Relationship Between Intra Ocular Pressure and Visual Acuity in Port Harcourt, Nigeria
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RETINAL DISORDERS Eye63 (1)
RETINAL DISORDERS Eye63 (1) Retinal Disorders Last updated: May 9, 2019 CENTRAL RETINAL ARTERY OCCLUSION (CRAO) ............................................................................... 1 Pathophysiology & Ophthalmoscopy ............................................................................................... 1 Etiology ............................................................................................................................................ 2 Clinical Features ............................................................................................................................... 2 Diagnosis .......................................................................................................................................... 2 Treatment ......................................................................................................................................... 2 BRANCH RETINAL ARTERY OCCLUSION ................................................................................................ 3 CENTRAL RETINAL VEIN OCCLUSION (CRVO) ..................................................................................... 3 Pathophysiology & Etiology ............................................................................................................ 3 Clinical Features ............................................................................................................................... 3 Diagnosis ......................................................................................................................................... -
Acquired Colour Vision Defects in Glaucoma—Their Detection and Clinical Significance
1396 Br J Ophthalmol 1999;83:1396–1402 Br J Ophthalmol: first published as 10.1136/bjo.83.12.1396 on 1 December 1999. Downloaded from PERSPECTIVE Acquired colour vision defects in glaucoma—their detection and clinical significance Mireia Pacheco-Cutillas, Arash Sahraie, David F Edgar Colour vision defects associated with ocular disease have The aims of this paper are: been reported since the 17th century. Köllner1 in 1912 + to provide a review of the modern literature on acquired wrote an acute description of the progressive nature of col- colour vision in POAG our vision loss secondary to ocular disease, dividing defects + to diVerentiate the characteristics of congenital and into “blue-yellow” and “progressive red-green blindness”.2 acquired defects, in order to understand the type of This classification has become known as Köllner’s rule, colour vision defect associated with glaucomatous although it is often imprecisely stated as “patients with damage retinal disease develop blue-yellow discrimination loss, + to compare classic clinical and modern methodologies whereas optic nerve disease causes red-green discrimina- (including modern computerised techniques) for tion loss”. Exceptions to Köllner’s rule34 include some assessing visual function mediated through chromatic optic nerve diseases, notably glaucoma, which are prima- mechanisms rily associated with blue-yellow defects, and also some reti- + to assess the eVects of acquired colour vision defects on nal disorders such as central cone degeneration which may quality of life in patients with POAG. result in red-green defects. Indeed, in some cases, there might be a non-specific chromatic loss. Comparing congenital and acquired colour vision Colour vision defects in glaucoma have been described defects since 18835 and although many early investigations Congenital colour vision deficiencies result from inherited indicated that red-green defects accompanied glaucoma- cone photopigment abnormalities. -
Intraocular Pressure During Phacoemulsification
J CATARACT REFRACT SURG - VOL 32, FEBRUARY 2006 Intraocular pressure during phacoemulsification Christopher Khng, MD, Mark Packer, MD, I. Howard Fine, MD, Richard S. Hoffman, MD, Fernando B. Moreira, MD PURPOSE: To assess changes in intraocular pressure (IOP) during standard coaxial or bimanual micro- incision phacoemulsification. SETTING: Oregon Eye Center, Eugene, Oregon, USA. METHODS: Bimanual microincision phacoemulsification (microphaco) was performed in 3 cadaver eyes, and standard coaxial phacoemulsification was performed in 1 cadaver eye. A pressure transducer placed in the vitreous cavity recorded IOP at 100 readings per second. The phacoemulsification pro- cedure was broken down into 8 stages, and mean IOP was calculated across each stage. Intraocular pressure was measured during bimanual microphaco through 2 different incision sizes and with and without the Cruise Control (Staar Surgical) connected to the aspiration line. RESULTS: Intraocular pressure exceeded 60 mm Hg (retinal perfusion pressure) during both standard coaxial and bimanual microphaco procedures. The highest IOP occurred during hydrodissection, oph- thalmic