Evidence map›Paper›PMID 33776895›Full record

SynthesisFrontiers in neurology2021

Dietary Management of Children With Super-Refractory Status Epilepticus: A Systematic Review and Experience in a Single UK Tertiary Centre.

Natasha E Schoeler, Zoe Simpson, Runming Zhou, Suresh Pujar, Christin Eltze, J H Cross

Registry-linked trialOpen access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05674552 (Efficacy of Exogenous Ketone Esters for Children With Refractory Convulsive Status Epileptics), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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.

NCT05674552 phase2 / phase3recruitingnot on this mapstarted 2023, after this paper: background citation

Efficacy of Exogenous Ketone Esters for Children With Refractory Convulsive Status Epileptics

TypeinterventionalSponsorSohag UniversityRan2023 to 2025Enrolled50ConditionsStatus EpilepticusArmsExogenous ketone ester
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Choice of pharmaceutical form as a key factor during ketogenic diet: a case report.European journal of hospital pharmacy : science and practice · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Stuttering: A Disorder of Energy Supply to Neurons?Frontiers in human neuroscience · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Natasha E SchoelerDevelopmental Neurosciences Research and Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
Zoe SimpsonDepartment of Dietetics, Great Ormond Street Hospital for Children, London, United Kingdom.
Runming ZhouDevelopmental Neurosciences Research and Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
Suresh PujarDepartment of Paediatric and Neurology, Great Ormond Street Hospital for Children, London, United Kingdom.
Christin EltzeDepartment of Paediatric and Neurology, Great Ormond Street Hospital for Children, London, United Kingdom.
J H CrossDevelopmental Neurosciences Research and Teaching Department, University College London Great Ormond Street Institute of Child Health, London, United Kingdom.
University College London · GBGreat Ormond Street Hospital · GB

Funding

Medical Research Council MC_PC_14140
6 · The paper itself

Abstract

Ketogenic diet therapies (KDT) are high-fat, low carbohydrate diets used as an effective treatment option for drug-resistant epilepsy. There is limited research on the efficacy of KDT for super-refractory status epilepticus (SRSE). We systematically review evidence for use of KDT in children with SRSE and present a single UK tertiary centre's experience. Thirty one articles were included, of which 24 were "medium" or "low" quality. One hundred and forty seven children with SRSE started KDT, of which 141 (96%) achieved ketosis. KDT was started mean 5.3 days (range 1-420) after status epilepticus (SE) started. SRSE resolved in 85/141 (60%) children after mean 6.3 days (range 0-19) post SE onset, but it is unclear whether further treatments were initiated post-KDT. 13/141 (9%) children died. Response to KDT was more likely when initiated earlier (

Indexed as

epilepsyketogenicseizuresuper-refractory status epilepticussystematic review

Identifiers

PMID33776895
PMCPMC7994594
OpenAlexW3139478696

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.