ENT Tests of function Flashcards

1
Q

NARROW BAND IMAGING - procedure
- patterns
- exam outcomes

A

A biologic endoscopy technique focusing on vascularisation of the lesion

  • Identifies neoangiogenic patterns inside and surrounding the target lesion
  • Initially developed to improve diagnosis/localisation of Barrett’s oesophagus

Procedure: Narrow band spectrum filters reduce illumination in all wavelengths except blue 415nm and green 540nm (the peaks of haemoglobin absorption) - Enhances visualisation of mucosal and submucosal microvascular patterns

Patterns:

  1. Normal — green vessels, parallel to epithelium then branch obliquely and end as intra-epithelial papillary capillary loop (IPCL)
  2. Premalignant/malignant — well demarcated brown areas within blue/green background, scattered dark spots (speckled pattern), increased micovascular density, winding/’earthworm’ vessels with abnormal IPCLs

Characterised into 5 patterns: Ni et al n=104 — sens=89%, spec=93%, PPV=992%, NPV=90%

  1. Normal
  2. Laryngitis (enlarged diameter of vessels)
  3. Hyperplasia, mild dysplasia (IPCLs may be obscured by white plaque)
  4. Hyperplasia, mild-mod dysplasia (IPCLs recognisd as small dots)
  5. Severe dysplasia (Va)-invasive carcinoma (Vb, Vc) —> speckled pattern, tortuous, irregular distribution, scattered across tumour surface
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2
Q

NARROW BAND IMAGING - applications

A

Applications: - Early detection of abnormal microvascular changes - Distinguishes low grade vs high grade dysplasia vs SCC - Pre-operative — ‘optical biopsy’, evaluate 2nd primary, 20% gain (upstaging, change surgical resection) - Intra-operative — peripheral extension of lesion, refine laser technique - Post-operative — detect persistent/recurrent disease - Retains sensitivity and specificity post-RT as well

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3
Q

SALIVARY FLOW TESTING xxx

A

TESTS: Chorda Tympani

PROCEDURE: 6% citric acid on anterior tongue Wharton’s duct cannulated and salivary flow measured Compare the two sides

OUTCOME: Reduction of 25% = abnormal

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4
Q

ASSESSMENT OF SWALLOWING - clinical

A

History:

  • Weight loss, haemoptysis etc

Examination:

  1. Oral cavity - dentures — poor sensation - CN function- IX, X, XII
  2. Neck - Masses
  3. FNE

Penetration = Saliva into trachea followed by clearance mechanisms

Aspiration = No clearance efforts observed

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5
Q

ASSESSMENT OF SWALLOWING - investigations

A
  1. FEES - FNE then observe swallow of various consistencies and observe pharyngeal phase of swallowing, pooling, penetration/aspiration - Detects presence of: penetration, aspiration, pooling, retained secretions, effectiveness of cough
    - Procedure: start with ice — water — pureed food — solids - Allows assessment of efficacy of compensatory strategies (e.g. head tuck, chin tuck) - Disadvantages: not good for oral phase, MBS better for quantifying pharyngeal movement 


  2. FEESST - FEES + sensory testing - Small puff of air in close proximity to laryngeal mucosa — elicits the Laryngeal Adductor Reflex (LAR) - Can be tested unilaterally - Grading of response, response elicited at: - 3mmHg = normal - 6mmHg = mild sensory impairment - 9mmHg = moderate impairment - Not elicited at 9mmHg = severe sensory impairment
  3. Modified Barium Swallow (MBS) - The gold-standard for swallowing complaints - Provides information regarding: - Anatomy - Function - safety of swallow, consistency of food, compensatory strategies
  4. Manometry - Assess for motility disorder e.g. achalasia

Management: - Diet modification, BioFEESback, swallowing exercises - Non-oral feeding (e.g. PEG)

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6
Q

LARYNGEAL EMG Def/technique/uses

A

Definition: A means of studying the electrical activity of the muscles of the larynx to provide diagnostic and prognostic information

Technique: Measure either spont activity or during phonation Monopolar needle into cricothyroid or thyroarytenoid muscle - T/A: percutaneous, midline through C/T membrane then head sup/lat - C/T: percutaneous, midline, then aim sup/lat along the cricoid to enter muscle

Uses:

