Dysphagia Grading Systems
The Dysphagia Outcome and Severity Scale (DOSS) is the recommended grading system for evaluating dysphagia severity, as it is a validated 7-point scale with high inter-rater (90%) and intra-rater (93%) reliability that systematically rates functional severity and provides specific recommendations for diet level, independence, and nutrition type. 1
Primary Grading Systems
DOSS (Dysphagia Outcome and Severity Scale)
The DOSS is the most widely validated and reliable scale for clinical use, rating dysphagia on a 7-point scale based on three critical assessment areas: 1
The scale has demonstrated strong criterion validity when used with both videofluoroscopic swallowing studies (VFSS) and flexible endoscopic evaluation of swallowing (FEES), with correlation coefficients of rs = 0.936 for DOSS and rs = 0.858 for FOIS. 2 Recent validation confirms DOSS can be reliably used with FEES, showing high inter-rater agreement (α = 0.891) and almost perfect intra-rater agreement (Kw = 0.945). 2
Alternative Validated Scales
Functional Outcome Swallowing Scale (FOSS) provides a simpler 6-stage system (0-V) based on functional outcomes: 3
- Stage 0: Normal function, asymptomatic 3
- Stage I: Normal function with episodic/daily symptoms 3
- Stage II: Compensated abnormal function with dietary modifications but no weight loss 3
- Stage III: Decompensated function with ≤10% weight loss or daily aspiration 3
- Stage IV: Severely decompensated with >10% weight loss or severe aspiration complications 3
- Stage V: Nonoral feeding for all nutrition 3
Dysphagia Severity Scale (DSS) rates severity based on: 4
- Laryngeal penetration/aspiration (scored by which food consistencies are aspirated) 4
- Pharyngeal retention (scored as none, minimal, moderate, or severe) 4
- Final score takes the higher of the two ratings, with correlation to clinical severity of r = 0.71 4
Clinical Application Algorithm
For Oropharyngeal Dysphagia Assessment
Step 1: Screening - Use validated questionnaires in specific populations:
- Parkinson's disease: Apply the Swallowing Disturbance Questionnaire (SDQ) with 81% sensitivity and 82% specificity, or the Munich Dysphagia Test-PD (MDT-PD) with 81% sensitivity and 71% specificity 5
- Multiple sclerosis: Use the Northwestern Dysphagia Patient Check Sheet, which identifies dysphagia in 31.7% of consecutive MS patients 5
Step 2: Clinical Identifiers - Recognize high-risk features requiring formal evaluation: 5
- Need for oral-pharyngeal suctioning 5
- Malnutrition or unintentional weight loss 5
- Feeding tube in place 5
- Abnormal chest x-ray (patchy opacity, lower lobe infiltrate, air space disease) 5
- Dysarthria or dysphonia 5
- Weak voluntary cough 5
- Reflexive cough or wet voice after water bolus 5
Step 3: Instrumental Assessment - Proceed to definitive testing:
- FEES is preferred over VFSS for oropharyngeal dysphagia, particularly in Parkinson's disease, as it avoids radiation, requires minimal patient cooperation, can be performed bedside, and directly identifies silent aspiration that occurs frequently in neurological conditions 5
- VFSS should be used if FEES is unavailable 5
For Esophageal Dysphagia Assessment
High-resolution manometry (HRM) is superior to standard manometry for evaluating dysphagia, with better reproducibility, faster performance, and easier interpretation. 5 HRM should be performed in all patients being considered for antireflux surgery to rule out achalasia and major motor disorders. 5
Critical Pitfalls to Avoid
Clinical experience significantly affects DOSS reliability: More experienced speech-language pathologists (>3 years VFSS experience) demonstrate significantly higher inter-rater reliability (κ = 0.342) compared to less experienced clinicians (κ = 0.298). 6
Audio-recording during VFSS improves DOSS accuracy: DOSS inter-rater reliability is significantly higher with audio-recorded VFSS clips (κ = 0.287) versus silent clips (κ = -0.0395). 6
Silent aspiration is common and dangerous: Up to 55% of patients who aspirate do so without a protective cough reflex, making clinical diagnosis unreliable without instrumental assessment. 7 In Parkinson's disease specifically, silent penetration and aspiration cannot be reliably detected by clinical assessment alone. 5
Subjective patient reports have limited specificity: In neurologically impaired patients, self-reported swallowing difficulty has 88% sensitivity but only 30% specificity for aspiration on videofluoroscopy, with a positive predictive value of just 52%. 5