Guide Line to Solve Eye Scenarios by Maryam Malik
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Optic Disc Drusen in Differential Diagnosis of Optic Neuritis Optik Nörit Ayrıcı Tanısında Optik Disk Druzeni
DO I:10.4274/tnd.56514 Images in Clinical Neurology Optic Disc Drusen in Differential Diagnosis of Optic Neuritis Optik Nörit Ayrıcı Tanısında Optik Disk Druzeni Erkingül Shugaiv1, Elif Aksoy Güzeller2, Sait Alim2 1Tokat State Hospital, Clinic of Neurology, Tokat, Turkey 2Tokat State Hospital, Clinic of Diases Eye, Tokat, Turkey Optic disc drusen is a condition where a hyaline-like calcific object is accumulated on the optical nerve ending, often bilaterally (1). Its prevalence in the general population is 0.34-3.7%. It can be confused with optic papillitis since it blurs the papillary border at the bottom of the eye. Drusens can be seen as opacity in B-scan ultrasonography and computerized tomography (2). Optic disc drusens present with slowly progressing visual field defects. The 21-year-old patient who complained of blurry vision on both eyes did not have a history of disease. Her vision was blurry for the past 10 days, especially on the left side. There was no history of eyeball pain, headache, infection or trauma. Her vision was 0.2 on the right and 0.1 on the left side. The papillary borders were undefined on both sides in the examination of the base of Figure 1. Optic disc drusen on both sides: Discs are protruded due the eyes (Figure 1). Due to the slow clinical decline over 10 days, to the drusen and their borders are not clearly defined. cranial and spinal magnetic resonance imaging was conducted in order to address any possible demyelinating disease but did not produce any remarkable findings. After this, cranial and orbital tomography was conducted with the pre-diagnosis of optic disc drusen. -
Traumatic Glaucoma: an Overview
Indian Journal of Clinical and Experimental Ophthalmology 2020;6(1):1–2 Content available at: iponlinejournal.com Indian Journal of Clinical and Experimental Ophthalmology Journal homepage: www.innovativepublication.com Editorial Traumatic glaucoma: An overview Rajendra Prakash Maurya1,* 1Regional Institute of Ophthalmology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India ARTICLEINFO © 2020 Published by Innovative Publication. This is an open access article under the CC BY-NC-ND Article history: license (https://creativecommons.org/licenses/by/4.0/) Received 11-03-2020 Accepted 12-03-2020 Available online 17-03-2020 of blunt trauma are (i) Trabecular meshwork disruption, Dear Friends (ii) Hyphaema: Accumulation of blood in the anterior chamber leads to obstruction of the trabecular meshwork Season’s Greeting!! with erythrocytes, fibrin, platelets and other inflammatory It is my humble privilege to present the special issue debris lead to prolonged increase in the IOP. 2 (iii) of IJCEO after successful journey of five years. This Inflammation: Trauma may also lead to direct inflammation issue of IJCEO has several interesting articles on vision of the trabecular meshwork (trabeculitis) causing decrease threatening morbidity, Glaucoma particularly on diagnosis in aqueous outflow. (iv) Choroidal hemorrhage: causing and management of primary glaucoma. a mass effect in the posterior segment leading to forward Traumatic glaucoma (TG) refers to a heterogeneous displacement of the lens-iris diaphragm and leads to acute group of post-traumatic secondary glaucoma with varying angle closure glaucoma. The pathophysiology of late underlying mechanisms. Traumatic glaucoma occurs onset TG are (i) Angle-Recession (tear which occurs commonly after mechanical injury of globe (blunt or between the longitudinal and circular layers of the ciliary penetrating injury). -
Posterior Uveitis Signs
