Abstract
Background/aims
Clinical trials suggest anti-vascular endothelial growth factor is more
effective than intravitreal dexamethasone as treatment for macular oedema
secondary to branch retinal vein occlusion. This study asks if ‘real world’
data from a larger and more diverse population, followed for a longer period,
also support this conclusion.
Methods
Data collected to support routine care at 27 NHS (National Health Service)
Trusts between February 2002 and September 2017 contained 5661 treatment-naive
patients with a single mode of treatment for macular oedema secondary to branch
retinal vein occlusion and no history of cataract surgery either during or
recently preceding the treatment. Number of treatment visits and change in
visual acuity from baseline was plotted for three treatment groups
(anti-vascular endothelial growth factor (anti-VEGF), intravitreal
dexamethasone, macular laser) for up to 3 years.
Results
Mean baseline visual acuity was 57.1/53.1/62.3 letters in the
anti-VEGF/dexamethasone/macular laser groups, respectively. This changed to
66.72 (+9.6)/57.6 (+4.5)/63.2 (+0.9) at 12 months. Adequate numbers allowed
analysis at 18 months for all groups (66.6 (+9.5)/56.1 (+3.0)/60.8 (-1.5)) and
for anti-VEGF at 36 months (68.0, +10.9) Mean number of treatments were
5.1/1.5/1.2 at 12 months, 5.9/1.7/1.2 at 18 months for all three groups and
10.3 at 36 months for anti-VEGF.
Conclusions
Visual acuity improvements were higher and more sustained with anti-VEGF.
Higher treatment burden occurred with anti-VEGF but this reduced over 36
months. Patients with better vision at baseline than those in the clinical
trials maintained high levels of vision with both anti-VEGF and
dexamethasone.
Funder
National
Institute for Health Research
Novartis
Foundation for the
National Institutes of Health
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Cited by
20 articles.
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