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1  proton pump inhibitors (PPIs) began 24-hour esophageal pH and impedance monitoring and esophagoscopy
2 8 unselected patients, consisting of 24-hour esophageal pH and lower esophageal sphincter manometry.
3                                           An esophageal pH electrode also was placed and fluoroscopy
4 rom the 49 recordings of 24-hour gastric and esophageal pH from the Stanford study as well as from an
5 annot reduce PPIs should consider ambulatory esophageal pH/impedance monitoring before committing to
6                                   Control of esophageal pH improved after TF (mean 9.3% before and 6.
7 imilar effect on the percentage of time with esophageal pH < 4 [mean reduction: 68.5% (30 mg), 54.2%
8  subjects treated with a PPI, measuring time esophageal pH < 4 will significantly overestimate the pr
9  to perform a cost analysis of the available esophageal pH-metry methods.
10 swallow, esophagogastroduodenoscopy, 48-hour esophageal pH monitoring (off PPIs), and high-resolution
11 omatic assessment, esophageal manometry, and esophageal pH monitoring (using a probe with 2 sensors l
12      At 6 months, patients underwent 48-hour esophageal pH monitoring and esophagogastroduodenoscopy.
13 agnostic accuracy and reliability of 24-hour esophageal pH monitoring and how best to interpret pH te
14               All patients underwent 24-hour esophageal pH monitoring and upper endoscopy before rand
15                           Ambulatory 24-hour esophageal pH monitoring documented abnormal reflux in 3
16 may strongly affect the results of prolonged esophageal pH monitoring in GERD patients.
17                             Twenty-four-hour esophageal pH monitoring led to the understanding of the
18                                              Esophageal pH monitoring results were classified as norm
19 copic airway survey, bronchoalveolar lavage, esophageal pH monitoring, and a swallowing study.
20                      During dual gastric and esophageal pH monitoring, we observed that postprandial
21  a URS questionnaire before dual-probe, 24-h esophageal pH monitoring.
22  than IPF underwent dual-channel, ambulatory esophageal pH monitoring.
23 tion; 2) esophageal motility; and 3) 24-hour esophageal pH monitoring.
24 ent Heller alone were studied with a 24-hour esophageal pH probe and had a median Johnson-DeMeester s
25 th lower reflux, 36% of subjects with normal esophageal pH studies, and 9% of normal volunteers repor
26 uated by esophagogastroduodenoscopy, 24-hour esophageal pH studies, gastric-emptying tests, electroga
27                  Among the 115 children with esophageal pH studies, the prevalence of GER was 43%.
28 stroesophageal reflux disease by an abnormal esophageal pH study (body mass index <35 kg/m, hiatal he
29                            A subgroup had an esophageal pH study before randomization.
30                                    A 24-hour esophageal pH study should be considered in patients who
31 patients had abnormal results on the 24-hour esophageal pH study.
32 sthma patients without reflux symptoms, 24-h esophageal pH testing is required.
33                        Patients referred for esophageal pH testing were randomly assigned to WC with
34 symptoms using esophageal manometry and 24-h esophageal pH testing.
35 phic variables did not predict abnormal 24-h esophageal pH tests in asthma patients with asymptomatic
36 aphic variables do not predict abnormal 24-h esophageal pH tests in asthma patients without reflux sy
37              The prevalence of abnormal 24-h esophageal pH tests in asthma patients without reflux sy
38                             Dual gastric and esophageal pH tracings were analyzed from 40 dyspeptic p
39                                              Esophageal pH was measured, and pH data were analyzed an
40                                Manometry and esophageal pH were recorded for 30 minutes, after which

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