topic 2: glaucoma part 2 Flashcards

1
Q

what is OHT?

what are the risk factors of OHT progessing to glaucoma? (who are at risk)

A

4 - 7% of individuals older than 40 years have IOPs > 21 mmHg without detectable glaucomatous damage

  1. IOP ≥ 30 mmHg, treat as for POAG
  2. Greater age
  3. Thinner central corneal thickness (CCT)
  4. Larger C/D ratio (OHT has 10% chances of progressing to POAG after 5 years)
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2
Q

what are the 6 characteristics of primary open angle glaucoma?

A
  1. AC angle=open
  2. outflow= slow
  3. Most common
  4. Chronic
  5. Usually bilateral (happens in both eyes)
  6. Asymmetrical dmg
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3
Q

what are the 8 risk factors of POAG? (who are at risk)

A
  1. Race: More prevalent in Blacks than in Whites and Orientals
  2. Age: 40 - 60 age group, risk increases with increasing age
  3. High Myopia
  4. FmHx: 1/10 risk for first degree relative
  5. Systemic diseases: Diabetes mellitus, Hypertension
  6. Smoking
  7. Steroid use
8. Ocular: 
Consistently high IOP
Large CD ratio
Higher Myopia
Retinal disease: CRVO, RP
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4
Q

what are the signs of POAG?

A

*High IOP: > 21 mmHg (28-32 mmHg)
POAG can occur with normal IOP while high IOP may not have POAG

Diurnal variation of > 4 - 6 mmHg

*Large C/D ratio: >0.5

C/D ratio asymmetry: > 0.2

*Notching or loss of neural rim

Bayoneting/baring/nasal sweep of BV

Drance hemorrhages

*NFL defect/loss

Peripapillary atrophy

*Glaucomatous VF loss

Open & normal filtration angle

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5
Q

what are the symptoms of POAG?

A

Usually asymptomatic

History taking important– ask about frequency of eye examination

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6
Q

what is the management for POAG?

A

IOP reduction: greater the damage, the greater the IOP should be reduced

Urgent referral for medical/surgical Tx

Regular follow up: 6 ~ 12 months

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7
Q

what is normal tension glaucoma commonly associated with? what are its 2 signs and 1 symptoms?

A

Associated with poor vascular perfusion of the ONH

signs:
IOP ≤ 21 mmHg

Glaucomatous disc damage and VF defect

symptoms
Asymptomatic

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8
Q

what is the management for NTG?

A

Take detailed history

Do IOP phasing (when IOP is monitored at different time)

May require drug treatment

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9
Q

what are the risk factors for angle closure glaucoma?

A
  1. Race: South-East Asians, Chinese, Eskimos
  2. Age: > 40
  3. Hyperopia
  4. Family History
  5. Shorter axial length
  6. Larger crystalline lens size
  7. Dim illumination
  8. Post pupil dilation
  9. Emotional disturbance
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10
Q

what are the signs and symptoms of ACG?

A
  1. Blur vision
  2. Haloes, hazy vision
  3. Severe eye pain, headaches
  4. Nausea, vomiting
  5. Conjunctival injection / ‘red eye’
  6. Oval non-reactive mid-dilated pupil
  7. Corneal epithelial oedema
  8. Shallow or closed AC angle
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11
Q

what is the pathogenesis of ACG? (relate to pupillary block)

A

Iris recedes during pupillary dilation (e.g. in a dim room)

Crystalline lens moves anteriorly

Iris buries itself into the lens when pupil tries to dilate

Relative pupil block

Aqueous cannot flow into the anterior chamber

Aqueous builds up in the posterior chamber

Iris bombe
Iridocorneal contact

Increase in IOP → causing eye pain, corneal oedema (hazy, seeing halos) and conjunctival injection/redness.

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12
Q

what is the mangement for ACG and sub-acute ACG?

A

Immediate referral to drop IOP

Normally require surgical tx, followed by drugs

Follow up: every 3 months

Peripheral Iridotomy is 1st choice

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13
Q

what is Sub-Acute Angle Closure Glaucoma?

