Evidence map›Paper›PMID 36223877›Full record

ReviewNeuropediatrics2023

Elective and Emergency Deep Brain Stimulation in Refractory Pediatric Monogenetic Movement Disorders Presenting with Dystonia: Current Practice Illustrated by Two Cases.

M Garofalo, M Beudel, J M Dijk, L A Bonouvrié, A I Buizer, J Geytenbeek, R H N Prins, P R Schuurman, L A van de Pol

Erratum issuedOpen access · hybridAbstract readReviewCase Reports
In one paragraph

Review in Neuropediatrics, 2023. 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dyskinetic crisis inFrontiers in neurology · 2024
    Article
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

M GarofaloDepartment of Child Neurology, Emma Children's Hospital, Amsterdam UMC Location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-1823-0109
M BeudelDepartment of Neurology, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.
J M DijkDepartment of Neurology, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.
L A BonouvriéAmsterdam UMC Location Vrije Universiteit Amsterdam, Rehabilitation Medicine, Amsterdam, the Netherlands.
A I BuizerAmsterdam UMC Location Vrije Universiteit Amsterdam, Rehabilitation Medicine, Amsterdam, the Netherlands.ORCID 0000-0001-5662-2843
J GeytenbeekAmsterdam UMC Location Vrije Universiteit Amsterdam, Rehabilitation Medicine, Amsterdam, the Netherlands.
R H N PrinsDepartment of Neurology, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.
P R SchuurmanDepartment of Neurosurgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.
L A van de PolDepartment of Child Neurology, Emma Children's Hospital, Amsterdam UMC Location University of Amsterdam, Amsterdam, the Netherlands.
Amsterdam University Medical Centers · NLAmsterdam Neuroscience · NLEmma Kinderziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDystonia is characterized by sustained or intermittent muscle contractions, leading to abnormal posturing and twisting movements. In pediatric patients, dystonia often negatively influences quality of life. Pharmacological treatment for dystonia is often inadequate and causes adverse effects. Deep brain stimulation (DBS) appears to be a valid therapeutic option for pharmacoresistant dystonia in children.

methodsTo illustrate the current clinical practice, we hereby describe two pediatric cases of monogenetic movement disorders presenting with dystonia and treated with DBS. We provide a literature review of similar previously described cases and on different clinical aspects of DBS in pediatric dystonia.

resultsThe first patient, a 6-year-old girl with severe dystonia, chorea, and myoclonus due to an

conclusionDBS can be effective in monogenetic pediatric dystonia and should be considered early in the disease course. To better evaluate the effects of DBS on patients' functioning, patient-centered therapeutic goals should be discussed in a multidisciplinary approach.

Indexed as

ChoreaDeep Brain StimulationDystoniaDystonic DisordersMovement DisordersChildFemaleGlobus PallidusGTP-Binding Protein alpha Subunits, Gi-GoHumansMaleQuality of LifeTreatment OutcomeGNAO1 protein, humanGTP-Binding Protein alpha Subunits, Gi-Go

Identifiers

PMID36223877
PMCPMC9842449
OpenAlexW4304756681

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.