  • Diagnostic - Site of lesion: SLN vs RLN (i.e. high vs low vagal) based on C/T vs T/A - Neurologic vs mechanical limitation - Mechanical will have normal EMG with fixed cord - CA joint arthritis, arytenoid dislocation, posterior glottic scarring
  • Prognostic - Predicting return of function after VC palsy
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7
Q

LARYNGEAL EMG Interpretations & treatment planning

A

Interpretation: - Spontaneous activity in normal muscle at rest is minimal - But not complete electrical silence (active with respiration) - Will have an initial negative deflection - Fibrillation potentials: presence of spontaneous, bizarre activity with initial positive deflection - Pathologic (denervation) - Polyphasic potentials: greater than 4 phases (N=2-3). - Hallmark of reinnervation

EMG findings after VC palsy: Timing is important - Initially: electrical silence (complete injury) vs reduced amplitude (incomplete, common in idiopathic lesions) - Fibrillation potentials occur by 3/52 (resting potential falls to near depol threshold) — perform 2-6/52 after injury - Then pattern is either reinnervation or no recovery - Reinnervation: polyphasic potentials. Motor unit weakness and asynchrony (can persist in long-term) - No recovery: spontaneous activity persists. muscle atrophies and replaced by CT

Guiding treatment: Subjective, difficult to interpret. Rarely used - Normal EMG - acute: reduce arytenoid sublux, chronic: look for fixation - Polyphasic potentials: observe/speech therapy vs temporary injection (gel foam, fat, restylane) - Based on patient factors: aspiration, vocal demand, patient desire - Fibrillation potentials (persisting): complete nerve injury. Manage either: Radiesse injection, MT +/- AA or nerve anastomosis or reinnervation

Good prognosis = recruitment, near normal wave morphology, absence of spontaneous activity

Poor prognosis = spontaneous activity (fibrillation potentials), absent recruitment

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8
Q

STROBOSCOPY xxx

A

Enables the human eye to visualise the vibratory pattern of the vocal fold during phonation

-Pulsed light source creates an illusion of continuous slow motion mucosal oscillation

Theory: Fundamental frequency: M=100Hz, F=200Hz Talbot’s law = human retina can only appreciate 5 images/sec (stay on retina min 0.2s). Faster than that — seen as a continuous image Light pulses are slightly different to freq of glottal cycle - Pattern averaged over many successive non-identical cycles

Remeber ‘SAPMuC’ Synchrony of movement between the two vocal cords Amplitude Periodicity Mucosal wave Closure (glottic)

Features on Stroboscopy: Synchrony Amplitude - Normal = 1/3 of width of vocal fold Periodicity - Jitter = cycle-cycle variation in frequency - Shimmer = cycle-cycle variation in amplitude Mucosal wave Closure (glottic) - Incomplete — motion impairment, scar, MTD - Posterior gap — common in females - Anterior gap —deficit of anterior VC (surgery, sulcus, SLN palsy), may be normal in males - Spindle-shaped — presbylarynx - Hourglass — bilateral pathology e.g. vocal cord nodules - Irregular

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9
Q

VII FUNCTION - all types

A
  1. Topodiagnostic testing: Site of lesion - Schirmer’s test — GSPN - Stapedial reflex — N to Stapedius - Electrogustatometry — Chorda Tympani - Salivary Flow — Chorda Tympani
  2. Electrophysiology Prognosis - NET (acute test after 3-4 days) - MST (acute test after 3-4 days) - ENoG (acute test after 3-4 days) - EMG (chronic test - after 3 weeks and onward)
  3. Intra-operative monitoring - Active = electrical stimulation of nerve and measures CAPs - Passive = facial movement with direct stimulation
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10
Q

VII FUNCTION - techniques electrophysiology tests

A
  1. Nerve Excitation Test Subjective - Transcutaneous DC stimulation of VII at SMF - Minimum stimulation required to elicit a muscle contraction - >3.5mA difference between sides is significant
  2. Maximal Stimulation Test Subjective - Set-up as per NET - Maximal stimulation (patient tolerance or maximum level on machine) - Observe the 2 sides — equal, slightly reduced, markedly reduced, absent - Loss of response in 10 days assoc with incomplete recovery

