Endophthalmitis means bacterial or fungal infection inside the eye involving the vitreousand/or aqueous humors. Most cases are exogenous and occur after eye surgery, after penetrating ocular trauma, or as an extension of corneal infection. An increasing number of cases are occurring after intravitreal injections of anti-vascular endothelial growth factor(VEGF) medications. Endophthalmitis may also be endogenous, arising from bacteraemic or fungaemic seeding of the eye. The infected eye never serves as a source of bacteraemia or fungaemia, however. The most common pathogens in endophthalmitis vary by category. Coagulase-negative staphylococci are the most common causes of post-cataract endophthalmitis, and these bacteria and viridans streptococci cause most cases of post-intravitreal anti-VEGF injection endophthalmitis, Bacillus cereus is a major cause of post-traumatic endophthalmitis, and Staphylococcus aureus and streptococci are important causes of endogenous endophthalmitis associated with endocarditis. In Taiwan and other East Asian nations, Klebsiella pneumoniae causes most cases of endogenous endophthalmitis, in association with liver abscess. Endogenous fungal endophthalmitis in hospitalized patients is usually caused by Candida species, particularly Candida albicans. Acute endophthalmitis is a medical emergency. The most important component of treatment is the intravitreal injection of antibiotics, along with vitrectomy in severe cases. Systemic antibiotics should be used in cases of endogenous endophthalmitis and exogenous fungal endophthalmitis, but their role in exogenous bacterial endophthalmitis is uncertain. Repeated intravitreal injections of antibiotics may be necessary if there is no response to the initial therapy. Many eyes that receive prompt and appropriate treatment will recover useful vision.
Bacterial endophthalmitisCandida endophthalmitisendogenous endophthalmitisendophthalmitisfungal endophthalmitiskeratitis-related endophthalmitismould endophthalmitispost-injection endophthalmitispostoperative endophthalmitispost-traumatic endophthalmitis
Endophthalmitis means bacterial or fungal infection inside the eye, involving the vitreousand/or aqueous humors. Most cases of endophthalmitis are exogenous, and organisms are introduced into the eye via trauma, surgery, or an infected cornea. Endogenous endophthalmitis occurs when the eye is seeded via the bloodstream. Patients usually have symptoms from their underlying systemic infection, but sometimes present only with eye symptoms.
Endophthalmitis does not serve as a source of bactaeremia or fungaemia. Infection remains confined to the eye. In panophthalmitis, infection spreads from the globe of the eye to the adjacent soft tissues of the orbit.
Most cases of endophthalmitis present acutely, with hours to a few days of symptoms. These cases are medical emergencies, as delay in treatment may result in permanent vision loss.
TABLE 1. Types of endophthalmitis, common pathogens, and treatment
TypeMost common pathogensIntial intravitreal treatmentaVitrectomy necessarycNeed to remove artificial intra-ocular lens?Initial systemic antibioticsbAcute post-cataractCoagulase-negative staphylococci (70% of cases), other Gram-positive cocci (25%)Intravitreal vancomycin plus ceftazidimeYes, if severe infection or fungal aetiologyNo, unless fungal aetiologyValue unknown, rarely givenChronic post-cataractPropionibacterium acnesIntravitreal vancomycinVariesYesNoPost-injectionCoagulase-negative staphylococci, viridans streptococciIntravitreal vancomycin plus ceftazidimeYes, if severe infectionNoMoxifloxacin or similar?Bleb-relatedStreptococci, Haemophilus influenzaeIntravitreal vancomycin plus ceftazidimeMost casesNoMoxifloxacin or similar?Post-traumaticBacillus cereus, coagulase-negative staphylococci (fungi in some cases)Intravitreal vancomycin plus ceftazidime (plus amphotericin if fungi suspected)Most casesVaries (always if fungal)Intravenous vancomycin plus either ceftazidime or ciprofloxacinEndogenous bacterialStaphylococcus aureus, streptococci, Gram-negative bacilli (e.g. Klebsiella)Intravitreal vancomycin plus ceftazidime (or amikacin)Yes, nearly all casesNoIntravenous antibiotics tailored to systemic infectionCandidaCandida speciesIntravitreal amphotericin (or voriconazole)Yes, if vitritisOftenYesMouldAspergillus, FusariumIntravitreal amphotericinYesYesYesa
Intravitreal antibiotics are given at the end of a vitrectomy case in the operating room, or as an office procedure without a vitrectomy (see text). Whereas initial therapy is empirical, subsequent injections may be tailored to culture results.
Systemic antibiotics alone are not effective in treating endophthalmitis, except for most cases of Candida chorioretinitis without vitritis. They are indicated in endogenous endophthalmitis and fungal endophthalmitis. Whether they are beneficial as adjunctive therapy in exogenous bacterial endophthalmitis is unknown (see text).
See text for exceptions.
Cataract surgery is one of the most common eye operations performed worldwide, and acute post-cataract endophthalmitis complicates this procedure in c. 0.1% of cases [1, 2, 3, 4, 5, 6, 7]. In the USA and Europe, nearly all cases are caused by bacteria, whereas in tropical regions such as India, 10–20% of cases are caused by fungi .
