eMedicine Specialties > Emergency Medicine > Ophthalmology

Ultraviolet Keratitis: Treatment & Medication

Author: Reed Brozen, MD, Director of Air Transport, Associate Professor, Department of Emergency Medicine, Dartmouth Medical School, Dartmouth-Hitchcock Medical Center
Coauthor(s): Christian Fromm, MD, FAAEM, FACEP, Assistant Professor, Department of Emergency Medicine, Mount Sinai School of Medicine; Director of Research, Attending Physician, Department of Emergency Medicine, Maimonides Medical Center
Contributor Information and Disclosures

Updated: Feb 4, 2008

Treatment

Prehospital Care

  • Flush eyes for several minutes with water or saline solution.

Emergency Department Care

  • Administer a short-acting cycloplegic drop (eg, cyclopentolate 1%) to relieve the pain of reflex ciliary spasm.
  • Administer a topical antibiotic ointment or drops, such as erythromycin or gentamicin. If an eye patch is used with an antibiotic ointment, the patient should use antibiotic drops after the eye patch has been removed.
  • Application of a semipressure dressing with the eye well closed underneath was once the standard of care, but today this method of treatment is controversial. While these dressings may offer good pain relief, they may also delay reepithelialization. Moreover, some patients find the loss of sight and depth perception (in the case of single-eye patching) more traumatic than the pain itself.
    • When used, the dressing is to be left on for 24 hours.
    • The dressing should not be replaced by the patient without professional assistance because excessive pressure can cause further damage to the eye.
  • Because of the severely painful nature of this type of injury, patients should be treated with nonsteroidal anti-inflammatory drugs and oral narcotic analgesics.
    • All patients without contraindications should take ibuprofen 600 mg qid and oxycodone with acetaminophen for breakthrough pain.
    • Topical anesthetic may be administered only in the ED; frequent use retards epithelial healing and may lead to corneal ulcer formation. The relief provided by topical anesthetics is so immediate and dramatic that patients are highly motivated to take a bottle home with them. Be careful not to allow the patient to take the bottle surreptitiously.
  • Topical NSAIDs are not approved for this indication but are used for many other painful and allergic eye conditions. Topical NSAIDs for UV keratitis and corneal abrasions is an off-label use but has become common practice in many places.

Consultations

Ophthalmologic consultation usually is not necessary for this condition but may be obtained at the discretion of the emergency physician in the ED or if substantial healing has not occurred within 24-48 hours.

Medication

The goal of therapy is to treat the pain associated with damage in the corneal epithelium resulting from UV light exposure and to prevent infection while the cornea heals. Some medications include ophthalmic antibiotics, topical cycloplegics, ophthalmic anesthetics, NSAIDs (both ophthalmic and parenteral), and other analgesics.

Ophthalmic anesthetics

These agents are indicated for pain relief. Local anesthetics stabilize the neuronal membrane and prevent the initiation and transmission of nerve impulses, thereby producing the local anesthetic action.


Proparacaine 0.5% (Alcaine, Ophthetic)

Has rapid onset of anesthesia that begins 13-30 sec after instillation. However, has short duration of action of about 15-20 min. Since prolonged eye anesthesia can eliminate patient's awareness of mechanical damage to the cornea, drug should not be used outside the ED. Frequent use of anesthetics may retard healing. Least irritating of all topical anesthetics. Prevents initiation and transmission of impulse at nerve cell membrane by stabilizing and decreasing ion permeability.

Adult

2-3 gtt in affected eye q15-20min during ED examination

Pediatric

Administer as in adults

Increases effects of phenylephrine and tropicamide

Documented hypersensitivity; prolonged use

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

Precautions

Caution in cardiac disease or hyperthyroidism and with abnormal or reduced levels of plasma esterases

Cycloplegics

These agents relax ciliary muscle spasm that can cause a deep aching pain and photophobia. Cycloplegics are used to facilitate eye examination and provide relief of symptoms in patients with moderate-to-severe eye injury. Cycloplegic agents also are mydriatics, thus before using them it is important to ensure that the patient does not have glaucoma. This medication could provoke an acute angle-closure glaucoma attack in a susceptible patient.


Cyclopentolate 0.5-1% (Cyclogyl)

Prevents muscle of ciliary body, and sphincter muscle of iris from responding to cholinergic stimulation. Induces mydriasis in 30-60 min and cycloplegia in 25-75 min.

