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   Table of Contents      
REVIEW ARTICLE
Year : 2020  |  Volume : 68  |  Issue : 9  |  Page : 1764-1773

Viral anterior uveitis


1 Department of Uveitis and Ocular inflammation, Vittala International Institute of Ophthalmology and Prabha Eye Clinic and Research Centre, Bangalore, Karnataka, India
2 Department of Uveitis and Ocular Inflammation, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India
3 Department of Ophthalmology, National University Hospital, Singapore
4 Singapore National Eye Centre; Singapore Eye Research Institute; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore; Duke-NUS Graduate Medical School Singapore, Singapore
5 Centre for Ophthalmology, University of Tuebingen, Germany

Date of Submission10-Apr-2020
Date of Acceptance11-Jun-2020
Date of Web Publication20-Aug-2020

Correspondence Address:
Dr. Kalpana Babu
504, 40th Cross, Jayanagar 8th Block, Bangalore - 560 070, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijo.IJO_928_20

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  Abstract 


Viral anterior uveitis (VAU) needs to be suspected in anterior uveitis (AU) associated with elevated intraocular pressure, corneal involvement, and iris atrophic changes. Common etiologies of VAU include herpes simplex, varicella-zoster, cytomegalovirus, and rubella virus. Clinical presentations can vary from granulomatous AU with corneal involvement, Posner-Schlossman syndrome, Fuchs uveitis syndrome, and endothelitis. Due to overlapping clinical manifestations between the different viruses, diagnostic tests like polymerase chain reaction and Goldmann-Witmer coefficient analysis on the aqueous humor may help in identifying etiology to plan and monitor treatment.

Keywords: Cytomegalovirus, herpes simplex virus, ocular hypertension, rubella virus, varicella-zoster virus, viral anterior uveitis


How to cite this article:
Babu K, Konana VK, Ganesh SK, Patnaik G, Chan NS, Chee SP, Sobolewska B, Zierhut M. Viral anterior uveitis. Indian J Ophthalmol 2020;68:1764-73

How to cite this URL:
Babu K, Konana VK, Ganesh SK, Patnaik G, Chan NS, Chee SP, Sobolewska B, Zierhut M. Viral anterior uveitis. Indian J Ophthalmol [serial online] 2020 [cited 2020 Sep 24];68:1764-73. Available from: http://www.ijo.in/text.asp?2020/68/9/1764/292596



Viral anterior uveitis (VAU) is characterized by anterior uveitis (AU) with elevated intraocular pressure (IOP) diffuse stellate keratic precipitates (KPs), presence of pigmentation in active KPs and iris atrophic changes.[1],[2],[3],[4] The most commonly implicated viruses include herpes simplex (HSV), varicella-zoster (VZV), cytomegalovirus (CMV), and rubella (RV).[5],[6] Herpetic AU is the most common cause of VAU accounting for 5–10% of all uveitis cases in the western world and 0.9–8.3% of all infectious uveitis in India.[7],[8],[9],[10] The severity and outcome of VAU depend on the type of the virus, clinical characteristics of the disease, immune status, and genetic makeup of the individual. In an aqueous-based polymerase chain reaction (PCR) study from South India, 2/3rd of cases were VZV, 19.4% were HSV-1, and 8.3% were CMV.[11] This review will focus on syndromes associated with viral etiology, different viruses causing AU, clinical features, diagnostic tools, and management of viral anterior uveitis.


  Methods Top


Literature search pertaining to VAU published in PubMed, EMBASE, and MEDLINE. For PubMed related search, MESH terms “viral anterior uveitis” and “Herpetic”/”Cytomegalovirus”/”Rubella”/”Fuchs heterochromic iridocyclitis”/”Posner Schlossman syndrome”/”Diagnosis”, and “Therapy”. A manual search of references cited by retrieved articles for additional references was also done. All authors independently conducted a systematic review of the literature and extracted data.


  Syndromes associated With Viral Aetiology Top


Posner Schlossman syndrome (PSS)

PSS is characterized by recurrent, acute attacks of unilateral mild AU with few granulomatous KPs, and severely elevated intraocular pressure (IOP).[12] Symptoms include mild blurring of vision and haloes. It affects young adults more frequently in the 3rd decade in the European population but later in the Asian population (3–5th decade).[13],[14],[15],[16],[17] Males are at a higher risk of developing PSS (50.5–71.4%).[18] CMV appears to be a major cause of PSS, especially in Asia.[14],[15],[19] HSV is also known to cause PSS.[20] Posterior synechiae and vitritis are absent. Mild iris atrophic changes may occur. Glaucoma develops in 26% of which 17% require filtration surgery.[14] The course is recurrent and often unpredictable.

