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- Publisher Website: 10.1016/j.jcjo.2015.01.007
- Scopus: eid_2-s2.0-84930160239
- PMID: 26040225
- WOS: WOS:000355555400015
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Article: Efficacy and safety of dexamethasone intravitreal implant for refractory macular edema in children
Title | Efficacy and safety of dexamethasone intravitreal implant for refractory macular edema in children |
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Authors | |
Issue Date | 2015 |
Citation | Canadian Journal of Ophthalmology, 2015, v. 50, n. 3, p. 236-241 How to Cite? |
Abstract | © 2015 Canadian Ophthalmological Society. Published by Elsevier Inc. All rights reserved.Objective To evaluate the efficacy and safety of dexamethasone (DEX) intravitreal implant (Ozurdex) in pediatric patients with cystoid macular edema (CME) refractory to conventional treatment. Design This study is a retrospective chart review. Participants Four pediatric patients (5 eyes) with CME caused by uveitis, type I idiopathic macular telangiectasia (IMT), or Coats disease treated with DEX intravitreal implant. Methods Medical records of the 4 pediatric patients (5 eyes) with CME included in this study were reviewed. Data collected included details of the underlying diseases, treatments, and pretreatment and post-treatment central retinal thickness (CRT) measured by time-domain optical coherence tomography, visual acuity (VA), intraocular pressure (IOP), and lens status. The median follow-up time was 65 weeks (range, 59-93 weeks). Results Fifteen DEX intravitreal implants were injected into 5 eyes over the follow-up period. Reduction of CME was achieved in all eyes within 12 weeks after the initial injection. VA improved in 4 eyes and was unchanged in 1 eye at 12 weeks; VA improved in 2 eyes, decreased in 2 eyes, and was unchanged in 1 eye at 52 weeks. Three of 5 eyes experienced IOP elevation ≥10 mm Hg during the follow-up period. IOP was ultimately controlled medically in all eyes. Significant lens opacification was documented in 2 eyes. Conclusions DEX intravitreal implant can be considered as an effective adjunctive off-label treatment to pediatric macular edema caused by uveitis or IMT/Coats disease; the safety profile of repeated treatment is acceptable. |
Persistent Identifier | http://hdl.handle.net/10722/228220 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 0.753 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lei, Shaobo | - |
dc.contributor.author | Lam, Wai Ching | - |
dc.date.accessioned | 2016-08-01T06:45:29Z | - |
dc.date.available | 2016-08-01T06:45:29Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Canadian Journal of Ophthalmology, 2015, v. 50, n. 3, p. 236-241 | - |
dc.identifier.issn | 0008-4182 | - |
dc.identifier.uri | http://hdl.handle.net/10722/228220 | - |
dc.description.abstract | © 2015 Canadian Ophthalmological Society. Published by Elsevier Inc. All rights reserved.Objective To evaluate the efficacy and safety of dexamethasone (DEX) intravitreal implant (Ozurdex) in pediatric patients with cystoid macular edema (CME) refractory to conventional treatment. Design This study is a retrospective chart review. Participants Four pediatric patients (5 eyes) with CME caused by uveitis, type I idiopathic macular telangiectasia (IMT), or Coats disease treated with DEX intravitreal implant. Methods Medical records of the 4 pediatric patients (5 eyes) with CME included in this study were reviewed. Data collected included details of the underlying diseases, treatments, and pretreatment and post-treatment central retinal thickness (CRT) measured by time-domain optical coherence tomography, visual acuity (VA), intraocular pressure (IOP), and lens status. The median follow-up time was 65 weeks (range, 59-93 weeks). Results Fifteen DEX intravitreal implants were injected into 5 eyes over the follow-up period. Reduction of CME was achieved in all eyes within 12 weeks after the initial injection. VA improved in 4 eyes and was unchanged in 1 eye at 12 weeks; VA improved in 2 eyes, decreased in 2 eyes, and was unchanged in 1 eye at 52 weeks. Three of 5 eyes experienced IOP elevation ≥10 mm Hg during the follow-up period. IOP was ultimately controlled medically in all eyes. Significant lens opacification was documented in 2 eyes. Conclusions DEX intravitreal implant can be considered as an effective adjunctive off-label treatment to pediatric macular edema caused by uveitis or IMT/Coats disease; the safety profile of repeated treatment is acceptable. | - |
dc.language | eng | - |
dc.relation.ispartof | Canadian Journal of Ophthalmology | - |
dc.title | Efficacy and safety of dexamethasone intravitreal implant for refractory macular edema in children | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jcjo.2015.01.007 | - |
dc.identifier.pmid | 26040225 | - |
dc.identifier.scopus | eid_2-s2.0-84930160239 | - |
dc.identifier.volume | 50 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 236 | - |
dc.identifier.epage | 241 | - |
dc.identifier.eissn | 1715-3360 | - |
dc.identifier.isi | WOS:000355555400015 | - |
dc.identifier.issnl | 0008-4182 | - |