RED EYE? EMERGENCY OR NOT? a Short Guide to Recognition and First Aid of Glaucoma and Uveitis
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Hypotony Following Intravitreal Silicone Oil Removal in a Patient with a Complex Retinal Detachment with Giant Retinal Tear
Open Access Case Report DOI: 10.7759/cureus.16387 Hypotony Following Intravitreal Silicone Oil Removal in a Patient With a Complex Retinal Detachment With Giant Retinal Tear Ilias Gkizis 1 , Christina Garnavou-Xirou 1 , Georgios Bontzos 1 , Georgios Smoustopoulos 1 , Tina Xirou 1 1. Ophthalmology, Korgialenio-Benakio General Hospital, Athens, GRC Corresponding author: Georgios Smoustopoulos, [email protected] Abstract Postoperative ocular hypotony after silicone oil removal in complex cases of retinal detachment is a complication that can occur in about 20% of cases and can prevent the successful management of retinal detachments. Thus, it is critical to understand the mechanisms of hypotony and the potential interventions that can be done in order to avoid irreversible tissue damage. We present a case of a 35-year-old man who underwent intraocular surgery for removal of silicone oil tamponade following a combined scleral buckling and pars plana vitrectomy (PPV) surgery for a rhegmatogenous retinal detachment associated with a giant retinal tear. On Day 1 after the operation, the patient was found to have hypotony with optic disc edema, chorioretinal folds, and visual acuity of ‘hand movement’ perception. Two weeks postop, the patient’s condition stabilized, with a visual acuity of 0.38 logMAR, an intraocular pressure (IOP) of 12 mmHg, and the absence of macular edema. Categories: Ophthalmology Keywords: hypotony, silicone oil removal, retinal detachment, vitrectomy, giant retinal tear Introduction Ocular hypotony is defined as intraocular pressure (IOP) of 5 mmHg or less. Depending on the duration and time of onset, it can be classified as acute, chronic, transient, or permanent. Whilst acute hypotony is not an uncommon phenomenon following intraocular surgery, it is generally reversible after 10-15 days [1]. -
MIOTICS in CATARACT SURGERY by Harold Beasley, MD
MIOTICS IN CATARACT SURGERY BY Harold Beasley, MD PROMPT MIOSIS OF the pupil after delivery of the lens in round pupil cataract surgery is recommended to protect the vitreous face, to prevent iris incarceration, and to facilitate the postplacement of corneoscleral sutures.1 It has been postulated that miosis also prevents the formation of peripheral anterior synechia, but this has not been demonstrated experimentally.2 An ideal miotic should produce prompt pupillary constriction and for a duration of 12 to 24 hours. It should also be nonirritating to anterior chamber structures. Acetylcholine ( 1.0 per cent)37 and a weak solution of carbachol (0.01 per cent) ,8 as well as pilocarpine, have been found to be satisfactory for this purpose. The purposes of this study were (1) to evaluate the effectiveness of miotics in preventing peripheral anterior synechia and in preserving the integrity of the vitreous face; and (2) to compare the effectiveness of acetylcholine 1 per cent and carbachol 0.01 per cent as miotics in round pupil cataract surgery. PROCEDURE This study compared three experimental treatments in a double blind procedure in which the code was left unbroken until all the data were accumulated. Selected patients were gonioscoped prior to surgery and only patients with grades Im or iv angles were chosen for this study. All patients were predosed with 2 per cent homatropine and 10 per cent phenylephrine. Prior to the injection of the test solution the pupillary diameters were measured before the section was made and immediately after lens extraction. Measurements were then made at two minutes and at five minutes after the intracameral instillation of 0.4- to 0.5-cc of the test solutions. -
BLINDNESS in MONGOLISM (DOWN's SYNDROME)*T by J
