What diagnostic tests are indicated for evaluating vertigo?

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Diagnostic Tests for Vertigo

The diagnostic evaluation of vertigo is fundamentally clinical and relies on bedside positional maneuvers—specifically the Dix-Hallpike and supine roll tests—rather than laboratory or imaging studies, which should be reserved only for patients with red-flag features suggesting central pathology. 1

Essential Bedside Maneuvers (First-Line Diagnostic Tests)

Dix-Hallpike Maneuver (Gold Standard for Posterior Canal BPPV)

  • Perform this test bilaterally on every patient presenting with positional vertigo by moving the patient from upright to supine with the head turned 45° to one side and neck extended 20° beyond horizontal. 1, 2
  • Positive findings include: torsional upbeating nystagmus with 5-20 second latency, crescendo-decrescendo pattern lasting <60 seconds, fatigability with repeated testing, and accompanying subjective vertigo. 1, 2
  • The test has 82% sensitivity and 71% specificity for posterior canal BPPV, though a negative result does not rule out BPPV and may require repeat testing at a separate visit. 1
  • A negative Dix-Hallpike mandates proceeding to the supine roll test to evaluate for lateral canal BPPV. 1

Supine Roll Test (For Lateral Canal BPPV)

  • Perform this test when the Dix-Hallpike is negative or shows horizontal nystagmus by rapidly rotating the patient's head 90° to each side while supine. 1, 2
  • Lateral canal BPPV accounts for 10-15% of BPPV cases and is commonly missed when this test is skipped. 1, 2
  • Observe for geotropic nystagmus (fast component toward the ground, most common) or apogeotropic nystagmus (fast component away from the ground). 1, 3

HINTS Examination (For Acute Vestibular Syndrome)

  • Use the Head Impulse, Nystagmus, Test of Skew examination to differentiate vestibular neuritis from posterior circulation stroke in patients with continuous vertigo lasting days. 3
  • This bedside test has 92.9% sensitivity and 83.4% specificity for central causes when performed by trained clinicians. 3

Nystagmus Assessment (Critical Diagnostic Feature)

Peripheral Vertigo Nystagmus Characteristics

  • Horizontal with rotatory component, unidirectional, suppressed by visual fixation, fatigable with repeated testing, and has brief latency before onset. 4

Central Vertigo Nystagmus Characteristics (Red Flags)

  • Pure vertical (upbeating or downbeating) without torsional component, direction-changing without head position changes, not suppressed by visual fixation, and does not fatigue with repeated testing. 4, 2
  • Downbeating nystagmus on Dix-Hallpike without torsional component mandates urgent MRI. 4
  • Baseline nystagmus present without provocative maneuvers is a red flag for central disease. 4, 2
  • Gaze-evoked nystagmus (direction changes with eccentric gaze) is typical of central lesions, especially vertebrobasilar insufficiency. 4

Imaging Studies (Only When Red Flags Present)

When Imaging Is NOT Indicated

  • Do not order radiographic imaging or vestibular testing in patients meeting diagnostic criteria for BPPV with typical nystagmus on Dix-Hallpike testing and no additional concerning symptoms. 1
  • CT head has <1% diagnostic yield for isolated dizziness and misses posterior fossa strokes in the acute phase. 1, 3
  • MRI has only 4% diagnostic yield in patients with isolated dizziness without neurologic findings. 1

When Urgent MRI Brain (With Diffusion-Weighted Imaging) Is Mandatory

  • Severe postural instability with falling 1, 4, 3
  • New-onset severe headache accompanying vertigo 4, 3
  • Any additional neurologic symptoms (dysarthria, dysmetria, dysphagia, sensory/motor deficits, diplopia, Horner's syndrome) 4, 3
  • Downbeating nystagmus on Dix-Hallpike without torsional component 4, 3
  • Purely vertical nystagmus without torsional component 4, 3
  • Failure to respond to appropriate peripheral vertigo treatments (e.g., canalith repositioning) 4, 3
  • Baseline nystagmus without provocative maneuvers 4, 3
  • Positive Romberg test (indicates central pathology requiring imaging before Dix-Hallpike) 3

Specialized Imaging

  • MRI head and internal auditory canal without contrast is first-line for persistent vertigo with neurologic symptoms and can detect acute brain lesions in 11% of patients with acute persistent vertigo even without focal neurologic deficits. 3
  • MRA head and neck can detect vertebrobasilar insufficiency in episodic vertigo that cannot be confidently categorized as peripheral. 3
  • CT temporal bone without contrast is indicated for conductive hearing loss without middle-ear mass to detect otosclerosis, ossicular chain erosion, or superior semicircular canal dehiscence—not for routine vertigo evaluation. 1, 3

Audiometric Testing

  • No recommendation for routine audiometry in diagnosed BPPV. 1
  • Consider audiometry when auditory symptoms suggest Ménière's disease (fluctuating hearing loss, tinnitus, aural fullness) or other inner ear pathology. 3
  • An abnormal Weber test mandates formal hearing evaluation to differentiate conductive from sensorineural loss. 4

Laboratory Testing

  • Routine blood tests (CBC, serum chemistry) are not recommended as standard practice for BPPV diagnosis, which accounts for 85-95% of vertigo cases and is diagnosed clinically. 3
  • Reserve laboratory tests for specific clinical scenarios: autoimmune panels for progressive fluctuating bilateral hearing loss with concurrent vision/skin/joint problems; serologic testing for suspected Lyme disease or otosyphilis presenting with vertigo and severe otalgia, fever, or sudden bilateral hearing loss. 3

Critical Pitfalls to Avoid

  • Do not assume a normal neurologic examination excludes stroke: 75-80% of posterior circulation strokes causing vertigo lack focal neurologic deficits initially, and approximately 10% of cerebellar strokes present identically to peripheral vestibular disorders. 4, 2, 3
  • Do not skip the supine roll test when Dix-Hallpike is negative, as lateral canal BPPV is commonly missed. 2, 3
  • Do not rely solely on patient descriptions of "spinning" or "dizziness"—focus on timing and triggers to categorize into acute vestibular syndrome (days), spontaneous episodic (minutes-hours), triggered episodic (<1 minute), or chronic (weeks-months). 3, 5, 6
  • Isolated transient vertigo may precede vertebrobasilar stroke by weeks to months, typically lasting <30 minutes without hearing loss, with gaze-evoked nystagmus and severe postural instability. 4
  • Multiple peripheral vestibular disorders can coexist (e.g., BPPV with Ménière's disease or vestibular neuritis), requiring careful evaluation. 4

Follow-Up Protocol

  • Reassess all patients within 1 month after initial observation or treatment to confirm symptom resolution or identify persistent BPPV or underlying peripheral vestibular/CNS disorders. 1, 3
  • Repeat the Dix-Hallpike test at follow-up to confirm ongoing BPPV or other vestibular pathology if symptoms persist. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Physical Examination for Vertigo

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Diagnostic Approach to Vertigo

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Differentiating Between Central and Peripheral Vertigo Clinically

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

A New Diagnostic Approach to the Adult Patient with Acute Dizziness.

The Journal of emergency medicine, 2018

Research

Acute Dizziness.

Seminars in neurology, 2019

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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