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VNG Report Interpretation — Jasleen Kapan, 48F (21/Apr/2026)
Summary of Findings
| Test | Result | Interpretation |
|---|
| Saccades (H & V) | Velocity, precision, latency all within normal limits | Central saccade pathways intact |
| Smooth Pursuit Horizontal (0.2 Hz) | Gain 0.28–0.45 (both eyes, both directions) | Significantly reduced (normal ≥ 0.8) |
| Smooth Pursuit Horizontal (0.4 Hz) | Gain 0.36–0.52 | Reduced (age-expected slight drop, but still below normal) |
| Smooth Pursuit Vertical (0.2 Hz) | Gain 0.50–0.55 | Borderline low-normal |
| Smooth Pursuit Vertical (0.4 Hz) | Gain 0.26–0.31 | Significantly reduced |
| Optokinetic (OKN) all directions | Gain 0.89–1.15 (10° and 20° stimuli) | Normal |
| Spontaneous nystagmus (light/dark) | None recorded | Normal |
| High-frequency head shake | No post-head shake nystagmus | Normal |
| Gaze tests (all positions) | No gaze-evoked nystagmus | Normal |
| Dix-Hallpike Right | No nystagmus in all positions | Negative |
| Dix-Hallpike Left — Supine Head Ext. & Left | Left eye: vertical nystagmus, SPV 19.96°/s, amplitude 7.62°, freq 0.96 Hz | Positive — left posterior canal BPPV |
| Dix-Hallpike Left — Return to Sit (second recording) | Left eye: vertical SPV −3.14°/s, amplitude 0.10°, freq 0.95 Hz | Minimal reversal nystagmus on return (consistent with BPPV) |
| Subjective Visual Vertical (SVV) | Deviations of 1° (clockwise) and −1° (anticlockwise/blank) | Within normal limits (normal < 2–2.5°) |
Key Abnormalities
1. Bilaterally Reduced Smooth Pursuit Gain (Horizontal > Vertical)
Horizontal smooth pursuit gain of 0.28–0.52 is well below the expected ≥ 0.80 for a 48-year-old. This is a bilateral, symmetric abnormality. Reduced smooth pursuit in isolation — without gaze-evoked nystagmus, without saccadic intrusions, and with normal OKN — points to a central vestibulo-cerebellar pathway dysfunction, specifically involving the flocculus/paraflocculus of the cerebellum, which normally drives smooth pursuit. However, it can also be seen in:
- Vestibular migraine (the most likely diagnosis in this clinical context — see below)
- Medications (sedatives, anticonvulsants, alcohol — must be excluded)
- Mild cerebellar or brainstem lesions
The OKN gain being fully preserved (0.89–1.15) while smooth pursuit is impaired is a significant dissociation: OKN is driven by a lower-level brainstem–retinal reflex arc and does not require cerebellar smooth pursuit circuits, so this pattern is consistent with a cerebellar/cortical pursuit pathway defect rather than a retinal or brainstem problem.
2. Left Posterior Canal BPPV
The Dix-Hallpike Left (supine, head extended and rotated left) produced:
- Vertical nystagmus in the left eye at 0.96 Hz, SPV 19.96°/s, amplitude 7.62°
- This is characteristic of left posterior semicircular canal BPPV — free-floating otoconia (canalith) in the left posterior canal generates geotropic, upbeat-torsional nystagmus when triggered by the provoking head position
- The minimal reversal nystagmus on sitting back up is further confirmatory
- Dix-Hallpike Right was completely negative
Clinical Correlation with Symptoms
| Symptom | Mechanism |
|---|
| Dizziness after prolonged walking | Low-level continuous head motion at ~2 Hz demands sustained vestibulo-ocular and cerebellar smooth pursuit compensation. In this patient, impaired smooth pursuit and a subclinical left BPPV combine to degrade gaze stability with repetitive head micro-movements during walking, causing dizziness/unsteadiness on prolonged ambulation. |
| Dizziness after returning from gym | Exercise causes sustained head movement, elevated cardiovascular output, and in susceptible patients (especially those with vestibular migraine), exercise is a well-documented trigger. Vigorous gym activity likely displaces the otolithic debris further or provokes a migraine-related episode through vascular/autonomic mechanisms. |
| Symptoms worsening during menstruation | Estrogen and progesterone fluctuations at menstruation have direct effects on labyrinthine fluid dynamics (endolymph volume regulation) and lower the central vestibular migraine threshold. Menstrual vestibular migraine is a recognised entity — estrogen withdrawal before menstruation drops the migraine threshold, and the inner ear is highly sensitive to these hormonal changes. This cyclical pattern in a 48-year-old woman also raises consideration of perimenopause, where hormonal fluctuation is maximal and worsens vestibular symptoms. |
| Dizziness during prolonged driving | Driving provides sustained optokinetic stimulation (visual flow from passing scenery) without corresponding vestibular/proprioceptive movement matching — a sensory mismatch or "visual dependency" state. Patients with smooth pursuit dysfunction rely excessively on visual input and are overwhelmed when visual-vestibular conflict is high (classic "highway driving" dizziness). The left BPPV can also be provoked by head turns while checking mirrors. |
Integrated Diagnosis
Primary diagnosis: Vestibular Migraine with left posterior canal BPPV
The overall pattern — bilaterally reduced smooth pursuit (central vestibular sign), left posterior canal BPPV (peripheral component), cyclical worsening with menstruation, symptom provocation with exercise and prolonged locomotion, and preserved gaze/saccades/OKN — is most consistent with vestibular migraine as the unifying diagnosis, with a concurrent left posterior canal BPPV explaining positional symptoms.
At age 48, perimenopause is a major contributing factor that amplifies both components through hormonal fluctuation.
Recommended Management
- Left posterior canal BPPV → Epley manoeuvre (left side) — highly effective canalith repositioning; expect resolution in 1–3 sessions
- Vestibular migraine evaluation — detailed headache/dizziness diary; assess for migraine history (even "silent" migraine without headache)
- Vestibular physiotherapy — gaze stabilisation exercises to address smooth pursuit deficit
- Hormonal assessment — gynaecological review for perimenopausal status; hormone fluctuation management may significantly reduce cyclical vestibular episodes
- Trigger avoidance — vigorous head-impact exercise (avoid high-impact gym activities during symptomatic periods), adequate hydration, sleep hygiene
- Migraine prophylaxis — if frequency warrants, consider propranolol, nortriptyline, or venlafaxine (all have evidence for vestibular migraine)
Note: This interpretation is based on the VNG data and clinical context provided. The formal report section (Impression/Clinical History) in the original document was left blank. A complete clinical assessment including audiometry, full neurological examination, and migraine history is essential before initiating management.