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Volume 10, Number 2

July 2001

 

 


Research Update and New Members Highlight Board Meeting

 

Inspiring words from Glaucoma Service Research Center Director Dr. William Steinmann and the introduction of three new Board members highlighted the June 5 meeting of the Board of Trustees of the Glaucoma Service Foundation.

 

Dr. Steinmann spoke to 24 Board members and guests about the Center’s great progress since moving into its new quarters at 901 Walnut Street, propelled by his vision of the research enterprise as the “Tiger Woods of clinical research.”  The Center, he explained, is young and attempting to do something that has not been done before and do it superbly well:  building a model of a great clinical research foundation focused on glaucoma.  An important aspect of this is what he referred to as a “transparence” between clinical and research activities:  every patient has something to teach us, and everything we learn from patients contributes to their care.

 

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Board member Mr. Stanley Tuttleman (left) and Wills Eye Hospital CEO D. McWilliams Kessler at the June 5 Board meeting.
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Board member Ms. Nettie Taylor (left) and Board Chairman Mr. S. Stoney Simons at the June 5 Board meeting in the Wills Eye Hospital auditorium.  Ms. Taylor has been active in promoting glaucoma screenings at area churches.  See Mr. Simons’ in article below.

Photos by Robert Curtin

 

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New Members Introduced

 

Three new Board members were introduced at the meeting:  Ms. Megan Brunner, Dr. Andrew Medcalf, and Ms. Bonnie Carr Long.  In addition to running her own marketing and public relations consulting business in Paoli, PA, for over 20 years, since 1993 Bonnie Carr Long has been Vice President, Marketing for Home-Nurse, Inc. in Wayne, PA.  Ms. Long has the distinction of having been one of Dr. George Spaeth’s first patients when he started the Glaucoma Service of Wills Eye Hospital now nearly 40 years ago.  Frequent headaches and a family history of glaucoma led her to Dr. Spaeth when she was 19, during her sophomore year in college.  The diagnosis: primary open-angle glaucoma.  The treatment: two different drops, four times a day.  The drops caused so much blurring that she found she could study for only short periods each day.  Ten years later she underwent trabeculectomy in both eyes.  Today she remains without any loss of visual field, on no medications.

 

“I am excited about the possibility of contributing to the Foundation’s mission of education and research about glaucoma.  I was lucky in the sense that my glaucoma was caught very early on.  We have to develop screening techniques to enable us to find people who are in the very early, most treatable stages of the disease.”

 

Born in England, Dr. Andrew Medcalf received his Ph.D. in Cancer Research from the University of London.  For 10 years he was a research scientist at the Institute of Cancer Research in London and at Michigan State University.  He subsequently founded and operated a consulting firm in the field of environmental toxicology.  For the past three years he has been a Financial Advisor at Legg Mason.  Dr. Medcalf has coached rowing at the University of London, the University of Rochester and now at the University of Pennsylvania.

 

It was while rowing in London when he was 27 that he noted a milky film develop across his right eye.  This disappeared but not long after he saw haloes with his right eye.  An acute attack of angle closure in his right eye brought him to the famous Moorfields Eye Hospital in London.  The pressure was 40 mm Hg.  Treatment with a laser to reduce the pressure was not as relatively painless and problemfree as it is today.  In 1979 it was painful and did not work immediately.  He was placed on Timoptic and pilocarpine, which kept his pressure in the mid-20s.  Later that year he underwent a trabeculectomy in his right eye.  At that point he learned ocular massage, which he still does daily.  Not long thereafter a trabeculectomy was done in his left eye.  When his ophthalmologist in Rochester, New York, heard he was moving to Philadelphia, he recommended Dr. Spaeth.  Now he is off medications, and his visual fields are stable.

 

Says Dr. Medcalf: “I am pleased that I may be able to use my medical research background and experience with glaucoma to further the Foundation’s goals.”

