A review of medical therapy for proton pump inhibitor nonresponsive gastroesophageal reflux disease

被引:40
|
作者
Hillman, L. [1 ]
Yadlapati, R. [2 ]
Thuluvath, A. J. [3 ]
Berendsen, M. A. [4 ]
Pandolfino, J. E. [2 ]
机构
[1] Northwestern Univ, Dept Med, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Med, Div Gastroenterol & Hepatol, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Johns Hopkins Bayview Med Ctr, Dept Med, Baltimore, MD USA
[4] Northwestern Univ, Feinberg Sch Med, Galter Hlth Sci Lib, Chicago, IL 60611 USA
来源
DISEASES OF THE ESOPHAGUS | 2017年 / 30卷 / 09期
关键词
adjunctive medication; rapid metabolizer; refractory gastroesophageal reflux disease; RANDOMIZED CLINICAL-TRIAL; ADD-ON THERAPY; DOUBLE-BLIND; CYP2C19; POLYMORPHISM; INTRAGASTRIC PH; GENETIC POLYMORPHISMS; AGONIST REVEXEPRIDE; PERSISTENT SYMPTOMS; EROSIVE ESOPHAGITIS; COST-EFFECTIVENESS;
D O I
10.1093/dote/dox055
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Up to 40% of patients report persistent gastroesophageal reflux disease (GERD) symptoms despite proton pump inhibitor (PPI) therapy. This review outlines the evidence for medical therapy for PPI nonresponsive GERD. A literature search for GERD therapies from 2005 to 2015 in PubMed, EMBASE, Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews identified 2928 unique citations. Of those, 40 unique articles specific to the impact of PPI metabolizer genotype on PPI response and the use adjunctive medical therapies were identified. Thirteen articles reported impacts on CYP genotypes on PPI metabolism demonstrating lower endoscopic healing rates in extensive metabolizers; however, outcomes across genotypes were more uniform with more CYP independent PPIs rabeprazole and esomeprazole. Twenty-seven publications on 11 adjunctive medications showed mixed results for adjunctive therapies including nocturnal histamine-2 receptor antagonists, promotility agents, transient lower esophageal sphincter relaxation inhibitors, and mucosal protective agents. Utilizing PPI metabolizer genotype or switching to a CYP2C19 independent PPI is a simple and conservative measure that may be useful in the setting of incomplete acid suppression. The use of adjunctive medications can be considered particularly when the physiologic mechanism for PPI nonresponse is suspected. Future studies using adjunctive medications with improved study design and patient enrollment are needed to better delineate medical management options before proceeding to antireflux interventions.
引用
收藏
页码:1 / 15
页数:18
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