November 2018

Background

The clinical value of cannabis in alleviating the symptoms of dry eye disease (DED) is limited at this time due to a lack of clinical evidence.

The Canadian Ophthalmological Society does not support the medical use of cannabis for the treatment of DED or its associated pain symptoms, due to its undesirable side-effects, including dry eye symptoms if smoked, and the absence of scientific evidence showing any beneficial effect at this time.

Other evidence-based, less harmful treatment modalities are available for DED and its associated symptoms.

Access Details

Read the full position statement and recommendations from the Canadian Ophthalmological Society (COS).

The CanMEDS 2015 Framework is an educational framework that describes the abilities physicians require to effectively meet the health care needs of the people they serve. CanMEDS is the basis for the educational and practice standards of the Royal College of Physicians and Surgeons of Canada (RCPSC). 

Watch the LEGO episode and enjoy the playful tutorial and overview of the CanMEDS roles:

How to obtain and claim MOC credits in ophthalmology – Opportunities for additional learning.

Dear COS members,

As ophthalmologists and physicians, lifelong learning through continuing professional development (CPD) is at the heart of what we do. Taking care of our patients requires us to keep up with current standards and maintain and enhance our competence, knowledge and skills.

As members of the Maintenance of Certification (MOC) committee, an arm of the COS Council on CPD, we would like to provide you with a list of CPD activities accessible to you. Below you will find a wealth of resources. They vary from online learning modules to live, interactive sessions.

Take advantage of these resources to earn all the credits you need to meet the annual requirements of the Royal College. Remember to enter your credits into MAINPORT as you complete CPD activities.

• Updates to the Royal College MOC program
• The MOC Framework
• To review information about MAINPORT

A big thanks to Cheryl Ripley for helping to synthesize these resources. Members of the COS MOC committee include: Dr. Colin Mann, Chair, Dr. Chloe Gottlieb, Dr. Phil Hooper, Dr. Rob Shertzer, and Dr. Glen Hoar.

How many CPD credits do you need?

New Cycle requirements are such that all Fellows and Maintenance of Certification (MOC) Program participants will be required to complete a minimum of 25 credits in each section of the MOC Program during their new 5-year MOC cycle. The annual minimum of 40 credits and a cycle overall minimum of 400 credits are still applicable.

This new policy will only apply to new cycles starting in January 1, 2014 or later. If currently completing your MOC cycle, the minimum credit requirements will not apply until your next cycle begins. Not sure when your current cycle ends? You can find out by logging into your MAINPORT account (your cycle dates appear on the dashboard, under your name). You may also contact the Royal College Services Centre to find out.

Further information on the types of activities you can claim can be found in each section.

October 2018

Background

The clinical utility of cannabis (sometimes referred to as marijuana or marihuana) for the treatment of glaucoma is limited by the inability to separate the potential clinical action from the undesirable neuropsychological and behavioural effects. The Canadian Ophthalmological Society does not support the medical use of cannabis for the treatment of glaucoma due to the short duration of action, the incidence of undesirable psychotropic and other systemic side effects and the absence of scientific evidence showing a beneficial effect on the course of the disease. This is in contrast to other more effective and less harmful medical, laser and surgical modalities for the treatment of glaucoma.

Access Details

Read the full policy statement from the Canadian Ophthalmological Society (COS) and the Canadian Glaucoma Society (CGS).

Position Statement

(December 2017)

Summary

Current surgical treatments for glaucoma are aimed at reducing intraocular pressure (IOP) through decreasing aqueous inflow or enhancing of aqueous outflow and thereby reducing the risk of visual field loss. While trabeculectomy and implantation of glaucoma drainage devices are the standard and more commonly performed surgical interventions for glaucoma, they are often reserved for patients with uncontrolled moderate to severe disease, due to their higher risk of severe complications. The COS & CGS recognize that there is a gap in treatment options that exists between medical and traditional surgical interventions for patients with more mild to moderate forms of glaucoma who may not be optimally treated with the traditional standard of care. The surgical risk to benefit ratio would favour a safer procedure in these patients.

During the past decade, novel medical devices and procedures, collectively referred to as MIGS (micro-invasive or minimally invasive glaucoma surgery), have emerged and become available to Canadian patients. Their cardinal features include an ab interno approach, modest efficacy, high safety profile, rapid postoperative recovery and minimal tissue trauma. These procedures are designed to improve the safety of surgical intervention for glaucoma, while providing the efficacy needed to slow or halt glaucoma progression. The trade-off of having a safer surgical profile is that these procedures, at their current stage of development, are not as effective in reducing IOP as the standard glaucoma procedures.

Demonstrated benefits of MIGS include lowering IOP, reducing medication need, rapid post-operative recovery and minimal complications. Additional benefits that continue to be studied include the delay or prevention of more invasive glaucoma surgery, improvement of quality of life, reduction in number of doctor visits, cost-effectiveness, and prevention of vision loss.

Current indications for MIGS include patients undergoing cataract surgery and requiring medical glaucoma therapy; patients unable to tolerate or adhere to medical glaucoma therapy; and patients with intraocular pressure not sufficiently controlled by medical and/or laser therapy while not clearly requiring invasive surgeries such as trabeculectomy and glaucoma drainage devices. The majority of the MIGS procedures are not indicated for patients with angle closure glaucoma.

