The Rothman Institute, Thomas Jefferson University Hospital, 925 Chestnut Street, 5th Floor, Philadelphia, PA 19107, USA.
Clin Orthop Relat Res. 2011 Mar;469(3):658-65. doi: 10.1007/s11999-010-1731-8.
Existing studies suggest a relatively high incidence of dysphagia after anterior cervical decompression and fusion (ACDF). The majority of these studies, however, are retrospective in nature and lack a control group.
QUESTIONS/PURPOSES: We therefore (1) prospectively determined the incidence and severity of dysphagia after ACDF using lumbar decompression patients as a control group; and (2) determined which factors, if any, are associated with increased postoperative dysphagia.
Patients undergoing either one- or two-level ACDF (n=38) or posterior lumbar decompression (n=56) were prospectively followed. Baseline patient characteristics were recorded. A dysphagia questionnaire was administered preoperatively and during the 2-week, 6-week, and 12-week postoperative visits. We found no differences in patient age, body mass index, or the preoperative incidence and severity of dysphagia between the cervical and lumbar groups. We compared the incidence and severity of dysphagia between the patients who had cervical and lumbar surgery.
Postoperatively, 71% of patients having cervical spine surgery reported dysphagia at 2 weeks followup. This incidence decreased to 8% at 12 weeks followup. The incidence and severity of dysphagia were greater in the cervical group at 2 and 6 weeks followup with a trend toward greater dysphagia at 12 weeks followup. Body mass index, gender, location of surgery, and the number of surgical levels were not related to the risk of developing dysphagia. We observed a correlation between operative time and the severity of postoperative dysphagia.
Dysphagia is common after ACDF. The incidence and severity of postoperative dysphagia decreases over time, although symptoms may persist at least 12 weeks after surgery.
Level II, prospective, comparative study. See Guidelines for Authors for a complete description of levels of evidence.
现有研究表明,前路颈椎减压融合术(ACDF)后吞咽困难的发生率相对较高。然而,这些研究大多是回顾性的,缺乏对照组。
问题/目的:因此,我们(1)前瞻性地确定了使用腰椎减压患者作为对照组的 ACDF 后吞咽困难的发生率和严重程度;(2)确定哪些因素与术后吞咽困难增加有关。
前瞻性随访接受单节段或双节段 ACDF(n=38)或后路腰椎减压(n=56)的患者。记录基线患者特征。在术前和术后 2 周、6 周和 12 周就诊时进行吞咽困难问卷。我们发现颈椎组和腰椎组患者的年龄、体重指数或术前吞咽困难的发生率和严重程度无差异。我们比较了行颈椎和腰椎手术的患者的吞咽困难发生率和严重程度。
术后 2 周随访时,71%接受颈椎手术的患者报告吞咽困难。这一发生率在 12 周随访时降至 8%。颈椎组在 2 周和 6 周随访时吞咽困难的发生率和严重程度更高,12 周随访时吞咽困难的严重程度呈上升趋势。体重指数、性别、手术部位和手术节段数量与发生吞咽困难的风险无关。我们观察到手术时间与术后吞咽困难严重程度之间存在相关性。
ACDF 后吞咽困难很常见。尽管术后症状可能至少持续 12 周,但术后吞咽困难的发生率和严重程度随时间逐渐降低。
II 级,前瞻性,比较研究。有关证据水平的完整描述,请参见作者指南。