 

Megan Brunner has worked for a financial services company in Oaks, PA, for the past eight years.  About 10 years ago, when she was being treated for cornea and other eye problems by Wills doctors Jonathan Belmont and Irving Raber, they referred her to Dr. Marlene Moster for a glaucoma evaluation.  She was on eye drops for about six years before she eventually had tube-shunt procedures in both eyes.  Her glaucoma has been under control for the last two years, but she still classifies herself as having low vision — she is unable to drive, and makes frequent use of a magnifying glass.

 

She states that she made a New Year’s resolution to get involved with a charitable organization.  Although she now sees her glaucoma as a “nuisance,” making her job and being mother of a two-year- old more difficult, she feels that she is fortunate.  She is looking forward to her work with the Foundation Board: “I hope I can be of some help to others struggling with glaucoma.”

 

 

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Megan Brunner
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Andrew Medcalf, PhD
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Bonnie Carr Long

Photos by Robert Curtin

 

 

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In Perspective

 

The Challenge and Promise of Glaucoma Research

George L. Spaeth, MD

 

Each May the Association for Research in Vision and Ophthalmology has its annual meeting.  This has grown from a get-together of research-minded ophthalmologists and Ph.D.’s meeting in several small, simple hotels on a beach in Sarasota to a meeting at which thousands and thousands of researchers from around the world congregate at Ft. Lauderdale to present the results of their studies, to discuss their findings with others, and to learn what others are doing.  There were hundreds of presentations in the section dealing just with glaucoma.

 

That so much attention is being focused on glaucoma is surely exciting news for all those whose lives have been touched by it.  At the same time, however, one would think that with all the effort going on the problem of glaucoma would long since have been solved.

 

Glaucoma: A Different Kind of Disease

 

This apparent paradox arises perhaps because we tend to think of disease on the model of small-pox, for example, a disease successfully eradicated by dedicated research.

 

But glaucoma is a dramatically different kind of disease.  Smallpox has a highly specific cause, is easily recognizable, and affects only one species, the human.  Smallpox is caused by a virus related to a different virus, which causes cowpox in cattle.  The two viruses are enough alike that when a human being is exposed to cowpox, that individual develops the antibodies that will allow it to prevent itself from getting smallpox if in the future it is exposed to the smallpox virus.  The World Health Organization recognized that if virtually everybody in the world were vaccinated for smallpox the number of individuals who would contract smallpox would become so small that it might be possible that there would not be enough individuals to infect other people.  And indeed that is what happened.  A massive campaign across the entire planet to vaccinate human beings to prevent them from contracting small-pox brought magnificent results:   smallpox as a disease no longer existed.

 

“With effective research, education, and medical systems, it is possible that in the future no person would ever lose vision as a result of glaucoma.”

 

Glaucoma is a very different kind of disease, requiring a very different kind of research strategy.  In the first place, glaucoma is not a specific disease, but rather a complex group of diseases affecting different tissues in different ways with different causes and different treatments. Secondly, none of the various kinds of glaucoma are caused by a virus, but rather are most likely the result of genetic defects.  The only way to eliminate the pain and disability caused by smallpox was to eliminate the disease entirely. This is not the case with glaucoma.

 

Let us consider the mechanism for one type of glaucoma, acute primary angle-closure glaucoma.  This condition is known to be related to a small front part of the eye, and in almost all individuals can be prevented by performing a peripheral iridotomy (making a small hole in the iris with a laser). Performing a peripheral iridotomy on every person predisposed to developing primary angle-closure glaucoma would almost completely eliminate the disease in those individuals in whom the iridotomy was performed.

Still, we cannot say that we have eliminated angle-closure glaucoma in the way that smallpox was eliminated. Individuals with small fronts of the eyes will still pass on the predisposition to this type of glaucoma to the next generation. However, what we have done, practically speaking, may be nearly as good: we have the knowledge enabling us to eliminate all of the disability and pain caused by angle-closure glaucoma.

