Trajectory of Health-Related Quality of Life After Pediatric Epilepsy Surgery.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 03 2023
Historique:
medline: 29 3 2023
entrez: 27 3 2023
pubmed: 28 3 2023
Statut: epublish

Résumé

Health-related quality of life (HRQOL) is regarded as a key outcome for evaluating treatment efficacy. However, it is uncertain how HRQOL evolves after epilepsy surgery compared with medical therapy, such as whether it continues to improve over time, improves and then remains stable, or deteriorates after a period of time. To assess trajectory of HRQOL over 2 years in children with drug-resistant epilepsy (DRE) treated with surgery compared with medical therapy. Prospective cohort study assessing HRQOL longitudinally over 2 years. Participants were children recruited from 8 epilepsy centers in Canada from 2014 to 2019 with suspected DRE aged 4 to 18 years who were evaluated for surgery. Data were analyzed from May 2014 to December 2021. Epilepsy surgery or medical therapy. HRQOL was measured using the Quality of Life in Childhood Epilepsy Questionnaire (QOLCE)-55. HRQOL and seizure frequency were assessed at baseline, 6-month, 1-year, and 2-year follow-ups. Clinical, parent, and family characteristics were assessed at baseline. A linear mixed model was used to evaluate HRQOL over time, adjusting for baseline clinical, parent, and family characteristics. There were 111 surgical and 154 medical patients (mean [SD] age at baseline was 11.0 [4.1] years; 118 [45%] were female). At baseline, HRQOL was similar among surgical and medical patients. HRQOL of surgical patients was 3.0 (95% CI, -0.7 to 6.8) points higher at 6-month, 4.9 (95% CI, 0.7 to 9.1) points higher at 1-year, and 5.1 (95% CI, 0.7 to 9.5) points higher at 2-year follow-ups compared with medical patients. Surgical patients experienced greater improvements in social functioning relative to medical patients, but not for cognitive, emotional, and physical functioning. At 2-year follow-up, 72% of surgical patients were seizure-free, compared with 33% of medical patients. Seizure-free patients reported higher HRQOL than those who were not. This study provided evidence on the association between epilepsy surgery and children's HRQOL, with improvement in HRQOL occurring within the first year and remaining stable 2 years after surgery. By demonstrating that surgery improved seizure freedom and HRQOL, which has downstream effects such as better educational attainment, reduced health care resource utilization, and health care cost, these findings suggest that the high costs of surgery are justified, and that improved access to epilepsy surgery is necessary.

Identifiants

pubmed: 36972050
pii: 2802766
doi: 10.1001/jamanetworkopen.2023.4858
pmc: PMC10043749
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e234858

Subventions

Organisme : CIHR
ID : MOP-133708
Pays : Canada

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Auteurs

Elysa Widjaja (E)

Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Neurology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Medical Imaging, Lurie Children's Hospital, Chicago, Illinois.

Klajdi Puka (K)

Institute for Mental Health Policy Research, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.

Kathy N Speechley (KN)

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

Mark A Ferro (MA)

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

Mary B Connolly (MB)

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

Philippe Major (P)

Division of Neurology, Department of Pediatrics, CHU Ste-Justine Hospital, University of Montreal, Quebec, Canada.

Anne Gallagher (A)

Centre de Recherche, CHU Ste-Justine Hospital, University of Montreal, Quebec, Canada.

Salah Almubarak (S)

Division of Pediatric Neurology, Department of Pediatrics, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Qatif Central Hospital, Qatif, Saudi Arabia.

Simona Hasal (S)

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

Rajesh Ramachandrannair (R)

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

Andrea Andrade (A)

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

Qi Xu (Q)

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

Edward Leung (E)

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

O Carter Snead (OC)

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

Mary Lou Smith (ML)

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

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