Updated: Jul 27, 2009
The cornea is a transparent cover over the anterior part of the eye that serves several purposes: protection, refraction, as well as filtration of some ultraviolet light. It has no blood vessels and receives nutrients through tears as well as from the aqueous humor. It is innervated primarily by the ophthalmic division of the trigeminal nerve as well as the oculomotor nerve.
The cornea is composed of 5 layers (anterior to posterior): the corneal epithelium, Bowman’s layer, corneal stroma, Descemet’s membrane, and the corneal endothelium. A corneal abrasion is a violation in the surface of the most superficial layer, the epithelium.
The cornea of the eye and, commonly, the bulbar conjunctiva, are affected. Minor or superficial abrasions involve only the corneal epithelium. Severe injuries also involve the deeper, thicker stromal layer.
The exact frequency of emergency department visits for corneal abrasions is unknown. A survey completed in 1985 showed that around 3% of all cases to general practitioners were corneal abrasions.1 In the United States, 65,000 work-related eye injuries and illnesses that cause missed time from work occur each year.2
The rates of corneal abrasions have been reported at 12.5% at eye casualty departments in the United Kingdom.3 A study by Wong et al looked at the incidence of ocular injury in US automobile workers between July 1989 and June 1992 at 33 UAW-Chrysler Corporation plants. A total of 1983 work-related eye injuries occurred, with 86.7% of cases being superficial foreign bodies and corneal abrasions.4
Corneal abrasions can lead to lost time from work. A large study completed in the automobile industry showed that 32% of workers with eye injuries were unable to resume their normal duties for at least one day. Unfortunately, only 25% of workers in this study were wearing eye protection at the time of injury.4 A retrospective review from Torino, Italy, showed that ocular injuries including corneal abrasions were associated with a significant morbidity.5
Nevertheless, significant morbidity is uncommon but can be seen with infectious complications. Recurrent erosions are a common complication of abrasions, particularly in patients with epithelial basement membrane dystrophy.
In addition, corneal abrasions associated with contact lenses can progress to bacterial keratitis and lead to further ocular damage (including perforation or corneal scarring) if not treated promptly.6
No evidence exists of a racial predisposition to corneal abrasions.
Looking at automotive workers, men have a higher incidence of injury when compared to women of all ages.4
Incidence of corneal abrasion is more common in younger, active individuals. Automotive workers between the ages of 20-29 years had the highest incidence of eye injuries.4
| Burns, Chemical | Glaucoma, Acute Angle-Closure |
| Conjunctivitis | Herpes Simplex |
| Corneal Erosion, Recurrent | Herpes Zoster Ophthalmicus |
| Corneal Foreign Body | Hordeolum and Stye |
| Corneal Laceration | Iritis and Uveitis |
| Corneal Ulceration and Ulcerative
Keratitis | Keratitis, Herpes Simplex |
Corneal foreign bodies
Corneal perforation (see Causes and Corneal Laceration)
Keratitis or keratoconjunctivitis (eg, epidemic keratoconjunctivitis [EKC])
Recurrent epithelial erosion
Conjunctivitis
Iritis (see Iritis and Uveitis)
Acute angle-closure glaucoma
If ocular penetration is a possibility, protect with an eye shield. Limit vomiting if possible. Do not remove perforating foreign bodies.
Emergent ophthalmologic consultation is warranted for suspected retained intraocular foreign bodies. Urgent consultation is needed for suspected corneal ulcerations (microbial keratitis).
Topical antibiotics are often used to treat corneal abrasions. Oral analgesics also may be indicated.
Routine use of topical antibiotics for corneal abrasions remains controversial. Many emergency physicians have stopped using these agents for minor injuries, although others continue treating corneal abrasions with broad-spectrum antibiotic ointments for infection prophylaxis and lubrication. Antibiotic use persists despite unproved efficacy and evidence that ointments may retard corneal epithelial healing.