 

Research Strategies

 

Angle-closure glaucoma is only one of many, many types of glaucoma.  Different strategies need to be developed for each of them.  Nevertheless, the fact that most of the glaucomas involve the injury and potential death of the ganglion cells of the retina suggests common, promising, research strategies.

For example, much research is being done on the nature of those ganglion cells and how they can be protected.  Very likely such research sooner or later will bear good fruit, allowing many patients with many different types of glaucoma to be helped.  A longer-term and more complicated strategy lies in genetics.  In his article in this issue of the Searchlight, Dr. Rhee talks about these and other research approaches.

 

True, none of these strategies will eliminate glaucoma in the way that smallpox was eliminated.  Glaucoma will probably be a part of human existence for as long as there are humans.  But with effective research, education, and medical systems, it is possible that in the future no person would ever lose vision or develop pain as a result of glaucoma.  That is worth working to achieve!

 

 

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What's Hot?

The New Phosphene Eye Pressure Monitor

Marlene R. Moster, MD

 

People with glaucoma usually have an intraocular pressure (IOP) too high for their eyes to tolerate, risking damage to the optic nerve and eventual loss of vision.  Lowering the pressure decreases the risk of damage.  Measuring intraocular pressure (IOP) is crucial in the diagnosis and treatment of glaucoma.

All glaucoma patients are familiar with the “pressure check” in which a drop of anesthetic is placed on the eyeball and a device to measure the pressure is placed directly on the eye.  The gold standard for IOP measurement is the Goldmann tonometer, which measures the force required to flatten a small area of the central cornea.  The accuracy of the Goldmann tonometer is well established to within 1 to 2 mm Hg.

 

The problem is that IOP tends to vary throughout the day and night, and the pressure the doctor measures in the office, maybe every month or even every week, cannot reflect this variation.  Until now the only way to get a more accurate picture has been to have the patient spend all day in the office, having the pressure checked at regular intervals.

 

Measure Your Own Intraocular Pressure

 

Wouldn’t it be nice if patients were able to measure their intraocular pressure at home as prescribed by their doctor and report the results to him or her?

 

Enter the new Proview™ phosphene eye pressure monitor marketed by Bausch and Lomb, scheduled to be released this summer.  It’s portable and requires no anesthetic or skilled technician.  Invented by Bernard Fresco, O.D., the instrument relies on a phenomenon known as “phosphene,” recognized as long ago as by Aristotle in ancient Greece.  A phosphene is a sensation of light produced in the eye by something other than light.  You can easily observe a phosphene caused by mechanical pressure by gently pressing with your finger on the eyelid where it meets the nose.  This pressure phosphene typically appears as a bright central area surrounded by a dark ring with an outer bright halo.

 

The Proview eye pressure monitor is a pencillike device which contains a small flat probe, an internal spring, and a readable pressure scale.  The IOP is measured through a half-closed eyelid by applying gentle pressure with the monitor in the upper portion of the eye near the nose. Because the IOP is measured through the lid it is painless and requires no anesthesia.  As soon as the patient sees his or her pressure phosphene ring, the indentation is stopped and the IOP can be read directly off the scale.  The phosphene eye pressure monitor never touches the eyeball directly, thus reducing the chance of infection or injury to the eye.

 

How Does the Phosphene Eye Pressure Monitor Compare?

 

Dr. Fresco reported the comparative results of IOP measurements obtained in 100 patients by both the phosphene eye pressure monitor and the Goldmann tonometer.  Impartial observers checked the IOPs, and the results obtained by each observer were not shared with any other observer.  Dr. Fresco found that in 51% of the eyes the differences in the pressures measured by the two devices were with-in ± 1 mm Hg of each other, in 74.9% within ± 2 mm Hg, and in 90% within ± 3 mm Hg.

 

Although the possibilities introduced by this handheld device are exciting, many questions remain.  At Wills, we will be conducting a prospective study to evaluate the device in terms of its accuracy, ease of use, and compatibility with patients’ lifestyles during home use.  After gathering these data, we will be able to determine if indeed the phosphene eye pressure monitor is “ready for prime time.”

