Iritis

Bharat Gurnani; Jessica Kim; Koushik Tripathy; Navid Mahabadi; Mary Ann Edens

Iritis

Author: Bharat Gurnani Author: Jessica Kim Author: Koushik Tripathy Author: Navid Mahabadi Editor: Mary Ann Edens Updated: 8/25/2023 3:04:42 AM

Introduction

The International Uveitis Study Group (IUSG) recommended the anatomical classification of uveitis into anterior uveitis, intermediate uveitis, posterior uveitis, and panuveitis.[1] The Standardization of Uveitis Nomenclature (SUN) working group endorsed the same anatomical classification.[2] This anatomical location is based on the actual site of inflammation and is not affected by the presence or absence of structural complications, including cystoid macular edema.[2] The primary location of inflammation in anterior uveitis is the anterior chamber (AC).[2] The anterior uveitis includes three entities, namely iritis, iridocyclitis, and anterior cyclitis.[2] The inflammation of the iris is termed as iritis, and that involving the anterior part of the ciliary body is known as anterior cyclitis.[3]

When both of these are involved, it is called iridocyclitis.[3] Anterior uveitis is the most common form of uveitis.[4] The most common clinical presentation is acute anterior uveitis (AAU).[5] The most common etiologies include HLA-B27 and idiopathic.[5] It is difficult to pinpoint the etiology in some cases, and it may be secondary to the cross-reactivity of microbial antigens in genetically predisposed patients.[6] The etiology of AAU can be varied, ranging from viral infections, bacterial infections, trauma, lens-related inflammation, keratitis, and scleritis. It can exist alone as AAU or in conjuction with intermediate uveitis, posterior uveitis, or panuveitis. Chronic anterior uveitis (CAU) is usually bilateral secondary to an underlying systemic pathology and is less common than AAU.[7] The prognosis is typically good in most idiopathic and HLAB27- related AAU cases, provided management is adequate.[8] Outcomes are more variable in CAU and cases with an underlying ocular or systemic disorder.[5]

Etiology

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Etiology

Most cases of iritis are idiopathic, while 20% are due to blunt trauma.[3]

Nontraumatic iritis often is associated with HLA- B27 systemic diseases, including:

Juvenile Rheumatoid Arthritis (JRA)[9]
Ulcerative Colitis[10]
Reiter syndrome[11]
Sarcoidosis[12]
Behcet's disease[13]
Tubulointerstitial Nephritis and Uveitis (TINU)[14]
Systemic Lupus Erythematosus (SLE)[15]
Multiple Sclerosis[16]
Ankylosing Spondylitis[17]

Infectious Causes

Tuberculosis[18]
Chlamydia[19]
Lyme's disease[20]
Herpes Simplex[21]
Toxoplasmosis[22]
Varicella-Zoster virus (herpes zoster ophthalmicus or shingles)[23]
Syphilis.[24][5][25].

Other Causes

Drug-induced[26]
Masquerade syndromes like lymphoma, leukemia, malignant melanoma[27]
Juvenile Xanthogranuloma[28]

After Idiopathic variety, HLA-B27 associated uveitic ranks as the second commonest cause of anterior uveitis.[6] It is responsible for 40-70% of anterior uveitis cases in varied geographical regions. It is more common in males than females.[29]

The Various HLA-B27 Associated Conditions with Ocular Involvement are Listed Below[30]

S. No	HLA-B27 associated condition	Ocular features
1	Ankylosing Spondylitis	Acute anterior uveitis, conjunctivitis, keratitis
2	Reiter's disease (reactive arthritis)	Anterior uveitis, intermediate uveitis, posterior uveitis, keratitis, conjunctivitis, papillitis, scleritis, cataract
3	Juvenile spondyloarthropathy	Anterior uveitis
4	Psoriatic arthritis	Anterior uveitis, keratitis, dry eyes, conjunctivitis, panuveitis, scleritis, cataract, papillitis, pigmentary retinopathy
5	Inflammatory bowel disease	Conjunctivitis, episcleritis, scleritis anterior uveitis, cataract, vitritis retinal vasculitis, peripheral ulcerative keratitis
6	Undifferentiated spondyloarthropathies	Acute anterior uveitis or chronic anterior uveitis, vitritis, retinal vasculitis

Rodriguez et al., from their large-scale analysis from a tertiary eye care center, listed the prevalence of various etiologies in all the anatomic forms of uveitis.[31]

The most common conditions were:

Idiopathic
Seronegative spondyloarthropathies
Sarcoidosis
JRA
SLE
Behcet's
HIV

Ankylosing spondylitis, Inflammatory bowel disease, psoriatic arthritis, and Reiter's syndrome are grouped under seronegative spondyloarthropathies.[32] As per Rodriguez et al., the most common form was anterior uveitis, with the most common etiology being idiopathic followed by seronegative arthropathy, JRA, herpes, sarcoidosis, SLE, and rheumatoid arthritis. The next was posterior uveitis, with common etiologies being toxoplasmosis, idiopathic, CMV, SLE, and sarcoidosis.[33]

