Abstract | PURPOSE: METHODS: This prospective observational study analysed treatment-naïve eyes with symptomatic PCV without MA at baseline which were followed up for 5 years. All eyes were initially treated with PDT, followed by a PRN regimen of anti- vascular endothelial growth factor ( VEGF) therapy and/or PDT. We assigned eyes with and eyes without development of MA involving the fovea 5 years after the initial treatment into MA and non-MA groups, respectively. Baseline parameters and the number of treatments were compared between the two groups. RESULTS: Seventy-two eyes of 69 consecutive patients were included, and 29 eyes of 29 patients were analysed. Twelve (41%) and 17 (59%) eyes were assigned into the MA and non-MA groups, respectively. There were significant differences in subfoveal choroidal thickness (226.2 ± 47.8 μm vs. 278.8 ± 68.1 μm, P = 0.03) and number of anti- VEGF injections (13.7 ± 9.6 vs. 5.4 ± 5.6, P = 0.007) between the MA and non-MA groups, but not in the number of PDT sessions (P = 0.71). Best-corrected visual acuity at 5 years in the MA group was lower than in the non-MA group (P = 0.048). CONCLUSION: Our long-term observation suggests that a thin subfoveal choroid at baseline and many followed anti- VEGF injections in a PRN regimen increase the risk for development of MA involving the fovea 5 years after PDT.
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Authors | Kentaro Kawai, Manabu Miyata, Sotaro Ooto, Hiroshi Tamura, Naoko Ueda-Arakawa, Ayako Takahashi, Akihito Uji, Yuki Muraoka, Masahiro Miyake, Kenji Yamashiro, Akitaka Tsujikawa |
Journal | Eye (London, England)
(Eye (Lond))
Vol. 37
Issue 6
Pg. 1067-1072
(04 2023)
ISSN: 1476-5454 [Electronic] England |
PMID | 35422494
(Publication Type: Observational Study, Journal Article)
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Copyright | © 2022. The Author(s), under exclusive licence to The Royal College of Ophthalmologists. |
Chemical References |
- Angiogenesis Inhibitors
- Vascular Endothelial Growth Factor A
|
Topics |
- Humans
- Angiogenesis Inhibitors
(therapeutic use)
- Vascular Endothelial Growth Factor A
(therapeutic use)
- Polypoidal Choroidal Vasculopathy
- Photochemotherapy
- Follow-Up Studies
- Intravitreal Injections
- Macular Degeneration
(drug therapy)
- Fluorescein Angiography
- Atrophy
- Retrospective Studies
- Tomography, Optical Coherence
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