Fuchs uveitis syndrome (FUS)

FUS is a chronic low-grade inflammation involving the anterior uveal tract and vitreous and is most commonly unilateral (90%).[4],[21] Fuchs initially described this condition as Fuchs heterochromic iridocyclitis, characterized by heterochromia, cyclitis with KPs, and cataract associated with vitreous involvement.[22] In the USA and Europe, RV is the main etiologic agent while CMV is the predominant cause in Asia.[23],[24],[25],[26],[27] Other associations include HSV, toxoplasmosis, toxocariasis, sarcoidosis, retinitis pigmentosa, Horner's syndrome, Ushers syndrome, and previous ocular trauma.[28],[29],[30] Clinical signs include mild with low-grade anterior chamber inflammation, absent ciliary injection, diffuse distribution of white stellate KPs over the entire endothelium, diffuse iris atrophy, posterior subcapsular cataract, presence of Koeppe nodules, absence of posterior synechiae, low-grade vitritis and with or without glaucoma.[31],[32] Heterochromia is seen in light colored irides (12.7–82%) and often absent in heavily pigmented eyes and maybe noticed before the development of visual symptoms.[31] The affected eye is hypochromic due to diffuse pigment loss but maybe hyperchromic when anterior stromal atrophy occurs exposing the darker iris pigment epithelium. In the case of the absence of heterochromia, the occurrence of iris nodules together with cataract, vitritis, or glaucoma should alert the clinician on the likelihood of FUS.[25] FUS may begin in early childhood, but the diagnosis is often delayed for years, as the characteristic findings may not be present at disease onset.[21]

Structural changes in iris occur earlier than heterochromia. Atrophy affects all layers and radial markings at the pupillary border are less prominent.[33] A motheaten appearance develops. In later stages, there is a loss of iris tone and sphincter muscle causing widened iridocorneal angle and increased anterior chamber depth.[34]

In addition, normal radial iris vessels may appear like neovascularization in FUS patients with diffuse iris atrophy. Rubeotic-like “bridging vessels” in the chamber angle extension may cause hyphema during cataract surgery (Amsler sign).[35] A modified Amsler sign has been described after minor trauma, peribulbar anesthesia, contact tonometry, and sexual intercourse.[35],[36],[37] Rarely, iris crystals are seen (Russel bodies), which may represent plasma cells filled with antibodies.[33],[38] Other ocular findings include peripheral chorioretinal scars (7.2–65% of FUS patients).[30],[39] Disc and macula edema, snow banking, retinal vasculitis are typically absent in FUS.


  Common Etiologies of Viral Anterior Uveitis Top


Herpes simplex virus

HSV AU is commonly caused by HSV-type 1 and accounts for a large proportion of viral AU in western populations.[40],[41],[42],[43],[44] It typically affects both genders and in the 4th–5th decades of life.[44] There may be a history of recurrent fever, blisters, grouped vesicles around the eyelid border with diffuse edema. HSV AU occurs more frequently during reactivation than in primary disease. The viral genome lying latent within the trigeminal ganglion reactivates. It is transported down the axon, manifesting in the periocular skin, cornea, or intraocular inflammation.[45] It is usually unilateral but can be bilateral in 18% cases.[3],[4] Symptoms include acute severe eye pain, redness, tearing, photophobia, blurring of vision.

The incidence of corneal involvement in HSV ranges from 33–41% and can present as active keratitis (epithelial, stromal, interstitial, and disciform), old corneal scar, endotheliitis, and reduced corneal sensation. HSV dendritic ulcers are branching with well-developed terminal bulbs. The ulcer base and borders are stained by fluorescein and rose bengal, respectively.[4],[5],[6]

