GERD is a common condition worldwide. Key mechanisms of disease include abnormal oesophagogastric junction structure and function, and impaired oesophageal clearance. A therapeutic trial of acid-suppressive PPI therapy is often the initial management, with endoscopy performed in the setting of alarm symptoms and to exclude other conditions. If symptoms persist and endoscopy does not reveal evidence of GERD, oesophageal function tests are performed, including oesophageal manometry and ambulatory reflux monitoring. However, reflux episodes can be physiological, and some findings on endoscopy and manometry can be encountered in asymptomatic individuals without GERD symptoms. The diagnosis of GERD on the basis of functional oesophageal testing has been previously reported, but no updated expert recommendations on indications and the interpretation of oesophageal function testing in GERD has been made since the Porto consensus over a decade ago. In this Consensus Statement, we aim to describe modern oesophageal physiological tests and their analysis with an emphasis on establishing indications and consensus on interpretation parameters of oesophageal function testing for the evaluation of GERD in clinical practice. This document reflects the collective conclusions of the international GERD working group, incorporating existing data with expert consensus opinion.
GERD consists of troublesome symptoms or mucosal damage resulting from retrograde movement of gastric content through an incompetent oesophagogastric junction (EGJ)1. GERD is one of the most common gastrointestinal ailments worldwide; up to 40% of the US population report oesophageal symptoms intermittently and 10–20% have at least weekly symptoms2,3.
Typical GERD symptoms consist of heartburn and regurgitation, and clinical diagnosis is made on the basis of typical symptoms, supported by symptom response from empiric PPI therapy4,5. Alarm symptoms (for example, dysphagia, weight loss, anaemia), atypical presentations (including chest pain, laryngeal symptoms) or lack of response to empiric therapy prompt further evaluation with an upper endoscopy (EGD; oesophagogastroduodenoscopy)4,6. If symptoms persist despite empiric therapy, and EGD does not reveal evidence of GERD (oesophagitis, peptic oesophageal stricture, Barrett mucosa), oesophageal function tests are performed, including oesophageal manometry and ambulatory reflux monitoring7. However, reflux episodes can be physiological, and some findings on endoscopy (Los Angeles (LA) classification grade A or B reflux oesophagitis8) and manometry (hypotensive EGJ, ineffective oesophageal manometry) can be encountered in asymptomatic individuals without GERD symptoms9. GERD diagnostic criteria on the basis of oesophageal testing have been previously reported7,10,11,12; however, no updated consensus on indications and interpretation of oesophageal function testing in GERD among experts in the field has been made since the 2004 Porto consensus13.
Under the auspices of the International Working Group for Disorders of Gastrointestinal Motility and Function (www.idigest.ch), the authors of this manuscript organized a consensus project to describe modern oesophageal physiological tests and their analysis. The aim of this consensus project was to obtain 'a standard of practice' for clinicians and motility laboratories worldwide, and to reorganize and reiterate existing knowledge regarding GERD evaluation, as it has been over a decade since the last consensus of its kind in Porto13. Throughout this process, emphasis was focused on establishing indications and agreeing on interpretation of oesophageal function testing for the evaluation of GERD in clinical practice. This Consensus Statement reflects the collective clinical conclusions of the international GERD working group evaluating modern GERD testing and interpretation, incorporating existing data with expert consensus opinion. Novel concepts and recommendations developed through this process are shown in Box 1 and will be further discussed throughout.
The GERD consensus steering committee (S.R., C.P.G., E.S., A.B.) was appointed by the International Working Group for Disorders of Gastrointestinal Motility and Function. Under the guidance of the steering committee, an international GERD working group performed focused literature searches using search terms pertaining to GERD (for example, “GERD testing”, “GERD diagnosis”, “ambulatory pH” and “pH-impedance monitoring”, “hiatus hernia”, “transient lower oesophageal sphincter (LES) relaxation”, “oesophageal dysmotility”, “oesophageal manometry”, “endoscopy”, “GERD phenotypes”) to identify pertinent statements relating to oesophageal pathophysiology and oesophageal function testing in the context of GERD. At consensus meetings attended by international GERD experts held in conjunction with international conferences (United European Gastroenterology week 2015–2017, Digestive Disease Week 2015–2016, Ascona II 2015), these statements were extensively discussed and debated. Consensus was achieved through careful evaluation using the GRADE concept14 to define the quality of the supporting evidence based on study design, study limitations, consistency, directness, precision, publication bias, other modifying factors and expert agreement when guidelines lacked supporting evidence.
Mechanisms of gastro-oesophageal reflux
Oesophagogastric junction barrier. An ineffective EGJ barrier is consistently present in GERD (Fig. 1), often combined with morphological abnormality (hiatus hernia). Transient lower oesophageal sphincter relaxation (TLESR) is a physiological response to gastric distension, and excessive reflux during TLESRs is the most common EGJ event seen in patients with GERD15. Modern high-resolution manometry (HRM) criteria for TLESRs include profound EGJ relaxation of >10 s in the absence of swallowing, with inhibition of crural diaphragm contraction16. TLESRs are not routinely evaluated on oesophageal HRM, although they do affect oesophageal reflux burden. By contrast, motor deficiency and abnormal morphology of the EGJ barrier are readily identified on HRM.
An intact EGJ barrier consists of superimposed LES and crural diaphragm, with adequate resting tone preventing retrograde migration of gastric content at rest (Fig. 1). EGJ morphology is characterized into three morphological subtypes: subtype 1 (normal), subtype 2 (<3 cm separation between LES and crural diaphragm) and subtype 3 (≥3 cm separation between LES and crural diaphragm)17. The intrinsic LES can independently have a low resting tone, with values <5 mmHg during the end expiratory phase being considered abnormal12. Inspiratory crural diaphragm augmentation provides adjunctive EGJ barrier function when intrathoracic pressures are at their lowest18,19; this phenomenon is an important element not well-assessed by basal and end expiratory LES pressure measurements. The EGJ contractile integral might overcome these drawbacks by combining EGJ anatomy, basal tone and variation with respiration into a single metric, calculated using an algorithm similar to the distal contractile integral that takes into account the length and vigour of the EGJ resting barrier function and corrected for respiratory variation20,21. Normative EGJ contractile integral values have been described and available data suggest reflux burden might be abnormal in the setting of a low EGJ contractile integral21,22,23. Thus, an abnormal EGJ barrier can be hypotensive (with reduced resting tone that can be overcome by increased intra-abdominal pressure), disrupted with separation of the two components of the EGJ barrier (hiatus hernia) or both. In the presence of a hiatus hernia, the resting tone of the intrinsic LES is typically hypotensive, with oesophageal reflux burden higher than with either abnormality alone24. Consequently, these two EGJ abnormalities can coexist and both can contribute to abnormal reflux burden.
Oesophageal hypomotility. When a reflux episode occurs, the refluxate is cleared by a combination of a secondary peristaltic contraction and a primary post-reflux swallow-induced peristaltic contraction that also brings saliva to neutralize oesophageal mucosal acidification25. In many patients with GERD, oesophageal motor function is intact and normal26; however, hypomotility can contribute to delayed oesophageal clearance and increases the likelihood of oesophagitis27,28,29. The spectrum of hypomotility consists of fragmented peristalsis, ineffective oesophageal motility and absent contractility, with increased prevalence of abnormal oesophageal bolus clearance towards the high end of this spectrum30,31,32.