Br J Ophthalmol: first published as 10.1136/bjo.47.6.331 on 1 June 1963. Downloaded from Brit. J. Ophthal. (1963) 47, 331. BLINDNESS IN MONGOLISM (DOWN'S SYNDROME)*t BY J. F. CULLENt The Wilmer Institute, Johns Hopkins University and Hospital, Baltimore, Maryland IN a previous communication (Cullen and Butler, 1963), the ocular abnor- malities encountered in a survey of 143 mongoloids at the Rosewood State Hospital in Maryland were enumerated, and particular attention was drawn to the occurrence of keratoconus in over 5 per cent. of these patients. The purpose of this paper is to elaborate the incidence and causes of blindness in this same group. In the earlier paper no mention was made of the fact that several blind mongoloids were discovered among those examined, and, as the cause of blindness was in all but one instance associated with cataract or keratoconus, they were classified under these aetiological headings. Earlier surveys of the ocular abnormalities in mongoloids by Ormond (1912), Lowe (1949), Skeller and Oster (1951), and Woillez and Dansaut (1960) do not list any patient as being blind. More recently Eissler and Longenecker (1962) reviewed the ocular findings in 396 mongoloids and, though they made no attempt to compile uncommon ocular conditions, they did not state whether any of this very large number of patients were blind. When one considers that serious ocular conditions occur so com- monly in mongoloids, and that the eyes of such patients might be expected to respond unfavourably to trauma or to surgical insult, it is surprising that http://bjo.bmj.com/ no reference has hitherto been made to the not unexpected occurrence of blindness, particularly if they survive for more than 30 years. -
Aetiology Ofsevere Visual Impairment and Blindness in Microphthalmos 333
332 BritishJournal ofOphthalmology 1994; 78: 332-334 Aetiology of severe visual impairment and blindness in microphthalmos Br J Ophthalmol: first published as 10.1136/bjo.78.5.332 on 1 May 1994. Downloaded from Mark J Elder Abstract a group of patients with microphthalmos who Microphthalmos occupies a spectrum from were bilaterally legally blind. a normal, but small globe, to a globe with multiple anterior and posterior segment abnor- malities. This study examines 54 eyes of 27 Patients and methods patients who had bilateral microphthalmos and All six academic blind schools of the West Bank severe visual impairment or blindness. Con- and Gaza strip were visited prospectively, and genital cataract was the commonest cause of the children examined. 6 There were 241 children severe visual impairment (44%), followed by aged from 5 to 25 years with visual acuities less presumed retinal or optic nerve displasia (30%) than 6/60, irrespective of their ocular diagnosis. and chorioretinal coloboma (22%). Lensec- There were no exclusion criteria. tomy was followed by phthisis bulbi in 3/23 Each school was visited by the 'Outreach' cases and retinal detachment in 2/23 cases. facility of the St John Ophthalmic Hospital, There were no cases of angle closure glau- Jerusalem, which is a well equipped mobile coma. The three clinical conditions associated clinic. A complete history was taken and the with a poor prognosis were cataract, chorio- previous medical records were reviewed. A full retinal coloboma, and a markedly reduced examination was conducted, including best cor- corneal diameter. A corneal diameter of 6 mm rected visual acuity with Sheridan-Gardner test or less was associated with a visual acuity ofno charts, colour vision assessment, visual field perception of light in 81% (21/26) compared testing by confrontation, slit-lamp biomicro- with 4% (1/28) ofthose with larger corneas. -
Ocular Complications of Endocarditis
7 Ocular Complications of Endocarditis Ozlem Sahin Middle East Technical University Health Sciences Department of Ophthalmology, Ankara Turkey 1. Introduction Cardiac complications are the most common complications in patients with infective endocarditis, and they can be related to significant mortality and morbidity. (1) Extra- cardiac manifestations along with their historical descriptions such as splinter hemorrhages, emboli, Osler’s nodes, Janeway and Bowman lesions of the eye, Roth’s spots, patechiae and clubbing generally result from thromboemboli or septic emboli. (2) Inflammatory complications may occur as a result of septic emboli, and these include endogenous (metastatic) endophthalmitis, focal abscess, and vasculitis. (3) In this chapter we mainly focus on the endogenous endophthalmitis arising as a complication of infective endocarditis. Endogenous (metastatic) endophthalmitis is an inflammatory condition of the intraocular structures including the aqueous, iris, lens, ciliary