For large or dirty abrasions, many practitioners prescribe broad-spectrum antibiotic drops, such as trimethoprim/polymyxin B (Polytrim) or sulfacetamide sodium (Sulamyd, Bleph-10), which are inexpensive and least likely to cause any complications. Alternatives are an aminoglycoside or a fluoroquinolone.
Contact lens-associated abrasions warrant antibiotic treatment due to their propensity for developing infectious corneal ulcers (microbial keratitis). Coverage for gram-negative organisms (especially pseudomonas) is recommended with agents such as gentamicin (Garamycin), tobramycin (Tobrex), norfloxacin (Chibroxin), or ciprofloxacin (Ciloxan).
Avoid antibiotics containing neomycin (eg, Neosporin) because of the higher incidence of allergy to neomycin in the general population.
Antibiotic drops are more comfortable than ointments but must be administered every 2-3 h. Ointments that retain their antibacterial effect longer can be used less often (every 4-6 h) but are more uncomfortable due to visual blurring.
Used for treatment of ocular infections involving cornea or conjunctiva.
Available as solution and ointment.
Solution: 1-2 gtt q2h in the affected eye while awake
Ointment: Apply 0.5-inch ribbon into conjunctival sac qid
<2 months: Not established
>2 months: Administer as in adults
None reported
Documented hypersensitivity; viral and mycobacterial infections of the eye; fungal diseases
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Do not use in deep ocular infections or in those likely to become systemic; prolonged use of antibiotics or repeated therapy may result in bacterial or fungal overgrowth of nonsusceptible organism
Interferes with bacterial growth by inhibiting bacterial folic acid synthesis through competitive antagonism of PABA.
Available as solution, ointment, and lotion.
Solution: 1-3 gtt q2-3h in the affected eye, while awake; less frequently at night
Ointment: Apply 0.5-inch ribbon 1-4 times/d into conjunctival sac
<2 months: Not established
>2 months: Administer as in adults
Effects decreased when used concurrently with gentamicin
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in severely dried eye; ointment may retard corneal epithelial healing
Aminoglycoside that interferes with bacterial protein synthesis by binding to 30S and 50S ribosomal subunits, causing a defective bacterial cell membrane.
Available as solution, ointment, and lotion.
Solution: 1-2 gtt q4h in the affected eye, while awake; less frequently at night
Severe infections: 2 gtt q30-60min for the first 24 h, followed by less frequent intervals
Ointment: Apply 0.5-inch ribbon bid/tid into conjunctival sac
Severe infections: Apply q3-4h
<2 years: Not established
>2 years: Administer as in adults
None reported
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use in deep-seated ocular infections or in those that may become systemic; prolonged use of antibiotics may result in bacterial or fungal overgrowth of nonsusceptible organisms
Inhibits bacterial growth by inhibiting DNA gyrase.
1-2 gtt qid for 7 d
Suspected corneal ulcers: 1-2 gtt qh for first 24 h, then qid for 7 d
<1 year: Not established
>1 year: Administer as in adults
None reported
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use in deep ocular infections likely to become systemic; prolonged use of antibiotics may result in bacterial or fungal overgrowth of nonsusceptible organisms
Inhibits bacterial growth by inhibiting DNA gyrase.
1-2 gtt qid for 7 d
Suspected corneal ulcers: 1-2 gtt qh for first 24 h, then qid for 7 d
<1 year: Not established
>1 year: Administer as in adults
None reported
Documented hypersensitivity; viral, mycobacterial, and fungal eye infections; avoid coadministration with steroid combinations after uncomplicated removal of a foreign body from cornea
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use in deep ocular infections likely to become systemic; prolonged use of antibiotics may result in bacterial or fungal overgrowth of nonsusceptible organisms
Aminoglycoside antibiotic used for gram-negative bacterial coverage.
Solution: 1-2 gtt q4h in the affected eye, while awake; less frequently at night
Severe infections: 2 gtt q30-60min for the first 24 h, followed by less frequent intervals
<2 years: Not established
>2 years: Administer as in adults
None reported
Documented hypersensitivity; mycobacterial, viral, and fungal infections of the eye; patients taking steroid combinations after uncomplicated removal of a foreign body from cornea
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
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 and may lead to a secondary infection
These agents are used for analgesia to facilitate an adequate examination. These agents should never be prescribed for home use because they may cause a secondary keratitis, compromise epithelial wound healing, and block effective corneal protective reflexes and sensation.
