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DIABETIC
RETINOPATHY
JKUAT BSC CLASS
introduction
 Diabetes mellitus describes a metabolic
disorder characterized by chronic
hyperglycemia resulting from defects in
insulin secretion , insulin action, or both.
 It is the leading cause of preventable
blindness in individual 40 to 60 years of
age.
 The rate of blindness among diabetic
persons is 20 times that of the general
population.
Diabetic Retinopathy
 This is the disease of the retina caused by
microangiopathy due to long term effect of
diabetes leading to the damage of the retina
and blindness
 It is the most important ocular complication of
diabetes.
 Prevalence of DR of any severity in the diabetic
population is 30%.
 Prevalence of blindness due to DR is
approximately 5%.
RISK FACTORS
 Duration of DM
 poor control of diabetes
 Hypertension
 Renal Disease
 Pregnancy
 Nephropathy
 others; Obesity, hyperlipidaemia,
smoking, anaemia
PATHOPHYSIOLOGY
 This is a Microangiopathy diseases
primarily affecting the precapillary
arterioles and capillaries , venules
and post capillary venules.
 The basic component of damaging is
microvascular occlusion and
microvascular leakages
PATHOPHYSIOLOGY OF
DIABETIC RETINOPATHY
pathogenesis
PATHOGENESIS
 DR is predominantly a microangiopathy in which small
blood vessels are particularly vulnerable to damage
from high glucose levels.
 Direct hyperglycemic effects on retinal cells are also
likely to play a role.
 Many angiogenic stimulators and inhibitors have been
identified; vascular endothelial growth factor (VEGF)
appears to be of particular importance.
Diabetic retinopathy
symptoms
 DR is asymptomatic in early stages but as the
disease progresses symptoms may include:
 Blurred vision
 Floaters
 Distorted vision
 Dark areas in the vision
 Poor night vision
 Impaired colour vision
 Partial or total loss of vision
Diabetic retinopathy signs
 Microaneurysms; these are localized
outpouchings, mainly saccular, of the capillary
wall that may form either by focal dilatation of
the capillary wall where pericytes are absent,
or by fusion of two arms of a capillary loop.
 Retinal hemorrhage
 Exudate
CLASSIFICATION
1.Non-proliferative DR
Mild
Moderate
Severe
Very severe
2.Proliferative DR
3.Diabetic maculopathy
4.Advanced diabetic eye disease
Cont.
NPDR
Mild :
 Indicated by the presence of at least 1 microaneurysm.
 Referral : review in 1-2 years
Cont.
Cont.
Moderate:
 Microaneurysm/ intraretinal hemorrhages in 2 or 3
quadrants.
• Early mild IRMA
• Hard or soft exudates may or may not be there
Cont.
Exudate
Microaneurysm
Cotton wool
Cont.
Severe:
 The (4-2-1) rule; any one of the following
 4 quadrants of microaneurysms and extensive
intraretinal haemorrhage
 2 quadrants of venous beading
 1 quadrant of IRMA
Cont….
Very severe
 The (4-2-1) rule; any two of the following
 4 quadrants of microaneurysms and extensive
intraretinal haemorrhage
 2 quadrants of venous beading
 1 quadrant of IRMA
Proliferative diabetic
retinopathy
Mild-moderate PDR
 New vessels on the disc (NVD) or new vessels
elsewhere(NVE), but extent insufficient to meet the
high-risk criteria
 Treatment considered according to severity of signs,
stability, systemic factors, and patient’s personal
circumstances such as reliability of attendance for
review
 If not treated, review in up to 2 months
NVD > 1/3 disc in area Less extensive NVD
+ haemorrhage
MILD MODERATE
High-risk PDR
• New vessels on the disc (NVD) greater than ETDRS
• Any NVD with vitreous haemorrhage
• NVE greater than 1/2 disc area with vitreous haemorrhage
• Treatment Should be performed immediately when possible,
and
• certainly same day if symptomatic presentation with
• good retinal view
High-risk PDR
Neovascularization
NVD
DIABETIC MACULOEDEMA
 Diabetic macular edema is the leading cause of legal
blindness in diabetics
 Diabetic macular edema can be present at any stage of
the disease, but is more common in patients with
proliferative diabetic retinopathy
International Clinical Diabetic
Macular Edema
Disease Severity Scale
 DME apparently absent -No apparent retinal thickening
or hard exudates in posterior pole
 DME apparently present -Some apparent retinal
thickening or hard exudates in posterior pole
 DME present ;
 Mild DME- Some retinal thickening or hard exudates in
posterior pole but distant from the center of the macula
 Moderate DME- Retinal thickening or hard exudates
approaching the center of the macula but not involving
the center
 Severe DME- Retinal thickening or hard exudates
involving the center of the macula
Advanced diabetic eye
disease
 Marked by complications like;
 Persistent VH
 Tractional retinal detachment
 Neovascular glaucoma
Cont.
