The Rothman Institute, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA.
Spine (Phila Pa 1976). 2011 Nov 15;36(24):2039-44. doi: 10.1097/BRS.0b013e31821795f1.
Prospective controlled clinical study.
To determine the incidence and severity of GERD in patients undergoing anterior cervical decompression and fusion (ACDF), using patients undergoing posterior lumbar decompression as a control group.
The incidence gastroesophageal reflux disease (GERD) after anterior cervical decompression and fusion (ACDF) has not previously been studied.
Patients undergoing either 1- or 2-level ACDF (n = 38) or posterior lumbar decompression surgery (control group, n = 56) were prospectively enrolled. Baseline patient characteristics were recorded. Intraoperative and postoperative medical records were reviewed. A validated GERD measurement tool (GERD Impact Scale, GIS) and a dysphagia questionnaire (including a dysphagia numeric rating score, range, 0-10) were administered preoperatively, and during the 2-week, 6-week, and 12-week postoperative visits.
Cervical patients had a significantly higher incidence of GERD at 2 weeks than the lumbar patients (78.9% vs. 42.9%, P = 0.001). Cervical patients had a higher incidence of GERD at 6 and 12 weeks as well, but these differences were not statistically significant. The change in GIS score from baseline was significantly higher in the cervical group at all follow-up time periods. On average, cervical patients required 1.2 doses of antacid medication in the postoperative period, compared to an average of 0.5 doses required by lumbar patients (P = 0.006). There was a significant correlation between the severity of dysphagia and the GIS score at 2 weeks, but no correlation at 6 or 12 weeks. Operative time did not correlate with the GIS score at any of the follow-up time periods. The number of surgical levels (i.e., one vs. two) and level of surgery (i.e., above C5-C6 vs. at or below C5-C6) had no effect on the GIS score.
Compared to the lumbar control group, patients in the cervical group had increased incidence, and severity of GERD-like symptoms in the early postoperative period.
前瞻性对照临床试验。
通过与后路腰椎减压术作对照,确定前路颈椎减压融合术(ACDF)患者胃食管反流病(GERD)的发生率和严重程度。
前路颈椎减压融合术后 GERD 的发生率尚未见研究报道。
前瞻性纳入行单节段或双节段 ACDF(n=38)或后路腰椎减压术(对照组,n=56)的患者。记录基线患者特征。回顾术中及术后病历。术前及术后 2 周、6 周和 12 周时采用经过验证的 GERD 测量工具(胃食管反流病严重程度指数,GIS)和吞咽困难问卷(包括吞咽困难数字评分,范围 0-10)进行评估。
颈椎组患者在术后 2 周时 GERD 的发生率显著高于腰椎组(78.9% vs. 42.9%,P=0.001)。颈椎组在术后 6 周和 12 周时 GERD 的发生率也更高,但这些差异无统计学意义。颈椎组在所有随访时间点的 GIS 评分变化均显著高于腰椎组。颈椎组患者平均在术后需要 1.2 剂抗酸药物,而腰椎组平均需要 0.5 剂(P=0.006)。在术后 2 周时,吞咽困难的严重程度与 GIS 评分之间存在显著相关性,但在术后 6 周和 12 周时无相关性。手术时间与任何随访时间点的 GIS 评分均无相关性。手术节段数(即 1 节 vs. 2 节)和手术部位(即 C5-C6 以上 vs. C5-C6 及以下)对 GIS 评分均无影响。
与后路腰椎减压术对照组相比,颈椎组患者在术后早期 GERD 样症状的发生率和严重程度更高。