Evidence map›Paper›PMID 32975748›Full record

ArticleSpine deformity2021

Surgical treatment of segmental spinal dysgenesis: a report of 19 cases.

Rodrigo G Remondino, Carlos A Tello, Ernesto S Bersusky, Alejandra Francheri Wilson, Mariano A Noel, Eduardo Galaretto, Lucas Piantoni

Abstract readCase Reports
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In one paragraph

Article in Spine deformity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 5 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

7 authors at 1 institution in 1 country.

Rodrigo G RemondinoSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina. rodrigoremondino@hotmail.com.ORCID 0000-0002-8388-298X
Carlos A TelloSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Ernesto S BersuskySpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Alejandra Francheri WilsonSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Mariano A NoelSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Eduardo GalarettoSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Lucas PiantoniSpine Unit, Juan P. Garrahan. Pediatric Hospital, 1881Combate de los Pozos. First floor, office 7484, Buenos Aires, Argentina.
Garrahan Hospital · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

designRetrospective review.

objectiveTo describe clinical presentation, surgical management, long-term results, and complications in patients with segmental spinal dysgenesis (SSD). In addition, we sought to emphasize early surgery for this complex congenital abnormality. SSD is a rare congenital malformation characterized by focal stenosis, spinal subluxation, kyphosis, and absence of the nerve roots. Neurologic function ranges from normal to complete paraplegia. Progression of the deformity and neurologic deterioration is the rule.

methodsAn independent spinal surgeon reviewed the complete records of 19 patients with SSD, between 1998 and 2015 at a single institution. Mean follow-up was 10 years and 6 months (2-14 years).

resultsWe evaluated 11 males and 8 females, with a mean age of 2 years and 9 months (5 months-15 years). The dysgenetic segment involved an average of 2.9 vertebrae (1-5); the upper thoracic region was most commonly involved in ten cases. Fifteen patients had severe spinal stenosis. 14 patients presented neurological deficits and 15 patients had associated organ and musculoskeletal anomalies.Twenty-seven surgeries were performed, a mean of 1.76 procedures (1-5) to obtain solid fusion. Neurologic function improved in four, deteriorated in three, and remained unchanged in 12 patients Seven complications were recorded.

conclusionWe strongly recommend decompression and fusion as soon as possible to preserve or prevent neurologic deterioration. Although challenging, it was possible to achieve a solid instrumented fusion in all cases; however, a high rate of patients may deteriorate or not recover neurological status after surgery. LEVEL OF EVIDENCE: Level IV evidence.

Indexed as

KyphosisSpinal FusionChild, PreschoolFemaleHumansLumbar VertebraeMaleRetrospective StudiesThoracic VertebraeCongenital subluxationDeformity progressionEarly surgeryNeurological impairmentSegmental spinal dysgenesis

Identifiers

PMID32975748
OpenAlexW3089199133

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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.