EMERGENCY:Seizure lasting more than 5 minutes (status epilepticus) or repeated seizures without recovery between them —call040-46324365immediately — 24 hours, 7 days— 24/7
KIMS Neuroscience Hyderabad delivers epilepsy classification, drug-resistant seizure surgery, video-EEG telemetry, and the ketogenic diet programme for adults and children.
65–70% (TLE Surgery)
040-46324365
Epilepsy is a neurological condition in which the brain produces repeated, unprovoked seizures — bursts of abnormal electrical activity disrupting awareness, movement, or sensation. Approximately 10 million people in India have epilepsy. As worldwide, focal epilepsy (starting in one region of the brain) is the most common type in India, with structural causes such as neurocysticercosis playing a large role. Carbamazepine — widely prescribed in India — is an effective first-line drug for focal epilepsy, but it can aggravate certain generalised syndromes (JME, absence epilepsy, Dravet). At KIMS Neuroscience Hyderabad, every consultation begins with syndrome identification because the syndrome determines the medication, the prognosis, and whether surgery should be considered.
| Fact | Details |
|---|---|
| India-specific fact | Focal epilepsy is the most common type in India (neurocysticercosis is a leading structural cause) · Carbamazepine is widely prescribed and effective for focal epilepsy, but can aggravate generalised syndromes such as JME, absence epilepsy, and Dravet |
| Conditions treated | JME · Childhood Absence · Lennox-Gastaut · Dravet · West Syndrome · Temporal Lobe Epilepsy · Status Epilepticus · Febrile Seizures · PNES |
| Surgical series | Temporal lobe resection · Largest in TG/AP · 65–70% seizure freedom · Corpus callosotomy · SEEG (Stealth AutoGuide robotic) |
| Advanced diagnostics | Video-EEG telemetry · Epilepsy-protocol MRI (thin-slice FLAIR) · fMRI language mapping · FDG-PET · Ictal SPECT/SISCOM |
| Emergency threshold | Seizure lasting >5 minutes = status epilepticus · Call 040-46324365 immediately · KIMS Neuro ICU 24/7 |
| Who should come | Drug-resistant epilepsy (2+ drugs failed) · Seizures worsening on current medication · Child with staring spells · No syndrome classification yet |
| Contact | 040-44885000 · No referral required · Emergency: 040-46324365 |
Epilepsy is a condition in which the brain produces repeated, unprovoked seizures — bursts of abnormal electrical activity that disrupt awareness, movement, sensation, or behaviour. Seizures are classified by where they begin: focal (one region of the brain) or generalised (both hemispheres at once).
At KIMS Neuroscience, every consultation begins with syndrome diagnosis — because the wrong medication can actively worsen seizures. For drug-resistant epilepsy, temporal lobectomy, corpus callosotomy, and the ketogenic diet can deliver outcomes that medication cannot.
• Morning arm jerks after waking
• Brief blank stares with no response
• Rising sensation from the stomach
• Sudden déjà vu or unexplained fear
• Lip smacking or hand fumbling
• Seizure lasting longer than 5 minutes
Both hemispheres seize together. JME, Lennox-Gastaut, Dravet — syndrome-specific medication is critical.
View Details →Most common focal epilepsy in adults. Surgery at KIMS achieves 65–70% seizure freedom.
View Details →Brief blank stares in childhood. Often mistaken for daydreaming — requires EEG diagnosis.
View Details →Prolonged seizure or seizures without recovery — a neurological emergency needing immediate ICU care.
View Details →Continued seizures despite two appropriately chosen drugs — trigger for surgical evaluation, video-EEG telemetry and the ketogenic diet programme.
View Details →Every patient is formally classified focal, generalised, or combined — the first step before any medication.
Temporal lobectomy, corpus callosotomy for LGS drop attacks, and SEEG for complex localisation.
Long-term monitoring to capture seizures, classify syndromes, and plan pre-surgical evaluation.
Dietitian-supervised ketogenic therapy for Dravet, LGS, GLUT1 deficiency, and refractory West syndrome.
Our multidisciplinary epilepsy team reviews every drug-resistant case. No referral required.
