I now have all the data I need to generate a detailed clinical interpretation report. Let me compile the comprehensive analysis.
Detailed VNG (Videonystagmography) Report - Clinical Interpretation
Patient Information
| Field | Details |
|---|
| Name | Surya Kumar Yadav (SK Yadav) |
| Patient ID | CCDA00422 |
| Age / Gender | 75 years / Male |
| Date of Test | 11 August 2026 |
| Facility | Priority Hearing Care Pvt. Ltd. |
| Chief Complaint | Continuous dizziness while walking |
Summary of All VNG Test Findings
1. SACCADE TEST (Rapid Eye Movement)
Saccades test the fast, voluntary gaze-shifting pathway (brainstem/cerebellum frontal eye fields).
| Parameter | 0.3 Hz Horizontal | 0.45 Hz Horizontal |
|---|
| Velocity (Right Eye) | 826 °/s | 781 °/s |
| Velocity (Left Eye) | 1677 °/s | 940 °/s |
| Precision (Right Eye) | 84.34 | 85.33 |
| Precision (Left Eye) | 132.57 | 84.33 |
| Latency (Right Eye) | 343 ms | 320 ms |
| Latency (Left Eye) | 315 ms | 337 ms |
Vertical Saccades (0.3 Hz / 0.45 Hz):
- Right Eye Velocity: 489 / 459 °/s
- Left Eye Velocity: 779 / 782 °/s
- Right Eye Precision: 73.49 / 71.52 (notably reduced)
- Right Eye Latency: 211 / 273 ms
Interpretation: There is an asymmetry in saccade velocity and precision - particularly, the right eye shows reduced precision and velocity in both horizontal (at 0.3 Hz) and vertical planes. Left eye saccade velocity appears higher at 0.3 Hz horizontal. Latencies are within acceptable range but the reduced precision of the right eye may reflect mild central or oculomotor pathway involvement. Normal saccade latency is 150-250 ms; latencies here are mildly prolonged, suggesting possible subcortical processing slowing consistent with age (75 years).
2. OPTOKINETIC TEST (OKN)
Tests the ability to follow a repeating moving visual field - a function of the brainstem and visual cortex.
| Direction | Right Eye Gain | Left Eye Gain |
|---|
| Left to Right (10°) | 1.05 | 0.95 |
| Right to Left (10°) | 0.87 | 0.96 |
| Top to Bottom (10°) | 0.86 | 0.87 |
| Bottom to Top (10°) | 1.02 | 0.96 |
Normal OKN gain range: 0.80 - 1.20
Interpretation: OKN gains are within normal limits in all four directions. This indicates that the central visual tracking pathways (visual cortex, parieto-occipital cortex, brainstem pursuit system) are functionally intact. No significant directional asymmetry or suppression of OKN is present. This effectively rules out significant central (posterior fossa) lesions affecting smooth pursuit/OKN symmetry.
3. SPONTANEOUS NYSTAGMUS
Spontaneous nystagmus in the absence of external stimulation indicates a tonic imbalance between left and right vestibular tone.
In Light (With Fixation):
| Channel | Right Eye | Left Eye |
|---|
| Horizontal SPV | - | - |
| Vertical SPV | 5.35 °/s | - |
| Amplitude (Vertical) | 1.93° | - |
| Frequency | 0.69 Hz | - |
In Dark (Without Fixation):
- No nystagmus recorded in any plane in either eye.
Interpretation - SIGNIFICANT FINDING:
- A low-amplitude vertical spontaneous nystagmus is present in the right eye in light, with a slow phase velocity of 5.35 °/s and amplitude of 1.93°. This is a subtle but real finding.
- The fact that it disappears in the dark (without fixation) suggests the nystagmus may be fixation-dependent or suppressed in darkness, a pattern sometimes seen in central/vertical nystagmus types.
