Diabetic Retinopathy Screening Program in the Cree Region of James Bay of Quebec

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RUIS McGILL VIRTUAL HEALTH AND SOCIAL SERVICES CENTRE (CvSSS) SIMPLIFYING TELEHEALTH! Diabetic Retinopathy Screening Program in the Cree Region of James Bay of Quebec Nurse and Imager Training Prepared and presented by: David E. Lederer, MD FRCSC Last updated June 20, 2014 CUSM

VIRTUAL HEALTH AND SOCIAL SERVICES CENTRE (CvSSS) SIMPLIFYING TELEHEALTH! Diabetic Retinopathy Screening Program in the Cree Region of James Bay of Quebec Nurse and Imager Training Prepared and presented by: David E. Lederer, MD FRCSC Last updated June 20, 2014 CUSM Copyright This presentation is designed to train health care professionals in screening diabetic retinopathy in region 18. The content as well as the images used in this presentation are solely for teaching purposes. They are not for redistribution or copy in any manner whatsoever. The McGill University Health Centre (MUHC) does not endorse nor is it liable for any redistribution or copying of the content of this presentation. 2

TOPICS Diabetes Refresher Ocular Anatomy Diabetic Retinopathy Other Ocular Diseases Diabetic Retinopathy Screening Procedures Diabetic Retinopathy Treatment Collective Prescription Procedures Hands-on Training 3 DIABETES MELLITUS - EPIDEMIOLOGY Every 2 seconds, 2 people are diagnosed with diabetes somewhere in the world 135 million people worldwide 300 million people projected by 2025 Canadian Statistics 1.8 million people in 2005 (5.5% of population) 2.4 million people projected by 2016 4

DIABETES MELLITUS - EPIDEMIOLOGY Cree Nation 2x more common Impact on Waskaganish (approximate) 2,000 persons 220 with diabetes (11%) 5 DIABETES MELLITUS Metabolic disorder characterized by the presence of hyperglycemia due to defective insulin secretion, defective insulin action or both 6

7 DIABETES MELLITUS Definition based on fasting plasma glucose Fasting plasma glucose > 7.0 mmol/l Casual plasma glucose > 11.1 mmol/l + symptoms of diabetes 2 hr plasma glucose in a 75g oral glucose tolerance test > 11.1 mmol/l 8

9 DIABETES MELLITUS TYPE 1 Result of pancreatic beta cell destruction Autoimmune Unknown etiology TYPE 2 Range of disease from insulin resistance with relative insulin deficiency to a predominant secretory defect with insulin resistance 10

DIABETES MELLITUS Leading cause of blindness in the working age population, end-stage renal failure and nontraumatic amputations Cardiovascular disease is 2-4x more common (leading cause of death) 11 ANATOMY 12

ANATOMY 13 ANATOMY 14

ANATOMY 15 ANATOMY 16 www.optos.com

ANATOMY 17 QUESTIONS? 18

BREAK 19 DIABETIC RETINOPATHY Any Retinopathy: prevalence=40% Proliferative retinopathy Type 1: 23% Type 2: 14% if on insulin ; 3% if on oral Rx Macular edema Type 1: 11% Type 2: 15% if on insulin ; 4% if on oral Rx 20

DIABETIC RETINOPATHY Visual loss associated with Falls Hip fractures 4-fold increase in mortality 21 HISTOPATHOLOGY 22

DIABETIC RETINOPATHY Defined as a clinical entity based on characteristic vascular and retinal changes Microaneurysms Intraretinal Hemorrhage Exudates Macular Edema Vascular Malformation Retinal Capillary Closure Abnormal Vessel Growth (Neovascularization) 23 MICROANEURYSMS 24

