Diabetes Mellitus Flashcards

1
Q

What are the 3 structural change in Diabetic retinopathy?

A
  1. Microvascular circulation changes from prolonged hyperglycaemia (due to compromise of the blood – retinal barrier)
  2. Microaneurysm
  3. Changes in haemodynamic
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2
Q

What is the pathogenesis of Diabetic Retinopathy

A
  • Vascular occlusion
    • Capillary occlusion: Loss of pericytes, thickening of basement membrane, damage, and proliferation of endothelial cells
    • Haematological: deformation and increased platelet aggregation leading to decreased oxygen transport
    o Results
    1. Retinal ischemia – initially developed in the mid – peripheral retinal. 30% of haemorrhages, microaneurysms (MA), IRMA and NVE occurred outside the 7 ETDRS zones (posterior pole and mid retina). Lesions observed outside the ETDRS zones increased DR severity grading in 10% of patients.
    2. Arteriovenous shunts (intraretinal micro – vascular abnormalities) = due to capillary occlusion that run from arterioles to venules
    3. Neovascularisation cause by growth factors released from hypoxic tissue in an attempt to revascularize hypoxic retina. Promotes neovascularisation of retina, optic nerve, iris (rubeosis iridis)
  • Vascular leakage
    • Pathogenesis = breakdown of inner blood-retinal barrier leads to leakage of plasma constituents into the retina
    • Leads to increased vascular permeability –development of intraretinal haemorrhages and oedema
    • 2 general types of retina oedema
    o Diffuse retinal oedema = due to capillary dilatation and leakage
    o Focal retinal oedema = Chronic retinal oedema leads to deposition of hard exudates
    • Hard exudates = occur at the border of normal and oedematous retina composed of lipoprotein and lipid-filled macrophages
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3
Q

What is HbA1c?

A

a measure of how much haemoglobin in the blood which is an index of long-term blood glucose control.

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4
Q

What are the risk factors for diabetic retinopathy?

A

Duration of Diabetes
Elevated HbA1c
Px with systemic hypertension
Px with hyperlipidaemia (high chlorestorol)
Pregnancy
Neuropathy
Gender - male
smoking status, ethnicity and type 1 DM

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5
Q

What are the systems of diabetic retinopathy?

A

Fluctuating vision, vision blurriness that cant be corrected with refraction, sudden eye pain and redness
acute onset flashes and/floaters

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6
Q

What are these symptoms indicative off:

Fluctuating vision, vision blurriness that cant be corrected with refraction, sudden eye pain and redness
acute onset flashes and/floaters

A

Diabetic retinopathy

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7
Q

What are the Anti VEGF treatments for Diabetic Macular Oedema?

A

1.Ranibizumab= binds and inhibits all identified VEGF isoforms

2.Bevacizumab = recombinant, humanized, antibody that binds to and inhibits the biologic activity of all isoforms of human VEGF. Originally approved by the FDA for use in patients with metastatic colorectal cancer.

3.Aflibercept= exhibits higher affinity for VEGF-A/-B and binds all the VEGF isoforms

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8
Q

What are the three Ophthalmology management for Clinically significant Macular Oedema?

A

Ophthalmology Management
1. Laser Photocoagulation
• Focal laser treatment applying laser burns (permanent structural damage to areas with MA or microvascular lesions. Treatment of lesions up to 300 µm from foveal centre
• Grid laser treatment used for areas of diffuse retinal thickening more than 500 µm
• Results: 70% achieve stable VA, 15% show improvement
2. Panretinal laser photocoagulation (PRP)
• Purpose: to induce involution of new vessels and prevent vision loss from vitreous haemorrhage (VH) and retinal detachment
• Treatment: 2000-3000 laser burns covering the peripheral retina in several session depending on pain threshold of patients.
3. Pars Plana Vitrectomy
• excision of posterior hyaloid face, relieving the vitreous/retinal traction and reattaching the retina and creating a vitreous cavity for filling with gas/silicone or internal tamponade
• Indication: Proliferative DR with VH or tractional Retinal detachment

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9
Q

What is the purpose of CSME ophthalmologic treatment?

