ophthalmology Flashcards

1
Q

What is conjunctivitis?

A

Conjunctivitis, also known as ““pink eye,”” is a common condition that involves inflammation or infection of the conjunctiva, the transparent membrane that lines the eyelid and covers the white part of the eye. This condition can be either infectious (caused by bacteria or viruses) or noninfectious (due to allergies or other irritants).

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2
Q

What are the three main types of conjunctivitis?

A

Allergic
Viral
Bacterial

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3
Q

What type of hypersensitivity reaction is allergic conjunctivitis?

A

Type I hypersensitivity

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4
Q

What is viral conjunctivitis most often caused by?

A

adenoviruses (65-90%) but can also be caused by herpes simplex virus. It is highly contagious and often associated with upper respiratory tract infections or colds. This is the most common acute infectious cause.

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5
Q

What common pathogens cause bacterial conjunctivitis?

A

Common pathogens include Staphylococcus aureus, Staphylococcus epidermis, Streptococcus pneumoniae and Haemophilus influenzae. Sexually transmitted infections like gonorrhoea or chlamydia can also cause bacterial conjunctivitis, so it is important to take a sexual history if suspected.

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6
Q

What are common signs and symptoms of conjunctivitis?

A

Eye redness
Itching
Irritation
Excessive tearing
Discharge from the eyes, which can vary in consistency based on the cause. For example viral aetiologies produce a more watery discharge, wheres bacterial causes produce purulent discharge.
Photophobia, which suggests corneal involvement (keratoconjunctivitis)

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7
Q

What should notably not be affected by conjunctivitis?

A

Visual acuity

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8
Q

What are red flag symptoms for a more serious cause of red eye?

A

Reduced visual acuity
Marked eye pain, headache, photophobia
Red sticky eye in a neonate
History of trauma or foreign body
Rapidly progressive discharge
Infection with herpes virus
Contact lens use
Pupil abnormalities or pain on constriction
Loss of red reflex
Blood or pus in the anterior chamber

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9
Q

What are the investigations for conjunctivitis?

A

The diagnosis of conjunctivitis is typically based on the patient’s history and physical examination. In certain cases, conjunctival swabs for bacterial cultures may be taken, particularly if the patient does not respond to initial treatment, presents severe or unusual symptoms, or in cases of suspected gonococcal or chlamydial conjunctivitis.

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10
Q

What is the management for allergic conjunctivitis?

A

Patients are advised to avoid allergens when possible and may be prescribed artificial tears, topical antihistamines, or mast cell stabilisers such as topical sodium cromoglycate.

1st line: topical mast cell stabilizer (sodium cromoglycate) and topical antihistamine (antazoline).

In this light, think of mast cell stabilisers as the ‘preventer’ of allergic conjunctivitis and antihistamines as the ‘reliever’

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11
Q

What is the management for viral conjunctivitis?

A

As this form is self-limiting, treatment focuses on symptom relief and prevention of spread through good hygiene practices.

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12
Q

What is the management for bacterial conjunctivitis?

A

This form is also generally self-limiting, but in severe cases, topical antibiotics like chloramphenicol and fusidic acid may be recommended.

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13
Q

How to manage conjunctivitis associated with contact lens wear?

A

Conjunctivitis associated with contact lense wear should be managed with an aminoglycoside (e.g. gentamycin) or a quinolone (e.g. levofloxacin or moxifloxacin), to cover for gram -ve organisms. Patients should immediately stop wearing contact lenses until symptom resolution and antibiotic course completion.

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14
Q

When should patients be told to seek further medical attention with conjunctivitis?

A

if their condition worsens or fails to improve after a week of treatment.
If there is evidence of any red flag signs (see above), patients should be referred urgently to ophthalmology.

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15
Q

What is prulent discharge and unilateral stomps a sign of in conjunctivitis?

A

bacterial infection whereas serous discharge is a more a sign of viral or allergic conjunctivitis

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16
Q

What is optic neuritis?

A

Optic neuritis (ON) is an inflammatory condition of the optic nerve that often results in visual impairment and ocular pain.

