Gastro-oesophageal reflux disease

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作者
Ronnie Fass
Guy E. Boeckxstaens
Hashem El-Serag
Rachel Rosen
Daniel Sifrim
Michael F. Vaezi
机构
[1] Case Western Reserve University,The Esophageal and Swallowing Center, Division of Gastroenterology and Hepatology, MetroHealth Medical System
[2] University of Leuven,Translational Research Center for Gastrointestinal Disorders (TARGID)
[3] Baylor College of Medicine,Department of Medicine
[4] Harvard Medical School,Division of Gastroenterology, Hepatology and Nutrition, Boston Children’s Hospital
[5] Queen Mary University of London,Wingate Institute of Neurogastroenterology, Royal London Hospital, Barts and The London School of Medicine and Dentistry
[6] Vanderbilt University Medical Center,Division of Gastroenterology, Hepatology, and Nutrition
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摘要
Gastro-oesophageal reflux disease (GERD) is a common disorder in adults and children. The global prevalence of GERD is high and increasing. Non-erosive reflux disease is the most common phenotype of GERD. Heartburn and regurgitation are considered classic symptoms but GERD may present with various atypical and extra-oesophageal manifestations. The pathophysiology of GERD is multifactorial and different mechanisms may result in GERD symptoms, including gastric composition and motility, anti-reflux barrier, refluxate characteristics, clearance mechanisms, mucosal integrity and symptom perception. In clinical practice, the diagnosis of GERD is commonly established on the basis of response to anti-reflux treatment; however, a more accurate diagnosis requires testing that includes upper gastrointestinal tract endoscopy and reflux monitoring. New techniques and new reflux testing parameters help to better phenotype the condition. In children, the diagnosis of GERD is primarily based on history and physical examination and treatment vary with age. Treatment in adults includes a combination of lifestyle modifications with pharmacological, endoscopic or surgical intervention. In refractory GERD, optimization of proton-pump inhibitor treatment should be attempted before a series of diagnostic tests to assess the patient’s phenotype.
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