Longitudinal changes in emotional functioning following pediatric resective epilepsy surgery: 2-Year follow-up.


Journal

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

Informations de publication

Date de publication:
01 2021
Historique:
received: 04 09 2020
revised: 20 10 2020
accepted: 21 10 2020
pubmed: 5 12 2020
medline: 20 4 2021
entrez: 4 12 2020
Statut: ppublish

Résumé

To examine longitudinal changes and predictors of depression and anxiety 2 years following resective epilepsy surgery, compared to no surgery, in children with drug-resistant epilepsy (DRE). This multicenter cohort study involved 128 children and adolescents with DRE (48 surgical, 80 nonsurgical; 8-18 years) who completed self-report measures of depression and anxiety at baseline and follow-up (6-month, 1-year, 2-year). Child demographic (age, sex, IQ) and seizure (age at onset, duration, frequency, site and side) variables were collected. Linear mixed-effects models controlling for age at enrolment found a time by treatment by seizure outcome interaction for depression. A negative linear trend across time (reduction in symptoms) was found for surgical patients, irrespective of seizure outcome. In contrast, the linear trend differed depending on seizure outcome in nonsurgical patients; a negative trend was found for those with continued seizures, whereas a positive trend (increase in symptoms) was found for those who achieved seizure freedom. Only a main effect of time was found for anxiety indicating a reduction in symptoms across patient groups. Multivariate regressions failed to find baseline predictors of depression or anxiety at 2-year follow-up in surgical patients. Older age, not baseline anxiety or depression, predicted greater symptoms of anxiety and depression at 2-year follow-up in nonsurgical patients. Children with DRE reported improvement in anxiety and depression, irrespective of whether they achieve seizure control, across the 2 years following surgery. In contrast, children with DRE who did not undergo surgery, but achieved seizure freedom, reported worsening of depressive symptoms, which may indicate difficulty adjusting to life without seizures and highlight the potential need for ongoing medical and psychosocial follow-up and support.

Identifiants

pubmed: 33272893
pii: S1525-5050(20)30765-4
doi: 10.1016/j.yebeh.2020.107585
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107585

Subventions

Organisme : Canadian Institutes for Health Research
ID : MOP-133708

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Natalie L Phillips (NL)

Neurosciences and Mental Health Program, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, The Hospital for Sick Children, Toronto, ON, Canada.

Elysa Widjaja (E)

Neurosciences and Mental Health Program, The Hospital for Sick Children, Toronto, ON, Canada; Division of Neurology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, ON, Canada.

Kathy Speechley (K)

Departments of Paediatrics and Epidemiology and Biostatistics, Western University, London, ON, Canada.

Mark Ferro (M)

School of Public Health and Health Systems, University of Waterloo, Waterloo, ON, Canada.

Mary Connolly (M)

Division of Neurology, Department of Pediatrics, BC Children's Hospital, Vancouver, BC, Canada.

Philippe Major (P)

Division of Neurology, Department of Pediatrics, Ste. Justine Hospital, Montreal, QC, Canada.

Anne Gallagher (A)

Centre de Recherche, Ste. Justine Hospital, Montreal, QC, Canada.

Rajesh Ramachandrannair (R)

Department of Pediatrics, McMaster University, Hamilton, ON, Canada.

Salah Almubarak (S)

Department of Pediatrics, Neurology Division, Royal University Hospital, Royal University Hospital, Saskatoon, SK, Canada; Department of Pediatrics, Neurology Division, Qatif Central Hospital, Qatif, Saudi Arabia.

Simona Hasal (S)

Department of Pediatrics, Neurology Division, Royal University Hospital, Royal University Hospital, Saskatoon, SK, Canada; Department of Pediatrics, Neurology Division, Qatif Central Hospital, Qatif, Saudi Arabia.

Andrea Andrade (A)

Department of Pediatrics, London Health Sciences Center, University of Western Ontario, London, ON, Canada.

Qi Xu (Q)

Department of Pediatrics, Health Sciences Centre, Winnipeg, MB, Canada.

Edward Leung (E)

Department of Pediatrics, Health Sciences Centre, Winnipeg, MB, Canada.

O Carter Snead (OC)

Division of Neurology, The Hospital for Sick Children, Toronto, ON, Canada.

Mary Lou Smith (ML)

Neurosciences and Mental Health Program, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, University of Toronto Mississauga, Mississauga, ON, Canada. Electronic address: marylou.smith@utoronto.ca.

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