Evidence map›Paper›PMID 40853387›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Prevalence of spinal deformities in myelomeningoceles treated in utero and postnatally, utilizing 3D external orthopedic system (EOS) panoramic radiographic technology.

Vinicius de Meldau Benites, Vinicius Santos Baptista, Matheus Galvão Valadares Bertolini Mussalem, Marcos Devanir Silva da Costa, Sergio Cavalheiro

Abstract read
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Vinicius de Meldau BenitesDepartment of Neurology and Neurosurgery, Universidade Federal de São Paulo, Rua Ibaiti, 145, São Paulo, SP, 03414-150, Brazil. drviniciusbenites@gmail.com.ORCID http://orcid.org/0000-0003-1693-9357
Vinicius Santos BaptistaDepartment of Neurology and Neurosurgery, Universidade Federal de São Paulo, Rua Ibaiti, 145, São Paulo, SP, 03414-150, Brazil. vinicius.baptista@unifesp.br.ORCID http://orcid.org/0000-0002-4017-6110
Matheus Galvão Valadares Bertolini MussalemDepartment of Neurology and Neurosurgery, Universidade Federal de São Paulo, Rua Ibaiti, 145, São Paulo, SP, 03414-150, Brazil.ORCID http://orcid.org/0000-0003-1123-9570
Marcos Devanir Silva da CostaDepartment of Neurology and Neurosurgery, Universidade Federal de São Paulo, Rua Ibaiti, 145, São Paulo, SP, 03414-150, Brazil.ORCID http://orcid.org/0000-0003-3552-6347
Sergio CavalheiroDepartment of Neurology and Neurosurgery, Universidade Federal de São Paulo, Rua Ibaiti, 145, São Paulo, SP, 03414-150, Brazil.

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001
6 · The paper itself

Abstract

purposeThis study analyzes the prevalence of spinal deformities in patients who underwent in utero myelomeningocele (MMC) repair compared to those who had postnatal surgery.

methodsPatients treated at Hospital São Paulo and Hospital e Maternidade Santa Joana between 2006 and 2021 were included. Selection was retrospective; external orthopedic system (EOS) imaging was performed prospectively. Only patients under 18 at the time of imaging were analyzed. Data collected included birth metrics, need for ventriculoperitoneal shunt, urinary/fecal incontinence, and postnatal complications. Radiographic analysis assessed scoliosis, pelvic parameters, and sagittal balance. Groups were compared using statistical tests (p < 0.05).

resultsSeventy patients were evaluated: 47 had in utero repair and 23 postnatal. Groups were similar in age (p = 0.089) and gender (p = 0.725), but the in utero group had lower birth weight (p = 0.024) and gestational age (p = 0.004). Ventriculoperitoneal shunt requirement (p = 0.001), scoliosis incidence (p = 0.020), and urinary incontinence (p = 0.009) were significantly lower in the in utero group. Cobb angle did not differ significantly. Most postnatal complications were comparable, except for lower axial pelvic rotation in the in utero group (p = 0.024).

conclusionIn utero MMC repair is associated with reduced rates of acquired scoliosis, need for shunting, and urinary incontinence, indicating a better overall prognosis compared to postnatal surgery.

Indexed as

Imaging, Three-DimensionalMeningomyeloceleScoliosisFemaleHumansInfantInfant, NewbornMalePregnancyPrevalenceRetrospective StudiesCongenital abnormalitiesMyelomeningocelePediatricsScoliosisSurgical procedures

Identifiers

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.