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GER in Cystic Fibrosis

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Gastroesophageal Reflux in Children

Abstract

Increased levels of gastroesophageal reflux (GER) are common among people with cystic fibrosis (CF). Multiple intraluminal impedance-pH (MII-pH) studies involving small sample sizes (n = 11–44) of children and adults with CF (not taking anti-reflux medications and no history of fundoplication) have shown that most children and adults with CF experienced increased GER. Among children, 46.4–81% were diagnosed with GERD disease (GERD). Among adults, 66.7–100% had GERD. Approximately two-thirds of the detected GER events were acidic (pH < 4) and a third of these events reached the proximal esophagus. The presence of proximally reaching GER episodes remains a constant concern for clinical management of GER in children and adults with CF. Data from the few available studies suggest that Nissen fundoplication decelerates lung function decline, improves weight gain, and reduces the frequency of pulmonary exacerbations. Future studies are needed to assess the impact of CFTR modulator therapy on GERD in people with CF.

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Woodley, F.W., Bass, R., Hayes, D., Kopp, B.T. (2022). GER in Cystic Fibrosis. In: Vandenplas, Y. (eds) Gastroesophageal Reflux in Children. Springer, Cham. https://doi.org/10.1007/978-3-030-99067-1_9

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