28天随机双盲安慰剂对照试验,使用预聚合交联硫糖铝屏障(esolgatate)治疗糜烂性反流

R. Mccullough
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引用次数: 0

摘要

背景:侵蚀性胃食管反流病(eGERD)的治疗以使用质子泵抑制剂(PPI)、组胺2受体拮抗剂(H2RA)和抗酸剂(AA)控制酸碱度为中心。然而,胃回流液中胆汁和丝氨酸蛋白酶的存在(PPI、H2RA或AA未解决)被怀疑与Barrett食管的发病和食管腺癌的发病有关。美国食品药品监督管理局首次将预聚合三氯蔗糖酯屏障疗法(PPSBT)视为一种医疗设备,它增强了生物粘附性,并阻断了酸性和非酸性刺激物进入粘膜。目的:评价PPSBT保护黏膜治疗糜烂性胃食管反流病的疗效。方法:在一项为期28天的统计支持、多中心随机双盲安慰剂对照试验中,19名eGERD患者被随机分为PPSBT或安慰剂组。每组都可以使用抗酸剂治疗突破性疼痛。评估对糜烂和eGERD症状(烧心和反流感)的治疗效果。对不良事件进行评估。结果:在服用PPSBT的患者中,89%和78%的患者胃灼热和反流症状得到缓解,而服用安慰剂的患者分别为25%和12.5%。服用PPSBT的患者中89%的患者完全治愈,而服用安慰剂的患者中这一比例为25%。未发生不良事件。结论:PPSBT增强的粘膜保护作用在eGERD患者中显示出有效的症状控制和侵蚀愈合。PPSBT对酸、胆汁和丝氨酸蛋白酶的无酸细胞保护作用可能是治疗eGERD的有用辅助手段,也是对未来的回归。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
28 Day Randomized Double-Blind Placebo Controlled Trial using Pre-Polymerized Cross-Linked Sucralfate Barrier (Esolgafate) for Erosive GERD
Background: Treatment of erosive gastroesophageal reflux disease (eGERD) centers on control of acid pH using proton pump inhibitors (PPI), histamine 2 receptor antagonists (H2RA) and antacids (AA). However, the presence of bile and serine proteases in gastric refluxate, not addressed by PPI, H2RA or AA, is suspected to be associated with onset of Barrett’s esophagus and rise of esophageal adenocarcinoma. Pre-polymerized sucralfate barrier therapy (PPSBT) recognized first by US FDA as a medical device has enhanced bio adherence and blocks access of acid and non-acid irritants to the mucosa. Aim: To evaluate the efficacy of mucosal protection by PPSBT for the treatment of erosive GERD. Methods: In a 28 day statistically powered, multi-center randomized double-blind placebo controlled trial, 19 patients with eGERD were randomized to receive PPSBT or placebo. Antacids were available to each group for breakthrough pain. Treatment effect on erosions and eGERD symptoms (heartburn & reflux sensation) were evaluated. Adverse events were assessed. Results: For patients taking PPSBT, 89% and 78% had relief of heartburn and reflux respectively compared to 25% and 12.5 % of those on placebo. Complete healing occurred in 89% taking PPSBT compared to 25% of those on placebo. No adverse events occurred. Conclusions: Enhanced mucosal protection by PPSBT demonstrates effective symptom control and erosion healing in patients with eGERD. Acid-indifferent cytoprotection from acid, bile and serine proteases by PPSBT may be a useful adjunct in management of eGERD, and a return to the past for the future.
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