Uveitis unplugged: sorting out infectious uveitis Hobart 2017 Peter McCluskey Save Sight Institute Sydney Eye Hospital Sydney Medical School University of Sydney Sydney Australia No financial or proprietary interest in any material discussed Immunosuppression for IED The fundamental principle for managing uveitis: Is the disease: infective inflammatory neoplastic What is the worst, most acute threat to vision this could be? Immunosuppression for IED The fundamental principle for managing uveitis: Is the disease: infective inflammatory neoplastic What is the worst, most acute threat to vision this could be? usually infection! Common Causes of Uveitis in Sydney 2015 Idiopathic 505 (50%) • idiopathic 424 Infective 203 (20%) • Fuchs 26 • Herpetic 105 • WDS 55 - anterior 83 - posterior 22 Inflammatory 358 (35%) • HLA B27 188 TB 40 (+systemic B27) 46 • • Toxoplasmosis 38 • sarcoid 56 • syphilis 10 (25) • Behcets 18 4 Assessing the patient with uveitis How do I sort this out??? • clinical assessment + carefully selected tests • clinical assessment is the key investigation • critical to take as comprehensive a history and review of systems as possible plus • thorough careful complete examination of each eye Sorting out Uveitis: anterior uveitis signs Anterior Uveitis Signs: • comprehensive a history and systems review • there are some unofficial “rules” can’t diagnose anterior uveitis without a normal fundus on dilated exam • anterior uveitis: mostly non specific signs • KPs, iris and pupil: useful clues Sorting out Uveitis: posterior uveitis -
A Case of Cerebral Granuloma and Optic Papillitis Due to Brucella Sp
Hindawi Case Reports in Infectious Diseases Volume 2020, Article ID 5216249, 3 pages https://doi.org/10.1155/2020/5216249 Case Report A Case of Cerebral Granuloma and Optic Papillitis due to Brucella sp. A. Chiappe-Gonzalez 1,2 and A Solano-Loza2 1Hospital Nacional Dos de Mayo, Lima, Peru 2Cl´ınica Angloamericana, San Isidro, Peru Correspondence should be addressed to A. Chiappe-Gonzalez; [email protected] Received 21 December 2019; Revised 18 April 2020; Accepted 29 June 2020; Published 18 July 2020 Academic Editor: Larry M. Bush Copyright © 2020 A. Chiappe-Gonzalez and A Solano-Loza. ,is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. We document a case of a 24-year-old woman who presented with cerebral granuloma and optic papillitis associated to Brucella sp. infection, whose diagnosis was made with a brain biopsy and serology tests, with clinical improvement following specific antibiotic therapy. ,e patient was followed up for over a year without evidence of relapse. 1. Introduction Seven months prior to presentation, she had been eval- uated for this complaint; a head computed tomography (CT) Brucellosis is a common zoonotic infection in many angiography was performed which showed a hypodense, right countries, including Mediterranean and Middle Eastern occipital lesion with ill-defined borders and peripheral con- countries. In Peru, the prevalence of brucellosis has been trast enhancement (Figure 1); the study was followed by a poorly documented, with higher frequency in the cities of brain magnetic resonance imaging (MRI), which confirmed Lima, Callao, and Ica probably due to the informal goat the presence of a solid cortical formation of about 0.7 cen- farming in these regions. -
Myelin Oligodendrocyte Glycoprotein-Igg-Positive Recurrent Bilateral Optic Papillitis with Serous Retinal Detachment: a Case Report
doi: 10.2169/internalmedicine.9840-17 Intern Med Advance Publication http://internmed.jp 【 CASE REPORT 】 Myelin Oligodendrocyte Glycoprotein-IgG-positive Recurrent Bilateral Optic Papillitis with Serous Retinal Detachment: A Case Report Tomoya Kon 1, Hiroki Hikichi 1, Tatsuya Ueno 1, Chieko Suzuki 1, Jinichi Nunomura 1, Kimihiko Kaneko 2, Toshiyuki Takahashi 2,3, Ichiro Nakashima 2 and Masahiko Tomiyama 1 Abstract: Autoantibodies against myelin oligodendrocyte glycoprotein (MOG-IgG) have been detected in inflamma- tory demyelinating central nervous system diseases. A 30-year-old woman had blurred vision, marked optic nerve disc swelling, serous retinal detachment at the macular on optic coherence tomography, and MOG-IgG seropositivity. The patient was thought to have optic papillitis associated with MOG-IgG. Her symptoms rap- idly improved after high-dose methylprednisolone therapy. We hypothesize that serous retinal detachment was secondary, arising from optic papillitis. This is the first report of the concurrence of optic papillitis with MOG-IgG and serous retinal detachment. MOG-IgG should be tested in patients with marked optic disc swelling. Key words: IgA nephropathy, MOG, myelin oligodendrocyte glycoprotein, optic neuritis, optic papillitis, serous retinal detachment (Intern Med Advance Publication) (DOI: 10.2169/internalmedicine.9840-17) inflammatory diseases, such as Vogt-Koyanagi-Harada dis- Introduction ease, sarcoidosis, and Behçet’s disease, disrupt the blood- retinal barrier, resulting in the development of serous retinal Autoantibodies against myelin oligodendrocyte glycopro- detachment (4, 5). However, to our knowledge, serous reti- tein (MOG-IgG) have been detected in patients with central nal detachment in a patient with MOG-IgG-positive optic nervous system demyelinating diseases, including acute dis- neuritis has not been reported to date. -
