Choroidal Thickness Changes After Intravitreal Ranibizumab and Photodynamic Therapy in Recurrent Polypoidal Choroidal Vasculopathy

Purpose To evaluate subfoveal choroidal thickness changes in cases with recurrent polypoidal choroidal vasculopathy (PCV) after combination therapy with intravitreal ranibizumab and photodynamic therapy (PDT). Design Retrospective observational case series study. Methods We measured subfoveal choroi...

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Veröffentlicht in:American journal of ophthalmology 2013-09, Vol.156 (3), p.548-556
Hauptverfasser: Maruko, Ichiro, Iida, Tomohiro, Oyamada, Hiroshi, Sugano, Yukinori, Ojima, Akira, Sekiryu, Tetsuju
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Sprache:eng
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Zusammenfassung:Purpose To evaluate subfoveal choroidal thickness changes in cases with recurrent polypoidal choroidal vasculopathy (PCV) after combination therapy with intravitreal ranibizumab and photodynamic therapy (PDT). Design Retrospective observational case series study. Methods We measured subfoveal choroidal thickness in PCV using optical coherence tomography (OCT) before and after PDT. In recurrent cases, the choroidal thickness was measured at the time of the recurrence. In nonrecurrent cases, choroidal thickness was measured 1 year after PDT. Results Combination therapy was performed in 27 eyes (27 patients). Polypoidal lesions regressed within 3 months after initial treatment in all eyes. Retreatment was needed in 10 of 27 eyes (37.0%) after more than 3 months of follow-up. In recurrent cases, subfoveal choroid decreased from 188 μm at baseline to 157 μm 3 months after PDT ( P < .01); however, choroidal thickness increased to 179 μm with recurrence ( P  = .54 compared to baseline; average, 8.0 months). In nonrecurrent cases, subfoveal choroid decreased from 257 μm at baseline to 210 μm 3 months after PDT and 212 μm 1 year after PDT ( P < .01, respectively). Conclusion Subfoveal choroidal thickness in PCV at the time of recurrence returned to the baseline level after choroidal thinning as a result of PDT treatment. Choroidal thickness changes after PDT examined using OCT may reflect disease activity in PCV.
ISSN:0002-9394
1879-1891
DOI:10.1016/j.ajo.2013.03.041