The mean quality scores of EEG1 and EEG2 were 6.4 [range, 1 (low) to 10 (high); both medians 7.0]. A total of 44 (29.5%) participants had epileptiform discharges (EDs) at EEG1 and 25 (16.8%) had EDs at EEG2. EDs were focal/multifocal (rather than generalized) in 70.1% of EEG1 and 72.5% of EEG2 interpretations. A total of 39 (26.2%) were recommended for neuroimaging after EEG1 and 22 (14.8%) after EEG2. Of participants without EDs at EEG1 (n = 53, 55.8%), seven (13.2%) had EDs at EEG2. Of participants with detectable EDs on EEG1 (n = 23, 24.2%), 12 (52.1%) did not have EDs at EEG2. Tablet-based EEG had a reproducible quality level on repeat testing and was useful for the detection of EDs. The incremental yield of a second EEG in this setting was ~13%. The need for neuroimaging access was evident.
Sections du résumé
BACKGROUND AND PURPOSE
Epilepsy is most common in lower-income settings where access to electroencephalography (EEG) is generally poor. A low-cost tablet-based EEG device may be valuable, but the quality and reproducibility of the EEG output are not established.
METHODS
Tablet-based EEG was deployed in a heterogeneous epilepsy cohort in the Republic of Guinea (2018-2019), consisting of a tablet wirelessly connected to a 14-electrode cap. Participants underwent EEG twice (EEG1 and EEG2), separated by a variable time interval. Recordings were scored remotely by experts in clinical neurophysiology as to data quality and clinical utility.
RESULTS
There were 149 participants (41% female; median age 17.9 years; 66.6% ≤21 years of age; mean seizures per month 5.7 ± SD 15.5). The mean duration of EEG1 was 53 ± 12.3 min and that of EEG2 was 29.6 ± 12.8 min. The mean quality scores of EEG1 and EEG2 were 6.4 [range, 1 (low) to 10 (high); both medians 7.0]. A total of 44 (29.5%) participants had epileptiform discharges (EDs) at EEG1 and 25 (16.8%) had EDs at EEG2. EDs were focal/multifocal (rather than generalized) in 70.1% of EEG1 and 72.5% of EEG2 interpretations. A total of 39 (26.2%) were recommended for neuroimaging after EEG1 and 22 (14.8%) after EEG2. Of participants without EDs at EEG1 (n = 53, 55.8%), seven (13.2%) had EDs at EEG2. Of participants with detectable EDs on EEG1 (n = 23, 24.2%), 12 (52.1%) did not have EDs at EEG2.
CONCLUSIONS
Tablet-based EEG had a reproducible quality level on repeat testing and was useful for the detection of EDs. The incremental yield of a second EEG in this setting was ~13%. The need for neuroimaging access was evident.
Identifiants
pubmed: 32359218
doi: 10.1111/ene.14291
pmc: PMC8830803
mid: NIHMS1752064
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1570-1577Subventions
Organisme : NINDS NIH HHS
ID : R21 NS098886
Pays : United States
Organisme : Hospital Corporation of America (HCA) International Foundation
Pays : International
Informations de copyright
© 2020 European Academy of Neurology.
Références
J Clin Neurophysiol. 2018 Jul;35(4):357
pubmed: 29851687
Epilepsy Behav. 2019 Mar;92:276-282
pubmed: 30731293
Sci Rep. 2017 Apr 03;7:45567
pubmed: 28367974
J Clin Neurophysiol. 2002 Dec;19(6):504-13
pubmed: 12488781
Continuum (Minneap Minn). 2013 Jun;19(3 Epilepsy):598-622
pubmed: 23739100
Seizure. 2019 Oct;71:93-99
pubmed: 31229939
Ann Neurol. 2016 Jun;79(6):871-81
pubmed: 27015883
J Child Neurol. 2012 May;27(5):625-31
pubmed: 22114217
J Neurol Neurosurg Psychiatry. 2005 Jun;76 Suppl 2:ii2-7
pubmed: 15961864
Epilepsy Behav. 2020 Feb;103(Pt A):106507
pubmed: 31645318
Neurol Clin Pract. 2017 Feb;7(1):35-44
pubmed: 29849234
Can J Neurol Sci. 2000 Nov;27(4):321-4
pubmed: 11097524
Seizure. 2009 Mar;18(2):133-8
pubmed: 18835193
Epilepsia. 2001 Feb;42(2):230-6
pubmed: 11240595
PLoS One. 2014 Feb 05;9(2):e86733
pubmed: 24505263