Ophthalmology Ophthalomolgy
Ophthalmology Ophthalomolgy Description ICD10-CM Documentation Tips Description ICD10-CM Documentation Tips Cataracts Code Tip Glaucoma Code Tip Cortical age-related cataract, right eye H25.011 Right, left, or bilateral; Presenile, Open angle with borderline H40.011 Suspect, Open angle, Primary senile, traumatic, complicated; findings, low risk, right eye angle closure; type; acute vs., specific type (cortical, anterior or chronic; mild, moderate, severe, Cortical age-related cataract, left eye H25.012 Open angle with borderline H40.012 posterior subcapsular polar, etc) indeterminate findings, low risk, left eye Cortical age-related cataract, bilateral eye H25.013 Open angle with borderline H40.013 findings, low risk, bilateral eye Anterior subcapsular polar age-related H25.031 Anatomical narrow angle, right H40.031 cataract,right eye eye Anterior subcapsular polar age-related H25.032 Anatomical narrow angle, right H40.032 cataract, left eye eye Anterior subcapsular polar age-related H25.033 Anatomical narrow angle, H40.033 cataract, bilateral bilateral Age-related nuclear cataract, right eye H25.11 Primary open-angle H40.11x2 glaucoma, moderate stage Age-related nuclear cataract, left eye H25.12 Globe Rupture Code Tip Age-related nuclear cataract, bilateral eye H25.13 Penetrating wound without S05.62xS Contusion vs. laceration; If foreign body of left eyeball, laceration, with or without sequela prolapsed or loss of intraocular tissue; penetrating wound, with or Combined forms of age-related cataract, H25.811 Contusion of eyeball and -
Fluorescein Angiography Reference Number: OC.UM.CP.0028 Coding Implications Last Review Date: 05/2020 Revision Log
Clinical Policy: Fluorescein Angiography Reference Number: OC.UM.CP.0028 Coding Implications Last Review Date: 05/2020 Revision Log See Important Reminder at the end of this policy for important regulatory and legal information. Description Intravenous Fluorescein Angiography (IVFA) or fluorescent angiography is a technique for examining the circulation of the retina and choroid using a fluorescent dye and a specialized camera. It involves injection of sodium fluorescein into the systemic circulation, and then an angiogram is obtained by photographing the fluorescence emitted after illumination of the retina with blue light at a wavelength of 490 nanometers. This policy describes the medical necessity guidelines for fluorescein angiography. Policy/Criteria I. It is the policy of health plans affiliated with Envolve Vision, Inc.® that fluorescein angiography is medically necessary for the following indications: A. Initial evaluation of a patient with abnormal findings of the fundus / retina on ophthalmoscopy exam including one of the following: 1. Choroidal Neovascular Membranes (CNVM) 2. Lesions of the Retinal Pigment Epithelium (RPE) a. Serous Detachment of the RPE b. Tears or rips of the RPE c. Hemorrhagic detachment 3. Fibrovascular Disciform Scar 4. Vitreous Hemorrhage (patient presents with sudden loss of vision) 5. Drusen 6. Diabetic Retinopathy B. Evaluation of patient presenting with symptoms of sudden vision loss (especially central vision), blurred vision, distortion, etc., which may suggest a subretinal neovascularization and abnormal findings of the fundus / retina on ophthalmoscopy exam. C. Evaluation of patients with nonproliferative (background) and proliferative diabetic retinopathy without macular edema. Frequency is determined by disease progression and the treatment performed. Fluorescein angiography may be performed on the treated eye only at 6 weeks post-treatment and as often as every 8-12 weeks to assist in management of the retinopathy. -
Doyne Lecture the Pathology of the Outflow System in Primary and Secondary Glaucoma
