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Volume
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August
2008
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OGS
PRESIDENT'S MESSAGE
We live in exciting times. I say this
not just because of the upcoming Olympics, or the grace and style that was Spain in Euro2008, the extraordinary
Wimbledon final (Spain again), or the way in which Tiger Woods won the US Open. Not even at the thought of
cracking open that last bottle of 2002 claret, sipping a favourite malt, or the prospect of new Coldplay music.
I say this because we live in an exciting time of discovery in the world of glaucoma. Our understanding of the
basic mechanisms of the disease is increasing exponentially, we have imaging techniques with a resolution that
could not have been imagined a decade ago, new perimetric techniques for early detection and better progression
analysis, and stand with the promise of clinically useful functional imaging. Although our clinical armamentarium
has not changed dramatically, there is an inevitable momentum that will fundamentally change our approach to
the disease and its management. But, in any time of discovery there is always confusion. The question is
whether such confusion serves to destroy morale and lower confidence, or whether it is seen as a challenge that
can lead to better patient care. The next question to be considered is how best we can learn and apply this new information?
We can meet: 1. In October the OGS holds its 7th annual meeting with a lineup of speakers as good as can be found anywhere,
including the 2008 honoree Dr. Robert Ritch (see http://www.optometricglaucomasociety.org for details). This year's
meeting boasts several innovations. There is a half day joint meeting with the Glaucoma Progression Scholars, and the
first joint meeting with the American
Academy of Optometry.
2. In July 2009 the 3rd World Glaucoma Congress will be held in Boston and all optometrists are encouraged to attend
and will be welcomed. The OGS will be holding a special meeting on the first day of the congress. Having attended
the first two WGCs in Vienna and Singapore I can highly recommend this meeting and look forward to seeing many of you there.
We can read: 1. The recent special glaucoma issue of Optometry and Vision Science (OVS) is truly exceptional. Under
the guidance of guest editor Brad Fortune, the authors and articles are of the highest quality. We owe OVS Editor Tony
Adams a debt of gratitude for nurturing the glaucoma special issues we have all come to enjoy. Let the tradition continue!
2. Very soon the latest edition of the OGS Glaucoma Handbook will be distributed through Review of Optometry.
With Murray Fingeret as Editor it is always a pleasurable read as well as being topical and relevant.
3. The outstanding OGS E-Journal. Amazingly this is the 10th edition and is as informative and entertaining as ever.
Great job Paul Spry and team.
We can practice: As informed clinicians we can make a difference. We can diagnose early and manage our patients with care,
compassion and knowledge.
Exciting times indeed!
John Flanagan PhD, MCOptom, FAAO
President, Optometric Glaucoma Society
jgflanag@quark.uwaterloo.ca
EDITORIAL
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Difficult questions need informed answers
What do you say when a patient asks, "Will my glaucoma make me go blind?" Providing
an appropriate answer to this question is absolutely critical because
no matter what you reply, there will be an inevitable impact on the individuals
perception of their own health. A negatively phrased answer may disproportionately
reduce their perceived quality of life. A positively phrased answer could
fail to provide sufficient impetus for the patient to regard glaucoma
seriously, and undermine his/her motivation to adhere to the treatment
and follow-up plan. An effective strategy for handling this question may
be to provide and discuss information about prognosis. Useful information
for this purpose was presented at this year's Annual meeting of the Association
for Research in Vision and Ophthalmology (ARVO) by Heijl et al. These
authors reported that the rate of progressive visual field decline, quantified
using Mean Deviation, in a large cohort of treated patient with chronic
open angle glaucoma followed over ~10 years was -1.2dB/year. On average,
reaching blindness would take 35 years. However, the spread of progression
rates was negatively skewed such that more patients progressed slowly.
Extrapolation from this evidence about the relationship between proportion
and rates implied that 17% of patients took ≤20 years to reach blindness,
whilst 4.8% of patients took ≤12 years. This information will, without
doubt, allow a patient to understand the timescale of glaucoma and therefore
their prognosis, especially because the power of this study’s findings
lies in the lack of selection bias. Unlike clinical trials, this study
included data from all patients receiving glaucoma care, with the only
drawback to generalisability being that the study population was almost
exclusively white and up to one third had pseudoexfoliative glaucoma and
such individuals may be more likely to exhibit higher progression rates
than primary open angle glaucoma and normal tension glaucoma.
Other information likely to assist patient’s understanding of the potential impact of glaucoma on their life
is how and when it may affect their driving ability. This issue of the E-journal reviews recent publications
on glaucoma
and driving.
One final consideration is that visual field testing appears unlikely to inform us about the relationship
between glaucoma and the many visual functions involved in daily life. This subject was explored at ARVO,
and highlights are featured in our ARVO
review.