Video-EEG Telemetry & SEEG
Corpus Callosotomy for LGS Drop Attacks
Ketogenic Diet Programme for Children
The distinction requires specialist assessment and EEG. Seizures with no aura, bilateral involvement of both arms from the start, onset in adolescence, morning jerks, and a family history of similar seizures all suggest generalised epilepsy. Focal epilepsy typically starts with one-sided symptoms or a specific aura. At KIMS every patient is formally classified focal, generalised, or combined as the first step in treatment planning.
Yes — seek urgent reassessment. Carbamazepine is effective for focal epilepsy but contraindicated in generalised syndromes like Juvenile Myoclonic Epilepsy and Dravet syndrome. If a patient with generalised epilepsy is on carbamazepine and seizures are increasing, the medication is almost certainly the cause. The solution is stopping it and starting a syndrome-appropriate medication.
Yes — you should be assessed to determine whether you are a surgical candidate. Drug-resistant epilepsy means seizures have continued despite two or more appropriately chosen medications. At that point, further medication has less than 5% probability of seizure freedom. Temporal lobectomy at KIMS achieves 65–70% seizure freedom for mesial TLE with hippocampal sclerosis.
Status epilepticus is any seizure lasting more than 5 minutes, or recurrent seizures without recovery of consciousness between them. It is a neurological emergency — call 040-46324365 immediately, 24 hours a day, 7 days a week. Treatment at KIMS follows a structured protocol: IV benzodiazepines first (lorazepam or midazolam) → second-line agents (levetiracetam, fosphenytoin, valproate) → anaesthetic induction with continuous EEG monitoring for refractory cases. The longer status continues, the harder it is to control and the higher the risk of permanent neuronal injury.
Video-EEG telemetry is a 3–7 day inpatient admission during which the patient is continuously monitored with EEG electrodes and a synchronised video camera. It captures actual seizures so the type, the syndrome, and the seizure-onset zone can be determined directly rather than inferred from history alone. It is essential for distinguishing epilepsy from psychogenic non-epileptic seizures, for confirming syndrome diagnosis, and for planning surgery. KIMS performs video-EEG telemetry on site.
Yes — KIMS has a dietitian-supervised ketogenic diet programme particularly effective for Dravet syndrome, Lennox-Gastaut syndrome, GLUT-1 deficiency, and refractory West syndrome (infantile spasms). The classical ketogenic diet is 4:1 fat to carbohydrate-and-protein ratio, supervised by a paediatric dietitian. Modified Atkins diet and low-glycaemic-index treatment are less restrictive alternatives. Effective ketogenic therapy requires precise calorie and ratio calculation, supplementation, and laboratory monitoring — it is not a home-cooked attempt.
Yes. KIMS Neuroscience performs temporal lobe resections — the largest series in Telangana and Andhra Pradesh — with 65–70% seizure freedom for mesial temporal lobe epilepsy with hippocampal sclerosis. The programme also includes corpus callosotomy for Lennox-Gastaut drop attacks (70–80% reduction), Vagus Nerve Stimulation, and SEEG with robotic guidance for complex MRI-negative cases. Patients in Hyderabad, Telangana, and Andhra Pradesh do not need to travel to another city for epilepsy surgery.
Yes — direct epilepsy clinic appointments are accepted. Outpatient: 040-44885000 (Mon–Sat). For a first seizure, please bring any video of the event captured on a phone — this is often the single most useful piece of evidence for classification. For ongoing status epilepticus, call 040-46324365 immediately.
Initial consultation 30–60 minutes. Routine EEG is usually performed on the same or next day. A video-EEG telemetry admission (typically 3–5 days inpatient) is scheduled if the syndrome classification or surgical workup needs it. MRI with epilepsy protocol is scheduled within 1–2 weeks. A complete diagnostic picture and a treatment plan are usually in place within 2–4 weeks.
Don't Wait for the Next Seizure
Correct syndrome classification and timely surgical evaluation change the trajectory of epilepsy. Speak with our specialists today.
International enquiries: info@kimsneurosciences.com