Refluxate. The acid pocket is a supernatant layer of gastric acid overlying an ingested meal immediately below the EGJ. In health, the transition from an acid to alkaline milieu occurs at the EGJ in the post-prandial period33. However, when the EGJ barrier is weak or disrupted, for example in presence of hiatus hernia, the acid pocket can migrate into the distal oesophagus, leading to pathological acid in the distal oesophagus34. Delayed gastric emptying and acid hypersecretory states, such as in gastrin-secreting tumours (gastrinomas), are additional downstream factors that contribute to oesophageal reflux burden35. Acid and other components of the refluxate (pepsin, bile acid) can participate in mucosal damage and in complications including Barrett metaplasia36.
Finally, the degree of proximal migration of the refluxate and differences in oesophageal perception of reflux (sensitivity) between individuals can contribute to symptom reporting in GERD37. Symptoms identical to typical GERD can be reported with reflux hypersensitivity and functional heartburn, in which oesophageal reflux burden is physiological; both can overlap with true GERD when symptoms persist despite reflux burden being rendered physiological with acid-suppressive therapy38.
Oesophageal manometry in GERD
The pathophysiology of GERD does not have a direct implication on initial GERD management, as treatment consists of acid suppression. However, if GERD symptoms persist despite empiric therapy and endoscopy is normal, further oesophageal testing is recommended (Box 2). Manometry is commonly performed for positioning of pH or pH-impedance catheters. When symptoms persist, manometry is also performed to exclude achalasia and alternate disorders that can mimic GERD, such as rumination, systemic sclerosis and supragastric belching26,39. Consequently, understanding motor mechanisms of GERD and identifying conditions mimicking GERD complement information obtained from ambulatory oesophageal reflux monitoring in planning management (Table 1). However, the Chicago Classification of oesophageal motor disorders targets abnormal bolus transit with symptomatic dysphagia and chest pain, but was not designed to assess motor function in the context of GERD40. Thus, the proposed classification, devised by this international GERD working group and detailed in the following subsections, represents an advance to previous classifications by attempting to provide structure in analysing HRM studies performed in the context of GERD40.
Most metrics (LES basal pressure, integrated relaxation pressure, distal contractile integral, hiatus hernia size) utilized in reporting oesophageal motor function in GERD are readily obtained from oesophageal HRM (Fig. 2) using a standard protocol of ten 5 ml water swallows in the supine position. Furthermore, when oesophageal peristaltic performance is abnormal, oesophageal body contraction reserve (potential for augmentation of oesophageal body contraction when ineffective oesophageal motility is found on routine water swallows) can be determined using provocative testing. The simplest provocative tests consist of either a series of five 2 ml water swallows in rapid succession, termed multiple rapid swallows41,42, or free drinking of 100–150 ml of water from a cup, termed rapid drink challenge43,44. During the series of swallows, inhibition of oesophageal body contraction and relaxation of the LES occurs. Following the final swallow of the sequence, there is augmented oesophageal body contraction and re-establishment of LES tone41,42. Augmentation of oesophageal body contraction is measured as the ratio between distal contractile integral (DCI) following multiple rapid swallows and the mean DCI during standard wet swallows. Contraction reserve indicates a DCI ratio >1, and enables phenotyping of oesophageal body peristalsis with implications on management outcome42,45. Absence of contraction reserve is associated with an increased likelihood of transit symptoms (dysphagia) following a 360° fundoplication42.
Evaluation and reporting of oesophageal motor function in GERD can be achieved through three hierarchical steps, as outlined in the following subsections. The first two steps can reveal abnormalities that can be independent of each other; however, the coexistence of abnormalities might predict an increased likelihood of abnormal oesophageal reflux burden. The final step only applies when oesophageal body motor function is abnormal and as an exploratory tool that might have implications on management outcome.
Integrity of the oesophagogastric junction barrier. EGJ hypomotility is defined as low EGJ resting tone, with end expiratory LES pressure <5 mmHg (Ref. 12), or EGJ contractile integral <39–47 mmHg per cm (Refs 20,21,22). EGJ morphology is based on the relationship between the intrinsic LES and crural diaphragm, and is described as one of the three EGJ subtypes described in the previous section. When the EGJ barrier is intact, the EGJ resting tone is normal and the LES and crural diaphragm are superimposed (EGJ morphology type 1). A hypotensive EGJ can sometimes occur as an isolated abnormality; however, this finding often coexists with a hiatus hernia (EGJ morphology types 2 or 3)17.
Oesophageal body motor function. Intact or normal oesophageal body motility consists of <50% of swallows with DCI <450 mmHg·cm·s (Ref. 40). Fragmented peristalsis is defined by the presence of ≥50% fragmented swallows, whereby DCI is >450 mmHg·cm·s but there are ≥5 cm breaks in the 20 mmHg peristaltic contour40. Ineffective oesophageal motility consists of ≥50% ineffective sequences, in which DCI is <450 mmHg·cm·s (Ref. 40). Absent contractility describes uniformly failed sequences, in which DCI is <100 mmHg·cm·s (Ref. 40).
Oesophageal body contraction reserve. This metric is evaluated when oesophageal body motor function is abnormal. Contraction reserve is present when multiple rapid swallow DCI is higher than the mean wet swallow DCI. For example, the ratio between multiple rapid swallow DCI and wet swallow DCI is >1 (Ref. 42).
Ambulatory reflux monitoring Proven versus unproven GERD. Ambulatory reflux monitoring is performed to document oesophageal reflux burden or to define the relationship between symptom events and reflux episodes. The most common settings consist of persisting oesophageal symptoms despite seemingly adequate acid-suppressive therapy, such as a failed PPI test or atypical symptoms (chest pain, cough, laryngeal symptoms) that might not directly implicate GERD but could improve with GERD therapy if pathological reflux is present4,5 (Fig. 3). In the typical clinical scenario, ambulatory reflux monitoring has either rule-in or rule-out value in defining abnormal oesophageal reflux burden46. The concepts of unproven GERD and proven GERD, deliberated extensively and defined here precisely during this consensus process, determine how reflux monitoring is performed. In the absence of prior evidence of reflux (unproven GERD; with no prior LA classification grade C or D oesophagitis, peptic stricture or Barrett mucosa on endoscopy, or no prior positive ambulatory reflux study), or before antireflux surgery (ARS; for example, Nissen or Toupet fundoplication), testing is performed off anti-secretory therapy for 7–10 days47. When irrefutable evidence of GERD exists (proven GERD; EGD evidence of LA classification grade C or D oesophagitis, peptic stricture, long-segment Barrett mucosa or prior abnormal ambulatory reflux monitoring), testing can be performed on anti-secretory therapy, in which the objective is to determine if ongoing symptoms can be explained by abnormal oesophageal reflux burden or linked to reflux episodes. In this setting, pH testing alone is insufficient in describing weakly acidic reflux episodes that predominate in patients on PPI therapy, therefore, pH-impedance testing is used48. When reflux monitoring is repeated after ARS or other invasive reflux therapy, the same testing method used before intervention is performed, typically off anti-secretory therapy. If suspicion of GERD is strong in the setting of negative 24 h reflux monitoring, repeated and prolonged monitoring using a wireless pH probe can be considered, as day-to-day variation in oesophageal reflux burden has been documented and some patients struggle to eat and behave normally with an oesophageal catheter in place49. Repeat testing in this context could improve diagnostic yield and the finding of abnormal reflux burden can affect management direction49,50.
As typical reflux symptoms are initially managed with an empiric PPI trial, persisting symptoms despite PPI therapy can be an indication for ambulatory reflux monitoring (Fig. 3). However, the PPI trial is not perfect, with a specificity of only 50–60% despite sensitivity of ∼80% in predicting erosive oesophagitis or an abnormal pH study51,52. Investigation of persisting reflux symptoms, or alarm symptoms, starts with an EGD with biopsies to exclude alternative mucosal processes, such as infectious oesophagitis or eosinophilic oesophagitis53. Persisting symptoms, both typical and atypical, necessitate ambulatory reflux monitoring to determine if antireflux therapy is indicated; the more atypical the symptoms, the greater the need for ambulatory reflux monitoring.
