CLINICAL CASE PRESENTATION
Dr. Samten Dorji
Your Logo Here
• 38 year old male complained of right eye pain
and redness for 5 days duration.
CHIEF COMPLAINT
Personal information
He is from Zhemgang, married with two children and is gardener by profession
• He developed slow onset of pain in his right eye
and increase progression of pain. He had
associated redness, photophobia, excessive
tearing and reduced vision.
HISTORY OF CHIEF COMPLAINT
• No joint pain
• No history of asthma or symptoms suggestive of
chest infection
• No gastro intestinal symptoms
• No history of haematuria or urethral discharge
• No skin conditions
SYSTEMIC REVIEW
• Past ocular history/ocular medications/systemic
medications/comorbidities/allergies/family
history/social history
• No pets in house
HISTORY CONT.
Examination
Right eye Left eye
Visual acuity 6/60 6/6
With pinhole 6/12 6/6
Color vision Normal Normal
Extraocular movements Normal Normal
Lids and adnexa Normal Normal
Conjunctiva and sclera Circumcorneal congestion Normal
Cornea Clear Clear
Anterior chamber Cells grade +4 and flare
grade +3
Normal
Iris and lens Posterior synechia Normal
Pupil Round regular and miotic Round regular and reactive
IOP by Icare 13 mmhg 11 mmhg
Dilated Funduscopy NAD NAD
• 38 year old male presented to eye OPD with
right eye pain with redness for 5 days duration
with associated photophobia, excessive tearing
and reduced vision. On examination there was
no significant findings in his left eye. On his right
eye his visual acuity was 6/12 with pin hole. He
had circumcorneal congestion and had grade +4
cells and grade +3 flare in anterior chamber with
posterior synechia and miosis. He doesn’t have
any clinical features suggestive of systemic
disorder.
CASE SUMMARY
DIAGNOSIS
Acute anterior uveitis
Supporting points
• Unilateral eye pain with
photophobia and redness with
excessive tearing for duration of 5
days.
• Circumcorneal congestion with
anterior chamber cells and flare
with posterior synechia and miosis.
• Fundus appeared normal
Non-Supporting points
• Slow onset
Aetiology
• Idiopathic
• HLA-B27 associated uveitis
• Behcet disease
• Lyme disease
Differential diagnosis
• Posterior uveitis with spill over into the anterior chamber
• Traumatic iritis
• Infectious keratouveitis
Chest X ray PA= NAD
• Cycloplegic drops
• Antibiotic drops
• Prednisolone drops
• Oral prednisolone
MANAGEMENT
SUBJECT REVIEW
Acute anterior uveitis
• Introduction
• Clinical features
• Investigation
• Treatment
OUTLINE
• Uveitis is the inflammation of the uveal tract
INTRODUCTION
Clinical course
Acute Chronic Recurrent
Aetiology
Infectious Noninfectious
Histology
Granulomatous Nongranulomatous
Anatomy
Anterior uveitis Intermediate
uveitis
Posterior
uveitis
Panuveitis
• In a large community-based study, the vast
majority of uveitis cases were anterior (71%),
followed by posterior uveitis (5%) and
intermediate and panuveitis (1% each).
• The most common causes of anterior uveitis are
idiopathic (38−56%), the seronegative
spondyloarthropathies (21−23%), juvenile
idiopathic arthritis (JIA; 9−11%), and herpetic
keratouveitis (6−10%).
• Presentation: sudden onset of unilateral pain,
photophobia and redness, which maybe
associated with lacrimation.
