Beckwitt Colin H, Monaco Spencer J, Gruen Gary S
Department of Pathology, University of Pittsburgh, School of Medicine, Pittsburgh, PA, USA.
Premier Orthopaedics, Kennett Square, PA, USA.
Foot Ankle Orthop. 2023 Aug 6;8(3):24730114231193391. doi: 10.1177/24730114231193391. eCollection 2023 Jul.
The treatment for highly comminuted pilon fractures remains controversial. The goal of this retrospective cohort study was to compare functional outcomes of primary arthrodesis of the tibiotalar joint (fusion) and open reduction internal fixation (ORIF).
Patients who underwent primary ORIF or fusion for pilon fractures at our institution since 2000 were identified by () code. Inclusion criteria for the ORIF cohort were patients with an AO/Orthopaedic Trauma Association type C3 pilon fracture. Additional inclusion criteria for the fusion cohort were patients whose fractures were deemed non-reconstructable by the treating surgeon. Outcome assessment was determined by the Foot and Ankle Outcome Score (FAOS) and Short Form 36-item health survey (SF-36), time to radiographic union or fusion, and wound-healing complications at a minimum of 2 years after their surgery.
Nineteen ORIF and 16 fusion patients completed the study's outcome assessments. A higher rate of nonunion was observed in patients treated by primary ORIF than primary fusion (5/19 vs 1/16). Posttraumatic arthritis was observed in 11 of 19 primary ORIF patients. Primary fusion patients exhibited increased symptoms, pain, and physical role limits but were equivalent to primary ORIF patients on all other functional metrics examined.
Primary ankle arthrodesis achieves a lower rate of nonunion and comparable functional outcomes to ORIF in patients with severely comminuted pilon fractures. The higher rate of nonunion observed in the primary ORIF group suggests that primary fusion should be considered an effective procedure for severe injuries to decrease the need for further operative intervention.
Therapeutic Level III, retrospective cohort.
高度粉碎性pilon骨折的治疗仍存在争议。这项回顾性队列研究的目的是比较胫距关节一期融合术(融合)和切开复位内固定术(ORIF)的功能结果。
通过()编码确定自2000年以来在我们机构接受pilon骨折一期ORIF或融合术的患者。ORIF队列的纳入标准是AO/骨科创伤协会C3型pilon骨折患者。融合队列的其他纳入标准是经治疗外科医生认为骨折不可重建的患者。结局评估由足踝结局评分(FAOS)和36项简短健康调查(SF-36)、影像学骨愈合或融合时间以及术后至少2年的伤口愈合并发症来确定。
19例接受ORIF和16例接受融合术的患者完成了研究的结局评估。与一期融合术相比,一期ORIF治疗的患者骨不连发生率更高(5/19比1/16)。19例一期ORIF患者中有11例出现创伤后关节炎。一期融合术患者的症状、疼痛和身体功能受限有所增加,但在所有其他检查的功能指标上与一期ORIF患者相当。
对于严重粉碎性pilon骨折患者,一期踝关节融合术的骨不连发生率较低,功能结果与ORIF相当。一期ORIF组观察到的较高骨不连发生率表明,一期融合术应被视为治疗严重损伤的有效方法,以减少进一步手术干预的需求。
治疗性III级,回顾性队列研究。