腿-小牛-珀特病儿童的骨骼成熟度新方法。

IF 1.5 3区 医学 Q3 ORTHOPEDICS
Journal of Pediatric Orthopaedics Pub Date : 2025-09-01 Epub Date: 2025-04-28 DOI:10.1097/BPO.0000000000003001
William Woodhams, K Aaron Shaw, Michael O'Sullivan, Chanhee Jo, J Anthony Herring
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引用次数: 0

摘要

背景:legg - calf - perthes病(LCPD)的预后在很大程度上取决于发病时的年龄和成熟度。在LCPD中,根据Greulich和Pyle (GP)成熟度图谱的成熟度评估,已知与受影响儿童骨骼成熟度延迟长达1.9年的关联。GP图谱是评估骨龄的标准,但需要获得单独的手部x线片。一种新的方法来评估骨骼成熟比较GP骨年龄在LCPD儿童寻求。方法:回顾性分析一项前瞻性、多中心研究,对1984年至1991年治疗的LCPD患者进行随访,直至骨骼成熟。如果患者在骨盆前后位x线片上诊断为LCPD,包括对侧髋关节,并在就诊时获得骨龄x线片,则纳入患者。如果患者表现为双侧LCPD,对侧髋关节在其呈现的x线片上没有显示,他们在呈现时缺乏骨龄x线片,或者他们在最优化牛津系统的范围之外,则排除患者。利用股骨粗隆高度与股骨头直径之比和患者性别(GT+性别)预测GP骨龄的公式被开发出来。将GP和GT+ Sex骨年龄与年代学年龄(CA)进行比较,以确定平均差异。结果:纳入71例患者(平均9.5±1.2岁,42.2%为女性)。通过GP骨年龄法进行的骨骼成熟度评估显示,平均差异比CA小1.4岁(95% CI: 1.01-1.76 y)。GT+性别骨龄评估显示平均差异比CA小1.4岁(95% CI: 1.03-1.75 y)。GP骨年龄与GT+性别评估骨年龄平均相差0.00岁(95% CI: -0.3 ~ 0.3 y)。GT+性别评估骨年龄与GP骨年龄有显著相关性(R=0.89, p)。结论:比较LCPD患儿GT+性别骨骼成熟度评估系统与GP骨年龄有显著相关性。GT+ Sex评估可以提供LCPD患者真实骨年龄的评估,而无需进行手部放射成像研究。证据等级:iii级——回顾性评价和分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A New Skeletal Maturity Methodology for Children With Legg-Calve-Perthes Disease.

Background: Legg-Calve-Perthes disease (LCPD) outcomes are largely determined by their age and maturity at onset. In LCPD, there is a known association with delayed skeletal maturity of up to 1.9 years in affected children based on maturity assessment with the Greulich and Pyle (GP) maturity atlas. The GP atlas is the standard for assessing bone age but requires obtaining a separate radiograph of the hand. A new methodology for assessing skeletal maturation in comparison to the GP bone age in children with LCPD was sought.

Methods: A retrospective review of a prospective, multicenter study of patients with LCPD treated from 1984 to 1991 and followed to skeletal maturity was performed. Patients were included if they had LCPD diagnosed on anteroposterior pelvis radiographs that included the contralateral hip who had bone age radiographs obtained at the time of presentation. Patients were excluded if they presented with bilateral LCPD, the contralateral hip was not visualized on their presenting radiographs, they lacked bone age radiographs at the time of presentation, or they presented outside the range for the Optimized Oxford system. A formula using the greater trochanteric height to femoral head diameter ratio and patient sex (GT+ Sex) for predicting GP bone age was developed. The GP and GT+ Sex bone ages were compared with the chronologic age (CA) to determine the mean discrepancy.

Results: Seventy-one patients were included (mean 9.5 ± 1.2 y at presentation, 42.2% females). Skeletal maturity assessment by the GP bone age method demonstrated a mean discrepancy of 1.4 years younger than CA (95% CI: 1.01-1.76 y). GT+ Sex bone age assessment demonstrated a mean discrepancy of 1.4 years younger than CA (95% CI: 1.03-1.75 y). The GP bone age was a mean of 0.00 years different than the GT+ Sex assessment bone age (95% CI: -0.3 to 0.3 y). The GT+ Sex assessment bone age correlated significantly with GP bone age ( R =0.89, P <0.0001). Male patients had a significantly younger GP bone age relative to CA compared with female patients (1.8 vs. 0.86 y, P = 0.02); however, there were fewer sex differences in the GT+ Sex assessment bone age relative to CA (male, 1.77 y younger vs. 1.12 y younger; P = 0.01).

Conclusions: The GT+ Sex skeletal maturity assessment system in children with LCPD significantly correlated with the GP bone age system when compared. The GT+ Sex assessment may provide an assessment of the true bone age in LCPD patients without the need for hand radiographic imaging studies.

Level of evidence: Level III-retrospective review and analysis.

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来源期刊
CiteScore
3.30
自引率
17.60%
发文量
512
审稿时长
6 months
期刊介绍: ​Journal of Pediatric Orthopaedics is a leading journal that focuses specifically on traumatic injuries to give you hands-on on coverage of a fast-growing field. You''ll get articles that cover everything from the nature of injury to the effects of new drug therapies; everything from recommendations for more effective surgical approaches to the latest laboratory findings.
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