HSV AU is characterized by small to medium-sized KPs, some of these fresh KPs may be pigmented. The location may be central, paracentral, or diffuse. In keratouveitis, they are located in the same distribution as the inflamed cornea. Elevated intraocular pressures occur due to trabeculitis and this can be episodic. These may cause secondary glaucomatous optic neuropathy. Iris atrophy occurs in 41–48%.[42],[43] During acute HSV, sectoral iridoplegia and flattening of the pupillary border occur in the affected area [Figure 1]. The presence of patchy or sectoral iris atrophy is seen in recurrent or chronic disease and may be absent in very early disease. Spiral atrophy is typically associated with HSV. Diffuse iris atrophy is rather an uncommon finding and noted in 10% cases.[45],[46],[47] HSV AU causes iris pigment epithelitis. In severe inflammation, hypopyon, transient hyphema, posterior synechiae (38%), and vitritis (43%) may occur.[47] Focal iris stromal hemorrhage may be seen in acute HSV. Cataract occurs later in the disease course.
Figure 1: Slit-lamp photograph of HSV AU showing granulomatous keratic precipitates adjacent to the inflamed cornea (a), iridoparesis (b) and diffuse iris stromal atrophy (c)

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Varicella Zoster virus

VZV lies dormant in the neural sensory ganglia following primary infection usually in childhood and reactivates when VZV specific immunity wanes, typically during the 6th or 7th decade of life.[4],[10],[48],[49],[50],[51],[52],[53],[54],[55],[56],[57],[58],[59] Alternatively, it may occur in young immunocompetent individuals, conditions causing immunosuppression like acquired immunodeficiency syndrome and immunosuppressive drugs.[60],[61],[62],[63],[64],[65] Herpes zoster ophthalmicus (HZO) presents with severe pain followed by a vesicular eruption in the dermatome of the ophthalmic division of the trigeminal nerve. If the tip of the nose is involved, it is a predictor for ocular inflammation (Hutchinson's sign). VZV AU occurs in 40–60% of HZO in immunocompetent patients and may be present for many months.[48],[50]

Typically, VZV AU presents 2 weeks following dermatological manifestations in the form of acute hypertensive AU with granulomatous or nongranulomatous uveitis. The inflammation in VZV is generally more severe than in HSV AU, possibly because VZV invades the root of iris epithelium and causes occlusive vasculitis. Segmental iris atrophy (triangular sectoral loss of iris pigment epithelium with the base at the iris root) may develop after the acute episode resolves causing transillumination defect (88%). It has been postulated that the severity of iris atrophy and pupil distortion is closely related to the viral load in aqueous [Figure 2].[23],[59] Corneal involvement has been reported in 25% of cases and includes nummular keratitis, limbal keratitis, and ring infiltrates. Profound reduced corneal sensation and coarse pseudo dendrites with an elevated appearance that lacks terminal bulbs may be seen. There may be associated episcleritis, scleritis, and choroidal vitiligo.[66] Posterior synechiae (40%) and vitritis (83%) can occur in VAV AU. Secondary glaucoma is noted in 15–43% of cases.[43],[56],[67] A detailed posterior segment examination is mandatory in all cases of herpetic uveitis.
Figure 2: Slit-lamp photograph of VZV AU showing pigmented active keratic precipitates and D shaped pupil at initial presentation (a) and development of sectoral iris atrophy in the same eye over 6 months (b). External photograph showing facial scars of herpes zoster ophthalmicus scars over the left side of the forehead and nose (c)

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Zoster sine herpete AU: At times, patients present with AU typical of viral AU in the absence of dermatological manifestations.[68],[69]

Cytomegalovirus

CMV is an important cause of hypertensive AU in immunocompetent individuals and there is likely a prominent immunological component as it is not seen in immunocompromised individuals.[15] Ocular tissues like iris and ciliary body may be a site of CMV latency as suggested by murine studies.[70] An intraocular immunocompromised state with impairment of both innate and adaptive immunity, especially the virus-specific T-cell response, may trigger CMV reactivation (Example: ocular corticosteroid implants, topical cyclosporine A 0.05% ophthalmic emulsion, topical prostaglandin analogs, ophthalmic surgery).[71],[72]

Most cases have been reported from Asia, particularly from Chinese and Japanese populations, which could be due to the higher seroprevalence of CMV in Asia.[15],[18],[40],[73] CMV has been identified as the causative virus for 75% of hypertensive AU in Singapore, 67% of the chronic idiopathic recurrent AU and ocular hypertension in Korea, 33% of the viral AU in Thailand, 8.3% of viral AU in south India and only 2% of viral AU in the United States of America.[11],[15],[16],[17],[19],[40],[70],[73],[74],[75],[76] CMV AU usually affects individuals from the 3rd decade onwards, particularly Asians and males, those in their 3rd–5th decade present with PSS while those in their 5th –7th decade present with chronic CMV AU resembling FUS. It is acute and recurrent in patients younger than 40 years of age or chronic in those above 40 years of age. It is unilateral in most of the cases and bilateral in 7% cases.[16],[17],[74],[75] The clinical manifestations of CMV AU vary.