Epidemiology

Anterior uveitis is the most common form of uveitis (occurring every 12 per 100 000 cases).[5] It predominantly occurs in young and middle-aged people. In western countries, 50% to 70% of all uveitis cases are classified as anterior uveitis. Uveitis is responsible for 10% of legal blindness in the USA, and it accounts for approximately 30,000 new patients with blindness every year.[34] The study from northern California on the epidemiology of uveitis revealed an incidence of 52.4 per 100000 persons per year and a prevalence of 115.3 per 100000 persons.[35]

The maximum incidence and prevalence were seen in elderly patients above 65 years and lowest in the pediatric age group. Women had a higher prevalence than men.[35] The study from Affairs Medical Centre, Northwest Pacific, reported an incidence of 25.6 cases per 100000 persons and a prevalence of 69 per 100000 persons.[36] The study in the elderly population from the care survey medicare cohort revealed an incidence of uveitis ranging from 302-424 per 100000 persons per year and an average of 340.9 per 100000.[37] The mean incidence of uveitis was 243.6 per 100000. The reported incidence of posterior uveitis was 76.6 per 100000, and panuveitis incidence was 41.7 per 100000.[37]

Pathophysiology

Eye pain is thought to be due to irritation of the ciliary nerves and ciliary muscle spasms. Photophobia is caused by irritation of the trigeminal nerve from the ciliary spasm.[38] Increased permeability of blood vessels in the anterior chamber allows proteinaceous transudate ("flare") and WBCs ("cells"), the characteristic 'flare and cells' seen with the slit lamp.[39] In traumatic uveitis, there can be microbial contamination and retention of necrotic debris at the site of trauma, resulting from a florid inflammatory response in the anterior segment of the eye. In infectious uveitis, the pathophysiological mechanism is immune-mediated destruction of foreign antigens that may cause damage to the uveal tissue, vessels, and cells.[40] There is immune complex deposition inside the uveal tract in autoimmune uveitic conditions, a form of hypersensitivity reaction.[41][39]

Uveal inflammation behaves similarly to inflammation in other body tissues, i.e., having a vascular and cellular response. But due to excessive vascularity and looseness of uveal tissue, there is heightened vascular response. Pathophysiologically, the uveal inflammation is subdivided into purulent (suppurative) and nonpurulent (non-suppurative) types.[41]

Wood’s Classification of Non-Suppurative Inflammation[42]

Non-granulomatous
Granulomatous

Suppurative Uveitis

It results from exogenous infections from pyogenic microorganisms. It is a part of the spectrum of endophthalmitis or panophthalmitis and is caused by Staphylococci, Streptococci, Pseudomonas, Pneumococcus. In suppurative inflammation, there occur outpouring of purulent exudates and an increase in polymorphonuclear cells. The uveal tissue increases in size, becomes thickened, and demonstrates necrosis and pus formation in the cavities.[43]

Non-granulomatous Uveitis

In non-granulomatous (NG) uveitis, diffuse inflammation is characterized by dilatation and increase in permeability of vasculature, blood-aqueous barrier breakdown, increase in exudates, increased infiltration by lymphocytes, plasma cells and, macrophages.[44] The iris becomes edematous, muddy in color, and waterlogging occurs. As a result, there occur loss of crypts and furrows. Further, there is iridoplegia; the pupil becomes small and sluggish due to the engorgement of iris vessels. The infiltration of exudates and lymphocytes manifests as cells and flare in the anterior chamber and KPs at the back of endothelium.[45] The exudates can also be seen in the posterior segment and manifest as posterior synechiae, where the posterior iris adheres to the anterior lens capsule. Sometimes exudates may occupy the ciliary body and result in a cyclitic membrane. In the healing phase, atrophy of the iris is evident, and there may be areas of necrosis. Further destructive changes manifest as necrosis, gliotic and fibrotic areas, resulting in adhesions, scar formation, and eventual destruction of uveal tissue.[46]

Granulomatous Uveitis

In granulomatous uveitis, there is increased infiltration by lymphocytes, plasma cells, epithelioid cells, and giant cells resulting in nodule formation. The nodules may be seen at the pupillary border, such as Koeppe's nodules) and nodules may be seen at the back of the cornea as mutton fat KP's. This may be followed by necrosis, gliotic and fibrotic areas which result in adhesions, scar formation, and eventual destruction of uveal tissue.[5]

Histopathology

The histopathological findings in uveitis vary with etiology.

