| Literature DB >> 29991945 |
Hongfei Fang1, Don C Codipilly1, Karthik Ravi2, Dale C Ekbom3, Jan L Kasperbauer3, Magnus Halland2.
Abstract
INTRODUCTION: Idiopathic subglottic stenosis represents a spectrum of subglottic disease without a clear underlying cause. Prior studies have implicated a pathogenic role of gastroesophageal reflux disease in idiopathic subglottic stenosis. The aim of this study was to examine the presence and pattern of gastroesophageal reflux in a large cohort of patients with idiopathic subglottic stenosis at a tertiary referral center.Entities:
Year: 2018 PMID: 29991945 PMCID: PMC6016176 DOI: 10.1155/2018/8563697
Source DB: PubMed Journal: Gastroenterol Res Pract ISSN: 1687-6121 Impact factor: 2.260
Patient demographics.
|
| |
|---|---|
| Mean age (years) | 54.8 ± 11.5 |
| % female | 97.6 |
| BMI | 30.9 ± 8.8 |
| On PPI | 24 (58.5%) |
| 20 mg/day | 1 |
| Airway symptoms | 46.3% |
BMI: body mass index; PPI: proton pump inhibitor; airway symptoms: shortness of breath and dyspnea.
Comparison between abnormal and normal pH impedance studies in idiopathic subglottic stenosis patients.
| Abnormal ( | Normal ( |
| |
|---|---|---|---|
| Acid exposure (pH) | |||
|
| |||
| Total | 8.9 ± 6.4 | 0.9 ± 1.4 | <0.0001 |
| Upright | 11.3 ± 9.5 | 1.25 ± 1.6 | 0.0002 |
| Supine | 4.8 ± 8.9 | 0.1 ± 0.3 | 0.0334 |
|
| |||
| Total | 84.9 ± 99.3 | 15.3 ± 14.0 | 0.0007 |
| Upright | 58.8 ± 33.3 | 13.2 ± 13.6 | <0.0001 |
| Supine | 26.4 ± 77.1 | 2.0 ± 5.8 | 0.1859 |
|
| 32.6 ± 26.0 | 3.6 ± 3.9 | 0.0001 |
| Reflux episode activity (impedance) | |||
|
| 81.47 ± 48.6 | 26.4 ± 18.1 | 0.0001 |
|
| |||
| Acid | 49 ± 36.3 | 8.2 ± 9.0 | 0.0001 |
| Nonacid | 27.5 ± 59.3 | 15.0 ± 12.4 | 0.3775 |
|
| |||
| Acid | 3.9 ± 5.0 | 0.7 ± 1.8 | 0.0148 |
| Nonacid | 1.1 ± 2.6 | 2.5 ± 5.7 | 0.3265 |
| Airway symptoms | 57.9% | 42.1% | 0.1715 |
| BMI | 30.4 ± 8.9 | 31.3 ± 8.9 | 0.7544 |
| On PPI | 47.4% | 68.2% | 0.1763 |
| MVV | |||
|
| 48.5 ± 19.7 | 44.6 ± 20.9 | 0.5430 |
|
| 56.5 ± 20.6 | 57.0 ± 21.9 | 0.9435 |
BMI: body mass index; PPI: proton pump inhibitor; MVV: maximum voluntary ventilation.
Figure 1Distribution of GERD phenotypes.
Figure 2Number of reflux events among patients with upright and supine GERD phenotypes.