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Intravitreal triamcinolone as an adjunct in the treatment of concomitant proliferative diabetic retinopathy and diffuse diabetic macular oedema

dc.contributor.authorKaderli, B.
dc.contributor.authorAvcı, R.
dc.contributor.authorGelişken, O.
dc.contributor.authorYücel, A.
dc.contributor.buuauthorKaderli, Berkant
dc.contributor.buuauthorAvcı, Remzi
dc.contributor.buuauthorGelişken, Öner
dc.contributor.buuauthorYÜCEL, AHMET ALİ
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGöz Hastalıkları Ana Bilim Dalı
dc.contributor.scopusid6507602756
dc.contributor.scopusid7004838001
dc.contributor.scopusid6602526353
dc.contributor.scopusid7005217049
dc.date.accessioned2025-05-13T14:15:17Z
dc.date.issued2005-12-01
dc.description.abstractPurpose: To investigate if triamcinolone acetonide (TA) can be an adjunct to laser treatment in patients with concomitant non-high-risk proliferative diabetic retinopathy (PDR) and diffuse clinically significant diabetic macular oedema (CSMO). Methods: This prospective, interventional and comparative clinical study included 32 eyes of 16 patients with bilateral concomitant non-high-risk PDR and diffuse CSMO. Each patient received 4 mg intravitreal TA for the eye with worse visual acuity (study group) and macular focal and grid laser photocoagulation (MP) for the other eye (control group). One month later, each patient received four sessions of panretinal photocoagulation for both eyes plus MP for the eyes in the study group. The visual and angiographic results of both groups were compared. Results: In the study group, the mean visual acuity (VA) improved from 0.12 ± 2.3 lines at the baseline to 0.19 ± 3.1 (P = 0.004), 0.20 ± 3.2 (P = 0.004), 0.19 ± 3.6 (P = 0.009) and 0.19 ± 3.3 lines (P = 0.091) at the 1-, 3-, 6- and 9-month follow-up intervals, respectively. The macular oedema was found to be resolved in 11 eyes (69%) and decreased in five eyes (31%). In the control group, the mean VA deteriorated progressively from 0.41 ± 3.1 lines at the baseline to 0.20 ± 3.1 lines (P = 0.026) at the end of the study and the macular oedema decreased only in three eyes (19%) at the sixth follow-up month. Conclusions: During the follow-up period of the study, intravitreal TA as an adjunct in the treatment of concomitant non-high-risk PDR and diffuse CSMO led to a more-favourable clinical outcome than conventional laser treatment. © Springer Science+Business Media, Inc. 2007.
dc.identifier.doi10.1007/s10792-007-9042-0
dc.identifier.endpage214
dc.identifier.issn0165-5701
dc.identifier.issue6
dc.identifier.scopus2-s2.0-33947264095
dc.identifier.startpage207
dc.identifier.urihttps://hdl.handle.net/11452/52828
dc.identifier.urihttps://link.springer.com/content/pdf/10.1007/s10792-007-9042-0.pdf
dc.identifier.volume26
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherSpringer
dc.relation.journalInternational Ophthalmology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectProliferative diabetic retinopathy
dc.subjectLaser photocoagulation
dc.subjectIntravitreal triamcinolone
dc.subjectDiffuse diabetic macular oedema
dc.subject.scopusDiabetic Macular Edema; Diabetic Retinopathy; Implant
dc.titleIntravitreal triamcinolone as an adjunct in the treatment of concomitant proliferative diabetic retinopathy and diffuse diabetic macular oedema
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Göz Hastalıkları Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublication34be4f44-59fb-4838-9179-a4b19b9575e6
relation.isAuthorOfPublication.latestForDiscovery34be4f44-59fb-4838-9179-a4b19b9575e6

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