Cataract Extraction in Retinitis Pigmentosa Patients
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Masqueraders of Age-Related Macular Degeneration
COVER STORY Masqueraders of Age-related Macular Degeneration A number of inherited retinal diseases phenocopy AMD. BY RONY GELMAN, MD, MS; AND STEPHEN H. TSANG, MD, PHD ge-related macular degeneration (AMD) is a leading cause of central visual loss among the elderly population in the developed world. The Currently, there are no published A non-neovascular form is characterized by mac- guidelines to prognosticate ular drusen and other abnormalities of the retinal pigment epithelium (RPE) such as geographic atrophy (GA) and Stargardt macular degeneration. hyperpigmented areas in the macula. The neovascular form is heralded by choroidal neovascularization (CNV), with subsequent development of disciform scarring. ABCA4 defect heterozygote carrier may be as high as This article reviews the pathologic and diagnostic char- one in 20.11,12 An estimated 600 disease-causing muta- acteristics of inherited diseases that may masquerade as tions in the ABCA4 gene exist, of which the three most AMD. The review is organized by the following patterns common mutations account for less than 10% of the of inheritance: autosomal recessive (Stargardt disease and disease phenotypes.13 cone dystrophy); autosomal dominant (cone dystrophy, The underlying pathology of disease in STGD involves adult vitelliform dystrophy, pattern dystrophy, North accumulation of lipofuscin in the RPE through a process Carolina macular dystrophy, Doyne honeycomb dystro- of disc shedding and phagocytosis.14,15 Lipofuscin is toxic phy, and Sorsby macular dystrophy); X-linked (X-linked to the RPE; furthermore, A2E, a component of lipofuscin, retinoschisis); and mitochondrial (maternally inherited causes inhibition of 11-cis retinal regeneration16 and diabetes and deafness). complement activation. -
Wildlife Ophthalmology
Wildlife Ophthalmology DR. HEATHER REID TORONTO WILDLIFE CENTRE TORONTO, ON CANADA Why understand eyes? Wildlife need to have excellent vision to survive in the wild Eye related problems are common in wildlife admitted to rehabilitation centers What we will cover Anatomy of the eye Differences between birds and mammals The eye exam Recognizing common problems Prognosis Treatment options When to see the vet Anatomy Around the Eye: Muscles & nerves Skin Eye lids Nictitating eyelid Conjunctiva & sclera Tear glands & ducts Ossicles (birds) Anatomy Front of the Eye: Cornea Iris Pupil Ciliary body Anterior Chamber Aqueous humor Anatomy Back of the Eye: Lens Retina Optic nerve Choroid Pecten (birds) Posterior Chamber Vitreous humor Fundus of the Eye Mammal Eye Bird Eye The Avian Eye - Differences Small eye size in most birds and small pupil size makes it hard to examine Can control the size of their pupil Lower eyelid more developed The nictitating membrane spreads the tears allowing birds to blink less Moves horizontally across eye The Avian Eye - Differences Eyes are not as protected by skull Less muscles around eye so less eye movement Boney ossicles support the eye Three main eye shapes; flat, globose & tubular The Avian Eye - Differences Four different color receptors compared to the three in mammals means better color detail Can see in the ultraviolet range Higher flicker rate – can detect lights that flicker at more than 100 flashes per second (humans detect at 50) The Avian Eye - Differences In some species the eye -
Cytomegalovirus Retinitis: a Manifestation of the Acquired Immune Deficiency Syndrome (AIDS)*
Br J Ophthalmol: first published as 10.1136/bjo.67.6.372 on 1 June 1983. Downloaded from British Journal ofOphthalmology, 1983, 67, 372-380 Cytomegalovirus retinitis: a manifestation of the acquired immune deficiency syndrome (AIDS)* ALAN H. FRIEDMAN,' JUAN ORELLANA,'2 WILLIAM R. FREEMAN,3 MAURICE H. LUNTZ,2 MICHAEL B. STARR,3 MICHAEL L. TAPPER,4 ILYA SPIGLAND,s HEIDRUN ROTTERDAM,' RICARDO MESA TEJADA,8 SUSAN BRAUNHUT,8 DONNA MILDVAN,6 AND USHA MATHUR6 From the 2Departments ofOphthalmology and 6Medicine (Infectious Disease), Beth Israel Medical Center; 3Ophthalmology, "Medicine (Infectious Disease), and 'Pathology, Lenox Hill Hospital; 'Ophthalmology, Mount Sinai School ofMedicine; 'Division of Virology, Montefiore Hospital and Medical Center; and the 8Institute for Cancer Research, Columbia University College ofPhysicians and Surgeons, New York, USA