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Intravenous thrombolysis in acute central retinal artery occlusion - A prospective interventional case series.
Schultheiss, Maximilian; Härtig, Florian; Spitzer, Martin S; Feltgen, Nicolas; Spitzer, Bernhard; Hüsing, Johannes; Rupp, André; Ziemann, Ulf; Bartz-Schmidt, Karl U; Poli, Sven.
Afiliação
  • Schultheiss M; Department of Ophthalmology, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
  • Härtig F; University Eye Hospital Tübingen, University of Tübingen, Tübingen, Germany.
  • Spitzer MS; Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany.
  • Feltgen N; Department of Ophthalmology, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
  • Spitzer B; University Eye Hospital Tübingen, University of Tübingen, Tübingen, Germany.
  • Hüsing J; Department of Ophthalmology, University Medical Center Goettingen, Goettingen, Germany.
  • Rupp A; Department of Experimental Psychology, University of Oxford, Oxford, United Kingdom.
  • Ziemann U; Coordination Center for Clinical Trials, University Hospital Heidelberg, Heidelberg, Germany.
  • Bartz-Schmidt KU; Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.
  • Poli S; Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Tübingen, Germany.
PLoS One ; 13(5): e0198114, 2018.
Article em En | MEDLINE | ID: mdl-29813111
BACKGROUND: No evidence-based therapy exists for non-arteritic central retinal artery occlusion (NA-CRAO). Retinal ischemic tolerance is low; irreversible damage occurs within four hours of experimental NA-CRAO. In previous randomized trials evaluating intra-arterial or intravenous thrombolysis (IVT) in NA-CRAO, only one patient was treated this early. In December 2013, the Departments of Neurology & Stroke and Ophthalmology at University Hospital Tuebingen, Germany, decided to treat patients using IVT within 4.5 hours of NA-CRAO, the therapeutic window established for ischemic stroke. MATERIALS AND METHODS: Consecutive NA-CRAO patients with severe visual loss received IVT after exclusion of intracranial hemorrhage. Follow-up was conducted at day 5 (d5) and day 30 (d30). Visual outcomes were compared to the conservative standard treatment (CST) arm of the EAGLE-trial. RESULTS: Until August 2016, 20 patients received IVT within 4.5 hours after NA-CRAO with a median onset-to-treatment time of 210 minutes (IQR 120-240). Visual acuity improved from baseline mean logarithm of the minimum angle of resolution 2.46±0.33 (SD) (light perception) to 1.52±1.09 (Snellen equivalent: 6/200) at d5 (p = 0.002) and 1.60±1.08 (Snellen equivalent: 6/240) at d30. Compared to the EAGLE CST-arm, functional recovery to reading ability occurred more frequently after IVT: 6/20 (30%) versus 1/39 (3%) at d5 (p = 0.005) and at d30 5/20 (25%) versus 2/37 (5%) (p = 0.045). Two patients experienced serious adverse events (one angioedema and one bleeding from an abdominal aortic aneurysm) but recovered without sequelae. CONCLUSIONS: IVT within 4.5 hours after symptom onset may represent an effective treatment of NA-CRAO. Randomized trials are warranted to evaluate efficacy and safety of early IVT in acute NA-CRAO.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veias / Oclusão da Artéria Retiniana / Terapia Trombolítica Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veias / Oclusão da Artéria Retiniana / Terapia Trombolítica Idioma: En Ano de publicação: 2018 Tipo de documento: Article