Literature DB >> 16210125

Gastroesophageal reflux (symptomatic and silent): a potentially significant problem in patients with cystic fibrosis before and after lung transplantation.

Brenda M Button1, Stuart Roberts, Tom C Kotsimbos, Bronwyn J Levvey, Trevor J Williams, Michael Bailey, Gregory I Snell, John W Wilson.   

Abstract

BACKGROUND: The significance of gastroesophageal reflux (GER) and aspiration are unclear in cystic fibrosis (CF) and may contribute to declining lung function before and after lung transplantation (LTx).
METHODS: We sought to establish whether GER occurs in patients with CF on the LTx waiting list and after LTx. We then investigated whether GER correlates with patients' symptoms. Adults with CF on the waiting list and after LTx were prospectively recruited. Completion of a valid, structured symptom questionnaire was followed by ambulatory, dual-probe, 24-hour esophageal pH monitoring.
RESULTS: Twenty-four patients were studied, including 11 (6 males) in the pre-LTx group and 13 (9 males) in the post-LTx group. The pre-LTx group was 29.3 +/- 8.2 years of age, and the post-LTx group was 32.7 +/- 8.2 years of age. DeMeester score (normal value <14.7) was 36.6 +/- 22.3 for the pre-LTx group and 40.0 +/- 37.3 for the post-LTx group. Proximal esophageal acid exposure was significantly higher in both CF groups compared with normal. Symptom scores (normal <4, range -2 to 18) were: pre-LTx group, 5.8 +/- 6.5; post-LTx group, 7.7 +/- 5.4. Percent forced expiratory volume in 1 second (FEV1%) predicted was: pre-LTx group, 31.3 +/- 7.8; post-LTx group, 65.2 +/- 29.3. In the pre-LTx group, 10 of 11 (90.9%) patients had significant GER on monitoring, including 4 (40%) with symptomatic GER and 6 (60%) with silent GER. In the post-LTx group, 11 of 13 (84.6%) had significant GER on monitoring, including 9 (82%) with symptomatic GER and 2 (18%) with silent GER.
CONCLUSIONS: GER, symptomatic and silent, is a significant problem in CF. This condition should be aggressively treated and surgery should be considered if GER persists on re-testing.

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Mesh:

Year:  2005        PMID: 16210125     DOI: 10.1016/j.healun.2004.11.312

Source DB:  PubMed          Journal:  J Heart Lung Transplant        ISSN: 1053-2498            Impact factor:   10.247


  31 in total

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Authors:  Michael Wilschanski; Peter R Durie
Journal:  Gut       Date:  2007-04-19       Impact factor: 23.059

Review 2.  Structure and function of the mucus clearance system of the lung.

Authors:  Brenda M Button; Brian Button
Journal:  Cold Spring Harb Perspect Med       Date:  2013-08-01       Impact factor: 6.915

3.  Adenosine A₂A agonist improves lung function during ex vivo lung perfusion.

Authors:  Abbas Emaminia; Damien J Lapar; Yunge Zhao; John F Steidle; David A Harris; Victor E Laubach; Joel Linden; Irving L Kron; Christine L Lau
Journal:  Ann Thorac Surg       Date:  2011-10-31       Impact factor: 4.330

4.  Neuroendocrine Cell Hyperplasia of Infancy. Clinical Score and Comorbidities.

Authors:  Deborah R Liptzin; Kaci Pickett; John T Brinton; Amit Agarwal; Martha P Fishman; Alicia Casey; Christopher T Towe; Jane B Taylor; Geoffrey Kurland; James S Hagood; Jennifer Wambach; Ruma Srivastava; Hani Al-Saleh; Sharon D Dell; Lisa R Young; Robin R Deterding
Journal:  Ann Am Thorac Soc       Date:  2020-06

5.  Early outcomes of antireflux surgery for United States lung transplant recipients.

Authors:  Arman Kilic; Ashish S Shah; Christian A Merlo; Christine G Gourin; Anne O Lidor
Journal:  Surg Endosc       Date:  2012-12-28       Impact factor: 4.584

6.  Gastrointestinal surgery in adult patients with cystic fibrosis.

Authors:  Abhiram Sharma; Alison Morton; Daniel Peckham; David Jayne
Journal:  Frontline Gastroenterol       Date:  2012-07-13

7.  Relevance of GERD in lung transplant patients.

Authors:  Veerle Mertens; Lieven Dupont; Daniel Sifrim
Journal:  Curr Gastroenterol Rep       Date:  2010-06

8.  Symptomatic gastroesophageal reflux disease after lung transplantation.

Authors:  Ezequiel J Molina; Scott Short; Glen Monteiro; John P Gaughan; Mahender Macha
Journal:  Gen Thorac Cardiovasc Surg       Date:  2009-12

Review 9.  Patterns of gastrointestinal disease associated with mutations of CFTR.

Authors:  Michael Wilschanski
Journal:  Curr Gastroenterol Rep       Date:  2008-06

10.  Cough in adult cystic fibrosis: diagnosis and response to fundoplication.

Authors:  Hosnieh Fathi; Tanya Moon; Jo Donaldson; Warren Jackson; Peter Sedman; Alyn H Morice
Journal:  Cough       Date:  2009-01-18
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