Evaluation of post-operative dysphagia following anti-reflux surgery

被引:9
作者
Greenberg, Jacques A. [1 ]
Stefanova, Dessislava, I [1 ]
Reyes, Fernando Valle [1 ]
Edelmuth, Rodrigo C. L. [1 ]
Harik, Lamia [1 ]
Thiesmeyer, Jessica W. [1 ]
Egan, Caitlin E. [1 ]
Palacardo, Federico [1 ]
Liu, Mengyuan [1 ]
Christos, Paul [2 ]
Schnoll-Sussman, Felice H. [3 ]
Katz, Philip O. [3 ]
Finnerty, Brendan M. [1 ]
Fahey, Thomas J., III [1 ]
Zarnegar, Rasa [1 ]
机构
[1] New York Presbyterian Hosp, Weill Cornell Med Coll, Dept Surg, Div Endocrine & Minimally Invas Surg, 525 East 68th St,K-836, New York, NY 10065 USA
[2] New York Presbyterian Hosp, Weill Cornell Med Coll, Dept Populat Hlth Sci, Div Biostat, New York, NY USA
[3] New York Presbyterian Hosp, Weill Cornell Med Coll, Dept Med, Div Gastroenterol & Hepatol, New York, NY USA
来源
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES | 2022年 / 36卷 / 07期
关键词
EndoFLIP (TM); Dysphagia; Hiatal hernia; Gastroesophageal reflux disease; OUTCOMES; MYOTOMY;
D O I
10.1007/s00464-021-08888-y
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Anti-reflux surgery (ARS) has known long-term complications, including dysphagia, bloat, and flatulence, among others. The factors affecting the development of post-operative dysphagia are poorly understood. We investigated the correlation of intra-operative esophagogastric junction (EGJ) characteristics and procedure type with post-operative dysphagia following ARS. Methods Robotic ARS was performed on 197 consecutive patients with pathologic reflux utilizing EndoFLIP (TM) technology. Intraoperative EGJ measurements including distensibility index (DI), cross-sectional area (CSA), and high-pressure zone (HPZ) length were collected. Dysphagia was assessed pre-operatively and at 3 months post-operatively. Results The median pre-operative DI for all procedures was 2.6 (IQR 1.6-4.5) mm(2)/mmHg. There was no difference in post-operative DI between procedures [Hill: 0.9 (IQR 0.7-1.1) mm(2)/mmHg, Nissen: 1.0 (IQR 0.7-1.4) mm(2)/mmHg, Toupet: 1.2 (IQR 0.8-1.5) mm(2)/mmHg, Linx: 1.0 (IQR 0.7-1.2) mm(2)/mmHg, p = 0.24], whereas post-operative HPZ length differed by augmentation type [Hill: 3 (IQR 2.8-3) cm, Nissen: 3.5 (IQR 3-3.5) cm, Toupet: 3 (IQR 2.5-3.5) cm, Linx: 2.5 (IQR 2.5-3) cm, p = 0.032]. Eighty-nine patients (45.2%) had pre-operative dysphagia. Thirty-two patients (27.6%) reported any dysphagia at their 3-month post-operative visit and 12 (10.3%) developed new or worsening post-operative dysphagia [Hill: 2/18 (11.1%), Nissen: 2/35 (5.7%), Toupet: 4/54 (7.4%), Linx: 4/9 (44.4%), p = 0.006]. The median pre-operative and post-operative DI of patients who developed new or worsening dysphagia was 2.0 (IQR 0.9-3.8) mm(2)/mmHg and 1.2 (IQR 1.0-1.8) mm(2)/mmHg, respectively, and that of those who did not was 2.5 (IQR 1.6-4.0) mm(2)/mmHg and 1.0 (IQR 0.7-1.4) mm(2)/mmHg (p = 0.21 and 0.16, respectively). Conclusions Post-operative DI was similar between procedures, and there was no correlation with new or worsening post-operative dysphagia. Linx placement was associated with higher rates of new or worsening post-operative dysphagia despite a shorter post-procedure HPZ length and similar post-operative DI when compared to other methods of LES augmentation.
引用
收藏
页码:5456 / 5466
页数:11
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