Ocular surface bacteria contaminate the aqueous humor in 7–43% of cataract operations, but endophthalmitis is rare [9, 10, 11]. This may be because the aqueous humor has a rapid turnover time (100 min). The vitreous humor does not regenerate, so it is more susceptible to infection. During cataract surgery, the lens pulp is removed but the posterior lens capsuleis left intact. Inadvertent breaks in this capsule increase the endophthalmitis risk 14-fold [6, 12]. Other endophthalmitis risk factors include clear corneal incision and silicone rather than acrylic intra-ocular lenses (IOLs) .
Symptoms occur within 1 week postoperatively in 75% of cases, and include decreased vision (95%), red eye (80%), and eye pain (75%) . Patients feel otherwise well and are afebrile. On physical examination, vision is decreased, eyelids are normal to slightly swollen, the conjunctiva is injected, and a hypopyon is present in >80% of cases . There are white blood cells in the aqueous humor and vitreous humor, so the view of the retina is hazy. In 80% of patients, the view is so obscured that retinal vessels cannot be seen .
Diagnosis. Endophthalmitis is a clinical diagnosis, supported by culture of intra-ocular fluids, although a negative culture occurs in 30% of cases. The differential diagnosis is sterile intra-ocular inflammation. This may occur as a reaction to surgery, and is typically greatest on the first postoperative day, whereas endophthalmitis usually occurs on day 2 or later. Toxic anterior segment syndrome, another sterile inflammatory condition, is associated with instrument-cleaning problems or with solutions used during surgery [17, 18].
The vitreous humor is sampled through either a vitrectomy or a needle aspirate; the aqueous humor is sampled through a needle aspirate. Needle aspirates can be performed as an office procedure. A vitrectomy is performed in the operating room with a vitrector, which cuts and aspirates the vitreous humor while this is being replaced by saline. The result is c. 100 mL of dilute vitreous washings, which may be vacuum-filtered through a 0.45-µm filter; the filter paper can then be cultured. Gram stains are positive in 40–50% of cases. Gram stains may reveal pigment granules from the iris or retinal pigment epithelium, and these may resemble Gram-positive cocci but are more refractile. Vitreous cultures are more likely to be positive after vitrectomy than vitreous aspirate (90% vs. 75%); aqueous cultures are positive in 40% . Only the aqueous humor is positive in 4% .
Molecular diagnostic techniques have been used to improve the sensitivity of pathogen detection. A multicentre European study of over 16 600 cataract operations evaluated 29 endophthalmitis cases by both culture and PCR, and found that PCR increased the detection of pathogens from 14 to 20 . In a study from France of 100 post-cataract endophthalmitis cases, the sensitivities of PCR and culture were similar with initial intra-ocular samples, before antibiotics had been injected . However, PCR was much more sensitive than culture (70% vs. 9%) in subsequent vitrectomy samples, reflecting either the inhibitory effect of the previously injected antibiotics, or the fact that PCR does not distinguish living from dead organisms. In a study from Brazil of 11 patients with endophthalmitis, cultures were positive in 75% and PCR was positive in 91% . This study also tried to evaluate the specificity of PCR; none of the 12 vitreous controls were positive, but two of 50 aqueous samples were. A study from Japan also found improved sensitivity with PCR: of 19 patients with endophthalmitis, 18 were positive by PCR and only ten by culture . Control samples were positive by PCR in 6% of 50 patients with uveitis, although in none of 40 patients without intra-ocular inflammation.
Microbiology. The major pathogens are coagulase-negative staphylococci (70%), Staphylococcus aureus (10%), streptococci (9%), other Gram-positive cocci, including enterococci and mixed bacteria (5%), and Gram-negative bacilli (6%). The fact that Gram-positive bacteria cause >95% of cases reflects the usual pathogenesis, i.e. contamination of the aqueous humor with surface bacteria during surgery. In tropical regions such as India, fungi may cause 10–15% of postoperative endophthalmitis cases.
Treatment. The most important component of therapy is the direct injection of antibiotics into the eye. The injection is performed after a sample of vitreous humor is taken for Gram staining and culture. Initially, broad-spectrum antibiotics are used empirically: intravitreal vancomycin 1 mg/0.1 mL normal saline plus either ceftazidime 2.25 mg/0.1 mL or amikacin0.4 mg/0.1 mL. If there is no improvement in 48 h, a repeat intravitreal injection may be given with either vancomycin or ceftazidime, depending on culture results. Repeated injections of amikacin are avoided, owing to concerns about retinal toxicity.
The second component of treatment is vitrectomy. Vitrectomy surgically debrides the vitreous humor, similarly to draining an abscess, and is the fastest way of clearing infection in eyes with fulminant endophthalmitis. However, vitrectomy is performed in the operating room, whereas a needle aspirate (for culture) is performed in the office: intravitreal antibiotics are given at the end of a vitrectomy case or after vitreous aspirate. A multicentre prospective trial, the Endophthalmitis Vitrectomy Study (EVS), tried to answer the question of whether a vitrectomy was necessary in the treatment of postcataract endophthalmitis, prior to intravitreal injection of antibiotics . The EVS randomized 420 patients into ‘tap' (needle aspirate or biopsy of vitreous humor) and vitrectomy groups, with both groups receiving intravitreal antibiotics after the procedures . Vitrectomy decreased the rate of severe vision loss from 47% (tap group) to 20% (vitrectomy group) in patients who presented with the worst vision (light perception only). No apparent benefit was seen in patients who presented with hand motion or better vision, although the study design may have obscured a possible benefit: two-thirds of patients in the ‘tap' group actually received a vitreous ‘biopsy' in the operating room, with a vitrector. We favour vitrectomy for all patients who present with severe vision loss or rapidly worsening vision, or who are likely to have endophthalmitis caused by virulent bacteria such as streptococci.
Systemic antibiotics are not effective in treating endophthalmitis: intravitreal antibiotics must always be given. Whether systemic antibiotics provide any additional benefit to intravitreal antibiotics is unknown. The EVS also tried to answer this question, but the choice of systemic antibiotics used in the study, amikacin plus ceftazidime, was poor . These antibiotics have poor activity against staphylococci, the cause of 80% of post-cataract endophthalmitis cases, and amikacin does not cross the blood–eye barrier, and so reaches minimal levels in the vitreous humor.
Visual outcome. The visual outcome is highly correlated with the bacteriology. Streptococci of any type produce severe endophthalmitis with a poor chance of visual recovery, whereas coagulase-negative staphylococci cause milder endophthalmitis in general. Overall, 50% of eyes with post-cataract endophthalmitis recover 20/40 vision, and 10% are left with no useful vision (5/200 or less).
Chronic post-cataract endophthalmitis is usually caused by Propionibacterium acnes, and presents as a persistent low-grade inflammation in the anterior chamber. Patients present with decreased vision in the affected eye, and half also have eye pain, which is usually mild. On examination, there are white blood cells in the aqueous humor, sometimes a hypopyon, a characteristic white plaque on the posterior lens capsule, and usually inflammation in the anterior vitreous humor.
Intra-ocular cultures may be negative, although culture of the white capsular plaque is often positive. Treatment with a combination of removal or exchange of the IOL, total capsulectomy, vitrectomy and intravitreal antibiotics (e.g. vancomycin) has been the most successful approach. Treatment regimens that leave the original IOL in place have a 40–50% relapse rate.
In rare cases, this entity is caused by fungi, and treatment is different (see below).
Intravitreal injections of anti-vascular endothelial growth factor agents (e.g. bevacizumab, ranibizumab, and pegaptanib) are given to treat neovascular macular degeneration. Injections may be repeated monthly for several months, and each injection carries a small risk of causing endophthalmitis. The number of cases of post-injection endophthalmitis is increasing as the use of this treatment increases, and at a tertiary eye centre in Australia there were more cases of post-injection endophthalmitis than of post-cataract endophthalmitis between 2007 and 2010 . The rate of endophthalmitis per injection is low, with reported rates varying from 0.025% to 0.2% [25, 26, 27, 28]. A study using a Medicare database of 40 903 injections found an endophthalmitis rate of 0.09% per injection .
Symptoms are eye pain and decreased vision, and examination reveals vitreal inflammation. In one large study, all 23 patients with presumed endophthalmitis had pain and vitritisdeveloping 1–6 days after injection (average: 3.4 days), and 78% had hypopyon . Cultures were positive in only seven cases. A study in England of 47 post-injection endophthalmitis cases found that patients presented an average of 5 days after injection (range: 1–39 days), and positive cultures occurred in 60% .
Gram-positive bacteria cause >95% of culture-positive cases . Coagulase-negative staphylococci cause c. 60% of cases and viridans streptococci cause 25% [24, 30]. This is a much higher rate of streptococcal endophthalmitis than in postcataract cases. Viridans streptococci (Streptococcus mitis/Streptococcus oralis) also caused an outbreak of 12 cases of post-injection endophthalmitis in Florida, owing to contamination of bevacizumab syringes made up by a single compounding pharmacy . Eleven of the 12 patients were left with minimal vision, count fingers, or worse.
Diagnosis and treatment are the same as for post-cataract endophthalmitis (see above). Visual outcomes are poor in cases caused by streptococci.
A filtering bleb is a treatment for glaucoma. It is a surgically created scleral defect, covered only with conjunctiva, that allows excess aqueous humor to be absorbed into the systemic circulation. Because only conjunctiva separates the ocular surface flora from the aqueous humor at the bleb, endophthalmitis may occur at any time. The risk of endophthalmitis is c.1.3% per patient-year . One study reported an average onset at 2 years postoperatively (range: 1 month to 8 years) . Streptococci, including Streptococcus pneumoniae, cause 50% of cases. Haemophilus influenzae, Moraxella catarrhalis, S. aureus and coagulase-negative staphylococci are other pathogens .
Vitrectomy and intravitreal antibiotics (e.g. vancomycin plus ceftazidime) are indicated. The value of a systemic agent as adjunctive therapy has not been studied, but it seems reasonable to give an oral quinolone, such as moxifloxacin, that achieves good vitreous levels and treats the major pathogens. The visual outcome varies, depending partly on the pathogen: 40% achieve 20/40 vision or better, whereas 30% lose all vision in the affected eye .
Endophthalmitis occurs in 3–10% of cases after penetrating trauma to the eye, although early surgical repair and prophylactic systemic antibiotics may reduce this incidence to <1% . Risk factors for the development of endophthalmitis include metal rather than glass or blunt trauma injuries, retained intra-ocular foreign bodies, disruption of the lens, and delay in primary repair of >24 h.
Bacillus cereus is a major pathogen in post-traumatic endophthalmitis, and causes a fulminant infection with very poor visual outcome . Onset of symptoms (eye pain, red eye, and decreased vision) usually occurs within 12–24 h of the injury. Findings include marked intra-ocular inflammation and often a ring corneal infiltrate. Other causes of post-traumatic endophthalmitis are coagulase-negative staphylococci, streptococci, Gram-negative bacilli such as Klebsiella and Pseudomonas, and moulds [37, 38].
Treatment should be aggressive, with vitrectomy, intravitreal antibiotics (e.g. vancomycin plus ceftazidime), and systemic therapy.
Endogenous bacterial endophthalmitis arises from bacteraemic seeding of the eye. Endocarditis, usually caused by S. aureus or streptococci, accounts for 40% of endogenous endophthalmitis cases in the USA, and other cases are associated with urinary tract infections, indwelling central venous catheters, illicit injection drug use, and procedures such as endoscopy that can cause transient bacteraemia. In Taiwan, Singapore, and other East Asian nations, liver abscess caused by Klebsiella pneumoniae is the source of 60% of cases of endogenous endophthalmitis .
Many patients present with eye symptoms (pain and blurred vision) rather than symptoms of their underlying infection; this was true of half of the patients in one study . Blood cultures are positive in 75% of cases, as are vitreous cultures . Common pathogens in western countries include S. aureus (25%), streptococci (30–50%, primarily Streptococcus pneumoniae, Streptococcus milleri group, and group A and B streptococci), and Gram-negative bacilli such as Escherichia coli (30%). In Asia, K. pneumoniae causes the majority of cases.
Treatment of the underlying source of bacteraemia with systemic antibiotics is necessary, but this will not effectively treat the endophthalmitis: intravitreal antibiotics and, usually, a vitrectomy are necessary.
Endogenous Candida endophthalmitis. Most cases of Candida endophthalmitis are endogenous, occurring as a complication of candidaemia. The candidaemia usually occurs in hospitalized patients, often as a complication of an indwelling central venous catheter. Other risk factors include total parenteral nutrition, broad-spectrum antibiotics, neutropenia, recent abdominal surgery, and glucocorticoid therapy.
Candidaemia seeds the highly vascular choroid first, so the initial manifestation is usually chorioretinitis or choroiditis. There may be minimal or no vitreous inflammation at first. Infection in the choroid and retina is often painless, so, unless the lesions are near the macula, patients with early Candida chorioretinitis may have no symptoms. As the infection worsens, vitritis develops, and patients develop decreased vision. With inflammation spreading to the aqueous humor, eye pain may also be a presenting symptom.
Often, the literature distinguishes Candida chorioretinitis from Candida endophthalmitis, the latter term being reserved for those cases with significant vitritis. A term that includes both Candida chorioretinitis and endophthalmitis (i.e. vitritis) is ocular candidiasis.
The prevalence of ocular candidiasis in candidaemia must be evaluated by prospective studies. In such studies, the incidence varies from 2% to 26%, with most cases being attributable to chorioretinitis and only 0–6% having significant vitritis (i.e. ‘endophthalmitis') [41, 42, 43, 44]. In a multicentre trial involving 370 patients with candidaemia, possible or probable ocular involvement occurred in 16%, with most having chorioretinitis as the manifestation and only 1.6% being classified as having endophthalmitis (i.e. with significant vitritis) .
Outpatients may also present with endogenous Candida endophthalmitis, and some of these patients have a recent history of hospitalization and a recent indwelling central venous catheter. However, most outpatients who present with Candida endophthalmitis have a history of illicit intravenous drug use. In a study from Australia, 70% of 27 patients presenting with fungal endophthalmitis between 2001 and 2007 were injection drug users . Candidaemia is often transient in injection drug users and in patients with recent indwelling central venous catheters, so patients may present with decreased vision as their only symptom. They may be misdiagnosed initially as having a sterile uveitis, unless a history of intravenous drug use or recent hospitalization is obtained.
The diagnosis of ocular candidiasis is made on the basis of eye examination and confirmed with vitreous culture. Vitreous culture is usually not necessary in patients who have known candidaemia and eye findings compatible with chorioretinitis. Funduscopic examination shows white fluffy lesions in the choroid or retina, sometimes with vitritis (endophthalmitis). There may be so much vitritis that the retina may be obscured. A ‘string of pearls' or ‘snowballs' may be seen in the vitreous humor, representing clumps of infection within the inflamed vitreous humor. In outpatients who present with eye findings but do not have a history of known candidaemia, diagnosis must be suspected by clinical appearance (fluffy white infiltrates in the retina or vitreous humor, often with marked vitritis), and confirmed by vitreous culture.
All patients with ocular candidiasis must be followed closely by an ophthalmologist, as some patients worsen despite therapy. In a multicentre study of 370 patients with candidaemia who received either voriconazole or amphotericin followed by fluconazole, 18% of the 60 ocular candidiasis cases developed while antifungal therapy was being given . For most patients with chorioretinitis alone, the lesions will respond to the systemic antifungal therapy. Patients who have significant vitritis (endophthalmitis) require a vitrectomy and intravitreal amphotericin (or voriconazole), in addition to systemic antifungal therapy with an agent that crosses the blood–eye barrier, such as fluconazole (if susceptible), voriconazole, or amphotericin.
Exogenous Candida endophthalmitis. Exogenous cases are rare, and most cases occur following surgery. Inflammation may initially be greatest in the anterior chamber, before involving the vitreous humor.
Candida parapsilosis is the most common species, especially in postsurgical outbreaks. The reason is most likely that this species appears to survive well in irrigation fluids and on prosthetic materials . An outbreak in the USA in 1983 affecting 13 patients in different states was traced to a balanced salt solution used during ophthalmic surgery that was contaminated during manufacture .