SUMMARY Two homosexual males with the 'gay bowel syndrome' experienced an acute unilateral loss of vision. Both patients had white intraretinal lesions, which became confluent. One of the cases had a depressed cell-mediated immunity; both patients ultimately died after a prolonged illness. In one patient cytomegalovirus was cultured from a vitreous biopsy. Autopsy revealed disseminated cytomegalovirus in both patients. Widespread retinal necrosis was evident, with typical nuclear and cytoplasmic inclusions of cytomegalovirus. Electron microscopy showed herpes virus, while immunoperoxidase techniques showed cytomegalovirus. The altered cell-mediated response present in homosexual patients may be responsible for the clinical syndromes of Kaposi's sarcoma and opportunistic infection by Pneumocystis carinii, herpes simplex, or cytomegalovirus. http://bjo.bmj.com/ Retinal involvement in adult cytomegalic inclusion manifestations of the syndrome include the 'gay disease (CID) is usually associated with the con- bowel syndrome9 and Kaposi's sarcoma. -
Utah Eye Centers Now Offers the Latest Advance in Laser Eye Surgery
Mark G. Ballif, M.D. Scott O. Sykes, M.D. Michael B. Wilcox, M.D. John D. Armstrong, M.D. Robert W. Wing, M.D., FACS Keith Linford, O.D. Jed T. Poll, M.D. Claron D. Alldredge, M.D. Devin B. Farr, O.D. Michael L. Bullard, M.D. Court R. Wilkins, O.D. Utah Eye Centers Now Offers the Latest Advance In Laser Eye Surgery The New VICTUS® Femtosecond Laser Platform, from Bausch + Lomb is Designed to Support Positive Patient Experience and Outstanding Visual Results in Cataract and LASIK Procedures FOR RELEASE April 17, 2015 Ogden, Utah— Utah Eye Centers, the leading comprehensive ophthalmology practice in northern Utah, announced today the Mount Ogden facility now offers eye surgery for cataracts and LASIK with an advanced laser system, the VICTUS® femtosecond laser platform. They are the only practice north of Salt Lake City with a fixed site femtosecond laser for cataracts and LASIK. The versatile VICTUS platform is designed to provide greater precision compared to manual cataract and LASIK surgery techniques. According to Scott Sykes, M.D., the Victus laser is the only laser approved to perform treatments for both cataract and LASIK surgeries. "With the VICTUS platform, we are able to automate some of the steps that we have commonly performed manually," said Mark Ballif, M.D. "While we have performed thousands of successful cataract and LASIK surgeries, the VICTUS platform helps us to improve the procedures to give our patients the best outcomes possible." The VICTUS platform features a sophisticated, curved patient interface with computer-monitored pressure sensors designed to provide comfort during the procedure. -
Genetic Defects of CHM and Visual Acuity Outcome in 24 Choroideremia
www.nature.com/scientificreports OPEN Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families Takaaki Hayashi1,2*, Shuhei Kameya3, Kei Mizobuchi2, Daiki Kubota3, Sachiko Kikuchi3, Kazutoshi Yoshitake4, Atsushi Mizota5, Akira Murakami6, Takeshi Iwata4 & Tadashi Nakano2 Choroideremia (CHM) is an incurable progressive chorioretinal dystrophy. Little is known about the natural disease course of visual acuity in the Japanese population. We aimed to investigate the genetic spectrum of the CHM gene and visual acuity outcomes in 24 CHM patients from 16 Japanese families. We measured decimal best-corrected visual acuity (BCVA) at presentation and follow-up, converted to logMAR units for statistical analysis. Sanger and/or whole-exome sequencing were performed to identify pathogenic CHM variants/deletions. The median age at presentation was 37.0 years (range, 5–76 years). The mean follow-up interval was 8.2 years. BCVA of the better-seeing eye at presentation was signifcantly worsened with increasing age (r = 0.515, p < 0.01), with a high rate of BCVA decline in patients > 40 years old. A Kaplan–Meier survival curve suggested that a BCVA of Snellen equivalent 20/40 at follow-up remains until the ffties. Fourteen pathogenic variants, 6 of which were novel [c.49 + 5G > A, c.116 + 5G > A, p.(Gly176Glu, Glu177Ter), p.Tyr531Ter, an exon 2 deletion, and a 5.0-Mb deletion], were identifed in 15 families. No variant was found in one family only. Our BCVA outcome data are useful for predicting visual prognosis and determining the timing of intervention in Japanese patients with CHM variants. -
Faculdade De Medicina Veterinária