A

Intermittent episodes of blurred vision and ocular discomfort, with narrow angles

Repeated sub acute attacks may result in Primary Angle Closure Glaucoma

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14
Q

what is congenital glaucoma?

A

glaucoma caused by mal-development of the AC angle

Usually manifest before 3rd birthday, other manifest before 16th birthday

Usually sporadic; primary happens at irregular intervals

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15
Q

what is commonly associated with congenital glaucoma?

A
Sturge-Weber syndrome
Corneal dysgenesis/mal-development
Rubella
Aniridia
Retinoblastoma
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16
Q

what are the signs and symptoms of congenital glaucoma?

A
High myopia
Photophobia
Lacrimation
Buphthalmos
Increased corneal diameter (megalocornea)
Corneal haze
High IOP
17
Q

what is the management for congenital glaucoma?

A

Refer to paediatric ophthalmologist

Require surgical tx

18
Q

what is Pigment Dispersion Syndrome? when is its onset?

A

Pigments from iris epithelium clogs filtration angle

Young and middle-aged onset

19
Q

what is commonly associated with pigment dispersion syndrome?

A

Moderate myopia
Genetic
Exercise
Mechanical friction from IOL

20
Q

what are the signs and symptoms of pigment dispersion syndrome?

A

Krukenberg spindle
Pigment granules on iris surface or trabecular meshwork/hyperpigmentation
Loss of pupillary ruff
Iris transillumination

21
Q

what is the management for pigment dispersion syndrome?

A

Same as POAG’s management:

IOP reduction: greater the damage, the greater the IOP should be reduced

Urgent referral for medical/surgical Tx

Regular follow up: 6 ~ 12 months

22
Q

what is Pseudoexfoliation? what is the inset, common where and which sex?

A

Grey-white granular material found on pupil margin, anterior lens and posterior cornea

Elderly onset
Usually in females
High incidence in Scandinavia

23
Q

what is the management for pseudoexfoliation?

A

Same as POAG’s management

IOP reduction: greater the damage, the greater the IOP should be reduced

Urgent referral for medical/surgical Tx

Regular follow up: 6 ~ 12 months

24
Q

what is Neovascular Glaucoma secondary to?

A

Secondary to iris rubeosis (neovas) due to chronic severe retinal ischemia

25
Q

what is the management for Neovascular Glaucoma?

A

Refer to Surgical Tx

26
Q

what are the 3 types of secondary glaucoma?

A

Phakolytic Glaucoma
Rupturing of Morgagnian cataract

Uveitic Glaucoma
Formation of posterior synechiae

Haemolytic Glaucoma
Secondary to hyphema

27
Q

what is steroid induced glaucoma caused by?

A

Ocular inflammation, using steroid

Steroid responders after weeks of usage

28
Q

what is the main goal of glaucoma treatment?

A

Decrease aqueous production or increase outflow

Lower IOP
Avoid nerve damage
Save sight

29
Q

what is the purpose of medical/drug treatment of glaucoma?

A

To lower IOP by Increase aqueous outflow/uveoscleral outflow.

30
Q

what are the 2 types of drugs for glaucoma treatment? (in terms of their action)

A

type 1: Increase aqueous outflow/uveoscleral outflow

type 2: Decrease aqueous production

31
Q

decribe th e process of drug treatment. what kind of drug do we start off with? when do we review? what do we review?

A

(Anti-glaucoma medication/drug)
Normally started with one drug with lower concentration & instilled infrequently, with a targeted IOP to achieve

(Can be multiple drugs if very high IOP)

Review 4-8 weeks. If ideal IOP achieved, review 3-6 months

things to Review: IOP, Optic disc, VF, anterior angle

32
Q

give 3 examples of anti glaucoma drugs

A

e.g of drugs
Betaxolol 0.5%, timolol 0.5%, Latanoprost 0.5%

(Normally accompanied by Local anaesthesia and miotic drug eg. pilocarpine)