Acute relapsing hypertensive anterior uveitis (Posner-Schlossman Syndrome)

CMV is thought to be the cause of PSS in Asian and western populations.[16],[19],[23],[40],[77],[78] The typical presentation is a patient in the 3rd–5th decade with an acute onset of haloes, unilateral mild blurring of vision associated with an ipsilateral headache, possibly with a history of similar episodes. The IOP often exceeds 50 mm Hg during the attack in the presence of subtle subepithelial edema. The severely elevated IOP is often out of proportion to the findings of mild anterior segment inflammation. KPs are medium to large (39%), white or gray colored, and few located centrally or in the peripheral cornea.[4],[6]

Chronic hypertensive CMV anterior uveitis

Chronic CMV AU more commonly affects older patients in the 5th –7th decade, at a mean of 65 years of age, who may present with ocular discomfort and blurring of vision. A geographic disparity is seen in the clinical presentation of chronic CMV AU in Asian and western populations. CMV is a major cause of FUS in East Asia, especially in Singapore, Taiwan and Japan.[14],[15],[18],[19] It presents with mild ocular injection, mild-to-moderate anterior chamber activity and diffuse, fine, stellate uniformly distributed KPs. Chronic CMV AU in eyes of European patients has fewer KPs that are brown (pigmented) and located inferiorly, with minimal flare. The IOP is typically persistently elevated in chronic CMV AU. The iris may appear moth-eaten due to stromal atrophy, which is more commonly diffuse, although patchy and rarely sectoral atrophy have been reported, and the posterior pigment epithelium is often relatively intact with no transillumination defects.[79] Although findings of CMV in the smooth muscle cells of the iris led some to postulate that the iris stromal atrophy was due to ischemic necrosis of the iris stroma as a result of the direct viral invasion, Sakai et al. have suggested that the diffuse iris atrophy which is not associated with dyscoria may develop as a consequence of persistently elevated IOP rather than tissue damage by CMV.[58] Heterochromia (in which a naturally darker iris appears lighter, and lighter irides, particularly blue or light green, appear darker) is uncommon but may be present.[80] The diffuse iris atrophy may also result in fragile iris vasculature, which can be visualized on gonioscopy in the iris and trabecular meshwork or iridocorneal angle. These fragile vessels may be prone to bleeding easily, giving rise to Amsler's sign.

A posterior subcapsular cataract occurs in 81.3% of eyes later in the disease course. Unlike RV, vitritis is rare in CMV infection. Unlike in PSS, the inflammation tends to recur when topical corticosteroids are tapered.

Recurrent or chronic iridocyclitis

Unlike Asian patients who present similarly to FUS or PSS, patients in the West often present with less distinct syndromes, or overlap of features from both syndromes, manifesting as a mild unilateral recurrent or chronic iridocyclitis.[14]

Corneal endotheliitis

Corneal endotheliitis is the inflammation of the corneal endothelium characterized by localized corneal stromal edema and KPs.[81] It can involve a focal area or even the entire endothelium that presents similarly to diffuse bullous keratopathy with severe stromal edema. An immune ring formation similar to that seen in HSV-related keratitis may sometimes be present. The IOP may be elevated.[82] CMV corneal endotheliitis may be associated with AU in 30% of Asian or European patients or may occur in isolation.[19],[80]

Other characteristic clinical signs

Coin-shaped lesions in which small-sized KPs are distributed in a ring pattern are pathognomonic of CMV with a positive predictive value of 90.9% and, maybe seen in both acute and chronic infection.[73] These coin-shaped KPs were seen in 53% of CMV AU cases in a recent Japanese study.[58] KPs may also be seen in a linear pattern in the peripheral cornea.[15] Nodular endothelial lesions, which possibly represent swollen endothelial cells, are white medium-sized nodular lesions with a surrounding translucent halo and may become pigmented over time. They are more common in chronic CMV AU and are significantly associated with CMV infection in eyes with presumed FUS [Figure 3].[17] The endothelial cell count is significantly reduced in CMV positive eyes, a feature that is less commonly seen in other VAU in the absence of frank keratitis.[76],[83]
Figure 3: Slit-lamp photograph of CMV AU in diffuse illumination showing a couple of granulomatous keratic precipitates in the center of the steamy cornea in an eye presenting acutely with elevated intraocular pressure typical of CMV associated Posner Schlossman syndrome (a) and diffusely distributed fine filiform keratic precipitates typical of Fuchs uveitis syndrome admixed with scattered pigmented, medium-sized keratic precipitates in an eye with cytomegalovirus chronic anterior uveitis (b)

