Anna Korsgaard Eltvedt
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Anna Korsgaard Eltvedt has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Alfred Peter Born
Department of Pediatrics, Rigshospitalet, University of Copenhagen, Denmark
2 shared publications - Amalie Wandel Klein-Petersen
Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Denmark
2 shared publications - Emilie Schou
Department of Neurology, Copenhagen University Hospital, Rigshospitalet Glostrup, Denmark
2 shared publications - Lau Caspar Thygesen
National Institute of Public Health, University of Southern Denmark Copenhagen Denmark
2 shared publications - Magnus Spangsberg Boesen
Department of Neurology, Zealand University Hospital, Roskilde, Denmark
2 shared publications - Malene Landbo Børresen
Department of Pediatrics, Copenhagen University, Rigshospitalet, Juliane Maries vej, 2100, Copenhagen, Denmark
2 shared publications
Latest Publications
- 24 December 2022
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 42, 75-81
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort study
- 24 December 2022
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 42, 75-81
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort study
- 20 May 2022
- Published by Springer Nature in Journal of Neurology
- Vol. 269 (9) , 4997-5007
School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort study
Background We aimed to determine school performance and psychiatric comorbidity in juvenile absence epilepsy (JAE), juvenile myoclonic epilepsy (JME), and generalized tonic–clonic seizures (GTCS) alone. Methods All children (< 18 years) fulfilled International League Against Epilepsy criteria after review of their medical records. Control groups were the pediatric background population or children with non-neurological chronic disease. Outcomes were on school performance and psychiatric comorbidity. We compared mean grade point averages using linear regression and estimated hazard ratios using Cox regression in the remaining analyses. We adjusted for the child’s sex, age, and year of birth; and parental highest education, receipt of cash benefits or early retirement. Results We included 92 JAE, 190 JME, 27 GTCS alone, 15,084 non-neurological chronic disease controls, and population controls. JAE had two times increased hazard for special needs education compared with age-matched population controls (hazard ratio 2.2, 95% CI = 1.1‒4.6, p = 0.03); this was not seen in JME. Compared with population controls, both JAE and JME had lower grade point average in secondary and high school (JME: 9th grade: – 0.5 points, 95% CI = −0.9 to −0.06, p = 0.03; high school: – 0.6 points, 95% CI = −1.3 to −0.1, p = 0.04), and 8% fewer JME and 15% fewer JAE attended high school. Both JME and JAE had higher hazard for redeeming sleep medication compared with non-neurological chronic disease; additionally, JAE had increased hazard for ADHD medicine redemptions. Conclusions Both JAE and JME had marginally poorer school performance; performance seemed worse in JAE than in JME. Both JAE and JME had increased use of sleep medication.
- 20 May 2022
- Published by Springer Nature in Journal of Neurology
- Vol. 269 (9) , 4997-5007
School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort study
Background We aimed to determine school performance and psychiatric comorbidity in juvenile absence epilepsy (JAE), juvenile myoclonic epilepsy (JME), and generalized tonic–clonic seizures (GTCS) alone. Methods All children (< 18 years) fulfilled International League Against Epilepsy criteria after review of their medical records. Control groups were the pediatric background population or children with non-neurological chronic disease. Outcomes were on school performance and psychiatric comorbidity. We compared mean grade point averages using linear regression and estimated hazard ratios using Cox regression in the remaining analyses. We adjusted for the child’s sex, age, and year of birth; and parental highest education, receipt of cash benefits or early retirement. Results We included 92 JAE, 190 JME, 27 GTCS alone, 15,084 non-neurological chronic disease controls, and population controls. JAE had two times increased hazard for special needs education compared with age-matched population controls (hazard ratio 2.2, 95% CI = 1.1‒4.6, p = 0.03); this was not seen in JME. Compared with population controls, both JAE and JME had lower grade point average in secondary and high school (JME: 9th grade: – 0.5 points, 95% CI = −0.9 to −0.06, p = 0.03; high school: – 0.6 points, 95% CI = −1.3 to −0.1, p = 0.04), and 8% fewer JME and 15% fewer JAE attended high school. Both JME and JAE had higher hazard for redeeming sleep medication compared with non-neurological chronic disease; additionally, JAE had increased hazard for ADHD medicine redemptions. Conclusions Both JAE and JME had marginally poorer school performance; performance seemed worse in JAE than in JME. Both JAE and JME had increased use of sleep medication.