- Alternatively, it may represent a very low-level peripheral tone imbalance. Vertical spontaneous nystagmus, however, is more characteristically associated with central vestibular pathology (e.g., cervicomedullary junction, cerebellum) rather than peripheral pathology, which typically produces horizontal nystagmus.
- SPV of 5.35 °/s is at the low end - anything >6 °/s is clearly abnormal, but values between 3 and 6 °/s warrant clinical correlation.
4. HIGH-FREQUENCY HEAD SHAKE TEST
- All values negative (no nystagmus) in horizontal or vertical planes.
- Interpretation: No head-shaking nystagmus. This is a normal finding and does not show the asymmetric vestibular loss pattern that produces post-shake nystagmus. This makes a significant unilateral peripheral vestibular hypofunction less likely as a sole cause.
5. GAZE TESTS
Tests whether nystagmus appears with sustained gaze in specific directions (with and without fixation).
WITH FIXATION (all gaze positions - Center, Left, Up, Right, Down):
- All nystagmus values negative/absent in all positions.
- Interpretation: No gaze-evoked nystagmus with fixation. Normal.
WITHOUT FIXATION:
| Position | Notable Finding |
|---|
| Center | No nystagmus |
| Left | No nystagmus |
| Up | No nystagmus |
| Right | SPV 3.46 °/s, Amplitude 4.09°, Freq 0.38 Hz - RIGHT EYE ONLY |
| Down | No nystagmus |
Interpretation - SIGNIFICANT FINDING:
- Right gaze-evoked nystagmus without fixation (SPV 3.46 °/s, Amplitude 4.09°): A low-amplitude nystagmus appears in the right eye when gazing right without fixation. This is a right-beating gaze-evoked nystagmus which is typically seen in:
- Peripheral vestibular uncompensated right-sided lesion (nystagmus beating toward the irritated side or away from the lesion depending on phase)
- Early cerebellopontine angle or cerebellar involvement
- It may also represent Alexander's Law - nystagmus intensity increases when gazing in the direction of the fast phase
6. DIX-HALLPIKE POSITIONAL TESTS (for posterior/anterior canal BPPV)
The Dix-Hallpike test places the head in a position to stress the posterior semicircular canal.
| Test Position | Slow Phase Velocity | Amplitude | Frequency | Significant? |
|---|
| DHP Right - Sit Head Right (1st trial) | Vertical 15.24 °/s | 8.03° | 0.88 Hz | YES - POSITIVE |
| DHP Right - Supine + Head Ext. Right | No nystagmus | - | - | Negative |
| DHP Right - Sit Head Right (2nd trial) | No nystagmus | - | - | Negative |
| DHP Left - Sit Head Left | No nystagmus | - | - | Negative |
| DHP Left - Supine Head Ext. Left | No nystagmus | - | - | Negative |
| DHP Left - Sit Head Left (2nd trial) | No nystagmus | - | - | Negative |
Interpretation - POSITIVE DIX-HALLPIKE RIGHT:
- The first Dix-Hallpike Right (sitting with head right) produced vertical nystagmus, SPV 15.24 °/s, amplitude 8.03°, frequency 0.88 Hz - this is a clearly positive and significant result.
- The finding was in the sitting phase (repositioning to upright), not in the supine position, suggesting the nystagmus may be triggered during the head movement into or out of the test position.
- The nystagmus disappeared on repeat testing (2nd DHP Right sit position = negative) - this fatigability is a hallmark of BPPV (canalolithiasis type).
- Right-sided provocation with vertical nystagmus and fatigability = Right Posterior Semicircular Canal BPPV is the primary diagnosis.
As noted in Adams and Victor's Principles of Neurology (12th Ed): "With repetition of the maneuver, vertigo and nystagmus become less apparent, and after three or four trials, they can no longer be elicited - referred to as 'fatigue'; they can be reproduced in their original severity only after a protracted period of rest." This classic fatigability pattern is present here.