body, vitreous, choroid and retina. (4-6) It results from the hematogenous spread of organisms from a distant source of infection, most commonly infective endocarditis, gastrointestinal tract and urinary tract infections and wound infections. (7-9) Other sources of infection have included pharyngitis, pneumonia, septic arthritis and meningitis. (10,11) Compared with endophthalmitis following trauma or surgery, endogenous endophthalmitis is relatively rare, accounting 2-8% of all reported endophthalmitis cases. (5) However, endogenous endophthalmitis carries with it the danger of bilateral infection in 15-25% of cases. (6,12) 2. Epidemiology Endogenous endophthalmitis has been reported to occur at any age and no sexual predilection. (13) However, in the recent years the mean age of endogenous endophthalmitis has shifted to 65 years possibly because of the reduction in the incidence of rheumatic heart disease. -
Clinical Practice Guidelines: Care of the Patient with Anterior Uveitis
OPTOMETRY: OPTOMETRIC CLINICAL THE PRIMARY EYE CARE PROFESSION PRACTICE GUIDELINE Doctors of optometry are independent primary health care providers who examine, diagnose, treat, and manage diseases and disorders of the visual system, the eye, and associated structures as well as diagnose related systemic conditions. Optometrists provide more than two-thirds of the primary eye care services in the United States. They are more widely distributed geographically than other eye care providers and are readily accessible for the delivery of eye and vision care services. There are approximately 32,000 full-time equivalent doctors of optometry currently in practice in the United States. Optometrists practice in more than 7,000 communities across the United States, serving as the sole primary eye care provider in more than 4,300 communities. Care of the Patient with The mission of the profession of optometry is to fulfill the vision and eye Anterior Uveitis care needs of the public through clinical care, research, and education, all of which enhance the quality of life. OPTOMETRIC CLINICAL PRACTICE GUIDELINE CARE OF THE PATIENT WITH ANTERIOR UVEITIS Reference Guide for Clinicians Prepared by the American Optometric Association Consensus Panel on Care of the Patient with Anterior Uveitis: Kevin L. Alexander, O.D., Ph.D., Principal Author Mitchell W. Dul, O.D., M.S. Peter A. Lalle, O.D. David E. Magnus, O.D. Bruce Onofrey, O.D. Reviewed by the AOA Clinical Guidelines Coordinating Committee: John F. Amos, O.D., M.S., Chair Kerry L. Beebe, O.D. Jerry Cavallerano, O.D., Ph.D. John Lahr, O.D. -
Ophthalmic Drugs
A Supplement to 22nd EDITION Randall Thomas, OD, MPH Patrick Vollmer, OD The Clinical Guide to Dr. Melton Ophthalmic[ [ Dr. Thomas Drugs Dispense as writ ten — no substit utions. Refills: unlimit ed. May 15, 2018 Dr. Vollmer Peer-to-peer advice to help boost your prescribing prowess. Supported by an unrestricted grant from Bausch + Lomb 001_dg0518_fc.indd 3 5/11/18 10:52 AM FROM THE AUTHORS DEAR OPTOMETRIC COLLEAGUES: Supported by an Welcome to the 2018 edition of our annual Clinical Guide to Ophthalmic unrestricted grant from Drugs. Herein, we provide updates on our collective clinical experiences and Bausch + Lomb heavily season them with pertinent excerpts from the literature. This guide is intended to bring solid, scientifically accurate and clinically relevant information to our optometric colleagues. If you want to understand CONTENTS how the three of us treat, and what factors led us to develop these methods, you’ll find it explained here. The methods and opinions represented are our own. We recognize that other doctors may use alternative approaches. That First-year Impressions ...........3 is true in all of health care. But this three-doctor writing team has logged over 75 combined years of clinical optometry, and we bring that ‘real-world’ spirit to the discussions that follow. Know that, above all, we are doctors who are genuinely concerned for our patients’ well-being and who endeavor to Glaucoma Care .......................... 6 provide them the best of care, and we write from that perspective. The two topics of greatest interest and need for most eye physicians right now are glaucoma and dry eye disease. -
Conjunctival Primary Acquired Melanosis: Is It Time for a New Terminology?
