posterior eye conditions Flashcards

1
Q

sudden VF loss investigations

A
  • Tailored History
  • Slit Lamp Assessment – excludes anterior causes, indicative of pathology in posterior structures
  • Visual Acuity, if no glasses or if there are media opacities use pinhole to see if actual visual loss
  • Visual Fields – better idea of abnormality location (monocular pre chiasmal – affecting retina or optic nerve), binocular chiasmal or post chiasmal
  • Pupils – RAPD (indicates an intraocular symmetry in visual input, so caused by abnormality which effects the optic nerve or RNFL, wouldn’t get RAPD in post chaismal defect as this would not result in asymmetrical visual input between the 2 eyes – would effect both eyes
  • Eye movements –if pain possibly optic neuritis
  • Dilated Fundoscopy (also OCT and fundus photos)
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2
Q

signs and symptoms of CRAO

A

Symptoms
* Sudden painless monocular loss in vision
Signs
* Profound RAPD present (can have amaurotic pupil – completely unresponsive)
* Emboli? ( could see, the primary cause, look for yellow plaque, could be at disc of CRAO, or if BRAO then at effected area)
* Whitish, oedematous retina (depends how long it has been)
* Cherry red spot (if established)
* Disc pallor
Retinal vasculature narrowing (arteriola attenuation) (in early and acute stages)
Check if px had/has stroke/ TIA – ask about signs.
Arterial fibrillation then greater risk of developing emboli

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3
Q

BRAO signs and symptoms

A

Symptoms
* Sudden painless monocular drop in vision…. However vision is often unaffected, depends which branch affected
Signs
* RAPD often present (depends on severity)
* Emboli at bifurnication points
* Whitish, oedematous sector of retina
* Retinal vasculature narrowing in area supplied by the affected branch
* Altitudinal or sectoral visual field defect

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4
Q

management by optom for CRAO and BRAO

A
  • College CMG - CRAO if less than 12 hours old same day referral to ophthalmology. Greater Glasgow - CRAO if less than 24 hours old same day referral to ophthalmology
  • Initiate Ocular Massage whilst patient lies supine in new cases
  • BRAO can also benefit from ocular massage
  • Ocular Massage dilates the ophthalmic and retinal arteries, can cause a thrombus to disintegrate and may cause an impacted emboli to move to a more peripheral part of retinal circulation, and reduces the IOP
  • CRVO if elevated IOPS refer within a week, if IOPS over 40 refer same day
  • Patients will be referred by ophthalmology for a stroke work up (greater risk of stroke if emboli from carotid artery)
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5
Q

Retinal vein occlusion RVO

A
  • Thrombus in the CRV or a branch of the CRV
  • Atheriosclerotic aetiology
  • Common associations - hypertension, older age, hyperlipidaemia, diabetes, glaucoma, contraceptive pill, smoking
  • Can result in neovascular glaucoma, happens faster in CRAO than CRVO (less common in branch)
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6
Q

signs RVO

A
  • Variable presentation – depends where, if beginning of vein then more visual loss– blurred vision, metamorphopsia, visual loss
  • Could have no/minimal symptoms (if thrombus has lodged not centrally)
  • Poorer prognosis if vision poor and greater risk of neovascular
  • Dilation and tortuosity of retinal veins
  • Blot and flame haemorrhage
  • Cotton wool spots and retina oedema
  • CMO (cystoid macular oedema) !! important to check depends management
  • Retinal whitening
  • Disc oedema
  • RAPD only in ischaemic CRVO
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7
Q

management RVO

A
  • Branch more common than central
  • Not as worried about stroke than CRAO
  • Optometric Management
  • BRVO 5-6 x more common than CRVO
  • Referral urgency depends on presentation
  • If CMO present secondary to BRVO/CRVO then intravitreal anti-vegf will generally be given so referral urgency is usually within 1-2 weeks
  • Depends on guidelines

Eg Lothian guidelines Any Branch retinal vein occlusion (BRVO) with a reduction in vision (i.e. cystoid macular oedema present) should be referred to PAEP ARC clinic for review in 1-2 weeks and possible listing for treatment with intra-vitreal anti-VEGF (lucentis)
Any BRVO with no reduction in vision (i.e. no CMO) should be referred routinely to PAEP outpatients and should be advised to attend their GP within 1-2 weeks for BP check and routine blood tests.
Routine investigations include: FBC, Electrolytes, Cholesterol/Lipids, Glucose and LFTs.