Lens induced uveitis - Macrophages, acute and chronic inflammatory cells[47]
Parasitic uveitis - Eosinophils, polymorphonuclear neutrophils, and parasites occasionally[48]
Masquerade syndrome - Cellular infiltrates in retinoblastoma, leukemia, etc. and malignant cells[49]
Phacoanaphylactic uveitis - Epithelioid cells, polymorphonuclear neutrophils, and giant cells[50]
Uveitis- Predominant lymphocytic infiltrate[51]
Late-onset Endophthalmitis - Propionibacterium on gram stain, culture plating, or PCR[52]
Endophthalmitis - Acute and chronic inflammatory cell infiltrate along with offending microorganism[53]
Lymphomas (large cell) - Cells with pleomorphism, oval or circular nuclei, and scanty cytoplasm. There is an occasional predominance of micronuclei[54]

History and Physical

Classification

The anatomical classification of uveitis is proposed by the Standardization of Uveitis Nomenclature (SUN) Working Group.

Anatomical

Anterior- Involving the iris and ciliary body[55]
Intermediate- Involving vitreous and pars plana[56]
Posterior- Involving retina and choroid[57]
Panuveitis- Anterior, intermediate and posterior[2]

The Etiological Classification of Uveitis is Proposed by the International Uveitis Study Group (IUSG)

Infectious- Viral, bacterial, parasitic, Lyme disease, etc. [58]
Non-infectious- Idiopathic or associated with systemic diseases[45]
Masquerade- Neoplastic and non-neoplastic[59]

SUN Working Group Proposed the Classification Based on the Timing of Inflammation

Timing of onset- Insidious or sudden[60]
Duration of inflammation- Limited (less than or equal to 3 months ) or persistent[61]

Clinical Activity

Acute- Insidious or sudden
Chronic- Persistent with relapse within three months after stopping the treatment
Recurrent- Repeated episodes with an in-between inactive period
Remission- No active episode for three months or more[3]

Anterior Uveitis

Acute

Pain, redness, photophobia, tearing, and decreased vision with pain developing over a few hours or days except in trauma cases.[3]

Chronic

Blurred vision, mild redness, and little pain or photophobia except during an acute episode.[62]

Slit Lamp Evaluation in Uveitis Patients

Circumciliary congestion or circumcorneal congestion (injection) gives the appearance of a purple hue due to involvement in conjunctival plexus and deeper vessels. It's a sign of AAU and may not be seen in CAU.

Pupillary miosis is due to iridoplegia and sphincter spasms, which lead to the formation of posterior synechiae.

Anterior chamber cells are estimated by SUN grading with the help of a 1x1 mm slit beam under adequate lighting and magnification. The cells and flare indicate inflammatory activity inside the anterior chamber. The cells and flare should be assessed before pupillary dilatation as dilatation invites pigment shedding into the aqueous. The cells can also be observed in the vitreous phase.[63]

SUN Grading of Cells in Anterior Chamber (1 mm x 1 mm Slit Beam)

S. No	Grade	Cells in the field
1	0	< 1
2	0.5+	1-5
3	1+	6-15
4	2+	16-25
5	3+	26-50
6	4+	>50

An anterior chamber or aqueous flare is the turbid appearance of the aqueous in the anterior chamber due to the proteins secondary to the breakdown of the blood-aqueous barrier. In children with JIA-associated CAU, flare is taken as the level of inflammatory activity more than cells and indicates complications in the long term. Flare is graded on a slit lamp by assessing the iris and lens details. Laser flare photometry is another modality for objective grading.[63]

SUN Classification of Flare in the Anterior Chamber

S. No	Grade	Description
1	0	None
2	1+	Faint
3	2+	Moderate- Clear iris and lens details
4	3+	Marked- Hazy iris and lens details
5	4+	Intense- Plastic or fibrin aqueous

Hypopyon is the presence of whitish purulent exudative material in the anterior chamber. It is composed of inflammatory material, and form appears as a horizontal level that is gravity-dependent. It is common in HLA B27 associated uveitis. The hypopyon is immobile due to high fibrin content, making it difficult to absorb. Behcet's disease patients have a characteristically mobile hypopyon due to low fibrin content.[64] Hypopyon is inflammatory cells deposited in the anterior chamber and is composed of leucocytes.[64] It is measured with the help of a slit lamp micrometer. The shape, color, and consistency of hypopyon are indicators of etiology. It can be mobile or fixed. To test the mobility of hypopyon, the patient is asked to lie down supine for 10 minutes. Then after 10 minutes, the level of hypopyon is tested. In the case of fixed hypopyon, there is no movement, but in the case of mobile hypopyon, the level or height is changed.[65]

Various Types of Hypopyon in Different Condition

S. No	Hypopyon characteristic	Diagnosis/etiology
1	Sterile	Behcet's disease
2	Mobile	Bacterial keratitis
3	Fixed/ Immobile	Fungal keratitis
4	Central	Pneumococcal keratitis
5	Haemorrhagic	Pneumococcus, herpetic keratitis, trauma
6	Other causes	Endophthalmitis, ranibizumab, JIA, histiocytosis, Leukemia, laser iridotomy, lens-induced, HLA-B27 uveitis, leptospirosis, phacolysis