Least irritating of all topical anesthetics. Prevents initiation and transmission of impulse at the nerve cell membrane by stabilizing it and decreasing ion permeability. Onset of action for this anesthetic takes place within 20 sec of application. Anesthetic effect may last up to 10-15 min.
1-2 gtt of 0.5% solution in the eye q5-10min for 5-7 doses
Administer as in adults
Increases effects of phenylephrine and tropicamide
Documented hypersensitivity; prolonged use
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in cardiac disease or hyperthyroidism and those with abnormal or reduced levels of plasma esterases
Local anesthetic that blocks both initiation and conduction of nerve impulses by decreasing neuronal membrane's permeability to sodium ions. Results are inhibition of depolarization, blocking conduction of impulse.
Available in solution and ointment. Onset of action takes place within 1 min of application and anesthetic effect may last up to 15-20 min.
This medication stings considerably on application.
Solution: 1-2 gtt
Ointment: Apply 0.5-inch ribbon into conjunctival fornix
Not established
Antagonizes effect of sulfonamides and aminosalicylic acid
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in cardiac disease and hyperthyroidism; use may delay wound healing
Some ophthalmologists are advocating that diclofenac (Voltaren) or ketorolac (Acular) drops and a disposable soft contact lens be used in addition to antibiotic drops. This therapy may prove to be an effective alternative to patching, permitting the patient to maintain binocular vision during treatment. Compared with patching, the contact lens used with the NSAID may reduce pain.
Inhibits prostaglandin synthesis by decreasing the activity of the enzyme cyclooxygenase, which results in decreased formation of prostaglandin precursors.
1 gtt into affected eye qid, continue for a maximum of 2 wk
<12 years: Not established
>12 years: Administer as in adults
None reported
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Corneal thinning may occur
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.
1 gtt into affected eye qid, continue for a maximum of 2 wk
<12 years: Not established
>12 years: Administer as in adults
None reported
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
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
All but the most minor abrasions usually require a strong oral narcotic analgesic.
Drug combination indicated for the relief of moderate to severe pain.
1-2 tab or cap PO q4-6h prn
<12 years: 10-15 mg/kg/dose PO acetaminophen q4-6h prn; not to exceed 2.6 g/d acetaminophen or 5 mg of hydrocodone bitartrate/dose
>12 years: 750 mg PO acetaminophen q4h; not to exceed 5 doses/d acetaminophen or 10 mg of hydrocodone bitartrate/dose
Coadministration with phenothiazines may decrease analgesic effects; toxicity increases with CNS depressants or tricyclic antidepressants
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Tabs contain metabisulfite, which may cause hypersensitivity; caution in patients dependent on opiates because this substitution may result in acute opiate-withdrawal symptoms; caution in severe renal or hepatic dysfunction
Drug combination indicated for the relief of moderate to severe pain.
1-2 tab or cap PO q4-6h or prn
Based on oxycodone dose: 0.05-0.15 mg/kg/dose PO q4-6h or prn; not to exceed 5 mg/dose of oxycodone
Phenothiazines may decrease analgesic effects; toxicity increases with coadministration of either CNS depressants or tricyclic antidepressants
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Duration of action may increase in elderly persons; be aware of total daily dose of acetaminophen patient is receiving; do not exceed 4000 mg/d of acetaminophen; higher doses may cause liver toxicity
No good evidence exists in the literature to support the common practice of using cycloplegics/mydriatics for the treatment of routine corneal abrasions. However, most ophthalmologists believe that the instillation of a long-acting cycloplegic agent can provide significant relief in patients who have extensive corneal abrasions, a large degree of photophobia, and blepharospasm. These agents relax any ciliary muscle spasm that may cause a deep, aching pain and photophobia.
