Evidence map›Paper›PMID 38926769›Full record

ReviewNeurological research and practice2024

Use of ketamine in Super Refractory Status Epilepticus: a systematic review.

Aayush Adhikari, Sushil Kumar Yadav, Gaurav Nepal, Roshan Aryal, Pratik Baral, Peter Neupane, Aadesh Paudel, Barsha Pantha, Sulav Acharya, Gentle Sunder Shrestha and 1 more

Erratum issuedAbstract readReview
In one paragraph

Review in Neurological research and practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  6. Treatment considerations for the management of neonatal onset seizures.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Aayush AdhikariManang Hospital, 33500, Chame, Manang, Nepal.
Sushil Kumar YadavIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal. skyadav136@iom.edu.np.ORCID http://orcid.org/0000-0003-3840-5161
Gaurav NepalIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal.
Roshan AryalIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal.
Pratik BaralIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal.
Peter NeupaneJibjibe Primary Health Care Centre, 45003, Dhaibung, Rasuwa, Nepal.
Aadesh PaudelNational Medical College, 44300, Birgunj, Nepal.
Barsha PanthaPost Graduate Institute of Medical Education and Research, 160012, Chandigarh, India.
Sulav AcharyaIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal.
Gentle Sunder ShresthaDepartment of Critical Care Medicine, Tribhuvan University Teaching Hospital, 44600, Maharajgunj, Kathmandu, Nepal.
Ramesh KhadayatIntern, Institute of Medicine, Tribhuvan University Teaching Hospital, 44600, Kathmandu, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis review specifically investigates ketamine's role in SRSE management.

methodsPubMed, EMBASE, and Google Scholar databases were searched from inception to May 1st, 2023, for English-language literature. Inclusion criteria encompassed studies on SRSE in humans of all ages and genders treated with ketamine.

resultsIn this systematic review encompassing 19 studies with 336 participants, age ranged from 9 months to 86 years. Infections, anoxia, and metabolic issues emerged as the common causes of SRSE, while some cases had unknown origins, termed as NORSE (New Onset RSE) or FIRESs (Febrile Infection-Related Epilepsy Syndrome). Most studies categorized SRSE cases into convulsive (N = 105) and non-convulsive (N = 197). Ketamine was used after failed antiepileptics and anesthetics in 17 studies, while in others, it was a first or second line of treatment. Dosages varied from 0.5 mg/kg (bolus) and 0.2-15 mg/kg/hour (maintenance) in adults and 1-3 mg/kg (bolus) and 0.5-3 mg/kg/hour (maintenance) in pediatrics, lasting one to 30 days. Ketamine was concurrently used with other drugs in 40-100% of cases, most frequently propofol and midazolam. Seizure resolution rate varied from 53.3 to 91% and 40-100% in larger (N = 42-68) and smaller case series (N = 5-20) respectively. Seizure resolution occurred in every case of case report except in one in which the patient died. Burst suppression in EEG was reported in 12 patients from two case series and two case reports. Recurrence was reported in 11 patients from five studies. The reported all-cause mortality varied from 38.8 to 59.5% and 0-36.4% in larger and smaller case series., unrelated directly to ketamine dosage or duration. SIGNIFICANCE: Ketamine demonstrates safety and effectiveness in SRSE, offering advantages over GABAergic drugs by acting on NMDA receptors, providing neuroprotection, and reducing vasopressor requirement.

Indexed as

Burst suppressionConvulsive Status Epilepticus (CSE)NeuroprotectionNMDA agonistNon-convulsive Status Epilepticus (NCSE)SRSESTESS score

Identifiers

PMID38926769
PMCPMC11210084

What OpenQuestion holds

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Registered trials

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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.