巴雷特食管内镜治疗前、中、后胃酸/胆汁反流的医学处理:叙述性回顾

T. Jaswani, Ashton Ellison, V. Konda
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引用次数: 1

摘要

:食管远端反流造成的持续性损伤是Barrett食管(BE)的一个已知原因。胃酸可通过炎症介质如环氧合酶-2、c-myc和促分裂原活化蛋白激酶信号传导引起食管远端炎症。胆汁酸暴露于食管粘膜也会通过在酸性pH下非电离、进入细胞和通过炎症细胞毒性途径造成粘膜损伤而造成损伤。胆汁酸还上调原癌基因和c-myc。阻抗pH监测定义的酸抑制不足是一个可改变的风险因素,如果不加以控制,将增加肠化生(IM)复发的风险。研究表明,严格的酸控制方案与内镜根除治疗(EET)相结合可以减少IM的复发。我们建议接受EET的患者采用以下药物治疗方案:继续每天两次质子泵抑制剂(PPI),服用液体制剂三氯福,胃肠道利多卡因混合物制剂,根据需要与膳食和零食一起局部使用,并在EET后1-2天进行流质饮食,然后一周内进行软性饮食。如果需要,可以使用对乙酰氨基酚和/或其他非NSAIDS产品进行镇痛。饮食和生活方式的改变也应该与这些建议一起讨论。在EET前后,我们推荐抗反流方案,包括每天两次PPI和优化饮食、生活方式和辅助药物。通过将巴雷特氏症的成功根除与警惕的监测和最佳的抗反流控制相结合,这最终可以改善患者的预后,减少发育不良和IM的复发。
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Medical management of acid/bile reflux before, during and after endoscopic therapy for Barrett’s esophagus: a narrative review
: Persistent injury from reflux to the distal esophagus is a known cause of Barrett’s esophagus (BE). Gastric acid can cause inflammation of the distal esophagus through inflammatory mediators such as cyclo-oxygenase-2, c-myc and mitogen-activated protein kinase signaling. Bile acid exposure to the esophageal mucosa can also exert damage by becoming non- ionized at acidic pH, entering cells and exerting mucosal injury through inflammation cytotoxic pathways. Bile acids also upregulate proto-oncogenes and c-myc. Inadequate acid suppression defined by impedance-pH monitoring is a modifiable risk factor and if left uncontrolled, will increase the risk of recurrence of intestinal metaplasia (IM). It has been shown that a rigorous acid control protocol in combination with endoscopic eradication therapy (EET) can reduce the recurrence of IM. We suggest the following medical treatment regimen for patients undergoing EET: to continue twice daily proton pump inhibitor (PPI), take liquid preparation sucralfate, a GI lidocaine cocktail mixture preparation for topical use as needed with meals and snacks, and a liquid diet for 1–2 days followed by a soft diet for up to a week after EET. Analgesia may be provided with acetaminophen and/or other non NSAIDS products if needed. Diet and lifestyle modifications should also be discussed alongside these recommendations. Both before and after EET, we recommend antireflux protocols including twice daily PPI and optimization of diet, lifestyle and adjunctive medications. By combining successful eradication of Barrett’s with a vigilant surveillance monitoring and optimal antireflux control, this can ultimately lead to improved patient outcomes and decrease recurrence of dysplasia and IM.
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