Keratic precipitates (KPs) are inflammatory cellular deposits at the back of the cornea (endothelium). The cellular aggregates include lymphocytes, plasma cells, and macrophages. Epithelial cells and giant cells are also common in KPs. The KPs are seen inferior one-third of the cornea in a triangular pattern with the apex pointing upwards (Arlt's triangle). The KPs are distributed in Arlt's triangle due to aqueous convection currents and the effect of gravity. In contrast, they can be seen diffusely distributed in Fuch's heterochromic iridocyclitis (FHIC) and viral uveitis (stellate KPs). The morphological appearance of KPs indicates the type of uveitis, like small KPs in non-granulomatous (NG) uveitis and large in granulomatous uveitis. Large glistening greasy KPs are seen as granulomatous uveitis and are called mutton fat KPs. Once the acute episode resolves, KP usually disappears. Pigmented KPs can be observed (NG variety). The granulomatous KPs may also become pigmented and are classically described as the ground-glass appearance of KPs. Sometime before the appearance of KP's diffuse pigment deposition is seen at the back of the cornea called endothelial dusting.[66]

S. No	Characteristic	Type of KP
Fresh	Old
1	Colour	White	Pigmented
2	Shape	Circular/ Round	Flat
3	Hydration	Fully hydrated	Dehydrated
4	Edges	Smooth	Crenated

The fibrinous membrane is a common entity in AAU and is seen in the anterior chamber.

Iris atrophy is another clinical sign of uveitic sequelae. Diffuse iris atrophy is observed in FHIC, and a patchy or sectoral pattern appears in herpetic uveitis. Sectoral iris atrophy can be seen more in herpes zoster uveitis, although both sectoral and diffuse patterns can be observed in both herpes simplex and zoster uveitis.[67]

Iris nodules are observable in both NG and the granulomatous variety.

Koeppe's nodules - These are present at the pupillary margin or the location of posterior synechiae. These are ectodermal nodules usually white and may be pigmented. They can be seen in granulomatous as well as non granulomatous uveitis.
Busacca's nodules - These involve the iris stroma and are predominantly seen in granulomatous variety.
Roseolae - These are yellow nodules are seen in Syphilis, resulting from dilatation of iris vessels.
Berlin nodules - These are seen in angles in cases with sarcoidosis.
Iris pearls - These are observed in lepromatous uveitis.
Russell bodies - These, also called iris crystals, are seen in FHIC and rare cases of chronic uveitis. They are thought to result from immunoglobin deposits.[68]

Posterior synechiae (PS) are another essential clinical finding in uveitic cases. They result from adhesion of the pupil margin to the anterior capsule secondary to uncontrolled inflammation. PS can be seen at the site of the Koeppe nodule. All cases should be instilled with a cycloplegic agent like atropine or homatropine to prevent PS formation.[69]

Types of Posterior Synechiae

Segmental - They are adhesions of the iris at some points over the lens
Annular (ring) - They are 360-degree adhesion of the iris to the anterior lens capsule
Total- These are plastered posterior surface of iris to the lens
Broad- They are seen in tubercular uveitis
Filiform-They are seen in non-tubercular uveitis
Seculusio pupillae- When synechiae cover the 360-degree pupil and prevent migration of aqueous from posterior to the anterior chamber
Occlusio pupillae- Formation of membrane over the lens surface
Festooned pupil- When synechiae are localized, and on dilatation, the pupil takes an irregular shape

Heterochromic iris is the difference in the color of the iris between the two eyes. Heterochromia is seen in FHIC.[70]

Neovascularization of the iris (rubeosis iris) can result from chronic inflammation. The vascularization seems to be less as compared to posterior segment pathologies. FHIC shows abnormal iris vessels but does not result in synechial angle closure. Iris's new vessels are also seen in posterior uveitis. Sometimes it becomes difficult to differentiate between new and normal iris vessels (pseudo-rubeosis of the iris). The differentiating point is new vessels show irregular branching in contrast to normal vessels, which are radial. Fluorescein angiography is used to assess the leakage from new vessels.[71]

Fundus evaluation is mandatory in each case to rule out masquerades like malignant melanoma, retinal detachment, cystoid macular edema, and other posterior segment complications.

