Epidemiology of Treated Epilepsy in New Zealand Children: A Focus on Ethnicity.


Journal

Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060

Informations de publication

Date de publication:
09 11 2021
Historique:
received: 27 04 2021
accepted: 03 09 2021
pubmed: 11 9 2021
medline: 7 4 2022
entrez: 10 9 2021
Statut: ppublish

Résumé

To determine the period prevalence and incidence of treated epilepsy in a New Zealand pediatric cohort with a focus on ethnicity and socioeconomic status. This was a retrospective cohort study. The New Zealand Pharmaceutical Collection database was searched for individuals ≤18 years of age dispensed an antiseizure medication (ASM) in 2015 from areas capturing 48% of the New Zealand pediatric population. Medical records of identified cases were reviewed to ascertain the indication for the ASM prescription. Population data were derived from the New Zealand 2013 Census. A total of 3,557 ASMs were prescribed during 2015 in 2,594 children, of whom 1,717 (66%) children had epilepsy. An indication for prescription was ascertained for 3,332/3,557 (94%) ASMs. The period prevalence of treated epilepsy was 3.4 per 1,000 children. Children in the most deprived areas had 1.9 times the rate of treated epilepsy (95% confidence interval [CI] 1.6-2.2) as those from the least deprived areas. Prevalence was similar for most ethnic groups (European/other: 3.7, 95% CI 3.4-3.9; Pacific Peoples: 3.6, 95% CI 3.2-4.1; Māori: 3.4, 95% CI 3.1-3.8) apart from Asians, who had a lower prevalence of 2.3 per 1,000 (95% CI 2.0-2.6). However, when adjusted for socioeconomic deprivation, the prevalence of epilepsy was highest in European and similar in Māori, Pacific, and Asian children. This is the largest pediatric epidemiology epilepsy study where diagnosis of epilepsy was confirmed by case review. This is the first study to provide epidemiologic information for pediatric epilepsy in Māori and Pacific children.

Sections du résumé

BACKGROUND AND OBJECTIVES
To determine the period prevalence and incidence of treated epilepsy in a New Zealand pediatric cohort with a focus on ethnicity and socioeconomic status.
METHODS
This was a retrospective cohort study. The New Zealand Pharmaceutical Collection database was searched for individuals ≤18 years of age dispensed an antiseizure medication (ASM) in 2015 from areas capturing 48% of the New Zealand pediatric population. Medical records of identified cases were reviewed to ascertain the indication for the ASM prescription. Population data were derived from the New Zealand 2013 Census.
RESULTS
A total of 3,557 ASMs were prescribed during 2015 in 2,594 children, of whom 1,717 (66%) children had epilepsy. An indication for prescription was ascertained for 3,332/3,557 (94%) ASMs. The period prevalence of treated epilepsy was 3.4 per 1,000 children. Children in the most deprived areas had 1.9 times the rate of treated epilepsy (95% confidence interval [CI] 1.6-2.2) as those from the least deprived areas. Prevalence was similar for most ethnic groups (European/other: 3.7, 95% CI 3.4-3.9; Pacific Peoples: 3.6, 95% CI 3.2-4.1; Māori: 3.4, 95% CI 3.1-3.8) apart from Asians, who had a lower prevalence of 2.3 per 1,000 (95% CI 2.0-2.6). However, when adjusted for socioeconomic deprivation, the prevalence of epilepsy was highest in European and similar in Māori, Pacific, and Asian children.
DISCUSSION
This is the largest pediatric epidemiology epilepsy study where diagnosis of epilepsy was confirmed by case review. This is the first study to provide epidemiologic information for pediatric epilepsy in Māori and Pacific children.

Identifiants

pubmed: 34504020
pii: WNL.0000000000012784
doi: 10.1212/WNL.0000000000012784
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1933-e1941

Informations de copyright

© 2021 American Academy of Neurology.

Auteurs

Shayma Ali (S)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia.

James Stanley (J)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia.

Suzanne Davis (S)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia.

Ngaire Keenan (N)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia.

Ingrid Eileen Scheffer (IE)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia. scheffer@unimelb.edu.au.

Lynette Grant Sadleir (LG)

From the Departments of Pediatrics and Child Health (S.A., S.D., N.K., L.G.S.) and Public Health (J.S.), University of Otago, Wellington, New Zealand; and the Departments of Medicine and Pediatrics (I.S.), Austin Health and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, University of Melbourne, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH