Evidence map›Paper›PMID 30223294›Full record

SynthesisEuropean journal of neurology2019

Refractory juvenile myoclonic epilepsy: a meta-analysis of prevalence and risk factors.

R Stevelink, B P C Koeleman, J W Sander, F E Jansen, K P J Braun

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in European journal of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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.

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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

R StevelinkDepartment of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht.ORCID 0000-0003-0214-7965
B P C KoelemanDepartment of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht.
J W SanderStichting Epilepsie Instellingen Nederland (SEIN), Heemstede, The Netherlands.
F E JansenDepartment of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht.
K P J BraunDepartment of Child Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht.
University Medical Center Utrecht · NLUCL Biomedical Research Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeJuvenile myoclonic epilepsy (JME) is a common epilepsy syndrome for which treatment response is generally assumed to be good. We aimed to determine the prevalence and prognostic risk factors for refractoriness of JME.

methodsWe systematically searched PubMed and EMBASE and included 43 eligible studies, reporting seizure outcome after antiepileptic drug (AED) treatment in JME cohorts. We defined refractory JME as persistence of any seizure despite AED treatment and performed a random-effects meta-analysis to assess the prevalence of refractory JME and of seizure recurrence after AED withdrawal in individuals with well-controlled seizures. Studies reporting potential prognostic risk factors in relation to seizure outcome were included for subsequent meta-analysis of risk factors for refractoriness.

resultsOverall, 35% (95% confidence interval, 29-41%) of individuals (n = 3311) were refractory. There was marked heterogeneity between studies. Seizures recurred in 78% (95% confidence interval, 52-94%) of individuals who attempted to withdraw from treatment after a period of seizure freedom (n = 246). Seizure outcome by publication year suggested that prognosis did not improve over time. Meta-analysis suggested six variables as prognostic factors for refractoriness, i.e. having three seizure types, absence seizures, psychiatric comorbidities, earlier age at seizure onset, history of childhood absence epilepsy and praxis-induced seizures.

conclusionOne-third of people with JME were refractory, which is a higher prevalence than expected. Risk factors were identified and can be used to guide treatment and counselling of people with JME.

Indexed as

AnticonvulsantsHumansMyoclonic Epilepsy, JuvenilePrevalencePrognosisRisk FactorsAnticonvulsantsepilepsyJanz syndromemeta-analysispharmacoresistancesystematic review

Identifiers

PMID30223294
PMCPMC6586162
OpenAlexW2889914777

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.