Published ahead of print on December 18, 2008, doi:10.1164/rccm.200808-1359OC Am. J. Respir. Crit. Care Med., Volume 179, Number 5, March 2009, 408-413 A more recent version of this article appeared on March 1, 2009
Submitted on August 28, 2008 Gastro-Esophageal Reflux and Pulmonary Fibrosis in Scleroderma: A Study Using pH-Impedance MonitoringEdoardo Savarino1*,1 Division of Gastroenterology, Department of Internal Medicine, University of Genoa, Genoa, Italy, 2 Division of Clinical Immunology, Department of Internal Medicine, University of Genoa, Genoa, Italy, 3 Division of Gastroenterology and Hepatology, Department of Internal Medicine, University Hospital Zurich, Zurich, Switzerland, 4 Department of Radiology, University of Genoa, Genoa, Italy * To whom correspondence should be addressed. E-mail: esavarino{at}libero.it.
Introduction:
Interstitial lung disease (ILD) in systemic sclerosis (SSc) patients is associated with increased morbidity and mortality. Gastro-esophageal reflux (GER) is considered a contributing factor in the pathogenesis of ILD.
Aim:
To characterize gastro-esophageal reflux (acid and non-acid) in SSc patients with and without ILD.
Methods:
Patients with SSc underwent pulmonary high-resolution computer tomography (HRCT) scan and 24-h impedance-pH monitoring off-PPI therapy. The presence of pulmonary fibrosis was assessed using validated HRCT-scores. Reflux monitoring parameters included number of acid and non-acid reflux episodes, proximal migration of the refluxate and distal esophageal acid exposure. Unless otherwise specified data are presented as median [25th -75th percentile].
Results:
Forty consecutive SSc patients (35 female; mean age 53 years; range 24-71; 15 diffuse and 25 limited SSc) were investigated. Eighteen (45%) SSc patients had pulmonary fibrosis (HRCT score Key words: systemic sclerosis pulmonary fibrosis impedance pH-metry acid and nonacid reflux
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