Article Date: 4/1/2011

Clinical Vignettes in Retinal Vascular Disease and Macular Edema
Controversies in Care

Clinical Vignettes in Retinal Vascular Disease and Macular Edema

Edited by Michael Colucciello, MD

As clinicians, we are confronted several times daily with a patient presenting with retinal vascular disease and macular edema. We communicate with the patient's primary care provider and any appropriate specialists (endocrinologist, cardiologist, nephrologist, etc.) to treat and optimize systemic contributing factors.

For several years, the only decision for local treatment was whether or not the patient was eligible for laser treatment based on the results of landmark studies such as the Early Treatment Diabetic Retinopathy Treatment Study and the Branch and Central Retinal Vein Occlusion studies.

Now, armed with the results from the Diabetic Retinopathy Clinical Research Network, the CRUISE and BRAVO studies, the FAME and RISE studies, and the Ozurdex GENEVA study group, retina specialists have more, and improved, options for our RVO patients.

In this month's column, I have given the participants, Sharon Fekrat, MD, and Dennis Marcus, MD, four clinical vignettes from which to comment. These cases represent some of the more common scenarios that we face daily as retina specialists.

1. How would you treat a 55-year-old Type 2 diabetes patient with vision of 20/25 with no subjective visual complaints, clinically significant diabetic macular edema and intraretinal fluid on SD-OCT?


In this clinical scenario, visual acuity is good and the patient is essentially asymptomatic. Thus, I would recommend observation with good systemic control of glucose, blood pressure, and lipids and reevaluation in four months. If the edema increased at the four-month follow-up visit and the VA decreased, I would offer focal/grid laser treatment initially. If there was concurrent severe NPDR or non–high-risk PDR in the same eye, I would then treat the CSME with focal/grid laser prior to the needed PRP.


After discussion of all the options of observation, macular photocoagulation, intravitreal anti-VEGF injections, intravitreal steroid injections and combination therapy, I would recommend macular photocoagulation as the first-line therapy in the above scenario. Given that the patient is asymptomatic with very good visual acuity, I would not want to commit the patient to the small risks of multiple intravitreal injections with anti-VEGF therapy or to the not-so-small risks of intravitreal steroids. I would favor macular photocoagulation over observation, as macular photocoagulation has a very favorable safety record and certainly will decrease the risk of visual loss.

2. How would you treat a 50-year-old patient with a nonischemic CRVO of three weeks duration, 20/30 vision and very mild macular edema?


Given the good safety profile and the effectiveness of anti-VEGF agents, I would treat with intravitreal bevacizumab every four weeks for a total of three injections in this case. I would treat on the day of presentation with no “waiting period”—early treatment was demonstrated to be superior to delayed treatment in CRUISE.

If there was no improvement in macular thickness four weeks after the third bevacizumab injection, I would then initiate intravitreal ranibizumab per CRUISE. Non-Medicare patients, such as this 50-year-old, are concerned about the out of pocket costs of ranibizumab and generally prefer a bevacizumab trial first. In my anecdotal experience, treatment with anti-VEGF agents may delay or prevent conversion to an ischemic perfusion status.


After discussion of all the options of observation, intravitreal anti-VEGF injections and intravitreal steroid injections (dexamethasone implant and triamcinolone), I would recommend intravitreal anti-VEGF therapy. I think the anti-VEGF data for treatment of CRVO is very positive and I would commit the patient to at least three or four monthly injections and then consider observation with as-needed dosing, treat and extend dosing, or continued monthly dosing based on the patient's response. The Horizon study data evaluating extended ranibizumab therapy in CRVO indicates that prn dosing may result in a loss of the visual gains obtained during more frequent dosing in the CRUISE study.

As the patient has mild edema, is young and is treated early, I would still consider treat and extend or prn dosing of anti-VEGF therapy after the three or four monthly injections, although continued monthly injections would always be an option. I discuss the similarities and differences between ranibizumab and bevacizumab with regard to FDA approval, efficacy data, safety concerns and cost. Patients often prefer bevacizumab due to cost concerns.

Because some hemorrhages can take months to clear, grid-pattern laser is not initially an option.

3. How would you initially manage a 70-year-old hypertensive woman with a perfused BRVO diagnosed one week ago, associated with a visual acuity of 20/200 and dense intraretinal hemorrhage?


In the presence of dense intraretinal hemorrhage, it is not possible to determine the perfusion status of the RVO, particularly the perfusion status of the macular edema. In order to determine the perfusion status of the BRVO and associated macular edema, there must be sufficient clearing of the hemorrhage to evaluate the retinal capillary perfusion on fluorescein angiography. I would question the validity of the perfusion status in this case. It is possible that once the hemorrhage clears that the macular edema is perfused; however, this is not likely.

