Xu Yongqing, Fan Xinyu, Wang Teng, Pu Shaoquan, Cai Xingbo, Shi Xiangwen, Lin Wei, Yang Xi, Li Jian, Liu Min
Institute of Orthopedic Trauma, 920th Hospital of Chinese PLA Joint Logistics Support Force, Kunming Yunnan, 650032, P. R. China.
Beijing Aikang Yicheng Medical Equipment Co., Ltd, Beijing, 102200, P. R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2025 May 15;39(5):521-528. doi: 10.7507/1002-1892.202502045.
To analyze the effectiveness of single three-dimensional (3D)-printed microporous titanium prostheses and flap combined prostheses implantation in the treatment of large segmental infectious bone defects in limbs.
A retrospective analysis was conducted on the clinical data of 76 patients with large segmental infectious bone defects in limbs who were treated between January 2019 and February 2024 and met the selection criteria. Among them, 51 were male and 25 were female, with an age of (47.7±9.4) years. Of the 76 patients, 51 had no soft tissue defects (single prostheses group), while 25 had associated soft tissue defects (flap combined group). The single prostheses group included 28 cases of tibial bone defects, 11 cases of femoral defects, 5 cases of humeral defects, 4 cases of radial bone defects, and 3 cases of metacarpal, or carpal bone defects, with bone defect length ranging from 3.5 to 28.0 cm. The flap combined group included 3 cases of extensive dorsum of foot soft tissue defects combined with large segmental metatarsal bone defects, 19 cases of lower leg soft tissue defects combined with large segmental tibial bone defects, and 3 cases of hand and forearm soft tissue defects combined with metacarpal, carpal, or radial bone defects, with bone defect length ranging from 3.8 to 32.0 cm and soft tissue defect areas ranging from 8 cm×5 cm to 33 cm×10 cm. In the first stage, vancomycin-loaded bone cement was used to control infection, and flap repair was performed in the flap combined group. In the second stage, 3D-printed microporous titanium prostheses were implanted. Postoperative assessments were performed to evaluate infection control and bone integration, and pain release was evaluated using the visual analogue scale (VAS) score.
All patients were followed up postoperatively, with an average follow-up time of (35.2±13.4) months. In the 61 lower limb injury patients, the time of standing, walk with crutches, and fully bear weight were (2.2±0.6), (3.9±1.1), and (5.4±1.1) months, respectively. The VAS score at 1 year postoperatively was significantly lower than preoperative one ( =-10.678, <0.001). At 1 year postoperatively, 69 patients (90.8%) showed no complication such as infection, fracture, prosthesis displacement, or breakage, and X-ray films indicated good integration at the prosthesis-bone interface. According to the Paley scoring system for the healing of infectious bone defects, the results were excellent in 37 cases, good in 29 cases, fair in 3 cases, and poor in 7 cases. In the single prostheses group, during the follow-up, there was 1 case each of femoral prostheses fracture, femoral infection, and tibial infection, with a treatment success rate of 94.1% (48/51). In lower limb injury patients, the time of fully bear weight was (5.0±1.0) months. In the flap combined group, during the follow-up, 1 case of tibial fixation prostheses screw fracture occurred, along with 2 cases of recurrent foot infection in diabetic patients and 1 case of tibial infection. The treatment success rate was 84.0% (21/25). The time of fully bear weight in lower limb injury patients was (5.8±1.2) months. The overall infection eradication rate for all patients was 93.4% (71/76).
The use of 3D-printed microporous titanium prostheses, either alone or in combination with flaps, for the treatment of large segmental infectious bone defects in the limbs results in good effectiveness with a low incidence of complications. It is a feasible strategy for the reconstruction of infectious bone defects.
分析单枚三维(3D)打印微孔钛假体及皮瓣联合假体植入治疗四肢大段感染性骨缺损的疗效。
回顾性分析2019年1月至2024年2月期间收治的76例符合入选标准的四肢大段感染性骨缺损患者的临床资料。其中男性51例,女性25例,年龄(47.7±9.4)岁。76例患者中,51例无软组织缺损(单假体组),25例伴有软组织缺损(皮瓣联合组)。单假体组包括胫骨骨缺损28例、股骨缺损11例、肱骨缺损5例、桡骨缺损4例、掌骨或腕骨缺损3例,骨缺损长度为3.5~28.0cm。皮瓣联合组包括足背广泛软组织缺损合并大段跖骨缺损3例、小腿软组织缺损合并大段胫骨骨缺损19例、手部及前臂软组织缺损合并掌骨、腕骨或桡骨缺损3例,骨缺损长度为3.8~32.0cm,软组织缺损面积为8cm×5cm~33cm×10cm。第一阶段,采用载万古霉素骨水泥控制感染,皮瓣联合组行皮瓣修复。第二阶段,植入3D打印微孔钛假体。术后进行评估以评价感染控制及骨整合情况,并采用视觉模拟评分(VAS)评估疼痛缓解情况。
所有患者均获术后随访,平均随访时间为(35.2±13.4)个月。61例下肢损伤患者站立、拄拐行走及完全负重时间分别为(2.2±0.6)、(3.9±1.1)、(5.4±1.1)个月。术后1年VAS评分显著低于术前(=-10.678,<0.001)。术后1年,69例患者(90.8%)未出现感染、骨折、假体移位或断裂等并发症,X线片显示假体-骨界面融合良好。根据Paley感染性骨缺损愈合评分系统,结果为优37例、良29例、可3例、差7例。单假体组随访期间,股骨假体骨折、股骨感染及胫骨感染各1例,治疗成功率为94.1%(48/51)。下肢损伤患者完全负重时间为(5.0±1.0)个月。皮瓣联合组随访期间,发生胫骨固定假体螺钉骨折1例,糖尿病患者足部反复感染2例,胫骨感染1例。治疗成功率为84.0%(21/25)。下肢损伤患者完全负重时间为(5.8±1.2)个月。所有患者总体感染清除率为93.4%(71/76)。
使用3D打印微孔钛假体单独或联合皮瓣治疗四肢大段感染性骨缺损疗效良好,并发症发生率低。是感染性骨缺损重建的一种可行策略。