J R Soc Med 2006;99:125-127
doi:10.1258/jrsm.99.3.125
© 2006 Royal Society of Medicine
A review of developments in the management of retinal diseases
Somnath Banerjee
Department of Ophthalmology, Leicester Royal Infirmary, Infirmary Road,
Leicester LE1 5WW, UK
E-mail:
pinkubanerjee2002{at}yahoo.co.uk
INTRODUCTION
Retinal disease continues to be a major contributor to poor vision
especially in the ageing population. Age related macular degeneration is the
main cause of registerable blindness in the developed world. Retinal vein
occlusions are the second most common retinal vascular disease following
diabetic retinopathy.
This article is a review of new advances in the management of these
conditions as well as an introduction to developments in the surgical
management of retinal disease using new technology.
METHODS
A review of the ophthalmic literature as well as material obtained from
presentations at national and international conferences was used to provide
the material in this article.
MANAGEMENT OF AGE RELATED MACULAR DEGENERATION
Age-related macular degeneration is the most common cause of poor vision in
those over 65 in the Western world. There are two types: dry (atrophic)
age-related macular degeneration which accounts for 85-90% of all cases but is
associated with a better prognosis; and wet (exudative) age-related macular
degeneration (Figure 1). Wet
age-related macular degeneration is associated with choroidal
neovascularization, a process similar to angiogenesis at other sites.
The benefit of thermal (argon) laser retinal photocoagulation
was
established for choroidal neovascular membranes away from
the fovea
(extrafoveal) in the Macular Photocoagulation Study
in the early
1990s.
1 In
photodynamic
therapy
2,3
a light-sensitive
agent (Verteporfin) is given by intravenous infusion over 10
min
at a dose of 6 mg/m
2 of body surface area. Fifteen minutes
after
the start of the infusion, a low-powered laser calibrated to
deliver a
set amount of energy at a specific wavelength is applied
over a circular area
slightly larger than the choroidal neovascular
membranes. The laser is not
powerful enough to cause any damage
on its own but activation of Verteporfin
by light absorption
results in formation of cytotoxic free radicals that
damage
the new blood vessels of the choroidal neovascular membranes.
photodynamic
therapy has been shown to reduce the rate of visual loss in
patients
with well-defined (classic) choroidal neovascular membranes
but this
accounts for no greater than 20% of patients with wet
age-related macular
degeneration. Recent studies have shown
that photodynamic therapy may be
beneficial for poorly defined
(occult) choroidal neovascular membranes.
Medicaid recently
agreed to reimburse practitioners for photodynamic therapy
for
occult choroidal neovascular membranes in the USA. If it is
advocated also
by the FDA, a very large number of patients will
be eligible with considerable
impact on manpower and resources.
In the UK, NICE has advocated photodynamic
therapy only for
predominantly classic choroidal neovascular membranes at
present.
This guidance will due for review in 2006-2007
Anecortave acetate is an angiostatic agent administered by posterior
juxtascleral injection close to the macula every 6 months. A recent 24-months
double-masked phase 2/3 study showed that it was superior to placebo in
stabilizing vision for all types of choroidal neovascular membranes. The
Anecortave Acetate Risk Reduction Trial (AARRT) is examining whether
anecortave reduces progression of dry age-related macular degeneration in
patients at high risk of progression to wet age-related macular degeneration.
Macugen is a highly selective inhibitor of vascular endothelial growth factor
with anti-angiogenic and anti-permeability effects. The vascular endothelial
growth factor Inhibition Study in Ocular Neovascularisation (VISION)
demonstrated improved visual outcome at 54 weeks in wet age-related macular
degeneration, regardless of lesion subtype. Macugen has to be delivered by
intra-vitreal injection every 6 weeks. Lucentis is a recombinant humanized
antibody fragment that binds to vascular endothelial growth factor and
inactivates all vascular endothelial growth factor isoforms. This is also
delivered by intravitreal injection on a monthly basis.
