Anatomy and physiology • 153

8

of Budge at the level of T1. Fibres then pass to, and synapse

in, the superior cervical ganglion before joining the surface of

the internal carotid artery and passing to the pupil along the

nasociliary and the long ciliary nerves (Fig. 8.6B).

in the midbrain and pons and then pass through the cavernous

sinus (Fig. 8.3).

Refractive elements of the eye

The major refracting elements of the eye are the tear film, the

cornea and the crystalline lens. The cornea possesses the greatest

refractive power and is the main refracting element of the eye;

the lens provides additional controllable refraction, causing the

light to focus on to the retina. When light is precisely focused on

to the retina, refraction is called emmetropia (Fig. 8.4A). When

the focus point falls behind the retina, the result is hypermetropia

(Fig. 8.4B, long-sightedness). When rays focus in front of the

retina, the result is myopia (Fig. 8.4C, short-sightedness). These

refractive errors can be corrected with lenses or with a pinhole

(Fig. 8.4D).

Visual pathway

The visual pathway consists of the retina, optic nerve, optic

chiasm, optic tracts, lateral geniculate bodies, optic radiations

and visual cortex (Fig. 8.5). Deficits in the visual pathway lead

to specific field defects.

Pupillary pathways

The pupil controls the amount of light entering the eye. The

intensity of light determines the pupillary aperture via autonomic

reflexes. Pupillary constriction is controlled by parasympathetic

nerves, and pupillary dilatation is controlled by sympathetic

nerves.

For pupillary constriction, the afferent pathway is the optic

nerve, synapsing in the pretectal nucleus of the midbrain. Axons

synapse in both cranial nerve III (Edinger–Westphal) nuclei, before

passing along the inferior division of the oculomotor nerve to

synapse in the ciliary ganglion. The efferent postganglionic

fibres pass to the pupil via the short ciliary nerves, resulting in

constriction (Fig. 8.6A).

For pupillary dilatation, the sympathetic pathway originates

in the hypothalamus, passing down to the ciliospinal centre

Cavernous sinus

Arachnoid mater

Subarachnoid space

Third ventricle Optic tracts

Anterior cerebral arteries

Oculomotor nerve

Trochlear nerve

Ophthalmic division

of trigeminal nerve

Maxillary division

of trigeminal nerve

Temporal

lobe

Anterior pituitary

Sphenoidal air sinuses

Internal carotid arteries Abducens nerve

Dura mater

Fig. 8.3 Cavernous sinus (coronal view). Neuroanatomy of cranial nerves III, IV and VI.

B

A

C

D

Fig. 8.4 Normal and abnormal refraction by the cornea and lens.

A Emmetropia (normal refraction). Cornea and lens focus light on the

retina. B Hypermetropia (long-sightedness). The eye is too short and the

image on the retina is not in focus. A convex (plus) lens focuses the image

on the retina. C Myopia (short-sightedness). The eye is too long and the

image on the retina is not in focus. A concave (minus) lens focuses the

image on the retina. D Myopia corrected using a pinhole. This negates

the effect of the lens, correcting refractive errors by allowing only rays from

directly in front to pass.

154 • The visual system

Fig. 8.5 Visual field defects. 1, Total loss of vision in one eye because of a lesion of the optic nerve. 2, Bitemporal hemianopia due to compression of

the optic chiasm. 3, Right homonymous hemianopia from a lesion of the optic tract. 4, Upper right quadrantanopia from a lesion of the lower fibres of the

optic radiation in the temporal lobe. 5, Lower quadrantanopia from a lesion of the upper fibres of the optic radiation in the anterior part of the parietal lobe.

6, Right homonymous hemianopia with sparing of the macula due to a lesion of the optic radiation in the occipital lobe.

Light source

Short ciliary nerve

Ciliary ganglion

III nerve

Edinger–Westphal nucleus

Lateral geniculate body

Posterior commissure Superior

colliculus

Midbrain

Optic nerve

A B Posterior

hypothalamus

First-order neuron

Second-order neuron

Internal carotid artery

Superior cervical ganglion

External carotid artery

Carotid plexus

Trigeminal nerve

Long ciliary

nerve

Müller’s muscle

Pupil dilator

Ciliospinal centre of Budge

(C8–T2)

Fig. 8.6 Pupillary innervation. A Parasympathetic pathway.

B Sympathetic pathway.

The history • 155

8

Red eye

The eye is covered in a network of vessels in the conjunctiva, episclera

and sclera. Ciliary vessels are also found around the cornea. Dilatation

or haemorrhage of any of these vessels can lead to a red eye.

Additionally, in uveitis, acute angle-closure glaucoma and corneal

irritation the ciliary vessels around the cornea become more prominent

(a ‘ciliary flush’). The appearance is distinct from conjunctivitis, in

which there is a relative blanching of vessels towards the cornea.

Ask:

if the eye is painful or photophobic

if vision is affected

if there has been any recent trauma

whether the eye is itchy

whether there is any discharge

whether there has been any recent contact lens wear or

foreign body exposure.

Box 8.4 summarises the features of the common causes of

a red eye on history and examination.

Double vision (diplopia)

Decipher whether the diplopia is monocular or binocular. Binocular

diplopia is caused by an imbalance in eye movement. Monocular

diplopia results from intraocular disease in one eye. There are

several causes of double vision (Box 8.5 and Figs 8.9 and 8.10).

Ask:

whether the double vision occurs in one or both eyes

about the character of the double vision, and whether the images

are seen side by side, one above the other or at an angle

whether the double vision is associated with any recent

trauma.

Test the eye movements (see Fig. 8.11), and use your

knowledge of the function of the extraocular muscles (see Fig. 8.2)

to work out which cranial nerve is affected in binocular diplopia.

Discharge

Increasing discharge from the eye results from either an increase

in production or a decrease in drainage from the ocular surface.

Irritation of corneal nerves activates cranial nerve V(I) and results

in a reflex tearing response.

Tears normally drain through the punctum at the medial end of

the lower eyelid into the nasolacrimal duct, which opens below the

inferior turbinate into the nasal cavity. Blockage of tear drainage

or abnormal lid position can also result in excessive discharge.

Ask:

whether the discharge is clear or opaque

whether there is associated pain, foreign body sensation

or itchiness

whether the patient has noticed other abnormalities, such

as red eye.

There are many causes of eye discharge, and their clinical

features are summarised in Box 8.6.

Swollen eyes

The orbit is an enclosed structure, except anteriorly. Any swelling

inside the orbit can lead to proptosis or anterior displacement

of the globe.

Ask if:

the swelling is unilateral or bilateral

the changes were acute or gradual

the swelling is painful

there is any itchiness or irritation

the swelling is associated with any double vision.

Box 8.7 summarises the common causes of swollen eyes.

The history

When taking an ophthalmic history, bear in mind the anatomy

of the eye and visual pathways. This will enable you to work

from ‘front to back’ to include or exclude differential diagnoses.

Common presenting symptoms

Start the ophthalmic history with open questions. This builds rapport

with the patient by allowing them to describe the condition in their

own words, and provides clues for more directed questions later.

The visual system has its own set of presenting symptoms,

which prompt specific sets of questions. The most common

are described here.

Altered vision

Vision may be altered by an intraocular disease that leads

to a change in the optical or refractive properties of the eye

and prevents incident light rays from being clearly focused on

the retina. Alternatively, it may result from extraocular factors

associated with damage to the visual pathway, which runs from

the optic nerve to the occipital lobe (see Fig. 8.5).

Establish whether the change in vision is sudden or gradual,

as these will have their own specific set of differential diagnoses

(Box 8.1 and Fig. 8.7; Box 8.2 and Fig. 8.8).

Vision may be not just reduced but also distorted. This

results from disruption to the normal structure of the macula,

the central part of the retina. The most common cause is macular

degeneration but it may also frequently stem from an epiretinal

membrane, vitreous traction or central serous retinopathy.

Flashes and floaters result from disturbance of the vitreous and

the retina, occurring most commonly in posterior vitreous detachment. This is usually found in older patients as the vitreous

gradually degenerates and liquefies, causing it to peel off from the

retina. The vitreous is attached to the retina in certain regions; in

these regions the vitreous either detaches with traction, resulting

in flashing lights, or detaches by tearing the retina, releasing

retinal pigment cells. Patients will see either of these as floaters.

Haloes are coloured lights seen around bright lights. They

occur with corneal oedema and are most commonly associated

with angle-closure glaucoma.

When patients present with a change in vision, ask:

Did the change in vision start suddenly or gradually?

How is the vision affected (loss of vision, cloudy vision,

floaters, distortion)?

Is it one or both eyes that are affected?

Is the whole or only part of the visual field affected?

If partial, which part of the visual field is affected?

Pain

Ask:

when the pain began

whether anything started the pain

about the character of the pain

how severe the pain is

if the pain is exacerbated or relieved by any factors

whether the pain is associated with any other symptoms.

