Welcome
to the first edition of the Optometric Glaucoma Societys electronic
journal. The journal's goal is to help all eye practitioners and scientists,
worldwide, stay up to date in regards to emerging ideas and developments
related to glaucoma. Paul Spry, MCOptom, PhD (Bristol, UK) will be our
editor in chief, with Brad Fortune, OD, PhD (Portland, OR), Shaban Demirel,
BSc (Optom), PhD (Portland, OR) and Algis Vingrys, PhD (Melbourne, Australia)
serving as associate editors. As you can see, our editorial staff has
an international flavor that we hope will allow us to tap into the different
ways glaucoma is practiced around the world.
The purpose of this journal is to bring up-to-date, useful and clinically relevant information direct to those interested in the glaucomas. We want to help clinicians stay informed about all aspects of glaucoma care: from detection, through treatment to monitoring with the ultimate aim of helping you to maintain high quality practice. The journal will promote best clinical practice and, we hope, will contribute to the evolution of future standards for glaucoma care. As you will see, the journal is divided up into digestible sections, each covering a key aspect of glaucoma practice. Many of these are practical and will review clinical cornerstones using examples, such as the quarterly disc, visual field, image and case reviews. Other sections will describe and discuss the evidence base that underpins glaucoma care (Clinical Trial Review) identify emerging concepts and promising techniques that may change the way we practice (New Ideas & New Papers) and provide the very latest glaucoma news from meetings. As the Optometric Glaucoma Society President has described, we have cultivated a global flavour and created an "International" column to provide an opportunity and forum for us all to learn from each other and think outside our own regional comfort zone. Also, if you have a glaucoma-related query that you'd like to canvas our opinion on, then please ask us using the 'Clinical Question and Answer' section. I very much hope you find the journal content to be informative, convenient, user-friendly and that you will subscribe to complimentary future issues. I would welcome any feedback that may help us provide you with the best resource available. Paul GD Spry, PhD MCOptom paul.spry@ubht.swest.nhs.uk One challenge facing clinicians is the question of whether to treat a patient suspected of having early glaucoma. Our common sense, clinical training, and now too, data from several prospective, longitudinal clinical trials, guides us to consider the relative risk associated with each individual patient (or eye). We consider age, race, IOP, corneal thickness and clinical status among other factors prior to recommending treatment (or follow-up). When the patient has reproducible, even if only "early" visual field abnormalities, this decision becomes less ambiguous. However, when the visual field is normal, the decision depends more on the apparent structural integrity of the optic disk. We know this can create uneasiness because of the degree of overlap between normal and glaucomatous eyes in terms of disk appearance. One recent paper by Medeiros and colleagues did an excellent job discussing this issue as they presented results of their study on the diagnostic utility of scanning laser polarimetry (SLP). In their study, the diagnosis of glaucoma was defined as progressive change in the clinical appearance of the optic disk, that is, glaucomatous optic neuropathy (GON). Using the GDx VCC to obtain SLP measurements, they found that the "nerve fiber indicator" (NFI) parameter had a diagnostic sensitivity of 83%, with a specificity greater than or equal to 80%, in eyes with "preperimetric" GON, (i.e., eyes with normal threshold visual fields). They elegantly discussed how the NFI parameter might best be used to assess risk by calculation of likelihood ratios. For example, eyes with an NFI score between 35 and 50 were nine times more likely in patients with preperimetric GON than in controls. To quote, "this indicates that an NFI value greater than 35 would substantially raise the suspicion of disease" in an eye with a normal visual fields but a suspicious optic disk appearance. Thus, aside from suggesting that SLP offers a potentially helpful aid in the diagnosis of glaucoma suspects (and for treatment recommendations), this paper also did an excellent job arguing that progressive change should define GON. Hence, we should all endeavor to carefully document the appearance of the optic disk at baseline, and regularly during follow-up of our patients. Probably the best current technique for doing this is simultaneous-stereo photography. Brad Fortune, OD, PhD 1. Medeiros FA, Zangwill LM, Bowd C, Sample PA, Weinreb RN. Use of progressive glaucomatous optic disk change as the reference standard for evaluation of diagnostic tests in glaucoma. Am J Ophthalmol. 2005;139:1010-1018.
