Institutional members access full text with Ovid®

Share this article on:

Safety and Efficacy of Wireless pH Monitoring in Patients Suspected of Gastroesophageal Reflux Disease: A Systematic Review

Kessels, Sharon J.M. MSc; Newton, Skye S. GDPH; Morona, Judy K. PhD; Merlin, Tracy L. PhD

Journal of Clinical Gastroenterology: October 2017 - Volume 51 - Issue 9 - p 777–788
doi: 10.1097/MCG.0000000000000843
Clinical Reviews

Introduction: The primary aim of this systematic review was to determine the safety, technical efficacy, and effectiveness of 48-hour wireless pH monitoring (WM) for gastroesophageal reflux disease (GERD), compared with no pH monitoring in patients who failed to tolerate a catheter. In the absence of eligible studies, the secondary aim was to determine these performance characteristics for WM relative to catheter-based pH monitoring (CBM) in patients suspected of GERD, who are able to tolerate a catheter.

Methods: A protocol was registered on the PROSPERO database (CRD42013005852) before conducting the systematic review, which included the study selection criteria, and critical appraisal methods. Several key databases were searched to identify eligible comparative studies.

Results: Chest pain occurred more often with WM compared with CBM; however, other adverse events were reported less frequently with WM. Technical failures, mostly due to attachment failures and early capsule detachments, were 3 times higher with WM, compared with CBM, [pooled relative risk (from meta-analysis)=3.3; 95% confidence interval, 1.63-6.81; I 2=0%; P=0.012; k=8). The sensitivity and specificity of WM varied widely, depending on type of analysis, monitoring time, capsule placement, reference standard, and diagnostic threshold.

Discussion: WM is usually better tolerated than CBM but has more technical problems. Test accuracy was highly variable between studies; therefore, conclusions could not be drawn regarding the performance of the 2 tests. To make meaningful comparisons between WM and CBM a consensus is needed on the diagnostic threshold for GERD, monitoring time, appropriate capsule positioning, and the reference standard.

Supplemental Digital Content is available in the text.

Adelaide Health Technology Assessment (AHTA), School of Public Health, The University of Adelaide, Adelaide, SA, Australia

S.J.M.K.: study concept and design, review and inclusion of studies, acquisition of data, analysis and interpretation of data, drafting of the manuscript. S.S.N.: critical review of study design (protocol) and findings, review and inclusion of studies, critical revision of the manuscript for important intellectual content, study supervision. J.K.M.: analysis and interpretation of data, revision of the manuscript for important intellectual content. T.L.M.: critical review of study design (protocol) and findings, revision of the manuscript for important intellectual content, study supervision.

The systematic review was commissioned by the Australian Government Department of Health.

The authors declare that they have nothing to disclose.

Address correspondence to: Sharon J.M. Kessels, MSc, Adelaide Health Technology Assessment (AHTA), School of Public Health, The University of Adelaide, Adelaide, SA 5000, Level 9, 57 North Terrace (Adelaide Health and Medical Sciences Building), Australia (e-mail: sharon.kessels@adelaide.edu.au).

Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved.