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Ординатура / Офтальмология / Английские материалы / Ophthalmic Drugs Diagnostic and Therapeutic Uses 5th edition_Hopkins, Pearson_2007

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268 OPHTHALMIC DRUGS

Figure 16.9 Contact-lens- induced giant papillary conjunctivitis (reproduced from Kanski 2003, with permission).

Treatment

Contact lens wear might need to be discontinued for up to 2 months in severe cases until the inflammatory tarsal conjunctival changes have resolved. The main plank of the treatment is the removal of the cause and the advent of monthly and daily disposable hydrogel lenses, which accumulate less surface deposits, has significantly reduced the prevalence of this problem. In some cases, it may be necessary to change the lens material, change the lens care system, or to institute more rigorous cleaning of non-disposable lenses.

Relief of symptoms can be obtained by the use of a mast cell stabilizer, such as lodoxamide, initially for four times a day then slowly tapered to less frequent administration. Alternatively, combined antihistamine/mast cell stabilizers such as ketotifen and olopatadine can be prescribed.

In severe cases, short-term use of a topical corticosteroid (four times daily for 2 weeks) might be necessary.

 

 

CORNEA

Bacterial keratitis

Key features

 

 

This is a very serious infection caused usually by an opportunist

 

 

 

 

microorganism that takes advantage of a breakdown of the normal

 

 

corneal defence barrier, the epithelium. This can occur as a result of

 

 

trauma, contact lens wear or from pre-existing corneal conditions such as

 

 

xerophthalmia, caused by the lack of vitamin A. Some organisms, such

 

 

as Neisseria gonorrhoeae, are invasive and can penetrate corneas with

 

 

intact epithelia.

 

 

The patient presents with a foreign body sensation, which intensifies

 

 

and progresses fairly rapidly to photophobia and loss of vision. Initially

 

 

there is conjunctival injection, which is followed in the absence of

 

 

intervention by corneal ulceration. The corneal signs include an infiltrate

 

 

and keratic precipitates; cells and flare might be present in the anterior

 

 

chamber (Fig. 16.10).

INDICATIONS AND CONTRAINDICATIONS FOR OPHTHALMIC DRUGS 269

Figure 16.10 Bacterial keratitis (reproduced from Kanski 2003, with permission).

Treatment

Immediate treatment is necessary because this is a sight-threatening condition. Most of the common, commercially available antibiotic drops do not have a sufficiently broad antibiotic spectrum to cope with the organisms normally present. It is possible that more than one organism is present, each with differing susceptibilities. Custom-made mixtures are usually employed along with systemic antibiotics. The fluoroquinolones, ciprofloxacin and ofloxacin can be used as monotherapy. However, whichever drop is used, frequent (i.e. hourly during the waking hours) dosing will be required to maintain sufficiently high levels of agent. A cycloplegic can be used to reduce pain and to prevent the development of posterior synechiae.

Topical steroid therapy is a contentious issue but can be used following at least 1 week’s treatment with antibiotics by which time cultures should be sterile.

In the case of contact lens wearers, no further use can be allowed of the current lenses, the storage case and all opened solutions.

Marginal keratitis/

Key features

staphylococcal

Multiple, peripheral corneal infiltrates occur. These are separated

hypersentitivity

from the limbus by a clear space and are thought to represent an

 

 

inflammatory, hypersensitive response to staphylococcal exotoxins. This

 

 

 

 

condition, which is also known as a catarrhal ulcer, is commonly

 

 

associated with chronic staphylococcal blepharitis and usually affects

 

 

middle-aged individuals rather than children. It is often associated

 

 

with chronic staphylococcal blepharitis. The patient complains of

 

 

slight ocular irritation, lacrimation, photophobia and slight blurring

 

 

of vision.

Treatment

In mild cases, treatment includes the use of warm compresses, atten-

 

 

tion to lid hygiene and a topical anti-staphylococcal agent such as

270 OPHTHALMIC DRUGS

Herpes simplex keratitis

Treatment

Figure 16.11 Large dendritic ulcer stained with fluorescein (reproduced from Kanski 2003, with permission).

chloramphenicol or ciprofloxacin. More severe cases will require a topical steroid such as prednisolone sodium phosphate four times daily for a week then slowly tapered as the condition resolves.

VIRAL KERATITIS

Key features

The eye, like the skin, can be affected by herpes viruses, usually herpes simplex and herpes zoster. Herpes simplex exists in two types: herpes simplex I and herpes simplex II. Type I affects structures above the waist and can produce viral keratitis and cold sores whereas type II is associated with sexually transmitted infections.

Initial infection occurs during childhood, often without producing symptoms. After initial infection, the virus travels along the axon of a sensory nerve to the trigeminal ganglion, where it resides in a dormant state until activated by a trigger such as trauma. In the re-activated state, the virus travels back down the axon to infect the surface structure, leading to keratitis.

The initial superficial punctate or stellate keratitis can be followed, with further loss of surface epithelium due to viral replication, by a branching dendritic ulcer and an amoeboid or geographic ulcer (Fig. 16.11). Symptoms include lacrimation, ocular discomfort and photophobia.

