5.1 Contact lenses
Laser therapy can be carried out either through the dilated pupil using a
contact lens or the indirect ophthalmoscope, or externally through the
sclera. Trans-pupillary laser is normally applied using the slit lamp
biomicroscope and a contact lens. The modern wide angle contact lenses
are superior to the three mirror contact lens. Lenses such as the Volk,
Mainster or Rodenstock lenses give a good view of the macula d the
peripheral retina. These lenses give an inverted image but provide easy
access to the post-equatorial region which is difficult to visualize with
a three mirror lens. Both the wide angle indirect lens system
(Panfunduscope, Mainster, Volk lens) and the laser indirect ophthalmoscope
allow laser to be delivered to otherwise inaccessible areas of the retina. It
is important to remember that the spot size may vary with different types
of lenses and the operator should be familiar with the lens used.
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5.2 Lasers
Optical radiation produced by gas or solid lasers are unique in that they
are emitted at effectively one wavelength. Dye lasers are produced in
organic dyes and have varying wavelengths. Gas laser (argon, krypton)
produce optical radiations in the visible spectrum, while the newer diode
lasers produce energy in the infrared band; argon, krypton and newer
diode lasers are used in the treatment of diabetic retinopathy.
Lasers act by inducing thermal damage after absorption of the energy by
tissue pigments. Blue/green lasers are absorbed by haemoglobin pigment
and may therefore act at the level of the retinal vessels, and particularly
microaneurysms which are one target for direct laser therapy in cases of
maculopathy with focal retinal damage. Most of the energy from lasers of
all types, including the long wavelength lasers, is absorbed by the melanin
in the retinal pigment epithelium where much of the tissue destruction is
induced.
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A variety of different lasers have been developed for retinal use. The
wavelengths range from 488-810nm through the spectrum of colours
from blue at 488nm, green at 532nm, yellow at 577nm, red at 640nm and
infrared at 810nm. As far as the effect of treatment is concerned, all of
these lasers have the effect of producing a coagulation at the level of the
pigment epithelium radiation both into the choroids and into the retina. The
only wavelength to be avoided is the blue wavelength (488nm) as this has
been shown to be reflected off the surface of the contact lens into the
operator’s eye causing reduction in blue vision which may be cumulative over
many years. This is also more likely to cause loss of blue colour perception by
the patient due to reflection within the eye. Because of the possible potential
hazard with shorter wavelengths, coaxial red aiming beams are now commonly
used on modern laser machines.
The yellow laser (577nm) is becoming more popular because of the
ease with which red lesions can be directly coagulated. This is because
red and infra-red wavelengths (dye lasers, krypton laser and diode lasers)
are better transmitted through haemoglobin pigments and will frequently
allow better uptake by the retinal pigment epithelium. Burns with these
lasers can also be produced with a lower power than blue/green lasers.
The diode laser in the infrared or invisible spectrum is a highly popular source
of laser because it is delivered via a portable machine and there is no flash
accompanying the laser application, thus being favoured by many patients.
However, with the diode laser the end-point is more difficult to appreciate,
being a greyish lesion at the level of the pigment epithelium rather than the
more obvious white lesion produced by other wavelengths. If the laser surgeon
is unaware of this difference, there may be the tendency to raise the power of
the diode laser to produce a white lesion which may cause pain and excessive
damage to the retina.
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5.3 Side effects of lasers
5.3.1 Pain
Delivery of laser energy to the ocular fundus may in some cases be associated
with significant pain. Diode lasers may be more painful than conventional lasers.
The cause of the pain is unclear but may be due to direct thermal damage to
branches of the posterior ciliary nerves. Pain may be prevented with the use of
simple analgesia but on occasion may require retro-bulbar anaesthesia or even
less frequently general anaesthesia, to achieve a satisfactory full PRP particularly
in patients with florid proliferative retinopathy in whom delayed therapy may be
risky.
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5.3.2 Vitreous haemorrhage
Excessive laser therapy in patients with forward new vessels may be sufficient
to cause marked regression of vessels which separate from the posterior hyaloid
face and produce vitreous and subhyaloid haemorrhage. In most cases this is a
rare event but patients require information concerning this risk prior to initiation
of therapy.
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5.3.3. Effect on visual function
There is now good evidence that the risk of causing reduction in visual field is
around 40% to 50% after full PRP (see later chapter). This has implications
fitness to drive and should form part of the information provided to patients
prior to treatment. There may also be other more subtle effects of PRP on
visual function such as some degree of loss of contrast sensitivity and reduction
in the ERG. Finally it must be remembered that visual function may be lost
through inadvertent laser application to the foveal parafoveal regions, or
through the development of secondary neovascular membranes after focal
treatment of microaneurysms.
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