Treatment includes intra-ocular injection of either amphotericin or voriconazole, vitrectomy, and systemic voriconazole or fluconazole (if the organism is susceptible). The dose of intravitreal amphotericin is 5–10 µg in 0.1 mL of sterile water, and the dose of intravitreal voriconazole is usually 100 µg in 0.1 mL of sterile water. If infection follows cataract surgery, it is often necessary to remove the IOL as well. Systemic therapy with high-dose fluconazole (400–800 mg daily, assuming normal kidney function) is also indicated for susceptible strains, or voriconazole for fluconazole-resistant but voriconazole-susceptible strains.
Two-thirds of patients with mould endophthalmitis lose useful vision, but the prognosis may be improving with the use of newer antifungal agents.
Exogenous mould endophthalmitis. Mould endophthalmitis is usually exogenous, occurring after eye surgery, after eye trauma, or as a result of keratomycosis (fungal corneal infection). Aspergillus and Fusarium are the most common aetiological agents.
Postoperative mould endophthalmitis is rare in western countries. When it does occur, it often presents subacutely, and diagnosis may be delayed. In one review that included ten cases of postoperative mould endophthalmitis, 60% presented ≥2 months after surgery . In tropical regions such as India, moulds have caused >20% of postoperative endophthalmitis cases in some series [8, 50], and 80% of cases present within 4 weeks of surgery. Outbreaks of postoperative mould endophthalmitis have also occurred.
Post-traumatic mould endophthalmitis is also more common in India than in the USA or Europe. Moulds caused 14% of 113 culture-positive post-traumatic endophthalmitis cases in a series from India . In another series from India, the average time to presentation after eye trauma was 7 days . Aspergillus was the most common mould isolated in both of these series.
Mould infection of the cornea (keratomycosis) may lead to endophthalmitis as the mould grows through the cornea and into the aqueous humor. Keratomycosis was the aetiology for half of all exogenous mould cases in a series from Florida, and eye surgery and trauma each accounted for 25% of cases . Many cases of keratomycosis are associated with contact lens wear. Fusarium is the most common cause of endophthalmitis resulting from keratomycosis in many series. Some of these cases reflect the international outbreak of Fusarium keratitis that occurred in 2004–2006, related to one brand of contact lens cleaning solution. In this outbreak, 6% of keratitis cases developed endophthalmitis [53, 54].
The clinical presentation of exogenous mould endophthalmitis may be subacute, as noted above. Slit lamp examination of the eye often shows hypopyon and clumps of thick white material in the anterior chamber, particularly after trauma or surgery. There may be vitritis. When endophthalmitis complicates keratitis, slit lamp examination will show the corneal infection, and often shows filaments extending from the back of the cornea into the aqueous humor.
Diagnosis is made by culture of the aqueous humor as well as the vitreous humor. Treatment requires surgery to clean out thick material, if present, in the aqueous humor, vitrectomy for significant vitritis, intracameral and intravitreal injections of antifungal agents (amphotericin or voriconazole), and systemic voriconazole therapy. Systemic voriconazole achieves very good intra-ocular levels, of c. 40% of serum levels. Unless the fungus is known, the initial intra-ocular injection should be amphotericin; subsequent injections may be voriconazole for sensitive fungi. Repeated intra-ocular injections of voriconazole (if the organism is susceptible) or amphotericin can be given, at least 48 h apart. Voriconazole is preferred for susceptible strains, as it appears to be less irritating than amphotericin. If there is an IOL, this must be surgically removed. In cases related to keratomycosis, a corneal transplant is almost always necessary.
Several case reports have described salvage with posaconazole for cases of Fusariumkeratomycosis-related endophthalmitis in which other therapies have failed [55, 56]. Itraconazole is not recommended, as it does not achieve good levels in the vitreous humor; and fluconazole should not be given, as it has poor activity against moulds. Systemic amphotericin has significant toxicity, and is rarely used to treat exogenous fungal endophthalmitis, but may be considered as adjunctive therapy in those rare cases of azole-resistant fungal endophthalmitis in which other therapies have failed.
Endogenous mould endophthalmitis. Endogenous mould endophthalmitis is rare. It usually occurs in severely immunocompromised patients with fungaemia, or in injection drug users. Aspergillus and Fusarium are common aetiological agents. Hospitalized patients with mould fungaemia are usually very ill, and may not be able to complain of eye symptoms. In a retrospective study at a Texas cancer centre, only 27% of the 15 patients with mould endophthalmitis survived for >4 weeks . Often, the diagnosis of mould endophthalmitis is missed during life. In an autopsy study of 85 orthotopic liver transplant recipients, Aspergillusendophthalmitis was noted in 7%, but only one of six patients was diagnosed ante-mortem . In contrast, injection drug users who have endogenous mould endophthalmitis are usually well except for their eye, with no evidence of systemic infection. In these patients, fungaemia is usually transient, occurring only at the time of intravenous drug injection.
In immunocompromised patients, treatment must include systemic antifungal therapy, with the choice (e.g. amphotericin or voriconazole) tailored to optimize treatment for the fungaemia. Vitrectomy and removal of any IOL, followed by intravitreal amphotericin or voriconazole (for susceptible strains), should be performed if the patient is able to tolerate surgery. If too ill for surgery, the patient should have intravitreal injection of amphotericin or voriconazole, with repeated injections as needed. In injection drug users with no evidence of ongoing fungaemia, vitrectomy, intravitreal antifungal injection and systemic therapy should be given.