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8
Q

Amaurosis Fugax management

A

Patients should be referred urgently to a TIA clinic for review within 48hrs if they present with the following symptoms:
* Amaurosis Fugax of sudden onset within 2 weeks, with no headache or associated pain and no ocular pathology/abnormality present, need seen in 48 hours
* Sudden onset previously undiagnosed visual field total scotoma of less than 2 weeks with no ocular pathology (i.e. homonymous hemianopia or quadrantopia)
To refer to a TIA clinic there is a direct phone number available 24 hours a day 7 days a week

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9
Q

retinal detachment differential diagnosis

A

Posterior Vitreous Detachment
Retinoschisis
Choroidal Mass

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10
Q

what to do when shaffers sign seen but no break or tear found

A

Shaffers Sign (pigmented particles in anterior vitreous) = retinal detachment , referral even if break/tear not found

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11
Q

what is retinoschsis

A

no symptoms, common in hyperopia, benign splitting of neurosensory retina at the level of the outer plexiform layer - OCT can be handy here – helps differentiate where retina detached ( if whole retina then retinal detachment)
no retinal break, idiopathic
inferior temporal peripheral area common, bilateral common
in 5% of the population – underdiagnosed

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12
Q

features or retinoschsis

A

no shaffers sign
dome shaped elevation
Leads to loss of visual function in this area but as peripheral rarely noticed

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13
Q

retinoschsis vs retinal detachment

A

haemorrhage or pigment in RD and not in retinoschisis

shifting fluid in RD and not in retinoschisis - ask px to move eye

retinoschisis has domed shaped and smooth and has absolute scotoma

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14
Q

retinoschisis mangement

A

not an emergency, usually not progressive, observe px and make sure doesn’t change overtime

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15
Q

emergency referral for what

A
  • retinal detachment
  • pigment in the anterior vitreous (tobacco dust)
  • vitreous, retinal or pre-retinal haemorrhage, or
  • lattice degeneration or retinal break, with symptoms.
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16
Q

what would the VFs reflect when vitreous haemorrhage in subhyaloid space

A

haemorrhage in subhyaloid space then maybe mild superior defect since all the blood settled inferiorly sub hyaloid cavity

if dispersed then maybe very extensive VF loss

17
Q

What are the mechanisms of vitreous haemorrhages

A

abnormal vessels:
Diabetic retinopathy (31–54 percent) of vitreous haemorrhages are caused by diabetes
Neovascularization from branch or central retinal vein occlusion (4–16 percent)
Sickle cell retinopathy (0.2–6 percent)

Rupture of normal vessels:
Retinal tear (11–44 percent)
Trauma (12–19 percent)
Posterior vitreous detachment with retinal vascular tear (4–12 percent)
Retinal detachment (7–10 percent)
Terson’s syndrome (0.5–1 percent)

blood from adjacent source:
Macroaneurysm (0.6–7 percent)
Age-related macular degeneration (0.6–4 percent)

18
Q

management on AION

A
  • Emergency Referral regardless of NAION or AION.
  • GCA strong association with arthritic condition, 50% of cases occur in these patients polymyalgia rheumatica (20% with this condition will get GCA
19
Q

Optic neuritis - what is it

A

Inflammatory demyelination of the nerve - either idiopathic or as a result of Multiple Sclerosis

  • Typically age 20-50
  • 75% female
20
Q

signs and symptoms of optic neuritis

A
  • Acute visual loss typically monocular (progresses over a number of days, usually not more than 7 days)
  • majority have peri ocular pain initially, often increased with eye movement (resolves in week 1-2)
  • May have history of demyelinating symptoms or known diagnosis of multiple sclerosis
  • decreased colour vision (red green)
  • decreased VA (decreased colour vision often proportional to decreased VA)
  • VF defect, diffuse, altitudinal, cecocentral or other
  • RAPD if unilateral or asymmetric (can be bilateral)
  • 2/3 normal disc appearance (retrobulbar – affected further back), 1/3 disc oedema (bulbar or papillitis – hyperemic oedematous disc ); if present, disc oedema is typically mild without haemorrhage or exudates
    Look at nerve for previous episode of optic neuritis – may or may have noticed symptoms before
21
Q

management of optic neuritis

A

Urgent referral to HES for confirmation of diagnosis and high dose IV prednisolone if within a week of symptoms onset – prognosis and outcome better
Consider need for investigation of potential underlying Multiple Sclerosis
(MRI, CT scan to confirm retrobulbar)

22
Q

TIA/stroke features

A
  • Stroke/TIA can be diagnosed from a concise history and reliable testimony from a witness eg px themselves or someone who was with the px
  • Direct referral from Optometry to Stroke teams in place in several health boards in Scotland
  • Optometry being first port of call has increased volume of patients attending optometry practices with TIA symptoms
  • Main reason for presentation to Optometry
  • Amaurosis Fugax
  • Transient sudden monocular vision loss that can last between 2 to 30 minutes,
  • Can involve the entire visual field or can be partial, can say dimming or curtain and then it went away
  • Patients often describe it as a “curtain coming down” in front of their eye or as a generalized darkening or shadow.