Difference between Granulomatous and Non-Granulomatous Uveitis

S. No	Characteristic	Type of Uveitis
Granulomatous	Non-Granulomatous
1.	Time of onset	Insidious	Acute
2	Pain severity	Mild	Marked
3	Photophobia	Mild	Marked
4	Congestion	Minimal	Marked
5	Keratic precipitates	Large- Mutton fat	Small
6	Anterior chamber flare	Mild	Marked
7	Iris nodules	Present	Absent
8	Posterior synechiae	Thick and broad	Thin and flat
9	Posterior segment	Patchy involvement	Diffuse involvement

Difference between Acute and Chronic Uveitis

S. No	Characteristic	Type of Uveitis
Acute	Chronic
1.	Time of onset	Sudden	Acute
2	Symptoms	Pain, redness, photophobia	Asymptomatic, reduced vision and floaters
3	Start date	Definite	Not definitive
4	Resolution	Self-resolving mostly	Long duration

Evaluation

Since iritis involves anterior uveitis per se, the evaluation and treatment are focussed on anterior uveitis only. Further laboratory tests or imaging may be required if systemic involvement or infectious disease is suspected to be the underlying cause.[72][73][74][75] In most uveitic cases, the investigations are normal, and no underlying etiology can be discerned. Tailored made investigations are needed in each patient to pinpoint the etiology based on the clinical signs. In some cases, the etiology is evident on the clinical examination, like uveitis in the case of endophthalmitis post-surgery. Most patients also need systemic evaluation and careful review by an internist.[76]

Visual Acuity

Visual acuity depends on the extent of inflammatory activity and associated complications. It is generally minimally reduced in AAU. Snellen's uncorrected and best-corrected visual acuity should be documented in each patient. The improvement in visual acuity is also an indicator of resolution of uveitis and reduction in inflammation.[77]

Intraocular Pressure

Intraocular pressure (IOP) can be raised in uveitic cases. The reduction in IOP is due to ciliary shutdown or reduction in aqueous secretion from the ciliary epithelium. The raised IOP can be due to angle closure, trabeculitis, steroid-induced, and other causes. The IOP can be measured by noncontact tonometry, ICARE tonometer, or Goldman applanation tonometer and should be documented on each visit.[78]

Cases of Uveitis where Investigations are Not Mandatory

The first episode of unilateral mild NG AAU with no previous ocular or systemic history

Classical clinical signs of a specific etiology for which investigation will not be helpful like FHIC

When the systemic signs and symptoms are indicative of a particular etiology associated with uveitis like sarcoidosis, tuberculosis, multiple sclerosis, etc. [79]

Cases of Uveitis where Investigations Will be Helpful

Bilateral cases of AAU
Severe cases AAU
Recurrent cases of AAU
Chronic A.U. resistance to treatment
Granulomatous AU
AAU associated with I.U. or posterior uveitis or panuveitis cases
Ocular and systemic signs indication underlying pathology[3]

Further laboratory tests or imaging may be required if systemic involvement or infectious disease is suspected to be the underlying cause.[72][73][74][75]

Imaging

Chest radiography may be considered if sarcoidosis or tuberculosis is the underlying cause of uveitis. In granulomatous uveitis cases, a high index of suspicion should be kept to rule out these treatable systemic conditions as well as syphilis. X-ray of the sacroiliac joint reveals bamboo spine and sacroiliitis in cases with ankylosing spondylitis and other seronegative spondyloarthropathies.[80]

Ocular Imaging

B Scan Ultrasound

A B scan should be performed in the fundus that is not visualized due to small pupil, anterior chamber reaction, fibrinous membrane, or vitreous haze.[81]

Optical Coherence Tomography

It's a handy tool to rule out cystoid macular edema and epiretinal membrane and look for cells and flare.[82]

Fundus Fluorescein Angiography

This is an essential investigation in chronic uveitis cases to rule out posterior segment pathology like vasculitis macular ischemia delineate capillary non-perfusion areas and white dot syndrome spectrum.[83]

Fundus Autofluorescence

Fundus autofluorescence (FAF) is essential in posterior segment pathologies to rule out white dot syndromes and severe inflammatory conditions.

Indocyanine Green Angiography

Indocyanine green angiography (ICGA) is needed in cases with uveitis-associated choroidal pathology.[84]

Ultrasound Biomicroscopy

Ultrasound biomicroscopy (UBM) is helpful to rule out hypotony (ciliary shutdown), choroidal effusion, cyclodialysis cleft, and cyclitic membrane.[85]

Laboratory Workup

Laboratory workup is usually not necessary. In mild unilateral non-granulomatous uveitis with trauma or no evidence of systemic disease, laboratory studies are unlikely to be helpful. If there is the presence of bilateral granulomatous or recurrent uveitis, a workup is indicated.[3] Tests to consider include:

Human Leucocyte Antigen tissue typing (HLA-B27)

HLA- B27 testing should be done in any patient with recurrent A.U. or chronic N.G. A.U. The various HLA types and their associations are detailed below.
HLA B27- Recurrent AAU
HLA-B51 and HLA B5- Behcet's disease
HLA-A29- Birdshot retinochoroiditis
HLA-DR4- Sympathetic Ophthalmia and Vogt-Koyanagi-Harada disease
HLA-B7 and HLA-DR- Presumed Ocular Histoplasmosis Syndrome[86]

Syphilis Serology

The various test implicated in syphilis is treponemal antibody tests such as ELISA- enzyme-linked immunosorbent assay, which has high specificity and sensitivity but takes approximately three months to show positivity. Anti-cardiolipin antibody tests (non-specific) like venereal research laboratory test (VDRL) and rapid plasma regain (RPR) demonstrate positive results in the acute phase of the disease and help to monitor the disease and treatment. The patients having features of ocular syphilis should be referred to an internist to rule out sexually transmitted syphilis.[87]

