Dorward Ian G, Buchowski Jacob M, Stoker Geoffrey E, Zebala Lukas P
Departments of *Neurosurgery†Orthopaedic Surgery, Washington University School of Medicine, Saint Louis, MO.
Clin Spine Surg. 2016 Jul;29(6):E276-81. doi: 10.1097/BSD.0b013e318286fa7e.
Retrospective case series.
The purpose of this study was to determine the fusion rate and evaluate the complications associated with the application of recombinant human bone morphogenetic protein-2 (rhBMP-2) in posterior cervical fusion.
The rates of fusion and complications associated with the use of rhBMP-2 in posterior cervical fusion is unclear, though recent work has shown up to a 100% fusion rate.
We independently reviewed consecutive series of patients who underwent posterior cervical, occipitocervical, or cervicothoracic instrumented fusion augmented with rhBMP-2. Two surgeons at a tertiary-referral, academic medical center performed all operations, and each patient had a minimum of 2-year follow-up. Fusion status was determined by bony bridging on computed tomography scans, absence of radiolucency around instrumentation, and absence of motion on lateral flexion/extension radiographs.
Fifty-seven patients with a mean age of 56.7±13.2 years and mean follow-up of 37.7±20.6 months were analyzed. Forty-eight patients (84.2%) had undergone previous cervical surgery, and 42.1% had a preexisting nonunion. Constructs spanned 5.6±2.6 levels; 19.3% involved the occiput, whereas 61.4% crossed the cervicothoracic junction. The mean rhBMP-2 dose was 21.1±8.7 mg per operation. Iliac crest autograft was used for 29.8% of patients. Six patients (10.5%) experienced nonunion; only 2 required revision. In each case of nonunion, instrumentation crossed the occipitocervical or cervicothoracic junction. However, none of the analyzed variables was statistically associated with nonunion. Fourteen patients (24.6%) suffered complications, with 7 requiring additional surgery.
The observed fusion rate of rhBMP-2-augmented posterior cervical, occipitocervical, and cervicothoracic fusions was 89.5%. This reflects the complicated nature of the patients included in the current study and demonstrates that rhBMP-2 cannot always overcome the biomechanical challenges entailed in spanning the occipitocervical or cervicothoracic junction.
回顾性病例系列研究。
本研究旨在确定融合率,并评估重组人骨形态发生蛋白-2(rhBMP-2)在颈椎后路融合术中应用的相关并发症。
rhBMP-2用于颈椎后路融合术的融合率及并发症情况尚不清楚,尽管近期研究显示融合率高达100%。
我们独立回顾了接受rhBMP-2辅助的颈椎后路、枕颈或颈胸段器械融合术的连续系列患者。在一家三级转诊学术医学中心,由两名外科医生实施所有手术,每位患者至少随访2年。通过计算机断层扫描上的骨桥接、器械周围无透亮区以及侧屈/后伸X线片上无活动来确定融合状态。
分析了57例患者,平均年龄56.7±13.2岁,平均随访37.7±20.6个月。48例患者(84.2%)曾接受过颈椎手术,42.1%存在既往不愈合。融合节段跨越5.6±2.6个节段;19.3%涉及枕部,61.4%跨越颈胸交界处。每次手术rhBMP-2平均剂量为21.1±8.7mg。29.8%的患者使用了髂嵴自体骨移植。6例患者(10.5%)出现不愈合;仅2例需要翻修。在每例不愈合病例中,器械均跨越枕颈或颈胸交界处。然而,分析的变量中没有一个与不愈合有统计学关联。14例患者(24.6%)出现并发症,7例需要再次手术。
rhBMP-2辅助的颈椎后路、枕颈和颈胸段融合术的观察到的融合率为89.5%。这反映了本研究中纳入患者的复杂性,并表明rhBMP-蛋白2不能总是克服跨越枕颈或颈胸交界处所带来的生物力学挑战。