Adult

1 gtt of 1% solution to induce cycloplegia; repeat in 5-10 min prn

Pediatric

<1 year: 1 gtt of 0.5% into each eye 5-10 min before examination
>1 year: 1 gtt of 0.5%, 1%, or 2% solution; repeat in 5-10 min prn

Decreases effects of carbachol and cholinesterase inhibitors

Documented hypersensitivity; narrow-angle glaucoma

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

Precautions

Caution in patients (eg, elderly patients) in whom increased intraocular pressure may be present; can cause toxic anticholinergic systemic adverse effects, but incidence is rare when used sparingly (more common in children, especially infants); compressing the lacrimal sac with digital pressure for 1-3 min following application may minimize systemic absorption

Antibiotics, ophthalmic

The routine use of topical antibiotics remains controversial. Many emergency physicians have stopped its use for minor injuries, although others continue routine treatment with a broad-spectrum antibiotic ointment for lubrication and infection prophylaxis. This treatment persists despite its unproven efficacy, discomfort, and evidence that ointments may retard corneal epithelial healing.


Erythromycin 0.5% ointment (Ilotycin, AK-Mycin)

Indicated for treatment of infections caused by susceptible strains of microorganisms and for prevention of corneal and conjunctival infections.

Adult

Apply 0.5-inch (1.25-cm) ribbon 2-8 times/d, depending on severity of the infection

Pediatric

Administer as in adults

Documented hypersensitivity; viral, mycobacterial, and fungal infections of the eye; patients using steroid combinations after the uncomplicated removal of a foreign body from the cornea should avoid using this product

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Not for use to treat ocular infections that are likely to become systemic; prolonged or repeated therapy may result in bacterial or fungal overgrowth of nonsusceptible organisms and may lead to a secondary infection; take appropriate measures if superinfection occurs


Gentamicin (Genoptic, Garamycin)

Aminoglycoside antibiotic used for gram-negative bacterial coverage.

Adult

Ointment: Apply 0.5-inch (1.25-cm) ribbon bid/tid to the affected eye q3-4h
Solution: 1-2 gtt in affected eye q2-4h, as often as q1h for severe infections

Pediatric

Administer as in adults

Documented hypersensitivity; mycobacterial, viral, and fungal infections of the eye; patients taking steroid combinations after uncomplicated removal of a foreign body from cornea should also avoid using this product

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

Precautions

Do not use to treat ocular infections that may become systemic; prolonged or repeated antibiotic therapy may result in bacterial or fungal overgrowth of nonsusceptible organisms that may lead to a secondary infection; take appropriate measures if superinfection occurs

Analgesics

Although most NSAIDs are used primarily for their anti-inflammatory effects, they are effective analgesics and are useful for the relief of mild to moderate pain. Pain control is essential to quality patient care. Although oral narcotics may be sedating they should be prescribed and are nearly always needed to gain adequate pain control. Prescribing adequate pain medications on the first visit is essential to prevent a revisit solely for pain control. Only a small quantity is needed since this is a self-limited problem with short duration.


Ibuprofen (Motrin, Advil, Nuprin, Rufen)

Usually the DOC for mild to moderate pain, if no contraindications exist; inhibits inflammatory reactions and pain, probably by decreasing cyclooxygenase activity, which results in the inhibition of prostaglandin synthesis

Adult

200-800 mg PO q4-6h, while symptoms persist; not to exceed 3.2 g/d

Pediatric

10-70 mg/kg/d PO divided tid/qid

Probenecid may increase the concentrations and possibly the toxicity; may decrease the effect of loop diuretics when administered concurrently; PT may increase when administered concurrently with anticoagulants (monitor PT closely, and instruct patients to watch for signs and symptoms of bleeding); may increase serum lithium levels and risk of methotrexate toxicity

Documented hypersensitivity; because of potential cross-sensitivity to other NSAIDs, do not give these agents to patients in whom aspirin, iodides, or other NSAIDs induce hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in congestive heart failure, hypertension, and decreased renal and hepatic function


Oxycodone and acetaminophen (Percocet, Tylox, Roxicet)

Drug combination indicated for the relief of moderate to severe pain.

Adult

1-2 tab or cap PO q4-6h prn

Pediatric

0.05-0.15 mg/kg/dose PO q4-6h prn; not to exceed 5 mg/dose of oxycodone

Phenothiazines may decrease analgesic effects; toxicity increases when administered concurrently with CNS depressants or tricyclic antidepressants

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

Precautions

Duration of action may increase in elderly patients; be aware of the total daily dose of acetaminophen; maximum dose of acetaminophen is 4,000 mg/d, higher doses may cause liver toxicity

Ophthalmic analgesic

Some ophthalmologists are advocating that diclofenac (Voltaren) or ketorolac (Acular) drops be used despite lack of official indications. These topical agents have been shown to relieve pain in multiple situations including corneal abrasions, allergies, and postsurgical pain.


Ketorolac tromethamine 0.5% (Acular)

Inhibits prostaglandin synthesis by decreasing activity of the enzyme, cyclooxygenase, which results in decreased formation of prostaglandin precursors, which, in turn, results in reduced inflammation.