Reflux metrics. Oesophageal acid exposure time (AET) is the most commonly used metric in defining abnormal oesophageal reflux burden. AET can be extracted from both pH and pH-impedance studies (Fig. 4) and is calculated as the percentage of time that pH is <4.0 in the distal oesophagus (5 cm above the LES) for the duration of the ambulatory study7,10. AET can be separately calculated for upright and supine periods. Pathological supine AET can implicate a disrupted EGJ barrier, as TLESRs are generally suppressed during sleep54. Symptom–reflux association is an essential part of interpretation. This process requires the patient to report symptoms during the ambulatory study, typically using an event monitor button on the reflux monitoring device worn by the patient55. Concurrent reflux episodes are identified by reflux software using pH drops below 4.0 or impedance-detected retrograde movement of gastric content (Fig. 4). A symptom event is considered associated with a reflux episode if the symptom occurs within 2 min following the reflux episode7.
Although AET and symptom reflux association are the two main metrics used in interpreting ambulatory reflux monitoring studies, additional metrics can be extracted, especially when pH-impedance testing is used. Number of reflux episodes is often reported, and impedance-detected reflux episodes are more reliable than those detected based on decreases in pH alone56. Proximal oesophageal and pharyngeal reflux monitoring using pH or impedance sensors is possible; however, this approach has limited value in directing anti-reflux therapy as symptom outcome cannot be predicted based on these metrics57,58. Baseline mucosal impedance, especially when measured at night when swallow-related artefacts are at a minimum (MNBI; mean nocturnal baseline impedance), correlates inversely with AET and can be a marker of abnormal mucosal integrity59,60. The post-reflux swallow-induced peristaltic wave (PSPW) is an antegrade impedance-detected bolus propagation reaching all distal impedance monitoring sites within 30 s of a reflux event, and is an assessment of clearance of refluxate that can be measured in patients studied on or off therapy. The PSPW index identifies the proportion of reflux events followed by PSPW compared with all other reflux events, and can be lower in erosive and nonerosive GERD compared with healthy individuals as controls59. Furthermore, this index might assist in distinguishing hypersensitive oesophagus from functional heartburn61,62.
Interpretation of reflux monitoring
Data acquisition. Catheter-based ambulatory reflux monitoring (pH or pH-impedance studies) is performed over a 24 h period, with the distal oesophageal pH sensor positioned 5 cm proximal to the manometrically measured LES. Wireless pH probes are typically positioned 6 cm proximal to the squamocolumnar junction during EGD. These single sensor probes can record and transmit distal oesophageal pH data for up to 96 h and are better tolerated than ambulatory catheter-based testing46. Catheter or probe placement is performed after an overnight fast and after withholding anti-secretory therapy for at least 7 days when testing off PPI is performed. Patients are recommended to maintain normal activities and meals, and keep a diary of meals, symptoms, and recumbency periods7,10.
Analysis of pH data. The key metric extracted from any pH or pH-impedance study is the AET, which requires at least 16 h of recording. Meal times are excluded and the study is scanned visually to identify artefacts, catheter displacement or wireless probe dislodgement that could affect AET calculations. Total AET is considered physiological when <4%, as determined from normative studies (Table 2), and pathological when >6%, whereas values in between are borderline and require additional clinical or physiological evidence to confirm GERD63,64,65,66,67,68,69,70. Total, upright and supine AET are separately calculated and reported. When a dual-probe pH catheter is used, proximal oesophageal AET can also be reported (Fig. 4b,c). With wireless pH testing, averaged AET and AET for each day of pH recording are separately available. Specificity increases with averaged AET, whereas sensitivity is increased with AET from the worst day during the study. AET is marginally higher with the wireless probe compared with catheter-based pH studies, but similar thresholds can be used for both modes of reflux monitoring49,71,72. AET is considered more statistically valid and reproducible than the composite DeMeester score that takes upright, supine and total AET, longest reflux episode, reflux episodes >5 min and the total number of reflux episodes into account73.
Symptom reflux association. Episodic symptoms with finite onset and offset can be subject to evaluation of symptom reflux association (Fig. 4d), whereas continuous symptoms cannot be assessed by this approach. The dominant or most bothersome symptom is utilized for primary evaluation, secondary symptoms can also be evaluated. A cough detector can count and time cough events; this objective can also be achieved with ambulatory manometry. A simple ratio of associated symptoms to all symptoms defines the symptom index, which is abnormal if >50%74. In addition, the number of symptoms should be reported for relevance, as the symptom index can be based on one event only. Symptom association probability (SAP) takes into account 2 min periods with and without reflux episodes and symptom events, and applies a statistical test (Fisher's exact test) on a two-by-two table generated with this data55. A P value <0.05 (or SAP >95%) corresponds to a <5% chance that symptoms and reflux episodes could have co-occurred just by chance55. A similar conclusion can be reached using the Ghillebert probability estimate, which utilizes post-hoc statistical modelling from parameters routinely collected during a pH study to define symptom reflux association75. The yield and diagnostic value of symptom reflux association is highest when many symptoms are recorded, with the patient recording the symptom promptly upon occurrence76. Multiple symptoms with the 2-min window are counted as a single symptom. Substantial day-to-day variability in reflux episodes and in symptom occurrence does occur, but the results of symptom reflux association are reproducible if sufficient symptom events are observed during the study77. Recording of symptoms represents the weakest element in symptom reflux association testing, as incomplete or delayed symptom recording by the patient can render this metric negative and of limited clinical value. Thus, careful instruction and explanation to the patient is essential for success. Nevertheless, when positive, symptom reflux association can augment the evidence that clinically relevant reflux is present and can define reflux hypersensitivity. Evidence for symptom reflux association is considered to be sound when both SAP and the symptom index are positive78,79,80.
Analysis of impedance data. Impedance monitoring was initially believed to provide improved accuracy of reflux evidence, but impedance-based parameters have generally not been predictive of reflux treatment outcomes81,82. Although infrequent reflux episodes (<40) could indicate physiological reflux, there is variability in the association of reflux episodes with oesophageal reflux burden83,84,85,86,87,88. High numbers of episodes (>80) could suggest pathological reflux burden, whereas borderline values (40–80) require alternate reflux evidence. By contrast, MNBI could provide complementary longitudinal evidence of oesophageal mucosal damage from reflux exposure. Normative MNBI thresholds have been defined (2,292 Ω), but low values are seen in oesophageal motility disorders with impaired clearance and in abnormal oesophageal mucosa (eosinophilic oesophagitis, Barrett mucosa), which can confound clinical utility59,89. Nevertheless, erosive and nonerosive GERD are both associated with lower MNBI values than healthy individuals as controls and patients with functional heartburn90. Low MNBI values have also been associated with improved medical and surgical outcome, suggesting relevance in GERD management60,91. MNBI could, therefore, represent a complementary or adjunctive metric, available in all settings in which pH-impedance monitoring is performed.
GERD phenotypes. The metrics described earlier have highest value in predicting reflux outcome when testing is performed off PPI therapy in unproven GERD81,82,92. Phenotypes with pathological reflux burden on ambulatory reflux monitoring, with or without symptom association, predict the highest likelihood of symptom improvement from antireflux therapy81,93. However, thresholds defining pathological from physiological reflux burden are not precise, and a 'grey area' exists, for example, in borderline reflux burden or inconsistent symptom index and SAP, in which the clinical presentation and alternate reflux evidence could complement ambulatory reflux monitoring findings. Symptomatic phenotypes with physiological oesophageal reflux burden can implicate a functional basis for symptoms, whereby symptom improvement is suboptimal with antireflux therapy38,93. Within these phenotypes, reflux hypersensitivity consists of symptom–reflux association in the setting of physiological reflux burden, whereas functional heartburn or functional chest pain implies a normal ambulatory reflux monitoring study with negative symptom reflux association38.
