May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Incidence and Risk Factors of Intraocular Pressure Elevation After Triamcinolone Acetonide Administration for Macular Disorders
Author Affiliations & Notes
  • Y. Hirano
    Department of Ophthalmology and Visual Science,Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • T. Ito
    Department of Ophthalmology and Visual Science,Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • M. Nozaki
    Department of Ophthalmology and Visual Science,Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • M. Yoshida
    Department of Ophthalmology and Visual Science,Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • Y. Ogura
    Department of Ophthalmology and Visual Science,Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
  • Footnotes
    Commercial Relationships  Y. Hirano, None; T. Ito, None; M. Nozaki, None; M. Yoshida, None; Y. Ogura, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 3418. doi:
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      Y. Hirano, T. Ito, M. Nozaki, M. Yoshida, Y. Ogura; Incidence and Risk Factors of Intraocular Pressure Elevation After Triamcinolone Acetonide Administration for Macular Disorders . Invest. Ophthalmol. Vis. Sci. 2006;47(13):3418.

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

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Abstract

Purpose: : To evaluate the incidence and risk factors of intraocular pressure (IOP) elevation following triamcinolone acetonide (TA) administration for macular disorders.

Methods: : Intravitreal or posterior sub–Tenon’s injection of TA was performed on 202 patients (224 eyes) with diffuse diabetic macular edema (66 eyes), branch retinal vein occlusion (39 eyes), central retinal vein occlusion (25 eyes), exudative age–related macular degeneration (49 eyes), myopic choroidal neovascularization (10 eyes), uveitis (30 eyes) and other reasons (5 eyes). Simultaneous intravitreal and sub Tenon’s injection was performed on 85 eyes. Mean follow–up after TA administration was 15.9.±10.4 (range 3–39) months. Risk factors for IOP elevation were analyzed. We studied the effect of following factors, history of vitrectomy, route of administration, frequencies of injection, refractive error and age of the patients.

Results: : IOP readings higher than 21, 30, 40 and 50 mmHg were measured in 82 eyes (37 %), 35 eyes (16 %), 12 eyes (5.4 %) and 2 eyes (0.9 %). Fifty seven eyes (25 %) were treated by antiglaucoma medication. Two eyes (0.9 %) required trabeculotomy to control the IOP. Risk factors for the IOP elevation included younger age (P=0.026), high myopia (P=0.013) and multiple injections (0.038).

Conclusions: : These findings may be useful for comparing risks and benefits of TAtherapy. Careful follow–up of the IOP is required after TA injections.

Keywords: clinical (human) or epidemiologic studies: risk factor assessment • corticosteroids • drug toxicity/drug effects 
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