Treatment Effects in Retinal Angiomatous Proliferation Imaged with OCT Angiography

Jan H. De Jong, Boy Braaf, Sankha Amarakoon, Maximilian Gräfe, Suzanne Yzer, Koenraad A. Vermeer, Tom Missotten, Johannes F. De Boer, Mirjam E.J. Van Velthoven

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Purpose: This prospective case series is aimed at exploring optical coherence tomographic angiography (OCT-A) as a treatment monitoring tool in patients treated for retinal angiomatous proliferation (RAP). Methods: Twelve treatment-naïve RAP patients were included, with a median age of 79 years (range 65-90). Patients were imaged with an experimental 1,040-nm swept-source phase-resolved OCT-A instrument before and after treatment. Treatment consisted of either intravitreal bevacizumab or triamcinolone injections with or without photodynamic therapy (PDT). Abnormal blood flow after treatment was graded as increased, unchanged, decreased, or resolved. Results: OCT-A images before and after treatment could be obtained in 9 patients. The median follow-up period was 10 weeks (range 5-19). After various treatments, the RAP lesion resolved in 7 patients, in 1 patient the OCT-A depicted decreased flow in the lesion, and 1 patient showed unchanged abnormal blood flow. Monotherapy with intravitreal bevacizumab injections resolved RAP in 1 out of 2 patients. Combined therapy of bevacizumab with PDT resolved RAP in 6 out of 7 patients. Conclusions: OCT-A visualized resolution of abnormal blood flow in 7 out of 9 RAP patients after various short-term treatment sequences. OCT-A may become an important noninvasive monitoring tool for optimizing treatment strategies in RAP patients.

Original languageEnglish
Pages (from-to)143-153
Number of pages11
JournalOphthalmologica
Volume241
Issue number3
Early online date18 Sept 2018
DOIs
Publication statusPublished - Mar 2019

Funding

This study was received from the following: Stichting Combined Ophthalmic Research Rotterdam (project No. 2.0.0), Rotterdam, The Netherlands; MaculaFonds (project No. 2012.8), Utrecht, The Netherlands; and Stichting Life Sciences Health TKI (project No. LSHM16001), Heidelberg Engineering, Heidelberg, Germany. Funding for this study was received from the following: Sticht-ing Combined Ophthalmic Research Rotterdam (project No. 2.0.0), Rotterdam, The Netherlands; MaculaFonds (project No. 2012.8), Utrecht, The Netherlands; and Stichting Life Sciences Health TKI (project No. LSHM16001), Heidelberg Engineering, Heidelberg, Germany. Johannes F. de Boer received the following research funding: government and government sponsored foundations – Vici-ZonMW (grant 918.10.628), STW (grant No. 12822, 13936), ZonMW (grant No. 91212061), and LaserLaB Europe (grant agreement No. 654148); foundations – Kika retinablastoom and ISAO; commercial company – Heidelberg Engineering; personal fees (income from lecture) – Heidelberg Engineering; intellectual property rights, royalties, patents, licenses – Massachusetts General Hospital.

FundersFunder number
LaserLaB Europe654148
Stichting Life Sciences Health TKILSHM16001
Massachusetts General Hospital
ZonMw91212061
Stichting Combined Ophthalmic Research Rotterdam2.0.0, 2012.8
Stichting voor de Technische Wetenschappen13936, 12822
Internationale Stichting Alzheimer Onderzoek
Heidelberg Engineering

    Keywords

    • Anti-VEGF therapy
    • Imaging
    • Optical coherence tomographic angiography
    • Photodynamic therapy
    • Retinal angiomatous proliferation
    • Treatment monitoring
    • Type 3 neovascularization

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