3. Electroneuronography EnoG Objective - Evoked electromyography - Supramaximal stimulus to VII at SMF — bipolar electrode measures CAPs at nasolabial groove - Amplitude is proportional to number of intact axons (normal difference between sides = 3%) - 10% amplitude — 90% axonal loss — poor prognosis for spontaneous recovery - Timing: 1st 4 days = Wallerian degeneration, after 3 weeks = nerve desynchronisation

4. Electromyography Objective - Electrodes within muscle - Records active motor unit potentials: rest and voluntary contraction - Diphasic/triphasic potentials = normal - Fibrillation = 2-3 weeks post-injury —> LMN denervation, viable motor end plates — suitable for reinnervation/surgical exploration - Polyphasic potentials = regenerative process underway. Precede clinical recovery by 6-12 weeks - Electrical silence = long-standing denervation —> surgical exploration not indicated
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11
Q

ELECTROGUSTATOMETRY xxx

A

TESTS Chorda Tympani

PROCEDURE: Tongue is stimulated electrically to produce a metallic taste Two sides are compared

OUTCOME: Threshold compared between the two sides

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12
Q

SCHIRMER’S TEST xxx

A

Tests GSPN / VII Blotting paper inferior fornix 5 mins Compare length of moistened paper Outcome: > 75% unilateral decrease < 10mm both sides @ 5 mins = bilateral decrease

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13
Q

EUSTACHIAN TUBE FUNCTION xxx

A
  1. Valsalva - +ve when intact TM observed to be moving OR air heard thru perforation - Anatomically patent
  2. Toynbee test - Visual inspection of TM while patient swallows with nose closed manually - Significant portion of normal population can’t achieve this
  3. Politzer test - Visual inspection of TM whilst compressing one nostril with a finger and the other with a rubber tube which injects air into nasal cavity - Repeat the letter K or swallow - +ve when the over pressure that develops in NPx is transmitted to ME
  4. Frenzel manouevre - Opposite of Valsalva - Hard to learn but effective at inflating ET
  5. Imaging - CT vs MRI

Tympanometry

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14
Q

ALLERGY TESTING xxx

A

Broad categories:

  1. In vivo Skin prick (epidermal), intradermal - Time consuming, some discomfort, risk of anaphylaxis - May be difficult in children - Cheap, immediate result
  2. in vitro RAST, ELISA - Delayed result, expensive, less sensitive - Safe. Not affected by treatment (e.g. antihistamine)



Skin prick testing - Epidermal injection of dilute antigen - 15-20mins observe for a wheal (qualitative)

Intradermal - Dermal injection of dilute antigen — more sensitive than skin prick testing - Can use a range of dilutions — quantitative

RAST Radioallergosorbent test - Attach test antigen to a surface then expose to patient’s serum - If patient has allergen-specific IgE it will remain bound to the antigen surface - Wash, then apply labeled anti-IgE IgG - Replaced by ImmunoCAP

Total IgE - 50% of AR patients have normal IgE - Doesn’t identify which allergens — can’t counsel re: allergen avoidance

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15
Q

SMELL ASSESSMENT xxx

A

History: most powerful tool - Nature, pattern, timing, onset, duration, degree - Improvement with vasoconstrictors suggests conductive cause - Antecedent events (URTI, trauma, AR, CRS) - Other sinonasal symptoms, PMHx, FHx, Medications, Occupation, Smoking

Examination: - Full ENT exam - FNE - Cranial Nerve exam 


Smell testing:

  1. Screening - alcohol pad used to test distance from nose it is detected
  2. Psychophysical - Threshold testing - Dilutional testing of butyl alcohol — lowest concentration of odourant that can be detected - Odour identification- UPSIT = University of Pennsylvania Smell Identification test - Commercially available, 40 micro encapsulated odorants scratch + sniff - Chance performance = 10/40. Very low UPSIT reflects avoidance — detect malingering
  3. Electrophysiological - Electro-Olfactogram (EOG) + Odour Event-Related Potentials (OERP) — research only
  4. Imaging - Unusual/ominous symptoms - Pattern doesn’t fit standard diagnosis - Expected resolution doesn’t occur - CT - CRS or post-head trauma - MRI - Tumours (assess integrity of dura/brain. Olfactory agenesis in Kallman’s syndrome)s
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16
Q

LACRIMAL FUNCTION xxx

A

Key points of lacrimal assessment in epiphora:

  • Exclude excessive tearing
  • Differentiate anatomical from functional obstruction
  • Exclude upper system obstruction (not amenable to DCR)

Excluding Excessive Tearing:

  1. Schirmer’s test

Clinical Examination

Jones I - 2% Fluorescein in each eye. Observe inf meatus (if no dye = functional obst)

Jones II - Irrigate inferior punctum with saline via lacrimal irrigation cannula. Still no flow at inf meatus = anatomical obst.

