ArticleCureus2026
Super-refractory Status Epilepticus in Febrile Infection-Related Epilepsy Syndrome Triggered by Influenza A: A Pediatric Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Febrile infection-related epilepsy syndrome (FIRES) is a rare cause of new-onset refractory status epilepticus following a febrile illness. We report the case of a previously healthy three-year-old boy who developed focal seizures in the context of a confirmed Influenza A infection, rapidly progressing to super-refractory status epilepticus. Initial investigations, including cerebrospinal fluid analysis and neuroimaging, were unremarkable. Despite early multimodal therapy with multiple antiseizure medications, continuous anesthetic infusions, immunomodulatory treatments, and a ketogenic diet, seizure control remained transient. Continuous EEG confirmed persistent super-refractory status epilepticus, while cytokine analysis demonstrated elevated interleukin-6 and interleukin-8 levels. Follow-up MRI showed bilateral claustrum and hippocampal involvement, later progressing to diffuse cerebral atrophy. Despite escalation of therapy, including intrathecal corticosteroids and vagal nerve stimulation, the patient showed no sustained improvement. Care was ultimately redirected toward palliation, and the patient died after 50 days of intensive care. This case highlights the fulminant and refractory nature of FIRES, supports a potential role of cytokine-driven neuroinflammation, and suggests a possible association with a preceding viral infection.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.