TY - JOUR
T1 - Injection burden and treatment intervals of aflibercept in observe-and-plan regimen for neovascular age-related macular degeneration
AU - Subhi, Yousif
AU - Schneider, Miklos
AU - Hajari, Javad Nouri
AU - la Cour, Morten
N1 - © 2024 Acta Ophthalmologica Scandinavica Foundation. Published by John Wiley & Sons Ltd.
PY - 2024/11
Y1 - 2024/11
N2 - PURPOSE: The Observe-and-Plan (O&P) regimen allows for individualised treatment. In this study, we evaluated injection burden and intervals using aflibercept in an O&P regimen for eyes with neovascular age-related macular degeneration (AMD).METHODS: This was a retrospective registry-based study of treatment-naïve eyes with neovascular AMD. Treatment data were compiled for 3 years after commencement of intravitreal aflibercept therapy. We evaluated clinical consequences at the first follow-up after loading dose, the proportion of patients who obtained and kept dry macula after loading dose, number of injections and intervals between injections.RESULTS: Data were obtained for 1103 eyes. After loading dose, 0.4% were lost to follow-up, 7.5% discontinued, 50.9% booked for further injections and 41.3% booked for monthly observations. After loading dose, the macula remained dry in 49.2% at 3 months, 34.0% at 6 months, 23.7% at 12 months and 15.2% at 24 months. For the entire population, median cumulative total number of injections was 7, 12 and 15, after 1, 2 and 3 years, respectively. After the 3rd year, the proportion of eyes in the short 4-6 weeks treatment interval was 51.1%, 8 weeks interval was kept in 14.4% and the extended treatment intervals of 10 and 12 weeks was possible in 34.4%.CONCLUSION: After loading dose, one in two eyes required further injections. A large proportion required therapy with shorter intervals than the label-recommended 8 weeks. The large majority of those who obtained a dry macula after loading dose turned exudative again, mostly within the first 3 months.
AB - PURPOSE: The Observe-and-Plan (O&P) regimen allows for individualised treatment. In this study, we evaluated injection burden and intervals using aflibercept in an O&P regimen for eyes with neovascular age-related macular degeneration (AMD).METHODS: This was a retrospective registry-based study of treatment-naïve eyes with neovascular AMD. Treatment data were compiled for 3 years after commencement of intravitreal aflibercept therapy. We evaluated clinical consequences at the first follow-up after loading dose, the proportion of patients who obtained and kept dry macula after loading dose, number of injections and intervals between injections.RESULTS: Data were obtained for 1103 eyes. After loading dose, 0.4% were lost to follow-up, 7.5% discontinued, 50.9% booked for further injections and 41.3% booked for monthly observations. After loading dose, the macula remained dry in 49.2% at 3 months, 34.0% at 6 months, 23.7% at 12 months and 15.2% at 24 months. For the entire population, median cumulative total number of injections was 7, 12 and 15, after 1, 2 and 3 years, respectively. After the 3rd year, the proportion of eyes in the short 4-6 weeks treatment interval was 51.1%, 8 weeks interval was kept in 14.4% and the extended treatment intervals of 10 and 12 weeks was possible in 34.4%.CONCLUSION: After loading dose, one in two eyes required further injections. A large proportion required therapy with shorter intervals than the label-recommended 8 weeks. The large majority of those who obtained a dry macula after loading dose turned exudative again, mostly within the first 3 months.
KW - Aged
KW - Aged, 80 and over
KW - Angiogenesis Inhibitors/administration & dosage
KW - Dose-Response Relationship, Drug
KW - Drug Administration Schedule
KW - Female
KW - Fluorescein Angiography/methods
KW - Follow-Up Studies
KW - Fundus Oculi
KW - Humans
KW - Intravitreal Injections
KW - Macula Lutea/pathology
KW - Male
KW - Receptors, Vascular Endothelial Growth Factor/administration & dosage
KW - Recombinant Fusion Proteins/administration & dosage
KW - Registries
KW - Retrospective Studies
KW - Time Factors
KW - Tomography, Optical Coherence/methods
KW - Treatment Outcome
KW - Vascular Endothelial Growth Factor A/antagonists & inhibitors
KW - Visual Acuity
KW - Wet Macular Degeneration/drug therapy
U2 - 10.1111/aos.16709
DO - 10.1111/aos.16709
M3 - Article
C2 - 38733136
SN - 1755-375X
VL - 102
SP - 821
EP - 827
JO - Acta ophthalmologica
JF - Acta ophthalmologica
IS - 7
ER -