INTRARETINAL HEMORRHAGE 25 EXUDATES 26

MACULAR EDEMA 27 VASCULAR MALFORMATION 28

RETINAL CAPILLARY CLOSURE 29 NEOVASCULARIZATION 30

NEOVASCULARIZATION 31 STAGES OF DIABETIC RETINOPATHY Nonproliferative Mild Moderate Severe Proliferative Macular Edema Present Absent Clinically Significant Macular Edema 32

QUESTIONS? 33 OTHER DISEASES FOR WHICH WE CAN SCREEN Age Related Macular Degeneration Cataract Glaucoma 34

AGE RELATED MACULAR DEGENERATION More common in Caucasian race Onset age 55 One of the most common causes of visual loss after age 55 Subtypes Atrophic or Dry 90% Exudative or Wet 10% 35 DRY WET 36

CATARACT Progressive opacification of the natural lens Many causes including age, systemic disease and medications 37 CATARACT 38

GLAUCOMA Optic neuropathy with characteristic optic nerve head and visual field changes Many risk factors but one of the major risk factors is INTRAOCULAR PRESSURE (IOP) 39 PRIMARY OPEN ANGLE GLAUCOMA (POAG) Chronic disease that effects progressively causes loss of vision Loss commences peripherally and moves centrally eventually causing blindness if left untreated 40

41 42

QUESTIONS? 43 DR SCREENING TYPE 1 5 years after diagnosis in all persons > 15 years TYPE 2 All individuals at diagnosis After 20 years 99% have DR (any grade) After 20 years 60% have DR (any grade) 44

SCREENING MODALITIES Direct ophthalmoscopy 45 SCREENING MODALITIES Indirect opthalmoscopy 46

SCREENING MODALITIES Color fundus photography 7 standard fields Pupil dilation 47 COLOR FUNDUS PHOTOGRAPHY With or without pupil dilation 48

WHY DILATION 49 COLOR FUNDUS PHOTOGRAPHY 7 fields vs <7 fields 50

WIDEFIELD VIEW OF RETINA 51 www.optos.com INTERNAL FIXATION 52

53 53 54

CHEAT SHEET : EITHER EYE 55 56 56

57 QUESTIONS? 58

INTERVALS FOR FOLLOW-UP (American Academy of Ophthalmology) Normal Yearly Mild 9-12 Months Moderate 6 Months Severe 4 Months Macular Edema 2-4 Months Proliferative 2-3 Months Pregnancy Pre-/Early Conception and every 3 months thereafter 59 TREATMENT Healthy lifestyle Medical control Glucose Blood Pressure Cholesterol Laser treatment Adjunctive medications (for the eye) 60

HEALTHY LIFESTYLE Smoking cessation Weight loss Nutrition Exercise 61 GLUCOSE No Baseline Retinopathy Intensive glucose control 27% reduction in developing DR 76% reduction in progression 62

BLOOD PRESSURE Tight glucose control + Blood pressure <150/85 mmhg resulted in 34% decrease in retinopathy progression Special consideration for use of ACE-inhibitors 63 CHOLESTEROL High cholesterol may be associated with increased macular exudates It is unclear if decreasing cholesterol will decrease exudates and improve visual prognosis BUT IT CAN T HURT 64

LASER TREATMENT Grid/Focal Laser Panretinal Photocoagulation (PRP) 65 GRID/FOCAL LASER 66

GRID/FOCAL LASER 67 PANRETINAL PHOTOCOAGULATION 68

VITREORETINAL SURGERY 69 ADJUNCTIVE MEDICATIONS (FOR THE EYE) Steroids Subtenon Intravitreal Anti-VEGF medications Avastin Others Rapidly growing area of research 70

QUESTIONS? 71 BREAK 72

THE SCREENING PROCESS Check visual acuity with glasses Check intraocular pressure Dilate the eyes Photography 73 HOW TO CHECK VISION 74

