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Retinal toxicity attributable to intravitreal use of aminoglycosides for endophthalmitis has been reported. Campochiaro and Conway reported 101 cases of retinal damage due to intravitreal aminoglycosides.1 Amikacin, an aminoglycoside, is in widespread use in the United Kingdom for the treatment of Gram negative organisms in endophthalmitis. We report a case of macular toxicity following the use of intravitreal amikacin for postoperative endophthalmitis, outline mechanisms of retinal toxicity, and offer alternatives to amikacin. We believe that enough evidence now exists to support a change in the current Royal College of Ophthalmologists' endophthalmitis treatment guidelines that are based on the Endophthalmitis Vitrectomy Study.2
A 69 year old white woman presented 1 day after uneventful right phacoemulsification and intraocular lens implantation with a vision of counting fingers (CF), a relative afferent pupil defect, hypopyon with anterior chamber fibrin, and normal intraocular pressure. We were unable to visualise the fundus although a red reflex was noted. Ultrasound examination showed patchy increased vitreous reflectivity with a flat retina and choroid. Pars plana vitreous tap of 0.2 ml was performed followed by injection of 1 mg/0.1 ml of vancomycin and 0.4 mg/0.1 ml of amikacin. Sterile dilution was conducted with typewritten instructions. The globe never became tense. The ocular inflammation resolved on a daily regimen of oral prednisolone 60 mg, oral ciprofloxacin 750 mg four times daily, topical ofloxacin 0.3% 2 hourly, topical dexamethasone 0.1% 2 hourly, and topical atropine 1% once daily. Vision however remained CF because of angiographically proved macular ischaemia and vascular occlusion (Figs 1 and 2). There was no microbiological growth from the vitreous sample.
The rationale for amikacin use relates to the relatively high incidence of Gram negative isolates in endophthalmitis (6.4–26.2%)3–5 and the broad spectrum of action with low resistance offered by this agent. Amikacin has largely superseded gentamicin because of its perceived safety profile. Our case and others reported in the literature6–8 serve to notify clinicians of the serious retinal toxicity occurring with amikacin use, which is possibly a class related phenomenon.
Hypotheses for toxicity include dilution errors, raised post-injection intraocular pressure, concomitant use of high concentrations of subconjunctival amikacin, and variations in vitreous concentration. Local variation in concentration may play a part if the agent is directly injected into the posterior vitreous space instead of the gel itself. Another possibility for macular predilection is that this is the dependent part in the supine patient during pars plana injection.
Large studies offer alternatives to aminoglycosides on the basis of culture sensitivities.3–5, 9 Suggestions include ceftazidime, cefotaxime, and ciprofloxacin. Sensitivities of Gram negative organisms to ceftazidime range from 61% to 100% according to published studies.3–5, 9 It appears that in most studies 2 mg (0.1 ml of 20 mg/ml solution) of ceftazidime has in vitro effectiveness equipotent to or greater than 0.4 mg amikacin.3–5, 9 Primate studies have shown that intravitreal ceftazidime is non-toxic at doses of 2.25 mg.10 Ceftazidime is already in clinical use in the United Kingdom.6 There have been no reported cases of retinal toxicity with intravitreal ceftazidime use in humans.11
With mounting evidence against amikacin we support a change in current UK treatment guidelines. Choices will remain controversial until the incidence of toxicity for both amikacin and ceftazidime is determined by a prospective randomised controlled study; however, on the evidence currently available we suggest that ceftazidime should replace amikacin as the first line agent of choice against Gram negative organisms in postoperative endophthalmitis.