Bacterial keratitis is a sight-threatening process. A particular feature of bacterial keratitis is its rapid progression; corneal destruction may be complete in 24-48 hours with some of the more virulent bacteria. Corneal ulceration, stromal abscess formation, surrounding corneal edema, and anterior segment inflammation are characteristic of this disease. (See image below.)
Human eye anatomy.
Bacterial keratitis remains one of the most important potential complications of contact lens use and refractive corneal surgery. Keeping this in mind, early diagnosis and treatment are key to minimizing any visual-threatening sequelae. In addition, close follow-up, attention to laboratory data, and changing antimicrobials if no clinical improvement is evident are important elements for successful outcome.
Interruption of an intact corneal epithelium and/or abnormal tear film permits entrance of microorganisms into the corneal stroma, where they may proliferate and cause ulceration. Virulence factors may initiate microbial invasion, or secondary effector molecules may assist the infective process. Many bacteria display several adhesins on fimbriated and nonfimbriated structures that may aid in their adherence to host corneal cells. During the initial stages, the epithelium and stroma in the area of injury and infection swell and undergo necrosis. Acute inflammatory cells (mainly neutrophils) surround the beginning ulcer and cause necrosis of the stromal lamellae.
Diffusion of inflammatory products (including cytokines) posteriorly elicits an outpouring of inflammatory cells into the anterior chamber and may create a hypopyon. Different bacterial toxins and enzymes (including elastase and alkaline protease) may be produced during corneal infection, contributing to the destruction of corneal substance.
The most common groups of bacteria responsible for bacterial keratitis are as follows: Streptococcus, Pseudomonas, Enterobacteriaceae (including Klebsiella, Enterobacter, Serratia, and Proteus), and Staphylococcus species.
Up to 20% of cases of fungal keratitis (particularly candidiasis) are complicated by bacterial coinfection.
Approximately 25,000 Americans develop bacterial keratitis annually.
Incidence of bacterial keratitis varies considerably, with less industrialized countries having a significantly lower number of contact lens users and, therefore, significantly fewer contact lens-related infections.
In cases of severe inflammation, a deep ulcer and a stromal abscess may coalesce, resulting in thinning of the cornea and sloughing of the infected stroma. These processes may create some of the following complications:
Patients with bacterial keratitis usually complain of rapid onset of pain, photophobia, and decreased vision. It is important to document a complete systemic and ocular history in these patients to identify any potential risk factors that would have made them susceptible to develop this infection, including the following:
External and biomicroscopic examination of these patients reveals some or all of the following features:
Any factor or agent that creates a breakdown of the corneal epithelium is a potential cause or risk factor for bacterial keratitis. Furthermore, exposure to some virulent bacteria that may penetrate intact epithelium (eg, Neisseria gonorrhoeae) also may result in bacterial keratitis.
During the initial stages, the epithelium and the stroma in the area of injury and infection swell and undergo necrosis. Acute inflammatory cells (mainly neutrophils) surround the beginning ulcer and cause necrosis of the stromal lamellae. In cases of severe inflammation, a deep ulcer and a deep stromal abscess may coalesce, resulting in thinning of the cornea and sloughing of the infected stroma.
As the natural host defense mechanisms overcome the infection, humoral and cellular immune defenses combine with antibacterial therapy to retard bacterial replication. Following this process, phagocytosis of the organism and cellular debris take place, without further destruction of stromal collagen. During this stage, a distinct demarcation line may appear as the epithelial ulceration and stromal infiltration consolidate and the edges become rounded.
Vascularization of the cornea may follow if the keratitis becomes chronic. In the healing stage, the epithelium resurfaces the central area of ulceration and the necrotic stroma is replaced by scar tissue produced by fibroblasts. The reparative fibroblasts are derived from histiocytes and keratocytes that have undergone transformation. Areas of stromal thinning may be replaced partially by fibrous tissue. New blood vessel growth directed toward the area of ulceration occurs with delivery of humoral and cellular components to promote further healing. The Bowman layer does not regenerate but is replaced with fibrous tissue.
New epithelium slowly resurfaces the irregular base, and vascularization gradually disappears. With severe bacterial keratitis, the progressive stage advances beyond the point in which the regressive stage can lead to the healing stage. In such severe ulcerations, stromal keratolysis may progress to corneal perforation. Uveal blood vessels may participate in sealing the perforation, resulting in an adherent vascularized leukoma.
If no organisms are identified on the slide smear, initiate broad-spectrum antibiotics with the following: tobramycin (14 mg/mL) 1 drop every hour alternating with fortified cefazolin (50 mg/mL) 1 drop every hour.
