Department of Neurosurgery, Stanford University School of Medicine, 300 Pasteur Drive, R291 MC 5327, Stanford, CA 94305-5327. E-mail address for J.K. Ratliff:
J Bone Joint Surg Am. 2014 Sep 3;96(17):1409-16. doi: 10.2106/JBJS.M.01016.
Usage of recombinant human bone morphogenetic protein (rhBMP) in anterior cervical discectomy and fusion (ACDF) procedures is controversial. Studies suggest increased rates of dysphagia, hematoma or seroma, and severe airway compromise in anterior cervical spine procedures using rhBMP. The purpose of the present study was to determine and describe national utilization trends and complication rates associated with rhBMP usage in anterior cervical spine procedures.
The MarketScan database from 2006 to 2010 was retrospectively queried to identify 91,543 patients who underwent ACDF with or without cervical corpectomy. Patient selection and outcomes were ascertained with use of ICD-9-CM (International Classification of Diseases, Ninth Revision, Clinical Modification) and CPT (Current Procedural Terminology) coding. A total of 3197 patients were treated with rhBMP intraoperatively. Mean follow-up was 588 days (interquartile range [IQR], 205 to 886 days) in the non-treated cohort and 591 days (IQR, 203 to 925 days) in the rhBMP-treated cohort. Multivariate logistic regression as well as propensity score analysis were used to evaluate the association of rhBMP usage with postoperative complications.
In propensity score-adjusted models, rhBMP usage was associated with an increased risk of any complication (odds ratio [OR] = 1.34, 95% confidence interval [CI] = 1.2 to 1.5) and specific complications such as hematoma or seroma (OR = 1.8, 95% CI = 1.4 to 2.3), dysphagia (OR = 1.3, 95% CI = 1.1 to 1.5), and any pulmonary complication (OR = 1.5, 95% CI = 1.2 to 1.8) within thirty days postoperatively. There were no significant differences in the rates of readmission, in-hospital mortality, referral to pain management, new malignancy, or reoperation between the two cohorts. Usage of rhBMP was associated with a mean increase of $5545 (19%) in total payments to the hospital and primary physician (p < 0.001).
We found an increased overall rate of postoperative complications in patients receiving rhBMP for cervical spinal fusion procedures compared with patients not receiving rhBMP. Hematoma or seroma, pulmonary complications, and dysphagia were also more common in the rhBMP cohort. Usage of rhBMP in a case was associated with $311 greater payments to the surgeon and $4213 greater payments to the hospital.
Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.
在颈椎前路椎间盘切除融合术(ACDF)中使用重组人骨形态发生蛋白(rhBMP)存在争议。研究表明,在使用 rhBMP 的颈椎前路手术中,吞咽困难、血肿或血清肿以及严重气道阻塞的发生率增加。本研究的目的是确定并描述 rhBMP 在颈椎前路手术中使用的全国使用趋势和并发症发生率。
回顾性查询 2006 年至 2010 年的 MarketScan 数据库,以确定 91543 例接受 ACDF 加或不加颈椎切除术的患者。使用 ICD-9-CM(国际疾病分类,第 9 版,临床修订版)和 CPT(当前程序术语)编码确定患者选择和结果。3197 例患者在术中接受 rhBMP 治疗。非治疗组的平均随访时间为 588 天(四分位距[IQR],205-886 天),rhBMP 治疗组为 591 天(IQR,203-925 天)。多变量逻辑回归和倾向评分分析用于评估 rhBMP 使用与术后并发症的关联。
在倾向评分调整模型中,rhBMP 使用与任何并发症(比值比[OR] = 1.34,95%置信区间[CI] = 1.2-1.5)和特定并发症(如血肿或血清肿[OR] = 1.8,95% CI = 1.4-2.3)、吞咽困难(OR = 1.3,95% CI = 1.1-1.5)和任何肺部并发症(OR = 1.5,95% CI = 1.2-1.8)的风险增加相关术后 30 天内。两组之间在再入院率、住院死亡率、转至疼痛管理、新发恶性肿瘤或再次手术方面无显著差异。rhBMP 的使用与医院和初级医生的总付款增加 5545 美元(19%)(p < 0.001)相关。
与未接受 rhBMP 治疗的患者相比,我们发现接受 rhBMP 进行颈椎脊柱融合术的患者总体术后并发症发生率增加。rhBMP 组的血肿或血清肿、肺部并发症和吞咽困难也更为常见。rhBMP 在一个病例中的使用与外科医生支付 311 美元,医院支付 4213 美元有关。
治疗水平 III。有关证据水平的完整描述,请参见作者说明。