7. MCCLURE-PAGNINI (SUPINE ROLL) TEST (for horizontal canal BPPV)
| Position | Significant Finding |
|---|
| Sit to Supine | No nystagmus |
| Right Lateral | No nystagmus |
| Supine Head Neutral (1st) | No nystagmus |
| Left Lateral | Horizontal nystagmus in LEFT EYE: SPV 6.69 °/s, Amplitude 11.27°, Freq 0.31 Hz |
| Supine Head Neutral (2nd) | No nystagmus |
Interpretation - SIGNIFICANT FINDING - POSITIVE MCCLURE-PAGNINI LEFT:
- Left lateral roll position produces a horizontal nystagmus exclusively in the left eye with SPV 6.69 °/s and amplitude 11.27°. This is a clearly positive roll test result.
- In the supine roll (McClure-Pagnini) test:
- Geotropic horizontal nystagmus (beats toward the ground/dependent ear) = Canalithiasis type horizontal canal BPPV
- Apogeotropic horizontal nystagmus (beats away from the ground) = Cupulolithiasis type horizontal canal BPPV
- The nystagmus appeared in the left eye with left lateral position - the direction needs correlation with the physical eye-movement trace to determine geotropic vs. apogeotropic, but the presence of nystagmus strongly indicates LEFT Horizontal Semicircular Canal BPPV.
8. SUBJECTIVE VISUAL VERTICAL (SVV)
The SVV tests otolith (utricle) function - the patient aligns a bar to perceived vertical.
| Condition | Deviation | Direction |
|---|
| Clockwise (CW) | -2° (Left) | AntiClockwise |
| AntiClockwise (ACW) | -3° (Left) | Clockwise |
| Blank Background | -1° (Left) | AntiClockwise |
Normal SVV: within ±2.5° of true vertical
Interpretation:
- All three trials show consistent left-sided tilt (the patient perceives vertical as tilted to the left).
- Deviations of -1° to -3° are borderline - the -3° value with blank background is approaching the abnormal range.
- SVV deviation to the left suggests possible dysfunction of the right otolith (utricular) system or the right descending vestibulospinal/otolithic pathways.
- Consistent left-tilt across all conditions supports a subtle right-sided vestibular imbalance affecting otolithic function.
Consolidated Abnormal Findings Table
| Test | Finding | Significance |
|---|
| Spontaneous Nystagmus (in light) | Vertical, right eye, SPV 5.35 °/s | Low-level vertical nystagmus - central or peripheral |
| Gaze Test (Right, without fixation) | Horizontal, right eye, SPV 3.46 °/s | Right gaze-evoked nystagmus |
| Dix-Hallpike RIGHT (1st trial) | Vertical nystagmus, SPV 15.24 °/s, fatigable | POSITIVE - Right Posterior Canal BPPV |
| McClure-Pagnini LEFT Lateral | Horizontal nystagmus, Left eye, SPV 6.69 °/s | POSITIVE - Left Horizontal Canal BPPV |
| SVV | -1° to -3° left tilt (all trials) | Borderline right otolith hypofunction |
PRIMARY DIAGNOSIS
Benign Paroxysmal Positional Vertigo (BPPV) - Multi-Canal Involvement
Specific canals implicated:
- Right Posterior Semicircular Canal BPPV (Canalithiasis) - Positive Dix-Hallpike Right with fatigable vertical nystagmus (SPV 15.24 °/s) - Primary finding
- Left Horizontal Semicircular Canal BPPV - Positive left lateral roll test (SPV 6.69 °/s) - Secondary finding
Multi-canal BPPV is well-recognized, occurring in approximately 15-20% of BPPV patients, and is more common in elderly patients (age 75 here). The two canals affected are on opposite sides, which is less common than same-side multi-canal involvement but reported.