Many different compounds have been used in the past for treatment of dendritic ulcers, but those used principally are topical aciclovir (ointment) and ganciclovir (eye gel). Either one should be applied five times a day for at least a week.

If topical steroids are used to suppress the inflammation, they must be tapered over a period of months to avoid a rebound response.

INDICATIONS AND CONTRAINDICATIONS FOR OPHTHALMIC DRUGS 271

Trifluorothymidine (F3T or trifluridine) has been used as drops but is not commercially available in the UK and is more toxic to the corneal epithelium and conjunctiva than aciclovir.

Debridement of infected epithelium might be required.

Herpes zoster ophthalmicus

Figure 16.12 Eyelid involvement in herpes zoster ophthalmicus (reproduced from Kanski 2003, with permission).

Key features

Although the herpes zoster virus is very similar to herpes simplex, the clinical effects are very different. The initial infection normally produces the well-defined condition of chickenpox. When the virus is re-activated, it affects the region supplied by the nerve in whose ganglion, the virus remained dormant. The eruptions, known as shingles, are thus constrained to a discrete region. If the virus has been resident in the trigeminal ganglion and travels down the ophthalmic division, the resulting condition is referred to as herpes zoster ophthalmicus. It does not always follow that there will be ocular involvement. Unlike herpes simplex infection, there is a general feeling of lassitude and the patient complains of being ‘off-colour’. This is followed by neuralgia in the region served by the sensory nerve. The cutaneous eruptions then follow the classic picture of macules followed by pustules, which then crust over. If lesions are seen at the tip of the nose then ocular involvement usually follows. During the vescicular stage, the condition is contagious and patients should particularly avoid contact with pregnant women. Shingles varies a great deal in severity and this is true for the eye. There can be an acute epithelial keratitis which clears up spontaneously in a few days or a more persistent inflammation involving the stroma and other ocular structures such as the cornea, sclera and anterior uvea.

Depending on the degree of ocular involvement, there may be symptoms of lacrimation, blurring of vision and photophobia (Fig. 16.12).

272 OPHTHALMIC DRUGS

Treatment Treatment is usually symptomatic aimed at relieving the worst of the symptoms. Systemic treatment can be with oral antiviral agents such as valaciclovir (1 g three times daily) or famciclovir (250 g three times daily) for a period of 1 week. At the onset of the condition, systemic treatment is more appropriate than topical treatment with antivirals such as aciclovir and penciclovir.

Mucolytic agents, such as N-acetylcysteine, and tear substitutes might be required in some cases.

Acanthamoeba keratitis Key features

Acanthamoebae have become very notable in the recent past because of their potential to be a sight-threatening risk especially for wearers of soft contact lenses. Normally a free-living single-celled organism, acanthamoeba has the ability to cause keratitis following a minor abrasion (e.g. from contact lens wear) or as a superinfection over an existing viral keratitis. Initially, the patient complains of blurred vision and severe pain, which seems out of proportion to the clinical signs. There is inflammation around the limbus, followed by epithelial and subepithelial infiltrates. Later, the infiltrates coalesce in the shape of a ring (Fig. 16.13).

Treatment Topically active amoebicides and trophozoicides are available and are effective treatments. Propamidine isethionate and polyhexanide biguamide are two examples. Antibiotics such as tetracycline and neomycin are useful adjuncts to this therapy.

Figure 16.13 Epithelial changes and pseudodendrite in acanthamoeba keratitis (reproduced from Kanski 2003, with permission).

Clinical note

In the case of contact lens wearers, no further use can be allowed of the current lenses, the storage case and all opened solutions. The patient’s

compliance with the recommended routine for lens care should be reviewed, together with the antimicrobial efficacy of the products being used.

INDICATIONS AND CONTRAINDICATIONS FOR OPHTHALMIC DRUGS 273

Figure 16.14 Conjunctival hyperaemia in acne rosacea (reproduced from Kanski 2003, with permission).

Rosacea keratitis

Key features

 

 

This is a very variable condition, associated with acne rosacea, a skin

 

 

 

 

condition affecting the facial skin. Ocular involvement is not necessarily

 

 

related to the extent of the skin condition. The patient, commonly a

 

 

middle-aged adult, presents with mild irritation, tearing and redness.

 

 

The ocular signs vary from marginal keratitis to corneal thinning and

 

 

possible perforation. Being a skin condition, the eyelids can also be

 

 

affected with posterior blepharitis and meibomian cysts. The lipid layer

 

 

of the tear film might be affected (Fig. 16.14).

Treatment

Topical treatments include a short course of steroids and a tear

 

 

substitute. An antibiotic ointment is required when, for example,

 

 

blepharitis is present. However, the principal form of treatment is with a

 

 

high initial dose of an oral antibiotic such as tetracycline which is slowly

 

 

tapered. Warm compresses and attention to lid hygiene can alleviate

 

 

accompanying blepharitis or meibomianitis.