If irrigation refluxes out upper punctum then indicates NLDO, if refluxes out same punctum then maybe common canaliulus obstruction (also, note ‘soft stop’ vs ‘hard stop’)

Radiological investigations

Lacrimal Scintilligraphy - Radiologic Jones I - passive - Technitium in conjunctival fornix and scan regularly for next 30mins - Delayed passage to nasal cavity = narrow segment - No penetration = pump failure or anatomical obstruction Dacryocystogram (DCG) - Radiologic Jones II - active - High pressure irrigation of lacrimal system (ie. if no flow —> anatomical obstruction, if flow into nose —> functional obstruction) - DCG maybe useful to see ‘filling defects’ i.e. stones or neoplasms - Screening test - failure to identify an anatomical obstruction in a symptomatic patient, necessitates Scintigraphy

17
Q

TESTS OF NASAL AiRWAY FUNCTION xxx

A
  1. Cross-Sectional Area - CT or MRI - Acoustic Rhinometry
  2. Nasal Airflow - Nasal Peak Inspiratory Flow - M = 130-150L/min, F = 110-130L/min - Rhinomanometry

Uses of Nasal Function Tests:

  1. Objective, reproducible measure - Reaffirm/improve diagnostic accuracy - Allergy testing - Challenge testing in AR —> directly tests organ affected by allergy - Test potential interventions - Stenting nasal alae/valve or decongesting mucosa - Assess effect of therapy - medical or surgical
18
Q

RHINOMANOMETRY xxx

A

Determines nasal patency in terms of how difficult it is to breathe

Functional measure of the nasal airway - Gold-standard measure of nasal airway resistance

Resistance = change in pressure/volume - Curvilinear association between pressure and airflow - The ratio of pressure to flow

Equipment: airflow sensor, pressure sensor, mask, computer inferface

Procedure: see next facet - Transnasal pressure measurement- anterior/posterior/pernasal. Tubes in the detection sites are attached to a pressure transducer - Passive: air pumped through nose - Active: patient’s own resp effort is source of pressure/flow - Better represents normal physiology of nasal respiration

  1. anterior rhinomanometry = transducer is placed into nostril not being tested, because as no airflow in this nostril then the pressure at the anterior end of this nostril is equal to the presssure at the posterior end of this nostril. (main limitation is in septal perfs) **PREFERRED TECHNIQUE**
  2. posterior rhinomanometry = transducer placed per oral into posterior oropharynx (only method that can assess the contribution of adenoid hypertrophy on airway obstruction but poorly tolerated)
  3. pernasal rhinomanometry = placement of a posterior nasopharyngeal tube by way of the test or non-test nostril (difficult pt tolerance)

Interpretation: - Increase nasal obstruction — curve rotates clockwise (i.e. pressure required to generate a particular flow rate is higher) - Can provide an indirect cross-sectional area of nasal cavity (in contast to direct measure of acoustic rhinometry) - A functional measure

Measurements: Resistance = change in pressure/volume Nasal airway resistance (NAR) = pressure/flow ratio at 150 Pa Maximum resistance = peak pressure/flow point

19
Q

ACOUSTIC RHINOMETRY xxx

A

Changes in acoustic energy reflect cross-sectional area of the nasal cavity

Equipment: Sound tube (hollow plastic tube) conducts a sound pulse (click) into the nasal cavity. An appropriate external nosepiece is placed against the nares, taking care not to distort the nasal alae.