• Visual acuity is usually good at presentation
except in eyes with severe hypopyon
CLINICAL FEATURES
External examination Miosis
Endothelial dusting Aqueous flare and cells
Cells in field Grade (anterior chamber cells)
<1 0
1-5 +-
6-15 +1
16-25 +2
26-50 +3
>50 +4
Description Grade (aqueous flare)
Nil 0
Just detectable +1
Moderate (iris and lens details clear) +2
Marked (iris and lens detail hazy) +3
Intense(fibrinous exudate) +4
Fibrinous exudate Hypopyon
Posterior synechiae
Low IOP
Investigation
INDICATIONS NOT INDICATED
Granulomatous inflammation Single attack of mild unilateral
AAU
Recurrent uveitis Sympathetic ophthalmitis and
Fuchs cyclitis
Bilateral disease When systemic disease is
already apparent
Systemic manifestation
Confirmation
Skin test
Tuberculin test Pathergy test
Lepromin test
1. Non-treponemal test= rapid
plasma reagin
2. Treponemal antibody test=
fluorescent treponemal
antibody absorption test and
microhaemagglutination
treponema pallidum test
3. Dark ground microscopy
Serology
Syphilis Toxoplasmosis
1. Dye test(Sabin-Feldman)= gold standard
2. Immunofluorescent antibody test
3. Haemagglutination tests
4. Enzyme linked immunosorbent assay (ELISA)
Enzyme assay
Sarcoidosis
Tuberculosis
Leprosy
Serum angiotensin
converting enzyme
Lysozyme assay
HLA tissue typing
HLA type Associated disease
B27 spondyloarthropathies
A29 Birdshot chorioretinopathy
B51 Behcet syndrome
Optical coherence tomography
Radiology
Chest X ray Sacro iliac joint X ray
CT and MR
1. Conjunctival and lacrimal gland biopsy
BIOPSY
Treatment
Mydriatics
Short acting Long acting
Tropicamide (6 hours) Homatropine (2 days)
Cyclopentolate(24 hours) Atropine(2 weeks)
Phenylephrine(3 hours)
Promote comfort
Break down
recently formed
posterior
synechiae
Prevent formation
of posterior
synechiae
Topical steroids
AAU CAU
• Frequent instillation of
drops at first
• The frequency is tapered
off once the inflammation
gets controlled
• Exacerbations treated as
AAU
• The intensity of flare can
also indicate an active
process
• Follow up of patient
regularly
Complication
Elevation of IOP
Periocular steroid injection
Advantages
• Therapeutic concentrations behind the lens
may be achieved
• Trans-sclerally entrance
• Prolonged effect
Indications
• First line therapy in unilateral
intermediate or posterior uveitis
• Supplement systemic therapy or when
systemic steroids are contraindicated
• Poor compliance
• At time of surgery
Complication
Globe penetration
Increased IOP
Ptosis
Sub dermal fat atrophy
Extraocular muscle paresis
Optic nerve injury
Retinal and choroidal vascular occlusion
Cutaneous hypopigmentation
Systemic steroids
• Oral prednisolone and intravenous infusion of methylprednisolone
Indications
• Intermediate uveitis unresponsive to
posterior sub tenon injection
• Posterior or panuveitis, particularly
with bilateral involvement
• Prior to intraocular surgery
• Anterior uveitis resistant to topical.
Contraindications
• Poorly controlled diabetes
• Peptic ulceration
• Osteoporosis
• Active systemic infection
• Psychosis on previous exposure to
steroids
Short term side effects Long term side effects
• Dyspepsia
• Mental changes
• Electrolyte imbalance
• Aseptic necrosis of the head of the
femur
• Cushingoid state
• Osteoporosis
• Limitation of growth
• TB reactivation
• Cataract
• Diabetes and myopathy
Antimetabolites
Azathioprine Methotrexate Mycophenolate mofetil
Indications Behcet syndrome
Vogt-Koyanagi-Harada
syndrome
Uveitis associated with
sarcoidosis and
Juvenile idiopathic
arthritis
Alternative to
azathioprine
Dose and
route
Starting dose=1-3mg/kg
After 1-2 weeks dose is
doubled
Stopped only after disease
has been inactive for over
1 year and the daily steroid
dose is under 7.5mg
Adult:10-25mg weekly
Children:30mg
Folic acid 2.5-5mg/ day
1-2 g daily orally
Side effects Bone marrow suppression,
hepatotoxicity and nausea
+ acute pneumonitis Gastrointestinal
disturbance and bone
marrow supression
Monitoring CBC and LFT CBC and LFT CBC
Calcineurin inhibitors
Ciclosporin Tacrolimus
Indications Behcet syndrome, intermediate
uveitis, birdshot choroidopathy,
Vogt-Koyanagi-Harada syndrome,
sympathetic ophthalmitis and
idiopathic retinal vasculitis
Alternative to Ciclosporin
Dose and route 2.5-7.5mg/kg daily orally 1-0.25mg/kg daily orally
Side effects Nephrotoxicity, hyperlipidaemia,
hepatotoxicity, hypertension,
hirsutism and gingival hyperplasia
Hyperglycaemia, neurotoxicity and
nephrotoxicity
monitoring Blood pressure, RFT and LFT + blood glucose
Biological blockers
Interleukin receptor antagonists Tumour necrosis factor alpha antagonist
Daclizumab and anakinra Infliximab and adalimumab
• Introduction
• Clinical features
• Investigation
• Treatment
SUMMARY
THANK YOU

clinical case presentation on anterior uveitis

  • 1.