 

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Using the new Proview™ phosphene eye pressure monitor.

Photo courtesy of Bausch and Lomb

 

 

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VOL10-2I.jpg - 3064 BytesGlaucoma Treatment: On The Frontier

What’s New in Glaucoma Treatment?

Douglas J. Rhee, MD


Dr. Rhee will be the newest member of the Glaucoma Service, when he arrives from the National Institutes of Health in August.  He is a Board-certified ophthalmologist, glaucoma specialist, and molecular biologist.  In addition to caring for his patients, Dr. Rhee is developing directed gene therapy for glaucoma and working to determine the cause of primary open-angle glaucoma.  His clinical research interests involve studying the effects of blood flow to the optic nerve.  He is also scientifically analyzing alternative medicine treatments for glaucoma.

 

In the news, there are so many new and exciting developments in medicine.  Every day, there seem to be new advances in health care.  What’s new in glaucoma?

 

Over the last 12 months, a number of new medications have been released for the treatment of glaucoma.  How new are these drugs? Most of them are updated versions of older medications which may be a little more effective with a slightly more favorable side effect profile than their predecessors.  These are all good things, but all of the drugs, laser and incisional surgeries follow the same paradigm of treatment we have used for the last 100 years — lower the intraocular pressure (i.e., pressure inside the eye).

 

At this time, lowering intraocular pressure is the only scientifically and clinically proven method to slow the progression of glaucoma.  Aside from lowering intraocular pressure, there have been no other proven strategies for the treatment of glaucoma.  This is because the cause of primary open-angle glaucoma is not known. 

 

In the last decade, our understanding of glaucoma has increased dramatically leading to the possibility of new treatment strategies and possible cures.  Most are still in the laboratory testing phase and will not be available for many years.  However, one is closer than you think.

 

Memantine

Memantine (pronounced mem-an- teen) is a medication which has been used for the treatment of Parkinson’s disease.  It does not lower intraocular pressure, but has been experimentally shown to prevent optic nerve damage from excitotoxicity.

 

Excitotoxicity has been shown in experimental animals to be an important component of optic nerve damage from glaucoma that is not dependent on intraocular pressure.  Memantine is now being tested in several selected hospitals to see if it can help prevent further damage from glaucoma.  It has been used safely in people since the 1960s.  If it is proven effective, it will represent the first new treatment strategy for glaucoma in the last 100 years.  The Glaucoma Service is one of the selected centers investigating memantine.  Dr. L. Jay Katz is spearheading our efforts but all of us are participating in this effort.

 

Gene Therapy

 

What about gene therapy? Many of you may have heard about the French researchers in the late 1990s who were the first people to ever successfully treat a human disease with gene therapy.  They cured some patients with SCIDS, Severe Combined Immune Deficiency Syndrome, an extremely rare congenital disease of the immune system.  (Some of you may remember reading about children who had to live in a plastic bubble because their immune system was so weak they would die from the slightest infection.) What about using gene therapy for glaucoma?

First of All, What Are Genes?

 

Genes are in your chromosomes and are made up of DNA.  Genes are in every cell of your body and help determine what makes you, you.  In conjunction with the environment in which you live, genes determine your hair and eye color, height, and likelihood that you will develop a disease – like glaucoma.  More than one gene is responsible for most diseases, including glaucoma.  This means that, although glaucoma can run in families, a person will not necessarily get it because one of his parents had it.  Nevertheless, people whose parents had glaucoma are at a much higher risk for developing it and should certainly see an ophthalmologist.

 

What Is Gene Therapy?

 

Gene therapy refers to inserting into the appropriate tissue a healthy copy of a defective gene that will help diseased cells function better.  When a disease is caused by only one gene, it may be possible to insert a healthy copy of the defective gene, once the gene responsible has been identified, as in the case of SCIDS.

