The Ishihara charts (Figure 4.3) are used to check colour vision. Colour blindness is most often hereditary, and there are two distinct patterns of impairment:

FIGURE 4.3 Ishihara sample chart

• If the patient is a protanope, colour blindness is characterised by defective perception of red and confusion of red with green or bluish green.

• If the patient is a deuteranope, color blindness is characterised by insensitivity to green.

Pathological colour blindness indicates disease in the optic nerves and can occur even in the absence of prior visual symptoms, typically with a demyelinating optic neuropathy associated with multiple sclerosis.

THE VISUAL FIELDS

Severe visual field loss: quadrantanopia, hemianopia, visual inattention

A simple screening test that will detect a severe visual field loss, such as a quadrantanopia (loss of vision in the same quarter of the visual field in both eyes) or a hemianopia (loss of vision in the same half of the visual field of both eyes), is to move a finger in the peripheral vision in both upper and then both lower visual fields. If with double simultaneous stimulation the patient cannot see the moving finger in one of the fields, the problem is either a visual field loss or visual inattention. Visual inattention is the inability to see objects moving in both visual fields simultaneously, although the moving object can be seen if each visual field is tested separately.

To differentiate between these two possibilities, the examiner’s finger is moved in one visual field at a time. If the visual disturbance is a loss of vision, the finger will not be seen until it reaches the midline. On the other hand, if the visual problem is inattention the single moving finger will be seen in the areas of vision where it could not initially be seen with double simultaneous stimuli. Once again, this is the principle of testing from the area of abnormality until normality is found to define the exact pattern of impairment.

Subtle visual field defects:

CENTRAL SCOTOMA: To detect more subtle defects of the visual fields at the bedside a 4-mm red pin is used. In this test the examiner holds the pin at a distance midway between himself and the patient. The visual field of the examiner is used as a normal control. The visual fields are tested with the patient covering the left eye, for example, while the examiner covers the right eye, directly opposite the patient’s closed eye. The patient and the examiner look directly into each other’s eye and in this way the examiner can tell if the patient’s eye is moving during the test. Initially the 4-mm red pin is placed in the centre of the visual field to detect if there is a loss of central vision, a central scotoma. If there is a loss of vision in the centre, the pin is moved slowly away in each of the 4 quadrants in turn until it is visualised by the patient, establishing the size of the central scotoma. This indicates a lesion of the fovea in the eye.

ENLARGED BLIND SPOT: An enlarged blind spot occurs with a lesion of the optic discs (either optic neuritis or papilloedema). To detect an enlarged blind spot, the examiner slowly moves the 4-mm red pin out laterally from the centre at the level of the equator of the eye until the blind spot is detected. Once found, the examiner moves the pin up, down, medially and laterally until the size of the patient’s blind spot is established and compared with that of the examiner.

SUBTLE HEMIANOPIA, QUADRANTANOPIA OR BITEMPORAL HEMIANOPIA: To test the visual fields for a subtle hemianopia, quadrantanopia or bi-temporal hemianopia, the examiner moves the pin slowly from the periphery to the midline in each of the 4 quadrants asking the patient to indicate when the red pin is first noticed. If a loss is detected with this technique, the pin is then moved slowly from the area of abnormal vision to normal vision to establish the exact pattern of visual loss. Testing the visual fields individually with the 4-mm red pin will NOT detect visual inattention.

A Goldman Perimeter or Bjerum Screen is used to formally test the visual fields.

EXAMINATION OF THE OPTIC FUNDI

The patient is instructed to look straight ahead, preferably at a small dot or mark on the wall. The examiner approaches from the side at about 30–45° lateral to the midline until a retinal blood vessel is visualised and this is traced back to the optic disc (Figure 4.4). The blood vessels can be traced outwards from the optic disc to detect any abnormality. To examine the fovea (central vision), the patient looks directly at the ophthalmoscope with the intensity of the light reduced.