PERSPECTIVE Conjunctival Primary Acquired Melanosis: Is It Time for a New Terminology? FREDERICK A. JAKOBIEC PURPOSE: To review the diagnostic categories of a CONCLUSION: All pre- and postoperative biopsies of group of conditions referred to as ‘‘primary acquired flat conjunctival melanocytic disorders should be evalu- melanosis.’’ ated immunohistochemically if there is any question DESIGN: Literature review on the subject and proposal regarding atypicality. This should lead to a clearer micro- of an alternative diagnostic schema with histopathologic scopic descriptive diagnosis that is predicated on an and immunohistochemical illustrations. analysis of the participating cell types and their architec- METHODS: Standard hematoxylin-eosin–stained sec- tural patterns. This approach is conducive to a better tions and immunohistochemical stains for MART-1, appreciation of features indicating when to intervene HMB-45, microphthalmia-associated transcription factor therapeutically. An accurate early diagnosis should fore- (MiTF), and Ki-67 for calculating the proliferation index stall unnecessary later surgery. (Am J Ophthalmol are illustrated. 2016;162:3–19. Ó 2016 by Elsevier Inc. All rights RESULTS: ‘‘Melanosis’’ is an inadequate and misleading reserved.) term because it does not distinguish between conjunctival intraepithelial melanin overproduction (‘‘hyperpigmenta- ONJUNCTIVAL MELANOMAS ARE SEEN IN 2–8 INDI- tion’’) and intraepithelial melanocytic proliferation. It viduals per million in predominantly white popula- is recommended that -
Findings of Perinatal Ocular Examination Performed on 3573
BJO Online First, published on February 20, 2013 as 10.1136/bjophthalmol-2012-302539 Br J Ophthalmol: first published as 10.1136/bjophthalmol-2012-302539 on 20 February 2013. Downloaded from Clinical science Findings of perinatal ocular examination performed on 3573, healthy full-term newborns Li-Hong Li,1 Na Li,1 Jun-Yang Zhao,2 Ping Fei,3 Guo-ming Zhang,4 Jian-bo Mao,5 Paul J Rychwalski6 1Maternal and Children’s ABSTRACT children who despite screening go undetected with Hospital, Kunming, Yunnan, Objective To document the findings of a newborn eye respect to vision and eye disorders. A careful China 2Beijing Tongren Ophthalmic examination programme for detecting ocular pathology review of Pubmed revealed no published literature Center, Capital University of in the healthy full-term newborn. on the universality, much less the sensitivity and Medical Sciences, Beijing, Methods This is a cross-sectional study of the majority false-negative rate of RRT of normal newborns. China 3 of newborns born in the Kunming Maternal and Child Further, this age group has not been studied exten- Shanghai Xinhua Hospital, Healthcare Hospital, China, between May 2010 and sively and the actual prevalence of ocular abnor- Shanghai, China 4Shenzhen Eye Hospital, Jinan June 2011. Infants underwent ocular examination within malities, transient and permanent, is largely University, Shenzhen, China 42 days after birth using a flashlight, retinoscope, hand- unknown. There are few previous studies looking 5Eye Hospital of Wenzhou held slit lamp microscope and wide-angle digital retinal at the incidence of retinal haemorrhages in healthy Medical College, Wenzhou, image acquisition system. -
Visual Impairment Age-Related Macular
VISUAL IMPAIRMENT AGE-RELATED MACULAR DEGENERATION Macular degeneration is a medical condition predominantly found in young children in which the center of the inner lining of the eye, known as the macula area of the retina, suffers thickening, atrophy, and in some cases, watering. This can result in loss of side vision, which entails inability to see coarse details, to read, or to recognize faces. According to the American Academy of Ophthalmology, it is the leading cause of central vision loss (blindness) in the United States today for those under the age of twenty years. Although some macular dystrophies that affect younger individuals are sometimes referred to as macular degeneration, the term generally refers to age-related macular degeneration (AMD or ARMD). Age-related macular degeneration begins with characteristic yellow deposits in the macula (central area of the retina which provides detailed central vision, called fovea) called drusen between the retinal pigment epithelium and the underlying choroid. Most people with these early changes (referred to as age-related maculopathy) have good vision. People with drusen can go on to develop advanced AMD. The risk is considerably higher when the drusen are large and numerous and associated with disturbance in the pigmented cell layer under the macula. Recent research suggests that large and soft drusen are related to elevated cholesterol deposits and may respond to cholesterol lowering agents or the Rheo Procedure. Advanced AMD, which is responsible for profound vision loss, has two forms: dry and wet. Central geographic atrophy, the dry form of advanced AMD, results from atrophy to the retinal pigment epithelial layer below the retina, which causes vision loss through loss of photoreceptors (rods and cones) in the central part of the eye. -
