Association between visual acuity, lesion activity markers and retreatment decisions in neovascular age-related macular degeneration
- PMID: 32066898
- PMCID: PMC7784949
- DOI: 10.1038/s41433-020-0799-y
Association between visual acuity, lesion activity markers and retreatment decisions in neovascular age-related macular degeneration
Abstract
Background/objectives: To investigate the association between optical coherence tomography (OCT) markers of lesion activity and changes in visual acuity (VA) during anti-vascular endothelial growth factor (anti-VEGF) therapy of eyes diagnosed with neovascular age-related macular degeneration (nAMD); and how VA and OCT markers are considered in physicians' decision to retreat with anti-VEGFs.
Subjects/methods: Retrospective, non-comparative, non-randomised cohort study involving electronic medical record data collected from 1190 patient eyes with nAMD diagnosis at two sites in the United Kingdom. Two sub-cohorts consisting of 321 and 301 eyes, respectively, were selected for analyses.
Results: In 321 eyes, absence of IRF or SRF at ≥2 clinic visits resulted in a gain of five ETDRS letters from baseline, compared with two letters gained in eyes with <2 clinic visits with absence of IRF (p = 0.006) or SRF (p = 0.042). Anti-VEGF treatment was administered at 421 clinic visits, and 308 visits were without treatment. Comparing treatment visits with non-treatment visits, the maximum difference in frequency of OCT markers of lesion activity were for intraretinal fluid (IRF; 24% versus 5%) and subretinal fluid (SRF; 32% versus 5%). Pigment epithelial detachment (PED) was reported in 58% of treatment visits compared with 36% in non-treatment visits. VA loss was not a consistent trigger for retreatment as it was present in 63% of injection visits and in 49% of non-injection visits.
Conclusions: Retreatment decision making is most strongly influenced by the presence of IRF and SRF and less by the presence of PED or VA loss.
Conflict of interest statement
UC has received honoraria from Novartis Pharma AG and Bayer AG. NP and LB are employees of IQVIA. CB, AnS and AS are employees of Novartis Pharma AG. IQVIA received funding from Novartis to conduct the study. The study was sponsored by Novartis Pharma AG, Basel, Switzerland. The sponsor had a role in the study design, data collection, data analysis, and paper preparation.
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