Khajanchee Yashodhan S, O'Rourke Robert, Cassera Maria A, Gatta Prakash, Hansen Paul D, Swanström Lee L
Minimally Invasive Surgery Program, Department of Surgery, Legacy Health System, 1140 NW 22nd Ave, Ste 560, Portland, OR 97210, USA.
Arch Surg. 2007 Aug;142(8):785-901; discussion 791-2. doi: 10.1001/archsurg.142.8.785.
Laparoscopy has become the standard approach for surgical treatment of uncomplicated gastroesophageal reflux disease. Laparoscopic reintervention following failure of primary antireflux surgery (ARS) remains controversial. The purposes of this study were to assess outcomes in patients operated on for failed ARS, to describe reasons for failure of the primary surgery, and to identify factors predictive of failure of the revision.
Retrospective analysis of prospectively collected data.
Tertiary-care teaching hospital.
A total of 176 patients (20 with multiple ARS) undergoing laparoscopic reintervention between September 12, 1993, and August 1, 2006, for failed ARS.
Patients had preoperative subjective and/or objective documentation of failure after primary ARS: 131 patients had reoperative Nissen fundoplication, 28 patients had a partial wrap, and 17 patients had other procedures.
Preoperative and postoperative symptom scores and results of objective studies were prospectively collected. Postoperative patients with symptom scores of 2 or greater and/or abnormal 24-hour pH study results (DeMeester score > 14.7) were considered to have treatment failures. Logistic regression was performed to identify variables significant for poor outcomes.
Median follow-up was 9.2 months in 145 patients (82.4%). One hundred eight patients (74.5%) demonstrated excellent symptomatic outcomes (P = .001). Twenty of 37 patients with failures had reflux symptoms and 23 experienced dysphagia. Sixty-seven patients had 24-hour pH and manometry studies; 18 (11 asymptomatic) patients had a DeMeester score greater than 14.7. Odds of failure were higher among patients presenting with dysphagia (odds ratio, 3.38; 95% confidence interval, 1.35-8.40; P = .009) or requiring an esophageal-lengthening procedure (odds ratio, 5.77; 95% confidence interval, 1.38-24.11; P = .02).
Laparoscopic reintervention following failed primary ARS provides excellent subjective and objective outcomes in most patients. Patients having laparoscopic reintervention for dysphagia relief or those requiring an esophageal-lengthening procedure have a significantly greater chance of a poor outcome.
腹腔镜检查已成为单纯性胃食管反流病手术治疗的标准方法。初次抗反流手术(ARS)失败后的腹腔镜再次干预仍存在争议。本研究的目的是评估ARS失败后接受手术治疗患者的预后,描述初次手术失败的原因,并确定预测翻修手术失败的因素。
对前瞻性收集的数据进行回顾性分析。
三级护理教学医院。
1993年9月12日至2006年8月1日期间,共有176例(20例接受多次ARS)因ARS失败而接受腹腔镜再次干预的患者。
患者术前有初次ARS失败的主观和/或客观记录:131例患者接受再次手术Nissen胃底折叠术,28例患者接受部分包裹术,17例患者接受其他手术。
前瞻性收集术前和术后症状评分及客观研究结果。术后症状评分为2分或更高和/或24小时pH值研究结果异常(DeMeester评分>14.7)的患者被认为治疗失败。进行逻辑回归以确定对不良预后有显著影响的变量。
145例患者(82.4%)的中位随访时间为9.2个月。108例患者(74.5%)症状改善良好(P = .001)。37例失败患者中有20例有反流症状,23例有吞咽困难。67例患者进行了24小时pH值和测压研究;18例(11例无症状)患者的DeMeester评分大于14.7。出现吞咽困难的患者失败几率更高(优势比,3.38;95%置信区间,1.35 - 8.40;P = .009)或需要进行食管延长手术的患者失败几率更高(优势比,5.77;95%置信区间,1.38 - 24.11;P = .02)。
初次ARS失败后的腹腔镜再次干预在大多数患者中提供了良好的主观和客观预后。因缓解吞咽困难而接受腹腔镜再次干预的患者或需要进行食管延长手术的患者预后不良的几率明显更高。