UNIVERSIDADE DE LISBOA Faculdade de Medicina Veterinária OCULAR BRACHYCEPHALIC SYNDROME Joana Veiga Costa CONSTITUIÇÃO DO JÚRI ORIENTADORA Doutora Maria Luísa Mendes Jorge Doutora Esmeralda Sofia da Costa Doutora Esmeralda Sofia da Costa Delgado Delgado Doutora Lisa Alexandra Pereira Mestrinho CO-ORIENTADORA Doutora Andrea Steinmetz 2019 LISBOA ___________________________________________________________________ UNIVERSIDADE DE LISBOA Faculdade de Medicina Veterinária OCULAR BRACHYCEPHALIC SYNDROME Joana Veiga Costa DISSERTAÇÃO DE MESTRADO INTEGRADO EM MEDICINA VETERINÁRIA CONSTITUIÇÃO DO JÚRI ORIENTADORA Doutora Maria Luísa Mendes Jorge Doutora Esmeralda Sofia da Costa Doutora Esmeralda Sofia da Costa Delgado Delgado Doutora Lisa Alexandra Pereira Mestrinho CO-ORIENTADORA Doutora Andrea Steinmetz 2019 LISBOA ___________________________________________________________________ ACKNOWLEDGEMENT I express my sincere gratitude towards my amazing parents for always supporting me in the pursue of my dreams. I am also immensely thankful to my sister and grandparents, not only for sharing this road with me, but also my whole life. I gratefully acknowledge and offer a special thanks to Professor Esmeralda Delgado for the valuable contribution, guidance, support and kind words throughout the last year. A big thank you to Dr. Susana Azinheira and Dr. Diogo Azinheira for all that I’ve learned during my stayings in your incredible hospital, and the opportunity to put my knowledge at practice. My warmest thanks to my colleagues Maria, Mariana, Pedro, Francisco, Diogo, Catarina, Cláudia, Inês, Sara and Marta for being by my side all these years and for their friendship. May it last forever. I am grateful to Ivo and Rafael for their guidance during the course, specially in the first year, when everything was completely new to me. -
Retinitis Pigmentosa Precision Panel Overview Indications Clinical
Retinitis Pigmentosa Precision Panel Overview Retinitis Pigmentosa (RP) comprises a complex group of inherited dystrophies characterized by degeneration and dysfunction of the retina, affecting photoreceptor and pigment epithelial function. RP can be an isolated finding or be part of a syndrome that can be inherited in a dominant, recessive or X-linked pattern. This disease presents as progressive loss of night and peripheral vision, leading to a constricted visual field and markedly diminished vision. The clinical presentation of these findings is highly variable, some patients being affected during childhood while others are asymptomatic well into adulthood. There is an increase in mortality rate due to psychiatric comorbidities. The Igenomix Retinitis Pigmentosa Precision Panel can be used to make an accurate and directed diagnosis as well as a differential diagnosis of blindness ultimately leading to a better management and prognosis of the disease. It provides a comprehensive analysis of the genes involved in this disease using next-generation sequencing (NGS) to fully understand the spectrum of relevant genes involved. Indications The Igenomix Retinitis Pigmentosa Precision Panel is indicated for those patients with a clinical suspicion or diagnosis with or without the following manifestations: - Family history of RP - Night blindness - Progressive constriction of the visual field, usually peripheral - Cataracts - Sensation of sparking lights (photopsias) - Headache Clinical Utility The clinical utility of this panel is: - The genetic and molecular confirmation for an accurate clinical diagnosis of a symptomatic patient. - Early initiation of multidisciplinary treatment in the form of medical care with vitamin A and other antioxidants and surgical care for potential cataract extraction or retinal prosthesis. -
Nd:YAG CAPS ULOTOMY AS a PRIMARY TREATMENT
