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Gastroesophageal Reflux in Cystic Fibrosis and Non-CF Bronchiectasis

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Part of the book series: Respiratory Medicine ((RM,volume 2))

Abstract

Gastroesophageal reflux (GER) or the retrograde flow of gastric contents into the esophagus is a physiologic phenomenon that occurs most often after meals and is restricted to the distal esophagus [1, 2]. These occasional GER episodes are of brief duration, cleared rapidly, and generally well tolerated [3]. GER can be accompanied by typical symptoms, like heartburn and regurgitation, but also by atypical symptoms such as noncardiac chest pain, cough, wheezing, and ear, nose, and throat symptoms [1, 2]. Pathological GER or GERD (GER disease) has been described as the increased frequency or duration of exposure of the esophagus to regurgitated gastric contents [4]. Reflux has been clearly associated with the presence of esophagitis and Barrett’s esophagus, and it has also been implied in the pathophysiology of different respiratory disorders [5, 6]. This chapter deals with the literature data on the prevalence, mechanisms, and role of GER in cystic fibrosis as well as in non-CF bronchiectasis.

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Correspondence to Lieven Dupont M.D., Ph.D. .

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Pauwels, A., Sifrim, D., Dupont, L. (2012). Gastroesophageal Reflux in Cystic Fibrosis and Non-CF Bronchiectasis. In: Meyer, K., Raghu, G. (eds) Gastroesophageal Reflux and the Lung. Respiratory Medicine, vol 2. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4614-5502-8_9

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