NHMRC Glaucoma Guidelines - ANZGIG
NHMRC Glaucoma Guidelines - ANZGIG
NHMRC Glaucoma Guidelines - ANZGIG
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<strong>NHMRC</strong> GUIDELINES FOR THE SCREENING, PROGNOSIS, DIAGNOSIS, MANAGEMENT AND PREVENTION OF GLAUCOMA<br />
Chapter 8 – Monitoring: long-term care<br />
Point of note<br />
Angle closure can develop with ageing and lens change in any individual. Experts indicate that<br />
gonioscopy be performed more frequently than recommended by current guidelines, at intervals<br />
of one to two years for most individuals labelled as having open angle glaucoma. Less frequent<br />
observation may be justified in some individuals following cataract extraction.<br />
Optic nerves<br />
Visible damage to the optic nerve occurs early in the disease process, usually before visual field<br />
(VF) loss is detectable. Once VF defects have been established and optic nerve damage is severe,<br />
there may be little optic nerve neural tissue remaining to change. Therefore whilst optic nerve<br />
changes are a sensitive indicator of early and moderate glaucomatous damage, sequential perimetry<br />
may be a more sensitive indicator for progressive advanced glaucomatous damage.<br />
The review process should aim to identify subtle changes in the optic nerve head including:<br />
• further focal or generalised thinning of the neuroretinal rim<br />
• increase in nerve fibre layer defect<br />
• new disc rim haemorrhages which confer increased risk of progression (Heijl, Leske, Bengtsson<br />
et al 2002; Leske, Heijl, Hyman et al 2004).<br />
Suitable techniques for examining the optic nerve are discussed in Chapter 7. Sequential photography<br />
or imaging enhancement technology can be particularly valuable to detect subtle changes in<br />
the optic nerve or nerve fibre layer. The Working Committee acknowledges that access to these<br />
technologies may not be widely available.<br />
Fundus photography can provide a clinically useful and resource-appropriate level of information<br />
on longitudinal change in optic nerve structure. Photography through a dilated pupil can facilitate<br />
detection of change. Digital imaging analysis of such photos may be a valuable adjunct. Current<br />
clinical and trial standards use flicker analysis of photographs (Heijl et al 2002; Leske et al 2004)<br />
or rapid side-by-side comparison of photos (Gordon, Beiser, Brandt et al 2002), with the greatest<br />
sensitivity coming from flicker analysis of simultaneous stereo photographs (Barry, Eikelboom,<br />
Kanagasingam et al 2000).<br />
There is less than perfect concordance between VF loss and disc damage (Artes & Chauhan 2005).<br />
Disc damage is more noticeable earlier in the disease. Of the available objective techniques to<br />
detect change, only confocal scanning laser tomography has been rigorously evaluated (Burgoyne<br />
2004). Although retinal nerve fibre layer defects are also seen in other neurological disorders as<br />
well as in normal individuals, examination of the retinal nerve fibre layer is useful to detect early<br />
glaucomatous damage.<br />
Nerve fibre layer<br />
Assessment of the nerve fibre layer is similar to an optic nerve assessment, however it uses<br />
red-free illumination. In the early stages of glaucoma, estimation of structural abnormalities from<br />
serial nerve fibre layer photographs may be more sensitive than assessment of the optic nerve<br />
(AOA 2002). Visible structural alterations of the optic nerve head or retinal nerve fibre layer, and<br />
development of peripapillary choroidal atrophy frequently occur before VF defects can be detected.<br />
Even with the most sensitive clinical test currently available, the earliest unequivocal indication of<br />
loss of function may not be detectable until at least one-fifth of the ganglion cell axons of the retina<br />
have been destroyed, and there is a uniform 5-decibel (dB) decrease in threshold across the entire VF.<br />
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