Updated: Jun 1, 2009
Bacterial conjunctivitis is a microbial infection involving the mucous membrane of the surface of the eye. This condition, which is usually a benign self-limited illness, sometimes can be serious or signify a severe underlying systemic disease. Occasionally, significant ocular and systemic morbidity may result.
The purpose of this article is to help the practitioner recognize the character and significance of the condition, to avoid pitfalls in diagnosis, and to convey appropriate treatment modalities.
The surface tissues of the eye and the ocular adnexa are colonized by normal flora such as streptococci, staphylococci, and Corynebacterium strains. Alterations in the host defense or in the species of bacteria can lead to clinical infection. An alteration in the flora can occur by external contamination, by spread from adjacent sites, or via a blood-borne pathway.
The primary defense against infection is the epithelial layer covering the conjunctiva. Disruption of this barrier can lead to infection. Secondary defenses include hematologic immune mechanisms carried by the conjunctival vasculature; tear film immunoglobulins and lysozyme; and the rinsing action of lacrimation and blinking.
Bacterial conjunctivitis is a common condition in all areas of the United States. It is likely that most people will experience an episode. Most of the benign cases probably are treated by primary physicians or resolve spontaneously.
Bacterial conjunctivitis is common worldwide. Community sequelae can be devastating in areas affected by blinding infections of newborns as well as in areas heavily affected by Chlamydia trachomatis.
Mortality in the setting of bacterial conjunctivitis is related to the failure to recognize and treat the underlying disease. Sepsis and meningitis caused by Neisseria gonorrhoeae can be life threatening. Chlamydial infection in the newborn can lead to pneumonia and/or otitis media. Morbidity in terms of discomfort, ocular discharge, and redness are common in benign cases and often lead to absence from work and school. Morbidity can be associated with misdiagnosis. Since many eye diseases cause the eye to be red, it is beneficial to have a solid approach to diagnosis.
Eliciting a clinical history from the patient is influenced by such factors as age and social habits and may occasionally focus on sensitive issues that can be embarrassing to discuss.
The physical examination should evaluate the following signs:
| Blepharitis, Adult | Gonococcus |
| Cellulitis, Preseptal | Herpes Simplex |
| Chlamydia | Herpes Zoster |
| Conjunctivitis, Acute Hemorrhagic | Hordeolum |
| Conjunctivitis, Allergic | Horner Syndrome |
| Conjunctivitis, Giant Papillary | Keratitis, Bacterial |
| Conjunctivitis, Neonatal | Keratitis, Fungal |
| Conjunctivitis, Viral | Keratitis, Herpes Simplex |
| Contact Lens Complications | Keratoconjunctivitis, Epidemic |
| Corneal Foreign Body | Keratoconjunctivitis, Superior Limbic |
| Corneal Graft Rejection | Molluscum Contagiosum |
| Dacryocystitis | Ocular Rosacea |
| Endophthalmitis, Bacterial | Pharyngoconjunctival Fever |
| Endophthalmitis, Fungal | Scleritis |
| Endophthalmitis, Postoperative | Squamous Cell Carcinoma, Conjunctival |
| Episcleritis | Subconjunctival Hemorrhage |
| Filtering Bleb Complications | Thyroid Ophthalmopathy |
| Fistula, Carotid Cavernous | Trachoma |
| Glaucoma, Angle Closure, Acute | Trichiasis |
| Glaucoma, Malignant | Uveitis, Anterior, Granulomatous |
| Glaucoma, Neovascular | |
| Glaucoma, Uveitic |
Nongranulomatous iritis
Gram and Giemsa stains in the presence of bacteria demonstrate the expected inflammatory cell response in the stroma. However, this consideration is only academic because the condition is not an indication for biopsy. Cultures and scrapings are usually diagnostic.
Many antibiotic eye preparations can be used as first-line therapy in bacterial conjunctivitis. The justification for treating this condition empirically with a broad-spectrum topical agent is that relatively high levels of the drug are delivered directly to the site of infection. This level of drug concentration exceeds what is normally achieved in body tissues by oral or parenteral routes. Therefore, the antibiotic spectrum of the individual drug is enhanced.
This list of medicines is limited to a few common choices. Many other agents are available. Combination antibiotic-steroid medications are not discussed in this article, as these medicines play a role in postoperative care and only are used with extreme care in the setting of bacterial conjunctivitis.
Therapy must be comprehensive and cover all likely pathogens in the context of this clinical setting. Most cases of routine bacterial conjunctivitis respond to the commercially available combination of antibiotics.
Although the aminoglycosides are used in other fields of medicine primarily to treat gram-negative bacteria, the spectrum of efficacy expands to include gram-positive bacteria when used topically for conjunctivitis.