There is broad agreement among Canadian and international glaucoma specialists, based on current evidence and practice patterns, that MIGS do have a role in the glaucoma treatment algorithm. With the aging population at increased risk for glaucoma, coupled with limited healthcare resources, we support equitable access to innovative new technology such as MIGS. These newer surgical treatments can fill the gap in treatment that exists today, deliver better outcomes to patients, and ideally will aid in optimizing health system utilization. This position paper represents the current position of the COS and CGS regarding MIGS. Both societies support new and innovative technologies within Ophthalmology and will continue to monitor this evolving area of practice and update this position statement accordingly.

The COS and CGS are currently working together with the Canadian Agency for Drugs and Technologies in Health (CADTH) to determine the optimal use of MIGS for adults with glaucoma based on current evidence.

Access Details

Read the full Position Statement from the Canadian Ophthalmological Society (COS) and the Canadian Glaucoma Society (CGS)
COS-CGS Position Statement on MIGSDownload

(2017)

Joint Position Statement

Read the full position statement from the Canadian Association of Optometrists (CAO) and the Canadian Ophthalmological Society (COS).

Position Statement

November 2016

Summary

Retinitis Pigmentosa (RP) is part of a group of rare genetic disorders that cause slow but progressive degeneration of photoreceptor cells in the retina. RP symptoms typically begin in childhood with decreased night vision, followed by loss of peripheral vision, and can eventually lead to complete loss of vision. There is currently no cure for RP.

Since 1992, doctors in Cuba have offered a treatment for RP at an initial cost of just over $10 000 CDN. The Cuban treatment comprises eye surgery, ozone therapy, electric stimulation, and drugs. However, no independent, peer-reviewed studies have been conducted to date that demonstrate the Cuban treatment improves or stabilizes retinal function.

The Canadian Ophthalmological Society does not recommend the Cuban treatment for patients with RP due to the absence of objective, peer-reviewed evidence to support its efficacy, safety, and the fact that in some cases the treatment appears to have worsened patients’ RP symptoms.

Full Position Statement

Retinitis Pigmentosa (RP) refers to a group of rare genetic disorders that cause slow but progressive degeneration of photoreceptor cells in the retina. RP affects approximately 1 in 3500 Canadians.¹ RP symptoms typically begin in childhood with decreased night vision, followed by loss of peripheral vision, and can eventually lead to complete loss of vision. RP typically affects both eyes and ranges in severity from no visual problems in some families to early blindness in others. There is currently no cure for RP.

Since 1992, doctors in Cuba have offered a treatment for RP, which is available at a cost of $10 000 CDN for the initial treatment, plus $4900 CDN for each subsequent annual ozone treatment.² The Cuban treatment is open to anyone seeking treatment, both locally and internationally, and is comprised of the following:

1. Eye surgery: A flap of orbital vascular adipose tissue is inserted into a sclerochoroidal pocket at the temporal side of the eye. The theory behind the surgery is that it will increase blood flow, which will stabilize the progression of RP. However, our current knowledge, based on continued research, indicates that RP is a cellular disease, not a disease of blood circulation.² Several complications have been reported, including photophobia, strabismus with diplopia post-operatively, and inadvertent rupture or perforation of the scleral wall during surgery.^3,4
2. Ozone therapy: Post-surgery, ozone is administered to patients for 14-21 days, either rectally or via the bloodstream. The theory behind the ozone therapy is that it boosts antioxidants, which minimizes damage caused by lipid peroxidation. The rationale here remains contentious in the scientific community.⁵ In addition, ozone is an unstable molecule and may break down even before it is administered into the body. When ozone is infused into human blood, it produces reactive oxygen species which has the potential to cause an opposite effect, inducing oxidative stress and damage to the cell.⁶
3. Electric stimulation: Post-surgery, patients undergo multiple sessions of electrical stimulation of their head, neck, soles, and palms over a period of 14-21 days.⁷
4. Drugs: Post-surgery, patients are occasionally administered a mixture of antiplatelets, antioxidants, immunomodulators, vitamins, and minerals. Information on the precise dosages and names of the medications is not readily available and varies on an individual basis.³

Despite the fact that the Cuban treatment has been available for more than 20 years, its proponents have failed to demonstrate the scientific reasoning behind the treatment, and they have not demonstrated their techniques to any peers in the field outside of their own clinic. Furthermore, the results of pre- and post-operative outcomes have not been published in any peer-reviewed medical journal, nor have any longitudinal studies been conducted, even though the Cuban treatment has been offered since the early 1990s.⁷

The few studies on RP that have been performed report an absence of any evidence that the Cuban treatment for RP improves or stabilizes retinal function. In fact, according to a 1996 study conducted by Berson et al., in some cases, the treatment resulted in a 12.9% decline in patients’ visual fields.⁸

Given the lack of objective, independent, peer-reviewed medical studies, the Canadian Ophthalmological Society does not recommend the Cuban treatment for patients with RP. Furthermore, the Canadian Ophthalmological Society strongly advises that patients with RP avoid the Cuban treatment due to the absence of evidence to support its efficacy, safety, and the fact that in some cases the Cuban treatment appears to have worsened patients’ RP symptoms.