A

Purpose:
• 1.Removal of vitreous gel: removes the stimulus for further fibrovascular tissue can proliferate
• 2.Removal of vitreous haemorrhage
• 3.Repair retinal detachment
• 4.Prevention of further neovascularization by applying laser photocoagulation

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10
Q

What are some complications that can arise from CSME surgery?

A

Complications
• 1.Rubeosis iridis
• 2.Cataract
• 3.Glaucoma secondary to rubeosis iridis
• 4.Recurrent VH
• 5.Retinal detachment

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11
Q

What is required for a diagnosis of Clinically Significant Macular Oedema?

A

One or more of the following
- Thickening of the retina ≤ 500 microns (1/3 DD) from the centre of the macula
- Hard exudates ≤ 500 microns (1/3 DD) from the centre of the macula with thickening of the adjacent retina
- Area of retina thickening ≥ 1 DA in size, any portion which ≤1 DD from the centre of the macula
- Microaneurysms, haemorrhages, IRMA and venous beading
- Non-Centre Involving (Mild) Macular Oedema
- Centre Involving (Severe) Macular Oedema
- Centre Approaching (Moderate) Macular Oedema
- Diabetic Maculopathy

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12
Q

What is required for a diagnosis of Diabetic Maculopathy>

A

Diabetic Maculopathy – macular oedema on/off centre with clinical features of ischemia
- Hard exudates
- Retinal oedema
- Cystoid retinal changes
- Dark haemorrhages

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13
Q

What are the features of Mild NPR - no macular oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Microaneursyms only

12 months

Communication with GP

no referral required

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14
Q

What are the features of Mild NPR - macular oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Microaneursyms only

4 - 6 months

Photo documentation

retinal ophthalmology review in 4 - 6 weeks

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15
Q

What are the features of Mild NPR - CSME?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Microaneursyms only

2 - 4 months

Photo documentation including GA or OCT - A

retinal ophthalmology review in 2 - 4 weeks

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16
Q

What are the features of Moderate NPR - No macular oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following
-retinal dot and blot haemorrhages
-hard exudates or cotton wool spots
- +/- microaneurysms
- no signs of severe non-proliferative diabetic retinopathy

6 - 8 months

Communicate with GP + Photo documentation

No referral required

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17
Q

What are the features of Moderate NPR - Macular Oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following
-retinal dot and blot haemorrhages
-hard exudates or cotton wool spots
- +/- microaneurysms
- no signs of severe non-proliferative diabetic retinopathy

4 - 6 months

Photo documentation

Retinal ophthalmology review in 2 - 4 weeks

18
Q

What are the features of Moderate NPR - CSME?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following
-retinal dot and blot haemorrhages
-hard exudates or cotton wool spots
- +/- microaneurysms
- no signs of severe non-proliferative diabetic retinopathy

2 - 4 months

Photo documentation including GA or OCT - A

Retinal ophthalmology review in 2 - 4 weeks

19
Q

What are the features of Severe NPR - no oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following:
-more than 20 intraretinal haemorrhages in each of the 4 quadrants
-definite venous beading in 2 or more quadrants
-prominent intra-retinal microvascular abnormality (IRMA) in 1 or more quadrants
- no signs of proliferative retinopathy

3 - 4 months

Photo documentation

Retinal ophthalmology review in 2 - 4 weeks

20
Q

What are the features of Severe NPR - Macular Oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following:
-more than 20 intraretinal haemorrhages in each of the 4 quadrants
-definite venous beading in 2 or more quadrants
-prominent intra-retinal microvascular abnormality (IRMA) in 1 or more quadrants
- no signs of proliferative retinopathy

2 - 3 months

Photo documentation FA or OCT

Retinal ophthalmology in 2 - 4 weeks

21
Q

What are the features of Severe NPR - CSME?