This is an example of a healthy optic disc with
a large cup. When confronted with a large cup, the first area to analyze
is the size of the optic disc. A large optic disc often has large cupping.
A large cup in an average or small disc is suspicious. The middle spot
on the direct ophthalmoscope is used to evaluate disc size and is placed
adjacent to the optic disc. The middle spot correlates with the average
optic disc size (5 degrees in diameter). A large disc will be larger
than the spot of light. Other ways to evaluate disc size are with imaging
devices such as the HRT or OCT or the vertical slit of the slit lamp.
Optic discs larger than 2.4 mm2 are considered
large. The neuroretinal rim is the second area to analyze. The ISNT
rule is used which says that the rim area of a healthy optic disc varies
by sector with the Inferior (I) being thickest, followed by the Superior
(S), Nasal (N) and Temporal (T) regions. A healthy optic cup often has
a horizontal oval appearance when the ISNT rule is obeyed. The third,
fourth and fifth steps are to look for zone beta peripapillary atrophy
(PPA), retinal nerve fiber layer (RNFL) dropout and flame hemorrhages
located at the disc border. In this case, the disc is large, ISNT rule
obeyed, only zone alpha PPA is present and without flame hemorrhages
or RNFL loss.
This is an example of an unreliable visual field
with a high number of false positive and false negative responses as
well as fixation losses. The first clue that something is amiss is that
the gray scale has white sections which correlate to very high sensitivities.
This is confirmed in the raw data section in which the actual responses
are in the 40-50 dB range. The normal individual sensitivity peaks around
36-38 dB. These results are due to a patient clicking the response button
when they are not actually observing the stimulus. Other indicators
of an unreliable field due to a "happy clicker" is that the
false positive response is at 26%, which is quite high (above 15%
is unreliable), more points are flagged on the pattern than total deviation
side of the printout and the Glaucoma Hemifield Test (GHT) reads abnormally
high sensitivity. Usually, unreliable fields associated with high false
positives appear better than they are in reality, and this particular
field provides no help in regards to understanding if a field defect
is present. The patient should be educated that they are not expected
to see all targets and possibly, with practice, a useable field may
result
This 53-year-old presented for a comprehensive
examination. He failed a screening visual field test, done as part of
the pre-test battery. During the examination, his intraocular pressure
was found to be elevated (Ta 25/28 mm Hg) and the corneas were thin
(528 um/ 529 um). The optic discs were average in size and in particular
the left optic nerve did not obey the ISNT rule. The rim was thin superiorly.
Zone beta was present in each eye, but more obvious in the left eye.
A 78-year-old white asymptomatic male patient
presented for examination. Questioning revealed that he was fit and
well, had no cardiovascular disease, diabetes or history of hemodynamic
crisis. He was not taking any systemic medication and did not experience
migraine or cold extremities. No family history of glaucoma or blindness
was reported.
"I have always felt that the argument about
which happens first, structural damage or functional loss, was a silly
question. When one axon is lost, there is some function lost as well,
assuming the axon was serving some purpose. The question is, can we
detect the loss of one axon structurally or by the functional loss that
occurred? The answer is NO, you would not expect to be able to detect
the loss of an axon by inspecting the nerve, nor by testing any visual
function. Well, what about 100 axons, 1000 axons, 10,000 axons, etc.?
