Ultrasound assessment of short-term ocular vascular effects of intravitreal injection of bevacizumab (Avastin®) in neovascular age-related macular degeneration
Article first published online: 26 JUN 2009
DOI: 10.1111/j.1755-3768.2009.01526.x
© 2009 The Authors. Journal compilation © 2009 Acta Ophthalmol
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How to Cite
Bonnin, P., Pournaras, J.-A. C., Lazrak, Z., Cohen, S. Y., Legargasson, J.-F., Gaudric, A., Levy, B. I. and Massin, P. (2010), Ultrasound assessment of short-term ocular vascular effects of intravitreal injection of bevacizumab (Avastin®) in neovascular age-related macular degeneration. Acta Ophthalmologica, 88: 641–645. doi: 10.1111/j.1755-3768.2009.01526.x
Publication History
- Issue published online: 27 AUG 2010
- Article first published online: 26 JUN 2009
- Received on June 24th, 2008. Accepted on December 2nd, 2008.
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Keywords:
- antiangiogenic therapy;
- age-related macular degeneration (AMD);
- central retinal artery;
- ciliary artery;
- ophthalmic artery;
- ultrasound imaging
Acta Ophthalmol. 2010: 88: 641–645
Abstract.
Purpose: Angiogenic inhibitors, alone or combined with other therapies, are believed to represent a promising treatment for neovascularization in age-related macular degeneration (wet AMD). They can maintain or improve visual acuity (VA), at least for the first 2 years. However, evolution to retinal atrophy cannot be ruled out and it may be useful to assess the effects of antiangiogenic therapy on retinal and choroidal circulation.
Methods: We carried out a pilot study in 15 patients with wet AMD. Time-averaged mean blood flow velocities (BFVs) in the central retinal, temporal posterior ciliary and ophthalmic arteries (CRA, TPCA and OA) were measured by ultrasound imaging before and 4 weeks after a single intravitreal injection of 1.25 mg bevacizumab in 0.05 ml. Patients underwent two ophthalmic examinations, before and 4 weeks after injection, including VA measurement and optical coherence tomography (OCT3) examination.
Results: In treated eyes, bevacizumab injection was followed by a significant improvement in VA (from 20/125 to 20/80; p = 0.0214), and a decrease in mean central macular thickness (from 392 ± 96 μm to 271 ± 50 μm; p = 0.0038). Mean BFV decreased by 10% in the CRA (p = 0.0226), 20% in the TPCA (p = 0.0026) and 20% in the OA (p = 0.0003). No effect was observed in fellow eyes.
Conclusions: Intravitreal bevacizumab acutely improved VA and reduced central macular thickness in wet AMD. Ultrasound imaging revealed that BFVs decreased in all retrobulbar arteries, suggesting that after local diffusion, bevacizumab exerts a short-term regional effect. Bevacizumab might therefore induce hypoperfusion of the whole eye, which may correspond to a vascular side-effect.

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