Angiotensin-Converting Enzyme

This is a non-specific test to rule out the cause of N.G. A.U. such as sarcoidosis, tuberculosis, and Hansen disease. Serum levels of ACE are elevated in approximately 80% of patients with sarcoidosis but come down to normal levels during remission.[88]

Serum Lysozyme Assay

Lysozyme, an enzyme, is found in neutrophils and tear secretion. It has antibacterial properties and can cause bacterial cell wall breakdown. This test has comparatively less sensitivity and specificity than serum ACE in diagnosing sarcoidosis, but the combined test may prove more beneficial.[76]

Complete Blood Count

A raised leucocyte count is indicative of infective may be a hematological malignancy. Eosinophils are raised in parasitic causes of uveitis.[3]

Inflammatory Markers

C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and acute phase reactants may be elevated in systemic inflammatory disorders.[89]

Lyme Disease Serology

Disease-specific serology is essential in endemic areas, including serology for other infections like brucellosis and leptospirosis.[90]

Antinuclear Antibody

Antinuclear antibody (ANA) is the most important marker for juvenile idiopathic arthritis in children. ANA positivity is an indicator of CAU.[91]

Antineutrophil Cytoplasmic Antibody

Antineutrophil cytoplasmic antibody (ANCA) is valuable for anterior uveitis associated with scleritis. It is a valuable marker for Wegner granulomatosis (c-ANCA) and Polyarteritis Nodosa (PAN) {p-ANCA}.[92]

Interferon-Gamma Release Assay

Interferon-gamma Release Assay such as QuantiFERON-TB Gold for diagnosis of tuberculosis.[93]

HIV Serology

HIV tridot test for suspected patients with immunosuppression.[94]

Anterior Chamber Tap

An anterior chamber aqueous tap can be performed, and a sample can be sent for a polymerase chain reaction in cases of suspected viral uveitis like herpes, varicella, and rubella. PCR will also distinguish Propionibacterium acne infection in chronic uveitis in pseudophakic eyes.[95]

Iris Biopsy

Iris biopsy is another critical investigation but is rarely done nowadays.[96]

Vitreous Biopsy

In the case of associated posterior segment involvement, especially in the case of suspected endophthalmitis.[97]

Conjunctival Biopsy

In case of suspected granulomas or infiltrative lesions, a conjunctival biopsy is indicated.[98]

Physician Referral

To rule out systemic pathologies, timely referral to an internist is essential to pinpoint the etiology—for example, HRCT in pulmonary tuberculosis and MRI in cases of multiple sclerosis.

Treatment / Management

Treatment is primarily aimed at reducing inflammation and pain and preventing complications. First-line treatment involves topical cycloplegics (dilate the pupil, prevent the ciliary body and pupillary spasm) and topical steroids (decrease inflammation). The patient should be referred to an ophthalmologist within 24 to 48 hours. The review frequency is decided based on the clinical presentation and degree of inflammatory activity. Those with severe inflammation need review within a day or two, and those with mild AAU may be seen after a week or so.

Sustained-release corticosteroid vitreous implants (fluocinolone acetonide, dexamethasone) are available to treat inflammation-induced cases of panuveitis, intermediate uveitis, and posterior uveitis.
Corticosteroids should be initiated only in conjunction with the approval of an ophthalmologist because uveitis is a diagnosis of exclusion.
Steroids can have adverse effects, such as causing intraocular pressure, cataract formation, steroid-induced glaucoma, and the development of herpes keratitis.
Potassium-sparing drugs should be used when chronic steroid use is required to control inflammation. Approximately half of the patients with uveitis need treatment beyond corticosteroid treatment to prevent vision loss.[5]

Topical Steroids

Corticosteroids decrease inflammation. Treatment should only be initiated after consultation with an ophthalmologist. Prednisolone 1% or dexamethasone 0.1% are potent steroids and are the first treatment choice for uveitis. They work by decreasing inflammation by reversing increased capillary permeability and suppressing the migration of polymorphonuclear leukocytes.

The other drugs used for iritis management are difluprednate 0.05% (lower frequency), prednisolone 0.5%, loteprednol etabonate 0.5% and 0.2%, betamethasone, fluorometholone, and rimexolone (moderate to low potency). Steroid regimen can be altered based on the response and intraocular pressure elevation. Betamethasone ointment can be used at bedtime. The steroid regimen varies according to the degree of inflammation, starting from an hourly regimen for three days to every two hours for three days, then 6/5/4/3/2/1 times one week each. The treatment is usually stopped after 6 to 8 weeks. Timely and regular follow-up is mandated in each case. In CAU cases, the target is the full resolution of inflammation. Low-grade persistent inflammation can result in a higher incidence of complications which can be reduced with regular and timely steroids instillation. Steroids can act as a bilateral sword, resulting in elevated IOP (steroid response), cataract, glaucoma, keratitis, and corneal melt.[99]

Cycloplegics

Cycloplegics block nerve impulses to the ciliary muscles and pupillary sphincter to decrease photophobia and pain. They are implicated in AAU and CAU exacerbations. These help to break down the already formed posterior synechiae prevent the formation of new synechiae.