The cornea is one of the most highly innervated regions of the

body. When the corneal nerves are activated, this leads to pain,

the sensation of foreign body, reflex watering and photophobia.

There are, however, many other causes of a painful eye. Box

8.3 summarises the history and examination findings associated

with these.

156 • The visual system

8.1 Common causes of an acute change in vision

Cause Clinical features Cause Clinical features

Unilateral

Giant cell

arteritis

• Painless loss of vision

• Age >50 years

• Weight loss

• Loss of appetite, fatigue

• Jaw or tongue claudication

• Temporal headache

• Pale or swollen optic disc

• RAPD

Vitreous

haemorrhage

• Painless loss of vision

• Risk in proliferative diabetic retinopathy

• History of flashing lights or floaters may precede

haemorrhage in posterior vitreous detachment

• Poor fundus view on examination

• Reduction or loss of the red reflex

• Usually no RAPD if retina is intact

Central

retinal vein

occlusion

• Acute, painless loss of vision

• May have RAPD if severe

• Greater risk if hypertensive

• Haemorrhages, exudates and tortuous retinal veins

(Fig. 8.7A)

Wet

age-related

macular

degeneration

• Sudden painless loss of central vision

• Age >55 years

• Increased risk in smokers

• Haemorrhage at the macula (Fig. 8.7E)

Retinal

detachment

• Painless loss of vision

• Association with flashing lights or floaters

• History of a curtain coming across vision

• Myopic patients at greater risk

• RAPD if macula is involved

• Pale raised retina usually with a retinal tear (Fig. 8.7B)

Anterior

ischaemic optic

neuropathy

• Painless loss of upper or lower visual field

• Increased risk in vasculopaths

• Examination may reveal optic disc swelling

Central

retinal arterial

occlusion

• Acute, painless loss of vision

• Carotid bruit may be heard

• RAPD

• Increased risk in vasculopaths

• Examination: pale retina with a cherry red spot at the

fovea (Fig. 8.7C)

Optic neuritis/

retrobulbar

neuritis

• Visual reduction over hours

• Usually aged 20–50

• Pain exacerbated by eye movement

• RAPD

• Reduced colour sensitivity

• Swollen optic disc in optic neuritis (Fig. 8.7F) or

normal appearances in retrobulbar neuritis

Corneal

disease

• Usual association with pain

• Foreign body sensation

• Corneal opacity may be visible (e.g. Fig. 8.7D)

Amaurosis

fugax

• Painless loss of vision for minutes

• History of cardiovascular disease

• May have associated atrial fibrillation or carotid bruit

• Normal ocular examination

Bilateral

Giant cell

arteritis

• Painless loss of vision

• Age >50 years

• Weight loss

• Loss of appetite, Fatigue

• Jaw or tongue, claudication

• Temporal headache

• Pale or swollen optic disc

Cerebral infarct • May have associated headache and/or neurological

signs

• Usually specific field defects dependent on how the

visual pathway is affected (Fig. 8.5)

• Normal fundus examination

• If post chiasmal visual pathway affected, bilateral

visual field abnormalities

Raised

intracranial

pressure

• Headache

• Often asymmetric

• Pulsatile tinnitus

• Swollen optic discs

Migraine • Gradually evolving usually bilateral visual loss

• Vision loss is usually preceded by visual aura

• Normal ocular examination

• Ocular examination: normal

• Vision usually returns to normal after hours

RAPD, relative afferent pupillary defect (p. 162).

8.2 Common causes of a gradual loss of vision

Cause Clinical features

Refractive error • No associated symptoms

• Normal ocular examination

• Vision can be improved by pinhole (Fig. 8.4D)

Glaucoma • Usually bilateral but asymmetric loss of visual field

• Cupped optic discs on examination

Cataract • Gradual clouding of vision

• May be associated with glare

• Usually seen in the elderly

• Examination: clouding of the pupil and altered red

reflex (see Fig. 8.8A and B)

Cause Clinical features

Diabetic

maculopathy

• History of diabetes

• Central vision reduced or distorted

• Haemorrhages and exudates at the macula on

examination (Fig. 8.17A)

Compressive

optic neuropathy

• Gradual unilateral loss of vision

• Pale optic disc on examination (Fig. 8.8D)

Retinitis

pigmentosa

• Gradual bilateral symmetric loss of peripheral

visual field

• Nyctalopia (poor vision in dim light)

• Family history

• Examination: bone spicule fundus, attenuated

blood vessels and waxy optic disc (Fig. 8.8E)

The history • 157

8

D E F

C A B

Fig. 8.7 Common causes of an acute change in vision. A Central retinal vein occlusion. B Retinal detachment. Elevation of the retina around

the ‘attached’ optic disc; the retina may even be visible on viewing the red reflex. C Central retinal arterial occlusion. D Herpes simplex virus keratitis.