Paul GD Spry, PhD, BSc, MCOptom DipGlauc
Editor-in-Chief
paul.spry@uhbristol.nhs.uk
NEW IDEAS AND PAPERS
Doctor-patient communication and adherence to glaucoma medication recommendations
In the most recent paper to report results from the ongoing Glaucoma Adherence and Persistency Study (GAPS),
David Friedman and colleagues (1) have identified eight variables that were each associated independently with
poorer patient adherence to prescribed topical glaucoma medication: 1) hearing all of what you know about glaucoma
from your doctor (compared with some or nothing); 2) not believing that reduced vision is a risk of not taking
medication as recommended; 3) having a problem paying for medications; 4) difficulty while traveling or away
from home; 5) not acknowledging stinging and burning; 6) being non-white; 7) receiving samples; and 8) not
receiving a phone call visit reminder.
These findings are important for all eye care professionals to consider because they reveal several potentially
modifiable barriers to effective glaucoma therapy and highlight elements of effective doctor-patient communication
that are essential to overcoming these barriers. The authors elaborate on the first variable in part by describing
three modes of patient learning: those patients who learned all they know about their disease and treatment from
their physician were characterized as doctor-dependent learners; those who learned most but not all were described
as collaborative learners; and those who learned not much or nothing from their physicians were characterized as
independent learners. The authors found that doctor-dependent learners had significantly lower adherence than
either the collaborative learners or the independent learners. Though this may seem counter-intuitive at first
glance, it speaks to the heart of effective doctor-patient communication.
For example, doctor-dependent
learners were less likely than the others to report that their physician asked if they had any questions
or if they understood what they had been told. They also had the lowest confidence (of the three groups)
in their knowledge about glaucoma.
The second variable regarding a patient's concern for vision loss also relates to effective doctor-patient
communication. As compared with the 86% of patients who believed that not taking their medications as
recommended placed them at risk for reduced vision, the 14% of patients who did not believe this exhibited
poorer adherence. These patients who were not concerned that poor adherence put them at risk for vision loss
also did not believe they would be at risk for optic nerve damage, increased intraocular pressure, or complete
vision loss. They were also less likely to report that someone close to them experienced vision loss because
of eye disease. Especially important to our focus here, the group of unconcerned patients was more likely to
report that their doctor did not tell them what to expect from the future regarding their glaucoma. The authors
report that this latter characteristic was shared with doctor-dependent learners.
Those unconcerned about potential vision loss also "reported receiving less information and fewer answers
to questions from their physicians and
were less likely to report receiving a demonstration on using drops or being told by their physician about
stinging and burning as a possible side effect. Finally, the unconcerned were more than twice as likely to
have a charted notation of a missed appointment."
Some of the other variables less directly related to doctor-patient communication still warrant our consideration
under the same light. Patients having difficulty paying for medications and/or taking medications while travelling
or away from home may still benefit from enhanced doctor-patient communication in that these barriers still need to
be detected and identified, and may be overcome by "physician-initiated problem solving". Those patients who
did not acknowledge stinging and burning had lower adherence than those who did acknowledge these adverse effects of
their medication. It is possible that a patient who does not acknowledge any adverse effects might not be taking their
medication correctly. This is another reason to be routinely asking patients about potential adverse effects and to
take the opportunity to properly demonstrate eye drop instillation.
The authors report that their multivariate model based on these eight variables explained 21% of the variance
in the outcome measure of adherence. Thus, there are still other variables that impact patient adherence and other
ways to measure adherence that are likely to help identify the most important barriers. Nonetheless, the important
results of this study led the authors to reiterate that: "physicians should ensure that all patients have an
understanding of their disease that supports appropriate concern about future consequences." The authors stress
that this is particularly important for patients who exhibit the more passive characteristics of doctor-dependent
learners, for example, those patients who "give the appearance of taking in the given information because they do
not ask clarifying questions and do not reveal confusion or lack of confidence in their knowledge." Indeed, the
authors state that, "Although doctor-dependent learners may be in the greatest need of being encouraged
to ask questions and to be asked directly if they understand, our analysis shows that they are the least
likely to report receiving these interventions." For these and perhaps all patients, the authors recommend
that, "Physicians can assess patients' understanding and concern about the consequences of glaucoma and
simultaneously can detect and activate passive doctor-dependent learners by applying an ask-tell-ask communication
strategy." For details of the ask-tell-ask strategy, as well as for the methods, results, limitations and
caveats of this study, readers of the of the OGS E-Journal are encouraged to seek out this and other papers on GAPS.
Brad Fortune OD, PhD
1. Friedman DS, Hahn SR, Gelb L, Tan J, Shah SN, Kim EE, Zimmerman TJ, Quigley HA.
Doctor-Patient Communication, Health-Related Beliefs, and Adherence in Glaucoma Results from the Glaucoma
Adherence and Persistency Study. Ophthalmology. 2008 Mar 3. [Epub ahead of print]
A major concern of glaucoma patients their fitness to drive.
The study of Bhargava et al (1) provides information about concerns that glaucoma patients have regarding their visual
status and their treatment. This is an interview-based study of 82 patients attending two glaucoma clinics. The authors
developed a statistic of importance based on the patients’ responses (score awarded to a factor divided by
the sum for all factors). As there were 10 factors in the questionnaire (8 real and 2 dummies), importance should be 10%
(1/10) in the absence of any association. This group found that the greatest concern among patients was the risk of moderate
visual impairment (38%) and blindness (27%) with an average 33% importance for vision loss. In contrast
the use of topical medications and surgery returned an importance of 13%, on average.
