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A Prospective Validation Study of the Functional Bedside Aspiration Screen with Endoscopy: Is It Clinically
Rebecca Kassubek1, Beate Lindner-Pfleghar1, Ioanna Eleni Virvidaki2
1Department of Neurology, University of Ulm, 89081 Ulm, Germany.
Journal of Clinical Medicine
|December 11, 2022
Summary
The Functional Bedside Aspiration Screen (FBAS) reliably predicts aspiration risk in acute stroke patients, aiding therapy decisions. This tool offers a time-efficient alternative when instrumentation is unavailable.
Area of Science:
- Neurology
- Swallowing Disorders
- Clinical Assessment
Background:
- Aspiration risk is a significant concern in acute stroke patients.
- Accurate and timely assessment is crucial for guiding dysphagia management.
- Existing assessment tools may require specialized equipment or expertise.
Purpose of the Study:
- To validate the reliability of the Functional Bedside Aspiration Screen (FBAS) in predicting aspiration risk.
- To assess the FBAS's utility in guiding initial therapy needs for acute stroke patients.
- To compare FBAS performance against established swallowing assessment scales.
Main Methods:
- Prospective validation study involving 101 acute ischemic stroke patients.
- Comparison of FBAS scores with the Penetration Aspiration Scale (PAS) using Flexible Endoscopic Swallowing Study.
- Correlation analysis with the Functional Oral Intake Scale (FOIS) and Therapy Requirement Scale (TRS).
Main Results:
- FBAS demonstrated 73% sensitivity and 62% specificity for predicting aspiration risk (PAS ≥ 6).
- For patients with mild neurological deficits (mRS 0-2), FBAS showed 66.7% sensitivity and 88.6% specificity.
- FBAS scores correlated negatively with PAS and positively with FOIS, indicating clinical relevance.
Conclusions:
- The Functional Bedside Aspiration Screen (FBAS) is a reliable tool for predicting aspiration risk in acute stroke.
- FBAS can serve as a time-efficient clinical support tool, especially where instrumentation is limited.
- Further research with larger cohorts, including severely affected stroke patients, is warranted.
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