75 76

QUESTIONS? 77 HOW TO CHECK IOP 78

HOW TO CHECK IOP 79 HOW TO CHECK IOP Technical Aspects Administer 1 drop Alcaine 0.5% to both eyes TAP tonopen on center of cornea 10 times in rapid succession in either eye Listen for the beeps to tell you the number has registered Record the results Repeat for other eye Be careful not to push on the eye 80

81 QUESTIONS? 82

RISKS Corneal Abrasion Blurred vision Painful (but self limited) Pain relieved with Alcaine 0.5% drops May give any antibiotic ointment/cream 4x per day for 4 days If pain worsens or vision does not improve call the doctor IF A PATIENT RETURNS WITH A COMPLICATION, ALWAYS RE-CHECK IOP IN BOTH EYES 83 HOW TO DILATE THE PUPILS Administer 1 drop Alcaine 0.5% to both eyes (if not already done) Administer 1 drop Mydriacyl 1% to both eyes Wait 5 minutes and repeat administration of Mydriacyl Wait 20 more minutes Record pupil size using provided card Proceed to photography 84

HOW TO MEASURE PUPIL SIZE 85 RISKS Intolerance To Drops Mildly blurred vision Itchy, irritated but not very painful Variable relief with Alcaine 0.5% drops May give any artificial tear drop 4x per day for 4 days If pain worsens or vision does not improve call the doctor IF A PATIENT RETURNS WITH A COMPLICATION, ALWAYS RE-CHECK IOP IN BOTH EYES 86

ACUTE ANGLE CLOSURE (AAC) Obstruction of the trabecular meshwork by the iris Pupillary Block: Aqueous fluid is impeded from passing between the lens and iris in its travel from the posterior to anterior chamber This incites a pressure gradient leading to iris bowing and obstruction of the trabecular meshwork 87 TERMINOLOGY Congenital glaucoma Primary open angle glaucoma Secondary open angle glaucoma Primary angle closure glaucoma Secondary angle closure glaucoma Acute angle closure 88

GLAUCOMA Optic neuropathy with characteristic optic nerve head and visual field changes Many risk factors but one of the major risk factors is INTRAOCULAR PRESSURE (IOP) 89 NORMAL AQUEOUS FLOW 90

IRIS-TRABECULAR MEMBRANE OBSTRUCTION & PUPILLARY BLOCK 91 RISK FACTORS Shallow anterior chamber Risks for a shallow anterior chamber Hyperopia Large cataracts Elevated intraocular pressure Fellow eye 92

DIAGNOSIS OF AAC 93 DIAGNOSIS Intraocular pressure > 40 OR 2x the initial measurement PLUS 1 major or 2 minor symptoms MAJOR SYMPTOMS Severe eye pain not relieved by Alcaine drops Sudden vision loss MINOR SYMPTOMS Sudden headache Decrease in vision Nausea and vomiting Eye ache Corneal haziness Eye redness 94

SYMPTOMS Corneal haziness Eye redness 95 TREATMENT Check pressure of both eyes Call the physician if criteria of AAC are met Proceed to treatment Verify allergies (caution SULFA) Diamox 500mg PO x 1 Glycerin 30ml PO with juice x 1 Pilocarpine 2% 1 drop both eyes REPEAT after 30 minutes and AGAIN 30 minutes later May repeat the above procedure in 8 hours if the patient has not seen the ophthalmologist 96

DEFINITIVE TREATMENT Laser or surgery to create a secondary opening in the iris to bypass the pupillary block and thus alleviate the pressure gradient 97 QUESTIONS? 98

CONCLUSION 99

The RUIS McGill Telehealth Expertise and Coordination Centre (CECoT) is the physical entity of the CvSSS that coordinates your requests. CECoT contact information Address : E-mail : MUHC-Montreal Children s Hospital 2300 Tupper Street - Room F-256 Montréal (Quebec) H3H 1P3 visio-cusm@muhc.mcgill.ca Telephone : 514 412-4294 (Toll free in Quebec : 1 877 536-3202) Fax : 514 412-4362 www.cvsss.ca