Homatropine

Induces cycloplegia in 30 to 90 minutes.
Induces mydriasis in 10 to 30 minutes.
Effects last 10 to 48 hours for cycloplegia and 6 to 96 hours for mydriasis, but the duration may be less if severe anterior chamber reaction.
Homatropine is an agent of choice for uveitis.

Cyclopentolate 0.5% to 2%

Induces cycloplegia in 25 to 75 minutes.
Induces mydriasis in 30 to 60 minutes.
Effects usually last one day.
Less attractive for treating uveitis than homatropine.

The other cycloplegics available are atropine which has a long duration of action of 7-10 days. In AAU, 2.5% or 10% phenylephrine can also break posterior synechiae. Bedtime administration of the drug should be promoted to avoid difficulties with accommodation during the daytime. Atropine has been known to cause toxic side effects like seizures amblyopia in children, and extra precautions should be taken while administering drugs to children.[3]

Mydricaine

Mydricaine is a preparation of 0.3 ml containing 0.12 mg adrenaline, 1mg atropine, and 6 mg procaine. Adrenaline and atropine break the posterior synechiae and procaine to improve comfort. The drug combination is given as a subconjunctival injection. Another installation method is cotton pledget dipped in Mydricaine and kept for 5 minutes in the superior and inferior fornices for 5 minutes. Mydricaine number 1 is used pediatric version, and mydricaine number 2 is used in adults. The side effect reported with Mydricaine is transient sinus tachycardia.[100](B3)

Tissue Plasminogen Activator

In severe fibrinous anterior uveitis cases, 12.5 to 25 ug of tissue plasminogen activator is injected in the anterior chamber in 0.1 ml solution with a 30 G needle under topical anesthesia. This will dissolve the fibrin membrane and break down the posterior synechiae.[101](B3)

Subconjunctival Steroids

Betamethasone sodium phosphate and acetate combination can be given for severe A.U. and patients with poor compliance subconjunctivally.[102]

Subtenons Injection of Steroids

Posterior sub tenons injection of methylprednisolone or triamcinolone acetonide can be given in cases with aggressive posterior segment inflammation and in patients with anterior uveitis having cystoid macular edema a complication. They can be instilled as an OPD procedure or given during the surgery to supplement the systemic steroids. The onset of action is four weeks, and the maximum duration is around three months. Varied complications have been reported like secondary glaucoma, globe perforation, subconjunctival hemorrhage, cataract, retrobulbar hemorrhage, and ptosis.[103](B2)

Intravitreal Steroids

Intravitreal triamcinolone acetonide (4 mg in 0.1 ml) is also implicated in cystoid macular edema after anterior uveitis, which is not responding to other therapy. The complications are similar to sub tenons administration except pseudohypopyon, exclusive to intravitreal steroids.[104](B3)

Systemic Steroids

When the inflammation is severe and response to topical treatment is inadequate, oral prednisolone is indicated. They are given in tapering doses, and each case should monitor side effects.[102]

Non- Steroidal Anti- Inflammatory Drugs (NSAIDs)

Naproxen and tolmetin are implicated in CAU cases and can be used for the long term under physician observation.[99]

Antimetabolites

Methotrexate is implicated in CAU secondary to juvenile idiopathic arthritic in children when steroids fail to control the inflammation.[105]

Tumor Necrosis Factor Blockers

Infliximab or adalimumab may be used as second-line treatment for patients with vision-threatening chronic uveitis caused by seronegative spondyloarthropathy.[106]

Differential Diagnosis

The differential diagnoses include

Acute angle-closure glaucoma
Conjunctivitis
Subconjunctival hemorrhage
Trauma
Episcleritis
Scleritis
Dry eyes
Pingueculitis
Inflammed pterygium
Corneal abrasion
Corneal ulcer
HSV keratitis
Intraocular foreign body
Scleritis
Ulcerative keratitis
Ultraviolet keratitis

Prognosis

The prognosis is good with appropriate treatment. To have the best prognosis, follow-up care with an ophthalmologist within 24 hours is imperative. Monitoring should include repeat slit-lamp and intraocular pressure checks every few days. When the condition is stable, monitoring can be every 1 to 6 months. If not diagnosed and treated on time and neglected cases usually develop complications like cataract, glaucoma, retinal detachment, and macular edema, and the prognosis is guarded in these cases.[107]

