Bacterial Conjunctivitis Medication

  • Author: Karen K Yeung, OD, FAAO; Chief Editor: Hampton Roy Sr, MD   more...
 
Updated: Nov 3, 2011
 

Medication Summary

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 are used only with extreme care in the setting of bacterial conjunctivitis.

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Antibiotics

Class Summary

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, although many bacterial-resistant strains are emerging. 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.

Gentamicin (Garamycin, Gentak)

 

Gentamicin is an aminoglycoside antibiotic used for gram-negative bacterial coverage. Most cases of bacterial conjunctivitis will respond to this agent, including those caused by pseudomonads, Staphylococcus aureus, group A streptococci, S pneumoniae, and H influenzae. Gentamicin is commercially available in solution or ointment form.

Erythromycin topical (Ilotycin)

 

Topical erythromycin is indicated for infections caused by susceptible strains of microorganisms and for prevention of corneal and conjunctival infections. It is effective in most cases of bacterial conjunctivitis, including those caused by S aureus, group A streptococci, S pneumoniae, and H influenzae.

Azithromycin ophthalmic (AzaSite)

 

This ophthalmic macrolide antibiotic is indicated for bacterial conjunctivitis caused by CDC coryneform group G bacteria, H influenzae, S aureus, Streptococcus mitis group, and S pneumoniae.

Bacitracin ophthalmic

 

Bacitracin 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.

Ciprofloxacin ophthalmic (Ciloxan)

 

Ciprofloxacin inhibits bacterial growth by inhibiting DNA gyrase. It is indicated for superficial ocular infections of the conjunctiva or cornea caused by strains of microorganisms susceptible to this agent. It is effective in most cases of routine conjunctivitis, including those caused by S aureus, group A streptococci, H influenzae, and Pseudomonas aeruginosa. It 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.

Trimethoprim and polymyxin B (Polytrim)

 

This combination is used for ocular infections, involving cornea or conjunctiva, resulting from strains of microorganisms susceptible to this antibiotic. It is 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.

Erythromycin (E.E.S., Ery-Tab, Erythrocin)

 

Erythromycin inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes causing RNA-dependent protein synthesis to arrest. It is effective in the treatment of chlamydial infections.

Doxycycline (Doryx, Vibramycin, Doryx)

 

Doxycycline inhibits protein synthesis and thus bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. Doxycycline is a tetracycline antibiotic that is effective in the treatment of adult chlamydial infections.

Penicillin G (Pfizerpen)

 

Penicillin interferes with synthesis of cell wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms. It is used in the hospital setting for neonatal gonorrheal infections.

Ceftriaxone (Rocephin)

 

A third-generation cephalosporin that is an adjunct in the treatment of adult gonorrhea infections, ceftriaxone arrests bacterial growth by binding to one or more penicillin-binding proteins.

Tobramycin ophthalmic (Tobrex, AK-Tob)

 

This agent interferes with bacterial protein synthesis by binding to 30S and 50S ribosomal subunits, which results in a defective bacterial cell membrane. It is available as a solution, ointment, and lotion.

Neomycin

 

Neomycin is used in the treatment of minor infections. It inhibits bacterial protein synthesis and growth.

Ofloxacin ophthalmic (Ocuflox)

 

A pyridine carboxylic acid derivative with broad-spectrum bactericidal effect, ofloxacin inhibits bacterial growth by inhibiting DNA gyrase. It is indicated for superficial ocular infections of the conjunctiva or cornea caused by susceptible strains of microorganisms.

Levofloxacin ophthalmic (Quixin, Iquix)

 

Levofloxacin is an S (-) enantiomer of ofloxacin. It inhibits DNA gyrase in susceptible organisms, thereby inhibiting relaxation of supercoiled DNA and promoting breakage of DNA strands.

Gatifloxacin ophthalmic solution 0.3% (Zymaxid)

 

A fourth-generation fluoroquinolone ophthalmic indicated for bacterial conjunctivitis, gatifloxacin 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.

Gatifloxacin is indicated for bacterial conjunctivitis due to Corynebacterium propinquum, S aureus, Staphylococcus epidermidis, Streptococcus mitis, S pneumoniae, or H influenzae.

Besifloxacin ophthalmic (Besivance)

 

Besifloxacin is a quinolone antimicrobial ophthalmic suspension indicated for bacterial conjunctivitis. Susceptible bacteria include CDC coryneform group G (Corynebacterium pseudodiphtheriticum, Corynebacterium stratum), H influenza, Moraxella lacunata, S aureus, S epidermidis, Staphylococcus hominis, Staphylococcus lugdunensis, S mitis, Streptococcus oralis, S pneumoniae, and Streptococcus salivarius. This agent is available as a 0.6% ophthalmic suspension.

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Contributor Information and Disclosures
Author

Karen K Yeung, OD, FAAO  Director of Optometry, Arthur Ashe Student Health and Wellness Center, University of California, Los Angeles, David Geffen School of Medicine

Karen K Yeung, OD, FAAO is a member of the following medical societies: American Academy of Optometry

Disclosure: Nothing to disclose.

Coauthor(s)

David S Marlin, MD  Consulting Staff, Department of Ophthalmology, Kaiser Foundation Hospital, Los Angeles Medical Center

Disclosure: Nothing to disclose.

Chief Editor

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.

Additional Contributors

Jerre Freeman, MD Founder, Chairman, Memphis Eye and Cataract Associates; Clinical Professor, Department of Ophthalmology, University of Tennessee Health Science Center College of Medicine

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 Associate Professor of Ophthalmology, Jules Stein Eye Institute, University of California, Los Angeles, David Geffen School of Medicine

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; Director of the Cornea Service, Co-Director 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; EyeGate Pharma Consulting; Inspire Consulting fee Consulting; Bausch & Lomb Honoraria Speaking and teaching; Bausch & Lomb Consulting fee Consulting

References
  1. Tabbara KF, Hyndiuk RA. Infections of the Eye. Little, Brown and Company; 1996.

  2. Rapoza PA, Quinn TC, Kiessling LA, Taylor HR. Epidemiology of neonatal conjunctivitis. Ophthalmology. Apr 1986;93(4):456-61. [Medline].

  3. 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].

  4. Schachter J, Lum L, Gooding CA, Ostler B. Pneumonitis following inclusion blennorrhea. J Pediatr. Nov 1975;87(5):779-80. [Medline].

  5. 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].

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