Predictive Role of Electroencephalography in Regard to Neurological and Cognitive Sequelae After Acute Central Nervous System Infection.

CNS diseases EEG cognitive manifestation

Journal

Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH
ISSN: 0353-8109
Titre abrégé: Acta Inform Med
Pays: Bosnia and Herzegovina
ID NLM: 101147064

Informations de publication

Date de publication:
Dec 2019
Historique:
entrez: 15 2 2020
pubmed: 15 2 2020
medline: 15 2 2020
Statut: ppublish

Résumé

Electroencephalography can also be used to monitor long-term recovery of the patient after acute phase of the disease. Impaired neurocognitive function after infection, similar to brain injury, may present a transient but also prolonged problem for the functioning of an individual. Some studies have shown that importance of EEG may not be significant in sequel monitoring, because the extensive changes in EEG seen with severe forms of CNS infection do not necessarily imply a longer-term poor outcome. To examine the predictive potential of electroencephalography (EEG) in regard to the emergence of neurological and cognitive sequelae of acute central nervous system (CNS) infection. The study included 62 patients treated at the Clinic for Infectious Diseases, Clinical Center of Sarajevo University, who were diagnosed with acute CNS infection. The EEG record was characterized as: normal, non-specific changes of mild, moderate and severe degree and specific changes. The sequelae (headache, cognitive dysfunction, neurological and neurophysiological disorders, audiological and behavioral disorders) was evaluated by combining neurological, psychiatric, pediatric, otolaryngological, ophthalmic and infectological examination in the Neuroinfective Counseling Department for up to 6 months after discharge. After a treatment of an acute CNS infection 25 (40.3%) patients had no sequelae and 37 (59.7%) were with sequelae. The EEG in the initial stage of the disease (Wald's coefficient = 12.8), followed by the age of the patients (Wald = 6.4), had the greatest influence on the prediction of sequela (p=0.0001). For each additional degree of verified pathological changes in the EEG, the risk of sequelae was increased by 5 degrees (OR = 5.3), respectively. There was no statistically significant association between changes in cerebrospinal fluid (CSF) findings, meningeal symptoms, and signs with sequelae development. Younger age, as well as severe clinical status of a patient, which implies a disorder of consciousness and seizures on admission, are associated with irreversible consequences on a previously mentally healthy individual. Pathological changes (Delta and Theta waves, spike slow complex wave) on the EEG finding significantly predicted presence of sequelae. .

Identifiants

pubmed: 32055089
doi: 10.5455/aim.2019.27.234-239
pii: AIM-27-234
pmc: PMC7004286
doi:

Types de publication

Journal Article

Langues

eng

Pagination

234-239

Informations de copyright

© 2019 Belma Gazibera, Enra Suljic-Mehmedika, Nafija Serdarevic, Rusmir Baljic, Refet Gojak.

Déclaration de conflit d'intérêts

There are no conflicts of interest.

Références

J Neurosci. 2014 Jan 29;34(5):1592-8
pubmed: 24478343
BMC Infect Dis. 2015 Jul 22;15:279
pubmed: 26198732
PLoS One. 2018 Nov 16;13(11):e0207440
pubmed: 30444898
PLoS One. 2011;6(6):e21472
pubmed: 21720546
An Sist Sanit Navar. 2008;31 Suppl 1:99-113
pubmed: 18528447
Crit Care Med. 2013 Feb;41(2):580-637
pubmed: 23353941
J Intensive Care Soc. 2015 Nov;16(4):330-338
pubmed: 28979440
Front Psychiatry. 2019 Jan 17;9:752
pubmed: 30705643
Clin Microbiol Rev. 2014 Oct;27(4):691-726
pubmed: 25278572
Emerg Med Clin North Am. 2016 Nov;34(4):917-942
pubmed: 27741995
Clin Infect Dis. 2012 May;54(10):1455-64
pubmed: 22460967
PLoS One. 2014 Nov 04;9(11):e111393
pubmed: 25369023
Pediatr Int. 2013 Aug;55(4):461-4
pubmed: 23480596
Crit Care Med. 2013 Apr;41(4):1094-103
pubmed: 23385103
Crit Care. 2015 Sep 21;19:345
pubmed: 26387515
PLoS One. 2017 Feb 3;12(2):e0171094
pubmed: 28158207
Front Neurol. 2018 Oct 24;9:903
pubmed: 30405525
Pediatrics. 2015 Apr;135(4):e974-84
pubmed: 25802349
Neurol Clin. 2011 Feb;29(1):35-47, vii
pubmed: 21172569
Infect Dis Clin North Am. 2008 Mar;22(1):33-52, v-vi
pubmed: 18295682
J Infect. 2012 Apr;64(4):347-73
pubmed: 22120595
J Atten Disord. 2007 Nov;11(3):336-8; discussion 339-40
pubmed: 17932384
J Cent Nerv Syst Dis. 2017 May 01;9:1179573517703342
pubmed: 28579869
Pediatr Neurol. 2014 Apr;50(4):318-23
pubmed: 24507696
QJM. 2010 Oct;103(10):749-58
pubmed: 20657024
Emerg Infect Dis. 2013;19(9):
pubmed: 23969035
Crit Care Clin. 2013 Jul;29(3):621-49
pubmed: 23830656

Auteurs

Belma Gazibera (B)

Clinic for Infectious Diseases, Clinical Centre University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Enra Suljic-Mehmedika (E)

Clinic of Neurology, Clinical Centre University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Nafija Serdarevic (N)

Clinical Chemistry and Biochemistry, Clinical Centre University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Rusmir Baljic (R)

Clinic for Infectious Diseases, Clinical Centre University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Refet Gojak (R)

Clinic for Infectious Diseases, Clinical Centre University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Classifications MeSH