Scleral melt following Retisert intravitreal fluocinolone implant
Authors Georgalas I, Koutsandrea C, Papaconstantinou D, Mpouritis D, Petrou P
Received 22 April 2014
Accepted for publication 8 May 2014
Published 28 November 2014 Volume 2014:8 Pages 2373—2375
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Ilias Georgalas,1 Chrysanthi Koutsandrea,1 Dimitrios Papaconstantinou,1 Dimitrios Mpouritis,1 Petros Petrou1,2
1Ophthalmology Department, University of Athens, Athens, Greece; 2Moorfields Eye Hospital, London, UK
Abstract: Intravitreal fluocinolone acetonide implant (Retisert) has a high potency, a low solubility, and a very short duration of action in the systemic circulation, enabling the steroid pellet to be small and reducing the risk of systemic side effects. Scleral melt has not been reported as a possible complication of Retisert implant. The authors describe the occurrence of scleral melt 18 months after the implantation of fluocinolone acetonide implant in a 42-year-old Caucasian woman. To the authors’ knowledge, this is the first report of this possible complication.
Keywords: Retisert, scleral melt, complication, surgical management
Inflammatory macular edema represents one of the main causes of significant vision loss in patients with uveitis, as a result of the breakdown of the blood–retinal barrier by inflammatory mediators such as tumor necrosis factor-alpha and interleukin-1beta.1 In an effort to intercept the circulation of these mediators, corticosteroids have been used in variable delivery forms (oral, intravitreal, sub-Tenon’s administration) as a treatment modality for macular edema on the background of various types of chronic posterior uveitis.
The repeated administration nature of periocular and intravitreal steroid injections as well as the increased incidence of side effects associated both with topically and systemically administered corticosteroids2–4 led to the development of slow-release therapeutic modalities. Based on a Phase III study showing that the 34-week risk of uveitic recurrence fell significantly from 51.4% to 6.1% and visual acuity improved significantly,5,6 the Food and Drug Administration approved an intravitreal fluocinolone acetonide (FA) implant that could deliver a sustained dose of corticosteroid (Retisert; Bausch & Lomb Incorporated, Bridgewater, NJ, USA) for the treatment of the posterior uveitis.
Since 2005, the use of FA implant gained popularity among ophthalmologists. Nonetheless, the identification and management of possible intraoperative or postoperative complications associated with its use remains an ongoing process. The purpose of the present work is to report the unusual but serious postoperative complication associated with the implantation of Retisert, which to the best of our knowledge has never been reported before, and describe the surgical management of scleral melt at the site of the Retisert implantation in a patient with posterior uveitis on the background of psoriatic arthritis.
A 42-year-old Caucasian woman was referred to our department complaining of sudden vision loss, watery discharge from her right eye (RE), and pain. She had a complex past ocular history that included the implantation of Retisert in her RE to treat persistent uveitis-associated cystoid macular edema on the background of psoriatic arthritis 18 months earlier. In addition, according to her notes, she had undergone combined phacoemulsification and vitrectomy with epiretinal membrane peeling 2 years before the FA implant. One year after the Retisert implantation, she underwent right trabeculectomy to treat persistently high intraocular pressure.
On examination, the intraocular pressure (IOP) was 2 mmHg, the anterior chamber was flat, and the visual acuity was counting fingers in the RE. An anterior segment examination revealed scleral melt with active leaking (positive Seidel test) at the site of the FA implant. The patient underwent urgent surgical repair under general anesthesia. Intraoperatively, an anterior chamber maintainer was used and surgical exploration confirmed significant scleral melt at the site of implantation with leaking aqueous humor (Figure 1). A scleral patch graft was sutured over the leaking sclerotomy.
Figure 1 Intraoperative photo of the right eye.
On the following day, the IOP was 9 mmHg and the fundus examination revealed that the FA implant had detached from the scleral sutures and was free floating in the vitreous cavity.
Three weeks later, the IOP was 18 mmHg, the visual acuity recovered to 20/30, and the patch graft was in good position (Figure 2). Benefits and risks of vitrectomy to remove the Retisert implant were discussed with the patient; however, she decided against surgery.
Figure 2 Anterior segment image of the right eye 3 weeks postoperatively.
Two years later, visual acuity remained 20/30 with no recurrence of the cystoid macular edema, and IOP within normal limits, without additional medication.
FA has a high potency, a low solubility, and a very short duration of action in the systemic circulation, enabling the steroid pellet to be small and reducing the risk of systemic side effects.
The implant consists of a tablet encased in a silicone elastomer cup containing a release orifice and a polyvinyl alcohol membrane positioned between the tablet and the orifice. The silicone elastomer cup assembly is attached to a polyvinyl alcohol suture tab with silicone adhesive, which is supported to the sclera with sutures. The most common side effects of Retisert are cataract formation (all patients require cataract surgery within 3 years) and significantly raised ocular pressure (40% of patients require trabeculectomy surgery). More rare side effects are vitreous hemorrhage, retinal detachment, vitreous bands, scleral thinning over the implant, and hypotony (IOP <6 mmHg in 9.4% of implanted eyes).2,6–9
Scleral melt has not been reported as a possible complication of FA implant. In a study aiming to evaluate whether intravitreal FA implantation (Retisert) leads to scleral thinning, Taban et al10 reported that FA implant appears to lead to overall statistically nonsignificant scleral thinning with few exceptions.
In our case, significant scleral melt developed 18 months after the implantation of FA implant, which to the best of our knowledge has never been reported before. Of course, the patient had previously undergone vitrectomy with epiretinal membrane peel before FA implant as well as a trabeculectomy post-Retisert implantation. It is possible that these procedures could represent an additional factor for the significant scleral melt observed in our patient, although no significant inflammation or infection had been recorded post-vitrectomy or post-trabeculectomy. Scleral patch graft appeared to be adequate for the surgical management in our case. No adverse events were observed to be associated with the presence of the free-floating implant in the vitreous cavity.
The authors report no conflicts of interest in this work.
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