MANAGEMENT OF RETINAL VEIN OCCLUSION
Central or branch retinal vein occlusion is the second most common retinal
vascular disease after diabetic retinopathy
(Figure 2) Current practise is
to follow the guidelines suggested by the Central Retinal Vein Occlusion
Study4 and the
Branch Retinal Vein Occlusion
Study.5 The
management of central retinal vein occlusion (central retinal vein occlusion)
involves identifying modifiable risk factors, such as systemic hypertension
and hyperlipidaemia, and treating ischaemic complications of the vascular
occlusion. Laser treatment (pan retinal photocoagulation) is indicated at the
earliest sign of iris neovascularization. Macular laser photocoagulation is
not beneficial to visual improvement although the oedema may regress. It is
therefore not recommended in central retinal vein occlusion. In branch retinal
vein occlusion a modified grid laser photocoagulation is indicated for macular
oedema persisting for three or more months and the visual acuity is 6/12 or
less in the absence of significant macular ischaemia.
There are a number of other suggested techniques to treat retinal
vein
occlusions, including creating an anastomosis between the
retina and choroid
using high energy argon
laser.
6 Surgically
incising
the nasal part of the optic nerve (radial optic neurotomy) is
based
on the theory that the site of occlusion in central retinal
vein occlusion is
in the substance of the optic nerve producing
a `compartment
syndrome'.
7 A
randomized study is currently taking
place (Radial Optic Neurotomy in Central
Vein Occlusion Study
sponsored by NIH). If an occlusion site can be identified
in
branch retinal vein occlusion, surgical incision of the common
adventitial
sheath around the retinal arteriole and vein (arterio-venous
sheathotomy) with
elevation of the arteriole from the vein is
being studied, because it is
thought that the vein is compressed
by the atherosclerotic artery. The
procedure now most commonly
performed for macular oedema following vein
occlusion is the
injection of intravitreal steroid
(triamcinolone).
8
However,
this procedure maybe associated with increased intraocular pressure
and
does not always result in visual improvement. Randomised controlled
trials
on the efficacy of intravitreal triamcinolone in the
management of retinal
vein occlusion are awaited.
SURGICAL ADVANCES-TRANSCONJUNCTIVAL SUTURELESS VITRECTOMY
Removal of the vitreous using an aspiration-cutting instrument inserted
through the pars plana (pars plana vitrectomy) is performed for a number of
conditions including retinal detachment, complications of diabetic retinopathy
and certain macular pathology. Machemer first performed pars plana vitrectomy
in the early 1970's using a 17-gauge (1.5mm diameter) instrument. This
required a 2.3mm scleral incision. In 1974 O'Malley designed a smaller
20-gauge (0.9mm) instrument, which is currently in widespread use. Since 1990,
De Juan et al. have been developing a 25 gauge (0.5mm)
system.9 More
recently, Eckhardt has modified this to a 23-gauge system. The advantages of
both these systems are faster entry and closure, as no suturing of entry sites
is required (transconjunctival sutureless vitrectomy), and quicker recovery
for the patient. Both are available in this country and are likely to be used
more widely with time.
CONCLUSION
This is an exciting time for the retinal specialist with treatment options
now available for conditions that were previously not amenable to any type of
therapy.
As with any new developments in medicine it is wise to err on the side of
caution when advising patients as to the potential benefits of these until
long-term outcomes become available.
As sutureless vitrectomy goes, this procedure which used to be associated
with long operating times and stay in hospital as well as recovery times this
may soon also be a thing of the past.
REFERENCES
- Macular Photocoagulation Study Group. Laser photocoagulation of
subfoveal neovascular lesions of age related macular degeneration. Updated
findings from two clinical trials. Arch Ophthalmol1993; 111:1200
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- Verteporfin In Photodynamic Therapy Study Group. Verteporfin
therapy of subfoveal choroidal neovascularisation in age-related macular
degeneration: two-year results of a randomized clinical trial including
lesions with occult with no classic choroidal neovascularisation.
Am J Ophthalmol2001; 131:541
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randomised clinical trials TAP Report No 5. Arch
Ophthalmol 2002;120:1307
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- The Central Vein Occlusion Study Group. Natural history and
clinical management of central retinal vein occlusion. Arch
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- The Branch Vein Occlusion Study Group. Argon laser photocoagulation
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- McAllister IL, Douglas JP, Constable IJ, et al. Laser
induced chorioretinal venous anastomosis for nonischemic central retinal vein
occlusion: evaluation of the complications and their risk factors.
Am J Ophthalmol1998; 126:219
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11 consecutive patients. Retina2001; 21:408
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acetonide as treatment of macular edema in central retinal vein occlusion.
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- Fujii GY, De Juan E Jr, Humayun MS, et al. Initial
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