December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Retinal Vein Cannulation with Prolonged Infusion of Tissue Plasminogen Activator (t-PA) for the Treatment of Experimental Retinal Vein Occlusion in Dogs
Author Affiliations & Notes
  • MK Tameesh
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • GY Fujii
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • MS Humayun
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • T Shelley
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • S D'Anna
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • A Barnes
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • E Margalit
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • E de Juan
    Doheny Retina Institute Doheny Eye Institute Los Angeles CA
  • Footnotes
    Commercial Relationships   M.K. Tameesh, None; G.Y. Fujii, MadLAB P; M.S. Humayun, MadLAB C, P; T. Shelley, None; S. D'Anna, None; A. Barnes, MadLAB E; E. Margalit, None; E. de Juan, MadLAB C, P.
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 1874. doi:
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    • Get Citation

      MK Tameesh, GY Fujii, MS Humayun, T Shelley, S D'Anna, A Barnes, E Margalit, E de Juan; Retinal Vein Cannulation with Prolonged Infusion of Tissue Plasminogen Activator (t-PA) for the Treatment of Experimental Retinal Vein Occlusion in Dogs . Invest. Ophthalmol. Vis. Sci. 2002;43(13):1874.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To evaluate the feasibility, safety and efficacy of local thrombolytic agents directly injected into the occluded retinal vein in an experimental model of retinal vein occlusion. Methods: Experimental branch retinal vein occlusion was created photo-chemically using intravenous injection of rose bengal followed by diode laser photocoagulation in 6 eyes of 6 dogs. Three eyes were treated by retinal vein cannulation and injection of t-PA using a specifically designed microcatheter and the remaining 3 eyes were left as an untreated control group. The total amount of t-PA injected intravenously was 1 cc (1 mg/cc) using an average pressure of 40 psi resulting in an average injected flow rate of 0.05 cc/min. Evaluation was performed by clinical examination, fluorescein angiography and histological examination. Main outcome measures: achievement of prolonged intravascular infusion of t-PA, changes in the fundus appearance, fluorescein angiography and histology. Results: Cannulation with subsequent infusion of t-PA for a period of at least 30 minutes was achieved in all-3 treated eyes without any complications observed in the follow-up period. . One week and one month postoperatively, marked decreases in retinal hemorrhage , retinal veins dilatation and tortuosity were noted in all treated eyes. All non-treated eyes presented with persistent retinal hemorrhage, vascular dilation and tortuosity within the same follow-up period. Histologic analysis confirmed the presence of thrombi in non-treated eyes while no thrombi was observed in t-PA treated eyes. Fluorescein angiography demonstrated improved circulatory flow in treated eyes. Conclusion: Retinal vein cannulation with prolonged intravascular injection of t-PA is feasible and safe. This surgical technique may offer a new treatment option for patients with retinal vein occlusion.

Keywords: 615 vascular occlusion/vascular occlusive disease 
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