Complications

Corneal scar (keratouveitis)
Band shaped keratopathy
Hyphema
Non-resolving hypopyon
Iris atrophy
Posterior synechiae
Cataract (Inflammation related, steroid-induced)
Secondary glaucoma (pupillary block, inflammation, or topical corticosteroid)
Occlusio pupillae
Festooned pupil
Seclusio pupillae
Cystoid macular edema
Optic neuropathy
Optic disc neovascularization
Macular scar
Hypotony
Vitreous hemorrhage (associated intermediate, posterior, or panuveitis)
Retinal detachment
Endophthalmitis[53]
Panophthalmitis
Permanent blindness
Strabismus[108]

Postoperative and Rehabilitation Care

In cases undergoing cataract surgery, postoperative care is required for complicated cataract of filtration surgery for non-resolving glaucoma or progressive glaucomatous changes. For patients undergoing cataract surgery, the usual regimen is topical steroids (1% prednisolone or 0.1% dexamethasone) or steroids and antibiotic combination (0.1% dexamethasone + 0.5% gatifloxacin) 6/5/4/3/2/1 times for one week each along with a cycloplegic like topical 5% homatropine or 1% atropine two times per day for 2 to 3 weeks.[3]

The patients should be regularly and closely followed to prevent any complications. In patients undergoing filtration surgery, the usual regimen is topical steroids (prednisolone 1% or dexamethasone 0.1%) or steroids and antibiotic combination (dexamethasone 0.1% + gatifloxacin 0.5%) 8/7/6/5/4/3/2/1 times for one week each along with a cycloplegic like topical homatropine 5% or atropine 1% two times per day for 2 to 3 weeks. These patients should be closely followed up to rule out complications like macular snuff out, hypotony, uncontrolled glaucoma and check for the normal functioning bleb.[109] The patients requiring retinal detachment repair are also treated post-operatively with the same regimen as glaucoma patients. Two to three months later, these patients will require silicon oil removal. All these patients should also be closely followed up to rule out re-detachment and other complications of retinal surgery.[110]

Consultations

Any patient presenting to the clinic with pain, redness, and photophobia should be meticulously evaluated by an Ophthalmologist with suspicion of iritis. In the case of keratouveitis, the patient should be referred to a cornea specialist for higher opinion and management to rule out infective and autoimmune keratitis. Non-resolving iritis, endophthalmitis, or cases with diagnostic dilemmas must be evaluated by a retina and uvea specialist for expert opinion and further management. The patient with underlying systemic pathology leading to iritis and uveitis should be referred timely to an internist to pinpoint the etiology and targeted systemic treatment. Iritis with trabeculitis, angle-closure, or open-angle glaucoma should be managed with a glaucoma specialist. Patients with complicated cataracts requiring surgical intervention should be ideally operated on by a cataract and IOL surgeon for an excellent visual outcome.[3]

Deterrence and Patient Education

Patients with iritis should be explained about the ocular pathology the importance of regular and timely treatment and follow-up. The patient should be educated about the underlying systemic pathology associated with iritis and the critical role of the internist in treating the condition. The patients should also be explained about the complications related to iritis and the side effects of irregular and long-term use of steroids.

Pearls and Other Issues

Anterior uveitis can present as an isolated entity or associated intermediate and posterior uveitis. There can be a spillover of anterior segment inflammation into the vitreous or posterior segment. All patients should undergo extensive evaluation to pinpoint the etiology. The internists have a key role to play in the diagnosis and management of uveitic cases. If untreated, complications can include decreased visual acuity and/or blindness, glaucoma, cataracts, and irregular pupil.[5]

Enhancing Healthcare Team Outcomes

The management of a patient with iritis is interprofessional. Whenever a patient presents with eye pain, tearing, photophobia, vision loss, and red-eye in the absence of trauma, the patient must be referred to an ophthalmologist as soon as possible. The treatment of iritis primarily aims to reduce inflammation and pain and prevent complications. First-line treatment involves topical cycloplegics (dilate the pupil, prevent the ciliary body and pupillary spasm) and topical steroids (decrease inflammation). Depending on the cause, most patients respond well to treatment and retain full vision. However, at least 10 to 30% of patients may need treatment beyond steroids to prevent vision loss.[24][111] [Level 5] Once discharged, the patient may follow up with the ophthalmic nurse, primary care provider, or ophthalmologist.[5]

Media

(Click Image to Enlarge)

Slit-lamp image of the patient of recurrent anterior uveitis depicting circumciliary congestion, corneal scarring, central band shaped keratopathy, hypopyon in anterior chamber and pseudophakia Contributed by Dr. Bharat Gurnani, MBBS, DNB, FCRS, FICO, MRCS Ed, MNAMS

(Click Image to Enlarge)

Slit- lamp image of the patient with recurrent uveitis depicting mild circumciliary congestion, nebular corneal scarring, few areas of iris atrophy along with a complicated cataract Contributed by Dr. Bharat Gurnani, MBBS, DNB, FCRS, FICO, MRCS Ed, MNAMS

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