Endophthalmitis is a medical emergency. The most important component of therapy is intravitreal injection of antibiotics. Vitrectomy is also important in many cases, and leads to improved visual outcomes in patients who present with significant visual loss. Vitrectomy should also be performed in cases that have failed to respond to initial intravitreal injection. Systemic antibiotics are necessary to treat the underlying infection in endogenous endophthalmitis, and as adjunctive therapy in exogenous fungal endophthalmitis. Visual prognosis is partly related to the virulence of the pathogen. The best outcomes usually occur in cases that are either culture-negative or are caused by coagulase-negative staphylococci, and the worst outcomes typically occur in endophthalmitis caused by streptococci, Bacillusspecies, and moulds. Even in cases of severe endophthalmitis caused by virulent pathogens, however, prompt therapy may save useful vision. Even light perception vision is considered to be useful to a blind patient.
This work was undertaken without funding support or study sponsors. The author received no compensation for the work, and has no relevant conflicts of interest to declare.
1L Keay, EW Gower, SD Cassard, JM Tielsch, OD ScheinPostcataract surgery endophthalmitis in the United States: analysis of the complete 2003 to 2004 Medicare database of cataract surgeriesOphthalmology, 119 (2012), pp. 914-922ArticleDownload PDFView Record in ScopusGoogle Scholar2P Lalitha, J Rajagopalan, K Prakash, K Ramasamy, NV Prajna, M SrinivasanPostcataract endophthalmitis in South India: incidence and outcomeOphthalmology, 112 (2005), pp. 1884-1889ArticleDownload PDFView Record in ScopusGoogle Scholar3M Jambulingam, SK Parameswaran, S Lysa, M Selvaraj, HN MadhavanA study on the incidence, microbiological analysis and investigations on the source of infection of postoperative infectious endophthalmitis in a tertiary care ophthalmic hospital: an 8‐year studyIndian J Ophthalmol, 58 (2010), pp. 297-302View Record in ScopusGoogle Scholar4TY Wong, SP CheeThe epidemiology of acute endophthalmitis after cataract surgery in an Asian populationOphthalmology, 111 (2004), pp. 699-705ArticleDownload PDFView Record in ScopusGoogle Scholar5SP Mollan, A Gao, A Lockwood, OM Durrani, L ButlerPostcataract endophthalmitis: incidence and microbial isolates in a United Kingdom region from 1996 through 2004J Cataract Refract Surg, 33 (2007), pp. 265-268ArticleDownload PDFView Record in ScopusGoogle Scholar6M Lundstrom, G Wejde, U Stenevi, et al.Endophthalmitis after cataract surgery: a nationwide prospective study evaluating incidence in relation to incision type and locationOphthalmology, 114 (2007), pp. 866-870ArticleDownload PDFView Record in ScopusGoogle Scholar7P Barry, DV Seal, G Gettinby, et al.ESCRS study of prophylaxis of postoperative endophthalmitis after cataract surgery: preliminary report of principal results from a European multicenter studyJ Cataract Refract Surg, 32 (2006), pp. 407-410ArticleDownload PDFView Record in ScopusGoogle Scholar8A Gupta, V Gupta, A Gupta, et al.Spectrum and clinical profile of post cataract surgery endophthalmitis in north IndiaIndian J Ophthalmol, 51 (2003), pp. 139-145View Record in ScopusGoogle Scholar9JB Dickey, KD Thompson, WM JayAnterior chamber aspirate cultures after uncomplicated cataract surgeryAm J Ophthalmol, 112 (1991), pp. 278-282ArticleDownload PDFView Record in ScopusGoogle Scholar10DR Sherwood, WJ Rich, JS Jacob, et al.Bacterial contamination of intraocular and extraocular fluids during extracapsular cataract extractionEye (Lond), 3 (Pt 3) (1989), pp. 308-312CrossRefView Record in ScopusGoogle Scholar11T Tervo, P Ljungberg, T Kautiainen, et al.Prospective evaluation of external ocular microbial growth and aqueous humor contamination during cataract surgeryJ Cataract Refract Surg, 25 (1999), pp. 65-71ArticleDownload PDFView Record in ScopusGoogle Scholar12JA Menikoff, MG Speaker, M Marmor, EM RaskinA case‐control study of risk factors for postoperative endophthalmitisOphthalmology, 98 (1991), pp. 1761-1768ArticleDownload PDFView Record in ScopusGoogle Scholar13Endophthalmitis Study Group, European Society of Cataract & Refractive SurgeonsProphylaxis of postoperative endophthalmitis following cataract surgery: results of the ESCRS multicenter study and identification of risk factorsJ Cataract Refract Surg, 33 (2007), pp. 978-988Google Scholar14Endophthalmitis Vitrectomy Study GroupResults of the Endophthalmitis Vitrectomy Study: a randomized trial of immediate vitrectomy and of intravenous antibiotics for the treatment of postoperative bacterial endophthalmitisArch