Interrogation of esophagogastric junction barrier function using the esophagogastric junction contractile integral: an observational cohort study.

Journal Article (Journal Article)

The esophagogastric junction contractile integral (EGJ-CI), designed similar to distal contractile integral (DCI), has been proposed as a metric to evaluate EGJ barrier function. We determined normative values and evaluated EGJ-CI in predicting esophageal acid exposure time (AET) and symptomatic outcome in this observational cohort study. High-resolution manometry (HRM) studies were reviewed in 188 patients (55.2 ± 0.9 years, 64% female) undergoing ambulatory pH monitoring off therapy. Dominant symptoms and global symptom severity (GSS) were determined on questionnaires initially and upon follow-up. EGJ-CI was measured using the DCI tool placed across the EGJ and compared to normal controls (n = 21, 27.6 ± 0.6 years, 52% female). EGJ-CI was calculated both for a single respiratory cycle (SRC, in and corrected for respiratory cycle (CRC, Univariate and multivariate analyses determined the predictive potential of EGJ-CI in terms of AET and post-therapy GSS at follow-up, controlling for medical versus surgical therapy. Mean EGJ-CI values were significantly lower when AET was abnormal; EGJ-CI/SRC and EGJ-CI/CRC were 86% concordant (r = 0.84). Using receiver operating characteristic analysis, values below 121.8 (EGJ-CI/SRC) and 39.3 (EGJ-CI/CRC) predicted abnormal AET best (sensitivity 0.61 and 0.65, specificity 0.61 and 0.57, respectively). On univariate and multivariate analysis, the EGJ-CI discriminated normal from abnormal AET better than conventional LES parameters (P ≤ 0.02). After 2.7 ± 0.1 years follow-up, EGJ-CI below identified thresholds predicted better symptom response to antireflux surgery compared to medical therapy (P = 0.009). EGJ-CI is a novel HRM metric that has potential to complement or replace currently used basal LES and EGJ parameters.

Full Text

Duke Authors

Cited Authors

  • Gor, P; Li, Y; Munigala, S; Patel, A; Bolkhir, A; Gyawali, CP

Published Date

  • October 2016

Published In

Volume / Issue

  • 29 / 7

Start / End Page

  • 820 - 828

PubMed ID

  • 26173375

Pubmed Central ID

  • PMC4757502

Electronic International Standard Serial Number (EISSN)

  • 1442-2050

Digital Object Identifier (DOI)

  • 10.1111/dote.12389


  • eng

Conference Location

  • United States