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Neurology

Will My Child Outgrow This? Prognosis and Long-Term Outlook

At a Glance

Approximately 60% to 90% of children with Childhood Absence Epilepsy (CAE) will completely outgrow the condition by mid-adolescence. Children who are seizure-free for two years with a normal EEG can often successfully taper off their medication under a doctor's supervision.

For many parents, the most pressing question after a diagnosis of Childhood Absence Epilepsy (CAE) is: “Will my child have to deal with this forever?” The answer for the vast majority of families is a hopeful one. CAE is one of the most likely forms of epilepsy to be “outgrown” [1][2].

The Road to Remission

In the context of epilepsy, remission means that the seizures have stopped entirely and the child no longer requires medication.

  • Success Rates: Approximately 60% to 90% of children with classic CAE achieve complete remission and outgrow the condition, usually by mid-adolescence [1][2].
  • The “Two-Year” Rule: Many doctors will consider tapering a child off medication if they have been completely seizure-free for at least two years and have a normal EEG [3].

Predictors of a Favorable Outcome

While every child is different, researchers have identified several “favorable predictors” that suggest a child is highly likely to outgrow CAE:

  1. Early Treatment Success: Children who respond quickly to their first medication (especially ethosuximide) have a very high likelihood of long-term success and a lower risk of developing other seizure types [4][2].
  2. Lack of Motor Symptoms: Seizures that consist only of a blank stare, without eye blinking or finger movements, are often associated with earlier remission [3].
  3. Normal EEG Background: A “clean” EEG (meaning the brain waves look normal in the seconds between seizure discharges) is a strong sign of a good prognosis [3].
  4. No History of Generalized Tonic-Clonic Seizures: Children who only ever experience absence spells have a better chance of total remission than those who also experience “grand mal” seizures [4].

CAE vs. Juvenile Absence Epilepsy (JAE)

The timing of when the epilepsy starts matters for the long-term outlook.

  • CAE (Starts ages 4–10): High rate of outgrowing the condition by the teenage years [5].
  • JAE (Starts ages 10–17): Remission is less certain. Patients with JAE are more likely to require lifelong medication and have a higher risk of developing generalized tonic-clonic seizures [6][7].

What if My Child Doesn’t Outgrow It?

About 20% to 30% of children do not achieve early remission or may experience pharmacoresistance (seizures that don’t respond well to medication) [8].

  • Extended Treatment: Some children may need to stay on medication longer than average, sometimes into their 20s.
  • Terminal Remission: Even if a child doesn’t outgrow the condition by age 15, research shows that the probability of terminal remission (permanent stopping of seizures) actually increases as a person gets older [7].
  • Comorbidities: Even if seizures persist, the goal of treatment remains high quality of life. Doctors will continue to monitor for cognitive or emotional impacts to ensure the child—and later, the adult—has the support they need [9][10].

While the journey can be long, the majority of children with CAE will eventually leave their “blank spells” behind and lead full, healthy lives. Prompt diagnosis and consistent treatment are the most powerful tools you have to help your child reach that finish line [2].

Common questions in this guide

Will my child outgrow childhood absence epilepsy?
Between 60% and 90% of children with classic Childhood Absence Epilepsy completely outgrow the condition. Most achieve full remission by mid-adolescence and no longer require daily medication.
When can a child stop taking medication for absence seizures?
Doctors typically consider tapering a child off medication if they have been completely seizure-free for at least two years and have a normal EEG. This weaning process should always be guided by a pediatric neurologist.
What is the difference between childhood and juvenile absence epilepsy?
Childhood Absence Epilepsy usually begins between ages 4 and 10 and has a high rate of remission. Juvenile Absence Epilepsy starts later, between ages 10 and 17, and these patients are more likely to require lifelong medication.
What signs indicate my child is likely to outgrow absence seizures?
Favorable predictors include early success with the first medication, seizures consisting only of a blank stare without motor movements, a normal EEG background, and no history of generalized tonic-clonic (grand mal) seizures.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Based on my child's early response to medication, what is the likelihood they will achieve terminal remission?
  2. 2.Does my child's current EEG show any 'polyspikes' or disorganized activity that might indicate a longer journey to remission?
  3. 3.If my child stays seizure-free for two years, what is your typical process for 'weaning' them off medication?
  4. 4.Are there any specific 'red flags' I should watch for that might suggest their epilepsy is evolving into a juvenile syndrome?
  5. 5.If my child is in the 20-30% who don't outgrow it by the teen years, what are the long-term options for adult management?

Questions For You

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References

References (10)
  1. 1

    Long-term prognosis of childhood absence epilepsy.

    Martínez-Ferrández C, Martínez-Salcedo E, Casas-Fernández C, et al.

    Neurologia 2019; (34(4)):224-228 doi:10.1016/j.nrl.2016.12.005.

    PMID: 28325560
  2. 2

    Childhood absence epilepsy: Electro-clinical manifestations, treatment options, and outcome in a tertiary educational center.

    Bashiri FA, Al Dosari A, Hamad MH, et al.

    International journal of pediatrics & adolescent medicine 2022; (9(2)):131-135 doi:10.1016/j.ijpam.2021.11.003.

    PMID: 35663781
  3. 3

    Long-term Prognosis of Childhood Absence Epilepsy.

    Yaşgüçlükal MA, Özçelik EU, Deniz Elmali A, et al.

    Noro psikiyatri arsivi 2024; (61(1)):85-89 doi:10.29399/npa.28583.

    PMID: 38496228
  4. 4

    Long-term outcomes of generalized tonic-clonic seizures in a childhood absence epilepsy trial.

    Shinnar S, Cnaan A, Hu F, et al.

    Neurology 2015; (85(13)):1108-14 doi:10.1212/WNL.0000000000001971.

    PMID: 26311751
  5. 5

    ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions.

    Hirsch E, French J, Scheffer IE, et al.

    Epilepsia 2022; (63(6)):1475-1499 doi:10.1111/epi.17236.

    PMID: 35503716
  6. 6

    Changes in awake and sleep electroencephalography characteristics after 1-year treatment for childhood and juvenile absence epilepsy.

    Edizer S, Baysal BT, Ünalp A, Yılmaz Ü

    Seizure 2023; (110()):244-252 doi:10.1016/j.seizure.2023.06.023.

    PMID: 37441906
  7. 7

    Absence epilepsy beyond adolescence: an outcome analysis after 45 years of follow-up.

    Holtkamp M, Janz D, Kirschbaum A, et al.

    Journal of neurology, neurosurgery, and psychiatry 2018; (89(6)):603-610 doi:10.1136/jnnp-2017-317052.

    PMID: 29348303
  8. 8

    Care of pharmaco-resistant absence seizures in childhood.

    Le Roux M, Benallegue N, Gueden S, et al.

    Revue neurologique 2024; (180(4)):251-255 doi:10.1016/j.neurol.2024.01.002.

    PMID: 38388226
  9. 9

    Refractory absence seizures: An Italian multicenter retrospective study.

    Franzoni E, Matricardi S, Di Pisa V, et al.

    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2015; (19(6)):660-4.

    PMID: 26239083
  10. 10

    Neuropsychological impairment in childhood absence epilepsy: Review of the literature.

    Verrotti A, Matricardi S, Rinaldi VE, et al.

    Journal of the neurological sciences 2015; (359(1-2)):59-66.

    PMID: 26671087

This page provides general prognosis and remission information for Childhood Absence Epilepsy. Always consult your pediatric neurologist before making any changes to your child's medication regimen.

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