May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Intravitreal Injection of Triamcinolone Acetonide for the Treatment of Macula Edema Due to Branch Retinal Vein Occlusion
Author Affiliations & Notes
  • Y. Ebihara
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • A. Mekada
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • M. Tajika
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • Y. Takihata
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • E. Sekii
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • A. Okada
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • M. Ohji
    Ophthalmology, Shiga Univercity of Medical Science, Otsu, Japan
  • Footnotes
    Commercial Relationships  Y. Ebihara, None; A. Mekada, None; M. Tajika, None; Y. Takihata, None; E. Sekii, None; A. Okada, None; M. Ohji, None.
  • Footnotes
    Support  Ministry of Education, Culture, Sports, Science and Technology of Japan
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 4264. doi:
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    • Get Citation

      Y. Ebihara, A. Mekada, M. Tajika, Y. Takihata, E. Sekii, A. Okada, M. Ohji; Intravitreal Injection of Triamcinolone Acetonide for the Treatment of Macula Edema Due to Branch Retinal Vein Occlusion . Invest. Ophthalmol. Vis. Sci. 2006;47(13):4264.

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

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Abstract

Purpose: : To evaluate the efficacy and safety of intravitreal injection of triamcinolone acetonide (TA) to treat macula edema secondary to branch retinal vein occlusion (BRVO).

Methods: : Twenty–five eyes of 25 consecutive BRVO patients with macula edema with best–corrected visual acuity (BCVA) of 20/30 or less were included. The patients received one 4–mg intravitreal injection of TA. The BCVA and intraocular pressure (IOP) were assessed at baseline and at 1, 3, and 6 months after the TA injection.

Results: : The mean logMAR visual acuity level was 0.60±0.45 at baseline and improved significantly to 0.28±0.37 at 1 month (p<0.01), 0.29±0.32 at 3 months (p<0.01), and 0.26±0.32 at 6 months (p<0.01). The BCVA improved by 3 lines or more in 14 patients (56%); no patient lost 3 or more lines of BCVA at 6 months. The IOP increased by greater than 10 mmHg compared with baseline in 4 patients (16%). No serious adverse effects developed.

Conclusions: : Intravitreal injection of TA achieved a significant improvement of BCVA in patients with macula edema secondary to BRVO for the short term after the injection. TA seems to be a safe and effective treatment for BRVO. Further follow–up is required to determine if macula edema recurs after the treatment of BRVO.

Keywords: vascular occlusion/vascular occlusive disease • macula/fovea • injection 
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