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Volume 108, Issue 4, Pages 759-764 (April 2001)


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Retinal toxicity of gentamicin after subconjunctival injection performed adjacent to thinned sclera

Anat Loewenstein, MD1, Esther Zemel, DSc2, Yafa Vered, PhD3, Moshe Lazar, MD1, Ido Perlman, PhD2Corresponding Author Information

Received 4 August 1999; accepted 28 November 2000.

Abstract 

Objective

To investigate the potential toxicity to the retina of gentamicin injected near surgically thinned scleral areas in a rabbit model.

Design

Experimental study.

Methods

Scleral scraping to half thickness was performed in the superotemporal scleral area in both eyes of adult rabbits (n = 10). Gentamicin sulfate was injected subconjunctivally to the right eye and saline to the left eye, which always served as a control eye. Four weeks after the procedure, electroretinography (ERG) was performed to assess retinal function. Then, the eyes were enucleated and prepared for histologic evaluation of structural damage. In four eyes of two additional rabbits, vitreous gentamicin concentrations were measured using a fluorescence polarization assay.

Main outcome measures

Dark- and light-adapted ERG responses and histopathologic damage.

Results

Dark- and light-adapted ERG responses in all rabbits were similar in the experimental and control eyes. Gentamicin levels were more than 10 μg/ml after subconjunctival injection of gentamicin with scraping and 0.29 μg/ml after subconjunctival injection of gentamicin with no scraping. Histopathologic examination revealed significant local damage to the photoreceptors adjacent to the area of scraping and subconjunctival injection. A significantly lesser degree of damage was seen if gentamicin was injected in pigmented rabbits or in albino rabbits, but only 4 weeks after scleral scraping.

Conclusions

Increased penetration of gentamicin through thinned sclera may lead to toxic levels of the drug in a localized area adjacent to the site of injection. These toxic effects are also influenced by the degree of pigmentation and acute inflammation.

Manuscript no. 99535.

1 Department of Ophthalmology, Tel-Aviv Medical Center, Tel-Aviv, Israel

2 Bruce Rappaport Faculty of Medicine, Technion—Israel Institute of Technology and the Rappaport Institute, Haifa, Israel

3 Clinical Biochemistry Laboratory Tel-Aviv Medical Center, Tel-Aviv, Israel

Corresponding Author InformationCorrespondence and reprint requests to Ido Perlman, PhD, Bruce Rappaport Faculty of Medicine, Technion, P.O. Box 9649, Haifa 31096, Israel

 Supported in part by the Wasserman trust given to the Ophthalmology Dept. at the Tel-Aviv Medical Center.

PII: S0161-6420(00)00641-2


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