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The pupil is usually round and posterior synechiae are notably absent. Associated posterior segment abnormalities are uncommon and include periphlebitis, disc, and macular edema and epiretinal membrane. Prolonged arm to retina time on fluorescein angiography has been hypothesized to reflect subclinical vasculitis.[84]

Rubella virus

RV AU is chronic, often unilateral but may be bilateral (14%) in the presentation.[6] It is a common cause of FUS in the western population. The definitive finding of anti-RV antibodies in the anterior chamber fluid of FUS patients clearly shows that rubella may be participating in the pathogenesis.[24],[46],[85],[86] On the other side, the very rare finding of RV-PCR may be a sign that FUS is less an infectious but more an immune response to rubella. The hypothesis of FUS as a RV-induced disease was supported by the decreased number of FUS patients after the introduction of the rubella vaccination program in the United States (from 4.48% to 1% FUS patients/year).[25] However, the question rises if a living attenuated vaccine or a subclinical RV infection before vaccination may induce FUS.[39] Analysis of the aqueous humor in FUS patients also showed elevated levels of the inflammatory cytokine (IL-6, IL-10), interferon-γ, and low IL-12 levels suggesting a Th1-type response.[87],[88]

RV AV usually presents in relatively younger patients (mean age 35 ± 12 years) with posterior subcapsular cataract (47%) with a chronic blurring of vision and or floaters with minimal redness and pain.[6] It has a chronic course and presents with diffuse stellate KPs (do not become pigmented and persist despite treatment), diffuse iris atrophy, and mild anterior chamber reaction. Koeppe nodules may be present. Low-grade vitritis is often present and frequently mistaken for intermediate uveitis [Figure 4].
Figure 4: Slit-lamp photograph of the right eye in a case of Fuchs heterochromic iridocyclitis syndrome showing fine to medium-sized keratic precipitates on the corneal endothelium and moth-eaten appearance of iris

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Absence of redness, pain, posterior synechiae, and cystoid macular edema are characteristic features. RV AU can be complicated by ocular hypertension (25%) leading to secondary glaucoma.

Other viral etiologies

Less common causes include, human T-cell lymphotropic virus-type 1 (Seen in southern Japan and Africa and frequently presents as intermediate uveitis), Human immunodeficiency virus (anterior segment inflammation is mild with small or medium-sized KPs on the corneal endothelium which disappear quickly with the administration of highly active retroviral therapy), Chikungunya virus (nongranulomatous AU or FUS like presentation with a history of systemic Chikungunya virus infection and, responds to topical corticosteroids), ZIKA virus (mild in adults and presents as AU with nonpurulent conjunctivitis and treated with topical steroids) and Ebola virus (AU with KPs, posterior synechiae, cataract and ocular hypertension and, is unclear if it is caused by a cytopathic effect or an immune response). The role of Epstein–Barr virus and parvovirus B19 virus (link with juvenile idiopathic arthritis) in VAU is uncertain [89],[90],[91],[92],[93],[94],[95],[96] Vitiligo iridis and secondary glaucoma may also be seen as a long term sequelae of smallpox.[97]

[Table 1] summarizes the clinical manifestations between HSV, VZV, CMV, and RV
Table 1: Comparison of the clinical features between the common viral anterior uveitis aetiologies

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  Investigations Top


Anterior chamber tap

Aqueous humor analysis is a useful method to determine the etiology and estimate the viral load as it may difficult to differentiate the etiology based on clinical manifestations in all cases. Tests done include PCR, Goldmann–Witmer coefficient (GWC) analysis, metagenome sequencing.[6],[25],[77],[98],[99]