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17
Q

Who mostly gets optic neuritis?

A

Optic neuritis predominantly affects adult women and is often the first clinical presentation of multiple sclerosis (MS).

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18
Q

What causes optic neuritis?

A

caused by inflammatory demyelination

Multiple Sclerosis (MS): The most common cause of demyelinating optic neuritis.
Neuromyelitis Optica (NMO): A demyelinating disease that can also affect the optic nerve, presenting similarly to MS-related optic neuritis but with distinct pathophysiology.
Autoimmune disorders: Disorders such as lupus or sarcoidosis can trigger optic nerve inflammation.
Infections: Viral or bacterial infections, particularly those affecting the central nervous system, may lead to optic neuritis.

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19
Q

What are the signs and symptoms of optic neuritis?

A

Acute, painful vision loss: This is often the hallmark symptom and can range from mild to severe.
Periocular pain: Pain around the eye, especially with eye movement
Dyschromatopsia: Loss of colour vision, particularly red desaturation
Relative afferent pupillary defect
Additional features may include impaired contrast sensitivity and visual field defects.

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20
Q

What are the investigations for optic neuritis?

A

Visual function tests: To assess visual acuity, color vision (especially red desaturation), and visual fields. Even after recovery, some deficits in contrast sensitivity, color vision, or visual fields may persist.
MRI of the brain and spine: To detect demyelinating lesions, particularly in cases associated with multiple sclerosis or neuromyelitis optica - definitive investigation
Lumbar Puncture: May be required if a diagnosis of Multiple Sclerosis (MS) is considered to assess for paired Oligoclonal Bands (OCB).

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21
Q

What is the management for optic neuritis?

A

Intravenous methylprednisolone is the first-line treatment for optic neuritis, based on the Optic Neuritis Treatment Trial (ONTT).
Although oral steroids are sometimes used, they have been associated with an increased risk of relapse in some studies.

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22
Q

What is the prognosis of optic neuritis?

A

The prognosis for optic neuritis is generally good, with most patients regaining near-normal visual acuity within six months.
However, some may continue to experience subtle deficits in color vision, contrast sensitivity, or visual fields.

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23
Q

Which drug is strongly associated with optic neuritis?

A

ethambutol

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24
Q

What is orbital cellulitis?

A

a sight- and life-threatening emergency. It describes infection of the structures behind the orbital septum.

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25
Q

What is the orbital septum?

A

a membranous sheet that forms the anterior border of the orbit, extending from the orbital rims (superior and inferior) and into the eyelids.

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26
Q

What is preseptal cellulitis?

A

Preseptal cellulitis refers to infection of tissue anterior to the orbital septum. It is much more common than orbital cellulitis and 80% of cases occur in children under the age of 10 years.

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27
Q

Is orbital cellulitis or preseptal cellulitis more worrying?

A

Orbital cellulitis

28
Q

What are the risk factors for orbital and preiorbital cellulitis?

A

Trauma
Surgical – ocular, adnexal or sinus
Sinus disease – ethmoidal sinusitis is the most common site of infection that spreads to the orbit
Other facial infections – preseptal, dental abscess or dacryocystitis

29
Q

What are the signs and symptoms of orbital cellulitis?

A

Periocular pain and swelling
Fever
Malaise
Erythematous, swollen and tender eyelid
Chemosis
Proptosis
Restricted eye movements +/– diplopia

30
Q

What is the typical patient presenting with for preseptal cellulitis?

A

a child with an erythematous swollen eyelid, mild fever and erythema surrounding the orbit

31
Q

What findings suggest preseptal cellulitis over orbital cellulitis?

A

No proptosis
Normal eye movements
No chemosis
Normal optic nerve function

32
Q

What are the investigations for orbital and preseptal cellulitis?

A

Blood tests: FBC, CRP to screen for raised inflammatory markers
Swabs sent for microscopy, culture and sensitivity
CT orbit is the gold standard investigation to distinguish orbital cellulitis from preseptal cellulitis

33
Q

What is the gold standard investigation to distinguish orbital cellulitis from preseptal cellulitis?

