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dc.contributor.authorLasave, Andres F.
dc.contributor.authorDiaz-Llopis, Manuel
dc.contributor.authorMuccioli, Cristina [UNIFESP]
dc.contributor.authorBelfort, Rubens [UNIFESP]
dc.contributor.authorFernando Arevalo, J.
dc.date.accessioned2016-01-24T14:05:26Z
dc.date.available2016-01-24T14:05:26Z
dc.date.issued2010-09-01
dc.identifierhttp://dx.doi.org/10.1016/j.ophtha.2010.01.028
dc.identifier.citationOphthalmology. New York: Elsevier B.V., v. 117, n. 9, p. 1831-1838, 2010.
dc.identifier.issn0161-6420
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/32882
dc.description.abstractPurpose: To report the anatomic and functional outcomes of intravitreal clindamycin and dexamethasone for the treatment of zone 1 toxoplasmic retinochoroiditis (TRC). Patients had 1 or more of the following indications for local therapy: intolerance to oral medication, contraindication to oral medication because of pregnancy, lack of response despite oral antimicrobial treatment, or treatment with concomitant oral and local therapy to avoid or limit foveal or optic disc involvement.Design: Noncomparative, retrospective, multicentric interventional case series.Participants: We reviewed the medical records of 12 consecutive patients (eyes) with posterior pole (zone 1) TRC who were treated weekly or every 4 weeks (during pregnancy) with intravitreal injections of clindamycin (1.5 mg/0.1 ml) and dexamethasone (400 mu g/0.1 ml).Methods: Ophthalmic evaluation included Early Treatment Diabetic Retinopathy Study (ETDRS) best-corrected visual acuity (BCVA); assessment of central macular thickness (CMT); resolution of inflammation by optical coherence tomography (OCT), clinical examination, and fluorescein angiography; and assessment of adverse events. Patients were followed for 24 months.Main Outcome Measures: Resolution of TRC, changes in BCVA, and OCT.Results: Resolution of TRC was achieved in all cases with a mean number of injections of 3.6 (range: 2-5 injections) with a mean interval of 15.5+/-4 days. At 24 months a significant reduction in CMT by OCT was observed, from 387.6+/-70.1 mu m to 185.2+/-44.7 mu m (P = 0.0004). Baseline BCVA was logarithm of the minimal angle of resolution (logMAR) 1+/-0.4 (20/200), which improved to 0.5+/-0.4 (20/63) (P = 0.002) at the end of follow-up. Ten eyes (83.3%) improved >= 2 ETDRS lines of BCVA, and 2 eyes (20%) remained stable at 24 months. One patient's vision was limited because of macular scarring. No ocular or systemic adverse events were observed. No recurrences at 24 months of follow-up were observed.Conclusions: the combination of intravitreal clindamycin and dexamethasone was associated with resolution of zone 1 TRC and functional and anatomic improvement in patients who did not tolerate, had contraindications to, or did not respond to oral medications.en
dc.description.sponsorshipArevalo-Coutinho Foundation for Research in Ophthalmology, Caracas, Venezuela
dc.format.extent1831-1838
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofOphthalmology
dc.rightsAcesso restrito
dc.titleIntravitreal Clindamycin and Dexamethasone for Zone 1 Toxoplasmic Retinochoroiditis at Twenty-four Monthsen
dc.typeArtigo
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.contributor.institutionClin Oftalmol Ctr Caracas
dc.contributor.institutionUniv Valencia
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationClin Oftalmol Ctr Caracas, Retina & Vitreous Serv, Caracas 1010, Venezuela
dc.description.affiliationUniv Valencia, La Fe Hosp, Valencia, Spain
dc.description.affiliationUniversidade Federal de São Paulo, Vis Inst, São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Vis Inst, São Paulo, Brazil
dc.identifier.doi10.1016/j.ophtha.2010.01.028
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000281518100024


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