Polymerase chain reaction

PCR can detect minimal amounts of viral DNA and enable rapid confirmation of diagnosis. Aqueous tap for PCR should be done during the IOP spike, preferably before initiation of therapy especially in CMV.[16] A negative PCR does not exclude a viral etiology. This could be due to the limited volume of aqueous sample, low intraocular viral load, transient rapid rise in IOP, and self-limiting tendency of ocular inflammation with rapid elimination of viral DNA and presence of inhibitory compounds in the sample or microorganism polymorphism.[6] In some cases, a positive result may only be obtained after repeated aqueous taps. Conversely, PCR may give a false positive result by detecting DNA from latent viruses in leukocytes present in the anterior chamber during inflammation. A qualitative multiplex PCR can be done to screen for viruses and subsequent real-time PCR can help to identify the causative virus and quantify the viral load as a marker of severity of the infection. Real-time PCR can also be used to monitor response to therapy and any drug resistance.[77],[83]

Goldmann–Witmer coefficient analysis

GWC helps to determine pathogen-specific intraocular antibody production. Unlike PCR which tends to be positive at the early reactivation, when the viral load is higher, GWC analysis may take up to 2 weeks to become positive but remains positive for longer periods and hence more useful when patients present later (chronic) as in RV AU. RV is commonly detected via positive GWC results but only sporadically by PCR. However, it is less specific than PCR due to possible cross-reactivity of antibodies. As the diagnostic utility of the above tests depends on the patient's immune status, the chronicity of infection and the time of aqueous sampling, it is best to perform both the tests in parallel to increase the diagnostic yield. GWC analysis is not widely available in most countries and hence most countries rely solely on PCR.[6],[40],[98]

Viral cultures are difficult and time-consuming. It is not commonly done.

Other investigations

Anterior segment imaging includes specular microscopy to demonstrate lowered endothelial cell counts (ECC) compared to the fellow eye is known to occur in CMV AU. The extent of endothelial cell loss is correlated with the viral disease burden.[67],[83] Anterior segment optical coherence tomography can demonstrate the nodular endothelial lesions as thickened, highly reflective endothelial cells layer. Confocal microscopy demonstrates the owl eye cells (large endothelial cells containing nuclei with a high reflection area surrounded by a halo of low reflection within the cornea) and to monitor the response to therapy.[100],[101] Serology has limited value as most adults have had prior exposure to the viruses. Metagenomic deep sequencing can detect deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) viruses in as little as 20 μL of intraocular fluid samples in a single assay and holds promise in diagnosis of infectious uveitis.[102]


  Treatment Top


Treatment of HSV AU

Though the management of HSV keratitis is well studied, the role of acyclovir in the treatment of HSV AU is not evaluated. Studies suggest that the duration of AU may be shortened by the prompt use of therapeutic doses of antiviral therapy and, maintenance therapy is effective in decreasing disease recurrence.[51]

Oral acyclovir 400 mg five times daily for 4 weeks in conjunction with topical corticosteroids that reduce the anterior segment inflammation, cycloplegics/mydriatic agents that reduce the pain and prevent posterior synechiae. In severe and recurrent disease, maintenance therapy of oral acyclovir 400 mg twice daily is useful to prevent a relapse. Alternatively, valacyclovir, which is a prodrug with better bioavailability, may also be used at a dose of 500 mg three times a day for 4 weeks followed by 500 mg twice a day for maintenance.[47] Systemic antiviral therapy combined with low-dose corticosteroid drops may have to be used for several years, to prevent relapses. In eyes with raised IOP, antiglaucoma medications are given topically. Severe elevation of IOP may require oral carbonic anhydrase inhibitors and filtration surgery. When preparing the eye with a viral AU for cataract surgery, the eye should be quiescent and prophylactic oral antiviral therapy is found to be useful. Lucy M Lu et al. noted the recurrence of herpes zoster in 23 (40.4%) patients after phacoemulsification cataract surgery. An increased risk for recurrence was associated with shorter periods of quiescence and a greater number of recurrences before surgery. Acyclovir prophylaxis protected against recurrences after cataract surgery and, may be required in cases with a history of multiple disease recurrences.[103]