Cont.
Cont.
Cotton wool
Exudate
s
OCT
MACULA EDEMA
NORMAL
Vitreous hemorrhage
Retinal detachment
↗
↘
↘
TREATMENT
GENERAL
 Patient education
 Diabetic control
 Control of risk factors
 Fenofibrate-200mg od(statin)
 Address modifiable factors-smoking,anaemia
INVESTIGATION
 Examination
 Photograph of the fundus
 Optical coherence tomography scanning
 B scan
 Fluorescein angiography (FA) allows differentiation
Treatment of diabetic
retinopathy and diabetic
maculo oedema
1.Laser photocoagulation treatment
 Focal-diode or argon burns are
applied to leaking microaneurysms
500-3000um from the foveola
 Grid-burns are applied to macula
areas of diffuse retinal
thickening,treating no closer than
500um from the foveola and 500um
from the disk
2.Subthreshold micropulse diode laser
 Uses very short laser pulse duration
combined with a loner interval
CT.
5.Pars plana vitrectomy-
 Indicated when macula oedema is
associated with tangential traction from a
thickened and taut posterior
hyaloid(vitreomacular traction)
 Intraocular injection treatment
 Steroid intravitrial implant treatment
REFERENCE
 Kanski 8th Edition
 AK Khurana
THANK YOU

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DIABETES AND THE EYE.pptx

  • 2. introduction  Diabetes mellitus describes a metabolic disorder characterized by chronic hyperglycemia resulting from defects in insulin secretion , insulin action, or both.  It is the leading cause of preventable blindness in individual 40 to 60 years of age.  The rate of blindness among diabetic persons is 20 times that of the general population.
  • 3. Diabetic Retinopathy  This is the disease of the retina caused by microangiopathy due to long term effect of diabetes leading to the damage of the retina and blindness  It is the most important ocular complication of diabetes.  Prevalence of DR of any severity in the diabetic population is 30%.  Prevalence of blindness due to DR is approximately 5%.
  • 4. RISK FACTORS  Duration of DM  poor control of diabetes  Hypertension  Renal Disease  Pregnancy  Nephropathy  others; Obesity, hyperlipidaemia, smoking, anaemia
  • 5. PATHOPHYSIOLOGY  This is a Microangiopathy diseases primarily affecting the precapillary arterioles and capillaries , venules and post capillary venules.  The basic component of damaging is microvascular occlusion and microvascular leakages
  • 8. PATHOGENESIS  DR is predominantly a microangiopathy in which small blood vessels are particularly vulnerable to damage from high glucose levels.  Direct hyperglycemic effects on retinal cells are also likely to play a role.  Many angiogenic stimulators and inhibitors have been identified; vascular endothelial growth factor (VEGF) appears to be of particular importance.
  • 9. Diabetic retinopathy symptoms  DR is asymptomatic in early stages but as the disease progresses symptoms may include:  Blurred vision  Floaters  Distorted vision  Dark areas in the vision  Poor night vision  Impaired colour vision  Partial or total loss of vision
  • 10. Diabetic retinopathy signs  Microaneurysms; these are localized outpouchings, mainly saccular, of the capillary wall that may form either by focal dilatation of the capillary wall where pericytes are absent, or by fusion of two arms of a capillary loop.  Retinal hemorrhage  Exudate
  • 11. CLASSIFICATION 1.Non-proliferative DR Mild Moderate Severe Very severe 2.Proliferative DR 3.Diabetic maculopathy 4.Advanced diabetic eye disease
  • 12. Cont.
