Confirm the diagnosis of epilepsy |
Confirm the diagnosis of epilepsy by seizure type and etiology of epilepsy |
History and examination are of pivotal importance |
A video taken by family members, by a smart phone or other gadgets, of the ictal events can be crucial and confirmatory in many cases. |
Interictal Electroencephalogram can be helpful in classification of the epilepsy type (but should always be interpreted in the clinical context). |
Video EEG capturing the ictal events may be considered a gold standard to diagnose and classify epilepsy, however, this may not be practically feasible in majority of cases, and patients having indications for this modality should be referred to centers that have the facility of epilepsy monitoring unit. |
Brain imaging, if indicated, is preferably done with a 3 tesla MRI machine. |
Counseling |
Should be done after confirmation of epilepsy by its etiology. |
It should be done along with other family members e.g., spouse, parents, siblings etc. |
Prognosis of epilepsy and possible duration of therapy should be carefully suggested. |
In case the patient is married or has plans to get married in near future, a planned pregnancy should be advised, and appropriate contraceptive methods should be suggested. |
Patient and spouse should be informed about the risks of teratogenicity and fetal growth restrictions associated with AED use. |
Patients should be given time to discuss their own fears and concerns about their diagnosis and its impact on their personal, social and professional life. |
Optimal therapy |
Optimal therapy is determined by the epilepsy etiology, and various other patient related factors. |
Valproic acid, phenytoin, phenobarbitone and Topiramate are least favorable |
Carbamazepine should not be used in idiopathic generalized epilepsy syndromes. |
Carbamazepine, Levetiracetam and lamotrigine may be preferred as they have lower risk of teratogenicity. |
Aim to use a single antiepileptic drug in the least possible dose. |
Serum drug levels whenever available should be monitored, and at least one trough level when the patient is completely seizure free should be obtained. |
Folic acid supplementation should be given. |
Patient should be seizure free for at least 9 months before conceiving |
During pregnancy |
Patient should be monitored by a combined team of gynecologist and neurologist / epileptologist. |
Drug levels may be monitored, on a monthly basis (particularly in case of lamotrigine). |
The pre-pregnancy drug level with total seizure control should be aimed for, during pregnancy. |
Folic acid supplementation should be continued at 4 to 5 mg /day |
A level II ultrasound at 18 to 20 weeks gestational age should be offered to the patient for a detailed anatomical evaluation of the fetus. |
WWE taking enzyme inducing AEDs and whose newborns are at risk of intracranial hemorrhage may be given Vitamin K supplementation in the last month of pregnancy. |
Normal vaginal delivery can be safely attempted with epidural anesthesia, if required, C-section may be considered in patients who are not able to cooperate during delivery process because of heavy sedation. |
Post- partum |
WWE should be advised to breast feed their newborns, (because of the usual benefits of breast feeding). |
Infants should be nursed and carried with some precautions (see text) |
If AED dose was stepped up during pregnancy then it should be stepped down gradually postpartum to avoid toxicity, while monitoring AED levels |
It is preferable to keep patient on a slightly higher dose that was before pregnancy (with full seizure control), but less than the pregnancy dose, for 1 to 3 months post-partum, to protect patients from effects of sleep deprivation. |