SECONDARY/INCIDENTAL FINDINGS
Possible Central Vestibular Component (requires further evaluation):
- Vertical spontaneous nystagmus (SPV 5.35 °/s in light, absent in dark): Vertical spontaneous nystagmus is atypical for purely peripheral BPPV. While mild, it warrants consideration of:
- Cerebellar or brainstem microangiopathy (common in elderly, hypertensive patients)
- Central positional nystagmus as a differential
- Right gaze-evoked nystagmus without fixation: May reflect incomplete vestibular compensation on the right side, but could also indicate cerebellar hemispheric dysfunction.
Borderline SVV left tilt:
- Consistent left tilt (-1° to -3°) suggests subtle right utricular dysfunction, consistent with a right-sided peripheral vestibular process.
INTERPRETATION SUMMARY
| Domain | Status |
|---|
| Ocular Motor (Saccades) | Mild asymmetry, age-related slowing |
| Optokinetic | Normal |
| Spontaneous Nystagmus | Low-grade vertical - significant |
| Head Shake | Normal |
| Gaze (with fixation) | Normal |
| Gaze (without fixation) | Right gaze nystagmus - mild abnormal |
| Dix-Hallpike | POSITIVE right |
| Roll Test (Horizontal canal) | POSITIVE left lateral |
| SVV (Otolith) | Borderline left tilt |
| Overall | Peripheral Vestibular Disorder (BPPV, multi-canal) with borderline central component |
DIFFERENTIAL DIAGNOSES TO CONSIDER
- BPPV (Multi-canal) - Most likely diagnosis, supported by positional tests
- Age-related peripheral vestibular degeneration (Presbyvestibulopathy) - Common at age 75, may co-exist with BPPV
- Central vestibular pathology (cerebellar/brainstem) - Must be excluded given the vertical spontaneous nystagmus; MRI brain with focus on posterior fossa is recommended
- Vestibular neuritis (partially compensated) - Less likely given no head-shake nystagmus and intact OKN
CLINICAL RECOMMENDATIONS
Immediate Treatment (BPPV):
- Epley Maneuver (Canalith Repositioning) - For the Right Posterior Canal BPPV - this is the first-line treatment with 80-90% success rate in a single session
- BBQ Roll (Log Roll) / Lempert Maneuver - For the Left Horizontal Canal BPPV
Further Investigations:
- MRI Brain with Posterior Fossa sequences (FLAIR, DWI) - To rule out cerebellar infarct or demyelinating lesion given the vertical spontaneous nystagmus and gaze-evoked nystagmus
- Audiometry (Pure Tone and Speech) - To assess cochlear function and rule out Meniere's disease
- Video Head Impulse Test (vHIT) if available - To quantify semicircular canal gain and detect any canal paresis not captured on this VNG
- Blood pressure (orthostatic) - Rule out orthostatic hypotension contributing to dizziness while walking at age 75
Lifestyle Advice:
- Fall risk precautions - the patient is 75 years old with active BPPV; dizziness while walking significantly increases the risk of falls
- Vestibular rehabilitation exercises post-repositioning maneuver
- Avoid sudden head movements until BPPV is treated
CONCLUSION
This VNG study in Mr. Surya Kumar Yadav, 75 M, performed at Priority Hearing Care on 11 August 2026, reveals:
Bilateral multi-canal BPPV with right posterior semicircular canal canalithiasis as the dominant lesion, and concurrent left horizontal semicircular canal BPPV. A borderline vertical spontaneous nystagmus and right gaze-evoked nystagmus (without fixation) raise the possibility of a mild central vestibular component that warrants MRI evaluation to exclude posterior fossa pathology.
The symptom of continuous dizziness while walking is most directly explained by the active bilateral BPPV - the constant head movements during gait repetitively trigger brief vertiginous episodes from the displaced otoconia in both the right posterior and left horizontal canals, producing a sensation of sustained unsteadiness.
This report is an AI-assisted clinical interpretation based on the raw VNG data. Final clinical diagnosis and treatment decisions should be made by a qualified ENT surgeon, neurotologist, or neurologist in conjunction with clinical history and examination.