  • 13. NPDR Mild :  Indicated by the presence of at least 1 microaneurysm.  Referral : review in 1-2 years
  • 14. Cont.
  • 15. Cont. Moderate:  Microaneurysm/ intraretinal hemorrhages in 2 or 3 quadrants. • Early mild IRMA • Hard or soft exudates may or may not be there
  • 17. Cont. Severe:  The (4-2-1) rule; any one of the following  4 quadrants of microaneurysms and extensive intraretinal haemorrhage  2 quadrants of venous beading  1 quadrant of IRMA
  • 18. Cont…. Very severe  The (4-2-1) rule; any two of the following  4 quadrants of microaneurysms and extensive intraretinal haemorrhage  2 quadrants of venous beading  1 quadrant of IRMA
  • 19. Proliferative diabetic retinopathy Mild-moderate PDR  New vessels on the disc (NVD) or new vessels elsewhere(NVE), but extent insufficient to meet the high-risk criteria  Treatment considered according to severity of signs, stability, systemic factors, and patient’s personal circumstances such as reliability of attendance for review  If not treated, review in up to 2 months
  • 20. NVD > 1/3 disc in area Less extensive NVD + haemorrhage MILD MODERATE
  • 21. High-risk PDR • New vessels on the disc (NVD) greater than ETDRS • Any NVD with vitreous haemorrhage • NVE greater than 1/2 disc area with vitreous haemorrhage • Treatment Should be performed immediately when possible, and • certainly same day if symptomatic presentation with • good retinal view
  • 24. DIABETIC MACULOEDEMA  Diabetic macular edema is the leading cause of legal blindness in diabetics  Diabetic macular edema can be present at any stage of the disease, but is more common in patients with proliferative diabetic retinopathy
  • 25.
  • 26. International Clinical Diabetic Macular Edema Disease Severity Scale  DME apparently absent -No apparent retinal thickening or hard exudates in posterior pole  DME apparently present -Some apparent retinal thickening or hard exudates in posterior pole  DME present ;  Mild DME- Some retinal thickening or hard exudates in posterior pole but distant from the center of the macula  Moderate DME- Retinal thickening or hard exudates approaching the center of the macula but not involving the center  Severe DME- Retinal thickening or hard exudates involving the center of the macula
  • 27. Advanced diabetic eye disease  Marked by complications like;  Persistent VH  Tractional retinal detachment  Neovascular glaucoma
  • 28. Cont.
  • 29. Cont.
  • 34. TREATMENT GENERAL  Patient education  Diabetic control  Control of risk factors  Fenofibrate-200mg od(statin)  Address modifiable factors-smoking,anaemia
  • 35. INVESTIGATION  Examination  Photograph of the fundus  Optical coherence tomography scanning  B scan  Fluorescein angiography (FA) allows differentiation
  • 36. Treatment of diabetic retinopathy and diabetic maculo oedema 1.Laser photocoagulation treatment  Focal-diode or argon burns are applied to leaking microaneurysms 500-3000um from the foveola  Grid-burns are applied to macula areas of diffuse retinal thickening,treating no closer than 500um from the foveola and 500um from the disk 2.Subthreshold micropulse diode laser  Uses very short laser pulse duration combined with a loner interval
  • 37. CT. 5.Pars plana vitrectomy-  Indicated when macula oedema is associated with tangential traction from a thickened and taut posterior hyaloid(vitreomacular traction)  Intraocular injection treatment  Steroid intravitrial implant treatment
  • 38. REFERENCE  Kanski 8th Edition  AK Khurana

Editor's Notes

  1. Referral : review in 6 months – 1 year ; or refer to ophthalmologist