Evidence map›Paper›PMID 40709418›Full record

ReviewThe Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi2025

[Clinical Significance of the Mean Nocturnal Baseline Impedance and Post-Reflux Swallow-Induced Peristaltic Wave Index in the Diagnosis of Gastroesophageal Reflux Disease].

Ju Yup Lee

Abstract readEnglish AbstractReview
In one paragraph

Review in The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. [Modern Diagnostic Strategies for Gastroesophageal Reflux Disease: Focus on Lyon Consensus 2.0].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Ju Yup LeeDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu, Korea.ORCID 0000-0003-0021-5354

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastroesophageal reflux disease (GERD) is a common condition characterized by the reflux of gastric contents into the esophagus, often leading to troublesome symptoms or complications. Although the acid exposure time (AET) has long been used as a key diagnostic marker, it may be insufficient in certain clinical situations, particularly in patients with borderline AET. Recently, two novel impedance-based parameters have emerged as useful adjuncts in the diagnostic evaluation of GERD: mean nocturnal baseline impedance (MNBI) and post-reflux swallow-induced peristaltic wave index (PSPW-I). These metrics reflect the esophageal mucosal integrity and chemical clearance, offering physiologically relevant insights beyond AET. Studies suggest that a low MNBI (<1,500 Ω) and PSPW-I (<61%) are associated with pathological reflux and favorable response to proton pump inhibitors. Moreover, the combined use of MNBI and PSPW-I may enhance diagnostic accuracy and aid in predicting the therapeutic outcomes. This review summarizes the physiological background, diagnostic thresholds, and clinical implications of MNBI and PSPW-I based on the current literature and highlights their potential role in GERD diagnosis and management. Nevertheless, future standardization and automation may further improve their clinical utility.

Indexed as

Gastroesophageal RefluxPeristalsisClinical RelevanceDeglutitionElectric ImpedanceEsophageal pH MonitoringHumansProton Pump InhibitorsProton Pump InhibitorsEsophageal pH monitoringGastroesophageal refluxImpedancePeristalsis

Identifiers

PMID40709418
PMCPMC12305085

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.