    CLINICAL CASE PRESENTATION Dr.Samten Dorji Your Logo Here
  • 2.
    • 38 yearold male complained of right eye pain and redness for 5 days duration. CHIEF COMPLAINT Personal information He is from Zhemgang, married with two children and is gardener by profession
  • 3.
    • He developedslow onset of pain in his right eye and increase progression of pain. He had associated redness, photophobia, excessive tearing and reduced vision. HISTORY OF CHIEF COMPLAINT
  • 4.
    • No jointpain • No history of asthma or symptoms suggestive of chest infection • No gastro intestinal symptoms • No history of haematuria or urethral discharge • No skin conditions SYSTEMIC REVIEW
  • 5.
    • Past ocularhistory/ocular medications/systemic medications/comorbidities/allergies/family history/social history • No pets in house HISTORY CONT.
  • 6.
    Examination Right eye Lefteye Visual acuity 6/60 6/6 With pinhole 6/12 6/6 Color vision Normal Normal Extraocular movements Normal Normal Lids and adnexa Normal Normal Conjunctiva and sclera Circumcorneal congestion Normal Cornea Clear Clear Anterior chamber Cells grade +4 and flare grade +3 Normal Iris and lens Posterior synechia Normal Pupil Round regular and miotic Round regular and reactive IOP by Icare 13 mmhg 11 mmhg Dilated Funduscopy NAD NAD
  • 7.
    • 38 yearold male presented to eye OPD with right eye pain with redness for 5 days duration with associated photophobia, excessive tearing and reduced vision. On examination there was no significant findings in his left eye. On his right eye his visual acuity was 6/12 with pin hole. He had circumcorneal congestion and had grade +4 cells and grade +3 flare in anterior chamber with posterior synechia and miosis. He doesn’t have any clinical features suggestive of systemic disorder. CASE SUMMARY
  • 8.
    DIAGNOSIS Acute anterior uveitis Supportingpoints • Unilateral eye pain with photophobia and redness with excessive tearing for duration of 5 days. • Circumcorneal congestion with anterior chamber cells and flare with posterior synechia and miosis. • Fundus appeared normal Non-Supporting points • Slow onset Aetiology • Idiopathic • HLA-B27 associated uveitis • Behcet disease • Lyme disease
  • 9.
    Differential diagnosis • Posterioruveitis with spill over into the anterior chamber • Traumatic iritis • Infectious keratouveitis
  • 11.
    Chest X rayPA= NAD
  • 12.
    • Cycloplegic drops •Antibiotic drops • Prednisolone drops • Oral prednisolone MANAGEMENT
  • 13.
  • 14.
    • Introduction • Clinicalfeatures • Investigation • Treatment OUTLINE
  • 15.
    • Uveitis isthe inflammation of the uveal tract INTRODUCTION
  • 16.
    Clinical course Acute ChronicRecurrent Aetiology Infectious Noninfectious
  • 17.
    Histology Granulomatous Nongranulomatous Anatomy Anterior uveitisIntermediate uveitis Posterior uveitis Panuveitis
  • 21.
    • In alarge community-based study, the vast majority of uveitis cases were anterior (71%), followed by posterior uveitis (5%) and intermediate and panuveitis (1% each). • The most common causes of anterior uveitis are idiopathic (38−56%), the seronegative spondyloarthropathies (21−23%), juvenile idiopathic arthritis (JIA; 9−11%), and herpetic keratouveitis (6−10%).
  • 22.
    • Presentation: suddenonset of unilateral pain, photophobia and redness, which maybe associated with lacrimation. • Visual acuity is usually good at presentation except in eyes with severe hypopyon CLINICAL FEATURES
  • 23.
    External examination Miosis Endothelialdusting Aqueous flare and cells
  • 24.
    Cells in fieldGrade (anterior chamber cells) <1 0 1-5 +- 6-15 +1 16-25 +2 26-50 +3 >50 +4 Description Grade (aqueous flare) Nil 0 Just detectable +1 Moderate (iris and lens details clear) +2 Marked (iris and lens detail hazy) +3 Intense(fibrinous exudate) +4
  • 25.
  • 26.
    Investigation INDICATIONS NOT INDICATED Granulomatousinflammation Single attack of mild unilateral AAU Recurrent uveitis Sympathetic ophthalmitis and Fuchs cyclitis Bilateral disease When systemic disease is already apparent Systemic manifestation Confirmation
  • 28.
