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
Clinical Snapshot
PICO Framework
| P — Population | Tracheostomized critically ill patients with suspected dysphagia/aspiration |
| I — Intervention | Modified Evan's Blue Dye Test (MEBDT) |
| C — Comparator | Fiberoptic Endoscopic Evaluation of Swallowing (FEES) as gold standard |
| O — Outcomes | Diagnostic accuracy (sensitivity, specificity, positive predictive value) for aspiration detection |
Bottom Line
This meta-analysis of six studies suggests the Modified Evan's Blue Dye Test has high specificity (95%) for detecting aspiration in tracheostomized ICU patients when compared to FEES. However, the evidence base is limited and imprecise, with very wide confidence intervals. The test appears useful as a 'rule-in' tool - when positive, it strongly suggests aspiration risk. However, sensitivity data is missing, limiting assessment of the test's ability to detect all cases of aspiration. The authors appropriately recommend that negative results should prompt further evaluation with FEES in high-risk patients. While MEBDT offers a practical bedside screening option, clinicians should interpret results cautiously given the limited evidence and use it as part of a comprehensive dysphagia assessment rather than a standalone diagnostic tool.
Key Findings
P Value: Not reported
Effect Size: Specificity 95.42%, PPV 95%
Primary Outcome: Diagnostic accuracy of MEBDT for aspiration detection
Nnt Or Sensitivity: Sensitivity not reported; high specificity suggests good rule-in test when positive
Confidence Interval: Specificity 95% CI [67.38%, 99.53%], PPV 95% CI [81%, 100%]
Clinical Application
Highly feasible as bedside, non-invasive test requiring minimal resources Relevant to Australian ICUs; complements existing dysphagia assessment protocols; no specific TGA or PBS considerations for this diagnostic test ICU patients with tracheostomies requiring dysphagia assessment
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.
References
- 1.Szőke, E., Szántó, I., Turan, C., Szabó, B., Papp, M., Horváth, G., Zubek, L., Hegyi, P., Molnár, Z., & Lovas, A. (2026). 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. PLoS One. https://doi.org/10.1371/journal.pone.0349092
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