Fluoroquinolones have gained popularity in ocular therapy due to their efficacy in the treatment of bacterial corneal ulcers. Fluoroquinolones have been used mostly as second-line agents in routine bacterial conjunctivitis.
Neonatal chlamydial infection is treated with oral erythromycin.
Doxycycline is used to treat the mother of a neonate with chlamydial infection as well as her at-risk contacts.
Intravenous penicillin G is used for neonatal gonorrhea infections.
Third-generation cephalosporins are used in the treatment of adult gonorrhea infections.
Effective in most cases of bacterial conjunctivitis including those caused by Streptococcus pneumoniae, Haemophilus influenzae, and group A Streptococcus pyogenes. It may have some local activity against Chlamydia. Available as a solution and ointment preparation.
Solution (10%): Instill 1-3 gtt q2-3h in affected eye, while awake, for 1 wk with less frequent administration at night
Ointment: Apply 0.5-ribbon into conjunctival sac qid for 1 wk
Administer as in adults; sometimes 5% preparation used
Effects decreased when used concurrently with gentamicin
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Practitioners should be aware of the toxicity of systemically administered sulfonamides including the rare hematologic effects of agranulocytosis and hemolytic anemia; therefore, it is advisable to treat only if clinically indicated; caution in severely dried eye; ointment may retard corneal epithelial healing
Aminoglycoside antibiotic used for gram-negative bacterial coverage. Most cases of bacterial conjunctivitis will respond to this agent including pseudomonads, Staphylococcus aureus, group A streptococci, S pneumoniae, and H influenzae. Commercially available in solution or ointment form.
Ointment: Apply 0.5-inch (1/25 cm) ribbon to affected eye(s) qid for 1 wk
Solution: Instill 1-2 gtt qid for 1 wk
Administer as in adults
None reported
Documented hypersensitivity; mycobacterial, viral, and fungal infections of the eye; steroid combinations after uncomplicated removal of a foreign body from cornea also should avoid using this product
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 infections
Indicated for infections caused by susceptible strains of microorganisms and for prevention of corneal and conjunctival infections. Effective in most cases of bacterial conjunctivitis including those caused by S aureus, group A streptococci, S pneumoniae, and H influenzae.
Apply 0.5-inch (1.25 cm) ribbon qid for 1 wk
Administer as in adults
None reported
Documented hypersensitivity; viral, mycobacterial, fungal infections of eye; patients using steroid combinations after uncomplicated removal of a foreign body from cornea also should avoid using this product
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Do not use topical antibiotics 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 (take appropriate measures if superinfection occurs); may not cover pseudomonads in the setting of immunocompromised patients
Ophthalmic macrolide antibiotic. Indicated for bacterial conjunctivitis caused by CDC coryneform group G bacteria, Haemophilus influenzae, Staphylococcus aureus, Streptococcus mitis group, and Streptococcus pneumoniae.
Instill 1 gtt in affected eye(s) bid (administer doses 8-12 h apart) for 2 d, then 1 gtt qd for next 5 d
<1 year: Not established
>1 year: 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
Thoroughly wash hands before using; for topical ophthalmic use only; prolonged use may result in resistant organisms; do not wear contact lenses until infection resolves; may cause eye irritation; less common adverse effects include burning, stinging, and/or irritation when instilled; other less common adverse effects include contact dermatitis, corneal erosion, dry eyes, dysgeusia, nasal congestion, ocular discharge, punctate keratitis, and sinusitis
Prevents transfer of mucopeptides into growing cell wall, inhibiting bacterial growth. Most cases of routine bacterial conjunctivitis will respond to bacitracin including those caused by group A streptococci, S aureus, S pneumoniae, and H influenzae.
Apply 0.25- to 0.5-inch ribbon bid/qid into conjunctival sac(s) for 1 wk
Administer as in adults
None reported
Documented hypersensitivity; vaccinia, varicella, epithelial herpes simplex keratitis, mycobacterial infections, fungal diseases of the eye; patients using steroid combinations after uncomplicated removal of a corneal foreign body
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Ophthalmic ointments may delay healing of corneal epithelia; in deep-seated infections of the eye, supplement with systemic medications; prolonged use may result in overgrowth of nonsusceptible organisms
Inhibits bacterial growth by inhibiting DNA gyrase. Indicated for superficial ocular infections of the conjunctiva or cornea caused by strains of microorganisms susceptible to ciprofloxacin. They are effective in most cases of routine conjunctivitis including those caused by S aureus, group A streptococci, H influenzae, and Pseudomonas aeruginosa. They may not cover all cases of S pneumoniae. Newer classes of fluoroquinolones (eg, gatifloxacin, moxifloxacin) are available and are sometimes used for conjunctivitis or a red eye, particularly in the perioperative period for eye surgery.
