Evidence map›Paper›PMID 39402700›Full record

ArticleOrthopaedic surgery2025

Classification of Emerging Scoliosis in Congenital Scoliosis After Hemivertebra Resection and Short Segmental Fusion.

Chenkai Li, Xiaohan Ye, Bingtai Han, You Du, Yiwei Zhao, Dihan Sun, Shengru Wang, Jianguo Zhang

Abstract read
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Article in Orthopaedic surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chenkai LiDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.
Xiaohan YeDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.
Bingtai HanDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.
You DuDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.ORCID https://orcid.org/0009-0007-2041-0786
Yiwei ZhaoDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.
Dihan SunDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.
Shengru WangDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.ORCID https://orcid.org/0009-0004-3749-4267
Jianguo ZhangDepartment of Orthopedics, Peking Union Medical College Hospital, Beijing, P. R. China.ORCID https://orcid.org/0000-0003-3129-5190

Funding

Beijing Municipal Natural Science Foundation 7222133National High Level Hospital Clinical Research Funding 2022-PUMCH-A-045National High Level Hospital Clinical Research Funding 2022-PUMCH-B-122National High Level Hospital Clinical Research Funding 2022-PUMCH-D-004National Natural Science Foundation of China 82172382Natural Science Foundation of Beijing Municipality L222096
6 · The paper itself

Abstract

objectiveEmerging scoliosis (ES) is a rare phenomenon after hemivertebra (HV) resection and short segmental fusion. Since the introduction of the ES, there have been rare in-depth studies. The aim of the present study was to further analyze the characteristics, risk factors, treatment, and prognosis of ES.

methodsA retrospective study analyzed patients with congenital scoliosis due to a single HV who underwent posterior correction and short fusion from 2002 to 2022. ES was defined as a Cobb angle ≥20° from its initial value and an apical vertebra located ≥2 levels away from the fusion region. ES patients and non-ES patients were matched at a 1:2 ratio. Both demographics and radiological parameters were compared. Univariate analysis and multivariate logistic analysis were used to identify the risk factors of ES.

resultsAmong 261 patients, 13 patients (5.0%) experienced ES. There were eight females and five males. The mean age of the ES patients at the time of primary surgery was 6.6 ± 3.7 years old (2.0-13.2 years old), with a mean follow-up of 64.2 ± 47.9 months (12-156 months). The ES could be further divided into three types: balance-related ES, complication-related ES, and separated ES. There were three balance-related ESs, six complication-related ESs, and four separated ESs. At the last follow-up, six patients were under observation, six patients underwent brace treatment, and one patient underwent revision surgery. Multivariate logistic analysis showed that the magnitude of postoperative compensatory curve (CC) was an independent risk factor for ES (OR = 1.172, p = 0.014).

conclusionsES is an extraordinary phenomenon after HV resection and short fusion, and it can be divided into three types. The magnitude of postoperative CC was an independent risk factor for ES. According to the severity of ES, observation, brace, or surgery can be chosen.

Indexed as

Postoperative ComplicationsScoliosisSpinal FusionAdolescentChildChild, PreschoolFemaleHumansMaleRetrospective StudiesRisk Factorscompensatory curvecongenital scoliosishemivertebra resectionshort fusion

Identifiers

PMID39402700
PMCPMC11735354

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