Department of Orthopaedic Surgery, University of Washington Medical Center, Seattle, WA 98195, USA.
Spine (Phila Pa 1976). 2012 Oct 15;37(22 Suppl):S40-51. doi: 10.1097/BRS.0b013e31826ca9b1.
A systematic review.
To determine whether different indications or reasons for spinal fusion are associated with different risks of subsequent adjacent segment pathology (ASP) in the lumbar and cervical spine.
Pre-existing degeneration at levels adjacent to an arthrodesis may play a role in the development of symptomatic adjacent segment pathology. Although most spinal arthrodeses occur in patients with degenerative spinal disease, spinal fusion occurs in the pediatric and trauma population, and also congenitally. Evaluating the risk of ASP in these populations may shed light on its etiology.
A systematic search was conducted in PubMed and the Cochrane Library for articles published between January 1, 1990, and December 31, 2011. We included all articles that described the risk of radiographical adjacent segment pathology (RASP) following surgical fusion for degenerative disease, for trauma, or for conditions requiring fusion in pediatrics in the lumbar or cervical spine. In addition, we included studies recording ASP in patients with congenital fusion.
Nineteen studies met our inclusion criteria. In patients who underwent fusion in the lumbar spine for degenerative reasons, the RASP rate averaged 12.4% during an average of 5.6-year follow-up. For patients who underwent fusion in the cervical spine for degenerative reasons, the average RASP rate was 25.3% during a 2.3-year follow-up. For patients with Klippel-Feil syndrome and congenital fusion, the RASP rate averaged 49.7% during an average of 23.5-years of follow-up. In patients who were fused for scoliosis, the average RASP rate was 20.3% of 3.9-year follow-up. However there is significant variation between studies in patient population, follow-up, and definition of RASP.
In the cervical spine, the rate of RASP in patients with fusion for degenerative reasons indications is greater than the rate of RASP in patients with congenital fusion suggesting that the pre-existing health and status of the adjacent level at the time of fusion may play a contributory role in the development of ASP. There is insufficient evidence in the literature to determine whether the indication/reason for fusion affects the risk of RASP in the lumbar spine
In the cervical spine, the rate of RASP in patients with fusion for degenerative reasons indications is greater than the rate of RASP in patients with congenital fusion suggesting that the pre-existing health and status of the adjacent level at the time of fusion may play a contributory role in the development of ASP. Strength of Statement: Weak.
系统回顾。
确定脊柱融合的不同适应证或原因是否与腰椎和颈椎后路相邻节段病变(ASP)的风险不同有关。
在融合相邻节段存在预先存在的退变可能在症状性相邻节段病变的发展中起作用。尽管大多数脊柱融合术发生在退行性脊柱疾病患者中,但脊柱融合术也发生在儿科和创伤人群中,也有先天性的。评估这些人群中 ASP 的风险可能有助于阐明其病因。
在 PubMed 和 Cochrane 图书馆中对 1990 年 1 月 1 日至 2011 年 12 月 31 日期间发表的文章进行了系统检索。我们纳入了所有描述退行性疾病、创伤或儿科脊柱融合适应证下手术融合后影像学相邻节段病变(RASP)风险的文章,包括腰椎或颈椎。此外,我们还纳入了记录先天性融合患者 ASP 的研究。
19 项研究符合纳入标准。在因退行性原因在腰椎接受融合的患者中,平均 5.6 年的随访中,RASP 发生率平均为 12.4%。在因退行性原因在颈椎接受融合的患者中,平均 2.3 年的随访中,RASP 发生率平均为 25.3%。在 Klippel-Feil 综合征和先天性融合患者中,平均随访 23.5 年,RASP 发生率平均为 49.7%。在因脊柱侧凸接受融合的患者中,平均 3.9 年的随访中,RASP 发生率平均为 20.3%。然而,在患者人群、随访和 RASP 定义方面,各研究之间存在显著差异。
在颈椎,退行性原因融合患者的 RASP 发生率高于先天性融合患者,这表明融合时相邻节段的预先存在的健康状况和状态可能在 ASP 的发展中起作用。文献中没有足够的证据来确定融合的适应证/原因是否会影响腰椎 RASP 的风险。
在颈椎,退行性原因融合患者的 RASP 发生率高于先天性融合患者,这表明融合时相邻节段的预先存在的健康状况和状态可能在 ASP 的发展中起作用。
弱。