Ophthalmol, 113 (1995), pp. 1479-1496Google Scholar15GA Lalwani, HW Flynn Jr, IU Scott, et al.Acute‐onset endophthalmitis after clear corneal cataract surgery (1996–2005). Clinical features, causative organisms, and visual acuity outcomesOphthalmology, 115 (2008), pp. 473-476ArticleDownload PDFView Record in ScopusGoogle Scholar16M Taban, A Behrens, RL Newcomb, et al.Acute endophthalmitis following cataract surgery: a systematic review of the literatureArch Ophthalmol, 123 (2005), pp. 613-620CrossRefView Record in ScopusGoogle Scholar17CM Cutler Peck, J Brubaker, S Clouser, C Danford, HE Edelhauser, N MamalisToxic anterior segment syndrome: common causesJ Cataract Refract Surg, 36 (2010), pp. 1073-1080ArticleDownload PDFView Record in ScopusGoogle Scholar18PK Kutty, TS Forster, C Wood‐Koob, et al.Multistate outbreak of toxic anterior segment syndrome, 2005J Cataract Refract Surg, 34 (2008), pp. 585-590ArticleDownload PDFView Record in ScopusGoogle Scholar19M Barza, PR Pavan, BH Doft, et al.Evaluation of microbiological diagnostic techniques in postoperative endophthalmitis in the Endophthalmitis Vitrectomy StudyArch Ophthalmol, 115 (1997), pp. 1142-1150CrossRefView Record in ScopusGoogle Scholar20D Seal, U Reischl, A Behr, et al.Laboratory diagnosis of endophthalmitis: comparison of microbiology and molecular methods in the European Society of Cataract & Refractive Surgeons multicenter study and susceptibility testingJ Cataract Refract Surg, 34 (2008), pp. 1439-1450ArticleDownload PDFView Record in ScopusGoogle Scholar21C Chiquet, PL Cornut, Y Benito, et al.Eubacterial PCR for bacterial detection and identification in 100 acute postcataract surgery endophthalmitisInvest Ophthalmol Vis Sci, 49 (2008), pp. 1971-1978CrossRefView Record in ScopusGoogle Scholar22GB Melo, PJ Bispo, AC Campos Pignatari, AL Höfling‐LimaReal‐time polymerase chain reaction test to discriminate between contamination and intraocular infection after cataract surgeryJ Cataract Refract Surg, 37 (2011), pp. 1244-1250ArticleDownload PDFView Record in ScopusGoogle Scholar23S Sugita, N Shimizu, K Watanabe, et al.Diagnosis of bacterial endophthalmitis by broad‐range quantitative PCRBr J Ophthalmol, 95 (2011), pp. 345-349CrossRefView Record in ScopusGoogle Scholar24MP Simunovic, RB Rush, AP Hunyor, AA ChangEndophthalmitis following intravitreal injection versus endophthalmitis following cataract surgery: clinical features, causative organisms and post‐treatment outcomesBr J Ophthalmol, 96 (2012), pp. 862-866CrossRefView Record in ScopusGoogle Scholar25DA Lyall, A Tey, B Foot, et al.Post‐intravitreal anti‐VEGF endophthalmitis in the United Kingdom: incidence, features, risk factors, and outcomesEye (Lond), 26 (2012), pp. 1517-1526CrossRefView Record in ScopusGoogle Scholar26SS Bhatt, KE Stepien, K JoshiProphylactic antibiotic use after intravitreal injection: effect on endophthalmitis rateRetina, 31 (2011), pp. 2032-2036CrossRefView Record in ScopusGoogle Scholar27M Inoue, S Kobayakawa, C Sotozono, et al.Evaluation of the incidence of endophthalmitis after intravitreal injection of anti‐vascular endothelial growth factorOphthalmologica, 226 (2011), pp. 145-150CrossRefView Record in ScopusGoogle Scholar28CP Shah, SJ Garg, JF Vander, et al.Outcomes and risk factors associated with endophthalmitis after intravitreal injection of anti‐vascular endothelial growth factor agentsOphthalmology, 118 (2011), pp. 2028-2034ArticleDownload PDFView Record in ScopusGoogle Scholar29S Day, K Acquah, P Mruthyunjaya, DS Grossman, PP Lee, FA SloanOcular complications after anti‐vascular endothelial growth factor therapy in Medicare patients with age‐related macular degenerationRetina, 31 (2011), pp. 2032-2036View Record in ScopusGoogle Scholar30NED Hoevenaars, D Gans, T Missotten, et al.Suspected bacterial endophthalmitis following intravitreal anti‐VEGF injection: case series and literature reviewOphthalmologica, 228 (2012), pp. 143-147CrossRefView Record in ScopusGoogle Scholar31RA Goldberg, HW Flynn Jr, RF Isom, D Miller, S GonzalezAn outbreak of Streptococcus endophthalmitis after intravitreal injection of bevacizumabAm J Ophthalmol, 153 (2012), pp. 204-208View Record in ScopusGoogle Scholar32PW Debry, TW Perkins, G Heatley, et al.Incidence of late‐onset bleb‐related complications following trabeculectomy with mitomycinArch Ophthalmol, 120 (2002), pp. 297-300CrossRefView Record in ScopusGoogle Scholar33S Waheed, DC Ritterband, DS Greenfield, et al.New patterns of infecting organisms in late bleb‐related endophthalmitis: a ten year reviewEye (Lond), 12 (Pt 6) (1998), pp. 910-915CrossRefView Record in ScopusGoogle Scholar34TA