 

I am developing a novel delivery system and approach to gene therapy for glaucoma.  At this stage, it is still in the laboratory phase of testing, but has shown great promise.  I am hopeful that it will one day be a cure for glaucoma. 

 

How Patients Can Help

  • Is there anything you the patient can do to help? You can volunteer to participate in a research trial.  Some trials simply take extra measurements of your eye.  Some trials involve trying a new medication.  When thinking about participating in a new medication trial, you should understand that years of research have been performed to assure the safety of new medications. 

  • You can donate money towards the research efforts of the Wills Glaucoma Service.  Research costs a lot of money in terms of materials, laboratory space, and personnel.  Even the smallest donation helps

  • Some of our patients have elected to give us the most precious gift of all, by donating their eyes to Wills after they pass away.  Without their donation, our research efforts would be greatly impeded. 

 

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Ways to Help Meet the Challenge of Glaucoma

Gifts in Memory of Loved Ones

Joseph Leive, Director of Development, Wills Eye Hospital

 

Many friends of the Glaucoma Service Foundation often ask what they can do to support our work.  Besides contributing to the Annual Fund, many individuals have found that making a memorial contribution in the name of a loved one can be a very meaningful gesture. 

 

Memorial gifts honor the memory of someone you care about and also provide the Foundation with support for its work in research, education, and patient care. 

 

DoveHere’s how a memorial contribution can be made.  Please make a check payable to the Glaucoma Service Foundation in any amount and tell us the name of the individual you are choosing to memorialize.  Please provide us, as well, with the name(s) and address(es) of that individual’s next of kin.  We will let the family know that you have made a memorial gift in their loved one’s name (we do not tell them the amount of your contribution). 

 

Many families are deeply appreciative that such gifts are made at a time of loss.  Please call the Foundation office at 215-503-2986 if you would like additional information.

 

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Share Your Experiences with Other Searchlight Readers

 

Do you have a story about dealing with glaucoma that might be helpful or inspiring to others?  Have you discovered ways of coping with everyday problems resulting from your glaucoma that others might find useful?  The Searchlight wants to be a forum for glaucoma patients to speak to each other.  If you have something to say but need help writing it, let us know and we will work with you.

 

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Searchlight Readers Ask

Link Between Glaucoma and Migraine Headaches?

 

 

Judi Holmes of Terry, Montana, writes: 


“I’d like to know if there is any link between glaucoma and migraine headaches.”

 

Dr. Spaeth answers:

 

The answer to that is a qualified “yes.”  Quite a few years ago a rheumatologist and an ophthalmologist at the University of Iowa noted that there was an increased incidence of a certain type of glaucoma in some patients who had migraine headaches.  That observation has been confirmed by others.  In a study we did, we also found that a certain type of glaucoma that we first described, so-called “focal glaucoma,” in which the optic nerve becomes damaged in a very specific area, appears to occur more frequently in individuals who have migraine than in individuals who do not have migraine.  This particular type of glaucoma affects women about three times as often as men, and is usually seen in people who have relatively low intraocular pressures.  Consequently, it is one of the so-called “low-tension glaucomas.”

 

Because of this apparent association between migraine and glaucoma, a considerable amount of research has been done to see if understanding the mechanisms for migraine would shed light on the mechanisms for glaucoma.  Spasm of the blood vessels was considered a possible common mechanism.  However, this line of research has not been particularly fruitful.  Nevertheless, there is continuing investigation to learn more about this intriguing relationship. 

 

For the moment, migraine should be considered a minor risk factor for the development of glaucoma.

 

 

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Chat Room Praised

 

 

The Foundation Web site recently received the following e-mail:

 

Hi,

 

I’m Helen Russell, 36 years old, from Sydney, Australia. 

 

Thank You, Thank You, Thank You, for your web site. 

 

On Wednesday, May 2, I was diagnosed with Chronic Narrow-Angle Glaucoma after going to see the specialist about my dry eyes. (I am adopted and had no way of knowing my family history.)  A provocative test for Glaucoma saw my pressures go from 11 to 21, and I also had evidence of a weakened corneal lining.