1-2 gtt in the eye(s) qid for 1 wk
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
Practitioners should be aware that the fluoroquinolones are not as effective against Pneumococcus as they are against other bacteria; do not use in ocular infections that may become systemic; superinfections may occur with prolonged or repeated antibiotic therapy
For ocular infections, involving cornea or conjunctiva, resulting from strains of microorganisms susceptible to this antibiotic. Available as a solution and ointment. This combination of drugs is effective against the common causes of bacterial conjunctivitis including group A streptococci, S aureus, H influenzae, S pneumoniae, and pseudomonads.
Solution: 1-2 gtt qid for 1 wk
Ointment: 0.5-ribbon into conjunctival sac qid for 1 wk
Administer as in adults
None reported
Documented hypersensitivity; viral, fungal, and mycobacterial infections of the eye
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
Inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes causing RNA-dependent protein synthesis to arrest. Effective in the treatment of chlamydial infections.
Adults are treated with doxycycline
50 mg/kg/d PO divided qid for 2 wk
Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis
Documented hypersensitivity; hepatic impairment
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Caution in liver disease; estolate formulation may cause cholestatic jaundice; GI side effects are common (give doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur
Inhibits protein synthesis and thus bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. Doxycycline is a tetracycline class of antibiotic that is effective in the treatment of adult chlamydial infections.
100 mg PO bid for 7-21 d
Not prescribed for pediatric patients
Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy
Documented hypersensitivity; severe hepatic dysfunction
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last one half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines
Interferes with synthesis of cell wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms. Used in the hospital setting for neonatal gonorrheal infections.
Adults use ceftriaxone/doxycycline regimen
100 U/kg/d IV divided qid for 1 wk
Probenecid can increase effects of penicillin; coadministration of tetracyclines can decrease effects of penicillin
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Caution in impaired renal function and in the setting of seizure disorders
Third-generation cephalosporin that is an adjunct in the treatment of adult gonorrhea infections. Arrests bacterial growth by binding to one or more penicillin-binding proteins.
125 mg IM single dose, followed by a 1-wk course of doxycycline 100 PO bid for 7-21 d
Not for use in pediatric population
Probenecid may increase ceftriaxone levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy; caution in breastfeeding women and in the setting of renal disease or seizure disorders
Interferes with bacterial protein synthesis by binding to 30S and 50S ribosomal subunits, which results in a defective bacterial cell membrane. Available as a solution, ointment, and lotion.
Solution: 1-2 gtt qid for 1 wk
Ointment: Apply 0.5-inch ribbon in conjunctival sac bid/tid qid for 1 wk
<2 years: Not established
>2 years: Administer as in adults
Effects decrease when used concurrently with gentamicin
Documented hypersensitivity; mycobacterial, viral, and fungal infections of the eye; steroid combinations after uncomplicated removal of a foreign body from cornea also should avoid using this product
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
Used in the treatment of minor infections. Inhibits bacterial protein synthesis and growth.
Apply 0.5-inch (1/25 cm) ribbon to affected eye(s) qid for 1 wk
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
Absorption of neomycin is possible and may cause nephrotoxicity and ototoxicity; prolonged use may result in overgrowth of nonsusceptible organisms; may irritate ocular surface, resulting in mild injection of the conjunctiva and punctate staining of the cornea
Pyridine carboxylic acid derivative with broad-spectrum bactericidal effect. Inhibits bacterial growth by inhibiting DNA gyrase. Indicated for superficial ocular infections of the conjunctiva or cornea caused by strains of microorganisms susceptible to ofloxacin.
1-2 gtt in affected eye(s) qid for 1 wk
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
Failure to respond after treating for 2-3 d may indicate presence of resistant organism or another causative agent; do not use in ocular infections that may become systemic; superinfections may occur with prolonged or repeated antibiotic therapy
S (-) enantiomer of ofloxacin. Inhibits DNA gyrase in susceptible organisms, thereby inhibiting relaxation of supercoiled DNA and promoting breakage of DNA strands.
1-2 gtt in affected eye(s) qid for 1 wk
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
Failure to respond after treating for 2-3 d may indicate presence of resistant organism or another causative agent; do not use in ocular infections that may become systemic; superinfections may occur with prolonged or repeated antibiotic therapy
Fourth-generation fluoroquinolone ophthalmic indicated for bacterial conjunctivitis. Elicits a dual mechanism of action by possessing an 8-methoxy group, thereby inhibiting the enzymes DNA gyrase and topoisomerase IV. DNA gyrase is involved in bacterial DNA replication, transcription, and repair. Topoisomerase IV is essential in chromosomal DNA partitioning during bacterial cell division. Indicated for bacterial conjunctivitis due to Corynebacterium propinquum, S aureus, Staphylococcus epidermidis, Streptococcus mitis, S pneumoniae, or H influenzae.
