Fig. 10.1
Constellation signs of endogenous endophthalmitis. (Top left) Minimal anterior segment inflammation in a patient with dense vitreous exudates due to endogenous endophthalmitis; (Top right) dense vitritis with hazy view of the disc; (Bottom left) Candida endophthalmitis of the left eye, showing subretinal exudates with a preretinal projection into the vitreous cavity. (Bottom right) Another case of Candida endophthalmitis with a preretinal exudate but minimal subretinal involvement
Neonatal endophthalmitis is a special form of endogenous endophthalmitis seen in newborns with sepsis, very low birth weight and retinopathy of prematurity. It has two distinct clinical presentations [9]. Focal retinal infections generally have good visual prognosis, while fulminant nosocomial infections have poor outcomes. Clinical suspicion is crucial for early diagnosis, and vitreous aspiration and intravitreal antibiotic administration can be considered under topical anaesthesia, when general anaesthesia is contraindicated.
Diagnosis
Endogenous endophthalmitis is essentially a clinical diagnosis, based on the presence of characteristic ocular signs and often systemic risk factors. The diagnosis may be aided by B-scan ultrasonography that, besides showing vitreous exudates, may also reveal choroidal abscesses that appear as dome-shaped choroidal lesions, underneath the vitreous exudates (Fig. 10.2, left). Rarely, optical coherence tomography may help delineate intra-retinal, subretinal or subretinal pigment epithelium location of infective foci.
Fig. 10.2
A 41-year-old man presented with decreased vision in right eye, 1 day following percutaneous transluminal coronary angioplasty. The affected eye right eye had anterior chamber hypopyon with dense vitreous exudates. Ultrasound B-scan revealed dome-shaped elevation arising from the choroid (notched arrow, a) (left). Three consecutive vitreous biopsies did not grow any organism. However, a subretinal biopsy, 1 month after initial presentation, revealed presence of fungal filaments (arrow, b). (Right) The patient was treated with intravitreal and oral voriconazole, but vision could not be salvaged (Courtesy: Rajeev K. Reddy, MD)
The key test for confirmation of diagnosis is diagnostic vitrectomy. Since the infection originates at the back of the eye, sampling the vitreous near the infective focus greatly increases the diagnostic yield of the procedure. Rarely, subretinal biopsy of the subretinal exudates can help in identifying the causative organism (Fig. 10.2, right). Vitreous samples are subjected to standard microbiological examination (microscopy and culture) protocols for bacteria and fungi. Recently, quantitative real-time polymerase chain reaction (rt-PCR) has shown excellent sensitivity in diagnosis of bacterial and fungal infections, as compared to culture. Sugita et al. described a procedure that can be performed as quickly as 90 min [10]. Despite these advantages, current molecular techniques lack the ability to test for the entire range of antibiotic susceptibility and are prone to false-positive results, especially if care is not taken to prevent contamination of test samples.
Additional tests are required to rule out presence of systemic infection that may have been missed during clinical evaluation. The most effective method is blood culture using blood drawn on three consecutive days under sterile precautions. It is also useful to sample other extraocular sites of infection such as urine or pus from skin or other abscesses. A thorough internist evaluation can help in identifying occult infections (Table 10.1).
Table 10.1
Etiological agents of bacterial and fungal endogenous endophthalmitis
Gram-positive bacteria | Gram-negative bacteria | Filamentous fungi | Yeast and yeast-like fungi | Other organisms |
---|---|---|---|---|
Streptococcus pneumonia | Listeria monocytogenes | Aspergillus fumigatus | Candida albicans | Toxoplasma gondii |
α-Hemolytic streptococci | Neisseria meningitidis | Aspergillus glaucus | Candida tropicalis | Toxocara canis |
β-Hemolytic streptococci (group A, B, G) | Escherichia coli | Aspergillus terreus | Candida stellatoidea | Pneumocystis carinii |
Staphylococcus aureus | Klebsiella pneumoniae | Fusarium spp. | Candida parapsilosis | |
Corynebacterium spp. | Haemophilus influenzae | Sporotrichum spp.
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