Monitoring using pH impedance is also used in proven GERD if symptoms persist, when testing is performed on maximal antisecretory therapy. In these instances, similar AET thresholds can be utilized and the yield of abnormal oesophageal acid burden is expected to be low (typically <1%)94. Management decisions will, therefore, need to be based on symptom–reflux association and number of reflux events. Utilizing these parameters, the possible phenotypes prompting escalation of antireflux therapy are as follows (Fig. 3): inadequate control of oesophageal acid burden with antisecretory therapy; persisting symptoms associated with impedance-detected reflux episodes; and abnormally high impedance-detected reflux episodes. By contrast, the following phenotypes could indicate adequate acid control or alternate mechanisms for symptom generation: normal (physiological) oesophageal acid burden; lack of association between persisting symptoms and reflux episodes; and low impedance-detected reflux episodes. Borderline reflux burden could also be encountered in proven GERD with similar implications as in unproven GERD. Additionally, reflux hypersensitivity or functional symptoms could overlap with true GERD. Under all these circumstances, clinical presentation and evidence from other tests for GERD evaluation will need to be combined with results from ambulatory reflux monitoring in planning management.
Other tests for evaluation of GERD
Several questionnaires with varying characteristics have been developed for the assessment of GERD95. A few of these have some diagnostic utility and two have been validated in multiple languages: the Reflux Disease Questionnaire (RDQ) and the GERDQ95,96,97. However, both have shown only modest accuracy (∼65–70%) for symptom-based diagnosis of GERD and, therefore, cannot be recommended as stand-alone diagnostic instruments96,97.
Endoscopy has high specificity but very low sensitivity for GERD diagnosis, as oesophageal mucosa is normal in up to 70% of patients with symptomatic GERD98,99. When performed following recent or current antisecretory therapy, the probability of a normal assessment increases to 90%100. Thus, endoscopy has very low sensitivity for initial GERD diagnosis, and is appropriate only in the presence of alarm symptoms, such as dysphagia or unintentional weight loss, multiple risk factors for Barrett oesophagus (>50 years of age, male sex, prolonged reflux symptoms, obesity) or failure to respond to appropriate antisecretory therapy6. Supplemental endoscopic tools such as narrow-band imaging and confocal laser endomicroscopy provide limited additional benefit in identifying mucosal damage consistent with reflux. Their use remains restricted to research given intrinsic limitations such as high costs, time-consuming procedures and weak interobserver and intraobserver agreement. Furthermore, there is higher clinical value with reflux monitoring than these newer tools101. Novel endoscopic probes for measurement of oesophageal mucosal impedance have been introduced, providing basal mucosal impedance estimates similar to that obtained from ambulatory pH-impedance monitoring102,103,104,105. These tools have shown promise in distinguishing reflux disease from functional oesophageal disorders and in monitoring treatment response. Future studies will determine the true potential of these methods as diagnostic tools106.
Oesophageal biopsies evaluating histological changes potentially related to reflux, such as dilated intercellular spaces, basal cell hyperplasia and papillary elongation, have shown moderate to good sensitivity and specificity in identifying GERD107,108,109,110. When findings are considered collectively as evidence of microscopic oesophagitis, particularly when combined into a global severity score, distinction of erosive oesophagitis and nonerosive reflux disease from functional heartburn and healthy individuals is possible with good accuracy111,112. Furthermore, some studies suggest usefulness of histological findings in monitoring response to medical and surgical therapies112,113. Conversely, there are several drawbacks, mainly related to limited specificity and interobserver and/or intraobserver agreement between pathologists114. These restrictions limit the usefulness of histological assessment in current clinical practice, although efforts are ongoing to resolve these limitations114.
The use of barium radiography in diagnosing GERD is not recommended. Data comparing radiographic diagnosis of GERD with that from reflux testing demonstrate that radiographic findings do not correlate with the prevalence or extent of reflux seen on ambulatory pH-impedance monitoring115. Thus, barium radiography alone cannot be used to diagnose GERD, although radiography can be accurate and useful in defining EGJ anatomy.
The use of impedance planimetry to measure cross-sectional area and distensibility at the EGJ (endoluminal functional lumen imaging probe or endo-FLIP) has shown no demonstrable value in the diagnostic work-up of GERD, although clinical data are scant116,117. Similarly, not enough evidence currently exists to recommend the clinical use of salivary pepsin in the diagnosis of GERD.
Oesophageal function testing implications
GERD phenotypes can be defined on the basis of clinical assessment, endoscopy and oesophageal function testing. The best use of GERD phenotypes lies in predicting outcomes from management, thereby enabling practitioners to choose the most ideal management options to maximize therapeutic outcome. In this regard, symptoms and PPI response do not adequately phenotype GERD into reliable therapeutic categories. Limited research is available describing prediction of therapy outcomes on the basis of presentation, morphology of the EGJ and oesophageal motor function.
Using EGD findings, GERD can be phenotyped into erosive and nonerosive disease, with clearly better symptomatic outcomes from PPI therapy in erosive GERD than nonerosive disease. For erosive GERD, LA classification grades C and D provide the most consistent evidence of GERD8,118. LA classification grade B oesophagitis also prompts medical management with acid suppression8; however, this grade might not be sufficient evidence for a recommendation of ARS in the absence of alternate phenotypic GERD evidence. LA classification grade A oesophagitis is frequently encountered in asymptomatic healthy volunteers and does not provide conclusive evidence for GERD119.
Evidence of reflux on ambulatory reflux monitoring prompts initiation or escalation of acid-suppressive therapy (Fig. 3), and pathological AET is a predictor of good outcome from both medical and ARS therapy81,92,93. Within abnormal AET cohorts, those with positive symptom–reflux association (Fig. 4d) have the highest likelihood of improvement from antireflux therapy78,79,80. Thus, the GERD phenotype with the strongest evidence consists of pathological AET associated with positive symptom–reflux association, especially if both SAP and symptom index are positive80,93. Antacids and alginates can treat infrequent or breakthrough reflux symptoms120. Baclofen, a γ-aminobutyric acid type B receptor agonist, can reduce reflux events by inhibiting TLESRs, with potential adjunctive symptomatic benefit when this drug is available121. ARS might be a consideration that can be explored in some patients, especially when EGJ disruption is documented. By contrast, physiological AET with no symptom–reflux association predicts suboptimal outcomes from antireflux therapy and can overlap with functional oesophageal syndromes. Coexisting functional syndromes (functional dyspepsia, IBS) might also predict suboptimal outcome from antireflux therapy122,123 and might prompt treatment with neuromodulators38.
Reflux hypersensitivity (physiological acid burden with positive symptom–reflux association) represents a challenge in interpretation and management. The prevalence of reflux hypersensitivity is higher when pH impedance is employed for reflux monitoring compared with pH monitoring alone124. When symptom–reflux association is recorded with impedance-detected reflux events, antireflux management approaches (including ARS) might be successful, especially if evidence for EGJ disruption and/or hiatus hernia exists125,126. Although true acid sensitivity (symptom associated with pH-detected reflux events alone) is relatively rare, this occurrence is associated with suboptimal response to antireflux therapy125 and treatments similar to those for functional oesophageal syndromes (for example, neuromodulators) might provide a better outcome than with antireflux therapy alone38.
