Physiotherapy assessment of cranial nerve examination

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Physiotherapy assessment of cranial nerves

Cranial nerve examination is part of a neurological screen in physiotherapy, especially after stroke, traumatic brain injury, concussion, dizziness, facial weakness, suspected central nervous system pathology, or unexplained balance problems.

Preparation

  • Explain the assessment and obtain consent.
  • Ensure the patient uses their usual glasses and hearing aids.
  • Compare right and left sides throughout.
  • Observe first: facial symmetry, eyelid position, speech, swallowing, head posture, involuntary eye movements, and use of mobility aids.
  • Stop and seek urgent medical review if there is an acute new deficit, particularly diplopia, dysphagia, facial weakness, unequal pupils, sudden visual loss, severe headache, or new ataxia.
Cranial nerveMain functionPhysiotherapy screening testAbnormal findings / relevance
I OlfactorySmellWith eyes closed, identify a familiar, non-irritant odour such as coffee or soap, one nostril at a time.Usually omitted unless there is relevant head trauma, frontal-lobe concern, or reported loss of smell. Do not use irritants such as ammonia.
II OpticVisionAsk about visual clarity; check reading of suitable print, visual fields by confrontation, and ability to detect fingers in each quadrant.Field loss can affect walking safety, obstacle avoidance, reading, and falls risk.
III OculomotorMost eye movements, pupil constriction, eyelid elevationObserve eyelid position and pupil size. Assess pupil response to light if within scope. Test eye tracking.Ptosis, diplopia, unequal pupils, impaired gaze, or poor visual tracking. New pupil asymmetry with headache or reduced consciousness needs urgent escalation.
IV TrochlearDownward and inward eye movementIncluded with eye-movement testing. Ask whether double vision occurs when looking down, such as on stairs.Diplopia on downward gaze can affect stair negotiation and mobility.
V TrigeminalFacial sensation and masticationTest light touch over forehead (V1), cheek (V2), and jaw (V3), comparing sides. Palpate masseter/temporalis while patient clenches teeth.Altered facial sensation or weak jaw clench. Corneal reflex is generally not a routine physiotherapy test.
VI AbducensLateral eye movementTest with H-pattern or tracking a target horizontally and vertically, keeping head still.Failure to abduct eye, horizontal diplopia, nystagmus. Important in vestibular and balance assessment.
VII FacialFacial expression; taste anterior tongueInspect face at rest. Ask patient to raise eyebrows, close eyes tightly, smile, show teeth, puff cheeks, and frown.Whole-side facial weakness suggests a peripheral pattern; lower facial weakness with preserved forehead movement may suggest a central pattern. Check ability to close eye fully and protect cornea.
VIII VestibulocochlearHearing and balanceScreen hearing with finger rub or whisper, one ear at a time. In dizziness, observe spontaneous/gaze-evoked nystagmus, gait, balance, and consider vestibular assessment within competence.Hearing asymmetry, vertigo, nystagmus, imbalance, nausea. Acute vestibular symptoms plus focal neurological signs require urgent referral.
IX GlossopharyngealPharyngeal sensation, swallowing contributionListen to voice quality, ask about choking/coughing with food or fluids, and observe swallowing only if appropriate.Wet/gurgly voice, cough after swallowing, nasal regurgitation, dysphagia. Refer promptly to speech and language therapy or medical team. Do not routinely elicit gag reflex.
X VagusPalatal movement, voice, swallowingAsk patient to say “ah”; observe palate elevation and uvula position. Listen for hoarseness or nasal speech.Palatal asymmetry, hoarseness, weak cough, swallowing difficulty. Aspiration risk needs escalation.
XI AccessorySternocleidomastoid and trapeziusShoulder shrug against resistance. Turn head against resistance to each side.Shoulder droop or weakness, difficulty with cervical control and upper-limb function.
XII HypoglossalTongue movementAsk patient to protrude tongue and move it side-to-side. Observe for deviation, wasting, or fasciculations.Tongue deviation, dysarthria, impaired bolus control, possible swallowing difficulty.

Eye movement test: practical method for CN III, IV and VI

  1. Position the target about 30-50 cm from the patient.
  2. Ask the patient to keep their head still and follow the target with the eyes only.
  3. Move the target in an H-pattern.
  4. Observe for:
    • Reduced range of eye movement
    • Diplopia
    • Nystagmus
    • Loss of smooth pursuit
    • Head movement used to compensate
  5. Ask, “Do you see one image or two?” and identify the gaze direction provoking diplopia.
Harrison's recommends a minimum neurological cranial-nerve screen that includes visual fields, pupils, extraocular movements, and facial movements; it also advises grouping CN III, IV and VI because of their shared ocular-motor role. Harrison's Principles of Internal Medicine, 22e, Cranial Nerve Examination section.

Documentation example

Cranial nerve screen: CN II visual fields grossly intact to confrontation. Pupils equal and reactive. Extraocular movements full; no diplopia or nystagmus. Facial sensation and facial movements symmetrical. Hearing grossly intact to finger rub bilaterally. Voice clear; no reported dysphagia. Palate elevates symmetrically. Shoulder shrug and head rotation strong and equal. Tongue protrudes midline.

Key physiotherapy implications

  • Visual-field loss or diplopia: assess transfers, mobility, stair safety, scanning strategies, and falls risk.
  • Vestibular signs: distinguish possible peripheral vestibular presentation from central warning signs.
  • Facial weakness: eye protection, communication, eating/drinking concerns, and appropriate referral.
  • Bulbar signs, CN IX, X, XII: treat as swallowing and airway-safety concerns, not simply as an exercise issue.
  • CN XI weakness: consider scapular position, neck pain, shoulder function, and upper-limb rehabilitation.
A recent systematic-review search did not identify evidence that changes the standard bedside cranial-nerve screen; the core approach remains clinical observation, side-to-side comparison, and prompt escalation of acute focal deficits.
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