Diabetic Retinopathy Flashcards

1
Q

Risk factor for DR

A
  • African and Hispanic ethnicity
  • T1DM (have diabetes for longer period, more time to develop DR complications)
  • Duration of diabetes - >10 years
  • High HbA1c - >8.0%.
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2
Q

Work up for DR

A
  1. Visual acuity (best corrected – distance and near, monocularly)
  2. Pupil reactions (direct/consensual and near pupil responses)
  3. Motility and cover test (correct any diplopia with prism)
  4. Visual field screening (minimum confrontation fields)
  5. Refraction (diabetes can lead to lens swelling and dioptric changes)
  6. Slit lamp Biomicroscopy (with dilation)
    a. Identify any NVC, cataracts, corneal changes.
  7. IOP (pre & post dilation)
  8. Stereoscopic fundus exam (using 0.5 or 1.0% tropicamide)
  9. Dilated retinal photography.
  10. Gonioscopy (assess glaucoma risk, narrow angle/NVC)
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3
Q

Signs for DR

A

decrease VA, decreased contrast sensitivity, increased central/paracentral retinal thickness, presence of intraretinal cysts.

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4
Q

Qs for DR classification and management

A
  1. How severe is the DR?
  2. Is there macula oedema?
  3. Is it clinically significant?
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5
Q

What is CSME

A

a. Macula thickening ≤500um (1/3 DD) from fovea
b. Hard exudate ≤500um from fovea with adjacent retinal thickening
c. Retina thickening ≥1 disc area in size, any portion of which is ≤1500um (1DD) from fovea.

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6
Q

Clinical findings for Mild NPDR

A

MA + retinal hb / CWS/ Hex

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7
Q

Clinical findings for Moderate NPDR

A

Hb/MA > photo 2A + CWS or venous beading + IRMA in 1/4

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8
Q

Clinical findings for Severe NPDR

A

One or more (4/2/1):
- Hb/MA Hb/MA > photo 2A in 4/4
- Venous beading in 2/4
- IRMA >Photo 8A in ¼

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9
Q

Clinical findings for Mild PDR?

A

NVD or NVE or Fibrous proliferation

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10
Q

Clinical findings for Moderate PDR?

A

NVD <Photo 10A (1/4 – 1/3 DA) or Vhb/PRhb and NVE <1/2 DA and NVD absent

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11
Q

Clinical findings for Severe PDR?

A

One or more (4/2/1):
- NVD>1/4 – 1/3 DA (Photo 10A)
- NVD and Vhb /PR hb
- NVE >1/2 DA and V hb /PR hb

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12
Q

Read follow up and referral timelines for DR

A

Read follow up and referral timelines for DR

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13
Q

Management for DR

A

Management:
1. Optimize cardiovascular risk factors.
a. Report to GP for intensive glycaemic control (recommended by DCCT) – aiming for <6.0%
b. Recommend intensive blood pressure control (UKPDS) - <130mmHg systolic target.
c. Recommend weight loss – 5 -10% reduction.
d. If px has high cholesterol recommend change from levato to fenofibrate (reduce DR risk)
2. Recommend regular aerobic training (30min 4x a week)
a. Exercise that make you puff
3. Referral to ophthalmologist for
a. Anti VEGF – Aflibercepts better for VA 6/15 or worse or PDR (DA VINCI + VISTA + VIVI DME study) May use Ranibizumab or Bevacizumab if needed.
b. Steroids: Dexamethasone (implant) may be used in alone or in combination with PRP. Triamcinolone 1mg or 4mg (worse VA than PRP, risk of endophthalmitis, retinal tear/detachment, elevated IOP, cataract). Fluocinolone Acetonide (surgical implant) – use alone or with PRP. Risk of elevate IOP and cataracts.
c. Panretinal Photocoagulation (PRP) – decrease demand for blood supply → decrease in new vessels. RISK of severe vision loss and progression of DR
d. Pars Plana Vitrectomy: beneficial for non-clearing vitreous hb and traction RD. Minimal functional improvements.

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14
Q

New emerging tx in DR

A
  1. Neuroprotective agent: doxycycline (50mg) or glycosaminoglycan. Prevent DR progression. Doxycycline has not significant functional/anatomical improvement.
  2. Angiopoietin 2 – antagonist of the tunica internal endothelial cell kinase (TIE2) receptor →increased vascular permeability and angiogenesis. Intravitreal injection TID for 4 weeks – multiple dosages available)
  3. Encapsulated cell technology (ECT) – allow a genetically modified group of cells lines expressing the gene of interest to encapsulate in synthetic semi-permeable capsules, allow diffusions of nutrients to these cells while protecting them from the hosts defence mechanism.
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