Liu Xi, Cen Shiqiang, Xiang Zhou, Zhong Gang, Yi Min, Fang Yue, Liu Lei, Huang Fuguo
Department of Othopedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R.China.
Department of Othopedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041,
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Jun 15;31(6):665-669. doi: 10.7507/1002-1892.201611127.
To evaluate the safety of conversion from external fixation to internal fixation for open tibia fractures.
Between January 2010 and December 2014, 94 patients (98 limbs) with open tibia fractures were initially treated with external fixators at the first stage, and the clinical data were retrospectively analyzed. In 29 cases (31 limbs), the external fixators were changed to internal fixation for discomfort, pin tract response, Schantz pin loosening, delayed union or non-union after complete wound healing and normal or close to normal levels of erythrocyte sedimentation rate (ESR), C reactive protein (CRP), and the leucocyte count as well as the neutrophil ratio (trial group); in 65 cases (67 limbs), the external fixators were used as the ultimate treatment in the control group. There was no significant difference in gender, age, side of the limbs, interval from injury to the first debridement, initial pathogenic bacteria, the limbs that skin grafting or flap transferring for skin and soft tissue defect between the two groups ( >0.05). The incidence of Gustilo type III fractures in the control group was significantly higher than that in the trial group ( =0.000). The overall incidence of infection was calculated respectively in the two groups. The incidence of infection according to different fracture types and whether skin grafting or flap transferring was compared between the two groups. The information of the pathogenic bacteria was recorded in the infected patients, and it was compared with the results of the initial culture. The incidence of infection in the patients of the trial group using different internal fixation instruments was recorded.
The overall incidences of infection for the trial and control groups were 9.7% (3/31) and 9.0% (6/67) respectively, showing no significant difference ( =0.013, =0.909). No infection occurred in Gustilo type I and type II patients. The incidence of infection for Gustilo type IIIA patients in the trial group and the control group were 14.3% (1/7) and 6.3% (2/32) respectively, showing no significant difference ( =0.509, =0.476); the incidence of infection for type IIIB patients in the two groups were 50.0% (2/4) and 14.3% (2/14) respectively, showing no significant difference ( =2.168, =0.141); and the incidence of infection for type IIIC patients in the two groups were 0 and 16.7% (2/12) respectively, showing no significant difference ( =0.361, =0.548). Of all the infected limbs, only 1 limb in the trial group had the same as the result of the initial culture. In the patients who underwent skin grafting or flap transferring, the incidence of infection in the trial and control groups were 33.3% (2/6) and 13.3% (2/15) respectively, showing no significant difference ( =1.059, =0.303). After conversion to internal fixation, no infection occurred in the cases that fixed with nails (11 limbs), and infection occurred in 4 of 20 limbs that fixed with plates, with an incidence of infection of 20%.
Conversion from external fixation to internal fixation for open tibia fractures is safe in most cases. However, for open tibia fractures with extensive and severe soft tissue injury, especially Gustilo type III patients who achieved wound heal after flap transfer or skin grafting, the choice of secondary conversion to internal fixation should carried out cautiously. Careful pre-operative evaluation of soft tissue status, cautious choice of fixation instrument and meticulous intra-operative soft tissue protection are essential for its safety.
评估开放性胫骨骨折从外固定转换为内固定的安全性。
回顾性分析2010年1月至2014年12月期间94例(98肢)开放性胫骨骨折患者的临床资料,这些患者均在第一阶段首先采用外固定架治疗。29例(31肢)患者在伤口完全愈合且红细胞沉降率(ESR)、C反应蛋白(CRP)、白细胞计数及中性粒细胞比例恢复正常或接近正常水平后,因不适、针道反应、斯氏针松动、延迟愈合或不愈合而将外固定架更换为内固定(试验组);65例(67肢)患者将外固定架作为最终治疗方式(对照组)。两组患者在性别、年龄、肢体侧别、受伤至首次清创间隔时间、初始病原菌、因皮肤和软组织缺损而行植皮或皮瓣转移的肢体等方面差异无统计学意义(P>0.05)。对照组Gustilo III型骨折的发生率显著高于试验组(P=0.000)。分别计算两组的总体感染发生率。比较两组不同骨折类型及是否行植皮或皮瓣转移时的感染发生率。记录感染患者的病原菌信息,并与初始培养结果进行比较。记录试验组使用不同内固定器械患者的感染发生率。
试验组和对照组的总体感染发生率分别为9.7%(3/31)和9.0%(6/67),差异无统计学意义(P=0.013,P=0.909)。Gustilo I型和II型患者未发生感染。试验组和对照组Gustilo IIIA患者的感染发生率分别为14.3%(1/7)和6.3%(2/32),差异无统计学意义(P=0.509,P=0.476);IIIB型患者的感染发生率分别为50.0%(2/4)和14.3%(2/14),差异无统计学意义(P=2.168,P=0.141);IIIC型患者的感染发生率分别为0和16.7%(2/12),差异无统计学意义(P=0.361,P=0.548)。在所有感染肢体中,试验组仅1肢的病原菌与初始培养结果一致。行植皮或皮瓣转移的患者中,试验组和对照组的感染发生率分别为33.3%(2/6)和13.3%(2/15),差异无统计学意义(P=1.059,P=0.303)。转换为内固定后,使用髓内钉固定的11例患者未发生感染,使用钢板固定的20例患者中有4例发生感染,感染发生率为20%。
多数情况下,开放性胫骨骨折从外固定转换为内固定是安全的。然而,对于软组织损伤广泛且严重的开放性胫骨骨折,尤其是经皮瓣转移或植皮后伤口愈合的Gustilo III型患者,二次转换为内固定的选择应谨慎。术前仔细评估软组织状况、谨慎选择固定器械及术中细致保护软组织对其安全性至关重要。