Literature DB >> 12118204

Frequency, consequences and pharmacological treatment of gastroesophageal reflux in children with cystic fibrosis.

Jacek Brodzicki1, Maria Trawińska-Bartnicka, Maria Korzon.   

Abstract

BACKGROUND: Gastroesophageal reflux (GER) may aggravate chronic bronchopulmonary diseases. The study evaluated GER frequency and characteristics in children with Cystic Fibrosis (CF) as well as its consequences and pharmacological treatment. MATERIAL/
METHODS: 40 CF children aged 1.3 to 20 years were examined. The study methodology involved: medical files analysis, anamnesis, physical examination, growth status estimation, esophageal pH-metry and upper gastrointestinal tract endoscopy with histological examination of esophageal biopsies.
RESULTS: Based on pH-metry results, the diagnosis of GER was established in 22 children (55%). Mild GER (Index Reflux - IR 5-10%) was found in 12 children (54.5%), moderate GER (IR 10-20%) in 7 (31.8%) and severe GER (IR>20%) in 3 (13.6%). Ten patients with moderate or severe GER underwent endoscopy, which revealed GER-related esophagitis in 8 cases. There was no statistical difference of GER frequency and degree according to: age, sex, growth status, presence of type DF508 mutation in CFTR genome and typical GERD symptoms. According to the ESPGAN proposition, cisapride or cisapride with ranitidine medication was instituted. Treatment analysis was performed in 19 cases after successful follow-up examinations carried out three months later, indicating a significant decrease in reflux index, the longest episode duration and the number of episodes longer than 5 minutes. Improvement of endoscopic picture was noticed after treatment.
CONCLUSIONS: High frequency of gastroesophageal reflux and its consequences among children with cystic fibrosis, as well as the possibility of well-tolerated and efficient treatment of GER, indicate that diagnostics of GER among children with CF should be obligatory.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12118204

Source DB:  PubMed          Journal:  Med Sci Monit        ISSN: 1234-1010


  12 in total

Review 1.  The Great ESKAPE: Exploring the Crossroads of Bile and Antibiotic Resistance in Bacterial Pathogens.

Authors:  Kevin S Gipson; Kourtney P Nickerson; Eliana Drenkard; Alejandro Llanos-Chea; Snaha Krishna Dogiparthi; Bernard B Lanter; Rhianna M Hibbler; Lael M Yonker; Bryan P Hurley; Christina S Faherty
Journal:  Infect Immun       Date:  2020-09-18       Impact factor: 3.441

2.  Monitoring of serum prolactin in pediatric patients with cystic fibrosis who are receiving domperidone.

Authors:  Eva Cho; Sharon Ho; Patricia Gerber; A George F Davidson
Journal:  Can J Hosp Pharm       Date:  2009-03

Review 3.  Gastroesophageal reflux disease in children with asthma: treatment implications.

Authors:  Mark D Scarupa; Nanako Mori; Brendan J Canning
Journal:  Paediatr Drugs       Date:  2005       Impact factor: 3.022

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.  Objective measurement of cough during pulmonary exacerbations in adults with cystic fibrosis.

Authors:  J A Smith; E C Owen; A M Jones; M E Dodd; A K Webb; A Woodcock
Journal:  Thorax       Date:  2006-01-31       Impact factor: 9.139

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.  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

8.  Effect of esomeprazole versus placebo on pulmonary exacerbations in cystic fibrosis.

Authors:  Emily Dimango; Patricia Walker; Claire Keating; Maria Berdella; Newell Robinson; Elinor Langfelder-Schwind; Diane Levy; Xinhua Liu
Journal:  BMC Pulm Med       Date:  2014-02-15       Impact factor: 3.317

9.  Microbiological profiles of sputum and gastric juice aspirates in Cystic Fibrosis patients.

Authors:  H Al-Momani; A Perry; C J Stewart; R Jones; A Krishnan; A G Robertson; S Bourke; S Doe; S P Cummings; A Anderson; T Forrest; S M Griffin; M Brodlie; J Pearson; C Ward
Journal:  Sci Rep       Date:  2016-06-01       Impact factor: 4.379

10.  Nontuberculous mycobacteria in gastrostomy fed patients with cystic fibrosis.

Authors:  H Al-Momani; A Perry; R Jones; S Bourke; S Doe; J Perry; A Anderson; T Forrest; I Forrest; M Griffin; M Brodlie; J Pearson; C Ward
Journal:  Sci Rep       Date:  2017-04-24       Impact factor: 4.379

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.