Cycloplegic agents are mydriatics; thus, to prevent an acute angle-closure attack, ensure that the patient does not have narrow-angle glaucoma.
Blocks the response of the iris sphincter muscle and the accommodative muscle of ciliary body to cholinergic stimulation. This results in dilation and loss of accommodation. Useful for patients with dark iris.
Induces mydriasis in 10-30 min and cycloplegia in 30-90 min. These effects last up to 48 h.
Instill 1-2 gtt of 2% solution or 1 gtt of 5% solution to induce cycloplegia; repeat in 15-20 min prn
For prolonged cycloplegia: 1-2 gtt up to q3-4h; if heavily pigmented irides, larger doses may be necessary
Apply 1 gtt of 2% solution immediately before the procedure; repeat at 10-min intervals prn
None reported
Documented hypersensitivity; narrow-angle glaucoma
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Exercise caution in patients who may have increased IOP (eg, elderly persons); toxic anticholinergic systemic adverse effects can occur, but are rare when used sparingly; adverse effects are more common in children, especially infants; compressing lacrimal sac by digital pressure for 1-3 min following instillation minimizes systemic absorption
DOC in the treatment of cornea abrasions. Prevents the muscle of the ciliary body and the sphincter muscle of the iris from responding to cholinergic stimulation, causing mydriasis and cycloplegia.
Induces mydriasis in 30-60 min and cycloplegia in 25-75 min. These effects last up to 24 h.
1 gtt of 1% solution is usually adequate to induce cycloplegia; repeat in 5-10 min prn
Infants: Before examination, instill 1 gtt of 0.5% into each eye q5-10min
>1 year: Instill 1 gtt of a 0.5%, 1%, or 2% solution to induce cycloplegia; repeat in 5-10 min prn
Decreases effects of carbachol and cholinesterase inhibitors
Documented hypersensitivity; narrow-angle glaucoma; albinotic patients
Exercise caution in patients who may have increased IOP (eg, elderly persons); can cause toxic anticholinergic systemic adverse effects (common in children, especially infants) but incidence rare when used sparingly; compressing lacrimal sac by digital pressure for 1-3 min following application may minimize systemic absorption
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corneal abrasion, corneal epithelial defect, corneal abrasion treatment, scratched cornea, scraped eye, scraped cornea, eye trauma, scratched eye, corneal surface
Feras H Khan, MD, Resident Physician, Department of Emergency Medicine, State University of New York Downstate, Kings County Hospital, Brooklyn
Feras H Khan, MD is a member of the following medical societies: American College of Emergency Physicians, Emergency Medicine Residents Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Mark A Silverberg, MD, FACEP, MMB, Assistant Professor, Assistant Residency Director, Department of Emergency Medicine, State University of New York Downstate College of Medicine; Consulting Staff, Department of Emergency Medicine, Staten Island University Hospital, Kings County Hospital, University Hospital, State University of New York Downstate at Brooklyn
Mark A Silverberg, MD, FACEP, MMB is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Council of Emergency Medicine Residency Directors, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Debra Slapper, MD, Consulting Staff, Department of Emergency Medicine, St Anthony's Hospital
Debra Slapper, MD is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
Douglas Lavenburg, MD, Clinical Professor, Department of Emergency Medicine, Christiana Care Health Systems
Douglas Lavenburg, MD is a member of the following medical societies: American Society of Cataract and Refractive Surgery
Disclosure: Nothing to disclose.
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.
Barry E Brenner, MD, PhD, FACEP, Professor of Emergency Medicine, Professor of Internal Medicine, Program Director, Emergency Medicine, University Hospitals, Case Medical Center
Barry E Brenner, MD, PhD, FACEP is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Chest Physicians, American College of Emergency Physicians, American College of Physicians, American Heart Association, American Thoracic Society, Arkansas Medical Society, New York Academy of Medicine, New York Academy of Sciences, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
I would like to thank Samala Khan, OD, for supplying the visual images.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Robert M Howell, MD, to the development and writing of this article.
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