Trang Jason, Kos Jennifer, Sears William
Department of Neurosurgery, Sydney Adventist Hospital, Sydney, Australia
Wentworth Spine Clinic, Sydney, Australia.
Int J Spine Surg. 2023 Feb;17(1):86-94. doi: 10.14444/8394. Epub 2023 Feb 2.
Recombinant human bone morphogenetic protein-2 (rhBMP-2) combined with an activated collagen scaffold (Infuse; Medtronic, MN) has been used to facilitate lumbar intervertebral fusion; however, data regarding its efficacy are inconsistent. We aimed to assess the efficacy of rhBMP-2 when used in posterior lumbar interbody fusion (PLIF) by analyzing the rate of reoperation for nonunion and patient-reported outcome measures in a large retrospective case series. We also aimed to assess the impact of patient and surgical factors on rates of reoperation and determine frequency of complications.
Prospectively collected data from a single-surgeon database of consecutive PLIFs (minimum 18-month follow-up) were retrospectively analyzed. PLIF was performed with pedicle screw instrumentation, intervertebral spacers, and locally harvested bone graft to which rhBMP-2 and bone marrow aspirate (BMA) were added. Multivariate logistic regression was used to determine the influence of patient and surgical factors on the primary outcome: reoperation for confirmed nonunion.
A total of 1019 operations at 1485 levels across 908 patients were analyzed. Mean duration of follow-up was 51.7 ± 30.0 months (range 18-172). Twelve patients required reoperation for nonunion (1.2%). Increasing body mass index was found to be significant in predicting reoperation (OR 1.114, = 0.046). Postoperative radiculitis was common (42%) but transient in most cases. There were significant and sustained improvements in patient-reported outcome measures postoperatively. Four cases of osteolysis and 5 of epidural cyst were recorded, and a reduction of rhBMP-2 dose seemed to ameliorate these sequelae.
In this large retrospective observational study, PLIF performed with rhBMP-2 and BMA resulted in a low rate of clinically significant nonunion and significant improvement in patient-reported outcomes. Transient radiculitis was common. Osteolysis and epidural cyst formation were rare and possibly related to dosage.
rhBMP-2 is effective when used in PLIF, resulting in a high rate of fusion and improved patient outcomes, and it has an acceptable safety profile.
重组人骨形态发生蛋白-2(rhBMP-2)与活性胶原支架(Infuse;美敦力公司,明尼苏达州)联合使用已被用于促进腰椎椎间融合;然而,关于其疗效的数据并不一致。我们旨在通过分析大型回顾性病例系列中不融合翻修率和患者报告的结局指标,评估rhBMP-2用于后路腰椎椎间融合术(PLIF)时的疗效。我们还旨在评估患者和手术因素对翻修率的影响,并确定并发症的发生率。
对前瞻性收集的来自单一外科医生的连续PLIF手术数据库(至少随访18个月)的数据进行回顾性分析。PLIF手术采用椎弓根螺钉内固定、椎间融合器,并添加局部采集的骨移植材料以及rhBMP-2和骨髓抽吸物(BMA)。多因素逻辑回归用于确定患者和手术因素对主要结局的影响:确诊不融合后的翻修手术。
共分析了908例患者的1485个节段的1019例手术。平均随访时间为51.7±30.0个月(范围18 - 172个月)。12例患者因不融合需要翻修(1.2%)。发现体重指数增加在预测翻修方面具有显著性(OR 1.114,P = 0.046)。术后神经根炎很常见(42%),但大多数情况下是短暂的。术后患者报告的结局指标有显著且持续的改善。记录到4例骨溶解和5例硬膜外囊肿,rhBMP-2剂量的减少似乎改善了这些后遗症。
在这项大型回顾性观察研究中,使用rhBMP-2和BMA进行的PLIF导致临床上显著不融合的发生率较低,且患者报告的结局有显著改善。短暂性神经根炎很常见。骨溶解和硬膜外囊肿形成罕见,可能与剂量有关。
rhBMP-2用于PLIF时有效,导致融合率高且患者结局改善,并且具有可接受的安全性。