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      Ocular findings in systemic lupus erythematosus

      review-article
      a , * , a , b , c
      Saudi Journal of Ophthalmology
      Elsevier
      SLE, Autoimmune, Ocular complications

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          Abstract

          Systemic lupus erythematosus (SLE) is a chronic multisystem autoimmune disease. Ocular complications occur in up to one-third of patients with SLE. The ocular findings may represent the initial manifestation of the disease and may lead to severe ocular morbidity and loss of vision. Early diagnosis and prompt management of patients with SLE are mandatory and require collaboration between the ophthalmologist and the rheumatologist.

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          Most cited references47

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          Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus.

          M Hochberg (1997)
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            Revised recommendations on screening for chloroquine and hydroxychloroquine retinopathy.

            The American Academy of Ophthalmology recommendations for screening of chloroquine (CQ) and hydroxychloroquine (HCQ) retinopathy were published in 2002, but improved screening tools and new knowledge about the prevalence of toxicity have appeared in the ensuing years. No treatment exists as yet for this disorder, so it is imperative that patients and their physicians be aware of the best practices for minimizing toxic damage. New data have shown that the risk of toxicity increases sharply toward 1% after 5 to 7 years of use, or a cumulative dose of 1000 g, of HCQ. The risk increases further with continued use of the drug. The prior recommendation emphasized dosing by weight. However, most patients are routinely given 400 mg of HCQ daily (or 250 mg CQ). This dose is now considered acceptable, except for individuals of short stature, for whom the dose should be determined on the basis of ideal body weight to avoid overdosage. A baseline examination is advised for patients starting these drugs to serve as a reference point and to rule out maculopathy, which might be a contraindication to their use. Annual screening should begin after 5 years (or sooner if there are unusual risk factors). Newer objective tests, such as multifocal electroretinogram (mfERG), spectral domain optical coherence tomography (SD-OCT), and fundus autofluorescence (FAF), can be more sensitive than visual fields. It is now recommended that along with 10-2 automated fields, at least one of these procedures be used for routine screening where available. When fields are performed independently, even the most subtle 10-2 field changes should be taken seriously and are an indication for evaluation by objective testing. Because mfERG testing is an objective test that evaluates function, it may be used in place of visual fields. Amsler grid testing is no longer recommended. Fundus examinations are advised for documentation, but visible bull's-eye maculopathy is a late change, and the goal of screening is to recognize toxicity at an earlier stage. Patients should be aware of the risk of toxicity and the rationale for screening (to detect early changes and minimize visual loss, not necessarily to prevent it). The drugs should be stopped if possible when toxicity is recognized or strongly suspected, but this is a decision to be made in conjunction with patients and their medical physicians. Copyright © 2011 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
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              Ocular Manifestations of Systemic Lupus Erythematosus: A Review of the Literature

              About one-third of patients suffering from systemic lupus erythematosus have ocular manifestations. The most common manifestation is keratoconjunctivitis sicca. The most vision threatening are retinal vasculitis and optic neuritis/neuropathy. Prompt diagnosis and treatment of eye disease is paramount as they are often associated with high levels of systemic inflammation and end-organ damage. Initial management with high-dose oral or IV corticosteroids is often necessary. Multiple “steroid-sparing” treatment options exist with the most recently studied being biologic agents.
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                Author and article information

                Contributors
                Journal
                Saudi J Ophthalmol
                Saudi J Ophthalmol
                Saudi Journal of Ophthalmology
                Elsevier
                1319-4534
                16 February 2016
                Apr-Jun 2016
                16 February 2016
                : 30
                : 2
                : 117-121
                Affiliations
                [a ]The Eye Center and The Eye Foundation for Research in Ophthalmology, Riyadh, Saudi Arabia
                [b ]Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia
                [c ]The Wilmer Ophthalmological Institute of The Johns Hopkins University, School of Medicine, Baltimore, MD, USA
                Author notes
                [* ]Corresponding author at: The Eye Center, PO Box 55307, Riyadh 11534, Saudi Arabia.The Eye CenterPO Box 55307Riyadh11534Saudi Arabia samir.shawki@ 123456hotmail.com
                Article
                S1319-4534(16)00024-2
                10.1016/j.sjopt.2016.02.001
                4908056
                27330388
                96407bd9-7a9f-4171-adbf-7202c34281b3
                © 2016 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 11 March 2015
                : 5 January 2016
                : 9 February 2016
                Categories
                Review Article

                sle,autoimmune,ocular complications
                sle, autoimmune, ocular complications

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