Conditions mimicking GERD
Of patients referred with refractory reflux symptoms, at least 30% have functional heartburn, rumination syndrome or achalasia rather than GERD127 (Table 1). In the achalasia spectrum disorders, retrosternal discomfort and regurgitation occur as a consequence of oesophageal outflow obstruction rather than from reflux127,128. Within patients referred for ARS, ∼1% are diagnosed with achalasia by oesophageal HRM, and an additional 1.5% have evidence of EGJ outflow obstruction26. The diagnosis of achalasia and EGJ outflow obstruction have profound clinical importance, as invasive management for these conditions (EGJ disruption) is contradictory to that performed in GERD (EGJ enhancement with ARS).
Rumination syndrome consists of voluntary contraction of abdominal wall musculature during periods of crural diaphragm relaxation, leading to a sharp increase in intra-abdominal pressure that forces gastric content through the oesophagus into the mouth129. This increase in intra-abdominal pressure can be identified in the form of an 'r' wave on prolonged HRM with impedance in the post-prandial period. Ambulatory pH-impedance monitoring, however, does not discriminate a rumination episode from a reflux episode130,131.
Supragastric belching starts with air forced into the oesophagus by contraction of the diaphragm, creating negative pressure in the oesophagus, followed by contraction of abdominal and thoracic muscles resulting in immediate expulsion in the form of a belch131. Less commonly, air is swallowed into the stomach and expelled out by a mechanism similar to rumination. In addition to careful history and clinical observation, supragastric belching can be identified on concurrent HRM with impedance.
Oesophageal symptoms can be associated with conditions such as eosinophilic oesophagitis, lichen planus and infectious oesophagitis (oesophageal candidiasis, herpes simplex oesophagitis, cytomegalovirus oesophagitis). Finally, functional disease can give rise to any oesophageal symptom, including symptoms similar to GERD38. Ambulatory reflux monitoring demonstrates physiological reflux parameters, but minor motor disorders and contraction-wave abnormalities on HRM are compatible with functional oesophageal disorders38.
Combining existing data on reflux testing with expert consensus opinion, this Consensus Statement describes the modern evaluation of GERD, especially when oesophageal symptoms persist despite empiric antisecretory therapy and when EGD does not identify an alternate mechanism for symptoms. In this setting, HRM identifies motor pathophysiology conducive to gastro-esophageal reflux and ambulatory reflux monitoring describes pathological oesophageal reflux burden and symptom–reflux association. Other novel parameters on pH testing or pH-impedance testing, including MNBI and the PSPW index, might complement conventional reflux parameters in improving confidence for a reflux diagnosis. In the future, understanding GERD pathophysiology in more detail, particularly the inter-relationship between GERD and oesophageal motor dysfunction, and evaluating oesophageal reflux burden with novel metrics could help identify GERD phenotypes better and improve management outcomes (Box 3). A need now exists for prospective and collaborative outcome studies to determine the clinical value of oesophageal function testing in predicting symptomatic outcome.
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Vakil, N. et al. The Montreal definition and classification of gastroesophageal reflux disease: a global evidence-ased consensus. Am. J. Gastroenterol. 101, 1900–1920 (2006).
Dent, J. et al. Epidemiology of gastro-oesophageal reflux disease: a systematic review. Gut 54, 710–717 (2005).
Zagari, R. M. et al. Gastro-oesophageal reflux symptoms, oesophagitis and Barrett's oesophagus in the general population: the Loiano-Monghidoro study. Gut 57, 1354–1359 (2008).
Katz, P. O., Gerson, L. B. & Vela, M. F. Guidelines for the diagnosis and management of gastroesophageal reflux disease. Am. J. Gastroenterol. 108, 308–328 (2013).
Vela, M. F. Diagnostic work-up of GERD. Gastrointest. Endosc. Clin. N. Am. 24, 655–666 (2014).
ASGE Standards of Practice Committee et al. The role of endoscopy in the management of GERD. Gastrointest. Endosc. 81, 1305–1310 (2015).
Pandolfino, J. E. & Vela, M. F. Esophageal-reflux monitoring. Gastrointest. Endosc. 69, 917–930.e1 (2009).
Lundell, L. R. et al. Endoscopic assessment of oesophagitis: clinical and functional correlates and further validation of the Los Angeles classification. Gut 45, 172–180 (1999).
Kahrilas, P. J. et al. American Gastroenterological Association Institute technical review on the management of gastroesophageal reflux disease. Gastroenterology 135, 1392–1413.e1-5 (2008).
Kahrilas, P. J. & Quigley, E. M. Clinical esophageal pH recording: a technical review for practice guideline development. Gastroenterology 110, 1982–1996 (1996).
Kahrilas, P. J. et al. American Gastroenterological Association Medical Position Statement on the management of gastroesophageal reflux disease. Gastroenterology 135, 1383–1391.e1-5 (2008).
Pandolfino, J. E., Kahrilas, P. J. & American Gastroenterological Association AGA technical review on the clinical use of esophageal manometry. Gastroenterology 128, 209–224 (2005).
Sifrim, D. et al. Gastro-oesophageal reflux monitoring: review and consensus report on detection and definitions of acid, non-acid, and gas reflux. Gut 53, 1024–1031 (2004).
Atkins, D. et al. Grading quality of evidence and strength of recommendations. BMJ 328, 1490 (2004).
Ribolsi, M. et al. Impedance-high resolution manometry analysis of patients with nonerosive reflux disease. Clin. Gastroenterol. Hepatol. 12, 52–57 (2014).
Roman, S. et al. Validation of criteria for the definition of transient lower esophageal sphincter relaxations using high-resolution manometry. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo.12920 (2016).
Pandolfino, J. E. et al. High-resolution manometry of the EGJ: an analysis of crural diaphragm function in GERD. Am. J. Gastroenterol. 102, 1056–1063 (2007).
Nicodeme, F. et al. Esophagogastric Junction pressure morphology: comparison between a station pull-through and real-time 3D-HRM representation. Neurogastroenterol. Motil. 25, e591–e598 (2013).
Nicodeme, F. et al. Adding a radial dimension to the assessment of esophagogastric junction relaxation: validation studies of the 3D-eSleeve. Am. J. Physiol. Gastrointest. Liver Physiol. 303, G275–G280 (2012).
Nicodeme, F. et al. Quantifying esophagogastric junction contractility with a novel HRM topographic metric, the EGJ-Contractile Integral: normative values and preliminary evaluation in PPI non-responders. Neurogastroenterol. Motil. 26, 353–360 (2014).
Gor, P. et al. Interrogation of esophagogastric junction barrier function using the esophagogastric junction contractile integral: an observational cohort study. Dis. Esophagus 29, 820–828 (2016).
Jasper, D. et al. Prolonged measurement improves the assessment of the barrier function of the esophago-gastric junction by high-resolution manometry. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo/12925 (2016).
Tolone, S. et al. Esophagogastric junction morphology is associated with a positive impedance-pH monitoring in patients with GERD. Neurogastroenterol. Motil. 27, 1175–1182 (2015).
Sloan, S. & Kahrilas, P. J. Impairment of esophageal emptying with hiatal hernia. Gastroenterology 100, 596–605 (1991).
Helm, J. F. et al. Effect of esophageal emptying and saliva on clearance of acid from the esophagus. N. Engl. J. Med. 310, 284–288 (1984).
Chan, W. W., Haroian, L. R. & Gyawali, C. P. Value of preoperative esophageal function studies before laparoscopic antireflux surgery. Surg. Endosc. 25, 2943–2949 (2011).
