May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Therapeutic Efficacy of Intravitreal Injection of Tissue Plasminogen Activator for Macula Edema Due to Central Retinal Vein Occlusion
Author Affiliations & Notes
  • S. Mizunoya
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • J. Uehara
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • Y. Nakamura
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • A. Hagiwara
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • H. Abe
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • S. Yamamoto
    Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chuo–ku, Chiba, Japan
  • Footnotes
    Commercial Relationships  S. Mizunoya, None; J. Uehara, None; Y. Nakamura, None; A. Hagiwara, None; H. Abe, None; S. Yamamoto, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 4280. doi:
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    • Get Citation

      S. Mizunoya, J. Uehara, Y. Nakamura, A. Hagiwara, H. Abe, S. Yamamoto; Therapeutic Efficacy of Intravitreal Injection of Tissue Plasminogen Activator for Macula Edema Due to Central Retinal Vein Occlusion . Invest. Ophthalmol. Vis. Sci. 2006;47(13):4280.

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

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Abstract

Purpose: : To evaluate the therapeutic efficacy of intravitreal injection of tissue plasminogen activator (tPA) for macular edema (ME) due to a central retinal vein occlusion (CRVO).

Methods: : Twenty one eyes of 21 patients with a CRVO–associated ME were treated with an intravitreal injection of tPA. The estimated duration of symptoms ranged from 2 to 24 weeks (mean 8 weeks). The tPA (40,000 units of monteplase) was injected into the vitreous cavity through the pars plana with a 30G needle following paracentesis. The best–corrected visual acuity (BCVA), OCT–determined foveal thickness, fluorescein angiography, and full–field electroretinography (ERG) were measured before and 1 week, 1, 3 and 6 months after tPA.

Results: : The BCVA was improved by more than 2 lines in 13 eyes (62%) and remained stable in 4 eyes (19%) at 6 month postoperatively. The ME was temporary increased in 4 eyes (19%) at 1month after tPA but was markedly reduced in all eyes at 6 months after the tPA injection. The preoperative mean foveal thickness was 776 µm which was significantly reduced to 499 µm at 1 week, 449 µm at 1 month, 368 µm at 3 month and 275 µm at 6 month postoperatively. The a– and b–wave amplitudes of the rod–cone ERG were significantly reduced at 1 month after tPA. The photopic b–wave amplitudes were reduced at 1 and 3 months after tPA injection.

Conclusions: : Intravitreal injection of tPA may be effective for treating ME associated with a CRVO but may be toxic to the retina. Additional careful investigations are needed to show the advantage of tPA over the natural course.

Keywords: vascular occlusion/vascular occlusive disease • electroretinography: clinical • vitreous 
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