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Weiss Microcannulation System

REVS for CRVO - Central Retinal Vein Occlusion Treatment

Jeffrey N. Weiss, M.D. , formerly Chief of Vitreoretinal Surgery at the Joslin Diabetes Center, Faculty member at Harvard Medical School and a Visiting Scientist at the Massachusetts Institute of Technology, has developed an operation to improve the eyesight of patients with Central Retinal Vein Occlusion.

The retina of the eye is the sensory organ for vision. If the eye is compared to a camera, the retina would be the film  where the “picture” is formed. Proper blood circulation is needed for the retina to function. Normally, blood flows into the retina through the Central Retinal Artery and leaves the eye through the Central Retinal Vein. Both of these blood vessels enter the eye through the optic nerve.

Central Retinal Vein Occlusion (CRVO) is caused by a blood clot in the vein that drains the blood from the retina of the eye. The arterial blood enters the retina but cannot leave it due to a blockage in the vein.

As a result, blood and fluid are backed up into the retina, whichcauses a loss in vision. With further damage, the blood vessels in the retina may close leading to further visual loss with the possible development of new abnormal blood vessels.

These new vessels may cause a very painful type of glaucoma and lead to blindness. Traditionally, there has been no reliably effective treatment to prevent the loss of vision or to improve vision once it is lost.

Patients with high blood pressure, diabetes, or glaucoma are at an increased risk for developing CRVO. One researcher estimates that approximately 60,000 people develop a CRVO each year in the United States.

A TREATMENT FOR CRVO
After a diagnosis of CRVO has been made, many patients are advised by their doctors that the vision may return on its own if nothing is done to the eye. However, spontaneous recovery of vision in CRVO is very uncommon and when it does occur, the amount of recovery is usually very small. The Central Vein Occlusion Study (the largest study of CRVO funded by the National Eye Institute of the National Institutes of Health) showed that only 6% of eyes with CRVO recover at least 3 lines of vision (a 2-fold improvement) within 1 year (i.e., if vision has dropped to 20/200, there is only a 6% chance of it improving to 20/100 or better). So the odds are not in favor of recovering vision after it is lost to CRVO.

Tissue plasminogen activator (t-PA) is a well known "clot busting" medication successfully used for treating heart attack and stroke patients. Dr. Weiss has developed the instruments to allow t-PA to be directly injected into the retinal vein. The t-PA causes the clot to dissolve, which helps blood flow through the Central Retinal Vein. The operation is performed on an outpatient basis and takes approximately one hour. Furthermore, the procedure is very similar to a standard vitrectomy, which has been employed by retinal surgeons for over 30 years to treat eye diseases that are much less severe than CRVO.

WHAT ARE THE RESULTS?
After a CRVO has been diagnosed, many patients are advised by their doctors that the vision may return on its own if nothing is done to the eye. However, spontaneous recovery of vision in CRVO is very uncommon and when it does occur, the amount of recovery is usually very small. The Central Vein Occlusion Study (the largest study of CRVO funded by the National Eye Institute of the National Institutes of Health) showed that only 6% of eyes with CRVO recover at least 3 lines of vision (a 2-fold improvement) within 1 year (i.e., if vision has dropped to 20/200, there is only a 6% chance of it improving to 20/100 or better). So the odds are not in favor of recovering vision after it is lost to CRVO.

However, the amount and rate of visual recovery in CRVO following our procedure is much higher than what occurs without treatment. To date, 90 patients with CRVO have undergone this procedure as part of our clinical study approved by the Institutional Review Board (which is monitored by the Food and Drug Administration). Of the 61 cases with at least 4 months of follow-up data, 30 (49%) have recovered at least 3 lines of visual acuity within the first 4 months following surgery (a 2-fold improvement), while 15 (25%) have recovered at least 6 lines (a 4-fold improvement; from 20/200 to 20/50, for example)!

Some of the more remarkable results include: 1) Recovery of vision from 20/400 (legally blind) to 20/40 (usual legal limit for driving an automobile) within 2 months following the surgical procedure, and 20/20 vision 4 months later; 2) an improvement in vision from 20/60 to 20/25 (4 lines) within 2 months following the procedure; 3) an improvement in vision from “count fingers” (just being able to discern how many fingers are held in front of one’s face) to 20/100 within one week following the procedure; and 4) a 8-line improvement in vision in a patient who had a severe CRVO for at least 4 months before the surgery. These results are very encouraging and shows this procedure may help recover vision that has been lost following CRVO. We presented our technique at the American Academy of Ophthalmology Annual Meeting in October 2000 and presented the most recent results at the Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting on May 3, 2001.

While we have had very positive results even in eyes with longstanding CRVO, the final visual acuity achieved following this procedure may be related to the duration of CRVO and the preoperative visual acuity. Therefore, if you are considering having the procedure, it is better to decide early, before the CRVO has progressed and caused irreversible damage to the retina.
 
 


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