小儿滑囊成形术-系统回顾。

The Iowa orthopaedic journal Pub Date : 2024-01-01
Nathan Chaclas, Kevin Orellana, Kevin Huang, Chad Amato, Brendan A Williams
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引用次数: 0

摘要

背景:滑车成形术是治疗高度滑车发育不良的一种手术方法。在骨骼发育不成熟的人群中,该手术的安全性仍不清楚,因为人们担心骨骼骤停和过早髌骨关节炎的发展。本研究的目的是系统地回顾文献,以评估滑囊成形术在儿科患者中的应用、结果和并发症。方法:根据PRISMA指南对PubMed、SCOPUS和Embase数据库进行系统评价。纳入标准是平均年龄≤18岁的研究,其中报告了滑囊成形术后的个体化患者特征和结果。患者的人口统计资料、不典型增生类型、手术类型和患者结果在可能的情况下被抽象出来,并用描述性统计进行总结。结果:我们的检索策略确定了2006-2020年发表的7项研究,包括108例患者(平均年龄= 14.3),平均随访时间为27.6个月(12-60个月)。除1例外,其余均为IV级证据(平均未成年人评分为10.5[6-13])。多数患者根据Dejour评分(107/108)进行分类。最常使用的是Bereiter技术(83/108)。在包括患者报告的结果测量的研究中,术后平均Kujala和Lysholm评分增加。滑车成形术后复发性不稳定1例(1%)。13%的患者出现术后并发症,最常见的是关节纤维化(14/108)。在一项使用Albee侧楔增强术的研究中发现了过早的影像学骨关节炎改变,并在23例患者中观察到4例(17.4%)。没有研究发现过早的生理停止或生长障碍。结论:关于滑车成形术在儿科患者中的应用,证据基础仍然有限。总的来说,观察到的良好结果是不常见的复发性不稳定,没有因生理停止而引起的生长障碍的报道。在一小部分接受单次滑骨成形术的患者中观察到髌骨关节炎的改变。需要进一步的工作来确定这是手术本身的结果还是正在治疗的潜在病理。随着儿童人群和骨骼发育不成熟的个体对滑车成形术的兴趣越来越大,有必要进一步研究这一人群的并发症,以便为患者提供适当的建议并为手术决策提供信息。证据水平:III。
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Trochleoplasty in Pediatric Patients - A Systematic Review.

Background: Trochleoplasty is a surgical consideration for the treatment of high-grade trochlear dysplasia. The safety profile of this procedure remains particularly unclear in the skeletally immature population where concerns exist regarding physeal arrest and the development of premature patellofemoral arthritis. The purpose of this study was to systematically review the literature to evaluate trochleoplasty use, outcomes and complications observed among pediatric patients.

Methods: A systematic review was performed in accordance with PRISMA guidelines reviewing PubMed, SCOPUS, and Embase databases. Inclusion criteria were studies with a mean cohort age ≤ 18 in which individualized patient characteristics and resultant outcomes were reported after trochleoplasty. Patient demographics, dysplasia type, procedure type and patient outcomes were abstracted when available and summarized with descriptive statistics.

Results: Our search strategy identified 7 studies published from 2006-2020 that included 108 patients (mean age = 14.3) with a mean follow up of 27.6 months (range 12-60 months). All but one were classified as Level IV evidence (mean MINORS score of 10.5 [6-13]). Most patients were classified according to Dejour (107/108). The Bereiter technique was used most often (83/108). In studies including patient-reported outcome measures, mean Kujala and Lysholm scores increased postoperatively. Recurrent instability occurred in 1 patient (1%) following trochleoplasty. Postoperative complications, most commonly arthrofibrosis, were observed in 13% of patients (14/108). Premature radiographic osteoarthritic changes were identified in a single study using the Albee lateral wedge augmentation and observed in 4 of 23 (17.4%) of patients. No study identified premature physeal arrest or growth disturbance.

Conclusion: There remains a limited evidence base regarding trochleoplasty use in pediatric patients. Overall, favorable outcomes have been observed with infrequent recurrent instability and no reported growth disturbance from physeal arrest. Patellofemoral arthritic changes were observed radiographically in a small subgroup of patients undergoing a single trochleoplasty technique. Further work is necessary to determine if this is a result of the procedure itself or the underlying pathology being treated. As interest grows in implementing trochleoplasty in the pediatric population and among skeletally immature individuals, further work is necessary to clarify the complication profile in this population to appropriately counsel patients and inform surgical decision-making. Level of Evidence: III.

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