Within this context of patient concern, it is worth noting that Owen et al. (2) report that older adults in the UK
view the surrender of a driving license as a significant life event, resulting in the loss of self-esteem as well
as mobility and social independence. Not surprisingly they note that those who have stopped driving are at greater
risk of worsening depression, which not only impacts on their own lives but that of their caregivers, family and friends (2).
In this context Owen et al argue that an appropriate position for glaucoma intervention is to prevent or delay
the onset of the loss of one’s driving license.
Fitness to drive in the UK not only requires a minimum subtense of peripheral visual field (120° width) but
also the absence of scotomata in the binocular central field. Here, Owen et al. suggest that clinicians should
consider visual capacity in terms of the binocular integrated visual field (IVF). These authors prefer the IVF
representation (3) to the Esterman binocular test because the former is a threshold outcome whereas the latter is
based on suprathreshold measures having limited central representation. The IVF is established on a point-wise
basis by using the highest sensitivity at a given location derived from both monocular fields. The authors propose
that any point in the IVF having a sensitivity <10dB should correspond with an Esterman outcome. However,
they also note that the IVF has a greater number of test points and propose the criterion for failing a driving
fitness assessment should be a cluster of at least 4 contiguous abnormal points (<10 dB) within the
central 20° with a further non-contiguous point within this region or two elsewhere.
Using the IVF analysis and the fail criterion given above, the authors reviewed the visual fields of 199 glaucoma patients
who had been followed in the glaucoma clinic of Moorfields Eye Hospital over a 17 year period (1986 to 2003). They found
that some 30% of glaucoma patients failed to meet this criterion after a 14 year follow up, making it likely that
these individuals would have been required to surrender their driving licenses. What is interesting in this data is
that the IVF is a good predictor for future loss of vision and that 1/3 of patients or, 10% of the total glaucoma
group, showed rapid deterioration over the first 2 years of follow-up. It needs to be mentioned that the authors did
not establish whether driving licenses were actually surrendered, only that they would have developed a vision loss
consistent with this potential, nor do they report on what the variability was in applying this diagnostic approach.
The take home message of this work is that many patients most fear a loss of vision to the point where they will have
to surrender their driving license, and that clinicians can use an IVF approach to monitor the prospect of this and
treat aggressively to prevent its occurence. An ancillary finding is that the first two years after diagnosis are
important in establishing future prospects of vision loss and the capacity to retain a driving license.
Algis Vingrys BScOptom, PhD
References
1. Bhargava JS, et al.
Views of glaucoma patients on aspects of their treatment.
Invest Ophthalmol Vis Sci, 2006: 47: 2885-88.
2. Owens VMF, et al. Glaucoma and fitness to Drive. Invest Ophthalmol Vis Sci, 2008: 49: 2449-55.
3. Crabb DP, et al. Simulating binocular visual field status in glaucoma. Br J Ophthalmol 1998; 82: 1236-41.

VISUAL FIELD REVIEW
How many tests are needed to detect significant glaucomatous visual field change?
If you manage patients with glaucoma, possibly the most important tool you can get your hands on this year
comes in the form of a paper by Chauhan et al. (1) A free, full-text
copy is available through the BMJ journals scheme and I highly recommend downloading one for yourself.
An impressive group of thought leaders jointly authored this paper, shining a light on that often-uttered question:
How many visual field tests will I need before I can tell if my patient’s glaucoma is progressing?
The paper commences with a compelling argument for the regular measurement of visual fields in general and the
use of standard automated perimetry (SAP) in particular. Generally, visual field damage is perhaps the best
functional predictor we have of a patient’s quality of life. In particular, SAP is the test that was used as
the primary functional endpoint in almost all of the large-scale randomized clinical trials and has the largest
amount and longest duration of clinical information available.
The main thrust of this paper is that you must "measure the rate of visual field
progression." Although it is acknowledged that there are several ways to do this,
there is no doubt that estimating the rate of change dictates that a threshold
test should be employed. The authors also suggest that examining mean deviation
or mean defect (MD) over time is probably the best compromise between sensitivity
to change and specificity in the face of variable results. Furthermore, you should
not chop and change. It is best to stick with the same thresholding algorithm
and visual field pattern if possible and changes should be made only when compelling
reasons exist. If resources are tight, no other functional (SWAP, FDT) or structural
(CSLT, OCT, SLP) test should be used in place of SAP. In other words, if you
can only do one test (other than IOP) then make it SAP.
Perhaps the most striking recommendation is that six visual field exams should be performed in the first two
years of management. The logic behind this suggestion is two-fold. First, it will afford the clinician a decent
chance of detecting those eyes bound for a very rapid rate of decline and second, it will establish a very good
baseline and thus enable some determination of the rate of change in those eyes that are going to have a more moderate
or slower course to be detected. However, six tests in two years represents a minimum. If your patient has major risk
factors for progression and visual impairment (i.e. suspicion of ONH change within the interval, poor IOP control,
morbidity in the fellow eye) or is slightly more variable than average, then it might be prudent to perform even more than six tests.