Lin, S. et al. Impaired esophageal emptying in reflux disease. Am. J. Gastroenterol. 89, 1003–1006 (1994).
Bredenoord, A. J., Hemmink, G. J. & Smout, A. J. Relationship between gastro-oesophageal reflux pattern and severity of mucosal damage. Neurogastroenterol. Motil. 21, 807–812 (2009).
Daum, C. et al. Failure to respond to physiologic challenge characterizes esophageal motility in erosive gastro-esophageal reflux disease. Neurogastroenterol. Motil. 23, 517–e200 (2011).
Ribolsi, M. et al. Weak peristalsis with large breaks is associated with higher acid exposure and delayed reflux clearance in the supine position in GERD patients. Am. J. Gastroenterol. 109, 46–51 (2014).
Reddy, C. A., Patel, A. & Gyawali, C. P. Impact of symptom burden and health-related quality of life (HRQOL) on esophageal motor disorders. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo.12970 (2017).
Savarino, E. et al. Oesophageal motility and bolus transit abnormalities increase in parallel with the severity of gastro-oesophageal reflux disease. Aliment. Pharmacol. Ther. 34, 476–486 (2011).
Beaumont, H. et al. The position of the acid pocket as a major risk factor for acidic reflux in healthy subjects and patients with GORD. Gut 59, 441–451 (2010).
Kahrilas, P. J. et al. The acid pocket: a target for treatment in reflux disease? Am. J. Gastroenterol. 108, 1058–1064 (2013).
Kessing, B. F. et al. Prucalopride decreases esophageal acid exposure and accelerates gastric emptying in healthy subjects. Neurogastroenterol. Motil. 26, 1079–1086 (2014).
Koek, G. H. et al. Multivariate analysis of the association of acid and duodeno-gastro-oesophageal reflux exposure with the presence of oesophagitis, the severity of oesophagitis and Barrett's oesophagus. Gut 57, 1056–1064 (2008).
Woodland, P. et al. Distinct afferent innervation patterns within the human proximal and distal esophageal mucosa. Am. J. Physiol. Gastrointest. Liver Physiol. 308, G525–G531 (2015).
Aziz, Q. et al. Functional esophageal disorders. Gastroenterology 150, 1368–1379 (2016).
Fuchs, K. H. et al. EAES recommendations for the management of gastroesophageal reflux disease. Surg. Endosc. 28, 1753–1773 (2014).
Kahrilas, P. J. et al. The Chicago Classification of esophageal motility disorders, v3.0. Neurogastroenterol. Motil. 27, 160–174 (2015).
Fornari, F. et al. Multiple rapid swallowing: a complementary test during standard oesophageal manometry. Neurogastroenterol. Motil. 21, e718–e741 (2009).
Shaker, A. et al. Multiple rapid swallow responses during esophageal high-resolution manometry reflect esophageal body peristaltic reserve. Am. J. Gastroenterol. 108, 1706–1712 (2013).
Elvevi, A. et al. Usefulness of low- and high-volume multiple rapid swallowing during high-resolution manometry. Dig. Liver Dis. 47, 103–107 (2015).
Ang, D. et al. Rapid Drink Challenge in high-resolution manometry: an adjunctive test for detection of esophageal motility disorders. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo.12902 (2016).
Mello, M. D. et al. Ineffective esophageal motility phenotypes following fundoplication in gastroesophageal reflux disease. Neurogastroenterol. Motil. 28, 292–298 (2016).
Richter, J. E. et al. Utilization of wireless pH monitoring technologies: a summary of the proceedings from the esophageal diagnostic working group. Dis. Esophagus 26, 755–765 (2013).
Jobe, B. A. et al. Preoperative diagnostic workup before antireflux surgery: an evidence and experience-based consensus of the Esophageal Diagnostic Advisory Panel. J. Am. Coll. Surg. 217, 586–597 (2013).
Vela, M. F. et al. Simultaneous intraesophageal impedance and pH measurement of acid and nonacid gastroesophageal reflux: effect of omeprazole. Gastroenterology 120, 1599–1606 (2001).
Pandolfino, J. E. et al. Ambulatory esophageal pH monitoring using a wireless system. Am. J. Gastroenterol. 98, 740–749 (2003).
Penagini, R. et al. Inconsistency in the diagnosis of functional heartburn: usefulness of prolonged wireless pH monitoring in patients with proton pump inhibitor refractory gastroesophageal reflux disease. J. Neurogastroenterol. Motil. 21, 265–272 (2015).
Fass, R. et al. Clinical and economic assessment of the omeprazole test in patients with symptoms suggestive of gastroesophageal reflux disease. Arch. Intern. Med. 159, 2161–2168 (1999).
Fass, R. et al. The omeprazole test is as sensitive as 24-h oesophageal pH monitoring in diagnosing gastro-oesophageal reflux disease in symptomatic patients with erosive oesophagitis. Aliment. Pharmacol. Ther. 14, 389–396 (2000).
Dellon, E. S. et al. ACG clinical guideline: evidenced based approach to the diagnosis and management of esophageal eosinophilia and eosinophilic esophagitis (EoE). Am. J. Gastroenterol. 108, 679–692 (2013).
Mittal, R. K. et al. Transient lower esophageal sphincter relaxation. Gastroenterology 109, 601–610 (1995).
Weusten, B. L. et al. The symptom-association probability: an improved method for symptom analysis of 24-hour esophageal pH data. Gastroenterology 107, 1741–1745 (1994).
Agrawal, A. et al. Ingestion of acidic foods mimics gastroesophageal reflux during pH monitoring. Dig. Dis. Sci. 50, 1916–1920 (2005).
Yadlapati, R. et al. Oropharyngeal pH testing does not predict response to proton pump inhibitor therapy in patients with laryngeal symptoms. Am. J. Gastroenterol. 111, 1517–1524 (2016).
Dulery, C. et al. A study with pharyngeal and esophageal 24-hour pH-impedance monitoring in patients with laryngopharyngeal symptoms refractory to proton pump inhibitors. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo.12909 (2017).
Frazzoni, M. et al. Analyses of the post-reflux swallow-induced peristaltic wave index and nocturnal baseline impedance parameters increase the diagnostic yield of impedance-pH monitoring of patients with reflux disease. Clin. Gastroenterol. Hepatol. 14, 40–46 (2016).
Patel, A. et al. Distal mean nocturnal baseline impedance on pH-impedance monitoring predicts reflux burden and symptomatic outcome in gastro-oesophageal reflux disease. Aliment. Pharmacol. Ther. 44, 890–898 (2016).
Frazzoni, M. et al. Impairment of chemical clearance and mucosal integrity distinguishes hypersensitive esophagus from functional heartburn. J. Gastroenterol. 52, 444–451 (2017).
Frazzoni, M. et al. The added diagnostic value of postreflux swallow-induced peristaltic wave index and nocturnal baseline impedance in refractory reflux disease studied with on-therapy impedance-pH monitoring. Neurogastroenterol. Motil. http://dx.doi.org/10.1111/nmo.12947 (2017).
Vitale, G. C. et al. Computerized 24-hour ambulatory esophageal pH monitoring and esophagogastroduodenoscopy in the reflux patient. A comparative study. Ann. Surg. 200, 724–728 (1984).
Schindlbeck, N. E. et al. Optimal thresholds, sensitivity, and specificity of long-term pH-metry for the detection of gastroesophageal reflux disease. Gastroenterology 93, 85–90 (1987).
Johnsson, F., Joelsson, B. & Isberg, P. E. Ambulatory 24 hour intraesophageal pH-monitoring in the diagnosis of gastroesophageal reflux disease. Gut 28, 1145–1150 (1987).
