Pars plana vitrectomy useful for post-injection endophthalmitis

Article

If improvement is not seen after 24 hours vitrectomy should be considered

Endophthalmitis is a serious threat to a patient's sight and can occur after any intraocular procedure. One such procedure that carries the risk of endophthalmitis is the administration of intravitreal injections. It has been reported that the risk of endophthalmitis post-injection can be as a result of the injection procedure itself or potentially as a result of drug contamination that may have occurred during preparation.

In all cases, early diagnosis and treatment of endophthalmitis is critical to avoid serious damage to the patient's visual acuity. However, the management of endophthalmitis that occurs after intravitreal injection has not been widely discussed and there are no guidelines set in place about the role of vitrectomy and silicone oil tamponade as treatment for this infection.

In a retrospective clinical study, Dr Pinarci and colleagues examined the records of just under 3000 patients who had been administered intravitreal injections between 2004 and 2011 at Baskent University Hospital. Out of this large group the team reviewed 8 patients (5 women and 3 men) who presented with acute endophthalmitis.

The initial treatment for all patients was a vitreous tap and intravitreal injections of both vancomycin and ceftazidime. In addition to this, topical antibiotics (vancomycin and ceftazidime) and an oral dose of moxifloxacin were also administered regularly. If this treatment did not improve the patient's symptoms or if they got any worse then they underwent pars plana vitrectomy with silicone oil tamponade.

Recent Videos
Thomas Aaberg, MD, gives an update on Neurotech Pharmaceuticals NT-501 device for the potential treatment of retinitis pigmentosa and age-related macular degeneration, including a projected PDUFA date from the FDA at the annual ASRS meeting in Stockholm, Sweden.
Sruthi Arepalli, MD, spoke with Modern Retina about her presentation, "Assessing retinal vascular changes in alzheimer disease with radiomics: A preliminary study of fundus photography" at the annual ASRS meeting in Stockholm, Sweden.
Nathan Steinle, MD, spoke with Modern Retina about the ongoing research on the durability of sozinibercept in combination therapy with anti-VEGF-A treatments at the annual ASRS meeting in Stockholm, Sweden.
Deepak Sambhara, MD, shared an overview of his paper-on-demand, which covered real-world safety and efficacy of aflibercept, 8 mg in the treatment of neovascular age-related macular degeneration at the annual ASRS meeting in Stockholm, Sweden.
Patrick C. Staropoli, MD, discusses clinical characterisation of Hexokinase 1 (HK1) mutations causing autosomal dominant pericentral retinitis pigmentosa
Richard B. Rosen, MD, discusses his ASRS presentation on illuminating subclinical sickle cell activities using dynamic OCT angiography
ASRS 2024: Socioeconomic barriers and visual outcomes in patients with rhegmatogenous retinal detachments, from Sally S. Ong, MD
Ashkan Abbey, MD, speaks about his presentation on the the CALM registry study, the 36-month outcomes of real world patients receiving fluocinolone acetonide 0.18 mg at the annual ASRS meeting in Stockholm, Sweden.
Nikoloz Labauri, MD, FVRS, speaks at the 2024 ASRS meeting about suspensory macular buckling as a novel technique for addressing myopic traction maculopathy
Jordana Fein, MD, MS, speaks with Modern Retina about the IOP outcomes with aflibercept 8 mg and 2 mg in patients with DME through week 48 of the phase 2/3 PHOTON trial at the annual ASRS meeting in Stockholm, Sweden.
© 2024 MJH Life Sciences

All rights reserved.