E Wet age-related macular degeneration. F Swollen optic nerve head in acute optic neuritis.

D E

C

A B

Fig. 8.8 Common causes of a gradual loss of vision. A Cataract. B Altered red reflex in the presence of cataract. C Dry age-related macular

degeneration. D Compressive optic neuropathy. Optic nerve sheath meningioma causing optic disc pallor and increased disc cupping with sparing of the

outer optic nerve rim. E Retinitis pigmentosa, with a triad of optic atrophy, attenuated retinal vessels and pigmentary changes. The latter typically start

peripherally in association with a ring scotoma and symptoms of night blindness.

8.2 Common causes of a gradual loss of vision – cont’d

Cause Clinical features

Dry age-related

macular

degeneration

• Gradual loss of central vision

• Usually bilateral

• Examination: drusen, atrophy and pigmentation at

the macula (Fig. 8.8C)

158 • The visual system

8.3 Causes of a painful eye

Cause Clinical features

Blocked gland

on lid

Pain on lid

Tenderness to touch

Ocular examination: redness and swelling of lid

Corneal foreign

body

Foreign body sensation

Watery eye

Photophobia

Ocular examination: foreign body visible or found

under the eyelid

Corneal

infection

Foreign body sensation

Photophobia

Red eye

Ulcer on cornea, which can be highlighted with

fluorescein staining (see Fig. 8.7D)

Ocular examination: white infiltrate may be visible

Scleritis Severe pain that keeps the patient awake at night

Soreness of the eye to touch

Association with recent infection, surgery or

rheumatic disease

Ocular examination: scleral injection

Angle-closure

glaucoma

Constant pain around the eye

Acute reduction in vision

Possibly, haloes seen around lights

Association with nausea and vomiting

Ocular examination: fixed mid-dilated pupil, hazy

cornea and usually a cataract

RAPD, relative afferent pupillary defect (p. 162).

Cause Clinical features

Conjunctivitis Increased clear or purulent discharge

Ocular examination: red eye

Vision is usually unaffected

Uveitis Floaters

Blurry vision

Photophobia

Ocular examination: ciliary flush

Optic neuritis Reduction in vision

Reduction in colour sensitivity

Constant pain worsened by eye movement

Ocular examination: swollen disc in optic neuritis

(see Fig. 8.7F), normal disc in retrobulbar neuritis

Orbital cellulitis Constant ache around the eyes

Reduced vision

Double vision

Association with a recent viral infection

Ocular examination: conjunctival chemosis and

injection, restricted eye movements; in severe cases,

visual reduction with RAPD

Thyroid eye

disease

Symptoms of hyperthyroidism (p. 197)

Sore, gritty eyes

Double vision

Ocular examination: lid retraction, proptosis,

restricted eye movements and conjunctival injection,

conjunctival chemosis (see Fig. 10.4)

8.4 Common causes of a red eye

Causes Clinical features

Allergic

conjunctivitis

Itchy eyes

Clear discharge

Possibly, more frequent occurrence at certain times

of year

Viral conjunctivitis Watery discharge

Possible itch

Swollen conjunctiva

Usually bilateral

Ocular examination: gland swelling and follicles

under the lid

Bacterial

conjunctivitis

Purulent discharge

Pain

Trauma History of trauma

Ocular examination: may reveal subconjunctival

haemorrhage or injection

Acute angleclosure glaucoma

Acute-onset reduction in vision

Pain

Blurring of vision

Haloes seen around lights

Nausea

Ocular examination: fixed, mid-dilated pupil with a

hazy cornea

Acute anterior

uveitis

Gradual onset of pain

Photophobia

Floaters

Ocular examination: ciliary flush

Causes Clinical features

Episcleritis Focal or diffuse injection

Possible association with a nodule

No pain

Vision not affected

Scleritis Focal or diffuse injection

Vision may be affected

Association with recent infection, surgery or

rheumatic disease

Severe pain that keeps the patient awake at night

Pain to touch

Dry eyes Gritty or burning sensation

Watery eyes

Ocular examination: corneal fluorescein staining

Subconjunctival

haemorrhage

No pain

Vision unaffected

Ocular examination: mildly raised conjunctiva with a

bleed

Corneal ulcer/

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