Diabetic Retinopathy Flashcards

1
Q

Examples of anterior segment complications of diabetes

A
  • Aqueous Deficient Dry eye – microvascular damage to lacrimal gland due to high blood sugar levels so reduced aqueous production, if underlying diabetic neuropathy then leads to reduced lacrimal innervation, reduced corneal sensitivity so reduced reflex tearing and can develop aqueous deficient
  • Diabetic neurotrophic keratopathy
  • Epithelial fragility
  • Delayed epithelial healing
  • Superficial punctate keratopathy
  • Persistent epithelial defects
  • Recurrent corneal erosions
  • Neurotrophic corneal ulceration
  • Filamentary keratitis
  • Descemet‘s folds
    Corneal involvement is a common factor, need to look at cornea thoroughly
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2
Q

what is Diabetic Keratopathy

A

Diabetic keratopathy is when the cornea that does not have normal wound healing or healing mechanism which can lead to persistent or recurrent corneal epithelial defects and unresponsive to treatment especially when person’s blood glucose level is out of control or really high

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3
Q

why do more diabetic patients suffer from corneal complications

A

70% of diabetic patients suffer from corneal complications
Since diabetic cornea experiences 4-fold higher glucose level in diabetics
Examples:
1. Superficial punctate keratitis
2. Recurrent corneal erosion
3. Persistent epithelial defect (corneal)
4. Diabetic neurotrophic keratopathy

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4
Q

Diabetic Neurotrophic Keratopathy - what is it

A
  • Occurs in up to 64% of diabetic patients
  • Involves reduction of corneal nerve density so impaired corneal sensitivity - not enough nerves in cornea
  • May lead to permanent vision loss
  • Characterised by structural and functional changes of cornea
    o Impaired corneal sensitivity
    o Epithelial defects (loss of protective function)
    o Impaired healing
    o Corneal ulceration
    o Loss of vision
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5
Q

what are the 3 stages of Diabetic Neurotrophic Keratopathy

A

o Three stages –
stage 1 could have no symptoms- could say eye is red than normal, reduced TBUT, could see punctate epithelial keratopathy. Need to catch at this stage.
cornea can be hazy in periphery
stage 3 stroma involved, ulceration, whole cornea oedematous, neovascularisation. High risk of perforation – could end up even more advanced infection – harder to control because of DM, such as endophthalmitis

When epithelial defect and does not heal properly and is slow healing or recurring, with the eye rubbing over it can lead to corneal ulceration and then vision loss.

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6
Q

corneal sensitivity in DM

A

Up to 55 % of diabetic patients have reduced corneal sensitivity.
Corneal sensitivity still difficult to measure and quantify. Need to consider if they want CLs!
When assessing cornea and adding NaFl,, does patient say eye is stingy once it goes in – shows cornea sensation, some reaction, does not mean if they don’t feel NaFl that they don’t have corneal sensitivity.
Not recommended to fit DM patients with CLs, fi already reduced corneal sensitivity and then training eye to forget anything on the eye with the cls, or only for occasional wear and monitor very frequently

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7
Q

Anterior Uveitis in DM

A
  • Presenting feature
  • Poor glycaemic control
  • Type 1
  • Advanced Type 2 (Neuropathy etc.)
  • Acute
  • Anterior
    can be a presenting feature of undiagnosed diabetes, recurrent, thought to be because of disruption in blood retina barrier – increases inflammation, increases risk of anterior uveitis, seen in poorly controlled diabetics, advanced type 2 in older patients and type 1 for younger patients usually
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8
Q

cataract in DM

A
  • Cortical
  • Nuclear
  • Snowflake
    More prone to develop cataract earlier in DM
    if someone had juvenile onset, type 1 mainly, and is difficult to control then snowflake cataract, would develop this at a young age as well
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9
Q