DOYNE LECTURE THE PATHOLOGY OF THE OUTFLOW SYSTEM IN PRIMARY AND SECONDARY GLAUCOMA W. R. LEE Glasgow On behalf of my specialty of ophthalmic pathology, I noted that since the contribution of Doyne himself, am indebted to the Master of the Oxford Congress few pathologists have been honoured. Professor for the invitation to present the Doyne Memorial Norman Ashton and the late Professor David Lecture on the pathology of the outflow system in Cogan were the only ophthalmic pathologists primary and secondary glaucoma. Although I regard included in the list. In 1960, Professor Ashton3 the Doyne Lecture as an awesome responsibility, it chose to lecture on the pathology of the outflow has been an enjoyable exercise in preparing for it to channels in glaucoma and I was interested to see that go through the contributions of previous Doyne in the final paragraph of his text he wrote 'no doubt lecturers and to read the remarks made by those who this topic will again be chosen by a Doyne Lecturer'. knew Doyne personally. From the various very Thus it is appropriate that the problem of glaucoma distinguished Doyne lecturers who have preceded should again be addressed by a pathologist some 35 me, I sense that the ethos of this lecture is that years later. In this lecture I have drawn freely on the speculation is an integral requirement of the speaker. research material which my colleagues and I have This is not so easy for a pathologist, but I hope that been studying in Glasgow for the past 25 years and I some of the text will be sufficiently controversial to have used this to re-interpret conventional morphol stimulate further research work. -
Clinical Medical Policy
CLINICAL MEDICAL POLICY Scanning Computerized Ophthalmic Imaging (SCODI) Policy Name: (L34601) Policy Number: MP-078-MC-NC Responsible Department(s): Medical Management Provider Notice Date: 06/10/2019 Issue Date: 07/15/2019 Effective Date: 07/15/2019 Annual Approval Date: 05/15/2020 Revision Date: N/A Products: North Carolina Medicare Assured All participating and nonparticipating hospitals and Application: providers Page Number(s): 1 of 26 DISCLAIMER Gateway Health℠ (Gateway) medical policy is intended to serve only as a general reference resource regarding coverage for the services described. This policy does not constitute medical advice and is not intended to govern or otherwise influence medical decisions. POLICY STATEMENT Gateway Health℠ may provide coverage under the medical-surgical benefits of the Company’s Medicare products for medically necessary scanning computerized ophthalmic imaging. This policy is designed to address medical necessity guidelines that are appropriate for the majority of individuals with a particular disease, illness or condition. Each person’s unique clinical circumstances warrant individual consideration, based upon review of applicable medical records. Policy No. MP-078-MC-NC Page 1 of 26 DEFINITIONS Abstract: Glaucoma is a leading cause of blindness, and a disease for which treatment methods clearly are available and in common use. Glaucoma also is diagnostically challenging. Almost 50% of glaucoma cases remain undetected. Elevated intraocular pressure is a clear risk factor for glaucoma, but over 30% of those suffering from the disease have pressures in the normal range. Further, most patients having abnormally high pressures will never suffer glaucomatous damage to their vision. Scanning computerized ophthalmic diagnostic imaging (SCODI) allows for early detection of glaucomatous damage to the nerve fiber layer or optic nerve of the eye. -
Diagnosis and Management of Vitreous Hemorrhage
American Academy of Ophthalmology OCAL CLINICAL MODULES FOR OPHTHALMOLOGISTS VOLUME XVIII NUMBER 10 DECEMBER 2000 (SECTION 1 OF 3) Diagnosis and Management of Vitreous Hemorrhage Andrew W. Eller, M.D. Reviewers and Contributing Editors Editors for Retina and Vitreous: Dennis M. Marcus, M.D. Paul Sternberg, Jr., M.D. Basic and Clinical Science Course Faculty, Section 12: Harry W. Flynn, Jr., M.D. Consultants Practicing Ophthalmologists Advisory Committee Dennis M. Marcus, M.D. for Education: Edgar L. Thomas, M.D. Rick D. Isernhagen, M.D. l]~ THE fOUNDATION [liO) LIFELONG EDUCATION ~OF THE AMERICAN ACADEMY FOR THE OPHTHALMOLOGIST OF OPHTHALMOLOGY Focal Points Editorial Review Board Diagnosis and Management of Michael W Belin, M.D., Albany, NY; Editor-in-Chief; Cornea, Vitreous Hemorrhage External Disease & Refractive Surgery; Optics & Refraction • Charles Henry, M.D., Little Rock, AR; Glaucoma • Careen Yen Lowder, M.D., Ph.D., Cleveland , OH; Ocular Inflammation & INTRODUCTION Tumors • Dennis M. Marcus, M .D., Augusta, GA; Retina & Vitreous • Jeffrey A. Nerad, M.D., Iowa City, IA; Oculoplastic, PATHOGENESIS Lacrimal & Orbital Surgery • Priscilla Perry, M.D., Monroe, Neovascularization