A

CT orbit

34
Q

What is the management for orbital cellulitis?

A

admission for IV antibiotics and close monitoring with input from the ophthalmology, ear, nose and throat and medical teams.

35
Q

What is the management for preseptal cellulitis?

A

Young or systemically unwell children should be admitted for IV antibiotics. Otherwise, treatment is with oral antibiotics and daily outpatient review.

36
Q

What is scleritis?

A

Scleritis is a severe inflammation of the sclera

37
Q

What systemic illnesses is scleritis associated with?

A

rheumatoid arthritis or granulomatosis with polyangiitis

infections such as Herpes zoster and syphilis.

38
Q

Photo of typical scleritis:

A

More diffuse across the eye

39
Q

Symptoms of scleritis?

A

Red eye
Severe pain in the orbit
Pain on eye movement
Bluish tinge to the white of the eye in severe or necrotising scleritis
Systemic symptoms in ~50% of patients

40
Q

What are the investigations for scleritis?

A

Urine dipstick to identify renal disease
FBC, CRP, U&Es, LFT to identify anaemia of chronic disease, neutrophilia, renal function
Autoimmune serology
Phenylephrine eye drops - these blanch the conjunctival and episcleral vessels but not the scleral vessels. So if there is no blanching this is suggestive of scleritis

41
Q

Management for scleritis?

A

NSAIDs such as fluriprofen PO 100 mg TDS for mild cases
Corticosteroids such as oral prednisolone or pulsed IV methylprednisolone for severe or necrotising cases
Steroid-sparing therapies for long-term treatment

42
Q

Prognosis for scleritis?

A

Less than 5% of patients lose useful vision long-term; however, vision deteriorates in 25% of patients in the years following scleritis and some patients develop cataracts.

43
Q

What is thyroid eye disease?

A

Thyroid eye disease (TED) is a complication of Grave’s disease, which is an autoimmune hyperthyroidism. An inflammatory process results in swelling of the extraocular muscles and orbital fat, which leads to multiple ocular complications.

44
Q

What is the pathophysiology of thyroid eye disease?

A

Evidence suggests that an autoimmune reaction to TSH receptors results in lymphocyte infiltration into orbital tissues, which initiates an inflammatory process.

45
Q

How long does the inflammatory phase of thyroid eye disease last?

A

The inflammatory phase of TED typically lasts 6–24 months and results in the swelling of extraocular muscles and orbital fat – it is only during this initial inflammatory phase that TED is responsive to medical management.

46
Q

What happens after the inflammatory phase of thyroid eye disease?

A

After the inflammatory phase, there is an inactive fibrotic phase, which is nonresponsive to medical therapy.

47
Q

What are the risk factors for thyroid eye disease?

A

Smoking – the most important risk factor for development and increased severity of TED in patients with Grave’s disease, so it is important to counsel patients on the importance of smoking cessation
Family history of Grave’s disease and other autoimmune disease
Female sex
Poor thyroid control

48
Q

What are the signs and symptoms of thyroid eye disease?

A

Ocular pain – often worse on movement
Dry, red eyes
‘Bulging eyes’
Painful eyelids
Proptosis/exophthalmos
Lid retraction and lid lag
Chemosis
Orbital fat prolapse
Exposure keratopathy

49
Q

What is the early management of thyroid eye disease?

A

Early medical management of TED has the potential to stabilise, slow or even reverse the disease process. Good control of thyrotoxicosis is essential and other medical therapies, such as steroids or other immunosuppressants, may be used.

50
Q

In sight threatening thyroid eye disease what is the management?

A

In sight-threatening TED, urgent surgical orbital decompression may be required, followed by intravenous corticosteroids.

51
Q

What is the conservative management of thyroid eye disease?

A

Conservative therapy consists of artificial tears, ointments and prisms to help with the symptoms of dry eye and diplopia.

52
Q

What are the sight threatening complications of thyroid eye disease?