If you are thinking that six tests in two years sounds like too many then take a look at what rate of change you can
reliably detect using such a schedule (their Tables 1 & 2). Given the expected test–retest variability for MD, a -2dB
change should just be statistically detectable with five or six tests in two years. This represents a -1dB per year
rate of decline. If we bear in mind the patient’s age, their life expectancy and that significant increases in rates
of driving accidents and falls occur even when relatively early visual field damage exists, it is easy to see the
increased risk this kind of patient is exposed to if we do not detect such a visual field trajectory quickly.
Even though Chauhan et al recommend using a trend based analysis, in this case the linear regression of MD over time,
event based analyses have been used in several of the large scale glaucoma clinical trials (OHTS, EMGT) and there may
be situations where event based analyses are preferable. Ease of implementation and clinicians’ comfort and understanding
of different analysis techniques may be part of the glaucoma progression equation that was not explored in this
important paper. However, a similar number (or density) of visual field exams would likely be required to reliably
detect change even when using event based analyses, nonetheless consistent with one of the essential recommendations
of this stimulating paper.
Shaban Demirel BScOptom, PhD.
1. Chauhan BC, Garway-Heath DF, Goñi FJ, Rossetti L, Bengtsson B, Viswanathan AC, Heijl A. Practical recommendations
for measuring Rates of visual field change in glaucoma. British Journal of Ophthalmology, 2008;92:569-573.
IMAGE REVIEW
Figure 1 and 2 show retinal photographs of the right eye. The image on the left ( Figure 1A, 1B)
shows the 2003 appearance while the image on the right (Figure 2A, 2B) shows the development of a retinal nerve fiber
layer (RNFL) defect at the 7 o’clock position that was visible in 2007. Figure 1B and 2B are magnified views of
Figure 1A and 2A. The rim tissue looks thinner both superiorly and inferiorly in 2007.
Figure 1a.
 |
Figure 2a.
 |
Figure 1b.
 |
Figure 2b.
 |
Figure 1A shows retinal photographs of the right eye. The image on
the left shows the 2003 appearance while the image on the right
shows the development of a retinal nerve fiber layer (RNFL) defect
at the 7 o’clock position that was visible in 2007. Figure 2B shows
a magnified view of Figure 2A. The rim tissue looks thinner both superiorly
and inferiorly in 2007.
The HRT OU report (Figure 3A- September 12, 2007) shows change in OD as seen by the
red-colored pixels at the inferior rim tissue. Asymmetry is noted as the right optic
disc is shown to have a larger cup, thinner rim tissue, and a greater
number of sectors flagged on the Moorfields Analysis. Figure 3B shows
the topographic change report with change first seen in 2005, and
confirmed over the next two visits. The red area on the reflectance
images at 7 o’clock confirms that this area has become thinner statistically
when compared to the baseline examinations. Figure 4 shows the OCT
image, which confirms that the RNFL is thinner inferiorly OD when
compared to the patient’s OS and the instrument’s
internal normative ranges. Although the OCT scans are in agreement
with the other imaging modalities, it should be noted that the
scan location relative to the optic disc cannot be confirmed in
the right eye because of artifact over the fundus image, and it
is decentered inferiorly in the left eye, which would cause the
RNFL to appear thinner inferiorly and thicker superiorly. The
TSNIT curve shows loss inferiorly for the right eye, which is
also seen in the sector and quadrant graphs. The OS appears to
be within normal limits. Figure 5A shows the GDx symmetry analysis
performed on an image taken in September 2007. The OD has an NFI
of 38 along with a dark region showing loss on the Right RNFL
map and pixels flagged in the OD superiorly and inferiorly. The
dark spot on the OS image inferonasally is due to a vitreous floater
obscuring the view of the retina. Other than this artifact, the
OS appears to be healthy. The printout found in the middle of
the page shows that the OD RNFL is reduced when compared to OS.
Figure 5B shows the GPA for the GDx, a recently released software
tool. Likely progression is noted in the image progression map,
TSNIT progression graph, and summary parameters. The image progression
map shows change in both the superior and inferior RNFL (red colors).
The TSNIT progression graph also shows change inferiorly and superiorly.
The inferior average summary parameter graph shows the steepest
slope, with significant change noted. The bottom of the printout
summarizes the changes found, with loss greatest inferiorly.
Figure 5a.
 |
Figure 5b.
 |
When progression is noted, reevaluation of the therapeutic regimen needs to occur. Often further IOP reduction
is indicated, either by the addition of medication if possible or the use of laser trabeculoplasty or
filtration surgery. In this case, dorzolamide (Trusopt) was added and the IOP was reduced by a further
2 mm Hg. Imaging in this case was done yearly but an option could be to image more frequently often
immediately after the diagnosis is made because at least five images are needed for the software
progression tools to work efficiently.
Murray Fingeret, OD

QUARTERLY CASE
Glaucoma discovered at comprehensive eye examination.
A 48-year-old white female presented for routine eye examination in November 2006. She had no ocular or visual complaints
other than blurred distance vision without correction. She reported no previous visual or ocular problems. She did report
that both maternal grandparents had been diagnosed with glaucoma. She wore primarily rigid gas-permeable (RGP) contact
lenses for myopia correction. She was unsure of the date of her previous eye examination.
