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Ophthalmology > SCLERA
Episcleritis
Article Last Updated: Mar 18, 2008
AUTHOR AND EDITOR INFORMATION
Section 1 of 10  
Author: Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences
Hampton Roy, Sr, is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, and Pan-American Association of Ophthalmology
Editors: Andrew A Dahl, MD, Director of Ophthalmology Teaching, Mid-Hudson Family Practice Institute; Assistant Professor of Surgery (Ophthalmology), New York College of Medicine; Simon K Law, MD, PharmD, Assistant Professor of Ophthalmology, Jules Stein Eye Institute; Chief of Section of Ophthalmology Surgical Services, Department of Veterans Affairs Healthcare Center, West Los Angeles; R Christopher Walton, MD, Professor, Director of Uveitis and Ocular Inflammatory Diseases Service, Assistant Department of Ophthalmology, Assistant Dean for Graduate Medical Education and Continuing Education, University of Tennessee College of Medicine; Consulting Staff, Regional Medical Center, Memphis Veterans Affairs Medical Center, St Jude Children's Research Hospital; Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri; James P Gills, MD, Founder, St Luke's Cataract and Laser Institute; Professor, Department of Ophthalmology, University of South Florida College of Medicine
Author and Editor Disclosure
Synonyms and related keywords:
simple episcleritis, nodular episcleritis, episcleral tissue, inflammation, conjunctiva, sclera
Background
Episcleritis is an inflammatory condition affecting the episcleral tissue that lies between the conjunctiva and the sclera. Episcleritis is usually a mild, self-limiting, recurrent disease. Most cases are idiopathic, although up to one third have an underlying systemic condition. Some cases may be caused by exogenous inflammatory stimuli.
Pathophysiology
The pathophysiology is poorly understood. The inflammatory response is localized to the superficial episcleral vascular network, and histopathology shows nongranulomatous inflammation with vascular dilatation and perivascular infiltration.
The 2 clinical types are simple and nodular.
The most common type is simple episcleritis, in which there are intermittent bouts of moderate-to-severe inflammation that often recur at 1- to 3-month intervals. The episodes usually last 7-10 days, and most resolve after 2-3 weeks. Prolonged episodes may be more common in patients with associated systemic conditions. Some patients note that episodes are more common in the spring or fall. The precipitating factor is rarely found, but attacks have been associated with stress and hormonal changes.
Patients with nodular episcleritis have prolonged attacks of inflammation that are typically more painful than simple episcleritis. Many patients with nodular episcleritis have an associated systemic disease.
Frequency
United States
True frequency is difficult to determine since many patients do not seek medical attention.
Sex
Some authors report no difference, while other authors report that up to 74% of cases occur in females.
Age
Episcleritis is most common in the fourth to fifth decades.
History
All patients should undergo a thorough history, including a review of systems. - Many patients complain of acute onset of mild-to-moderate discomfort, although some may notice an area of painless injection.
- Photophobia and watery discharge may be noted.
Physical
- A diffuse or localized injection of the bulbar conjunctiva is often present.
- A watery discharge is observed in some patients.
- A freely moveable nodule may be present in nodular episcleritis.
- Corneal findings are uncommon and include dellen formation as well as peripheral corneal infiltrates.
- An associated anterior uveitis may occur in as many as 10% of patients.
Causes
Most cases are idiopathic; however, up to one third of cases may have an underlying systemic condition. - Collagen vascular diseases
- Miscellaneous
- Gout
- Atopy
- Foreign bodies
- Chemicals
- Infectious diseases
- Other rare causes/associations
- T-cell leukemia
- Paraproteinemia
- Paraneoplastic syndromes - Sweet syndrome, dermatomyositis
- Wiskott-Aldrich syndrome
- Adrenal cortical insufficiency
- Necrobiotic xanthogranuloma
- Progressive hemifacial atrophy
- Following transscleral fixation of posterior chamber intraocular lens
- Insect bite granuloma
- Malpositioned Jones tube
Conjunctivitis, Viral
Keratoconjunctivitis, Superior Limbic
Scleritis
Lab Studies
- All patients should undergo a thorough history, including a review of systems. Results of this review and findings from the physical examination are used to determine the need for specific laboratory studies. In most patients with mild self-limited disease, laboratory studies are not useful.
