Department of Orthopaedic Surgery, Childrens's Hospital and Medical Center and University of Nebraska Medical Center, Omaha, NE 68114, United States of America.
Head of Bone and Joint Infection, International Center for Limb Lengthening, Rubin Institute for Advanced Orthopedics, Sinai Hospital of Baltimore, 2401 West Belvedere Ave, Baltimore, MD 21215, United States of America.
Injury. 2022 Feb;53(2):376-380. doi: 10.1016/j.injury.2021.11.024. Epub 2021 Nov 12.
Segmental bone defects are a challenging clinical problem. In animal studies and craniomaxillofacial surgery, resorbable polylactide membrane (OrthoMesh; DePuy Synthes, West Chester, PA) shows promise for treatment of bone defects. This study presents the results of the treatment of segmental bone defects with resorbable polylactide membrane, bone morphogenic protein-2 (BMP-2), and autograft.
This study was approved by the institutional review board. All patients with a segmental bone defect treated with a resorbable polylactide membrane by a single surgeon from 2010 to 2019 were retrospectively reviewed. Data related to demographic variables, surgical details, and union were collected.
Eleven patients with median age of 37 years (range 22-62 years) were included in the study with segmental bone defects in the tibia (n = 3), femur (n = 4), or forearm (n = 4). Median bone defect size was 6 cm (range 3-12 cm). Etiology of bone defects included osteomyelitis (n = 7), oncologic resection (n = 3), and post-traumatic aseptic nonunion (n = 1). Flap coverage was performed in two patients. Median radiographic follow-up was 24 months (range 5-75 months). Ten patients (10/11) achieved union at a median of 17 months (range 5-46 months). Seven patients required reoperation for any reason with six patients requiring repeat grafting.
To our knowledge, this study is the largest series of patients with segmental bone defects treated with resorbable polylactide membrane. Resorbable polylactide membrane in combination with BMP-2 and autograft represents a safe and effective method of bone graft containment in segmental bone defects measuring up to 12 cm in this series. Ten of 11 patients achieved union at a median time of 16 months with 6 patients requiring repeat grafting. These results compare favorably with the induced membrane technique. This study is limited by its retrospective design, absence of control and comparison groups, and low patient numbers. Future prospective randomized study of the induced membrane technique and resorbable polylactide membrane should be undertaken to determine preferred approaches for treatment of segmental bone defects.
节段性骨缺损是一个具有挑战性的临床问题。在动物研究和颅面外科中,可吸收聚乳酸膜(OrthoMesh;DePuy Synthes,West Chester,PA)在治疗骨缺损方面显示出了希望。本研究报告了使用可吸收聚乳酸膜、骨形态发生蛋白-2(BMP-2)和自体移植物治疗节段性骨缺损的结果。
本研究获得了机构审查委员会的批准。对 2010 年至 2019 年间由一位外科医生使用可吸收聚乳酸膜治疗的所有节段性骨缺损患者进行了回顾性研究。收集了与人口统计学变量、手术细节和愈合相关的数据。
本研究共纳入 11 例患者,中位年龄 37 岁(范围 22-62 岁),胫骨(n=3)、股骨(n=4)或前臂(n=4)存在节段性骨缺损。中位骨缺损大小为 6cm(范围 3-12cm)。骨缺损的病因包括骨髓炎(n=7)、肿瘤切除术(n=3)和创伤后无菌性不愈合(n=1)。两名患者进行了皮瓣覆盖。中位影像学随访时间为 24 个月(范围 5-75 个月)。10 例患者(10/11)在 17 个月(范围 5-46 个月)的中位时间实现了愈合。7 例患者因任何原因需要再次手术,其中 6 例需要再次植骨。
据我们所知,这是使用可吸收聚乳酸膜治疗节段性骨缺损患者的最大系列研究。在本系列中,可吸收聚乳酸膜联合 BMP-2 和自体移植物是一种安全有效的节段性骨缺损骨移植容纳方法,适用于长度达 12cm 的骨缺损。11 例患者中有 10 例(10/11)在中位时间 16 个月时实现了愈合,其中 6 例需要再次植骨。这些结果与诱导膜技术相当。本研究受到其回顾性设计、缺乏对照和比较组以及患者数量少的限制。应进行诱导膜技术和可吸收聚乳酸膜的前瞻性随机研究,以确定治疗节段性骨缺损的首选方法。