 

I walked out of the rooms in shock and by the time my brain was working it was the weekend.  I started searching the web for information and came across your wonderful site.  Your site answered a lot of my questions, which I rediscussed with my specialist on Tuesday, May 8.  What was so wonderful about your site is that it taught me about my condition when I came out of the shock/ denial stage.  I could then ask my specialist intelligent questions and not waste his time looking for standard information.

 

A peripheral iridotomy was performed on both eyes (May 11 and May 18) and plugs inserted in my tear ducts. 

 

To my delight the digital clock and the microwave oven clock no longer ‘glows’ at night, another surprise that this was not ‘normal’.

 

Once again, thank you.

 

Helen Russell

 

 

 

 

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View from the Boardroom

Glaucoma Research at Wills Eye Hospital

S. Stoney Simons

 

Mr. Simons has been the Chairman of the Glaucoma Service Foundation Board since 1997.  He brings to the Foundation a background of 20 years’ leadership experience at SmithKline Beecham in marketing, research and development, service on a variety of Boards, including those of Chestnut Hill Hospital and Fox Chase Cancer Center, and key positions in health consultancy, insurance, and banking.

 

For generations the Wills Eye Hospital has been a world-class institution whose physicians have provided the best compassionate care for patients and have trained succeeding generations of physicians to treat local and international patients.

 

More recently, the physicians of the Glaucoma Service have recognized that even greater benefits to a greater number of patients can be achieved through organized clinical research, that is, by organizing, combining, and analyzing the findings of many physicians.  The results are impressive.  Just as impressive, they are being widely shared with clinicians and researchers through publications, conference presentations, and through the Glaucoma Service Web site, reaching physicians and patients near and far.

 

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Practical Information for the Glaucoma Patient

Tips for Using Eye Drops

Jeffrey Henderer, MD

 

 

Physicians commonly treat disease with medications, and glaucoma specialists are no exception.  One of the mainstays of treatment is medication designed to lower eye pressure.  Unfortunately, this can be easier said than done.  Despite studies showing that patients frequently do not use glaucoma eye drops as instructed, little attention has been paid to improve this problem.  One reason may be that the patient forgets.  Another may be that the drops are too difficult to get into the eye.  This article will offer tips to overcome these problems.

 

Hints for Remembering

 

Forgetting drops is a common problem.  Generally, the more drops per day, the more chance of forgetting.  Fortunately, most glaucoma drops are used twice a day, although some are used three or four times, and some are used just once.  How should one remember when to use the drops?

First, make a schedule and post it in a prominent place like the refrigerator door.  Check off each drop as the day progresses.  Second, attach the bottle of once-a-day medication to your toothbrush with a rubber band.  This makes taking the prescribed drops easier to remember in the morning or at night . You can place twice-a-day medications near food that you will eat for breakfast and dinner — even in the refrigerator.  This will space the doses about 12 hours apart.

 

Three-times-a-day drops should be used once in the early morning, once in the early to midafternoon and once in the mid to late evening.  Very often the afternoon dose is the hardest to remember.  Placing the bottle in your lunchbox might be a helpful prompt. Placing it on your desk at work might be an option, or in a jacket pocket or purse.  Just be careful that the bottle does not get too hot, however.

 

Four-times-a-day drops are most often given only during waking hours.  Often this means with meals and at bedtime.  After glaucoma surgery, some drops are given up to eight times a day.  This should usually be interpreted as with meals, between meals and at bedtime unless your doctor tells you otherwise.

 

What should you do if you miss a drop?  If it is not too long after you were supposed to put it in, go ahead and do so.  If you missed a dose completely, do not panic.  Just put the next drop in as normal.

 

Hints for Getting Drops in the Eye

 

Once you remember to use the medicine, you must still get the drop in your eye.  This can be a complicated task, especially for those with arthritis. The best way to put the drops in is to have someone else do it for you.