Treatment of VZV AU

Acyclovir given 800 mg five times daily for 10 days given within 72 h of the onset of skin lesions in HZO reduces the incidence and severity of episcleritis, dendritiform keratopathy, stromal keratitis, and anterior uveitis. Topical steroids and cycloplegics/mydriatic agents are used to alleviate inflammation and pain. However, the duration of treatment for chronic VZV AU should be as long as the uveitis is active. Oral acyclovir 400 mg twice a day is used as prophylaxis for recurrent uveitis. Owing to the predictability of its resorption, oral valacyclovir is generally preferred to oral acyclovir. A thrice daily dose of 0.5-1 gm for 10-14 days is the standard protocol. Thereafter a prophylactic course of thrice-weekly dose of 500 mg or 500 mg daily should be continued for 3–12 months depending upon the topical demand for corticosteroids. Acyclovir and valacylovir need to be used with caution in HIV as they may cause thrombocytopenia.[51] Acute renal failure is a known complication with these drugs. Alternatively famciclovir 500 mg three times daily or brivudin 125 mg once a day may be used.[104] Topical steroids are given to control the inflammation and need to be tapered very slowly to avoid rebound inflammation.

Treatment of CMV AU

The acute recurrent phenotype of CMV AU frequently exhibits quiescence without antiviral treatment. However, it is reported that early antiviral treatment seems to lower the risks of sight-threatening complications that may develop from recurrent and chronic inflammation. CMV AU responds to oral valganciclovir, ganciclovir, and foscarnet. Ganciclovir and valganciclovir diffuse into CMV infected cells and inhibit CMV's DNA polymerase UL54 following phosphorylation by CMV'S viral kinase encoded by the UL97 gene while, foscarnet is a direct inhibitor of the viral DNA polymerase and does not require phosphorylation.[105],[106],[107] At present, there are no clear guidelines regarding the management of CMV AU. Studies have evaluated the efficacy of systemic (intravenous ganciclovir or foscarnet, oral ganciclovir) and local therapy (intravitreal ganciclovir, topical ganciclovir drops and gel) and have compared the various forms of antiviral therapy.

The induction regimen of oral valganciclovir followed is, 900 mg twice daily for 3 weeks followed by, a maintenance regimen of 450 mg twice daily for a minimum of 4 weeks.[108] CMV AU may require long term antiviral therapy to reduce the risk of recurrences. Regular laboratory monitoring for bone marrow suppression, renal and hepatic toxicity and the cost of treatment makes it less feasible as long-term therapy in developing countries.[98] Intravitreal ganciclovir has a lower risk of systemic toxicity and has been explored as an alternative to systemic ganciclovir. However, the recurrence rates were high. Topical ganciclovir is an alternative form of antiviral therapy in CMV AU. The topical concentration ranged between 0.15%–2% and applied 6–8 times/day for induction and 1–4 times/day for maintenance.[109],[110] Ganciclovir 2% eye drops have reported good results in CMV corneal endotheliitis and AU. Ganciclovir ophthalmic gel 0.15% is well tolerated with minimal toxicity. As this is less expensive and does not require laboratory monitoring, this may be a more viable option for long term antiviral therapy. The systemic and topical control of CMV anterior uveitis-treatment outcomes (STACCATO) is an ongoing randomized trial comparing the efficacy of oral valganciclovir and 2% topical ganciclovir along with placebo which, may provide further insight of effective routes of antiviral therapy in CMV AU.[110] Some authors favor the administration of intravitreal ganciclovir. An injection of 2 mg/0.05–0.1 ml is given weekly for 3 months either with or without adjunctive oral valganciclovir. The treatment of CMV induced endotheliitis with either topical or systemic ganciclovir has been reported to be partially successful.[51] Topical nonsteroidal anti-inflammatory drugs (NSAIDs) may also be considered in CMV AU recalcitrant to topical steroids.[108]

Treatment of Rubella AU

Topical steroids may not be necessary due to the low-grade inflammation. Prolonged use can hasten cataract and glaucoma formation. Systemic immunosuppressive therapy is not recommended. Topical NSAIDs are considered to retard progression especially if required long term. Antiglaucoma medications may be used for secondary glaucoma. In glaucoma cases resistant to topical treatment, filtration surgeries are recommended.


  Conclusion Top


A high index of suspicion for a viral etiology is required in the presence of the following features: Raised IOP at presentation, corneal scars, fresh pigmented KPs, and iris atrophy. HSV, VZV, CMV, RV are common etiologies. Variable clinical presentations with overlapping manifestations in different viruses may require diagnostic tests like PCR, GWC analysis for confirmation of etiology. This is important for planning therapy. Glaucoma is the most common vision-threatening complication of VAU.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
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