At some point you can recognize the loss, and it depends on the method
used. And this may change over time, with better ways to evaluate both
structure and function, so that at one time in history one method may
out-perform another. Moreover, cases differ, and if a very discrete
bundle is lost, you may not recognize that by structure, but be able
to find a small, deep scotoma. On the other hand, with more diffuse
loss, one may recognize cup enlargement, but the field may be depressed,
maybe fully still in the normal range. So as glaucoma is emerging to
the level of severity of clinical recognition, there may always be some
cases that are first recognized by a field abnormality or change and
others first recognizable by a structural abnormality or change. We
see that in OHTS, that some endpoints resulted from recognizing disc
change, and others with field change, and only a few in which both occurred
at the same time."
The North American Perimetry Society (NAPS) meeting
was held on September 22 and 23, 2005 in Skaneateles, New York. The
main theme of the meeting was perimetry in neuro-ophthalmologic conditions.
However, there were also a number of presentations directed towards
new test procedures and evaluation strategies for perimetric evaluation
of glaucoma, the relationship between structural and functional damage
in glaucoma, sources of variability in the assessment of glaucomatous
visual field loss and modeling of the mechanisms underlying glaucomatous
visual field loss. The presentations were of high caliber and generated
a considerable amount of discussion and debate among the attendees.
INTERNATIONAL
COLUMN: GLAUCOMA MANAGEMENT DOWN-UNDER The role of optometry in glaucoma detection and
management is undergoing change in Australia. In all states optometrists
have a primary care role, detecting glaucoma and referring on to ophthalmologists
for diagnosis and treatment, as and when needed. However, in some states,
notably Victoria, a secondary care aspect has been approved following
the recent promulgation of therapeutic legislation in 1996 and its enactment
in 1998. The law has allowed post-graduate certification after an approved
training course, and this has been achieved by some 200 practitioners
so far. The certification allows treating and monitoring glaucoma patients
with confirmed disease on a co-management basis. In these cases the
certified optometrists have access to, and can prescribe, all classes
of topical glaucoma drugs as approved by the Minister (some drugs are
not available in Australia to medicine or optometry). However, Victorian
optometrists cannot provide prescriptions via the Pharmaceutical Benefits
Scheme (PBS). This places the patients of certified optometrists at
a significant, financial disadvantage as the government substantially
subsidizes the costs of PBS drugs for diseases requiring chronic intervention
e.g. in some cases, a PBS script can be 20-25% of the non-PBS price.
Nevertheless, certified Victorian optometrists are now much more integrated
in glaucoma care by working alongside ophthalmologists. Their major
role is in monitoring suspects or patients with active disease and suggesting
treatment interventions when progression is detected. Under this co-management
model, the managing group (optometrist/ophthalmologist) agree on a target
pressure and intervention modality and patients are monitored for their
capacity to achieve and sustain this target with minimal change in nerve
or fields. Baseline topographic optic disc measurements
are associated with the development of primary open-angle glaucoma.
The Confocal Scanning Laser Ophthalmoscopy Ancillary Study to the Ocular
Hypertension Treatment Study. (Zangwill et al, Arch Ophth 123, Sept
2005).
PERSISTENCE
OF DRUG USAGE IN GLAUCOMA CARE We are all intimately familiar
with the issue of "compliance" being the weak link in the
glaucoma care chain. However, the bigger picture centers around "persistency;"
that is, do our patients persist in returning to the pharmacy to continue
to purchase their medicines? A recently published study on this issue
reports: "Nearly one-half of the individuals who had a glaucoma
prescription discontinued all topical ocular hypotensive therapy within
six months, and just 37% of these individuals recently had refilled
their initial medication at three years after first dispensing."
This is abysmal, and we, as a profession, need to be cognizant of such
poor patient performance so we can mount an aggressive and sustained
effort to improve our care and thus, our patients quality of life.
CLINICAL
NEWS QUESTIONS & ANSWERS In future issues this section will contain answers
and comments from our editorial board that relate to questions from
our readers. If you would like us to answer a clinical question, please
send it to paul.spry@ubht.swest.nhs.uk.
The questions can concern anything related to glaucoma, for example
analysis of an optic nerve image, optic disc, a challenging case or
side effect of a medication. We welcome your questions and we will try
to address as many as possible in each issue.
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