viscosurgical device injection, and intraocular lens insertion. For the 8 stages of the phaco- emulsification procedure delineated in this study, IOP was lower for at least 1 of the bimanual microphaco eyes compared with the standard coaxial phaco eye in 4 of the stages (hydro steps, nu- clear disassembly, irritation/aspiration, anterior chamber reformation). CONCLUSION: There was no consistent difference in IOP between the bimanual microphaco eyes and the eye that had standard coaxial phacoemulsification. Bimanual microincision phacoemul- sification appears to be as safe as standard small incision phacoemulsification with regard to IOP. J Cataract Refract Surg 2006; 32:301–308 Q 2006 ASCRS and ESCRS Bimanual microincision phacoemulsification, defined as capable of insertion through these microincisions become cataract extraction through 2 incisions of less than 1.5 mm more widely available. -
17-2021 CAMI Pilot Vision Brochure
Visual Scanning with regular eye examinations and post surgically with phoria results. A pilot who has such a condition could progress considered for medical certification through special issuance with Some images used from The Federal Aviation Administration. monofocal lenses when they meet vision standards without to seeing double (tropia) should they be exposed to hypoxia or a satisfactory adaption period, complete evaluation by an eye Helicopter Flying Handbook. Oklahoma City, Ok: US Department The probability of spotting a potential collision threat complications. Multifocal lenses require a brief waiting certain medications. specialist, satisfactory visual acuity corrected to 20/20 or better by of Transportation; 2012; 13-1. Publication FAA-H-8083. Available increases with the time spent looking outside, but certain period. The visual effects of cataracts can be successfully lenses of no greater power than ±3.5 diopters spherical equivalent, at: https://www.faa.gov/regulations_policies/handbooks_manuals/ techniques may be used to increase the effectiveness of treated with a 90% improvement in visual function for most One prism diopter of hyperphoria, six prism diopters of and by passing an FAA medical flight test (MFT). aviation/helicopter_flying_handbook/. Accessed September 28, 2017. the scan time. Effective scanning is accomplished with a patients. Regardless of vision correction to 20/20, cataracts esophoria, and six prism diopters of exophoria represent series of short, regularly-spaced eye movements that bring pose a significant risk to flight safety. FAA phoria (deviation of the eye) standards that may not be A Word about Contact Lenses successive areas of the sky into the central visual field. Each exceeded. -
Final Version (2017-06-28) of the Vision Camp
Young Researcher VisionCamp An international Career building Symposium 2017 Castle Wildenstein Leibertingen Germany www.vision-camp.eu Contact: Jugendherberge Burg Wildenstein 88637 Leibertingen-Wildenstein Tel: +49 7466-411 Fax: +49 7466-417 E-Mail: [email protected] www.leibertingen-wildenstein.jugendherberge-bw.de Preamble Dear Colleagues, Dear Participants of the Young Researcher Vision Camp 2017, The aim of this camp is to give young investigators (MSc and PhD students, young MDs and post-docs) an opportunity to present themselves and their work to fellow researchers, to allow them to build and strengthen personal networks in an international environment. Take the time for professional and social networking Take the time for new views on career paths to shape your future Take the time to bridge the gap between basic and clinical research Take the time to revive a medieval castle ENJOY THE YOUNG RESEARCHER VISION CAMP Thomas Wheeler-Schilling on behalf of the organising committee (in alphabetical order) Michaela Bitzer Sigrid Diether Philipp Hunger Norbert Kinkl Arne Ohlendorf Francois Paquet-Durand Vera Schmid Timm Schubert 3 Agenda FRIDAY, JUNE 30th, 2017 until 16:00 Arrival (for details see ‘How to get there’) 16:25 - 16:30 Welcome 16:30 - 17:00 Keynote Lecture I ‘Primary Cilia in the Visual System’ Helen May-Simera 17:00 - 18:00 Scientific Session I: ‘Retinal development and homeo- stasis’ Chair: Jérôme Roger • Elena Braginskaja: “Glycogen Synthase Kinases 3 are Critical for Retinal Develop- ment and Homeostasis” -
New Developments in Glaucoma Therapy
