Diabetic retinopathy is a leading cause of blindness that is associated with both type 1 and type 2 diabetes. It results from glycation and damage to the retinal blood vessels over time. Early stages are asymptomatic, but can progress to cause vision loss through edema, hemorrhage, or the growth of abnormal new blood vessels. Risk increases with longer duration of diabetes. Management focuses on tight glycemic control through medication and lifestyle changes, as well as regular eye exams and treatments such as laser photocoagulation or anti-VEGF injections to prevent vision loss.
2. Objectives
• Diabetic retinopathy implications as a public health issue
and a leading cause of blindness in industrialized countries
• Discuss risk factors
• Discuss pathophysiology and the different stages
• Discuss management approach
- Prevention – risk factor control and annual dilated
retinal examinations
- Treatment modalities
4. Diabetes Mellitus
Hyperglycemia resulting from body’s inability to produce and/or utilize
insulin
•Type 1
- children and young adults
- immune prone
- no insulin production
- 5% of DM pts
• Type 2
- mostly adult onset (increase incidence at earlier age)
- insulin resistance followed by decreased production
- MC
- obesity
5. Diabetic Retinopathy (DR)
• Implicated by both types of DM
• Progressive glycation on retinal blood vessel wall
• Initially asymptomatic
• Microvascular leakage
• Microvascular occlusion
21. Symptoms
• Asymptomatic in early stages
• Blurred vision - myopic shift (lens changes)
• VA fluctuation Distorted vision
• Partial or total loss of vision
25. • Intraretinal microvascular abnormalities (IRMA)
- tortuous dilated capillaries that
- project anteriorly
- do not leak on FA
- adjacent to CWS
- Sign of hypoxia
IRMA
IRMA
IRMA
CWS
26. • Venous Beading (VB)
- focal dilation of the veins
- adjacent to occluded arterioles
/ areas of capillary of nonperfusion
- reflects increasing retinal ischemia
/hypoxia
- strong predictor of development
of PDR
27. • 4/2/1 Rule
- > 20 intraretinal hemorrhages in each of four quadrants
- VB in two or more quadrants
- IRMA in one or more quadrants
Severe NPDR
28. Proliferative Diabetic Retinopathy (PDR)
• Increased levels VEGF
• Disc new vessels (NVD)
• Peripheral new vessels (NVE)
• Vitreous or preretinal hemorrhages
• High risk
of severe
VAL
NVDVitreous
Fibrosis
NVE
29. • DME /Clinical Significant Diabetic Macular Edema (CSDME)
- not a criterion of severity of NPDR
- leading cause of legal blindness in diabetics
- present at any stage, more in PDR
3 criteria of CSDME
34. The Best Measure for Prevention of Vision
Loss is Strict Glycemic Control
35. • Treatments exist but work best before vision
is lost
RECOMMENDED EYE EXAMINATION
SCHEDULE
Diabetes Type Recommended Time of First
Examination
Recommended Follow-up*
Type 1 3-5 years after diagnosis Yearly
Type 2 At time of diagnosis Yearly
Prior to pregnancy (type 1
or type 2)
Prior to conception and
early in the first trimester
No retinopathy to mild
moderate NPDR every 3-12
months
Severe NPDR or worse every
1-3 months.
Ophthalmology Myron Yanoff MD and Jay S. Duker
Basic and Clinical Science Course, Section 12: Retina and Vitreous AAO
http://www.aao.org/eyecare/news/upload/Eye-Health-Fact-Sheet.pdf -