| Literature DB >> 29110162 |
Yu-Min Kung1,2, Wen-Hung Hsu1,3, Meng-Chieh Wu1,4, Jiunn-Wei Wang1,4, Chung-Jung Liu1, Yu-Chung Su1,3, Chao-Hung Kuo1,3, Fu-Chen Kuo5, Deng-Chyang Wu1,3,4, Yao-Kuang Wang6,7.
Abstract
The management of proton pump inhibitor-refractory GERD (rGERD) is a challenge in clinical practice. Since up to one-third of patients with typical GERD symptoms (heartburn and/or acid regurgitation) are not satisfied with proton pump inhibitor (PPI) therapy, new drug development targeting different pathophysiologies of GERD is imperative. At present, no other drugs serve as a more potent acid suppression agent than PPIs. As an add-on therapy, histamine type-2 receptor antagonists, alginates, prokinetics and transient lower esophageal sphincter relaxation inhibitors have some impact on the subgroups of rGERD, but greater effectiveness and fewer adverse effects for widespread use are required. Visceral hypersensitivity also contributes to the perception of GERD symptoms, and neuromodulators including antidepressants play a role in this category. Esophageal pH-impedance monitoring helps to distinguish functional heartburn from true GERD, and psychologic medication and cognitive behavior therapy are further therapy options instead of PPIs.Entities:
Keywords: Alginate; CB1 receptor agonist/antagonist; Gastroesophageal reflux disease; Histamine type-2 receptor antagonist; Proton pump inhibitor
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Year: 2017 PMID: 29110162 DOI: 10.1007/s10620-017-4830-5
Source DB: PubMed Journal: Dig Dis Sci ISSN: 0163-2116 Impact factor: 3.199