Evidence map›Paper›PMID 34297200›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2021

Spontaneous third ventriculostomy in patients undergoing fetal surgery for myelomeningocele correction.

Sergio Cavalheiro, Marcos Devanir Silva da Costa, Emmanuel de Oliveira Sampaio Vasconcelos E Sá, Patricia Alessandra Dastoli, Jardel Nicácio Mendonça, Renato Luis da Silveira Ximenes, Stéphanno Gomes Pereira Sarmento, Antonio Fernandes Moron

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Sergio CavalheiroDepartment of Neurology and Neurosurgery, Federal University of São Paulo, Sao Paulo, Brazil.
Marcos Devanir Silva da CostaDepartment of Neurology and Neurosurgery, Federal University of São Paulo, Sao Paulo, Brazil. marcoscostaneuro@gmail.com.ORCID http://orcid.org/0000-0003-3552-6347
Emmanuel de Oliveira Sampaio Vasconcelos E SáDepartment of Neurology and Neurosurgery, Federal University of São Paulo, Sao Paulo, Brazil.
Patricia Alessandra DastoliDepartment of Neurology and Neurosurgery, Federal University of São Paulo, Sao Paulo, Brazil.
Jardel Nicácio MendonçaDepartment of Neurology and Neurosurgery, Federal University of São Paulo, Sao Paulo, Brazil.
Renato Luis da Silveira XimenesLatin American Fetal Medicine Foundation, Campinas, Sao Paulo, Brazil.
Stéphanno Gomes Pereira SarmentoDepartment of Fetal Medicine, Santa Joana Hospital and Maternity Care, Sao Paulo, Brazil.
Antonio Fernandes MoronDepartment of Fetal Medicine, Santa Joana Hospital and Maternity Care, Sao Paulo, Brazil.
Hospital Santa Paula · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSpontaneous third ventriculostomy (STV) is characterized by the spontaneous rupture of one of the ventricle walls due to increased pressure in the third ventricle caused by obstructive hydrocephalus. Clinically, STV results in resolution of signs and symptoms of intracranial hypertension and head circumference stabilization. No spontaneous STV cases in patients with myelomeningocele have been reported in the literature. The objective of this study was to report three cases of STV in patients with type 2 Chiari malformation who underwent intrauterine treatment. CASE PRESENTATION: All patients presented clinically with increased head circumference during outpatient follow-up. Only one patient required a ventriculoperitoneal shunt implantation. The other patients did not require further intervention.

conclusionSTV is a rare entity that is difficult to diagnose and should always be suspected in spontaneous hydrocephalus resolution, especially in early childhood. STV is not synonymous with hydrocephalus resolution.

Indexed as

HydrocephalusMeningomyeloceleThird VentricleChild, PreschoolFemaleHumansTreatment OutcomeVentriculoperitoneal ShuntVentriculostomyFetal surgeryHydrocephalusMyelomeningoceleSpontaneous ventriculostomyType 2 Chiari malformationVentriculoperitoneal shunt

Identifiers

PMID34297200
OpenAlexW3186638678

What OpenQuestion holds

Textmetadata
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.