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Updated: Dec 21, 2025

Pupillary Response as Assessment of Effective Seizure Induction by Electroconvulsive Therapy
Published on: April 11, 2019
Methylprednisolone pulse therapy in 31 patients with refractory epilepsy: A single-center retrospective analysis
Tomokazu Kimizu1, Yukitoshi Takahashi2, Taikan Oboshi1
1National Epilepsy Center, NHO, Shizuoka Institute of Epilepsy and Neurological Disorders, Japan.
Purpose:
We investigated the efficacy of methylprednisolone pulse therapy (MP) and responder characteristics in patients with refractory epilepsy.
Methods:
We reviewed medical records of our center to identify patients with refractory epilepsy treated with MP other than continuous spikes and waves during slow sleep (CSWS), Landau-Kleffner syndrome (LKS), or Rasmussen's syndrome (RS) between 2004 and 2015. A course of MP consisted of intravenous methylprednisolone (30 mg/kg/day) on three consecutive days. Patients received multiple courses at intervals of four weeks. We examined seizure outcome, developmental outcome, antibodies to N-methyl-d-aspartate (NMDA)-type glutamate receptors (GluRs), cerebral spinal fluid (CSF)-albumin/serum-albumin ratio, and interictal electroencephalograms (EEGs). Responder to MP was defined as maintaining seizure reduction rate (SRR) ≥50% for three months after the first course of MP.
Results:
Thirty-one consecutive patients treated with MP at our center were studied. Seizure types were focal onset impaired awareness seizure (FIAS) only (n = 23), FIAS with epileptic spasms (ES) (n = 7), and ES only (n = 1). Responder rate was 32.2% (10/31 patients), and seizure-free rate was 9.7% (3/31). Responders constituted 43.5% of patients without ES. No patient with ES was responder. Behavior and cognition also improved in 6 of 10 responders. History of seizure aggravation after inactivated vaccine before MP was found significantly higher rate in responder patients, comparing with nonresponder patients (p = 0.01).
Conclusion:
Methylprednisolone pulse therapy may be considered for possible treatment in patients with focal epilepsy with drug-resistant seizures without ES, and it may improve cognitive function and behavioral comorbidities.
Insights
Methylprednisolone pulse therapy (MP) showed a 32.2% response rate in refractory epilepsy patients without epileptic spasms (ES). This treatment may improve cognitive and behavioral outcomes in select epilepsy cases.
Area of Science:
- Neurology
- Epileptology
- Pharmacology
Background:
- Refractory epilepsy presents significant treatment challenges.
- Identifying effective therapies for drug-resistant epilepsy is crucial.
- Methylprednisolone pulse therapy (MP) is an option for severe epilepsy cases.
Purpose of the Study:
- To evaluate the efficacy of methylprednisolone pulse therapy (MP) in patients with refractory epilepsy.
- To identify characteristics of patients who respond to MP treatment.
- To explore potential benefits beyond seizure control.
Main Methods:
- Retrospective review of 31 refractory epilepsy patients treated with MP between 2004 and 2015.
- MP involved intravenous methylprednisolone (30 mg/kg/day) for three consecutive days, repeated monthly.
- Outcomes assessed included seizure reduction rate (SRR ≥50%), seizure freedom, developmental status, antibody levels, CSF-albumin/serum-albumin ratio, and EEG findings.
Main Results:
- Overall responder rate to MP was 32.2% (10/31), with a 9.7% seizure-free rate.
- Patients with focal onset impaired awareness seizures (FIAS) without epileptic spasms (ES) had a higher responder rate (43.5%).
- No patients with ES responded to MP; however, 6 responders showed improved behavior and cognition. A history of seizure aggravation after inactivated vaccine was more common in responders.
Conclusions:
- Methylprednisolone pulse therapy (MP) may be a viable treatment option for drug-resistant focal epilepsy, particularly in patients without epileptic spasms (ES).
- MP treatment can potentially improve cognitive function and behavioral comorbidities in responders.
- Further research is warranted to optimize MP use and understand its mechanisms in refractory epilepsy.
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