Glaucoma 1 - introduction Flashcards

1
Q

What is glaucoma’s?

A

Group of ocular conditions that produces a characteristic of optic neuropathy

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2
Q

What are two way glaucoma is classified?

A

Primary - not associated with any other ocular disorders
Secondary- the increased IOPs are due to another condition

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3
Q

What percentage of glaucoma’s are primary?

A

95%

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4
Q

What is an example of secondary glaucoma?

A

Steroid induced glaucoma

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5
Q

What are the three classifications of primary glaucoma?

A

Open angle, closed angle, congential

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6
Q

What % of primary glaucoma is open?

A

85%

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7
Q

Which is easier to detect POAG or PCAG?

A

PCAG

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8
Q

What is the mechanism for open angle glaucoma?

A

Mechanism is unknown
possibility include:
Chronic injury to axons of the retinal ganglion cells and other optic nerve tissues mainly at the OD and lamina cribrosa causes IOPs to raise above average levels

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9
Q

What is the mechanical pathogenesis of the glaucomatous optic disc?

A

Axon damage within the optic nerve is caused by pressure induced deformation of the lamina cribrosa causing retinal ganglion cell death

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10
Q

What is the vasogenic pathogenesis of the glaucomatous optic disc?

A

The quality of blood supply to the optic nerve head is impaired which leads to hypoxia and reduced nutrient to the ONH —> retinal ganglion cell death.

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11
Q

What is meant by characteristic but not diagnostic visual field defects?

A

The typical VF defect is a arcuate shape, which take the path of the retinal ganglion cells. There is a nasal step as well
*glaucoma is not only disease that causes this- NOT DIAGNOISTIC

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12
Q

Why is central 20-30 so important, for early open angle glaucoma?

A

Because Glaucoma will first effect the 20 -30 degrees on the VF at tis earliest stage

And the px will not be able to notice, as no symptoms

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13
Q

What are the important risk factors for OAG?

A

1.Age
2.IOP (huge RF)
3.Race
4.FH
5.Myopia
6.Genetics

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14
Q

What increases with the prevalence of OAG?

A

Increased IOPs, increased VF loss

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15
Q

If IOPs are reduced with someone with OAG, what happens?

A

Optic nerve head damage risk reduced (IOPs should be reduced to the target pressure)

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16
Q

According to NICE guidelines what is the prevalence of OAG in over 40s?

A

2%

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17
Q

According to NICE guidelines what is the prevalence of OAG in over 75s?

A

10%

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18
Q

What is normal tension glaucoma (three situations where this is apparent)?

A
  • A glaucomatous optic neuropathy but IOP never exceeds 21mmHG
  • A glaucomatous optic neuropathy with mean IOP over a 24hr period of <21mmHg & peak pressure of <24mmHG
  • chronic OAG where IOP is rarely above 21mmHg (NICE Definition)
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19
Q

What does the Bedford glaucoma study show?

A

21mmHG comes from the mean IOP of 16mmHG +2 standard deviation
IOP is NOT normally distributed

SD is 2.5. 2 SD = 5. 16+5 = 21 21mmHg.

The value of 21 is more statistical not clinical

20
Q

Is normal tension glaucoma rare?

A

NO

21
Q

What percentage of pxs will have IOPs in the normal range at the time of diagnosis?

A

40-50%

22
Q

What is high tension glaucoma?

A

A glaucomatous optic neuropathy with IOP outside statically Normal range

23
Q

What are the three types of primary angle CLOSURE glaucoma ?

A

Acute, subacute and chronic
(Makes up 15% of primary glaucomas)

24
Q

Is the prevalence of PCAG and POAG similar everywhere around the world?

A

No- it is more prevalent in some places more than others for example in china PCAG is more prevalent than POAG

25
Q

What percentage of congential glaucomas make up primary glaucomas?

A

<0.5%

26
Q

What % of child blindness is caused by Priamry congenital glaucoma ?

A

2.5-10%

27
Q

What causes congenital glaucoma?

A

Mal-development of the anterior chamber angle and as a result incomplete development of the TM

28
Q

What is shown in severe cases of congenital glaucoma + what would treatment be?

A

Buphthalmos - visible enlargement of the eyeball due to controlled glaucoma
Treatment= surgical to open up drainage angle

29
Q

Are we involved in the diagnosis of congenital glaucoma?

A

No- normally the paediatrician

30
Q

Do people with ocular hypertension (OHT) have glaucoma?

A

No

31
Q

What signs do people with OHT have?

A

-IOP>21mmHg CONSISTENTLY
- Normal discs
- Normal VF
- Open anterior chamber angle

32
Q

According to the Norfolk Eye study, what is the prevalence of the population having OHT?

A

10%

33
Q

Why is the Norfolk Eye Study good?

A

Because it is fairly recent but also a study in the UK

34
Q

According to NICE (2009) what percent of those over 40 have OHT?

A

3-5%

35
Q

What are people with OHT at risk of?

A

Developing POAG

36
Q

If one identical twin developed OAG what is the chance that the other one gets it too?

A

98%

37
Q

Why is it important to ask for a family history of glaucoma?

A

There is a distinct genetic link, 10-50% of OAG report FH of glaucoma (but lots of people under report so it’s probably a higher %)

38
Q

If we are able to identify specific gene defects then what should this lead to?
(There are 3 points)

A
  • Better understanding of mechanism
  • Better conventional treatments
  • Wide spread screening for disease esp those at risk which could reduce risk of visual loss
39
Q

Do we screen for glaucoma as optometrists?

A

No- we do opportunistic surveillance or case finding

40
Q

Why is OAG difficult to detect?

A

Px nly get symptoms until late stages of the disease

41
Q

What are the three main tests we do to detect glaucoma?

A

Measure IOPs
Assessment of VF
Examination of the optic disc

42
Q

Are the screening tests for glaucoma perfect?

A

No- there’s many factors affecting accuracy for each of the tests e.g thick cornea affects IOPs, DISC assessment is subjective , FP & FN on VF

43
Q

What does sensitivity mean?

A

The proportion of all diseased pxs who are correctly classified as diseased by the test (should be 100%)

44
Q

What does specificity mean?

A

The proportion of all normal pxs who correctly classified as normal by the test (this should be 100%)

45
Q

What are the 3 stages / types of Congenital Glaucoma?

A

1.) Neonatal or newborn onset (0-1m)
2.) infantile onset (>1m until 24m)
3.) late onset or late recognised (>2yrs to puberty )
FYI for Anisha specifically: m stands for month x

46
Q

What could identification of specific gene defects lead to? (3)

A

1.) better understanding of mechanisms of disease esp as largely unknown in glauc
2.) better conventional treatments
3.) widespread screening for disease, esp in affected families- early risk identification could mean family members have reduced risk of Visual loss in life