Days 1-2: Instill 1 gtt into affected eye(s) q2h while awake; not to exceed 8 administrations/d
Days 3-7: Instill 1 gtt into affected eye(s) up to 4 times/d while awake
<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
For ophthalmic use only; commonly causes conjunctival irritation, increased lacrimation, corneal inflammation, and papillary conjunctivitis; less common adverse effects include conjunctival hemorrhage, dry eye, eye discharge, eye irritation, eye pain, eyelid swelling, headache, red eye, reduced visual acuity, and taste disturbance
Quinolone antimicrobial ophthalmic susp indicated for bacterial conjunctivitis. Susceptible bacteria include CDC coryneform group G (Corynebacterium pseudodiphtheriticum, Corynebacterium stratum), Haemophilus influenza, Moraxella lacunata, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus hominis, Staphylococcus lugdunensis, Streptococcus mitis, Streptococcus oralis, Streptococcus pneumoniae, and Streptococcus salivarius. Available as a 0.6% ophthalmic suspension.
Instill 1 gtt in affected eye(s) tid (4-12 h between doses) 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
In clinical trials, adverse effects occurred in <3% of patients and included redness of eyes, blurred vision, eye pain, eye irritation, eye itching, and headache; do not use with contact lens (remove and do not wear contacts during course of therapy and with symptoms of bacterial conjunctivitis); for topical ophthalmic use only; prolonged use may lead to bacterial resistance
Hammerschlag MR, Cummings C, Roblin PM, Williams TH, Delke I. Efficacy of neonatal ocular prophylaxis for the prevention of chlamydial and gonococcal conjunctivitis. N Engl J Med. Mar 23 1989;320(12):769-72. [Medline].
Rapoza PA, Quinn TC, Kiessling LA, Taylor HR. Epidemiology of neonatal conjunctivitis. Ophthalmology. Apr 1986;93(4):456-61. [Medline].
Schachter J, Lum L, Gooding CA, Ostler B. Pneumonitis following inclusion blennorrhea. J Pediatr. Nov 1975;87(5):779-80. [Medline].
Tabbara KF, Hyndiuk RA. Infections of the Eye. Little, Brown and Company; 1996.
Ullman S, Roussel TJ, Culbertson WW, Forster RK, Alfonso E, Mendelsohn AD, et al. Neisseria gonorrhoeae keratoconjunctivitis. Ophthalmology. May 1987;94(5):525-31. [Medline].
bacterial conjunctivitis, eye infection, pink eye, red eye
David S Marlin, MD, Consulting Staff, Department of Ophthalmology, Kaiser Foundation Hospital, Los Angeles Medical Center
Disclosure: Nothing to disclose.
Jerre Freeman, MD, Founder, Chairman, Memphis Eye and Cataract Associates; Clinical Professor, Department of Ophthalmology, University of Tennessee Health Science Center
Jerre Freeman, MD is a member of the following medical societies: American Academy of Ophthalmology, American Medical Association, American Society of Cataract and Refractive Surgery, and Tennessee Medical Association
Disclosure: Nothing to disclose.
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
Simon K Law, MD, PharmD is a member of the following medical societies: American Academy of Ophthalmology, American Glaucoma Society, and Association for Research in Vision and Ophthalmology
Disclosure: Nothing to disclose.
Christopher J Rapuano, MD, Professor, Department of Ophthalmology, Jefferson Medical College of Thomas Jefferson University; Co-Chairman of the Cornea Service, Co-Chairman of Refractive Surgery Department, Wills Eye Institute
Christopher J Rapuano, MD is a member of the following medical societies: American Academy of Ophthalmology, American Society of Cataract and Refractive Surgery, Contact Lens Association of Ophthalmologists, Cornea Society, Eye Bank Association of America, International Society of Refractive Surgery, and Pan-American Association of Ophthalmology
Disclosure: Allergan Honoraria Speaking and teaching; Allergan Consulting fee Consulting; Alcon Honoraria Speaking and teaching; Inspire Honoraria Speaking and teaching; RPS Ownership interest Other; Vistakon Honoraria Speaking and teaching
Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri
Disclosure: Nothing to disclose.
Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences
Hampton Roy Sr, MD is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, and Pan-American Association of Ophthalmology
Disclosure: Nothing to disclose.
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