Dr. Wilson Heriot A/Prof

Practice: Retinology Institute

Location: Glen Iris, Victoria

Website: https://retinology.com.au

Phone: 03 8823 9000

Email: info@retinology.com.au

Associate Professor Wilson Heriotis a vitreo-retinal specialist based in Melbourne, Australia and the director of Retinology Institute. After completing his general ophthalmic training in Melbourne, he investigated phototoxic retinal injury and choroidal neovascularization during a two-year Medical retinal research fellowship with Paul Henkind in New York. This was followed by a vitreoretinal surgical fellowship with Robert Machemer at Duke University also investigating RPE repair.

  • His current research projects include a translation to clinical care program for a new method of retinal detachment repair called Retinal Thermofusion funded by a USA Department of Defense Award. Another project with colleagues at the Department of Optometry and Vision Sciences and University of Melbourne measuring retinal capillary autoregulation changes in diabetic patients, which received a Bayer GOAP award in 2020. Associate Professor Heriotis also a principle investigator for a number of local and international clinical trials in areas of Diabetic Retinopathy and Age-related macular denegation.

    • Associate Professor (Clinical), Ophthalmology, Department of Surgery, University of Melbourne

    • Associate Professor (Clinical), Department of Optometry and Vision Sciences, University of Melbourne

    • Principal Investigator in Vitreoretinal Research, Centre for Eye Research Australia

    • Honorary Consultant Retinal Surgeon, Royal Children’s Hospital and Royal Women’s Hospital, Melbourne, Australia

    • Medical Advisory Board member at Roche, Novartis and Bayer

  • I see clinical medicine not only as an opportunity to help patients but also as a test bed for assessing the effectiveness of current management strategies and the improvements offered by new treatments. It is also an opportunity to consider how to do things better. I particularly love filling in gaps in our knowledge and identifying potentially better solutions. Every patient has unique features that defines their individual response to therapy but, importantly, those features offer clues that can trigger the clinical insights necessary for a deeper understanding of disease. It is a very rewarding challenge to devise the optimised care strategy for each individual. We are always striving to be at the cutting edge and offer the best care for each patient.

FAQ

At the Jack McGovern Coats’ Disease Foundation, we are often contacted by anxious parents or patients who are seeking information after receiving a diagnosis of Coats’ Disease. The questions below are provided as a resource to assist you as you and your doctor decide the best approach for treatment. These questions do not constitute any form of medical advice or diagnosis. Each patient is unique. An experienced retinal specialist who has examined the patient is the best source of information for diagnosis and treatment. We always recommend getting a second opinion.

Questions to Ask Your Doctor (Download PDF)

  • Ahead of any treatments or procedures, it is important to ask yourself and the doctor the following questions:

    • How do you know that this is Coats’ Disease?

    • Has your doctor treated other patients with Coats’ Disease?

    • Have you sought a second opinion? If not, please consult our Doctor Directory for knowledgeable doctors in your area.

    • What Stage of Coats’ Disease is he/she in?

    • Will his/her vision get worse over time?

    • Will the eye have pain?

    • Will his/her eye start to turn out? Is muscle corrective surgery an option?

    • Are cataracts likely?

    • How likely is glaucoma? (due to retinal detachment)

    • Is there calcification?

    • What is the anticipated disease progression?

    • Is there a thorough vision exam available?

    • Where is the vision affected? (central/peripheral/distance)

    • Does he/she have depth perception? (3D visibility)

    • What about the non-Coats’ eye?

    • To what extent is his/her vision affected?

    • Will we be able to use this as a baseline to measure progress/decline?

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