Because dense intraretinal hemorrhage can take months to clear, grid-pattern laser is not initially an option. As a result, I would initiate treatment on the day of presentation with an anti-VEGF agent to promote more rapid clearance of intraretinal hemorrhage than with observation alone and to also concurrently promote resolution of associated macular edema. I begin my anti-VEGF treatment with intravitreal bevacizumab because it is less expensive than ranibizumab, particularly for the non-Medicare patient and for the Medicare-only patient.

I would suggest a second intravitreal bevacizumab injection four weeks later and a third another four weeks later. If there is no improvement in the macular edema on OCT, I would switch to intravitreal ranibizumab per BRAVO. When the intraretinal hemorrhage has sufficiently cleared and determination of the macular edema as perfused on fluorescein angiography, combination treatment with the addition of grid-pattern laser photocoagulation per BVOS would be recommended.

I would continue to treat with intravitreal ranibizumab monthly, and then use the treat and extend approach until the effect of the grid-pattern laser is realized. This can take as long as one year, as demonstrated in SCORE.


My approach would be similar to scenario number 2 for CRVO but I would include laser therapy monotherapy or combined therapy as additional therapeutic options for discussion. Given the dense hemorrhages and severity for this BRVO, I would recommend at least three to four monthly loading doses of anti-VEGF therapy and would prefer treatment over observation despite the short duration of disease. With BRVO, I would certainly consider a treat and extend or prn dosing regimen if the patient responded with visual acuity gain and OCT thinning. Continued monthly dosing would be considered if edema persists, especially for a more severe BRVO, as described. With clearing of retinal hemorrhage, and residual edema, laser would also be considered later as an adjunctive therapy.

4. A 74-year-old hypertensive has had seven monthly bevacizumab in jections to treat macular edema associated with CRVO. Acuity had improved from 20/200 to 20/40 with resolution of macular edema (890 μm initially, improved to 210 μm). The photoreceptor IS/OS junction and ELM are only mildly disrupted. The edema has returned (370 μm) and vision is now 20/80. How would you proceed?


I would be interested to know how much time has passed from the last intravitreal bevacizumab injection until the recurrence of macular edema—one month or longer? I would suggest another intravitreal bevacizumab injection and repeat at monthly intervals until the edema has resolved. Then I would follow a treat and extend protocol using intravitreal bevacizumab to determine how long the treatment interval can be extended prior to the development of recurrent edema. If the patient is pseudophakic and does not have glaucoma and the treatment interval cannot be extended beyond six weeks, I would consider combination treatment with 1 mg of intravitreal triamcinolone per SCORE as an adjunct to decrease the number of injections of bevacizumab required. Good blood pressure control would be emphasized. If reinstitution of the intravitreal bevacizumab in this case did not result in resolution of the macular edema, I would use intravitreal ranibizumab per CRUISE. If this individual was a Medicare-only patient, out of pocket costs might pose some difficulty with the use of intravitreal ranibizumab.


Given the previous excellent response to bevacizumab, I would recommend continuing monthly bevacizumab therapy. I would explain to the patient that CRVO patients often require chronic therapy and that monthly therapy will likely result in the best visual outcome. Given the CRVO Horizon Study data demonstrating that prn dosing of ranibizumab results in a loss of visual gains in CRVO, I would recommend resuming monthly therapy for at least three to four months and then contemplate a treat and extend approach. If the edema returns or persists with monthly anti-VEGF therapy, I would discuss intravitreal steroid as a second-line option in a pseudophake. RP

How would you manage the clinical situations described in this article? You can comment as well by e-mail at after reading how Drs. Fekrat and Marcus approached these problems.

—Michael Colucciello, MD

Michael Colucciello, MD, is a partner at South Jersey Eye Physicians and a clinical associate at the University of Pennsylvania/Scheie Eye Institute. He is a member of the Retina Society and the American Society of Retina Specialists. He has no financial disclosures to report.

Sharon Fekrat, MD, is associate professor of vitreoretinal surgery at Duke University School of Medicine and chief of ophthalmology at the Durham, NC Veterans' Affairs Hospital. She reports a minimal financial interest in Genentech and Allergan in the past.

Dennis Marcus, MD, is professor of clinical ophthalmology at the University South Carolina School of Medicine in Columbia, SC and also practices at Southeast Retina Center in Augusta, GA. He reports significant financial interest in Genentech and moderate financial interest in Allergan.

Retinal Physician, Issue: April 2011