Division of Plastic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California.
Division of Orthopedic Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
J Reconstr Microsurg. 2020 Jun;36(5):386-396. doi: 10.1055/s-0040-1702147. Epub 2020 Feb 23.
In the pediatric population, bony defects of the extremities pose a significant challenge for which free vascularized fibular grafts (FVFGs) represent a valuable reconstructive option. The purpose of this study was to explore surgical outcomes, complications, and long-term functionality of FVFG for this patient group.
Using MEDLINE and PubMed databases, studies were identified of pediatric extremity reconstruction using FVFG which reported functional outcomes and/or complications. The operative logs at a tertiary pediatric center were then reviewed for cases of FVFG between January 2000 and 2017. Demographic characteristics, surgical indications, operative details, graft survival, bony union, complications, and functionality of the reconstruction were recorded.
A total of 366 studies were identified with 23 ultimately meeting inclusion criteria in the systematic review. In the institutional series, 29 patients were included with mean age of 9.7 years (1-17 years). Indications for reconstruction included malignant bone tumor ( = 11), osteomyelitis ( = 9), congenital pseudoarthrosis ( = 6), and osteofibrous dysplasia ( = 3). Major postoperative complications included graft nonunion (24.1%), fracture (17.2%), and hardware failure (17.2%). Thirteen patients (44.8%) experienced delayed complications, while two (6.8%) experienced an immediate complication. Complications occurred in the donor site in 2 cases and the recipient site in all 13 cases. Long-term graft survival was achieved in 27 patients (93.1%), and 23 (79.3%) had full functional recovery, with an average Musculoskeletal Tumor Society score of 90% (60-100%). Mean follow-up was 5.17 years (2-12 years).
This review and institutional series demonstrate the versatility of FVFG to facilitate limb reconstruction in large defects or serve as a salvage option in complex cases. While immediate and donor-site complications are uncommon, delayed recipient-site complications are frequent, and patients and families should be counseled regarding this expectation. Though technically challenging, excellent long-term graft viability and functional recovery can be achieved in the large majority of patients.
在儿科人群中,四肢的骨缺损是一个重大挑战,游离腓骨血管化移植(FVFG)是一种有价值的重建选择。本研究旨在探讨 FVFG 治疗该患者群体的手术结果、并发症和长期功能。
使用 MEDLINE 和 PubMed 数据库,确定了使用 FVFG 进行儿童四肢重建的研究,这些研究报告了功能结果和/或并发症。然后,回顾了 2000 年 1 月至 2017 年期间在一家三级儿科中心进行的 FVFG 手术记录。记录了人口统计学特征、手术适应证、手术细节、移植物存活率、骨愈合、并发症和重建的功能。
共确定了 366 项研究,其中 23 项在系统综述中最终符合纳入标准。在机构系列中,纳入了 29 例患者,平均年龄为 9.7 岁(1-17 岁)。重建的适应证包括恶性骨肿瘤(11 例)、骨髓炎(9 例)、先天性假关节(6 例)和骨纤维发育不良(3 例)。主要术后并发症包括移植物骨不连(24.1%)、骨折(17.2%)和内固定失败(17.2%)。13 例(44.8%)患者发生迟发性并发症,2 例(6.8%)患者发生即刻并发症。并发症发生在供区 2 例,发生在受区 13 例。27 例(93.1%)患者长期保留移植物,23 例(79.3%)患者完全恢复功能,平均肌肉骨骼肿瘤学会评分 90%(60-100%)。平均随访时间为 5.17 年(2-12 年)。
本综述和机构系列研究表明,FVFG 具有多功能性,可促进大缺损的肢体重建,或作为复杂病例的挽救选择。虽然即刻和供区并发症并不常见,但迟发性受区并发症很常见,应向患者及其家属说明这一预期。尽管技术上具有挑战性,但在绝大多数患者中可以实现长期移植物的良好存活和功能恢复。