Adult

1 gtt into each affected eye qid, continue for a maximum of 2 wk

Pediatric

<12 years: Not established
>12 years: Administer as in adults

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

Precautions

Perform ophthalmologic studies in patients who develop eye complaints during therapy; discontinue therapy if changes are noted; changes may include blurred or diminished vision, corneal deposits and retinal disturbances, scotomata, changes in color vision, and macula degeneration


Diclofenac (Voltaren)

Inhibits prostaglandin synthesis by decreasing the activity of the enzyme cyclooxygenase, which results in decreased formation of prostaglandin precursors.

Adult

1 gtt into affected eye qid, continue for a maximum of 2 wk

Pediatric

<12 years: Not established
>12 years: Administer as in adults

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

Precautions

Corneal thinning may occur

More on Ultraviolet Keratitis

Overview: Ultraviolet Keratitis
Differential Diagnoses & Workup: Ultraviolet Keratitis
Treatment & Medication: Ultraviolet Keratitis
Follow-up: Ultraviolet Keratitis
Multimedia: Ultraviolet Keratitis
References

References

  1. Belin MW, Catalano RA, Scott JL. Burns of the eye. In: Catalano RA, ed. Ocular Emergencies. Philadelphia, Pa: WB Saunders Co; 1992:192-4.

  2. Brown MD, Cordell WH, Gee AS. Do ophthalmic nonsteroidal anti-inflammatory drugs reduce the pain associated with simple corneal abrasion without delaying healing?. Ann Emerg Med. Oct 1999;34(4 Pt 1):526-34. [Medline].

  3. Brunette DD, Ghezzi K, Renner GS. Ophthalmologic disorders. In: Rosen P, Barkin R, eds. Emergency Medicine: Concepts and Clinical Practice. 4th ed. St. Louis, Mo: Mosby Year Book; 1998:2704.

  4. Crumpton KL, Shockley LW. Ocular trauma: a quick illustrated guide to treatment, triage, and medicolegal implications. Emerg Med Rep. 1997;18:223-34.

  5. Daxecker F, Blumthaler M, Ambach W. Ultraviolet exposure of cornea from sunbeds. Lancet. Sep 24 1994;344(8926):886. [Medline].

  6. Schein OD. Phototoxicity and the cornea. J Natl Med Assoc. Jul 1992;84(7):579-83. [Medline].

  7. Spencer WH. The Cornea. Ophthalmic Pathology. 4th ed. Philadelphia, Pa: WB Saunders Co; 1996:233-35.

  8. Weaver CS, Terrell KM. Evidence-based emergency medicine. Update: do ophthalmic nonsteroidal anti-inflammatory drugs reduce the pain associated with simple corneal abrasion without delaying healing?. Ann Emerg Med. Jan 2003;41(1):134-40. [Medline].

  9. Wittenberg S. Solar radiation and the eye: a review of knowledge relevant to eye care. Am J Optom Physiol Opt. Aug 1986;63(8):676-89. [Medline].

  10. Yen YL, Lin HL, Lin HJ, et al. Photokeratoconjunctivitis caused by different light sources. Am J Emerg Med. Nov 2004;22(7):511-5. [Medline].

Further Reading

Keywords

actinic keratitis, snow blindness, flash burn, welder's flash, arc eye, ultraviolet keratitis, UV keratitis, UV radiation injury, corneal damage, corneal abrasion, corneal ulceration, corneal laceration, superficial punctate keratitis, SPK, UV keratoconjunctivitis, ultraviolet keratoconjunctivitis 

Contributor Information and Disclosures

Author

Reed Brozen, MD, Director of Air Transport, Associate Professor, Department of Emergency Medicine, Dartmouth Medical School, Dartmouth-Hitchcock Medical Center
Reed Brozen, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, New Hampshire Medical Society, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Christian Fromm, MD, FAAEM, FACEP, Assistant Professor, Department of Emergency Medicine, Mount Sinai School of Medicine; Director of Research, Attending Physician, Department of Emergency Medicine, Maimonides Medical Center
Christian Fromm, MD, FAAEM, FACEP is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Eric M Kardon, MD, FACEP, Attending Emergency Physician, Georgia Emergency Medicine Specialists; Physician, Division of Emergency Medicine, Athens Regional Medical Center
Eric M Kardon, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

James Steven Walker, DO, MS, Clinical Professor of Surgery, Department of Surgery, University of Oklahoma Health Sciences Center
James Steven Walker, DO, MS is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, and American Osteopathic Association
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Rick Kulkarni, MD, Medical Director, Assistant Professor of Surgery, Section of Emergency Medicine, Yale-New Haven Hospital
Rick Kulkarni, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: WebMD Salary Employment

 
 
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