- Some patients with an unremarkable review of systems may benefit from a limited workup. This includes patients with nodular episcleritis or those with severe and recurrent/persistent simple episcleritis. Useful laboratory studies in this group of patients include serum uric acid, complete blood count with differential, antinuclear antibody, rheumatoid factor, erythrocyte sedimentation rate, Venereal Disease Research Laboratory (VDRL) test, fluorescent treponemal antibody absorption (FTA-ABS) test, and chest x-ray.
Histologic Findings
Histologic findings include nongranulomatous inflammation with perivascular infiltrates and vascular dilatation.
Medical Care
- Episcleritis is a self-limiting disease producing little or no permanent damage to the eye. Therefore, many, if not most, patients with episcleritis will not require any treatment. However, some patients with mild symptoms demand treatment and may benefit from the use of artificial tears.
- Occasionally, a clear history of an exogenous sensitization can be obtained, and removal of this agent will prevent recurrent attacks.
- Ocular therapy
- Simple episcleritis often requires no treatment. Artificial tears are useful for patients with mild-to-moderate symptoms. Patients with severe or prolonged episodes may require artificial tears and/or topical corticosteroids.
- Nodular episcleritis is more indolent and may require local corticosteroid drops or anti-inflammatory agents.
- Topical ophthalmic 0.5% prednisolone, 0.1% dexamethasone, or 0.1% betamethasone daily may be used.
- Systemic therapy
- If nodular episcleritis is unresponsive to topical therapy, systemic anti-inflammatory agents may be useful.
- Flurbiprofen (100 mg tid) is usually effective until inflammation is suppressed.
- If there is no response to flurbiprofen, indomethacin should be used; 100 mg daily and decreased to 75 mg when there is a response.
- Many patients who do not respond to one nonsteroidal anti-inflammatory agent (NSAID) may respond to another NSAID.
Activity
Sunglasses may be useful for patients with sensitivity to light.
The goals of pharmacotherapy are to reduce morbidity and to prevent complications.
Drug Category: Corticosteroids
Have anti-inflammatory properties and cause profound and varied metabolic effects. Corticosteroids modify the body's immune response to diverse stimuli.
| Drug Name | Dexamethasone sodium phosphate (Ocu-Dex) |
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| Description | Suppresses the inflammatory response to a variety of agents and probably delays healing. Used for steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe; when the inherent hazard of steroid use is accepted; and corneal injury from chemical or thermal burns or penetration of foreign bodies has occurred. Duration of treatment will vary from a few days to several weeks, according to therapeutic response. |
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| Adult Dose | Instill 1-2 gtt in conjunctival sac qh during the day and q2h during the night as initial therapy; further reduction in dosage to 1 gtt 3-4 times daily may suffice to control symptoms |
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| Pediatric Dose | Not established |
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| Contraindications | Documented hypersensitivity; most viral diseases of the cornea and conjunctiva, including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella; mycobacterial infections of the eye; fungal diseases of the ocular structures; may increase intraocular pressure (monitor patients with glaucoma) |
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| Interactions | None reported |
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| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
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| Precautions | Prolonged use may increase hazard of secondary ocular infection; suspect fungal invasion in any persistent corneal ulceration where a corticosteroid has been used or is in use (obtain fungal cultures when appropriate); may increase intraocular pressure; may cause cataract |
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| Drug Name | Prednisolone acetate 1% (Pred Forte) |
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| Description | Sterile ophthalmic suspension that is a topical anti-inflammatory agent for treating steroid responsive inflammation of palpebral and bulbar conjunctiva as well as cornea and anterior segment. Shake well prior to use. Do not discontinue therapy prematurely. |
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| Adult Dose | Instill 1-2 gtt bid/qid into conjunctival sac; during initial 24-48 h, dosage may be increased in frequency, prn |
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| Pediatric Dose | Not established |
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| Contraindications | Documented hypersensitivity; most viral diseases of the cornea and conjunctiva, including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella; mycobacterial infections of the eye; fungal diseases of the ocular structures |
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| Interactions | None reported |
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| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
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| Precautions | Fungal infections of the cornea are prone to develop coincidentally with long-term local corticosteroid use; suspect fungal invasion in any persistent corneal ulceration where a corticosteroid has been used or is in use (obtain fungal cultures when appropriate); if used for 10 d or longer, monitor intraocular pressure; steroid use in episcleritis may increase the risk of recurrence |
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Drug Category: Nonsteroidal anti-inflammatory agents
Their mechanism of action is not known but may inhibit cyclooxygenase activity and prostaglandin synthesis. Other mechanisms may exist, such as inhibition of leukotriene synthesis, lysosomal enzyme release, lipoxygenase activity, neutrophil aggregation, and various cell membrane functions.