PSEUDOPHAKIC MALIGNANT GLAUCOMA: Nd:YAG CAPS ULOTOMY AS A PRIMARY TREATMENT B. C. LITTLE and R. A. HITCHINGS London SUMMARY anisms of ciliolenticular block of aqueous flow leading to Malignant glaucoma is one of the most serious but rare the misdirection of aqueous posteriorly into or in front of complications of anterior segment surgery. It is best the vitreous gel leading to the characteristic diffuse shal known following trabeculectomy but has been reported lowing of the anterior chamber accompanied by a precipi following a wide variety of anterior segment procedures tous rise in intraocular pressure. The mechanistic including extracapsular cataract extraction with pos understanding of its pathogenesis has led to the use of the terior chamber lens implantation. It is notoriously refrac synonyms 'ciliolenticular block',7 'ciliovitreal block', tory to medical treatment alone and surgical intervention 'iridovitreal block',8 'aqueous misdirection' and 'aqueous has had only limited success. An additional treatment diversion syndrome'. Although probably more precise option in pseudophakic eyes is that of peripheral these are unlikely to succeed the original term 'malignant Nd:YAG posterior capsulotomy, which is minimally glaucoma', which more accurately evokes the fulminant invasive and can re-establish forward flow of posteriorly nature of the condition as well as the justified anxiety asso misdirected aqueous through into the drainage angle of ciated with it. Medical treatment alone is rarely successful the anterior chamber. We report our experience of seven in establishing control of the intraocular pressure.2•8 Pars cases of malignant glaucoma in pseudophakic eyes and of plana vitrectomy has been used in the surgical managment the successful use of Nd:YAG posterior capsulotomy in of malignant glaucoma with some definite but limited suc re-establishing pressure control in' five of these eyes, cess in phakic as well as pseudophakic eyes.9•10 thereby obviating the need for acute surgical However, when malignant glaucoma develops in intervention. -
Electroretinography 1 Electroretinography
Electroretinography 1 Electroretinography Electroretinography measures the electrical responses of various cell types in the retina, including the photoreceptors (rods and cones), inner retinal cells (bipolar and amacrine cells), and the ganglion cells. Electrodes are usually placed on the cornea and the skin near the eye, although it is possible to record the ERG from skin electrodes. During a recording, the patient's eyes are exposed to standardized stimuli and the resulting signal is displayed showing the time course of the signal's Maximal response ERG waveform from a dark adapted eye. amplitude (voltage). Signals are very small, and typically are measured in microvolts or nanovolts. The ERG is composed of electrical potentials contributed by different cell types within the retina, and the stimulus conditions (flash or pattern stimulus, whether a background light is present, and the colors of the stimulus and background) can elicit stronger response from certain components. If a flash ERG is performed on a dark-adapted eye, the response is primarily from the rod system and flash ERGs performed on a light adapted eye will reflect the activity of the cone system. To sufficiently bright flashes, the ERG will contain an A patient undergoing an electroretinogram a-wave (initial negative deflection) followed by a b-wave (positive deflection). The leading edge of the a-wave is produced by the photoreceptors, while the remainder of the wave is produced by a mixture of cells including photoreceptors, bipolar, amacrine, and Muller cells or Muller glia.[1] The pattern ERG, evoked by an alternating checkerboard stimulus, primarily reflects activity of retinal ganglion cells. -
Outcome of Lens Aspiration and Intraocular Lens Implantation in Children Aged 5 Years and Under
540 Br J Ophthalmol 2001;85:540–542 Outcome of lens aspiration and intraocular lens implantation in children aged 5 years and under Lorraine Cassidy, Jugnoo Rahi, Ken Nischal, Isabelle Russell-Eggitt, David Taylor Abstract However, final refraction is variable, such that Aims—To determine the visual outcome emmetropia in adulthood cannot be guaran- and complications of lens aspiration with teed, as there are insuYcient long term studies. intraocular lens implantation in children There have been many reports of the visual aged 5 years and under. outcome and complications of posterior cham- Methods—The hospital notes of all chil- ber lens implantation in children.4–12 Most of dren aged 5 years and under, who had these have been based on older children, undergone lens aspiration with intraocu- secondary lens implants, a high number of lar lens implantation between January traumatic cataracts, and many have reported 1994 and September 1998, and for whom early outcome. We report visual outcome and follow up data of at least 1 year were avail- complications of primary IOL implantation at able, were reviewed. least 1 year after surgery, in children aged 5 Results—Of 50 children who underwent years and under, with mainly congenital or surgery, 45 were eligible based on the juvenile lens opacities. follow up criteria. 34 children had bilat- eral cataracts and, of these, 30 had surgery Methods on both eyes. Cataract was unilateral in 11 SUBJECTS cases; thus, 75 eyes of 45 children had sur- We reviewed the notes of all children aged 5 gery. Cataracts were congenital in 28 years and under, who had undergone lens aspi- cases, juvenile in 16, and traumatic in one ration with primary posterior chamber in- case. -
