影响腰骶部脂肪瘤患儿独立行走的因素:基于 5 年解拴系列的回顾性队列研究

IF 1.7 Q2 PEDIATRICS
Clinical Medicine Insights-Pediatrics Pub Date : 2024-09-25 eCollection Date: 2024-01-01 DOI:10.1177/11795565241281334
Chiaki Takeuchi, Shiro Sugiura, Remi Fujita, Noriatsu Tatematsu, Hideshi Sugiura
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引用次数: 0

摘要

背景:照护者非常关心儿童能否实现独立行走,以证据为基础的康复支持是有益的。然而,目前的研究仅限于对脊柱裂畸形的单一研究,对腰骶部脂肪瘤患者独立行走时机的了解还存在空白:本研究旨在探讨影响腰骶部脂肪瘤患儿独立行走的因素:设计:回顾性队列研究:这项回顾性队列研究纳入了124名接受腰骶部脂肪瘤松解手术的儿童。研究分析了潜在的影响因素,包括脊柱脂肪瘤的类型、脂肪瘤的切除范围、磁共振成像特征、先天性异常并发症、排尿/排便管理要求、足/趾症状和矫形器的制作:多元逻辑回归分析显示,延迟独立行走的最重要影响因素是存在全身性合并畸形(调整后的几率比=15.5,P .001),而非全身性畸形,如尿道下裂,影响有限。对94名无全身合并畸形的患者进行的亚组分析表明,存在畸形的延髓与独立行走延迟有显著相关性(P = .014)。莫罗塔分类2型患儿独立行走的中位年龄为14个月,比其他类型患儿晚1个月,但差异不显著(P = .055):我们的研究结果表明,全身性合并畸形引起的并发症和畸形圆锥髓质的存在是导致无系带腰骶部脂肪瘤患儿独立行走延迟的影响因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influencing Factors on Independent Walking in Children With Lumbosacral Lipomas: A Retrospective Cohort Study Based on a 5-Year Untethering Series.

Background: Caregivers are deeply concerned about children achieving independent walking, and evidence-based rehabilitation support is beneficial. However, current research is confined to a single study on spina bifida aperta, leaving a gap in understanding the timing of independent walking for lumbosacral lipomas.

Objectives: This study aimed to examine the factors influencing independent walking in children with lumbosacral lipomas.

Design: Retrospective cohort study.

Methods: This retrospective cohort study included 124 children who underwent untethering surgery for lumbosacral lipomas. The age (in months) at which the children walked independently was used as the primary endpoint, and potential influencing factors, including the type of spinal lipoma, extent of lipoma removal, magnetic resonance imaging features, congenital anomaly complications, urinary/defecation management requirements, foot/toe symptoms, and orthotic device fabrications were analyzed.

Results: Multiple logistic regression analysis showed that the most significant influencing factor for delayed independent walking was the presence of systemic combined anomalies (adjusted odds ratio = 15.5, P<.001), while non-systemic malformations, such as suburethral cleft, had limited effects. A subgroup analysis of 94 patients without systemic combined anomalies showed that the presence of a malformed conus medullaris was significantly associated with delayed independent walking (P=.014). The median age of independent walking in children with Morota's classification type 2 was 14 months, which is 1 month later compared to other types, although this difference was not significant (P=.055).

Conclusion: Our findings suggest that complications arising from systemic combined anomalies and the presence of malformed conus medullaris are influencing factors in delays in independent walking in children with untethered lumbosacral lipomas.

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