Literature DB >> 19966579

Characteristics of gastroesophageal reflux and potential risk of gastric content aspiration in children with cystic fibrosis.

K Blondeau1, A Pauwels, Lj Dupont, V Mertens, M Proesmans, R Orel, J Brecelj, M López-Alonso, Mj Moya, A Malfroot, E De Wachter, Y Vandenplas, B Hauser, D Sifrim.   

Abstract

OBJECTIVES: Increased gastroesophageal reflux (GER) is common in children with cystic fibrosis (CF). We studied the occurrence of acid, weakly acidic (WA), and weakly alkaline (WALK) reflux in children with CF and evaluated a possible surrogate marker for risk of gastric content aspiration. PATIENTS AND METHODS: Twenty-four children with CF underwent impedance-pH monitoring for detection of acid (pH < 4), WA (pH 4-7), and WALK-GER (pH > or = 7). In 11 children, cough was objectively recorded with esophageal manometry and the symptom association probability was calculated to determine the reflux-cough relation. Presence of bile acids (BA) was measured in the saliva of 65 patients with CF and 23 healthy children, respectively.
RESULTS: Sixteen of the 24 children had increased GER (esophageal acid exposure). The majority of reflux events were acidic in nature. WA reflux was less common and WALK reflux was rare. The sequence reflux-cough was found in 8 of the 11 children and 1 of 11 children had a positive symptom association probability for reflux-cough. The sequence cough-reflux was found in only 3 of the 11 children. Only a small fraction of the total esophageal acid and volume exposure was secondary to cough. Twenty-three of the 65 children with CF had BA in saliva compared with none of the healthy controls.
CONCLUSIONS: Although WA-GER is uncommon, acid GER is prevalent in children with CF. It is a primary phenomenon and is not secondary to cough. One third of the children with CF have BA in saliva, which may indicate an increased risk for aspiration. However, the impact of salivary BA and potential aspiration on CF pulmonary disease needs further investigation.

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Year:  2010        PMID: 19966579     DOI: 10.1097/MPG.0b013e3181acae98

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  18 in total

1.  [Gastroesophageal reflux diseases in childhood. Diagnosis and therapy].

Authors:  P Ahrens
Journal:  HNO       Date:  2012-03       Impact factor: 1.284

Review 2.  Canadian Digestive Health Foundation Public Impact Series: gastroesophageal reflux disease in Canada: incidence, prevalence, and direct and indirect economic impact.

Authors:  Richard N Fedorak; Sander Veldhuyzen van Zanten; Ron Bridges
Journal:  Can J Gastroenterol       Date:  2010-07       Impact factor: 3.522

3.  Gastroesophageal reflux causing nutritional failure and vomiting in a teenager with cystic fibrosis and respiratory failure.

Authors:  Alexandra Higton; Sarah Collins; Diana Bilton
Journal:  J R Soc Med       Date:  2011-07       Impact factor: 5.344

Review 4.  Gastroesophageal reflux in cystic fibrosis: current understandings of mechanisms and management.

Authors:  Hayat M Mousa; Frederick W Woodley
Journal:  Curr Gastroenterol Rep       Date:  2012-06

5.  Ion transport mechanisms linked to bicarbonate secretion in the esophageal submucosal glands.

Authors:  Solange Abdulnour-Nakhoul; Hani N Nakhoul; Medhat I Kalliny; Alex Gyftopoulos; Edd Rabon; Rienk Doetjes; Karen Brown; Nazih L Nakhoul
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-04-06       Impact factor: 3.619

6.  Children with cystic fibrosis have prolonged chemical clearance of acid reflux compared to symptomatic children without cystic fibrosis.

Authors:  Frederick W Woodley; Rodrigo S Machado; Don Hayes; Carlo Di Lorenzo; Ajay Kaul; Beth Skaggs; Karen McCoy; Alpa Patel; Hayat Mousa
Journal:  Dig Dis Sci       Date:  2013-11-28       Impact factor: 3.199

7.  Bile acids repress hypoxia-inducible factor 1 signaling and modulate the airway immune response.

Authors:  Claire Legendre; F Jerry Reen; David F Woods; Marlies J Mooij; Claire Adams; Fergal O'Gara
Journal:  Infect Immun       Date:  2014-06-09       Impact factor: 3.441

Review 8.  Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis.

Authors:  Diana A Freitas; Gabriela Ss Chaves; Thayla A Santino; Cibele Td Ribeiro; Fernando Al Dias; Ricardo O Guerra; Karla Mpp Mendonça
Journal:  Cochrane Database Syst Rev       Date:  2018-03-09

9.  Gastroesophageal reflux in cystic fibrosis across the age spectrum.

Authors:  Frederick W Woodley; Don Hayes; Benjamin T Kopp; Melissa Moore-Clingenpeel; Rodrigo Strehl Machado; Christopher J Nemastil; Sudarshan Jadcherla; Carlo Di Lorenzo; Ajay Kaul; Hayat Mousa
Journal:  Transl Gastroenterol Hepatol       Date:  2019-09-16

10.  Respiratory pathogens adopt a chronic lifestyle in response to bile.

Authors:  F Jerry Reen; David F Woods; Marlies J Mooij; Claire Adams; Fergal O'Gara
Journal:  PLoS One       Date:  2012-09-26       Impact factor: 3.240

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