Safety of intravitreal ketorolac and diclofenac: an electroretinographic and histopathologic study.
Kim Stephen J, Adams Neal A, Toma Hassanain S, Belair Marie-Lyne, Thorne Jennifer E, Green W Richard, Jabs Douglas A
AI Summary
This rabbit study found high-dose intravitreal ketorolac and diclofenac were toxic, but lower doses (3000 µg ketorolac, 300 µg diclofenac) were safe, suggesting potential steroid-sparing alternatives for ocular inflammation.
Abstract
Objective
To determine the clinical, histologic, and electroretinographic effects in the rabbit retina of escalating doses of two intravitreally delivered nonsteroidal anti-inflammatory drugs (NSAIDs): ketorolac and diclofenac.
Methods
Right eyes received a single 0.1 mL injection of either ketorolac (500-6000 microg/0.1 mL) or diclofenac (300-1500 microg/0.1 mL) prepared in balanced salt solution (BSS). Left eyes served as controls and received BSS. Dark- and light-adapted electroretinograms (ERG) were obtained at baseline and 4 and 8 weeks postinjection. Enucleated eyes were examined histologically.
Results
Ophthalmic examinations demonstrated no signs of intraocular inflammation or retinal toxicity. Intraocular pressure measurements remained similar between NSAID injected and control eyes. Histologic and ERG studies of eyes injected with 6000 microg ketorolac and >or=500 microg diclofenac demonstrated toxicity. In contrast, doses up to 3000 microg ketorolac demonstrated enhanced b-wave amplitude responses. Delayed drug toxicity was observed for the highest doses of both NSAIDs.
Conclusions
Intravitreal 3000 microg ketorolac and 300 microg diclofenac were nontoxic in this animal study, and may offer an effective and safer alternative to intravitreal corticosteroids.
MeSH Terms
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