9.1 Corneal Topography and Tomography
9.2 Confocal Microscopy
9.3 Optical Coherence Tomography - Macula
9.4 Optical Coherence Tomography Angiography (OCT-A)
9.5 Optical Coherence Tomography - Glaucoma
9.6 Optical Coherence Tomography – Anterior Segment
9.7 Fundus Autofluorescence Imaging
9.8 Fundus Angiography - Fluorescein
9.9 Fundus Angiography - Indocyanine Green
9.10 B-scan Ultrasonography & UBM
9.11 Electrophysiology
9.12 Automated Visual Fields
9.13 Neuroimaging
Humphrey Visual Fields (HVFs) are often presented at data stations. Visual fields that are commonly tested include glaucomatous (usually respecting the horizontal meridian) and neuro-ophthalmic (usually respecting the vertical meridian) pathology. Candidates should pay special attention to reliability, artefacts and describing visual fields in general terms. Ideally, all HVFs should be correlated with clinical examination.
30-2
Tests central 30° of fixation. This may be preferable for monitoring disease progression
24-2
24-2 Tests central 24° superior, inferior and temporal; 30° nasal
10-2
Tests central 10° of fixation. Better for conditions with a small central scotoma such as can occur in optic neuritis and drug-induced optic neuropathies
NB: -2 strategy involves grid test points 6° apart offset from vertical and horizontal meridian
i. Fixation monitor
ii. Fixation target
iii. Fixation losses
iv. False Positive Errors
v. False Negative Errors
vi. Test Duration
vii. Gaze Tracker
Glaucomatous visual field changes usually respect the horizontal midline. The Glaucoma Hemifield Test assesses the probability of glaucoma by comparing the superior and inferior visual fields. It should never be used alone to diagnose glaucoma. The result may be:
These provide comparisons with age-matched normative values.
Mean Deviation (MD)
A weighted average of the total deviation is compared with the normal population. Negative values indicate overall sensitivity is lower than normal
Pattern Standard Deviation (PSD)
General indicator of the degree of localized visual field loss. A high PSD is indicative of irregularities in field
Analyse both the left and right visual fields and describe the defects. Look for patterns of loss:
A. Glaucomatous Patterns
B. Neurological Patterns
Optic Nerve (Unilateral)
Enlarged blind spot (disc swelling)
Altitudinal hemianopia e.g. non-arteritic anterior ischaemic optic neuropathy
Optic Chiasm
Bitemporal hemianopia
Optic Tract
Homonymous (matching defects)
Become more congruous towards the occipital lobe
Inexperienced Patient
Many patients will demonstrate an improvement in visual fields after one or two attempts. Always be cautious in over-interpretation of the first visual field
Ptosis
Reduced sensitivity in the superior portion of the central field (gray scale)
Lens Artefact
A high plus lens will contract the visual field. This may manifest as a marked, sudden reduction in peripheral sensitivity
Cloverleaf
Sensitivity is better in the central points of each quadrant but poor elsewhere.
This characteristic pattern is indicative of patients who fail to respond after the early testing period.
“Trigger Happy” Patient
This is evident by high false positives, a “white” greyscale, normal total deviation but abnormal pattern deviation and an “Abnormally High Sensitivity”
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9.11 Electrophysiology
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9.13 Neuroimaging
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