Mattioli, S. et al. Reliability of 24-hour home esophageal pH monitoring in diagnosis of gastroesophageal reflux. Dig. Dis. Sci. 34, 71–78 (1989).
Smout, A. J. et al. Physiological gastroesophageal reflux and esophageal motor activity studied with a new system for 24-hour recording and automated analysis. Dig. Dis. Sci. 34, 372–378 (1989).
Masclee, A. A. et al. Ambulatory 24-hour pH-metry in the diagnosis of gastroesophageal reflux disease. Determination of criteria and relation to endoscopy. Scand. J. Gastroenterol. 25, 225–230 (1990).
Richter, J. E. et al. Normal 24-hr ambulatory esophageal pH values. Influence of study center, pH electrode, age, and gender. Dig. Dis. Sci. 37, 849–856 (1992).
Kasapidis, P. et al. Differences in manometry and 24-H ambulatory pH-metry between patients with and without endoscopic or histological esophagitis in gastroesophageal reflux disease. Am. J. Gastroenterol. 88, 1893–1899 (1993).
Ayazi, S. et al. Bravo catheter-free pH monitoring: normal values, concordance, optimal diagnostic thresholds, and accuracy. Clin. Gastroenterol. Hepatol. 7, 60–67 (2009).
Wenner, J. et al. Wireless oesophageal pH monitoring: feasibility, safety and normal values in healthy subjects. Scand. J. Gastroenterol. 40, 768–774 (2005).
Johnson, L. F. & DeMeester, T. R. Development of the 24-hour intraesophageal pH monitoring composite scoring system. J. Clin. Gastroenterol. 8 (Suppl. 1), 52–58 (1986).
Wiener, G. J. et al. The symptom index: a clinically important parameter of ambulatory 24-hour esophageal pH monitoring. Am. J. Gastroenterol. 83, 358–361 (1988).
Ghillebert, G. et al. Ambulatory 24 hour intraoesophageal pH and pressure recordings v provocation tests in the diagnosis of chest pain of oesophageal origin. Gut 31, 738–744 (1990).
Kushnir, V. M. et al. Assessment of concordance of symptom reflux association tests in ambulatory pH monitoring. Aliment. Pharmacol. Ther. 35, 1080–1087 (2012).
Aanen, M. C. et al. Reproducibility of symptom association analysis in ambulatory reflux monitoring. Am. J. Gastroenterol. 103, 2200–2208 (2008).
Prakash, C. & Clouse, R. E. Wireless pH monitoring in patients with non-cardiac chest pain. Am. J. Gastroenterol. 101, 446–452 (2006).
Hersh, M. J., Sayuk, G. S. & Gyawali, C. P. Long-term therapeutic outcome of patients undergoing ambulatory pH monitoring for chronic unexplained cough. J. Clin. Gastroenterol. 44, 254–260 (2010).
Kushnir, V. M., Sayuk, G. S. & Gyawali, C. P. Abnormal GERD parameters on ambulatory pH monitoring predict therapeutic success in noncardiac chest pain. Am. J. Gastroenterol. 105, 1032–1038 (2010).
Patel, A., Sayuk, G. S. & Gyawali, C. P. Parameters on esophageal pH-impedance monitoring that predict outcomes of patients with gastroesophageal reflux disease. Clin. Gastroenterol. Hepatol. 13, 884–891 (2015).
Zerbib, F. et al. Clinical, but not oesophageal pH-impedance, profiles predict response to proton pump inhibitors in gastro-oesophageal reflux disease. Gut 61, 501–506 (2012).
Shay, S. et al. Twenty-four hour ambulatory simultaneous impedance and pH monitoring: a multicenter report of normal values from 60 healthy volunteers. Am. J. Gastroenterol. 99, 1037–1043 (2004).
Zerbib, F. et al. Normal values and day-to-day variability of 24-h ambulatory oesophageal impedance-pH monitoring in a Belgian-French cohort of healthy subjects. Aliment. Pharmacol. Ther. 22, 1011–1021 (2005).
Tutian, R. et al. Normal values for ambulatory 24-h combined impedance pH-monitoring on acid suppressive therapy [abstract]. Gastroenterology 130 (Suppl. 2), a171 (2006).
Savarino, E. et al. The role of nonacid reflux in NERD: lessons learned from impedance-pH monitoring in 150 patients off therapy. Am. J. Gastroenterol. 103, 2685–2693 (2008).
Zerbib, F. et al. Normal values of pharyngeal and esophageal 24-hour pH impedance in individuals on and off therapy and interobserver reproducibility. Clin. Gastroenterol. Hepatol. 11, 366–372 (2013).
Kawamura, O. et al. Liquid-containing refluxes and acid refluxes may be less frequent in the Japanese population than in other populations: normal values of 24- hour esophageal impedance and pH monitoring. J. Neurogastroenterol. Motil. 22, 620–629 (2016).
Kandulski, A. et al. Esophageal intraluminal baseline impedance differentiates gastroesophageal reflux disease from functional heartburn. Clin. Gastroenterol. Hepatol. 13, 1075–1081 (2015).
Kessing, B. F. et al. Esophageal acid exposure decreases intraluminal baseline impedance levels. Am. J. Gastroenterol. 106, 2093–2097 (2011).
Martinucci, I. et al. Esophageal baseline impedance levels in patients with pathophysiological characteristics of functional heartburn. Neurogastroenterol. Motil. 26, 546–555 (2014).
Patel, A., Sayuk, G. S. & Gyawali, C. P. Acid-based parameters on pH-impedance testing predict symptom improvement with medical management better than impedance parameters. Am. J. Gastroenterol. 109, 836–844 (2014).
Patel, A. et al. GERD phenotypes from pH-impedance monitoring predict symptomatic outcomes on prospective evaluation. Neurogastroenterol. Motil. 28, 513–521 (2016).
Charbel, S., Khandwala, F. & Vaezi, M. F. The role of esophageal pH monitoring in symptomatic patients on PPI therapy. Am. J. Gastroenterol. 100, 283–289 (2005).
Bolier, E. A. et al. Systematic review: questionnaires for assessment of gastroesophageal reflux disease. Dis. Esophagus 28, 105–120 (2015).
Dent, J. et al. Accuracy of the diagnosis of GORD by questionnaire, physicians and a trial of proton pump inhibitor treatment: the Diamond Study. Gut 59, 714–721 (2010).
Jones, R. et al. Development of the GerdQ, a tool for the diagnosis and management of gastro-oesophageal reflux disease in primary care. Aliment. Pharmacol. Ther. 30, 1030–1038 (2009).
Fass, R. Erosive esophagitis and nonerosive reflux disease (NERD): comparison of epidemiologic, physiologic, and therapeutic characteristics. J. Clin. Gastroenterol. 41, 131–137 (2007).
Savarino, E., Zentilin, P. & Savarino, V. NERD: an umbrella term including heterogeneous subpopulations. Nat. Rev. Gastroenterol. Hepatol. 10, 371–380 (2013).
Poh, C. H. et al. Upper GI tract findings in patients with heartburn in whom proton pump inhibitor treatment failed versus those not receiving antireflux treatment. Gastrointest. Endosc. 71, 28–34 (2010).
Savarino, E. et al. Novel insights into esophageal diagnostic procedures. Ann. NY Acad. Sci. 1380, 162–177 (2016).
Ates, F. et al. Mucosal impedance discriminates GERD from non-GERD conditions. Gastroenterology 148, 334–343 (2015).
Weijenborg, P. W. et al. Hypersensitivity to acid is associated with impaired esophageal mucosal integrity in patients with gastroesophageal reflux disease with and without esophagitis. Am. J. Physiol. Gastrointest. Liver Physiol. 307, G323–G329 (2014).