If the corneal ulcer is small, peripheral and no impending perforation is present, intensive monotherapy with fluoroquinolones is an alternative treatment. Other antimicrobials can be used, depending on the clinical progress and laboratory findings.
The fourth-generation ophthalmic fluoroquinolones include moxifloxacin (VIGAMOX, Alcon Laboratories, Inc, Fort Worth, TX) and gatifloxacin (Zymar, Allergan, Irvine, CA), and they are now being used for the treatment of bacterial conjunctivitis. Both antibiotics have better in vitro activity against gram-positive bacteria than ciprofloxacin or ofloxacin. Moxifloxacin penetrates better into ocular tissues than gatifloxacin and older fluoroquinolones; in vitro activity of moxifloxacin and gatifloxacin against gram-negative bacteria is similar to that of older fluoroquinolones. Moxifloxacin also has better mutant prevention characteristics than other fluoroquinolones. These findings support the use of the newer fluoroquinolones for the prevention and treatment of serious ophthalmic infections (eg, keratitis, endophthalmitis) caused by susceptible bacteria.
In view of these findings, moxifloxacin or gatifloxacin may be a preferred alternative to ciprofloxacin as the first-line monotherapy in bacterial keratitis.
Additionally, 0.5% moxifloxacin and, to a lesser extent, levofloxacin and ciprofloxacin have demonstrated significant effectiveness for reducing the number of Mycobacterium abscessus in vivo, suggesting the potential use of these agents in prevention of M abscessus keratitis.
Three patients with Acanthamoeba keratitis were successfully treated with a topical application of 0.1% riboflavin solution and 30 minutes of UV irradiation focused on the corneal ulcer.
The frequency of antibiotic administration should be tapered off according to the clinical course using some of the following parameters:
The most common cause of corneal perforation is infection by bacteria, virus, or fungus, accounting for 24-55% of all perforations, with bacterial infections being the most common. PK, sclerocorneal patch, or application of cyanoacrylate tissue adhesive may be necessary in cases of corneal perforation or imminent perforation, following the guidelines provided below.
Consultation with vitreoretinal colleagues may be helpful if the diagnosis of endophthalmitis is considered.
Topical antibiotics constitute the mainstay of treatment in cases of bacterial keratitis, with subconjunctival antibiotics used only under unusual circumstances, and systemic antibiotics used only in cases of perforation or specific organisms (eg, N gonorrhoeae). The use of topical corticosteroids remains controversial; however, when they are used, strict guidelines and close follow-up care are mandatory to ensure the best ultimate outcome of these patients.
Clinical Context: Interferes with bacterial protein synthesis by binding to 30S and 50S ribosomal subunits, which results in a defective bacterial cell membrane. Add 2 mL of parenteral tobramycin (40 mg/cc) to 5 mL commercial 0.3% tobramycin solution. Refrigerate (expires in 7 d)
Clinical Context: When mycobacteria are suspected. Irreversibly binds to 30S subunit of bacterial ribosomes; blocks recognition step in protein synthesis; causes growth inhibition.
Clinical Context: First-generation cephalosporin with excellent gram-positive but narrow gram-negative activity. To prepare for topical use, dilute 500 mg parenteral cefazolin powder in sterile water to form 10 mL solution. Refrigerate (preparation expires in 7 d).
Clinical Context: Third-generation cephalosporin has slightly less activity against gram-positive pathogens but more activity against gram-negative bacteria compared to a first-generation cephalosporin. To prepare, add 1 g parenteral ceftazidime powder to 9.2 cc of artificial tears. Add 5 cc of dilution to 5 cc of artificial tears, and shake well.
Clinical Context: Acts by inhibiting bacterial protein synthesis. Binds reversibly to the 50S subunit of bacterial 70S ribosome and prevents attachment of the amino acid-containing end of the aminoacyl-tran to acceptor site on ribosome. Active in vitro against a wide variety of bacteria, including gram-positive, gram-negative, aerobic, and anaerobic organisms.
Clinical Context: Ophthalmic ointment applied hs can be used in combination with a fluoroquinolone to improve coverage against streptococci and other gram-positive bacteria when dealing with small ulcers and outpatient treatment.
Clinical Context: To prepare for topical administration, dilute 500 mg of parenteral vancomycin powder in 10 mL sterile water, artificial tears, or normal saline (0.9%). Refrigerate (preparation expires in 4 d). The 25 mg/mL concentration appears to be just as effective as the 50 mg/mL concentration but is much better tolerated by patients.
Clinical Context: Laboratory diagnosis of Nocardia keratitis. Exerts bacteriostatic action by competitive antagonism of PABA, an essential component of folic acid synthesis.