of Retina and Disc LA; Cataract Surgery; Liaison for Practicing Ophthalmologists Rupture of a Normal Retinal Vessel Advisory Committee for Education • Lyn A. Sedwick, M.D., Diseased Retinal Vessels Orlando, FL; Neuro-Ophthalmology • Kenneth W. Wright, M.D., Los Angeles, CA; Pediatric Ophthalmology & Strabismus Extension Through the Retina CLINICAL MANIFESTATIONS Focal Points Staff History Susan R. Keller, Managing Editor • Kevin Gleason and Victoria Vandenberg, Medical Editors Ocular Examination DIAGNOSTIC STUDIES Clinical Education Secretaries and Staff Thomas A. Weingeist, Ph.D., M.D., Iowa City, IA; Senior B-Scan Ultrasound Secretary • Michael A. -
Traumatic Glaucoma in Children 1Savleen Kaur, 2Sushmita Kaushik, 3Surinder Singh Pandav
JOCGP Savleen Kaur et al 10.5005/jp-journals-10008-1162 REVIEW ARTICLE Traumatic Glaucoma in Children 1Savleen Kaur, 2Sushmita Kaushik, 3Surinder Singh Pandav ABSTRACT different causes, common presenting signs and symptoms, Young patients are more prone to ocular trauma but most of the visual outcomes, and most frequent management modalities published studies describe complicated cataract as a result of of traumatic glaucoma in children. This chapter aims to trauma with its treatment modality. As a result, little is known study the demographical profile, presentation, management about the different causes, common presenting signs and and outcome of traumatic glaucoma in children as well as symptoms, visual outcomes, and most frequent management modalities of traumatic glaucoma in children. This review aims to the various factors associated with advanced glaucomatous study the demographical profile, presentation, management and changes. outcome of traumatic glaucoma in children as well as the various factors associated with advanced glaucomatous changes. Definition of Traumatic Glaucoma Keywords: Trauma, Childhood, Glaucoma, Penetrating, Blunt. The definition is quite vague, usually defined by the judg How to cite this article: Kaur S, Kaushik S, Pandav SS. Traumatic Glaucoma in Children. J Curr Glaucoma Pract 2014; ment of the treating physician. Any posttrauma raised 8(2):58-62. intraocular pressure (IOP) more than 21 mm Hg post Source of support: Nil trauma which may be acute or chronic in onset, and blunt or penetrating in nature, in children less than 12 years of age Conflict of interest:None supplemented with/without establishment of glaucomatous INTRODUCTION optic neuropathy on visual field testing wherever possible is the acceptable definition. -
Ghost Cell Glaucoma After Intravitreous Injection of Ranibizumab in Proliferative Diabetic Retinopathy Jun Xu, Meng Zhao*, Ji Peng Li and Ning Pu Liu
Xu et al. BMC Ophthalmology (2020) 20:149 https://doi.org/10.1186/s12886-020-01422-z RESEARCH ARTICLE Open Access Ghost cell glaucoma after intravitreous injection of ranibizumab in proliferative diabetic retinopathy Jun Xu, Meng Zhao*, Ji peng Li and Ning pu Liu Abstract Background: The development of ghost cell glaucoma in patients with proliferative diabetic retinopathy (PDR) after intravitreous injection (IV) was rare. Here we reported a series of patients with PDR who received Intravitreous Ranibizumab (IVR) and developed ghost cell glaucoma and analyzed the potential factors that might be related to the development of ghost cell glaucoma. Methods: Retrospective case series study. The medical records of 71 consecutive eyes of 68 PDR patients who received vitrectomy after IVR from January 2015 to January 2017 were reviewed. The development of ghost cell glaucoma after IVR was recorded. Characteristics of enrolled patients were retrieved from their medical charts. Factors associated with ghost cell glaucoma were compared between eyes with the development of ghost cell glaucoma and eyes without the development of ghost cell glaucoma. Variables were further enrolled in a binary backward stepwise logistic regression model, and the model that had the lowest AIC was chosen. Results: There were 8 out of 71 eyes of the PDR patients developed ghost cell glaucoma after they received IVR. The interval between detection of elevation of intraocular pressure (IOP) and IV ranged from 0 to 2 days. Among them, after IVR, there were two eyes had IOP greater than 30 mmHg within 30 min, four eyes showed normal IOP at 30 min, and then developed ghost cell glaucoma within 1 day, two eyes developed ghost cell glaucoma between 24 and 48 h.