Intracrystalline Ozurdex®: therapeutic effect maintained for 18 months
Autor: | Francisco Farías-Rozas, Antonio Duch-Samper, Paulina Neira-Ibáñez, R. Clemente-Tomás, Raúl Torrecillas-Picazo, Delia Hernández-Pérez, Vanesa Osorio-Alayo |
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Rok vydání: | 2017 |
Předmět: |
medicine.medical_specialty
Intraocular pressure Visual acuity genetic structures business.industry medicine.medical_treatment Intraocular lens Phacoemulsification medicine.disease eye diseases Vein occlusion 03 medical and health sciences Ophthalmology 0302 clinical medicine Cataracts 030221 ophthalmology & optometry medicine Branch retinal vein occlusion sense organs Implant medicine.symptom business 030217 neurology & neurosurgery |
Zdroj: | International Ophthalmology. 39:207-211 |
ISSN: | 1573-2630 0165-5701 |
DOI: | 10.1007/s10792-017-0780-3 |
Popis: | Ozurdex® is a sterile, sustained-release implant of dexamethasone. The device dissolves within the vitreous body and releases dexamethasone. Here we present a clinical case that demonstrates the sustained therapeutic efficacy of Ozurdex® when accidentally injected into the crystalline lens. Case report. Sixty-three-year-old male in which we decided to prescribe the intravitreal injection of a dexamethasone implant (Ozurdex®) in the left eye because of macular oedema after branch retinal vein occlusion. Best-corrected visual acuity (BCVA) was 0.4. At 15 days post-implantation, the slit-lamp examination revealed the dexamethasone implant was located in the crystalline lens. Given there was no inflammation in the anterior pole, no cataracts had developed, the intraocular pressure (IOP) was normal and the macular oedema had been resolved, we decided to assess the efficacy and safety of the dexamethasone implant located in the crystalline lens. The BCVA improved until 14 months post-accidental injection. At 18 months post-Ozurdex® injection the BCVA worsened until 0.05 because of the cataract evolution. Phacoemulsification and intraocular lens placement in sulcus was performed. Once the complication has occurred, most authors advocate the early withdrawal of the implanted Ozurdex® device by means of crystalline phacoemulsification and then repositioning it in the vitreous body. However, as long as there are no signs of inflammation in the anterior pole, the IOP is within normal limits, the device does not affect the visual axis and there is no cataract development, we can evaluate the potential therapeutic effect of Ozurdex® in this non-indicated, abnormal location. |
Databáze: | OpenAIRE |
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