Infectious EO is an inflammatory reaction that poses a high risk of severe visual loss. During any intraocular procedure, prevention of EO should be a priority because of the multiple sources of contamination 10–12.
A number of authors and studies addressed the problem of RD due to EO and its surgical treatment. In the EVS, the rate of postoperative RD was 7.8% in the 20-gauge vitrectomy subgroup. Later then, due to the advancement of surgical techniques and technology, re-evaluation of this study’s results is needed 13, 14.
The evolution of the PPV technique with the introduction of 23-gauge and 25-gauge systems have made surgery less invasive. Nelsen et al 6 reported RD rates of 21% after PPV treatment and 9% in eyes not treated with PPV, with an overall RD rate of 16% after surgical treatment of EO. Olson and colleagues 8 reported an overall RD rate of 10% following post-surgical treatment, with a higher rate of 14% in post PPV eyes as well and Sridhar et al reported a high RD rate of 21.4 % in cases of acute EO at the time of initial PPV or during follow up 15, 16. Altan et al. reported that 13.8% of the subgroup treated with 20-gauge PPV led to a postoperative RD, while no RD developed in the subgroup treated with 25-gauge vitrectomy 17. In a study by Almanjoumi et al., the rate was 10% after a 23-gauge PPV 18.
EO cases should be treated immediately after diagnosis in order to minimize retinal damage. In our study all cases were treated at the same day of presentation. Even after the inflammation has subsided, strict follow-up examinations are necessary due to onset of late RD. Cases of late RD up to a year after successful treatment of EO have been reported. This could have been caused by the production of various cytokines released into the vitreous cavity over a long period of time, due to the blood-ocular barrier breakdown. Retinal necrosis with tangential traction of retinal membranes can lead to formation of retinal breaks and rhegmatogenous RD. Tori et al reported a rapid progression of proliferative vitreoretinopathy after endogenous bacterial endophthalmitis caused by meningitis 2, 19, 20. The results of our study can verify this point of late onset RD and of necessary strict follow ups.
The use of silicone oil has been reported by a number of authors in cases of intraoperative retinal breaks after post-surgical or following traumatic EO 21–24. Dave et al reported high rates of RD at presentation and during follow up after initial surgery for EO. All patients with RD were treated with silicone oil and the reattachment rates were deemed satisfactory 25. Sridhar et al reported a high RD rate of 21.4 % in cases of acute EO at the time of initial PPV or during follow up. Silicone oil proved to be effective in stabilizing the retina but the BCVA was poor in almost all patients due to the severity of the cases 15. Previously, due to the fear of infection behind the silicone oil bubble, there had been a reluctance to use silicone oil as a tamponade agent for EO 26. Later, silicone oil was proved to have an antibacterial and antifungal effect in vitro. The possible mechanisms of its antimicrobial activity that were reported are nutritional deprivation and toxicity 27. The dosage of intravitreal antibiotics in eyes treated with silicone oil injection still remains controversial. Hegazy’s study demonstrated a retinal toxicity in silicone oil-filled rabbit eyes, when the full dose of intravitreal antibiotics was used 28. Nevertheless, those results still might not apply to the human eyes. Still we believe it is wise to reduce the dose of intravitreal drugs to about 25% of the dose that is usually injected because all intravitreal drugs will only distribute in the small aqueous phase surrounding the silicone bubble.
On the microbiological side, the results of the organisms identified in our study are in accordance with other studies and there was no statistically significant correlation between the microbiological findings and the occurrence of RD or the initial BCVA (no statistical significance between Gram + bacteria and severity of EO, BCVA and rate of RD) 29, 30.
The treatment strategy of a severe EO is complicated and there is no clear protocol. Of essence is time and the goal is to evacuate the infection and administer antibiotics. The intravitreal injection of antibiotics and the vitrectomy are the standard and main therapeutic options. Every option has advantages and disadvantages. While vitrectomy allows the as complete as possible evacuation and removal of the infection, it is often not possible, since vitreoretinal surgeons and vitreoretinal operating rooms are relatively fewer. The VTB and intravitreal antibiotics injection have their own advantage. For example, they offer a smaller sample, permit earlier intravitreal antibiotics injection and microbiology tests 31. Vitrectomy has evolved over the years after the EVS study (smaller gauges, faster surgical procedures, minimal invasive) but the rates of RD vary and can be still high in severe cases of EO as demonstrated not only from the EVS study but from other authors using modern PPV techniques (23 and 25 gauge systems) 15, 17, 18, 25.
The high rate of RD in our cohort cannot be attributed to iatrogenic intraoperative breaks or to the vitreous sampling. No shaving of the vitreous base was performed (in combination with detailed indentation search of the peripheral retina) and the posterior hyaloid was not actively detached because it was already detached in all cases. We also did not use for vitreous sampling undiluted vitreous but diluted. Chiquet et al have reported that undiluted vitreous sampling at the start of PPV leads to hypotony, with a potential risk of vitreoretinal tractions, haemorrhages and RD. This can be avoided using diluted samples, since both samples have the same microbiological efficiency using PCR 32.
In our study, retinal detachment is statistically significant associated with preoperative visual acuity, which is similar to the findings of Doft et that RD is more likely to develop in patients who have the most severe presentation with visual acuity of LP only9. On the other hand, Chiquet et reported that other risk factors for RD in patients who had a vitrectomy after cataract surgery were diabetes and vasculitis 16. Our study could not find a statistical significant correlation between microbiological findings (especially Gram + bacteria), diabetes mellitus, immunosuppression and severity of EO, and RD rate. Vitrectomy offers the advantage of as complete as possible evacuation of the infection but is associated with a spectrum of complications like RD.
One of the limitations of most of the studies in the literature today dealing with this very complex problem are the retrospective nature, lack of a defined treatment protocol, treatment by multiple vitreoretinal surgeons and exclusion of cases due to the complexity of the disease and poor visual prognosis of this condition. These facts apply to our study also, but the large number of cases, the inclusion of two retinal centers, gives us optimism that our conclusions could shed some light on this complex issue.