Her medical history was unremarkable except for a hemithyroidectomy for which she has taken Synthroid (levothyroxine,
50 mcg/day) since 1977. Thyroid function had been in the normal range. Her vision was corrected to 20/20 in each eye.
With monovision RGP contact lenses, she functioned optimally.
A screening visual field examination (FDT, C-20-1) revealed inferior depressions in the right eye and normal sensitivity
in the left eye. (Figure 1) Applanation tonometry was 16/16 mm Hg (OD/OS). All other aspects of the dilated fundus exam
were normal, with a cup-to-disc ratio (CDR) of 0.5 and average optic disc diameters in each eye. The cup appearance was
felt to be within the range of normal variability. Photographs were not taken at this time. She was asked to return for
further testing to determine the nature of the apparent visual field depressions shown by FDT.
|
Figure 2.
 |
The patient did not return until February, 2008, at which time a reproducible visual field defect (FDT) was confirmed for the
right eye with and without the contact lens; the left eye was normal again. (Figure 2) Intraocular pressure (IOP)
was 16/17 mm Hg (OD/OS). All other aspects of the dilated fundus exam were again within normal limits, and a CDR of
0.5 was recorded for each eye. Again, the discs exhibited normal appearances, with neither disc pallor nor RNFL defects
observed. A reliable full threshold central 24-2 visual field test was completed during the same month. The inferior
visual field defect (OD) was present at this examination with a full visual field (OS) recorded. (Figure 3)
Figure 3a.
 |
Figure 3b.
 |
In April, 2008, the patient returned for optical coherence tomography (OCT) to determine whether RNFL losses were associated
with the visual field defects. Scans of the right RNFL showed significant thinning of the nerve fiber layer in the superior
quadrant, and markedly decreased rim tissue in the superior optic nerve. (Figure 4) All parameters were within normal range
for the left eye. (Figure 5) IOP was 17/17 mm Hg (OD/OS).
Figure 4.
 |
Figure 5.
 |
The patient returned in May, 2008 for a review of findings. IOP was 19/19 mm Hg (OD/OS) at this visit. Pachymetry
measurements taken at this time were 520/528 microns (OD/OS). The ciliary body was visible in 4 quadrants of each
eye on gonioscopy. Findings for the right eye included the presence of repeatable VF depressions, superior RNFL thinning,
with subtle shelving of the superior neuroretinal rim in the corresponding sector of the disc. For the left eye, no
visual field depressions or RNFL defects were evident. There appears to be a RNFL defect in the inferior temporal
aspect of the left eye. This is not seen with the OCT, so it is possible that it could be attributed to photographic
artifact. However it does arouse suspicion given the right eye presentation, and will therefore need to be followed closely.
A diagnosis of open-angle glaucoma was made. She was placed on timolol maleate
0.5%, one drop in the morning in both eyes. This regimen was chosen for simplicity
in the absence of contraindications and for cost considerations. The patient
accepted the recommendation to treat both eyes rather than just the one that
demonstrated the repeatable perimetric changes. Target IOP was set to the low
teens.
Figure 6a.
 |
Figure 6b.
 |
The possibility that the patient had non-glaucomatous field loss was considered. However, the close correspondence
between the optic disc appearance and field defects in May 2008 made neuro-imaging a more remote consideration.
At a follow-up visit two weeks later, intraocular pressure was unresponsive. The patient was asked to return in a
further two weeks under the same dosing regimen prior to consideration of changing dosing frequency or drug class.
The plan was dependent on outcome at that time: the choice of whether to continue the current regimen, to increase
dosing frequency or to change to a prostaglandin analog will be made at that subsequent visit. (1)
This case illustrates that in primary care practice, undiagnosed glaucoma patients can present for routine eye
examination. This patient was a contact-lens wearer without an immediate family history or other risk factors for glaucoma.
Although it is less common for visual field changes to precede optic disc changes
in glaucoma, it is not unprecedented. In the Ocular Hypertension Treatment Study,
conversion to glaucoma amongst untreated individuals was identified more commonly
by optic disc changes (57.3%) than visual field changes (32.6%), with concurrent changes occurring in 10.1%,
although OHTS study data are not generalisable to this case because IOP was not
found to be elevated (2).
It has become well known that glaucoma remains unidentified in roughly half of
all cases in the United States, although some suggest that as many as 90% of cases are undiagnosed (2-4).
It is likely that this applies broadly to all types of open-angle glaucoma in reports from around the world (5).
As recently as 2008, results of the Thessaloniki Eye Study revealed 50% of
glaucoma was undiagnosed. The most common reason reported from that study was
patients not attending for periodic routine eye care. Dependence on elevated
intraocular pressure alone, rather than visual field testing and careful scrutiny
of the optic nerve head and RNFL will inevitably lead to failure to detect glaucoma.
In this case, periodic eye examination was the reason for the visit to the optometrist
and further testing, suggested by screening visual field results and corroborated
by careful optic disc examination at follow-up, revealed early stage glaucoma.
