Evidence map›Paper›PMID 42127078›Full record

SynthesisPloS one2026

Evaluation of the diagnostic value of the Modified Evan's Blue Dye Test for assessing aspiration in tracheostomized critically ill patients: A systematic review and meta-analysis.

Eszter Szőke, Ildikó Szántó, Caner Turan, Bence Szabó, Márton Papp, Gábor Horváth, László Zubek, Péter Hegyi, Zsolt Molnár, András Lovas

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Eszter SzőkeCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0009-0009-7408-8897
Ildikó SzántóCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Caner TuranCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-8200-7569
Bence SzabóCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Márton PappCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Gábor HorváthCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
László ZubekCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Péter HegyiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0003-0399-7259
Zsolt MolnárCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
András LovasCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-8320-1515

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysphagia and aspiration are common complications in tracheostomized critically ill patients. The Modified Evan's Blue Dye Test (MEBDT) is a non-invasive, bedside, adjunctive rule-in signal for aspiration when positive. However, its diagnostic accuracy compared to the gold standard Fiberoptic Endoscopic Evaluation of Swallowing (FEES) in these patients remains unclear. We conducted a systematic review and meta-analysis to evaluate the diagnostic accuracy of the MEBDT for the detection of aspiration in tracheostomized critically ill patients. Study protocol was prospectively registered on PROSPERO (CRD:42023479920). A systematic search was performed across three databases (PubMed, Cochrane Central, and Embase), followed by a systematic screening process against predetermined selection criteria and included studies that provided data on the sensitivity and specificity of MEBDT versus FEES. The risk of bias and the level of evidence certainty in the included papers were assessed by the QUADAS-2 tool and GRADE approach respectively. Six out of 2227 screened studies were included. We found that MEBDT had a high specificity 95.42% (95% CI [67.38%, 99.53%]) and positive predictive value 95% (95% CI [81, 100]). In conclusion, the MEBDT can serve as a bedside adjunctive tool that indicates a potential aspiration risk when the result is positive. However, if the result is negative, further diagnostic assessments, like FEES, are recommended for high-risk patients.

Indexed as

Coloring AgentsDeglutition DisordersEvans BlueRespiratory AspirationTracheostomyCritical IllnessHumansSensitivity and SpecificityColoring AgentsEvans Blue

Identifiers

PMID42127078
PMCPMC13170877

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Registered trials

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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.