June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Long-term results of Intravitreal Bevacizumab for the Treatment of Choroidal Neovascular Membranes associated with Presumed Ocular Histoplasmosis Syndrome
Author Affiliations & Notes
  • Sarah Escott
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Susie Chang
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Ahmad Tarabishy
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Mark Barsamian
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • John Christoforidis
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Frederick Davidorf
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Alan Letson
    Ophthalmology, The Ohio State University Wexner Medical Center, Columbus, OH
  • Footnotes
    Commercial Relationships Sarah Escott, None; Susie Chang, None; Ahmad Tarabishy, None; Mark Barsamian, None; John Christoforidis, None; Frederick Davidorf, None; Alan Letson, Genentech (F)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 2935. doi:
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      Sarah Escott, Susie Chang, Ahmad Tarabishy, Mark Barsamian, John Christoforidis, Frederick Davidorf, Alan Letson; Long-term results of Intravitreal Bevacizumab for the Treatment of Choroidal Neovascular Membranes associated with Presumed Ocular Histoplasmosis Syndrome. Invest. Ophthalmol. Vis. Sci. 2013;54(15):2935.

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

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Abstract

Purpose: To assess the long-term efficacy of intravitreal bevacizumab therapy for choroidal neovascularization (CNV) in patients with presumed ocular histoplasmosis syndrome (POHS).

Methods: All patients diagnosed with CNV associated with POHS and treated with intravitreal bevacizumab (1.25 mg) between December 2005 and September 2012 were included. Baseline best-corrected visual acuity (BCVA) was compared with first post-treatment visit BCVA and final visit BCVA. Fluorescein angiography confirmed the presence of CNV prior to initial treatment.

Results: Seventeen eyes of 12 patients received intravitreal bevacizumab. Nine eyes were newly diagnosed; the remaining 8 previously treated eyes received prior therapy for CNV more than 1 year before initiation of intravitreal bevacizumab treatment. Mean follow-up was 45.24 months (3.77 years) with a range of 2.4 to 6.4 years. Overall there was a statistically significant improvement in mean logMAR VA after 1 treatment (0.16, Snellen equivalent of 20/29) when compared to mean baseline logMAR VA (0.35, Snellen equivalent of 20/45). At final visit, treatment effect was sustained in 15 of 17 study eyes. The improvement between baseline and final BCVA outcome in both the treatment naive and previously treated groups were not statistically significant; however the overall improvement in vision was greater in those naive to treatment (-0.16 versus -0.04 log MAR improvement). Eyes with subfoveal lesions (n=13) as a group demonstrated a statistically significant improvement of BCVA from baseline to both first post-treatment visit and final visit.

Conclusions: Long-term visual outcomes are favorable for patients treated with intravitreal bevacizumab for CNV associated with POHS. In patients with POHS, intravitreal bevacizumab may be more effective as initial therapy for new onset CNV and without other previous treatment. Furthermore, we demonstrate that in the majority of treatment naive eyes, the visual acuity is sustained over a period of at least four years. These findings suggest intravitreal bevacizumab is an appropriate first-line therapy for the management of CNV in patients with POHS.

Keywords: 453 choroid: neovascularization • 585 macula/fovea • 466 clinical (human) or epidemiologic studies: treatment/prevention assessment/controlled clinical trials  
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