Laryngopharyngeal Reflux Study Group of Young-Otolaryngologists of the International Federations of Oto-rhino-laryngological Societies (YO-IFOS), Paris, France.
Department of Human Anatomy and Experimental Oncology, Faculty of Medicine, UMONS Research Institute for Health Sciences and Technology, University of Mons (UMons), Mons, Belgium.
Ann Otol Rhinol Laryngol. 2021 Sep;130(9):996-1003. doi: 10.1177/0003489420986347. Epub 2021 Jan 19.
To study the profile and the therapeutic response of patients with laryngopharyngeal reflux (LPR) at the hypopharyngeal-esophageal multichannel intraluminal impedance-pH monitoring (HEMII-pH) according to the initial pepsin saliva concentration.
From January 2018 to January 2020, patients with positive LPR diagnosis at the HEMII-pH were consecutively recruited from 3 European Hospitals. Saliva pepsin concentration (Peptest™) was measured during the HEMII-pH testing period and patients were classified into 2 groups: negative versus positive Peptest. The clinical outcomes, that is, gastrointestinal and HEMII-pH findings, reflux symptom score-12 (RSS-12), and 3-month therapeutic response, were compared between groups.
A total of 124 patients completed the study. Among them, 30 patients had negative Peptest. Pharyngeal reflux events occurred outside 1-hour post-meal time in 74.0%, after the meals in 20.5% and nighttime in 5.5%. The pepsin saliva level was not significantly associated with the reflux events preceding the sample collection. Patients with positive Peptest had better improvement of RSS-12 digestive and respiratory subscores and oral, pharyngeal, and laryngeal findings compared with patients with negative Peptest.
Patients with high saliva pepsin concentration had no stronger gastrointestinal, HEMII-pH, or clinical outcomes compared with those with low or undetectable saliva pepsin concentration.
根据初始唾液胃蛋白酶浓度,研究喉咽反流(LPR)患者在食管多通道腔内阻抗-pH 监测(HEMII-pH)中的特征和治疗反应。
本研究纳入了 2018 年 1 月至 2020 年 1 月期间在欧洲 3 家医院连续就诊的 HEMII-pH 阳性的 LPR 患者。在 HEMII-pH 检测期间测量唾液胃蛋白酶浓度(Peptest™),并将患者分为 2 组:Peptest 阴性组和阳性组。比较两组间的临床结局,即胃肠道和 HEMII-pH 结果、反流症状评分-12(RSS-12)和 3 个月的治疗反应。
共有 124 例患者完成了研究。其中,30 例患者 Peptest 阴性。74.0%的患者发生在餐后 1 小时以外的咽部反流事件,20.5%的患者发生在餐后,5.5%的患者发生在夜间。胃蛋白酶唾液水平与样本采集前的反流事件无显著相关性。与 Peptest 阴性患者相比,Peptest 阳性患者的 RSS-12 消化和呼吸亚评分以及口腔、咽部和喉部发现均有更好的改善。
与低水平或无法检测到唾液胃蛋白酶浓度的患者相比,高唾液胃蛋白酶浓度的患者在胃肠道、HEMII-pH 或临床结局方面并没有更强的表现。