One item significant in the patient’s history is hypothyroidism. Although medically-regulated thyroid
function may represent a risk factor for glaucoma, there is controversy surrounding this connection. This patient’s
hypothyroidism was surgically induced at age 19. Since that time she has taken
thyroid supplementation. While most of the recent literature concerning hypothyroidism
and glaucoma seems confusing, one postulate is that hypothyroidism may cause
increased corneal thickness that results in artificially elevated estimates of
IOP. In this study, no correlation between thinned RNFL was made with elevated
IOP (6). Also, several IOP readings were taken before therapy was initiated.
Time of day unfortunately was not recorded in the chart.
James D. Fisk, OD, PhD and Leo Semes, OD
References
1. Singh K, Lee BL, Wilson MR; Glaucoma Modified RAND-Like Methodology Group. A panel assessment of glaucoma management:
modification of existing RAND-like methodology for consensus in ophthalmology. Part II: Results and interpretation. Am J Ophthalmol. 2008;145:575-581
2. Kass MA, Heuer DK, Higginbotham EJ, Johnson CA, Keltner JL, Miller JP, Parrish RK 2nd, Wilson MR, Gordon MO.The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002 Jun;120(6):701-13;
3. Sommer A, Tielsch JM, Katz J, Quigley HA, Gottsch JD, Javitt J, Singh K. Relationship between intraocular pressure and primary open angle glaucoma among white and black Americans. The Baltimore Eye Survey. Arch Ophthalmol. 1991;109:1090-5.
4. Topouzis F, Coleman AL, Harris et al. Factors associated with undiagnosed open-angle glaucoma: the Thessaloniki Eye Study.Am J Ophthalmol. 2008 ;145:327-335.
5. Sakata K, Sakata LM, Sakata VM, et al. Prevalence of glaucoma in a South Brazilian population: Projeto Glaucoma. Invest Ophthalmol Vis Sci. 2007; 48:4974-9.
6. Bahçeci UA, Ozdek S, Pehlivanli Z, Yetkin I, Onol M. Changes in intraocular pressure and corneal and retinal nerve fiber layer thicknesses in hypothyroidism. Eur J Ophthalmol. 2005; 15: 556-61.
For a full reference list for this case please click here.
MELTON AND THOMAS THEIR VIEWS
Switch or add in glaucoma therapy?
Medical therapy for the glaucomas is thoroughly heterogeneous. As most therapies in all fields of medicine,
the "art/science" continuum
varies widely. We long for the day when "science" is 90%, and "art" is only 10% of the
equation in our patient care decision making, but for now, "art" is the predominant factor in glaucoma care.
For all the wonderful studies published over the past decade, the care of individual patients remains largely
a physician’s decision.
"Adding" medical therapy is clearly the observable modus operandi of glaucoma care. Face it, adding is just
plain easy; just keep stacking on the medicines until the target IOP is reached. Combination medicines further
fuel this "throw the sink at it" mentality.
"Switching" requires relatively laborious effort, a little extra cerebral energy, and probably more office
visits; however, patients merit the very best of our clinical efforts.
Scenario A could be: initial therapy with a once-a-day medicine such as a prostaglandin analog (PGA) or a
non-selective beta-blocker (with a sufficiently long half-life such as timolol of levobunolol). If at least
a 20% reduction in IOP is achieved, this medicine can be considered "effective." If, however, the initial
drug does not achieve target IOP, then we recommend setting the initial drug aside (at least temporarily), and
trying the other "once-daily" medicine alone to see if it can achieve target IOP. If both medications achieve
at least 20% IOP reduction, then try using the beta-blocker in the mornings and the PGA in the
evenings thus yielding twice daily therapy.
Scenario B could be: the beta-blocker did not achieve more than a 10% effect (or, for whatever reason,
it could not be used). The PGA performed as expected, but failed to achieve target IOP. Now the question is
whether to choose a topical carbonic anhydrase inhibitor (CAI) or an alpha-adrenergic agonist. Either way,
the patient will now be instilling three drops per day. In our experience, our success rate is roughly
equal between these two drug classes. We typically start with a topical CAI, and default to an alpha-agonist
if the CAI does not achieve target IOP.
Scenario C could be: the PGA did not provide more than a 10% reduction in IOP, and therefore would be
considered a PGA failure. We do not switch intraclass. The beta-blocker came close, but failed to achieve target.
Now and only now would it be prudent to try adding either Cosopt or Combigan to the PGA, since we
have already established the efficacy of the beta-blocker component. We would never add any combination drug to a
PGA, unless we had established lack of target IOP achievement with at least one component of the combination drug.
As can readily be seen, intelligence and thoughtful switching is superior to adding in most cases. At a time
when "polypharmacy" is observably epidemic, we encourage all glaucoma clinicians to strive for a minimally
invasive, maximally simple therapy.
There are many such "switching" (and "adding") possibilities. We hope this brief overview will stimulate our
colleagues to strive for utopic therapeutic intervention.
Randall K. Thomas, OD Ron Melton, OD
MEETING REVIEWS
ARVO 2008 Round-Up. How glaucoma affects functions required for daily life.