Frequency of follow up?

Management plan?

Appropriate referral?

A

Any of the following:
-more than 20 intraretinal haemorrhages in each of the 4 quadrants
-definite venous beading in 2 or more quadrants
-prominent intra-retinal microvascular abnormality (IRMA) in 1 or more quadrants
- no signs of proliferative retinopathy

2 - 3 months

Photo documentation including FA and OCT - A

Retinal ophthalmology review in 2 - 4 weeks

22
Q

What are the features of PDR - no macular oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

One or both of the following: neovascularisation and vitreous/pre retinal haemorrhage

2 - 3 months

Photo documentation

Retinal ophthalmology review in 24 - 48 hours

23
Q

What are the features of PDR - Macular Oedema?

Frequency of follow up?

Management plan?

Appropriate referral?

A

One or both of the following: neovascularisation and vitreous/pre retinal haemorrhage

2 - 3 months

Photo documentation FA or OCT

Retinal ophthalmology review in 24 - 48 hours

24
Q

What are the features of PDR - CSME?

Frequency of follow up?

Management plan?

Appropriate referral?

A

One or both of the following: neovascularisation and vitreous/pre retinal haemorrhage

2 - 3 months

Photo documentation including FA or OCT - A

Retinal ophthalmology review in 24 - 48 hours

25
Q

What are the vision functional changes that can occur with Diabetes Mellitus?

A

Dry eye syndrome, corneal changes, rubeosis iridis, cataracts, colour vision defects, refractive error and accommodative dysfunction, visual field effects, EOM palsies and afferent pupillary defects

26
Q

What is management for Dry Eye?

A

Prescription of artificial tears, lubricants, and dry eye management techniques. Monitoring for corneal complications

27
Q

What is management for corneal changes?

A

Monitoring for keratitis, ulceration, delayed wound healing if contact lens wearer

28
Q

What is management for rudeosis iridis?

A

Gonioscopy evaluation to rule out anterior chamber involvement and neovascularization. Tonometry to rule out secondary glaucoma

29
Q

What is the management for cataracts?

A

Monitoring lens opacification and status of associated retinopathy; extraction is necessary if visualization of retina becomes inadequate

30
Q

What is the management of a colour vision defect?

A

Tritan colour vision loss –Dilated fundus exam to screen for Clinically Significant Macular Edema (CSME)

31
Q

What is the management for Refractive error and accommodative dysfunction

A

Consultation with GP regarding glucose control and updating spectacles

32
Q

What is the management for Visual field defect?

A

Low vision evaluation, orientation and mobility training

33
Q

What is the management for EOM palsies?

A

Neuro-ophthalmology consultation, prism prescription, eye patching

34
Q

What is the management for Afferent pupillary defects?

A

Workup to rule out optic neuropathy

35
Q

What sign of DR can be found in the lids and conjunctiva?

A

Infection, inflammation, ulcerative Blepharitis, styes, chalazion, conjunctivitis

36
Q

What sign of DR can be found in the cornea ?

A

Corneal Keratopathy, decreased corneal sensitivity/nerve density, corneal ulcers, corneal edema and altered epithelium Basement Membrane (can lead to Recurring corneal erosion)

37
Q

What sign of DR can be found in the lens?

A

Fluctuation myopia, cataracts, light sensitivity

38
Q

What sign of DR can be found in the extra ocular muscles?

A

Cranial Nerve Palsy, 3rd CN: affect eye lid closed/smaller aperture; eye movement cannot move adduct and upwards; pupil can be enlarged and abnormal light reactivity. 4th CN: vertical diplopia, head tilt, ipsilateral hypertropia. 6th CN: double vision, affected eye cannot abduct

39
Q

What sign of DR can be found in the pupil and iris?

A

Autonomic neuropathy, rubeosis iridis and neovascular glaucoma

40
Q

What sign of DR can be found in the Optic Nerve?

A

Optic neuritis, diabetic papillopathy