A longitudinal cohort study of mediators of health‐related quality of life after pediatric epilepsy surgery or medical treatment

Author:

Smith Mary Lou12ORCID,Puka Klajdi3,Speechley Kathy N.34ORCID,Ferro Mark A.5,Connolly Mary B.6,Major Philippe7,Gallagher Anne8,Almubarak Salah910,Hasal Simona9,Ramachandrannair Rajesh11ORCID,Andrade Andrea4,Xu Qi12,Leung Edward12,Snead O. Carter13,Widjaja Elysa214ORCID

Affiliation:

1. Department of Psychology University of Toronto Mississauga Mississauga Ontario Canada

2. Neurosciences and Mental Health Program The Hospital for Sick Children Toronto Ontario Canada

3. Department of Epidemiology and Biostatistics Western University London Ontario Canada

4. Department of Paediatrics, Schulich School of Medicine and Dentistry Western University London Ontario Canada

5. School of Public Health Sciences University of Waterloo Waterloo Ontario Canada

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

7. Division of Neurology, Department of Neurosciences, CHU Ste‐Justine Hospital University of Montreal Montréal Quebec Canada

8. Centre de Recherche, CHU Ste‐Justine Hospital University of Montreal Montréal Quebec Canada

9. Division of Pediatric Neurology, Department of Pediatrics University of Saskatchewan Saskatoon Saskatchewan Canada

10. Qatif Central Hospital Qatif Saudi Arabia

11. Department of Pediatrics McMaster University Hamilton Ontario Canada

12. Department of Pediatrics and Child Health University of Manitoba Winnipeg Manitoba Canada

13. Division of Neurology The Hospital for Sick Children Toronto Ontario Canada

14. Department of Medical Imaging Lurie Children's Hospital Chicago Illinois USA

Abstract

AbstractObjectivesThe purpose of this longitudinal cohort study was to examine the variables that influence health‐related quality of life (HRQOL) after epilepsy surgery in children. We examined whether treatment type (surgical vs medical therapy) and seizure control are related to other variables that have been shown to influence HRQOL, namely depressive symptoms in children with epilepsy or their parents, and the availability of family resources.MethodsIn total, 265 children with drug‐resistant epilepsy were recruited from eight epilepsy centers across Canada at the time of their evaluation for candidacy for epilepsy surgery and were assessed at baseline, 6‐month, 1‐year, and 2‐year follow‐up. Parents completed the Quality of Life in Childhood Epilepsy Questionnaire (QOLCE‐55) and measures of family resources and depression; children completed depression inventories. Causal mediation analyses using natural effect models were used to evaluate the extent to which the relationship between treatment and HRQOL was explained by seizure control, child and parent depressive symptoms, and family resources.ResultsOverall, 111 children underwent surgery and 154 were treated with medical therapy only. The HRQOL scores of surgical patients were 3.4 points higher (95% confidence interval [CI]: −0.2, 7.0) relative to medical patients at the 2‐year follow‐up after adjusting for baseline covariates, with 66% of the effect of surgery attributed to seizure control. Child or parent depressive symptoms and family resources had negligible mediation effects between treatment and HRQOL. The effect of seizure control on HRQOL was not mediated by child or parent depressive symptoms, or by family resources.SignificanceThe findings demonstrate that seizure control is on the causal pathway between epilepsy surgery and improved HRQOL in children with drug‐resistant epilepsy. However, child and parent depressive symptoms and family resources were not significant mediators. The results highlight the importance of achieving seizure control to improve HRQOL.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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