Stigma in psychogenic nonepileptic seizures.


Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
10 2020
Historique:
received: 12 05 2020
revised: 03 06 2020
accepted: 13 06 2020
pubmed: 11 7 2020
medline: 18 3 2021
entrez: 11 7 2020
Statut: ppublish

Résumé

There is scarce literature on stigma in families living with psychogenic nonepileptic seizures (PNES). Using a cohort of patients with epileptic seizures (ES) and their caregivers as controls, we aimed to quantify the level of patient and caregiver stigma in PNES and identify associations of patient and caregiver characteristics with it. Patients with PNES and ES and their caregivers completed surveys about demographic, clinical, and psychosocial characteristics. Multivariate regression analysis was used to identify correlates of patient and caregiver stigma. Forty-three patients with PNES and 165 patients with ES were recruited. Compared with patients with ES, patients with PNES had shorter disease duration, higher seizure frequency, normal diagnostic data, poorer psychosocial health, and fewer antiseizure medications (ASMs). A total of 76.5% of patients with PNES and 59.5% of patients with ES felt stigmatized. Patient stigma level was higher in patients with PNES compared with those with ES, and it was negatively associated with patient quality of life (QOL). Additionally, 28 caregivers of patients with PNES and 99 caregivers of patients with ES were recruited. There were no significant demographic, caregiving, or psychosocial differences between the two caregiver cohorts. Seventy-two percent of caregivers of patients with PNES and 47% of caregivers of patients with ES felt stigmatized. Caregiver stigma level was also higher in caregivers of patients with PNES compared with caregivers of patients with ES, and it was negatively associated with patient QOL and positively associated with patient and caregiver anxiety. Compared with those with ES, patients and caregivers living with PNES experience stigma more frequently and to a higher extent. Patient QOL emerges as a consistent correlate of that stigma.

Identifiants

pubmed: 32650291
pii: S1525-5050(20)30448-0
doi: 10.1016/j.yebeh.2020.107269
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107269

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest None of the authors has any pertinent declarations of interest to disclose to this study. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Auteurs

Ioannis Karakis (I)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA. Electronic address: ioannis.karakis@emory.edu.

Nicholas J Janocko (NJ)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Matthew L Morton (ML)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Olivia Groover (O)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Diane L Teagarden (DL)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Hannah K Villarreal (HK)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

David W Loring (DW)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

Daniel L Drane (DL)

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA; Department of Neurology, University of Washington, Seattle, WA, USA.

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Classifications MeSH