Management of Bi-occipital Spike and Slow Wave Activity
Bi-occipital spike and slow wave activity on EEG requires neurological consultation and anti-seizure medication therapy in patients with associated seizures, as this pattern is frequently associated with epileptic disorders, particularly occipital epilepsy of childhood. 1, 2, 3
Diagnostic Approach
EEG Characteristics and Interpretation
- Bi-occipital spike and slow wave activity is an EEG pattern characterized by:
Clinical Correlation
- The pattern is associated with several clinical presentations:
Management Algorithm
Step 1: Determine if the pattern is associated with clinical seizures
- If seizures are present:
Step 2: Neuroimaging
- MRI is the preferred imaging modality for patients with suspected epilepsy 5
Step 3: Additional diagnostic testing
- Consider simultaneous EEG and hemodynamic monitoring during tilt-table testing to distinguish between syncope, pseudosyncope, and epilepsy 5
- Evaluate for metabolic abnormalities:
Step 4: Treatment approach
- For patients with seizures:
- Initiate appropriate anti-seizure medication therapy
- Prognosis is generally good for benign occipital epilepsy, though less favorable than rolandic epilepsy 2
- For patients without seizures but with neurovegetative symptoms:
- Symptomatic management of headaches or dizziness
- Regular follow-up with repeat EEG to monitor for development of seizures
Special Considerations
Age and Gender Factors
- Bi-occipital spike and wave patterns show:
Associated Conditions
- This EEG pattern may be seen in:
Prognostic Factors
- Factors suggesting better prognosis:
- Factors suggesting poorer prognosis:
Pitfalls and Caveats
- Avoid routine neurological testing (EEG, CT, MRI) in patients with uncomplicated syncope as diagnostic yield is low with high cost per diagnosis 5
- Do not confuse this pattern with the 6/sec spike and wave complex, which has different clinical correlations 4
- Remember that this EEG pattern can occur in patients without clinical seizures (20% of cases) 3
- The pattern may be a nonspecific epileptiform abnormality that occurs in various epilepsy syndromes 3