New Developments in Glaucoma Therapy 100 - Oral Author: Ganesh Prasanna Presenter: Ganesh Prasanna Institution: Alcon Research Ltd Department: Glaucoma Research Ganesh Prasanna, Ph.D. Ocular Biology, Pfizer Global R&D, San Diego, CA 92121 Current affiliation: Alcon Research Ltd., Fort Worth, TX 76134 EFFECT OF PF-04217329 A PRO-DRUG OF A SELECTIVE PROSTAGLANDIN EP2 AGONIST ON INTRAOCULAR PRESSURE IN PRECLINICAL MODELS OF GLAUCOMA Purpose: While prostaglandin FP analogs are leading the therapeutic intervention for glaucoma, new target classes also are being identified with new lead compounds being developed for IOP reduction. One target class currently being investigated includes the prostaglandin EP receptor agonists. Recently PF-04217329 (Taprenepag isopropyl), a prodrug of CP-544326 (active acid metabolite), a potent and selective EP2 receptor agonist, was successfully evaluated for its ocular hypotensive activity in a clinical study involving patients with primary open angle glaucoma. The preclinical attributes of CP-544326 and PF-0421329 will be presented. Methods: PF-04217329 and active acid metabolite, CP-544326 were evaluated in cell based assays for receptor binding and EP2 receptor functional activity were used. Rabbits were used for assessing corneal permeability, ocular pharmacokinetic studies, EP2 receptor activation and IOP, whereas normal dogs and lasered ocular hypertensive cynomolgus monkeys were also used for IOP studies. Results: CP-544326 was found to be a potent and selective EP2 agonist (receptor binding IC50 = 10 nM; functional activity EC50 = 0.25 nM) whose corneal permeability and ocular bioavailability were significantly increased when the compound was dosed as the isopropyl ester prodrug, PF-04217329. Topical ocular dosing of PF-04217329 was well tolerated in preclinical species and caused an elevation of cAMP in aqueous humor/iris-ciliary body indicative of in-vivo EP2 target receptor activation. -
Visual Acuity
Diagnostic Procedures in OPHTHALMOLOGY Diagnostic Procedures in OPHTHALMOLOGY SECOND EDITION HV Nema Former Professor and Head Department of Ophthalmology Institute of Medical Sciences Banaras Hindu University Varanasi, Uttar Pradesh, India Nitin Nema MS Dip NB Assistant Professor Department of Ophthalmology Sri Aurobindo Institute of Medical Sciences Indore, Madhya Pradesh, India ® JAYPEE BROTHERS MEDICAL PUBLISHERS (P) LTD New Delhi • Ahmedabad • Bengaluru • Chennai • Hyderabad Kochi • Kolkata • Lucknow • Mumbai • Nagpur • St Louis (USA) Published by Jitendar P Vij Jaypee Brothers Medical Publishers (P) Ltd Corporate Office 4838/24 Ansari Road, Daryaganj, New Delhi - 110 002, India, +91-11-43574357 (30 lines) Registered Office B-3 EMCA House, 23/23B Ansari Road, Daryaganj, New Delhi 110 002, India Phones: +91-11-23272143, +91-11-23272703, +91-11-23282021, +91-11-23245672, Rel: +91-11-32558559 Fax: +91-11-23276490, +91-11-23245683 e-mail: [email protected], Website: www.jaypeebrothers.com Branches • 2/B, Akruti Society, Jodhpur Gam Road Satellite Ahmedabad 380 015 Phones: +91-79-26926233, Rel: +91-79-32988717 Fax: +91-79-26927094 e-mail: [email protected] • 202 Batavia Chambers, 8 Kumara Krupa Road, Kumara Park East Bengaluru 560 001 Phones: +91-80-22285971, +91-80-22382956, +91-80-22372664 Rel: +91-80-32714073, Fax: +91-80-22281761 e-mail: [email protected] • 282 IIIrd Floor, Khaleel Shirazi Estate, Fountain Plaza, Pantheon Road Chennai 600 008 Phones: +91-44-28193265, +91-44-28194897, Rel: +91-44-32972089 Fax: +91-44-28193231 e-mail: [email protected] • 4-2-1067/1-3, 1st Floor, Balaji Building, Ramkote Cross Road Hyderabad 500 095 Phones: +91-40-66610020, +91-40-24758498, Rel:+91-40-32940929 Fax:+91-40-24758499 e-mail: [email protected] • No. -
A1the Eye in Detail
A. The Eye A1. Eye in detail EYE ANATOMY A guide to the many parts of the human eye and how they function. The ability to see is dependent on the actions of several structures in and around the eyeball. The graphic below lists many of the essential components of the eye's optical system. When you look at an object, light rays are reflected from the object to the cornea , which is where the miracle begins. The light rays are bent, refracted and focused by the cornea, lens , and vitreous . The lens' job is to make sure the rays come to a sharp focus on the retina . The resulting image on the retina is upside-down. Here at the retina, the light rays are converted to electrical impulses which are then transmitted through the optic nerve , to the brain, where the image is translated and perceived in an upright position! Think of the eye as a camera. A camera needs a lens and a film to produce an image. In the same way, the eyeball needs a lens (cornea, crystalline lens, vitreous) to refract, or focus the light and a film (retina) on which to focus the rays. If any one or more of these components is not functioning correctly, the result is a poor picture. The retina represents the film in our camera. It captures the image and sends it to the brain to be developed. The macula is the highly sensitive area of the retina. The macula is responsible for our critical focusing vision. It is the part of the retina most used. -
DISSERTATION COLOR VISION DURING PREGNANCY Submitted by Melissa Pfohl Department of Psychology in Partial Fulfillment of The