Laser Learning Lecture and Lab: YAG Caps, LPI, And
5/9/17 Overview Laser Learning Lecture and Lab: • Why we use lasers YAG caps, LPI, and SLT • YAG capsulotomy • Laser Peripheral Iridotomy (LPI or PI) Aaron McNulty, O.D., F.A.A.O. • Argon Laser Peripheral Iridoplasty (ALPI) Nate Lighthizer, O.D., F.A.A.O. • Argon Laser Trabeculoplasty (ALT) • Selective Laser Trabeculoplasty (SLT) • Other Laser Trabeculoplasty Why do we use lasers? Posterior Capsular Opacification (PCO) • Vision is decreased from PCO following cataract surgery • Lens capsular bag has an anterior and • Narrow angles/angle closure posterior surface • Glaucoma is progressing in a pt on max meds – Anterior surface usually removed w/ capsulorhexis – Something else needs to be done – Surgery not wanted yet • PCO is the formation of a cloudy membrane • Compliance issues on the posterior surface of the capsular bag • Cost issues following ECCE • Convenience issues – AKA: Secondary cataract • Doctor preference PCO YAG Laser • Incidence: • Nd: YAG laser – Most common complication of post ECCE – Neodymium: Yttrium aluminum garnet laser – 10-80% of eyes following cataract surgery – Can form anywhere from a few days to years post surgery • Tissue interaction: Photodisruptive laser – Younger patients higher risk of PCO – High light energy levels cause the tissues to be reduced – IOL’s to plasma, disintegrating the tissue • Silicone > acrylic – A large amount of energy is delivered into very small focal spots in a very brief duration of time • Prevention: • 4 nsec – – Capsulotomy during surgery No thermal reaction/No coagulation when bv’s are hit – Posterior capsular polishing – Pigment independent* 1 5/9/17 YAG Cap Risks, Complications, YAG Cap Pre-op Exam Contraindications • Visual acuity, glare testing, PAM/Heine lambda Contraindications Risks/complications – Vision 20/30 or worse 1. -
Myopia: More Than a Refractive Error − Lasik and Retinal Dystrophies
MYOPIA: MORE THAN A REFRACTIVE ERROR − LASIK AND RETINAL DYSTROPHIES WALRAEDT S.1*, LEROY B.P.1,2*, KESTELYN P.H.1, DE LAEY J.J.1 SUMMARY SAMENVATTING Three patients who had undergone laser in situ Drie patiënten die een correctie van myopie hadden keratomileusis (LASIK) correction for myopia were ondergaan met laser in situ keratomileusis (LASIK) first seen because of suboptimal visual acuity (VA) werden onderzocht omwille van postoperatieve sub- and night blindness and/or photophobia. After a com- optimale visus en nachtblindheid en/of fotofobie. Na prehensive examination including psychophysical uitgebreid onderzoek met inbegrip van psychofysi- and electrophysiological tests, two of the three pa- sche en electrofysiologische testen werd een dia- tients were shown to suffer from a progressive cone- gnose van progressieve kegeltjes-staafjesdystrofie ge- rod dystrophy. The third patient had retinitis pig- steld bij twee patiënten. De derde patiënt leed aan mentosa. These cases illustrate the need for in depth retinitis pigmentosa. Deze gevallen illustreren de preoperative evaluation in myopic patients about to noodzaak van een doorgedreven preoperatief onder- undergo LASIK when signs or problems of night blind- zoek bij myope patiënten die LASIK zullen onder- ness and/or photophobia are present. gaan met klachten van nachtblindheid en fotofobie. KEY WORDS RÉSUMÉ Retinal dystrophy, cone-rod dystrophy, Trois patients sont présentés ayant été examinés pour retinitis pigmentosa, photophobia, night une acuité visuelle sous-optimale et une héméralo- blindness, laser in situ keratomileusis, pie et/ou photophobie, après correction d’une myo- preoperative evaluation pie suivant la technique du laser in situ keratomi- leusis (LASIK). Sur base d’une évaluation élaborée, MOTS-CLÉS y inclus des tests psychophysiques et éléctrophysio- logiques, un diagnostic de dystrophie des cônes et Dystrophie rétinienne, dystrophie de type bâtonnets a été établi chez deux patients.