Is the clavicla pro humero a reliable reconstruction for paediatric proximal humerus sarcomas?

IF 2 3区 医学 Q2 ORTHOPEDICS
International Orthopaedics Pub Date : 2025-01-01 Epub Date: 2024-10-11 DOI:10.1007/s00264-024-06345-8
Zhuoyu Li, Daoyang Fan, Qing Zhang, Weifeng Liu
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引用次数: 0

Abstract

Purpose: The proximal humeral reconstruction is challenging. This study aims to investigate the survival, function and complications of clavicla pro humero (CPH) for pediatric proximal humeral reconstruction.

Methods: A retrospective cohort study was conducted on eight patients (4 males, and 4 females) who underwent clavicla pro humero reconstruction between January 2009 and December 2020 in our institution. The average age was 10.4 ± 2.7 years (range, 6 to 14 years). The functional outcomes were assessed by the Musculoskeletal Tumor Society Score (MSTS-93), the Toronto Extremity Salvage Score (TESS), the American Shoulder and Elbow Surgeons (ASES) score and the range of motion (ROM) of the shoulder. The complications and overall survivorship of clavicla pro humero were recorded in the follow-up.

Results: The mean follow-up of all patients was 54.6 ± 23.9 months (range, 24 to 84 months) and 73.3 ± 8.5 months (range, 72 to 84 months) in all survivors. All patients had a bone union at an average of 3.8 months after the initial procedure. Only one patient had no complications in the follow-up. The most common complications were clavicle fracture (87.5%, 7/8), followed by pseudarthrosis (62.5%, 5/8), proximal clavicle osteolysis (37.5%, 3/8) and skin flap necrosis (12.5%, 1/8). The average MSTS-93 score was 79% (range, 73-86%), the average TESS was 82% (range, 76-86%) and the average ASES was 70% (68-73%), respectively.

Conclusions: The clavicla pro humero procedure provides rapid bone union but has a high complication rate. Therefore, we do not recommend this technique as a routine surgical procedure for paediatric proximal humeral reconstruction when other methods are available.

Level of evidence: level IV therapeutic study.

对于小儿肱骨近端肉瘤,肱骨近端锁骨是否是一种可靠的重建方法?
目的:肱骨近端重建具有挑战性。本研究旨在探讨小儿肱骨近端重建术(CPH)的存活率、功能和并发症:我院对2009年1月至2020年12月期间接受肱骨近端重建术的8名患者(4男4女)进行了回顾性队列研究。平均年龄为 10.4 ± 2.7 岁(6 至 14 岁)。功能结果通过肌肉骨骼肿瘤协会评分(MSTS-93)、多伦多肢体救治评分(TESS)、美国肩肘外科医生评分(ASES)和肩关节活动范围(ROM)进行评估。随访记录了肱骨锁骨前路手术的并发症和总体存活率:所有患者的平均随访时间为(54.6±23.9)个月(24至84个月),所有幸存者的平均随访时间为(73.3±8.5)个月(72至84个月)。所有患者在初次手术后平均 3.8 个月实现骨结合。只有一名患者在随访期间没有出现并发症。最常见的并发症是锁骨骨折(87.5%,7/8),其次是假关节(62.5%,5/8)、锁骨近端骨溶解(37.5%,3/8)和皮瓣坏死(12.5%,1/8)。MSTS-93平均得分率为79%(范围为73-86%),TESS平均得分率为82%(范围为76-86%),ASES平均得分率为70%(68-73%):结论:肱骨前锁骨术可快速实现骨结合,但并发症发生率较高。因此,在有其他方法可用的情况下,我们不建议将该技术作为小儿肱骨近端重建的常规手术方法。
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来源期刊
International Orthopaedics
International Orthopaedics 医学-整形外科
CiteScore
5.50
自引率
7.40%
发文量
360
审稿时长
1 months
期刊介绍: International Orthopaedics, the Official Journal of the Société Internationale de Chirurgie Orthopédique et de Traumatologie (SICOT) , publishes original papers from all over the world. The articles deal with clinical orthopaedic surgery or basic research directly connected with orthopaedic surgery. International Orthopaedics will also link all the members of SICOT by means of an insert that will be concerned with SICOT matters. Finally, it is expected that news and information regarding all aspects of orthopaedic surgery, including meetings, panels, instructional courses, etc. will be brought to the attention of the readers. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted. Reports of animal experiments must state that the "Principles of laboratory animal care" (NIH publication No. 85-23, revised 1985) were followed, as well as specific national laws (e.g. the current version of the German Law on the Protection of Animals) where applicable. The editors reserve the right to reject manuscripts that do not comply with the above-mentioned requirements. The author will be held responsible for false statements or for failure to fulfil the above-mentioned requirements.
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