 

 

Systemic treatments, i.e. oral and parenteral preparations, have a

 

 

place in the treatment of ophthalmic conditions but are beyond the

 

 

scope of this book. This chapter concentrates on the use of topical

 

 

treatments.

Phlyctenulosis

Key features

 

Phlyctenulosis is a rare condition generally found in children. It is

 

 

caused by a hypersensitivity to certain microorganisms, principally

 

Staphylococcus aureus, but might also be associated with tuberculosis. The

 

phlyctens appear as a small raised nodule in the limbal region, which

 

break down leaving a scar. Some resolve spontaneously. The symptoms

 

are tearing and photophobia with some irritation (Fig. 16.15).

274 OPHTHALMIC DRUGS

Figure 16.15 Limbal phlycten (reproduced from Kanski 2003, with permission).

Treatment

Episcleritis

Figure 16.16 Simple diffuse episcleritis (reproduced from Kanski 2003, with permission).

The condition normally responds to a topical course of steroids such as fluoromethalone, although any associated bacterial infection should be treated.

SCLERA

Key features

Episcleritis is a common, localized inflammation of the episclera, which can be sectorial or diffuse and often resolves spontaneously, especially when there are no nodules. Nodular episcleritis as its name suggests is associated with the development of small raised nodules. The condition is frequently unilateral and the patient, typically a young adult, complains discomfort, tearing and redness (Fig. 16.16).

INDICATIONS AND CONTRAINDICATIONS FOR OPHTHALMIC DRUGS 275

Treatment Treatment is normally symptomatic and can involve the use of artificial tears or vasoconstrictors. If necessary, topical steroids can be used but their use should be limited to short courses. Rarely, when the condition is recurrent, an oral non-steroidal anti-inflammatory drug (NSAID) is required.

Scleritis

Treatment

Uveitis

Figure 16.17 Diffuse nonnecrotizing anterior scleritis (reproduced from Kanski 2003, with permission).

Key features

Scleritis is less common and more serious than episcleritis. It can range from minor self-resolving events to extreme sight-threatening attacks. Scleritis normally affects the anterior sclera in diffuse, nodular and necrotizing forms and can result from a variety of causes, such as trauma from surgery or infection. It is particularly associated with rheumatoid arthritis and other systemic diseases, including Wegener’s granulomatosis, polyarteritis nodosa and systemic lupus erythematosus. In the less frequent posterior scleritis, the inflammation is mostly posterior to the equator. The patient experiences more discomfort than in episcleritis, the eye appears inflamed and the severity of the symptoms reflects the degree of inflammation (Fig. 16.17).

Topical treatments are ineffective and oral non-steroidal antiinflammatory agents or steroids are required.

UVEA

Key features

The term ‘uveitis’ spans a range of conditions, covering some or all parts of the uvea. Anterior uveitis can involve the iris (iritis) or the iris and ciliary body (irido-cyclitis). Acute attacks are associated with ocular pain, redness, photophobia and slightly decreased vision. Aqueous cells

276 OPHTHALMIC DRUGS

Figure 16.18 Ciliary injection in acute anterior uveitis (reproduced from Kanski 2003, with permission).

Treatment

and flare are present in the anterior chamber and keratitic precipitates might be seen on the endothelium of the cornea.

There is a circumcorneal hyperaemia of the perilimbal blood vessels which is termed ciliary injection or flush. Posterior synechiae can occur as complications (Fig. 16.18).

Treatment must be initiated promptly and is aimed at relieving symptoms, and preventing or breaking down if they are formed, of posterior synechiae. Cycloplegics are used to relax the iris sphincter muscle and prevent constriction of the pupil in the inflamed iris. In the past atropine drops were used, but normally, cyclopentolate produces sufficiently a mydriasis, of sufficiently long duration. Short courses of steroids (e.g. prednisolone) are used, with frequent instillation at the outset, which is tailed off gradually over several weeks.

CHRONIC CONDITIONS

The major chronic ocular conditions in which drug treatment plays a principal part are dry eye (keratoconjunctivitis sicca) and glaucoma. These are dealt with in Chapters 15 and 14, respectively.

POSTOPERATIVE USE OF DRUGS

On a daily basis, optometrists see patients who have undergone ophthalmic surgery most commonly for cataract, glaucoma and refractive errors. These patients will experience inflammation as a result of the trauma of the operation and will be at risk from infection at the operating sites.

INDICATIONS AND CONTRAINDICATIONS FOR OPHTHALMIC DRUGS 277

Commonly, the drugs prescribed for use following the surgical procedures are a broad-spectrum antibiotic such as chloramphenicol (four drops a day for 1 week) and a moderate strength corticosteroid, for example, dexamethasone, (four times a day for 1 week, then two times a day for 2 weeks). Alternatively, a combination product of tobramycin and dexamethasone can be employed.

References

Bruce A S, Loughnan M S 2003 Anterior eye disease and

Kanski J J 2003 Clinical ophthalmology, 5th edn.

therapeutics A–Z. Butterworth-Heinemann, Oxford

Butterworth-Heinemann, Oxford