References

1. Foundation Fighting Blindness. http://ffb.ca/learn/eye-diseases/
2. Richard F. Tourisme médical. Hôpital sous les tropiques. Journal de la rue 2009;1^er août. http://journaldelarue.wordpress.com/2009/08/01/tourisme-medical-hopital-sous-les-tropiques/.
3. Parmeggiani F, Sato G, De Nadai K, Romano MR, Binotto A, Costagliola C. Clinical and rehabilitative management of retinitis pigmentosa: up-to-date. Current Genomics. 2011, 12, 250-259.
4. Berger RW, Haase W, Gerding H. Original papers: Ocular motility disorders after surgery for retinitis pigmentosa ‘Cuba-therapy’. Strabismus 1995;3(1): 13-20.
5. Copello, M, Eguía, F, Menéndez, S, Menéndez, N. Ozone therapy in patients with retinitis pigmentosa. Ozone: Science & Engineering. 2003, 25(3), 223-232.
6. Fishman GA. A historical perspective on the early treatment of night blindness and the use of dubious and unproven treatment strategies for patients with retinitis pigmentosa. Survey of Ophthalmology 2013;58(6):652-663.
7. Duquette J. Is there evidence supporting the Cuban treatment for RP? Institut Nazareth & Louis-Braille, 2010. http://www.inlb.qc.ca/recherche-publ/is-there-evidence-supporting-the-cuban-treatment-for-rp/.
8. Berson EL, Remulla JC, Rosner B, Sandberg MA, Weigel-DiFranco C. Evaluation of Patients with Retinitis Pigmentosa Receiving Electric Stimulation, Ozonated Blood, and Ocular Surgery in Cuba. Arch Ophthalmol. 1996;114(5):560-563. doi:10.1001/archopht.1996.01100130552009.

Reviewed August 2022

The Canadian Ophthalmological Society (COS) and its subspecialty society, the Canadian Cornea, External Disease & Refractive Surgery Society (CCEDRSS), are committed to excellence in ophthalmology. Excellence requires adherence to the highest ethical standards in all professional activities, including marketing and advertising. Our guiding principle is that the welfare of the patient is paramount. Advertising is ethical when it informs and educates the patient, when it does not confuse or mislead, and when it augments – but does not substitute for – a full conversation between the patient and the surgeon. There is no substitute for patient counseling, which can only be provided in a one-on-one setting.

COS and the CCEDRSS believe that, as a form of patient education, advertising is governed by the ethical guidelines and policies that cover patient education, including the guidelines of the Provincial Colleges of Physicians and Surgeons.

In particular, we agree with the American Academy of Ophthalmology (AAO) that good patient education:

• Is clear, accurate, up-to-date and thorough;
• Avoids misleading statements;
• Is not overstated and does not instill unrealistic expectations in patients; and
• Serves as a springboard for the oral conversation with the patient.

COS and the CCEDRSS would recommend that our members conform to these standards.

We also agree with and would recommend that our members give consideration to the joint statement of the American Academy of Ophthalmology, the American Society of Cataract and Refractive Surgeons (ASCRS), and the International Society of Refractive Surgery of the American Academy of Ophthalmology entitled Guidelines for Refractive Surgery Advertising Policy.

No set of guidelines can anticipate every possible advertising claim or expression. Ultimately, advertising is an ethical matter, and we expect our members to conform to the highest ethical standards in advertising as in every other aspect of their practices.

April 2012

The Canadian Ophthalmological Society’s (COS) expert working group on driving and vision standards provided recommendations on the visual acuity and visual field needed for safe driving in Canada.

These recommendations are published in Section 12: Vision of the Canadian Medical Association Driver’s Guide, 8th edition.

COS’s Vision Standards for Driving Committee revisited the vision section of the guide in April 2012 and indicated no changes were required at this time.

Background

When a patient is visually impaired, the physician should inform the patient of the nature and extent of the visual defect and, if required, report the problem to the appropriate authorities.

When minor visual defects are not accompanied by cognitive defects or neglect, most drivers are capable of compensating for partial defects. For example, most people adapt to the loss of an eye in a period of several months.

Recent studies indicate that experienced drivers can compensate for a loss of visual acuity if they are in familiar surroundings and they limit their speed.  In these circumstances, functional assessments are indicated.

Section 12 presents information about the recommended visual acuity and visual field needed for safe driving (section 12.2). Actual standards for these functions are set by provincial or territorial licensing authorities and may vary among jurisdictions as well as varying from the recommendations in Section 12, which are based on expert opinion.

Section 12 also presents information about other important visual functions that should be taken into consideration in determining fitness to drive (section 12.3) and recommendations for exceptional cases that require individual assessment (section 12.4).

It also provides further detail on recommended testing procedures (addendum 1), a list of medical conditions with increased risk for vision problems and a discussion of the use of vision aids in driving (addendum 2).