This year's annual meeting of the Association of Research in Vision and Ophthalmology (ARVO)
was again held in Fort Lauderdale, Florida, from April 27th to May 1st. Over 4500 abstracts
were registered for presentation and you can search these online at ARVO's website. Although information on glaucomatous
loss of visual function, such as central visual field testing, is an essential tool for each
patient's clinical management, the poor and variable relationship between visual field
test outcome with conventional quality of life measures strongly suggest that
neither are useful at informing us about how glaucoma affects functions required
for daily life. A number of presentations at this year's ARVO explored this theme,
investigating the degree to which glaucoma impacts on life, both in terms of
aspects of vision not commonly measured in clinical situations, and also more
generally. An investigation of the impact of glaucoma on reading was reported
by Ramulu et al. of the Wilmer Eye Institute (program no 5447). This study was
part of a population-based, cross-sectional evaluation of visual function and
disability in the elderly. Both reading impairment (defined as reading <=90 words/minute) and
reading speed were evaluated at four different text sizes. Univariate analysis revealed a
significantly (p=0.006) greater proportion of reading impairment in individuals with
bilateral glaucoma (28.4%) than individuals without glaucoma (16%). For all text sizes,
average reading speed was slowest amongst study participants with bilateral glaucoma, and fastest
for individuals without glaucoma. Although the differences were not statistically significant when
all degrees of glaucoma were grouped together, they became highly significant (p=0.005)
when those with worst field loss only ('bilateral glaucoma, highest quartile visual field damage')
were compared with controls, with such individuals reading on average 37 words less per minute
than those without glaucoma, representing a reduction in reading speed of approximately 25%.
These data appear powerful due to the cross-sectional 'population study' design, although the
completeness of the sample was not reported, and as such some selection bias may be present.
Another study by Smith et al of City University, London (program number 1110) considered a different
type of visual outcome, that being an exploration of eye movements in glaucomatous patients when
viewing photographs. Their study used a case-control design with controls being age-matched to the
glaucoma patient group, who were recruited such that binocular field loss was present, with at
least two depressed Humphrey Field Analyzer test locations on binocular fields (integrated threshold
sensitivity levels of <20dB). Eye movements were measured using a head-mounted gaze-tracking device.
Two specific experiments were performed. Firstly, subjects were asked to look passively at a series of
photographs as they would when viewing a slideshow. Under these circumstances, subjects with glaucoma
had a decreased number of saccades, viewing area and increase in fixation duration compared to controls.
The second experiment comprised a search task and subjects were asked to locate a specific item or
location in an image in each of a series of photos. In this viewing scenario, glaucoma patients made, on
average, significantly fewer saccades had greater saccade amplitude and fixation duration than controls
and took longer to find the search item. The investigators concluded that patients with glaucoma exhibited
altered eye movements and search patterns compared with controls. Discussion with the author at the poster
provided some insight into the research group’s ongoing and future work which includes investigation of
the relationship between the point of regard and spatial location of binocular field defects.
Black et al. from Queensland University, Brisbane, Australia investigated the relationship between visual
field loss and falls amongst older patients with
glaucoma (program number 5458). Amongst a sample of 74 glaucoma patients aged
over 65 years, they found that 35% of participants had fallen on at least
one occasion in the previous twelve months, although no control data was available
for comparison. Postural instability was measured on even and uneven surfaces
using a Swaymeter and
was found to be significantly associated with binocular field loss, with the
rate of falls doubling for every 9dB reduction in Mean Deviation of a subject's
24-2 Sita-Standard HFA result in their better-eye. Potential confounders, such
as general health or systemic medication were not controlled by the observational
study design.
An exploratory study of eye-hand coordination deficits in glaucoma was presented by Kotecha et al
(program number 1158), also from City University. This case-control study investigated the reaching
and grasping behaviour amongst a group of glaucoma patients with early to moderate visual field loss
in their better eye (MD range =-3.5 to -10.2dB). Hand movement kinematics were initially captured
on digital video and converted into digital 3D plots from which spatial behaviour (such as position
and velocity) of predefined points on each patients hand could be quantified when the subject was asked
to move their hand to grasp a given object in a set location.
A digitised
3D plot from Kotecha et al. The large green object is
a cylinder which subjects were asked to grasp. Movements
of fixed locations on each subjects hand (shown as red,
blue and black circles) were used to quantify hand movements.
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Patients with glaucoma were found to
have significantly slower hand movement initiation and poorer reaching dynamics, such as the time to reach
peak hand velocity and a prolonged duration of the deceleration phase of movement occurring when a hand
homes-in on an object ('low velocity profile'). The authors concluded that patients with asymmetric
visuals field loss and relatively minor binocular field defects show deficits in prehension compared
to controls with normal visual fields.
These studies show that we are only beginning to figure out how daily tasks are affected by
glaucoma and that other outcomes, in addition to visual fields help to provide more detailed
information on this subject.