 

If that is not an option, I tell patients about a technique that I learned from Dr. Paul Palmberg at the Bascom Palmer Eye Institute in Miami.  To place a drop in your right eye, hold the bottle between your left thumb and first finger with the tip pointing down.  Take your right hand and curl your fingers halfway toward your palm to make a “C.”  Tip your head back, and use the tips of the fingers of your right hand to pull your right lower eyelid down.  Then rest the heel of your left hand on the back of your right hand.  The bottle should be positioned above your eye, pointing down.  Squeeze the bottle gently and let the drop fall into your eye.  One drop is sufficient.

 

If you keep the medication in the refrigerator, the coolness of the drop will let you know that you got it into your eye.  More than likely, some of the drop will run down your cheek.  This is normal and does not mean that you “missed” or that you need another drop.

 

After putting in the drop, it is generally a good idea to close your eye for a couple minutes while putting pressure on the inner corner of your eye against your nose.  This will close the tear duct and both maximize the drops’ absorption into the eye and minimize the absorption into the rest of your body.

 

Side Effects

 

If you believe that the drops are causing you a problem, call your doctor right away.  Both your eye doctor and your regular medical doctor should be aware of all medicines you are taking.  Eye medications have a wide variety of side effects that can affect both the eye and your body.  Be on the alert for problems of burning, redness, blurred vision, fatigue, sleepiness, trouble breathing and any aches and pains.  All these problems, and more, can be the result of the drops. If your have any problems, stop the drop!  Call your eye doctor and discuss the situation.

 

Even if you are having no side effects, make sure you talk about the drops when you see your doctor. Items to discuss include any changes to your oral medications and unusual or new problems with your eyes.  Mention if you are having difficulty putting the drops in your eye. Be honest about how often you use the drops. If you just can’t remember to use them, another form of treatment may be better.

 

Medication is one of the mainstays of glaucoma treatment.  These tips will hopefully make it easier to use correctly to maximize its benefits.

 

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What’s Up, Doc?

News from the Glaucoma Staff

Jonathan Myers, MD

  • One source of excitement for the physicians on the Glaucoma Service is the release a couple of months ago of the two new anti-glaucoma medications, Lumigan (bimatoprost) (Allergan) and Travatan (travoprost) (Alcon).  These two new medications have both proven to be very effective in clinical trials and our clinicians have been anxious to get a chance to try them for their patients.  Although it is still quite early, several of the staff have noted positive experiences with these agents, with some patients achieving significantly lower pressures.

  • Many of the staff were able to attend the annual meeting of the American Glaucoma Society (AGS) in April.  Several presented results from recent research and everyone enjoyed seeing Dr. Spaeth recognized as “Honored Guest” for his enormous contributions to the field of glaucoma, including being the first President of the Society.

  • Most staff members also attended the annual meeting of the Association for Research in Vision and Ophthalmology (ARVO) in May. Glaucoma Service clinicians and fellows presented nine posters.  New thoughts on neuroprotection, optic nerve imaging, genetics, and surgery were some of the myriad subjects presented at the conference.  This exciting but nearly overwhelming event each year allows the Wills staff and research and clinical fellows to present and discuss their recent findings with those of other researchers and clinicians throughout the world.

  • The Service enjoyed one of Glaucoma Service Research Center Director Dr. William Steinmann’s regular visits in June.  During these bimonthly visits from his main office at Tulane he spends three days meeting with the physicians and research staff to assess current projects and to plan for the future.  Currently on the docket is coordination of research and clinical pursuits in the new Wills facility.  The new facility’s steel skeleton is now in place, stretching eight floors up from the Walnut Towers building, across Ninth Street from the current Wills Eye Hospital.  Scheduled to open in July of 2002, the new facility promises great opportunities or improvement and expansion of the mission of the Glaucoma Service:  world-class clinical care, teaching, and research.

