Response of Laryngopharyngeal Symptoms to Transoral Incisionless Fundoplication in Patients with Refractory Proven Gastroesophageal Reflux

被引:6
作者
Snow, Grace E. [1 ]
Dbouk, Mohamad [2 ]
Akst, Lee M. [1 ]
Ihde, Glenn [3 ]
Zarnegar, Rasa [4 ]
Janu, Peter [5 ]
Murray, Michael [6 ]
Eskarous, Hany [7 ]
Sohagia, Amit [7 ]
Dhar, Shumon I. [1 ]
Irene Canto, Marcia [8 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Div Laryngol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Div Gastrointestinal & Liver Pathol, Baltimore, MD 21205 USA
[3] Matagorda Reg Med Grp, Dept Gen Surg, Bay City, TX USA
[4] Weill Cornell Med Coll, New York, NY USA
[5] Fox Valley Surg Associates, Dept Surg, Appleton, WI USA
[6] Northern Nevada Med Ctr, Dept Surg, Sparks, NV USA
[7] Easton Hosp, Dept Med, Easton, PA USA
[8] Johns Hopkins Univ, Sch Med, Dept Med & Oncol, Div Gastroenterol, Baltimore, MD USA
关键词
laryngopharyngeal reflux; gastroesophageal reflux disease; transoral incisionless fundoplication; PUMP INHIBITOR THERAPY; TIF; 2.0; MANAGEMENT; DIAGNOSIS;
D O I
10.1177/00034894211037414
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Patients with laryngopharyngeal reflux (LPR) symptoms may not respond to proton pump inhibitors (PPI) if they have an alternative laryngeal diagnosis or high-volume reflux. Transoral incisionless fundoplication (TIF) or TIF with concomitant hiatal hernia repair (cTIF) are effective in decreasing symptoms of gastroesophageal reflux disease (GERD) but are not well studied in patients with LPR symptoms. This prospective multicenter study assessed the patient-reported and clinical outcomes after TIF/cTIF in patients with LPR symptoms and proven GERD. Methods: Patients with refractory LPR symptoms (reflux symptom index [RSI] > 13) and with erosive esophagitis, Barrett's esophagus, and/or pathologic acid reflux by distal esophageal pH testing were evaluated before and after a minimum of 6 months after TIF/cTIF. The primary outcome was normalization of RSI. Secondary outcomes were >50% improvement in GERD-Health-Related Quality of Life (GERD-HRQL), normalization of esophageal acid exposure time, discontinuation of PPI, and patient satisfaction. Results: Forty-nine patients had TIF (n = 26) or cTIF (n = 23) with at least 6 months follow-up. Mean pre- and post TIF/cTIF RSI were 23.6 and 5.9 (mean difference: 17.7, P < .001). Post TIF/cTIF, 90% of patients had improved GERD-HQRL score, 85% normalized RSI, 75% normalized esophageal acid exposure time, and 80% discontinued PPI. No serious procedure-related adverse events occurred. Patient satisfaction was 4% prior to TIF/cTIF and 73% after TIF/cTIF (P < .001). Conclusion: In patients with objective evidence of GERD, TIF, or cTIF are safe and effective in controlling LPR symptoms as measured by normalization of RSI and improvement in patient satisfaction after TIF/cTIF.
引用
收藏
页码:662 / 670
页数:9
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