DISSERTATION COLOR VISION DURING PREGNANCY Submitted by Melissa Pfohl Department of Psychology In partial fulfillment of the requirements For the Degree of Doctor of Philosophy Colorado State University Fort Collins, Colorado Summer 2012 Doctoral Committee: Advisor: Vicki J. Volbrecht Co-Advisor: Janice L. Nerger Edward Delosh Paul Laybourn ABSTRACT COLOR VISION DURING PREGNANCY Color vision deficiencies, both congenital and acquired, are well documented. Acquired color vision deficiencies can arise from a variety of systemic and ocular problems. Previous research has shown that modulation of hormone levels leads to changes in visual perception. Pregnancy involves predictable increases in hormone levels, so this study examined how naturally occurring changes in endogenous levels of steroid hormones during pregnancy may affect color perception and visual acuity. Color vision testing was conducted at regular time intervals over the duration of pregnancy for 6 women as well as a control group of non-pregnant, non-contraceptive using women. As levels of hormones increased over the course of pregnancy, error scores were predicted to increase, indicating increasing losses in color perception. No significant differences were found between pregnant and control participants for any of the color vision tests conducted across any of the time periods tested; however, four of the pregnant participants did show increases in error scores in the shorter wavelengths as time elapsed. The lack of significant differences could indicate that there are compensatory mechanisms for the body to adjust to increasing levels of endogenous hormones from pregnancy. This study has opened up myriad possibilities for future research examining the relationship of hormones and neurosteroids and their effects on color vision. -
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. -
Clinical Significance of Central Corneal Thickness in the Managementof Glaucoma
CLINICAL SCIENCES Clinical Significance of Central Corneal Thickness in the Management of Glaucoma Carolyn Y. Shih, MD; Joshua S. Graff Zivin, PhD; Stephen L. Trokel, MD; James C. Tsai, MD Objective: To evaluate the effect of central corneal thick- Results: Using the linear correction scale, 105 (55.9%) ness determination on the clinical management of pa- of 188 patients had at least a measurement-significant ad- tients with glaucoma and glaucoma suspect. justment in their IOP measurements: 67 (35.6%) had ad- justments between 1.5 and 3.0 mm Hg, while 38 (20.2%) Methods: A cross-sectional retrospective study was per- had an outcomes-significant IOP adjustment (Ն3.0 formed on 188 consecutive patients. Mean ultrasound mm Hg). Among the 188 patients, 16 (8.5%) had a change pachymetry measurements of central corneal thickness in eyedrop therapy, 4 (2.1%) had a change regarding laser and corresponding Goldmann applanation tonometry therapy, and 6 (3.2%) had a change in the decision re- measurements were obtained. Intraocular pressures (IOPs) garding glaucoma surgery. Using the exponential cor- were corrected using linear and mathematical (Orssengo- rection (Orssengo-Pye) scale, similar percentages were Pye) algorithms. Measurement-significant outcomes were obtained. defined as an IOP adjustment of 1.5 mm Hg or greater and outcomes-significant results as an IOP adjustment of Conclusion: Pachymetry-measured central corneal thick- 3.0 mm Hg or greater. Changes in therapy such as the ness has a significant effect on the clinical management use of eyedrops and addition or cancellation of laser of patients with glaucoma and glaucoma suspect. -
UNIT 11 Special Senses: Eyes and Ears Pathological Conditions Eye ACHROMATOPSIA
UNIT 11 Special Senses: Eyes and Ears Pathological Conditions Eye ACHROMATOPSIA Congenital deficiency in color perception; also called color blindness. Achromatopsia is more common in men. ASTIGMATISM Defective curvature of the cornea and lens, which causes light rays to focus unevenly over the retina rather than being focused on a single point, resulting in a distorted image. CATARACT Degenerative disease in which the lens of the eye becomes progressively cloudy, causing decreased vision. Cataracts are usually a result of the aging process, caused by protein deposits on the surface of the lens that slowly build up until vision is lost. Treatment includes surgical intervention to remove the cataract. CONJUNCTIVITIS Inflammation of the conjuctiva that can be caused by bacteria, allergy, irritation, or a foreign body; also called pinkeye. DIABETIC RETINOPATHY Retinal damage marked by aneurysmal dilation and bleeding of blood vessels or the formation of new blood vessels, causing visual changes. Diabetic retinopathy occurs in people with diabetes, manifested by small hemorrhages, edema, and formation of new vessels leading to scarring and eventual loss of vision. GLAUCOMA Condition in which aqueous humor fails to drain properly and accumulates in the anterior chamber of the eye, causing elevated intraocular pressure (IOP). Glaucoma eventually leads to the loss of vision and, commonly, blindness. Treatment for glaucoma includes miotics (eyedrops) that cause the pupils to constrict, permitting aqueous humor to escape from the eye, thereby relieving pressure. If miotics are ineffective, surgery may be necessary. OPEN-ANGLE GLAUCOMA Most common form of glaucoma that results from degenerative changes that cause congestion and reduce flow of aqueous humor through the canal of Schlemm.