Oct 2026· The New Zealand medical journal· Vol 139 1643, pp.
24-31
· 0 citations
Medicine
TL;DR
High early cessation due to end-stage disease suggests possible late presentation, underscoring the need for earlier detection and referral in neovascular age-related macular degeneration patients.
Abstract
Aim
The aim of this study was to evaluate long-term real-world outcomes of anti-vascular endothelial growth factor (anti-VEGF) therapy for neovascular age-related macular degeneration (nAMD) at a regional New Zealand centre, with a primary focus on treatment duration and reasons for cessation.
Methods
A retrospective cohort study was conducted at Palmerston North eye clinic, including all newly diagnosed eyes with nAMD initiating anti-VEGF therapy between November 2017 and August 2023. Demographic data, visual acuity, treatment duration and documented reasons for cessation were extracted from a prospectively maintained database and validated against electronic health records.
Results
Among 527 eyes from 446 patients, 39.8% ceased treatment. The most common reasons were end-stage disease (44.8%), patient death (21.9%), logistical factors (17.6%) and injection intolerance (8.1%). Mean treatment duration was 421 days. Visual outcomes were favourable overall with 20.2% of eyes improving and 59.5% remaining stable. Better baseline visual acuity strongly predicted better final vision.
Conclusions
High early cessation due to end-stage disease suggests possible late presentation, underscoring the need for earlier detection and referral. Addressing logistical barriers and supporting adherence will be increasingly important as demand for anti-VEGF therapy grows with an ageing population.
Background: Neovascular age-related macular degeneration (nAMD) is a leading cause of irreversible vision loss among older adults. Although randomised controlled trials have demonstrated the robust efficacy of intravitreal anti-vascular endothelial growth factor (anti-VEGF) therapy, real-world outcomes often differ mar...
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Introduction This study evaluated 12-month anatomical and functional outcomes of Faricimab in Italian patients with neovascular age-related macular degeneration (nAMD). Methods 30 eyes from 30 participants who completed the 12-month follow-up were retrospectively analyzed at “Luigi Vanvitelli” University Eye Clinic (Na...
Settimio Rossi, C. Gesualdo, M. Trotta et al.· Frontiers in Medicine· 0 citations
INTRODUCTION
The aim of this work is to evaluate the early real-world effectiveness, anatomical outcomes, and safety of intravitreal aflibercept 8 mg in neovascular aged-related macular degeneration (nAMD) eyes.
METHODS
This retrospective single-center study included consecutive nAMD eyes treated with at least one af...
J. Fricker, L. Sejournet, J. Prange et al.· Ophthalmology and Therapy· 0 citations
PURPOSE
To assess one-year real-world outcomes of faricimab therapy in patients with neovascular age-related macular degeneration (nAMD) previously treated with anti-VEGF agents and managed using a treat-and-extend (TAE) regimen.
METHODS
Patients with treatment-resistant nAMD were switched to faricimab. Functional an...
Sebastian Hoffmann, Constance Liegl, Isabel Stasik et al.· Graefe's archive for clinica...· 0 citations
OBJECTIVE
To understand management of patients with neovascular age-related macular degeneration (nAMD) in routine US clinical practice to identify gaps in patient care.
DESIGN
Retrospective analysis of electronic medical records from the Vestrum database.
PARTICIPANTS
Treatment-naive eyes newly diagnosed with nAMD...
John D. Pitcher, Ehsan Rahimy, Steven Sherman et al.· Ophthalmology Retina· 0 citations
OBJECTIVE
To investigate the demographic, clinical, and treatment-related risk factors associated with being lost to follow-up (LTFU) among patients with neovascular age-related macular degeneration (nAMD) receiving antivascular endothelial growth factor (anti-VEGF) intravitreal injections (IVIs).
METHODS
We conducte...
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