Evidence map›Paper›PMID 41303121›Full record

ReviewJournal of clinical medicine2025

Congenital Scoliosis: A Comprehensive Review of Diagnosis, Management, and Surgical Decision-Making in Pediatric Spinal Deformity-An Expanded Narrative Review.

Paweł Grabala

Abstract readReview
In one paragraph

Review in Journal of clinical medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

1 author.

Paweł GrabalaDepartment of Neurosurgery, Polish-Mother's Memorial Hospital Research Institute, Rzgowska 281/289, 93-338 Lodz, Poland.ORCID 0000-0001-7059-2935

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital scoliosis is a complex spinal deformity caused by abnormal vertebral development during embryogenesis, occurring in roughly 0.5-1.0 per 1000 live births. It encompasses a wide spectrum of anomalies that arise from failures in vertebral formation or segmentation, or mixed defects during the fourth to sixth weeks of gestation. Managing this condition requires careful consideration of growth dynamics, associated systemic anomalies, and individualized decisions regarding surgical timing. In this review, current evidence on the epidemiology, pathophysiology, diagnostic strategies, and treatment of congenital scoliosis is synthesized, with special attention to surgical decision-making between hemivertebrectomy and growth-preserving methods such as growing rods. Recent surgical techniques-including magnetically controlled growing rods and posterior vertebral column resection-have expanded therapeutic options, while greater recognition of the psychosocial impacts has underscored the importance of family-centered care. Successful management relies on striking a balance between early deformity correction and preserving long-term spinal and thoracic growth. Multidisciplinary collaboration and thorough family counseling remain central to optimizing both structural and psychosocial outcomes.

Indexed as

congenital scoliosisgrowing rodshemivertebra resectionpediatric spinal deformityposterior spinal fusionposterior vertebral column resection (PVCR)thoracic insufficiency syndromevertebral malformations

Identifiers

PMID41303121
PMCPMC12653983

What OpenQuestion holds

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LicenceCC BY
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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.