Pigmented Epibulbar Lesions
igmentar f P y D o i l so a r n d Alena et al., Pigmentary Disorders 2014, 1:3 r e u r o s J Journal of Pigmentary Disorders DOI: 10.4172/jpd.1000121 World Health Academy ISSN: 2376-0427 Review Article Open Access Pigmented Epibulbar Lesions: Overview Furdova Alena*, Alsalman Ali Jameel, Krcova Ivana, Horkovicova Kristina and Furdova Adriana Department of Ophthalmology, Medical School, Comenius University, Bratislava, Slovakia Abstract Eyes can be affected by a wide variety of epibulbar lesions. The incidence and prevalence of the epibulbar lesions is significantly high, with an incidence of 89.8% of the benign lesions as compared to the malignant lesions that accounted for 10.2% of the lesions. Considering the significance of the knowledge of the different types of epibulbar lesions, there is a need to perform a brief discussion of these lesions to develop the information of these lesions among the general population and the healthcare professionals. This would enable the successful diagnosis of the different types of epibulbar lesions. Epibulbar pigmented lesions include conjunctival epithelial melanosis, conjunctival freckle, primary acquired melanosis, conjunctival nevus, congenital ocular melanocytosis, and malignant melanoma. Keywords: Conjuntival pigmented tumor; Nevus; Melanoma; fold) is present nasally, medial to which lies a fleshy nodule (caruncle) Primary acquired melanosis; Racial melanosis consisting of modified cutaneous tissue containing hair follicles, accessory lacrimal glands, sweat glands and sebaceous glands. Introduction Microscopically conjunctiva consists of three layers- epithelium, The complexity of the structure of eyes is extreme as they have adenoid layer and fibrous layer [2]. Epithelial layer is the most superficial a vital function that requires several small structures to perform the layer of the conjunctiva and is made up of epithelial cells arranged functioning of vision. -
Onchocerciasis in Ecuador: Ocular Findings in Onchocerca Volvulus Infected Individuals Br J Ophthalmol: First Published As 10.1136/Bjo.79.2.157 on 1 February 1995
British Journal of Ophthalmology 1995; 79: 157-162 157 Onchocerciasis in Ecuador: ocular findings in Onchocerca volvulus infected individuals Br J Ophthalmol: first published as 10.1136/bjo.79.2.157 on 1 February 1995. Downloaded from P J Cooper, R Proaflo, C Beltran, M Anselmi, R H Guderian Abstract which is largely absent from the rain Little is known of the epidemiology and forest.7 clinical picture ofocular onchocerciasis in In the Americas, foci of disease have been South America. A survey of onchocercal described in Mexico, Guatemala, Colombia, eye disease was performed in the hyper- Venezuela, Brazil, and Ecuador. Earlier endemic area of a rain forest focus of reports from Guatemala58 and Venezuela9 onchocerciasis in Esmeraldas Province in indicated ocular pathology attributable to Ecuador. A total of 785 skin snip positive onchocerciasis. The absence of comprehensive individuals from black and Chachi reports on the current status of ocular Amerindian communities were examined. onchocerciasis in any of these foci has made it The blindness rate attributable to difficult to evaluate if blinding onchocerciasis onchocerciasis was 0.4%, and 8.2% were remains a major problem in these regions. visually impaired. Onchocercal ocular The epidemiology of the rain forest focus of lesions were seen in a high proportion of onchocerciasis in Esmeraldas Province of the study group: 33.6% had punctate Ecuador has been extensively studied.'0 keratitis, microfilariae in the anterior Current evidence suggests that the prevalence chamber and cornea were seen in 2890/o and intensity of infection and its geographical and 33.5% respectively, iridocyclitis was boundaries are expanding.11 12 This is because seen in 1.5%, optic atrophy in 5.1%, and of migration of infected individuals and the chorioretinopathy in 28.0%.