Paul GD Spry PhD BSc MCOptom DipGlauc
International Perimetric Society focussing beyond the visual field
The International Perimetric Society (IPS) biannual
meeting was held at Nara, Japan on May 21-24, 2008. In general, the meeting and the accompanying social program
were exceptionally good. Nara is the historical and spiritual center of Japan, and the Convention Center is located
in the center of Nara Park. Attendees and accompanying persons were treated to an opening banquet that included
entertainment from a drum and percussion group, a Japanese dinner with musical entertainment, a feeding of the
deer, a Noh dramatic performance, a walking tour of the grounds in Nara park, and a magnificent closing banquet
complete with its tradition of singing in national groups.
In my opinion, the quality and content of the presentations at this IPS meeting were the best of any IPS meeting.
Sessions incorporating papers and posters related to structure/function relationships, optic nerve head and nerve
fiber imaging, brain changes in monkey models of glaucoma, new perimetric techniques, comparison of tests, visual
field analysis procedures, and glaucomatous progression were presented. In many instances, the papers included
empirical results, statistical analysis, mathematical modeling and well-constructed experimental designs. It
was clear that all presenters had conducted a creative and thorough evaluation of their research topic. Although
the presentations were of high relevance and quality, none stood out from all the others, which is an indication
of the high caliber of this meeting. In particular, several keynote presentations were given by Drs. Michael Patella,
Anders Heijl, Yijun Huang, Fritz Dannheim, Masaaki Sasaoka, Ron Harwerth, Ulrich Schiefer and Yoshi Kitazawa.
Dr. Dannheim was the IPS lecturer and spoke about the history of optic disc evaluation in glaucoma, and Dr. Heijl
was the Aulhorn lecturer and spoke about the rate of visual field progression in glaucoma. In an attempt to
encourage attendance by other investigators with related interests, the name of the group was changed to
the Imaging and Perimetric Society, embracing the new focus while keeping the several decades old acronym (IPS).
In all, the 2008 IPS meeting was a most worthwhile intellectual encounter blended with generous amounts of
entertainment, social interaction and collegiality among its members and guests. It is my sincere hope
that this excellence will continue to grow for succeeding IPS meetings.
Chris A. Johnson PhD
CLINICAL QUESTIONS AND ANSWERS
If you would like us to answer a clinical question, please
send it to paul.spry@uhbristol.nhs.uk with "OGS question"
as the subject. 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.
NEWS
All Eyes on Glaucoma Website
A new online resource to help clinicians was recently launched.
The Optic Nerve Resource Center, www.alleyesonglaucoma.com, is
a tool that will be useful to optometrists to learn about the latest technologies available to examine the optic nerve to detect anatomic damage, potentially before functional vision loss. The goals of the site are to provide online educational resource for eye health
professionals to review optic imaging technologies, highlight the role of optic nerve imaging techniques in detecting ongoing
structural changes in glaucoma and reinforce the importance of ongoing optic nerve assessment in management of glaucoma.
The site will be updated as new technologies become available.
Joint Meeting of the Optometric Glaucoma Society and the American Academy of Optometry
On Wednesday morning, October 22, 2008, the Optometric Glaucoma Society (OGS) will hold its first joint meeting
with the American Academy of Optometry (AAO). All attendees of both the OGS and AAO meetings are invited to attend,
with the symposium occurring as part of the AAO annual meeting. Brad Fortune, the program chair, has put together
a stellar program with the 8-10am session titled Pathogenic Mechanisms of Glaucoma. The different mechanisms for
why glaucoma may develop will be presented by Douglas Anderson, Claude Burgoyne, John Morrison and Jack Cioffi.
The second session (10am-12pm) is titled Clinical Implications: Pathogenic Mechanisms of Glaucoma with the same
speakers explaining why understanding the different pathogenic mechanisms is important for the clinician.
The program will take place at the Anaheim Convention Center in room 207 A/B.
World Glaucoma Congress 2009
The Optometric Glaucoma Society and the World Glaucoma Association
would like to invite optometrists to attend the 2009 World Glaucoma
Congress (WGC), to be held in Boston, MA from July 8-11th. Clinicians
and scientists from around the world will come together to discuss
and learn about glaucoma. The world’s experts will be present in a
forum only seen every other year. This is the first time the WGC is
being held in North America, and should provide a great learning environment
for all ODs.
i2i: Conversations to Enhancing Adherence
A program titled i2i:Conversations to Enhance Adherence will take place during the upcoming American Academy of
Optometry annual meeting.
The program will take place on Wednesday evening, October 22, 2008 at the Sheraton Park Hotel in Anaheim, CA.
Steven R. Hahn, MD and David S. Friedman, MD will be the presenters with Murray Fingeret, OD the moderator.
This program is similar to one presented at the AAO in Denver that was very well received.

Editor
in Chief
Paul Spry PhD MCOptom
Associate Editors
Brad Fortune, OD,
PhD
Shaban Demirel, BScOptom,
PhD
Algis Vingrys BScOptom,
PhD
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Editorial Board
Douglas Anderson MD
Paul Artes PhD MCOptom
Dick Bennett OD
Murray Fingeret, OD
Ron Harwerth, PhD
Chris Johnson, PhD
Tony Litwak, OD
John McSoley, OD
Ron Melton, OD
Bruce Onofrey, OD, RPh
Leo Semes, OD
Randall Thomas, OD
Thom Zimmerman, MD, PhD
Art/Production Director
Joe Morris
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