Procedure: Acoustic pulses are generated outside the nose - Anatomic structures within the nose cause changes/distortions in the reflected wave Microphone analyses changes in reflected sound wave - Cross-sectional area measured by the magnitude of distortions

Interpretation: cross-sectional area correlates with CT measures CSA1 = nasal valve area (aka I-notch) CSA2 = inf turbinate/head of middle turbinate (aka C-notch) CSA3 = mid area of middle turbinate

*These measures represent normal narrowings

Normal CSA = 0.7cm2 (decongested nose 0.9cm2)

20
Q

Peak nasal inspiratory flow (PNIF) xxx

A

Simple

Measures both nasal passages together Measure response to treatments – Medical and surgical Dependent on cooperation / effort

Equipment: Peak flow meter, mask

Technique: Sitting pt Use adapted peak flow meter with anaesthetic mask placed over nose Ensure adequate seal Maximal insp effort with mouth closed Best result of 3 attempts recorded Pre/post decongestion

Interpretation: MCID of 20L/min is recommended when NPIF is used as an outcome tool. PNIF change of < 20L/min after decongestion —> Consider structural cause

21
Q

SACCHARIN TEST xxx

A

Small tablet of Saccharin placed on anterior end of inferior turbinate

  • Patient should taste it in 5-15mins
  • Delay > 20 mins —> possibility of mucociliary dyskinesia
22
Q

SLEEP STUDY xxxx

A

Types:

  1. In laboratory - 7 channels (4 - ‘G’s, 3 - Resp. related, 1 positional, 1 oesophageal) EEG - define sleep stage EOG - detect REM sleep = rapid eye movements EMG (chin, leg) - measure muscle tension, sleep = ↓ muscle tension, REM = ↓↓ muscle tension, legs = PLMD ECG SaO2 Resp effort - chest wall and upper abdominal wall movement Airflow - measure resp rate, interruptions in breathing Also measure: Position, Oesophageal manometry Advantages: presence of a technician — fix technical issues and encourage supine sleeping, diagnosis of non-OSA sleep disorders (narcolepsy, PLM, parasomnias) Disadvantages: doesn’t replicate normal sleeping environment
  2. Home study Normally 4 channel study - need EEG at least to determine stage Advantages: Convenience, cost, replicate normal sleeping patterns, prevents hospital admission Disavantages: Unable to address technical issues during study, may under-estimate severity
  3. CPAP titration study
23
Q

INTERPRETING A SLEEP STUDY xxx

A

Patient demographics: Age, sex, BMI, symptoms, ESS

Sleep efficiency: 6hrs, >70% efficiency, REM:NREM (normally 20:80), latency < 20 mins

Sleep latency: normal = 10-25mins - Reduced in sleep deprivation and SDB - Increased in restless legs, insomnia, shift workers etc

AHI: - Type - obstructive vs central vs mixed - Position - supine vs lateral - Phase - REM vs NREM

RERAs:

SaO2:

Nadir and time below 90%

ECG arrythmias

Limb movements- PLM = repetitive, NREM sleep, not rel to resp events

24
Q

SLEEP STUDY x SB version

A

Types:

  1. In laboratory - 7 channels- EEG, EOG, ECG, EMG (chin, leg), SaO2, resp effort, airflow - Advantages: presence of a technician — fix technical issues and encourage supine sleeping, diagnosis of non-OSA sleep disorders (narcolepsy, PLM, parasomnias) - Disadvantages: doesn’t replicate normal sleeping environment
  2. Home study - Normally 4 channel study- need EEG at least to determine stage - Advantages: convenience, cost, replicate normal sleeping patterns, prevents hospital admission - Disavantages: unable to address technical issues during study, may under-estimate severity
  3. CPAP titration study

Components of the sleep study:

EEG- electrical wave patterns to define sleep stage EMG - chin: defines sleep stage — reduced during REM - legs: PLM (periodic limb movement) Chest/abdominal sensors - Discoordinated chest/abdo movements are consistent with obstructive events

25
Q

PULMONARY FUNCTION TESTS xxx

A

Test battery consists of: - History - Examination - CXR - ABG - Spirometry - Measures: volume and flow of air - Obstructive vs Restrictive patterns of disease - FEV1 = maximum air expired in 1sec - FVC = maximum amount of air than can be expired - FEV1:FVC — 0.8-1 = normal or restrictive, <0.6 = obstructive - Note in restrictive pattern both FEV1 and FVC are reduced - Other tests

26
Q

MINOR’S STARCH IODINE TEST xxx

A

Used in Dx of Frey’s syndrome

Paint face with iodine solution then allow to dry Area is dusted with starch powder Patient given a sialogogue (e.g. lemon wedge) Gustatory sweating —> dark blue-black spots appear as sweat dissolves the starch powder and it reacts with iodine

Alternative: Use a single ply tissue paper Lay over the skin area - Wet areas identify affected areas of skin - Unaffected areas remain dry

27
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