European Portuguese version of the Gugging Swallowing Screen-Intensive Care Units: reliability and validity
DOI:
https://doi.org/10.29352/mill0224e.44207Keywords:
deglutition disorders; intensive care units; sensitivity and specificity; nursing assessment; screeningAbstract
Introduction: Post-extubation dysphagia (PED) is a frequent complication of prolonged mechanical ventilation, increasing the risk of aspiration and malnutrition. Early screening with validated tools is essential, especially when instrumental assessments are unavailable. Although it has been translated and adapted into European Portuguese, the Gugging Swallowing Screen for Intensive Care Units (GUSS-ICU) has not been clinically validated.
Objective: To evaluate the reliability and concurrent validity of the European Portuguese version of the Gugging Swallowing Screen for Intensive Care Units (GUSS-ICU).
Methods: A cross-sectional study of 92 adult ICU patients in Portugal who received mechanical ventilation for over 24 hours and were eligible for oral intake. The GUSS-ICU was applied within one hour after extubation, followed by structured clinical swallowing evaluation within 24 hours. Inter-rater reliability and diagnostic accuracy (sensitivity, specificity, ROC) were assessed.
Results: GUSS-ICU identified dysphagia in 76.1% of patients, versus 70.7% by clinical evaluation. At a cut-off of 10, the instrument showed high accuracy (AUC = 0.912), sensitivity (75.9%), and specificity (96.9%). Scores negatively correlated with intubation duration (ρ = –0.353, p < 0.001). Inter-rater reliability was moderate (κ = 0.533).
Conclusion: Despite methodological limitations, GUSS-ICU showed acceptable agreement with structured clinical swallowing assessment and moderate inter-rater reliability, warranting further validation with instrumental reference standards.
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