Clinical Context: Fluoroquinolone with activity against pseudomonads, streptococci, MRSA, S epidermidis, and most gram-negative organisms, but no activity against anaerobes. Inhibits bacterial DNA synthesis, and consequently growth.
Clinical Context: A pyridine carboxylic acid derivative with broad-spectrum bactericidal effect.
Clinical Context: Quinolone that has antimicrobial activity based on ability to inhibit bacterial DNA gyrase and topoisomerases, which are required for replication, transcription, and translation of genetic material. Quinolones have broad activity against gram-positive and gram-negative aerobic organisms. Differences in chemical structure between quinolones have resulted in altered levels of activity against different bacteria. Altered chemistry in quinolones result in toxicity differences.
Aminoglycosides have a broad range of bactericidal activity against many bacterial species, particularly gram-negative rods. They have a selective affinity to bacterial 30S and 50S ribosomal subunits to produce a nonfunctional 70S initiation complex that results in inhibition of bacterial cell protein synthesis. Unlike other antibiotics that impair protein synthesis, they are bactericidal. Their clinical activity is limited severely in anaerobic conditions. They have a low therapeutic/toxic ratio.
Cephalosporins have a broad spectrum of activity, including effective action against Haemophilus species. They contain a beta-lactam ring similar to penicillins, and a dihydrothiazine ring that makes them resistant to the action of penicillinases produced by staphylococci. They inhibit the third and final stage of bacterial cell wall formation by preferentially binding to one or more penicillin-binding proteins that are in the cytoplasmic membrane beneath the cell walls of susceptible bacteria. They are well tolerated topically.
Chloramphenicol usually is reserved for specific infections such as those associated with H influenzae. Its use has been limited by toxicity, including a dose-dependent bone marrow depression.
Macrolides are bacteriostatic agents (eg, erythromycin, tetracycline) that can suppress the growth of susceptible gram-positive cocci. This class of drugs works by inhibition of bacterial protein synthesis.
Glycopeptides have activity against gram-positive bacteria, and methicillin and penicillin-resistant staphylococci. They inhibit the biosynthesis of peptidoglycan polymers during the second stage of bacterial cell wall formation, at a different site of action from that of the beta-lactam antibiotics. They also have an excellent activity against a variety of gram-positive bacilli.
Sulfonamides have a structure similar to para -aminobenzoic acid (PABA), a precursor required by bacteria for folic acid synthesis. They competitively inhibit the synthesis of dihydropteroic acid, the immediate precursor of dihydrofolic acid from PABA pteridine. This inhibition does not affect mammalian cells because they lack the ability to synthesize folic acid and require preformed folic acid. They are active against gram-positive and gram-negative bacteria, and they are the preferred drugs against Nocardia keratitis.
Fluoroquinolones variably inhibit the action of bacterial DNA gyrase an enzyme essential for bacterial DNA synthesis. They have activity against most aerobic gram-negative bacteria and some gram-positive bacteria. Concern has been generated regarding the emerging resistance to fluoroquinolones among staphylococci. Emerging resistance to these antimicrobials has been reported in nonocular and ocular isolates. A study by Haas et al has revealed that among patients with ocular bacterial pathogens, resistance to 1 or more antibiotics is prevalent. They have limited efficacy against streptococci, enterococci, non-aeruginosa Pseudomonas, and anaerobes. Two multicenter trials compared the efficacy of ciprofloxacin 0.3% and ofloxacin 0.3% solution versus fortified cefazolin and tobramycin showing favorable efficacy for a single agent fluoroquinolone therapy.
They also have a record for low toxicity, good ocular surface penetration, and prolonged tear film penetration. Monotherapy for bacterial keratitis using these classes of antibiotics has been proved to be effective in large clinical trials. However, emerging resistance to the fluoroquinolones is now being reported in nonocular and ocular isolates. One randomized trial of 500 patients with bacterial corneal ulcer who received the fluoroquinolone moxifloxacin found a higher resistance to the agent was associated with worse clinical outcomes. Results show a rate of 1 line of vision loss per 32-fold increase in minimum inhibitory concentration.
Clinical Context: Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability.
As the keratitis is controlled with antimicrobials, increase corticosteroids and decrease antibiotics.
Anti-inflammatory agents that may impair host defenses and enhance microbial proliferation, but can reduce host inflammatory response that contributes to conjunctival or corneal scarring. Should not be used until specific antimicrobial therapy has controlled microbial proliferation, and clear clinical improvement is evident. Judicious corticosteroid use entails dosage adjustment according to severity of ocular inflammation and occurrence of side effects. Discontinuation should be gradual to minimize rebound of inflammation.