2014
DOI: 10.2147/dddt.s66634
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Scleral melt following Retisert intravitreal fluocinolone implant

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 i… Show more

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Cited by 4 publications
(3 citation statements)
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“…In one randomized trial (ClinicalTrials.gov number, NCT00132691), the inflammation of NIU was controlled better with 0.59 mg FA implant than systemic treatment at 24 months [ 81 ]. However, the side effects related to Retisert also include cataracts and glaucoma [ 78 , 79 , 82 ]. Less common side effects are retinal detachment, vitreous hemorrhage, and scleral thinning over the implant [ 83 87 ].…”
Section: Pathogenesis and Experimental Models Of Niumentioning
confidence: 99%
“…In one randomized trial (ClinicalTrials.gov number, NCT00132691), the inflammation of NIU was controlled better with 0.59 mg FA implant than systemic treatment at 24 months [ 81 ]. However, the side effects related to Retisert also include cataracts and glaucoma [ 78 , 79 , 82 ]. Less common side effects are retinal detachment, vitreous hemorrhage, and scleral thinning over the implant [ 83 87 ].…”
Section: Pathogenesis and Experimental Models Of Niumentioning
confidence: 99%
“…Additional implants can be inserted extending the duration of treatment available with this sustained release drug delivery implant [ 84 ]. Due to the wound size required for implantation, associated scleral thinning and rare reports of scleral melt, scleral integrity should be monitored, particularly in patients undergoing reimplantation [ 85 , 86 ].…”
Section: Surgical Implantsmentioning
confidence: 99%
“…Although ILUVIEN® has the convenience of a suture-less procedure, there are reports of implant migration into the anterior chamber, blocking the visual axis, and dislodgement into the infusion cannula during vitrectomy (Andreatta et al 2017;El-Ghrably et al 2015;Moisseiev and Morse 2016;Papastavrou et al 2017). Reported Retisert® adverse effects are mostly sclerotomy-related: hypotony, temporary decrease in visual acuity, cataract formation, choroidal detachment, retinal detachment, vitreous hemorrhage, wound dehiscence, implant dislocation, and scleral melt (FDA Reference ID: 2955048) (Almeida et al 2015;Chang et al 2015;Freitas-Neto et al 2015;Petrou et al 2014;Yasin et al 2014). For these reasons, the doctor performs indirect ophthalmoscopy to verify correct placement of the implant, adequate central retinal artery perfusion, and absence of complications (FDA Reference IDs: 2955048; 3635981) (Bausch & Lomb n.d.;Yasin et al 2014).…”
Section: Intraocular Placementmentioning
confidence: 99%