Kangas, DS Greenfield, HW Flynn Jr, et al.Delayed‐onset endophthalmitis associated with conjunctival filtering blebsOphthalmology, 104 (1997), pp. 746-752ArticleDownload PDFView Record in ScopusGoogle Scholar35CM Andreoli, MT Andreoli, CE Kloek, et al.Low rate of endophthalmitis in a large series of open globe injuriesAm J Ophthalmol, 147 (2009), pp. 601-608View Record in ScopusGoogle Scholar36JJ Miller, IU Scott, HW Flynn Jr, et al.Endophthalmitis caused by Bacillus speciesAm J Ophthalmol, 145 (2008), pp. 883-888ArticleDownload PDFView Record in ScopusGoogle Scholar37AM Abu el‐Asrar, SA al‐Amro, AA al‐Mosallam, S al‐ObeidanPost‐traumatic endophthalmitis: causative organisms and visual outcomeEur J Ophthalmol, 9 (1999), pp. 21-31View Record in ScopusGoogle Scholar38DV Alfaro, DB Roth, RM Laughlin, et al.Paediatric post‐traumatic endophthalmitisBr J Ophthalmol, 79 (1995), pp. 888-891CrossRefView Record in ScopusGoogle Scholar39JS Wong, TK Chan, HM Lee, et al.Endogenous bacterial endophthalmitis: an east Asian experience and a reappraisal of a severe ocular afflictionOphthalmology, 107 (2000), pp. 1483-1491ArticleDownload PDFView Record in ScopusGoogle Scholar40AA Okada, RP Johnson, WC Liles, et al.Endogenous bacterial endophthalmitis. Report of a ten‐year retrospective studyOphthalmology, 101 (1994), pp. 832-838ArticleDownload PDFView Record in ScopusGoogle Scholar41AM Oude Lashof, A Rothova, JD Sobel, et al.Ocular manifestations of candidemiaClin Infect Dis, 53 (2011), pp. 262-268CrossRefView Record in ScopusGoogle Scholar42SP Donahue, CM Greven, JJ Zuravieff, et al.Intraocular candidiasis in patients with candidemia. Clinical implications derived from a prospective multicenter studyOphthalmology, 101 (1994), pp. 1302-1309ArticleDownload PDFView Record in ScopusGoogle Scholar43S Kannangara, D Shindler, DY Kunimoto, et al.Candidemia complicated by endophthalmitis: a prospective analysisEur J Clin Microbiol Infect Dis, 26 (2007), pp. 839-841CrossRefView Record in ScopusGoogle Scholar44LJ Rodriguez‐Adrian, RT King, LG Tamayo‐Deret, et al.Retinal lesions as clues to dissemiated bacterial and candidal infections: frequency, natural history, and etiologyMedicine (Baltimore), 82 (2003), pp. 187-202CrossRefView Record in ScopusGoogle Scholar45PP Connell, EC O'Neill, FM Amirul Islam, et al.Endogenous endophthalmitis associated with intravenous drug abuse: seven‐year experience at a tertiary referral centerRetina, 30 (2010), pp. 1721-1725CrossRefView Record in ScopusGoogle Scholar46A Lingappan, CC Wykoff, TA Albini, et al.Endogenous fungal endophthalmitis: causative organisms, management strategies, and visual acuity outcomesAm J Ophthalmol, 153 (2012), pp. 162-166View Record in ScopusGoogle Scholar47JJ Weems JrCandida parapsilosis: epidemiology, pathogenicity, clinical manifestations, and antibiotic susceptibilityClin Infect Dis, 14 (1992), pp. 756-766CrossRefGoogle Scholar48E McCray, N Rampell, SLO Solomon, et al.Outbreak of Candida parapsilosis endophthalmitis after cataract extraction and intraocular lens implantationJ Clin Microbiol, 24 (1986), pp. 625-628View Record in ScopusGoogle Scholar49CC Wycoff, HW Flynn Jr, D Miller, et al.Exogenous fungal endophthalmitis: microbiology and clinical outcomesOphthalmology, 115 (2008), pp. 1501-1507Google Scholar50AR Anand, KL Therese, HN MadhavanSpectrum of aetiological agents of postoperative endophthalmitis and antibiotic susceptibility of bacterial isolatesIndian J Ophthalmol, 48 (2000), pp. 123-128View Record in ScopusGoogle Scholar51DY Kunimoto, T Das, S Sharma, et al.Microbiology and susceptibility of isolates. Part II. Posttraumatic endophthalmitis. Endophthalmitis Research GroupAm J Ophthalmol, 128 (1999), pp. 242-244ArticleDownload PDFView Record in ScopusGoogle Scholar52A Chakrabarti, MR Shivaprakash, R Singh, et al.Fungal endophthalmitis: fourteen years’ experience from a center in IndiaRetina, 28 (2008), pp. 1400-1407CrossRefView Record in ScopusGoogle Scholar53AB EpsteinIn the aftermath of the Fusarium keratitis outbreak: what have we learned?Clin Ophthalmol, 1 (2007), pp. 355-366View Record in ScopusGoogle Scholar54KD Rosenberg, HW Flynn Jr, EC Alfonso, D MillerFusarium endophthalmitis following keratitis associated with contact lensesOphthalmic Surg Lasers Imaging, 37 (2006), p. 310View Record in ScopusGoogle Scholar55WE Sponsel, JR Graybill, HL Nevarez, D DangOcular and systemic posaconazole (SCH‐56592) treatment of invasive Fusarium solani keratitis and endophthalmitisBr J Ophthalmol, 86 (2002), pp. 829-830CrossRefView Record in ScopusGoogle Scholar56EY
Copyright © THE RETINA INSTITUTE, New Orleans, LA - All Rights Reserved.