INCIDENCE OF PRESUMED ENDOPHTHALMITIS AFTER INTRAVITREAL INJECTION PERFORMED IN THE OPERATING ROOM

A Retrospective Multicenter Study

Abstract

Purpose: 

To evaluate the incidence of presumed endophthalmitis (EO) after intravitreal injection (IVI) of anti–vascular endothelial growth factor agents performed in the operating room.

Methods: 

Retrospective study at 2 Swiss eye hospitals between 2004 and 2012. Hospital records were used to identify patients treated with an IVI of an anti–vascular endothelial growth factor agent between 2004 and 2012 and those treated for EO, defined as any intraocular inflammation treated with intravitreal antibiotics. All IVIs were performed using standard sterile technique in a Swiss Class 1 operating room. No patient received preinjection topical antibiotics. Postinjection topical antibiotics were used only in one hospital.

Results: 

A total of 40,011 IVIs were performed at the 2 centers during the study period. Of the IVIs, ranibizumab was injected in 36,398 (91%), bevacizumab in 3,518 (9%), aflibercept in 89 (0.2%), and pegaptanib in 6 (<0.1%). Three cases of post-IVI presumed EO occurred, yielding a combined incidence of 0.0075% per injection (95% confidence interval: 0.0026–0.0220%) or 1 case per 13,337 IVIs. Two of the three cases of EO occurred in patients using post-IVI antibiotics. All three cases followed ranibizumab injection and were culture negative by anterior chamber tap or vitreous biopsy.

Conclusion: 

The risk of EO after IVI performed under the sterile conditions of the operating room was very low.

In Brief

Performing intravitreal injections of anti–vascular endothelial growth factor agents in the operating room under laminar airflow is associated with a very low risk of endophthalmitis (0.0075% per injection, or 1 per 13,337 injections).