    Skin test Tuberculin testPathergy test Lepromin test
  • 29.
    1. Non-treponemal test=rapid plasma reagin 2. Treponemal antibody test= fluorescent treponemal antibody absorption test and microhaemagglutination treponema pallidum test 3. Dark ground microscopy Serology Syphilis Toxoplasmosis 1. Dye test(Sabin-Feldman)= gold standard 2. Immunofluorescent antibody test 3. Haemagglutination tests 4. Enzyme linked immunosorbent assay (ELISA)
  • 30.
    Enzyme assay Sarcoidosis Tuberculosis Leprosy Serum angiotensin convertingenzyme Lysozyme assay HLA tissue typing HLA type Associated disease B27 spondyloarthropathies A29 Birdshot chorioretinopathy B51 Behcet syndrome
  • 31.
  • 32.
    Radiology Chest X raySacro iliac joint X ray CT and MR
  • 33.
    1. Conjunctival andlacrimal gland biopsy BIOPSY
  • 34.
    Treatment Mydriatics Short acting Longacting Tropicamide (6 hours) Homatropine (2 days) Cyclopentolate(24 hours) Atropine(2 weeks) Phenylephrine(3 hours) Promote comfort Break down recently formed posterior synechiae Prevent formation of posterior synechiae
  • 35.
    Topical steroids AAU CAU •Frequent instillation of drops at first • The frequency is tapered off once the inflammation gets controlled • Exacerbations treated as AAU • The intensity of flare can also indicate an active process • Follow up of patient regularly
  • 36.
  • 37.
    Periocular steroid injection Advantages •Therapeutic concentrations behind the lens may be achieved • Trans-sclerally entrance • Prolonged effect Indications • First line therapy in unilateral intermediate or posterior uveitis • Supplement systemic therapy or when systemic steroids are contraindicated • Poor compliance • At time of surgery
  • 38.
    Complication Globe penetration Increased IOP Ptosis Subdermal fat atrophy Extraocular muscle paresis Optic nerve injury Retinal and choroidal vascular occlusion Cutaneous hypopigmentation
  • 39.
    Systemic steroids • Oralprednisolone and intravenous infusion of methylprednisolone Indications • Intermediate uveitis unresponsive to posterior sub tenon injection • Posterior or panuveitis, particularly with bilateral involvement • Prior to intraocular surgery • Anterior uveitis resistant to topical. Contraindications • Poorly controlled diabetes • Peptic ulceration • Osteoporosis • Active systemic infection • Psychosis on previous exposure to steroids Short term side effects Long term side effects • Dyspepsia • Mental changes • Electrolyte imbalance • Aseptic necrosis of the head of the femur • Cushingoid state • Osteoporosis • Limitation of growth • TB reactivation • Cataract • Diabetes and myopathy
  • 40.
    Antimetabolites Azathioprine Methotrexate Mycophenolatemofetil Indications Behcet syndrome Vogt-Koyanagi-Harada syndrome Uveitis associated with sarcoidosis and Juvenile idiopathic arthritis Alternative to azathioprine Dose and route Starting dose=1-3mg/kg After 1-2 weeks dose is doubled Stopped only after disease has been inactive for over 1 year and the daily steroid dose is under 7.5mg Adult:10-25mg weekly Children:30mg Folic acid 2.5-5mg/ day 1-2 g daily orally Side effects Bone marrow suppression, hepatotoxicity and nausea + acute pneumonitis Gastrointestinal disturbance and bone marrow supression Monitoring CBC and LFT CBC and LFT CBC
  • 41.
    Calcineurin inhibitors Ciclosporin Tacrolimus IndicationsBehcet syndrome, intermediate uveitis, birdshot choroidopathy, Vogt-Koyanagi-Harada syndrome, sympathetic ophthalmitis and idiopathic retinal vasculitis Alternative to Ciclosporin Dose and route 2.5-7.5mg/kg daily orally 1-0.25mg/kg daily orally Side effects Nephrotoxicity, hyperlipidaemia, hepatotoxicity, hypertension, hirsutism and gingival hyperplasia Hyperglycaemia, neurotoxicity and nephrotoxicity monitoring Blood pressure, RFT and LFT + blood glucose
  • 42.
    Biological blockers Interleukin receptorantagonists Tumour necrosis factor alpha antagonist Daclizumab and anakinra Infliximab and adalimumab
  • 43.
    • Introduction • Clinicalfeatures • Investigation • Treatment SUMMARY
  • 44.