FIGURE 4.4 Normal optic disc and the more common abnormalities of the optic discs
A Normal optic disc
B Papilloedema
The visual acuity is normal unless the papilloedema is chronic, and the blind spot is enlarged. The visual fields are otherwise normal. The pupillary responses are normal.
C Acute optic neuritis
The visual acuity is markedly impaired; colour vision is abnormal if the patient can read the chart (severe visual impairment will prevent the patient from seeing the numbers on the chart). The blind spot is enlarged. The direct pupillary response is slow and there is a Marcus–Gunn pupillary phenomenon (the pupil contracts promptly when the light is shone in the normal eye and when the light is shone in the abnormal eye the pupil initially dilates and then slowly contracts). Retrobulbar neuritis is the term applied to an inflammatory optic nerve lesion within the optic nerve but not affecting the optic nerve head, the part of the optic nerve that is visualised on examination of the fundus. In this situation, the visual acuity and colour vision are impaired, the visual field defect is usually a central scotoma although it may be a diffuse, lateral, superior or inferior defect. The fundus looks normal [3].
D Long-standing optic neuritis with pallor of the optic disc
The visual acuity is reduced, colour vision is abnormal, and a Marcus–Gunn pupillary phenomenon is present (see 4C for an explanation of this abnormality).
E Anterior ischaemic optic neuropathy (AION)
AION is the most common cause of acute optic neuropathy among older persons. It can be non-arteritic (nonarteritic anterior ischaemic optic neuropathy [NAION]) or arteritic, the latter being associated with giant cell arteritis. Visual loss usually occurs suddenly, or over a few days at most, and it is usually permanent. The optic disc is pale and swollen and there are flame haemorrhages.

THE 3RD, 4TH AND 6TH CRANIAL NERVES

The oculomotor (3rd) nerve

ANATOMY

The 3rd nerve nucleus is in the midbrain close to the midline, and the nerve exits the brainstem at the junction of the midbrain and pons just lateral to the midline (see Figure 1.6). It then crosses the subarachnoid space and, after traversing the cavernous sinus, it enters the orbit through the superior orbital fissure. The posterior communicating artery lies close to the nerve and this artery is a common site for berry aneurysm formation which can cause a 3rd nerve palsy.

The 3rd nerve supplies the following muscles:

• levator palpebrae superioris, one of the two muscles that elevate the eyelid

• medial rectus (MR) that adducts the eye towards the nose

• superior rectus (SR) and inferior rectus (IR) that cause the eye to look up and down, respectively, when the eye is in abduction.

The 4th nerve nucleus is in the paramedian midbrain. The fibres of the 4th nerve cross the midline in the posterior aspect of the midbrain and emerge adjacent to the crus cerebri (see Figure 1.6). The 4th nerve passes through the cavernous sinus and enters the orbit via the superior orbital fissure. It supplies the superior oblique (SO) muscle that depresses the eye when it is in the adducted position and internally rotates the eye when it is looking laterally (abducted) and down. Fourth nerve palsies are commonly associated with lesions of the other oculomotor nerves due to their proximity in the cavernous sinus and orbit; an isolated 4th nerve palsy is rare but can be congenital in origin or the result of trauma.

METHOD OF TESTING

The trochlear nerve is tested by asking the patient to look towards the nose and then down. However, if the patient also has a 3rd nerve palsy and cannot adduct the eye towards the nose, the method of testing the 4th nerve is to ask the patient to look laterally and then down. If the 4th nerve is intact there will be internal rotation of the eye as it looks down; if the 4th nerve is impaired the eye will not internally rotate.

The abducent (6th) nerve

ANATOMY

The 6th nerve nucleus lies within the pons (encircled by the 7th cranial nerve). It exits the pons laterally at the junction of the pons and medulla (see Fig. 1.6). It crosses the subarachnoid space, passes through the cavernous sinus and enters the orbit via the superior orbital fissure to supply the lateral rectus (LR) muscle. The close proximity between the 6th nerve nucleus and the 7th nerve within the pons means it is very unusual to have an isolated 6th nerve lesion with disease within the pons. Most often a 6th nerve palsy indicates a lesion directly affecting the nerve, but occasionally it can be a false localising sign due to raised intracranial pressure. A 6th nerve palsy results in an inability to abduct (move the eye laterally within the orbit) the eye fully (see Figure 4.5).