A

Sight-threatening complications include:
Exposure keratopathy – where corneal damage and infection occur as the patient is unable to close their eyes
Compressive optic neuropathy – occurs when the retro-orbital swelling begins to compress on the optic nerve
suspect this when signs of optic nerve involvement occur – reduced visual fields, reduced colour vision, reduced visual acuity, relative afferent pupillary defect
Diplopia – due to fibrosis of the extraocular muscles limiting gaze in various directions

53
Q

Which hyperthyroid disease treatment is contraindicated in grave’s disease?

A

Radioactive iodine ablation therapy worsens thyroid eye disease. The mechanism is proposed to centre on an initial increase in the number of thyroid antigens in the circulation following iodine ablation. These antigens then react with antibodies which go on to cross react with similar antigens in the extraocular muscles and fibroblasts

54
Q

What are the three parts of the uveal tract?

A

iris, ciliary body, and choroid

55
Q

What is uveitis?

A

Uveitis is an umbrella term for conditions causing inflammation of the uveal tract, including the iris, ciliary body, and choroid, along with associated structures in the eye. It is categorized into four types: anterior uveitis, intermediate uveitis, posterior uveitis, and panuveitis, based on the anatomical location of inflammation

56
Q

What is the most common type of uveitis?

A

anterior uveitis

57
Q

What does the global distribution of uveitis depend on?

A

The global distribution of uveitis differs according to the prevalence of HLA-B27 positivity.

58
Q

What is the underlying cause of uveitis?

A

Autoimmune diseases:
Ankylosing spondylitis
Behçet’s disease (associated with HLA-B51 positivity)
Juvenile idiopathic arthritis
Multiple sclerosis
Systemic lupus erythematosus (SLE)
Inflammatory bowel disease - ulcerative colitis
Granulomatosis with polyangiitis
Reactive arthritis
Other causes:
Infections (e.g., herpes, tuberculosis, syphilis, HIV)
Trauma
Iatrogenic causes (e.g., ocular surgery or medications)
Ischaemic conditions

59
Q

Signs and symptoms of anterior uveitis?

A

Symptoms:
Painful red eye worsening over several days
Photophobia
Blurred vision
Headache

Signs:
Conjunctival injection
Hypopyon - inflammatory cells can be seen as pus in the anterior chamber
Keratic precipitates
Posterior synechiae and irregular pupil
Anterior chamber flare
Anterior chamber cells

60
Q

Signs and symptoms of intermediate uveitis?

A

Symptoms:
Often painless
Floaters
Blurred vision
No external signs of inflammation in some cases

Signs:
Inflammatory cells within the vitreous

61
Q

Signs and symptoms of posterior uveitis?

A

Symptoms:
Blurred vision
Progressive vision loss
Flashes or floaters

Signs:
Yellow/white appearance of the retina
Cystoid macular oedema

62
Q

Signs and symptoms of panuveitis?

A

Patients typically exhibit a combination of all of the symptoms and signs of anterior, intermediate and posterior uveitis

63
Q

Investigations for uveitis?

A

Complete ocular examination including slit-lamp testing
Blood tests for autoimmune markers
Infectious disease screening

64
Q

What is the treatment for the acute phase of uveitis?

A

In the acute phase, management typically involves:
Cycloplegic mydriatic drops e.g. cyclopentolate
These cause iris dilation and help to break/prevent posterior synechiae
Corticosteroids (topical, oral, IV, or IM), typically starting on an hourly regimen and then gradually tapered
Analgesia

65
Q

What is the treatment for chronic uveitis?

A

Chronic uveitis may necessitate systemic steroid-sparing immunosuppressants, such as methotrexate or mycophenolate. Evidence also supports the use of biologic therapies targeting specific elements of the inflammatory cascade, such as adalimumab.

66
Q

What is the prognosis of uveitis?

A

Prognosis varies with the underlying aetiology, but often uveitis is self-limiting. With early intervention, treatment outcomes are generally favourable, recovering normal vision in 90% of patients; however, relapse occurs in two-thirds of cases.

67
Q

Name a disease which causes severe ocular inflammation

A

Behçet’s disease often leads to severe ocular inflammation, including retinal vasculitis, which requires systemic immunosuppressive therapy to control inflammation and prevent vision loss.