how many diabetics have DR

A

a third

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10
Q

main risk factors of DR

A
  • Hyperglycemia – poor blood glucose level control, or varied control
  • Hypertension – another vascular issue
  • Diabetes duration – generally the longer the more likely to have DR
  • Ethnicity (African, Hispanic, South Asian)
  • Puberty and pregnancy (DM type 1) – if significant change in body then higher risk of DR
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11
Q

clinical signs of DR

A
  • Microaneurysms
  • Retinal haemorrhages – flame, dot or blot, dot haemorrhages are smaller and rounder, blot are larger and uneven
  • Hard exudates – causes by lipid leaking from BVs due to damaged blood retinal barrier
  • Cotton-wool spots – accumulation of axoplasmic debris within the bundles of ganglion cell axons, tells us those areas in the retina are ischemia – not enough blood and oxygen – indication of underlying nerve fiber layer damage
  • Venous tortuosity and beading
  • Neovascularisation in retina or in posterior vitreous, which can lead to tractional RD
  • Tractional retinal detachment
  • Macular oedema
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12
Q

History and Symptom: First Presentation DM

A
  • Px may tell you that their vision fluctuates throughout the day – may be worse when they are hungry or after exercise.
    General Health:
  • Px may tell you they are being investigated for diabetes – prediabetic
  • They may be diet controlled (no meds)
    Family History:
  • Who (immediate family) had DM? TYPE? Age of Onset? Any effect on this family members eyes?
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13
Q

History and Symptoms: Monitoring, General Health:
If Px is already diagnosed, you need to ask:

A
  • Type
  • Duration – shows risk, longer
  • Medications
  • Stability with meds/lifestyle
  • Who monitors it? – may monitor themselves with home monitor or could be GP if new or uncontrolled.
  • When was the last check-up with GP? – even if monitored by themselves, since have annual check up in most cases
  • Are they attending DRS?
  • If yes – when was it? Were they advised of any changes in the back of their eye?
  • If no – any reason why not – accesses issue, nervous on going, any vlaid reason? Consider putting them on annual recall and monitoring them within your practice.
    if they don’t want to go to DRS then should consider seeing them sooner like 12/12
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14
Q

refraction signs DM

A

Biggest indication (of blood sugar level vascular issue): Fluctuating visual acuity throughout refraction.
You should consider DM as part of your differential diagnosis whilst refracting if this is the case, especially if there are other risk factors.

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15
Q

anterior eye health DM

A
  • Quantitative and qualitative evaluation of tear film
  • Measurement of corneal sensitivity
  • Treat any dry eye and monitor corneal defects
  • Look for inflammation in the anterior chamber – may be asymptomatic
  • Look for any structural changes in the lens
  • Refer if persistent visual impairment
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16
Q

posterior eye DM and when to dilate

A

Fundoscopy Assessment
Consider dilation (irrespective of px’s age) if:
* Small pupils (<2mm)
* >1 year since Px attended DRS
* Poor blood glucose level control (H+S, Refraction)
* First eye exam since diagnosis (yet to attend DRS)
Assessment can be aided with fundus photography
* The best way to detect retinopathy early—when still treatable and before vision is irreversibly lost

17
Q

further tests that couldbe done

A
  • Visual fields eg amsler – if distortion sign of macular issue , could do Sita fast, or 10-2 for testing centra foveal sensivity if screening or suspecting macular oedema
  • Octomap - wide image of fundus
  • Digital retinal photography
  • OCT imaging
18
Q

how can a tractional RD occur

A

retinal neovascularisation -vessels grow out towards the vitreous

the fibrous tissue over the top of the vessel and fibrous tissue or new vessel can attach itself to the posterior vitreous, overtime that can results in a tractional RD

19
Q

how to monitor patients with DM

A
  • Every 2 years if Px is under a DRS scheme and seen annually
  • Annually, if Px does not under a DRS scheme and seen annually
    (This can vary depending on health board)
20
Q

how to refer patients -to GP and HES

A

Letter to GP send by optometrist:
* To reassess blood glucose level and/or medication if clinically indicated, eg vision fluctuating in refraction or indication if glucose level is not stable eg new background retinopathy

