Original article
Subfoveal Retinal and Choroidal Thickness After Verteporfin Photodynamic Therapy for Polypoidal Choroidal Vasculopathy

https://doi.org/10.1016/j.ajo.2010.10.030Get rights and content

Purpose

To evaluate the morphologic retinal and choroidal changes after verteporfin photodynamic therapy (PDT) with and without ranibizumab for polypoidal choroidal vasculopathy using spectral-domain optical coherence tomography.

Design

Retrospective, comparative series.

Methods

The enhanced depth imaging optical coherence tomography technique was used in this retrospective, comparative series to measure the subfoveal retinal and choroidal thicknesses before and after treatment.

Results

Twenty-seven eyes with polypoidal choroidal vasculopathy were examined retrospectively. Sixteen eyes were treated with PDT monotherapy (PDT group). Eleven eyes were treated with PDT after intravitreal ranibizumab injection (ranibizumab plus PDT group). The polypoidal lesions regressed in all cases at 3 months. The mean retinal thickness, including the retinal detachment, increased from 401 ± 157 μm before treatment to 506 ± 182 μm 2 days after PDT (P < .001) and decreased to 365 ± 116 μm by 1 week after treatment (P = .03) and 265 ± 127 μm by 6 months after treatment (P < .001). The mean choroidal thickness increased from 269 ± 107 μm before treatment to 336 ± 96 μm 2 days after PDT treatment (P < .001 compared with baseline) and decreased to 262 ± 96 μm by 1 week after treatment (P = .24) and 229 ± 104 μm by 6 months (P < .001). Although the choroidal thickness showed a similar trend with both therapies, the retinal thickness in the ranibizumab plus PDT group remained thinner than that in the PDT group until 6 months after treatment.

Conclusions

PDT was associated with decreased retinal and choroidal thicknesses. Combination therapy reduced the transient exudation after PDT in some cases, and monthly intravitreal ranibizumab injections maintained retinal thinning and seemed to improve vision better than PDT monotherapy.

Section snippets

Methods

The clinical examinations for diagnosis of PCV included indirect ophthalmoscopy, slit-lamp biomicroscopy with a contact lens or noncontact lens, digital fluorescein angiography, and indocyanine green angiography (ICGA). We used a digital imaging system with an infrared camera and standard fundus camera (TRC-50 IX/IMAGEnet H1024 system; Topcon, Tokyo, Japan) and a confocal laser scanning system (HRA-2; Heidelberg Engineering, Dossenheim, Germany). The best-corrected visual acuity (BCVA) was

Results

Twenty-seven eyes of 27 consecutive patients with newly diagnosed PCV were included. Sixteen eyes of 16 patients (12 men, 4 women; mean age, 71.8 years) comprised the PDT group. Eleven eyes of 11 patients (6 men, 5 women; mean age, 71.0 years) comprised the ranibizumab plus PDT group. The lesion area included the fovea in all cases. The mean GLD for PDT was 3013 ± 1059 μm in the PDT group and 2905 ± 1122 μm in the ranibizumab plus PDT group. ICGA showed that the polypoidal lesions in all cases

Discussion

In the current study, PDT occluded the polypoidal lesions and decreased the retinal and choroidal thicknesses in eyes with PCV. The combination therapy of ranibizumab and PDT reduced the exudation just after PDT and maintained the retinal thinning until 6 months after treatment. Consequently, the BCVA after combination therapy was relatively better than that after PDT monotherapy.

PCV is more common in Asia than in white persons39, 40 and is thought to account for approximately half of patients

Ichiro Maruko, MD, was born and raised in Japan. He is a graduate of the Fukushima Medical University School of Medicine, Fukushima, Japan in 1999. He worked at College of Optometry, University of Houston, Houston, Texas, USA from 2002 to 2004. He received MD and PhD at Fukushima Medical University School of Medicine. His major interest includes retinal and choroidal imaging.

Dr Maruko is currently a Research Associate of the Department of Ophthalmology, Fukushima Medical University School of

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    Ichiro Maruko, MD, was born and raised in Japan. He is a graduate of the Fukushima Medical University School of Medicine, Fukushima, Japan in 1999. He worked at College of Optometry, University of Houston, Houston, Texas, USA from 2002 to 2004. He received MD and PhD at Fukushima Medical University School of Medicine. His major interest includes retinal and choroidal imaging.

    Dr Maruko is currently a Research Associate of the Department of Ophthalmology, Fukushima Medical University School of Medicine, Fukushima, Japan.

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