| Drug Name | Flurbiprofen (Ansaid) |
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| Description | May inhibit cyclooxygenase enzyme, which, in turn, inhibits prostaglandin biosynthesis. These effects may result in analgesic, antipyretic, and anti-inflammatory activities. Available in 50- and 100-mg doses. |
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| Adult Dose | 100 mg PO tid until suppressed |
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| Pediatric Dose | Not established |
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| Contraindications | Documented hypersensitivity |
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| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
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| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
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| Precautions | Category D in third trimester of pregnancy; may cause gastrointestinal disturbances and fluid retention and should not be used in patients with congestive heart failure; can mask symptoms of infection; other adverse effects, such as platelet aggregation and liver dysfunction, exist with long-term use but should not be a factor in a relatively short duration of treatment |
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| Drug Name | Indomethacin (Indocin, Indochron E-R) |
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| Description | Rapidly absorbed; metabolism occurs in liver by demethylation, deacetylation, and glucuronide conjugation; inhibits prostaglandin synthesis. For use with episcleritis that has been nonresponsive to topical treatment. |
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| Adult Dose | 100 mg PO qd; decrease to 75 mg when a response is seen |
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| Pediatric Dose | Not established |
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| Contraindications | Documented hypersensitivity |
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| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related side effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
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| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
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| Precautions | Category D in third trimester of pregnancy; acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia, and renal papillary necrosis may occur; patients with preexisting renal disease or compromised renal perfusion risk acute renal failure; may cause gastrointestinal disturbances; should not be used in patients with congestive heart failure; other adverse effects, such as platelet aggregation and liver dysfunction, exist with long-term use but should not be a factor in a relatively short duration of treatment |
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Further Outpatient Care
- Approximately 30% of patients with episcleritis may have an associated underlying systemic disease. Of these, up to 11% of patients with episcleritis may have hyperuricemia.
- Other diseases with high degrees of association with episcleritis are connective tissue disease, herpes zoster, rosacea, syphilis, underlying vasculitic disease, and atopy.
- Infectious diseases other than herpes (eg, tuberculosis, syphilis, Lyme disease, bacterial infections) are seen but are relatively uncommon.
- In patients with gout, recurrent episcleritis may be associated with attacks of arthritis.
- Long-term continuous therapy with steroid preparations should be avoided because of the danger of inducing cataract and glaucoma. Also, steroid use in episcleritis may increase the risk of recurrence.
Deterrence/Prevention
- In patients with gout, control uric acid levels.
Prognosis
- The prognosis is favorable.
Patient Education
- Episcleritis is usually self-limited. The patient is usually comforted to know that it does not progress to a more serious disorder.
Medical/Legal Pitfalls
- Hyperuricemia may be overlooked.
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- Minas TF, Podos SM. Familial glaucoma associated with elevated episcleral venous pressure. Arch Ophthalmol. 1968;80:202-213. [Medline].
- Roy FH. Ocular Differential Diagnosis. Vol 1. 7th ed. Baltimore: Williams & Wilkins; 2002.
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Episcleritis excerpt Article Last Updated: Mar 18, 2008
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