Intravitreal triamcinolone for diffuse diabetic macular oedema.
dc.contributor.author | Gibran, S K | |
dc.contributor.author | Cullinane, A | |
dc.contributor.author | Jungkim, S | |
dc.contributor.author | Cleary, P E | |
dc.date.accessioned | 2012-02-03T15:06:51Z | |
dc.date.available | 2012-02-03T15:06:51Z | |
dc.date.issued | 2012-02-03T15:06:51Z | |
dc.identifier.citation | Eye (Lond). 2006 Jun;20(6):720-4. Epub 2005 Jul 8. | en_GB |
dc.identifier.issn | 0950-222X (Print) | en_GB |
dc.identifier.issn | 0950-222X (Linking) | en_GB |
dc.identifier.pmid | 16021193 | en_GB |
dc.identifier.doi | 10.1038/sj.eye.6701992 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10147/208899 | |
dc.description.abstract | AIM: To evaluate the efficacy of intravitreal triamcinolone (IVTA) for the treatment of diffuse diabetic macular oedema (DME) refractory to conventional argon macular laser therapy. METHODS: A prospective, consecutive, and noncomparative case series was undertaken involving 38 eyes of 38 patients with refractory DME. Triamcinolone acetonide (4 mg) in 0.1 ml was injected intravitreally. LogMar visual acuity (VA) and macular thickness measured by ocular coherence tomography (OCT) were assessed preoperatively and postoperatively at 1, 3, and 6 months. RESULTS: All patients completed 6 months of follow up. VA (mean+/-SD) improved from 0.905+/-0.23 to 0.605+/-0.28, 0.555+/-0.29, and 0.730+/-0.30 at 1, 3, and 6 months, respectively. Macular thickness baseline (mean+/-SD) on OCT was 418.7+/-104.2 microm and this decreased to 276.9+/-72.6 microm, 250.6+/-53.1 microm, and 308.8+/-87.3 microm at 1, 3, and 6 months, respectively. CONCLUSIONS: IVTA may be a potential temporary treatment for refractory DME. It is effective in decreasing macular thickness and improving VA but the effect lasts approximately for 6 months in the majority of patients. Further investigations are required to establish the safety of IVTA for the treatment of DME. | |
dc.language.iso | eng | en_GB |
dc.subject.mesh | Aged | en_GB |
dc.subject.mesh | Anti-Inflammatory Agents/*therapeutic use | en_GB |
dc.subject.mesh | Diabetic Retinopathy/*drug therapy/pathology/physiopathology | en_GB |
dc.subject.mesh | Female | en_GB |
dc.subject.mesh | Humans | en_GB |
dc.subject.mesh | Macula Lutea/pathology | en_GB |
dc.subject.mesh | Macular Edema/*drug therapy/pathology/physiopathology | en_GB |
dc.subject.mesh | Male | en_GB |
dc.subject.mesh | Middle Aged | en_GB |
dc.subject.mesh | Prospective Studies | en_GB |
dc.subject.mesh | Treatment Outcome | en_GB |
dc.subject.mesh | Triamcinolone Acetonide/*therapeutic use | en_GB |
dc.subject.mesh | Visual Acuity/drug effects | en_GB |
dc.subject.mesh | Vitreous Body | en_GB |
dc.title | Intravitreal triamcinolone for diffuse diabetic macular oedema. | en_GB |
dc.contributor.department | Department of Ophthalmology, Cork University Hospital, Cork, Ireland., syedgibran@yahoo.com | en_GB |
dc.identifier.journal | Eye (London, England) | en_GB |
dc.description.province | Munster | |
html.description.abstract | AIM: To evaluate the efficacy of intravitreal triamcinolone (IVTA) for the treatment of diffuse diabetic macular oedema (DME) refractory to conventional argon macular laser therapy. METHODS: A prospective, consecutive, and noncomparative case series was undertaken involving 38 eyes of 38 patients with refractory DME. Triamcinolone acetonide (4 mg) in 0.1 ml was injected intravitreally. LogMar visual acuity (VA) and macular thickness measured by ocular coherence tomography (OCT) were assessed preoperatively and postoperatively at 1, 3, and 6 months. RESULTS: All patients completed 6 months of follow up. VA (mean+/-SD) improved from 0.905+/-0.23 to 0.605+/-0.28, 0.555+/-0.29, and 0.730+/-0.30 at 1, 3, and 6 months, respectively. Macular thickness baseline (mean+/-SD) on OCT was 418.7+/-104.2 microm and this decreased to 276.9+/-72.6 microm, 250.6+/-53.1 microm, and 308.8+/-87.3 microm at 1, 3, and 6 months, respectively. CONCLUSIONS: IVTA may be a potential temporary treatment for refractory DME. It is effective in decreasing macular thickness and improving VA but the effect lasts approximately for 6 months in the majority of patients. Further investigations are required to establish the safety of IVTA for the treatment of DME. |