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Sponsored by:

Glaucoma Service
To Prevent Blindness
900 Walnut Street
Philadelphia, PA  19107

Introducing Our

Support Group for Parents of Children with Glaucoma

Sunday, September 30th, 2001
Wills Eye Hospital 1st Floor Auditorium
1:30 PM to 3:30 PM

An Overview of Glaucoma in Children

By:  Dr. Courtland Schmidt

Childcare is available. Please call the Foundation office before September 28th to let us know how many children you will be bringing with you and their ages. We will have an appropriate number of chaperones. Thank you for your consideration.

 

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Glaucoma Patient Support Group

 

The first meeting of the 6th season of the Glaucoma Patient Support Group will take place Sunday, October 21, 2001, from 1:30 to 3:00 PM in the Wills Eye Hospital auditorium on the 1st floor of the Hospital. Dr. Jeffrey Henderer of the Glaucoma Service will speak about visual field examinations — the latest techniques, what the results mean and do not mean, and important points to remember when taking the test. As always, there will be plenty of time for questions and answers on all topics related to glaucoma. The monthly sessions are free, with light refreshments served.

 

On Sunday, November 18, again from 1:30 to 3:00 PM, new Wills Glaucoma Service staff member Dr. Douglas Rhee will continue the series speaking about what glaucoma patients should know about genes and glaucoma.

 

The program for the rest of the season will appear in the next Searchlight in November.

 

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Dr. Wilson Discusses “Living with Glaucoma” with Chat Support Group

 

On Wednesday, June 13, Dr. Richard Wilson of the Glaucoma Service staff discussed “Living with Glaucoma” with the Chat Support Group.  Here are some highlights from that session:

 

Dr. Rick Wilson:  You all are the experts on this topic.  Everyone please chime in and give advice about what works best for you.

Participant (P):  Asking questions, and not stopping until I get an answer I understand! 

P:   Good point.  But I get upset when I hear other glaucoma patients saying their doctor didn’t explain things to them.  I say, then get an answer you can understand.

Dr. Wilson: I agree.  I would like family there for important discussions.  It is too easy for the patient to focus in on one point and hear nothing thereafter.

Moderator:  Dr. Wilson, do most of your patients come with someone or do they come alone to your office?

Dr. Wilson:  Probably 30 to 40% bring someone.

Moderator:  I try to take someone with me anytime I see the eye doctor, even if it is a routine visit.  Sometimes two people hear two different things.

P:  I am very disciplined about taking my drops (Alphagan twice a day and Xalatan once a day).  But sometimes it seems so futile.  Nothing seems to have any effect.

Dr. Wilson: I spoke about that in a lecture I gave Friday in San Francisco.  It is hard to remember to take medications when you won’t see the results of not taking them for months to years.  My wife would do terribly with that scenario.  She takes medicine as long as she feels terrible.  As soon as she feels better, she forgets to take the medication.

P:  When I was first diagnosed, I thought for sure I would go blind.  But over the years, as Dr. Wilson said, most patients do not.

Dr. Wilson:  Keep a positive attitude, because the majority of vision lost to glaucoma occurs before the patients see the eye doctor, and are diagnosed and treated.  Once treated, most patients suffer only slow deterioration over long periods and die with close to the vision they had at the time of diagnosis.  Exercise, eat right, stop smoking, lose weight and keep yourself in as good health as possible.  It makes a huge difference in the long-term prognosis, especially in patients as they age.

P:  Dr. Wilson, this site, and those who contribute to it, have helped to reassure me that this mystery of glaucoma and the non-specific treatment regimes are the best that I can do.  It keeps me from lying awake at night thinking I should be trying some magic elixir.

P:  After more than 30 years on drops, a detached retina, a couple of trabeculectomies in both eyes, needling, blood injections, Holmium laser, and cataracts removed from both eyes, I am now off drops because I followed my doctor’s instructions.  I didn’t fight it.  I am not out of the woods yet, as the pressure in the left eye has dropped to five.

Dr. Wilson:  Nice going. But what a struggle!

 

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