Hall Jeremy A, Beuerlein Murray J, McKee Michael D
Division of Orthopaedics, Department of Surgery, St. Michael's Hospital and the University of Toronto, 55 Queen Street East, Suite 800, Toronto, ON M5C 1R6, Canada.
J Bone Joint Surg Am. 2009 Mar 1;91 Suppl 2 Pt 1:74-88. doi: 10.2106/JBJS.G.01165.
Standard open reduction and internal fixation techniques have been successful in restoring osseous alignment for bicondylar tibial plateau fractures; however, surgical morbidity, especially soft-tissue infection and wound necrosis, has been reported frequently. For this reason, several investigators have proposed minimally invasive methods of fracture reduction followed by circular external fixation as an alternative approach. To our knowledge, there has been no direct comparison of the two operative approaches.
We performed a multicenter, prospective, randomized clinical trial in which standard open reduction and internal fixation with medial and lateral plates was compared with percutaneous and/or limited open fixation and application of a circular fixator for displaced bicondylar tibial plateau fractures (Schatzker types V and VI and Orthopaedic Trauma Association types C1, C2, and C3). Eighty-three fractures in eighty-two patients were randomized to operative treatment (forty-three fractures were randomized to circular external fixation and forty to open reduction and internal fixation). Follow-up consisted of obtaining a history, physical examination, and radiographs; completion of the Hospital for Special Surgery (HSS) knee score, the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and the Short Form-36 (SF-36) General Health Survey; and recording of complication and reoperation rates.
There were no significant differences between the groups in terms of demographic variables, mechanism of injury, or fracture severity and/or displacement. However, patients in the circular fixator group had less intraoperative blood loss than those in the open reduction and internal fixation group (213 mL and 544 mL, respectively; p = 0.006) and spent less time in the hospital (9.9 days and 23.4 days, respectively; p = 0.024). The quality of osseous reduction was similar in the groups. There was a trend for patients in the circular fixator group to have superior early outcome in terms of HSS scores at six months (p = 0.064) and the ability to return to preinjury activities at six months (p = 0.031) and twelve months (p = 0.024). These outcomes were not significantly different at two years. There was no difference in total arc of knee motion, and the WOMAC scores at two years after the injury were not significantly different between the groups with regard to the pain (p = 0.923), stiffness (p = 0.604), or function (p = 0.827) categories. The SF-36 scores at two years after the injury were significantly decreased compared with the controls for both groups (p = 0.001 for the circular fixator group and p = 0.014 for the open reduction and internal fixation group), although there was less impairment in the circular fixator group in the bodily pain category (a score of 46) compared with the open reduction and internal fixation group (a score of 35) (p = 0.041). Seven (18%) of the forty patients in the open reduction and internal fixation group had a deep infection. The number of unplanned repeat surgical interventions, and their severity, was greater in the open reduction and internal fixation group (thirty-seven procedures) compared with the circular fixator group (sixteen procedures) (p = 0.001).
Both techniques provide a satisfactory quality of fracture reduction. Because percutaneous reduction and application of a circular fixator results in a shorter hospital stay, a marginally faster return of function, and similar clinical outcomes and because the number and severity of complications is much higher with open reduction and internal fixation, we believe that circular external fixation is an attractive option for these difficult-to-treat fractures. Regardless of treatment method, patients with this injury have substantial residual limb-specific and general health deficits at two years of follow-up.
标准切开复位内固定技术已成功用于恢复双髁胫骨平台骨折的骨对线;然而,手术并发症,尤其是软组织感染和伤口坏死,经常被报道。因此,一些研究者提出了微创骨折复位方法,随后采用环形外固定作为替代方法。据我们所知,尚未对这两种手术方法进行直接比较。
我们进行了一项多中心、前瞻性、随机临床试验,将标准切开复位并用内外侧钢板内固定与经皮和/或有限切开固定并应用环形固定器治疗移位双髁胫骨平台骨折(Schatzker V型和VI型以及骨科创伤协会C1、C2和C3型)进行比较。82例患者的83处骨折被随机分配接受手术治疗(43处骨折随机分配至环形外固定组,40处骨折随机分配至切开复位内固定组)。随访包括获取病史、体格检查和影像学检查;完成特种外科医院(HSS)膝关节评分、西安大略和麦克马斯特大学骨关节炎指数(WOMAC)以及简明健康调查问卷(SF - 36);并记录并发症和再次手术率。
两组在人口统计学变量、损伤机制或骨折严重程度和/或移位方面无显著差异。然而,环形固定器组患者术中失血量少于切开复位内固定组(分别为213 mL和544 mL;p = 0.006),住院时间也更短(分别为9.9天和23.4天;p = 0.024)。两组的骨复位质量相似。环形固定器组患者在6个月时的HSS评分(p = 0.064)、6个月(p = 0.031)和12个月(p = 0.024)时恢复到伤前活动能力方面有早期结果更好的趋势。两年时这些结果无显著差异。膝关节总活动弧度无差异,伤后两年时两组在疼痛(p = 0.923)、僵硬(p = 0.604)或功能(p = 0.827)类别方面的WOMAC评分无显著差异。伤后两年时两组的SF - 36评分均较对照组显著降低(环形固定器组p = 0.001,切开复位内固定组p = 0.014),尽管环形固定器组在身体疼痛类别中的损伤程度(评分为46)低于切开复位内固定组(评分为35)(p = 0.041)。切开复位内固定组的40例患者中有7例(18%)发生深部感染。切开复位内固定组的非计划再次手术干预次数及其严重程度高于环形固定器组(37次手术)(环形固定器组为16次手术)(p = 0.001)。
两种技术均能提供令人满意的骨折复位质量。由于经皮复位并应用环形固定器可缩短住院时间,功能恢复略快,且临床结果相似,并且切开复位内固定的并发症数量和严重程度更高,我们认为环形外固定是治疗这些难处理骨折的一个有吸引力的选择。无论采用何种治疗方法,该损伤患者在随访两年时均存在明显的残肢特异性和总体健康缺陷。