Weijenborg, P. W. et al. Electrical tissue impedance spectroscopy: a novel device to measure esophageal mucosal integrity changes during endoscopy. Neurogastroenterol. Motil. 25, 574–578; (e457–e458) (2013).
Weijenborg, P. W., Smout, A. J. & Bredenoord, A. J. Esophageal acid sensitivity and mucosal integrity in patients with functional heartburn. Neurogastroenterol. Motil. 28, 1649–1654 (2016).
Vaezi, M. F. & Choksi, Y. Mucosal impedance: a new way to diagnose reflux disease and how it could change your practice. Am. J. Gastroenterol. 112, 4–7 (2017).
Vela, M. F. et al. Refractory heartburn: comparison of intercellular space diameter in documented GERD versus functional heartburn. Am. J. Gastroenterol. 106, 844–850 (2011).
van Malenstein, H., Farre, R. & Sifrim, D. Esophageal dilated intercellular spaces (DIS) and nonerosive reflux disease. Am. J. Gastroenterol. 103, 1021–1028 (2008).
Zentilin, P. et al. Reassessment of the diagnostic value of histology in patients with GERD, using multiple biopsy sites and an appropriate control group. Am. J. Gastroenterol. 100, 2299–2306 (2005).
Vieth, M. et al. Epithelial thickness is a marker of gastroesophageal reflux disease. Clin. Gastroenterol. Hepatol. 14, 1544–1551.e1 (2016).
Savarino, E. et al. Microscopic esophagitis distinguishes patients with non-erosive reflux disease from those with functional heartburn. J. Gastroenterol. 48, 473–482 (2013).
Fiocca, R. et al. Long-term outcome of microscopic esophagitis in chronic GERD patients treated with esomeprazole or laparoscopic antireflux surgery in the LOTUS trial. Am. J. Gastroenterol. 105, 1015–1023 (2010).
Calabrese, C. et al. Reversibility of GERD ultrastructural alterations and relief of symptoms after omeprazole treatment. Am. J. Gastroenterol. 100, 537–542 (2005).
Yerian, L. et al. Refinement and reproducibility of histologic criteria for the assessment of microscopic lesions in patients with gastroesophageal reflux disease: the Esohisto Project. Dig. Dis. Sci. 56, 2656–2665 (2011).
Saleh, C. M., Smout, A. J. & Bredenoord, A. J. The diagnosis of gastro-esophageal reflux disease cannot be made with barium esophagograms. Neurogastroenterol. Motil. 27, 195–200 (2015).
Smeets, F. G. et al. Does measurement of esophagogastric junction distensibility by EndoFLIP predict therapy- responsiveness to endoluminal fundoplication in patients with gastroesophageal reflux disease? J. Neurogastroenterol. Motil. 21, 255–264 (2015).
Tucker, E. et al. Measurement of esophago-gastric junction cross-sectional area and distensibility by an endolumenal functional lumen imaging probe for the diagnosis of gastro-esophageal reflux disease. Neurogastroenterol. Motil. 25, 904–910 (2013).
Vakil, N. B., Traxler, B. & Levine, D. Dysphagia in patients with erosive esophagitis: prevalence, severity, and response to proton pump inhibitor treatment. Clin. Gastroenterol. Hepatol. 2, 665–668 (2004).
Ronkainen, J. et al. High prevalence of gastroesophageal reflux symptoms and esophagitis with or without symptoms in the general adult Swedish population: a Kalixanda study report. Scand. J. Gastroenterol. 40, 275–285 (2005).
De Ruigh, A. et al. Gaviscon Double Action Liquid (antacid & alginate) is more effective than antacid in controlling post-prandial oesophageal acid exposure in GERD patients: a double-blind crossover study. Aliment. Pharmacol. Ther. 40, 531–537 (2014).
Cossentino, M. J. et al. Randomised clinical trial: the effect of baclofen in patients with gastro-oesophageal reflux — a randomised prospective study. Aliment. Pharmacol. Ther. 35, 1036–1044 (2012).
Sifrim, D. & Zerbib, F. Diagnosis and management of patients with reflux symptoms refractory to proton pump inhibitors. Gut 61, 1340–1354 (2012).
Garros, A. et al. Factors associated with nonresponse to proton pump inhibitors therapy in patients referred for esophageal pH-impedance monitoring. Dis. Esophagus 29, 787–793 (2016).
Savarino, E. et al. The added value of impedance-pH monitoring to Rome III criteria in distinguishing functional heartburn from non-erosive reflux disease. Dig. Liver Dis. 43, 542–547 (2011).
Patel, A., Sayuk, G. S. & Gyawali, C. P. Prevalence, characteristics, and treatment outcomes of reflux hypersensitivity detected on pH-impedance monitoring. Neurogastroenterol. Motil. 28, 1382–1390 (2016).
Broeders, J. A. et al. Oesophageal acid hypersensitivity is not a contraindication to Nissen fundoplication. Br. J. Surg. 96, 1023–1030 (2009).
Herregods, T. V. et al. Patients with refractory reflux symptoms often do not have GERD. Neurogastroenterol. Motil. 27, 1267–1273 (2015).
Gyawali, C. P. Achalasia: new perspectives on an old disease. Neurogastroenterol. Motil. 28, 4–11 (2016).
Tack, J. et al. Functional gastroduodenal disorders. Gastroenterology 130, 1466–1479 (2006).
Rommel, N. et al. Rumination or belching-regurgitation? Differential diagnosis using oesophageal impedance-manometry. Neurogastroenterol. Motil. 22, e97–e104 (2010).
Bredenoord, A. J. et al. Aerophagia, gastric, and supragastric belching: a study using intraluminal electrical impedance monitoring. Gut 53, 1561–1565 (2004).
The International Working Group for Disorders of Gastrointestinal Motility and Function initiated the consensus meetings and provided material support for the consensus process. Five separate groups reviewed the current state-of-the-art in clinical measurement of gastrointestinal motility and function: oropharynx, esophagus, reflux disease, stomach / intestine and anorectum. This process was endorsed by the European Society of Neurogastroenterology and Motility (ESNM) and the European Society of Colo-Proctology (ESCP) with representation and support from the American Neurogastroenterology and Motility Society (ANMS), South and Latin American Neurogastroenterology and Motility Society (SLNG), Asian Neurogastroenterology and Motility Association (ANMA) and members of the Australasian Neurogastroenterology and Motility Association (ANGMA). Financial support was provided by the United European Gastroenterology (UEG) Education Committee, registration fees for meetings and sponsorship from all major manufacturers of physiological measurement equipment.
E.S. has served as consultant for Medtronic and Sandhill Scientific. A.B. received research funding from Endostim, as well as speaker and consulting fees from Medical Measurement Systems. M.F. received research funding from AstraZeneca, Medtronic and Reckitt Benckiser, and educational grants or speaker fees from Medical Measurement Systems, Medtronic, Mui Scientific, Reckitt Bencki and Sandhillser. J.E.P. has served as a consultant and speaker for Medtronic and Sandhill Scientific, a speaker for Astra Zeneca and Takeda, and a consultant for Ironwood. He also has stock options from Trimedyne Inc. S.R. has served as consultant for Medtronic and Sandhill Scientific and received research grant from Crospon. C.P.G. has served as a consultant for Ironwood, Medtronic and Torax, he is a speaker for Allergan and Medtronic, and has received research funding from Medtronic.
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Savarino, E., Bredenoord, A., Fox, M. et al. Advances in the physiological assessment and diagnosis of GERD. Nat Rev Gastroenterol Hepatol 14, 665–676 (2017). https://doi.org/10.1038/nrgastro.2017.130
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