Childhood Absence Epilepsy (Typical Absence Seizures)
The most likely diagnosis is childhood absence epilepsy, characterized by typical absence seizures. 1
Clinical Features That Support This Diagnosis
The presentation is classic for typical absence seizures:
- Brief staring episodes lasting 3-5 seconds with abrupt onset and termination are the hallmark of typical absence seizures 2, 3
- Immediate return to baseline without post-ictal confusion distinguishes absence seizures from other seizure types 1, 2
- Age of 2.5 years falls within the typical onset range for childhood absence epilepsy, which usually begins between 6 months and 5 years 4, 2
- Head shaking and atypical eye movements represent motor automatisms commonly seen during typical absence seizures, with myoclonic components (particularly facial) being the most frequent motor manifestation 2, 3
Diagnostic Evaluation Required
EEG is mandatory and the single most important diagnostic test for any child with suspected absence seizures 1:
- The characteristic EEG pattern shows generalized 3-4 Hz spike-and-wave discharges during the clinical event 2, 3
- Hyperventilation provokes absence seizures in approximately 90% of untreated patients, making it a valuable diagnostic maneuver 2
- EEG should be obtained promptly and not delayed 1
Laboratory testing should be selective, not routine 1:
- Order labs only when clinical circumstances suggest metabolic derangements such as vomiting, diarrhea, dehydration, or failure to return to baseline 1
- Fingerstick glucose should be checked if there is any concern for hypoglycemia 1
Neuroimaging is not typically indicated for uncomplicated absence seizures where the child has returned to baseline 1:
- MRI is the preferred modality if neuroimaging is obtained 1
- Non-urgent MRI should be considered only in children with significant cognitive or motor impairment of unknown etiology, unexplained abnormalities on neurologic examination, or in children aged less than 1 year 1
Key Differentiating Features
This presentation is not consistent with:
- Febrile seizures – no fever present, and simple febrile seizures do not require imaging 4
- Atypical absence seizures – these typically last longer (15-30 seconds or more), occur in children with developmental delay or mental retardation, and have a less favorable prognosis 5, 3
- Benign paroxysmal torticollis – episodes last minutes to days, onset before 3 months of age, and present as head tilt rather than staring 4
- Sandifer syndrome – episodes occur after eating and are secondary to gastroesophageal reflux 4
Treatment Considerations
Once the diagnosis is confirmed by EEG, first-line treatment options include 2:
- Valproic acid controls absences in 75% of patients and also controls generalized tonic-clonic seizures (70%) and myoclonic jerks (75%) 2
- Ethosuximide controls 70% of absences but is unsuitable as monotherapy if other generalized seizures coexist 2
- Lamotrigine may control absences and generalized tonic-clonic seizures in 50-60% of patients 2
Disposition
Outpatient management is appropriate if the child has returned to baseline, has a normal neurologic examination, and no concerning features on history 1:
- Arrange outpatient EEG if not performed in the emergency department 1
- No hospital admission is required for uncomplicated first-time absence seizures when the child has returned to baseline 1
Critical Pitfalls to Avoid
- Do not routinely order extensive laboratory panels in otherwise healthy children who have returned to baseline, as these are very low yield 1
- Do not delay EEG, as it is the single most important diagnostic test and should be obtained promptly 1
- Do not confuse brief absence seizures with attention lapses – the presence of motor automatisms (head shaking, eye movements) and the stereotyped nature of the episodes point toward seizures rather than behavioral inattention 2, 3