Referral:
* GP – If first presentation at eye exam, for assessment and diagnosis
* Ophthalmology - If clinically indicated
(no specific guidance on management for DR on college of optometrists – but emphasis we should encourage pxs to attend their local NHS retinal screening screens and choosing the correct recall)

21
Q

GP responsibility

A

Responsible for Investigation and confirmation of diagnosis
Assessment of Blood Glucose Level (done by either):
* Blood Test
* Urine Test
Once diagnosed, Px name goes on diabetes list
All diabetic patients are invited to attend annual retinal screening

22
Q

Optometrists’ role at the Diabetic Retinal Screening Service

A
  • Medical Retina Specialisation from college of optometrists
  • Advanced grading of digital fundus images
  • Run slit-lamp clinics
  • Clinical decision-making/referrals to ophthalmology

Management
* Any images that may require referral will be graded at least by two graders (2 optoms check it before referral)
* Referral from DRS directly to ophthalmology outpatient clinic
* Screening result letter will be sent to patient and GP
* If image quality at screening appointment inadequate: patient to be booked for appointment at slit-lamp clinic eg due to corneal issues or lens opacities

23
Q

what is DRS

A
  • Nation-wide service
  • All diabetic patients over 12 years of age will be invited annually.
  • Screening based primarily on digital fundus images. Just fundus photos
  • Non-mydriatic fundus photo (technicians, nurses)
  • Dilation if required (approx 25% of patients)
  • All images will be graded by an Optometrist.
24
Q

Refer to Ophthalmology only if graded as:

A
  • R3 (advanced background retinopathy)
  • R4 (proliferative retinopathy)
  • M2 (severe maculopathy)
25
Q

Ophthalmologist – management of proliferative DR

A

Pan-retinal Photocoagulation (PRP) – gold standard treatment for proliferative DR and retinal ischemia.

Anti-Vascular Endothelial Growth factor treatments
* Anti-VEGF agents can arrest, or even reverse, proliferative retinopathy and macular oedema

Intravitreal Corticosteroids - used for macular oedema, long acting steroid implant may be used

Vitrectomy - May be useful in advanced diabetic retinopathy

26
Q

DRS criteria and recall

A

Diabetic Retinal Screening
Optometrist (with medical retina specialisation certificate)
Perform (dilated) fundus photography in these patients annually and report any changes to GP/Ophthalmologist.

Routine Eye Examination
Annual recall for these patients IF they are not seen annually. If under DRS annually already – you see these Px’s every 2 years

27
Q

optometrist goal in this

A

is to identify anyone with pre-proliferative diabetic eye disease
* With early diagnosis and laser photocoagulation, vision loss may be prevented/reduced
* In case of vision loss, some sight may be regained by with anti-vascular endothelial growth factors or vitrectomy

28
Q

what does cotton wool spot mean

A

there is ischaemia
but can go away once blood sugar in control

29
Q

what other conditions could cause px to self inject

A

Generally, DM in needing to self-inject daily
Rheumatoid Arthritis (usually not daily), allergies, could cause px to self-inject

30
Q

example of management plan for diabetic px with HSK

A
  • Refer to GP for work up and compliance issues maybe. Refer to HES
  • Need to say as optom, that is really important and eyes are irreplaceable,
  • Important to know if cls wearer, which px is
  • Since bilateral, IP cannot manage, since when it is bilateral it is a very big systemic issue
  • Herpetic ulcers are generally unilateral and IP cannot manage bilateral cases
  • Ganciclovir concern contraception, affects sperm
31
Q

corneal arcus

A

caused by cholesterol

Corneal arcus is deposition of lipid in the peripheral cornea and is generally considered a concomitant of normal ageing process and expected in the elderly patient. (ring around cornea)
However could indicate health issues in younger patients