Acute Visual Loss
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Un-Explained Visual Loss Following Silicone Oil Removal
Roca et al. Int J Retin Vitr (2017) 3:26 DOI 10.1186/s40942-017-0079-6 International Journal of Retina and Vitreous ORIGINAL ARTICLE Open Access Un‑explained visual loss following silicone oil removal: results of the Pan American Collaborative Retina Study (PACORES) Group Jose A. Roca1, Lihteh Wu2* , Maria Berrocal3, Francisco Rodriguez4, Arturo Alezzandrini5, Gustavo Alvira6, Raul Velez‑Montoya7, Hugo Quiroz‑Mercado7, J. Fernando Arevalo8, Martín Serrano9, Luiz H. Lima10, Marta Figueroa11, Michel Farah10 and Giovanna Chico1 Abstract Purpose: To report the incidence and clinical features of patients that experienced un-explained visual loss following silicone oil (SO) removal. Methods: Multicenter retrospective study of patients that underwent SO removal during 2000–2012. Visual loss of 2 lines was considered signifcant. ≥ Results: A total of 324 eyes of 324 patients underwent SO removal during the study period. Forty two (13%) eyes sufered a signifcant visual loss following SO removal. Twenty three (7.1%) of these eyes lost vision secondary to known causes. In the remaining 19 (5.9%) eyes, the loss of vision was not explained by any other pathology. Eleven of these 19 patients (57.9%) were male. The mean age of this group was 49.2 16.4 years. Eyes that had an un-explained visual loss had a mean IOP while the eye was flled with SO of 19.6 6.9 mm± Hg. The length of time that the eye was flled with SO was 14.8 4.4 months. In comparison, eyes that± did not experience visual loss had a mean IOP of 14 7.3 mm Hg (p < 0.0002)± and a mean tamponade duration of 9.3 10.9 months (p < 0.0001). -
Acute Hydrops Following Penetrating Keratoplasty in a Keratoconic Patient
Acute Hydrops following PK • Baradaran-Rafiee et al Iranian Journal of Ophthalmology • Volume 20 • Number 4 • 2008 Acute Hydrops following Penetrating Keratoplasty in a Keratoconic Patient Alireza Baradaran-Rafiee, MD1 • Manijeh Mahdavi, MD2 • Sepehr Feizi, MD3 Abstract Purpose: To report a case with history of penetrating keratoplasty (PK) for keratoconus that developed acute hydrops in the recipient and donor cornea Methods: A 46-year-old man, with history of bilateral keratoconus, who had undergone corneal transplantation in his left eye, presented with complaints of sudden visual reduction, photophobia, redness and pain of the left eye. Results: Review of his clinical course, slit-lamp biomicroscopy, laboratory evaluations including confocal microscopy and ultrasound biomicroscopy revealed acute hydrops in the graft. Second corneal transplantation was done for his left eye and pathologic examination confirmed the diagnosis. Conclusion: Acute hydrops can occur after PK in patients with keratoconus. Although this condition is not common, it should be considered as a differential diagnosis of graft rejection. Keywords: Acute Hydrops, Keratoconus, Corneal Transplantation Iranian Journal of Ophthalmology 2008;20(4):49-53 Introduction Keratoconus is a degenerative, One of the complications of advanced non-inflammatory disease of the cornea, with keratoconus is acute hydrops. Affected onset generally at puberty. It is progressive in patients suffer from acute visual loss with pain 20% of cases and can be treated by lamellar and photophobia. On slit-lamp examination, or penetrating keratoplasty (PK). Its incidence conjunctival hyperemia and diffuse corneal in general population is reported to be about edema with intrastromal cystic spaces are 1/2000.1 Changes in corneal collagen visible. -
Red Spot • Important Is the Time Period from the Event • Therapy Is Reasonable If the Patient Is Treated Within the First 6 Hours
ACUTE VISUAL LOSS KAROLÍNA SKORKOVSKÁ VISUAL LOSS • CENTRAL RETINAL ARTERY OCCLUSION • CENTRAL RETINAL VEIN OCCLUSION • RETINAL DETACHMENT • VITREOUS HAEMORRHAGE • OPTIC NEURITIS • AION VISUAL LOSS - PATIENT´S HISTORY • UNILATERAL / BILATERAL • SUDDEN / SLOWLY PROGRESSIVE • PAIN • COMPLAINTS (FOGGY VISION, FLOATERS, CURTAIN…) • OTHER SYMPTOMS (FEVER, WEIGHT LOSS, REFRACTIVE CHANGE, …) CATARACT • SLOWLY PROGRESSIVE VISUAL LOSS • FOGGY VISION • CHANGE IN REFRACTIVE ERROR (INDEX MYOPIA) • CATARACT VISIBLE ON SLIT LAMP • THERAPY: CATARACT EXTRACTION RETINAL ARTERY OCCLUSION • SUDDEN, UNILATERAL, PAINLESS LOSS OF VISION • VISUAL ACUITY MAY BE „NO LIGHT PERCEPTION“ • BRANCH / CENTRAL RETINAL ARTERY OCCLUSION • RETINAL ISCHEMIA WITH CHERRY RED SPOT • IMPORTANT IS THE TIME PERIOD FROM THE EVENT • THERAPY IS REASONABLE IF THE PATIENT IS TREATED WITHIN THE FIRST 6 HOURS RETINAL ARTERY OCCLUSION - COMPLICATIONS • POOR PROGNOSIS • PERMANENT LOSS OF VISION • OPTIC DISC ATROPHY • NEOVASCULARISATION GLAUCOMA RETINAL ARTERY OCCLUSION - THERAPY • LOWERING OF INTRAOCULAR PRESSURE • RETROBULBAR INJECTION OF VASODILATORS • PARACENTHESIS • SYSTEMIC TROMBOLYSIS (DEPARTMENT OF INTERNAL MEDICINE) • CHECK-UP OF RISK FACTORS OF ISCHEMIA / TROMBOSIS RETINAL VEIN OCCLUSION • SUDDEN, PAINLESS, UNILATERAL VISUAL LOSS • VISUAL ACUITY USUALLY NOT AS MUCH AFFECTED AS IN CRAO • BRANCH / CENTRAL RETINAL VEIN OCCLUSION • OFTEN CARDIOVASCULAR RISK FACTORS (HYPERTENSION, DIABETES, HYPERLIPIDEMIA, ISCHEMIC HEART DISEASE,…) • RETINAL HAEMORHAGES, OPTIC NERVE HEAD OEDEMA, RETINAL -
A Review of Central Retinal Artery Occlusion: Clinical Presentation And
Eye (2013) 27, 688–697 & 2013 Macmillan Publishers Limited All rights reserved 0950-222X/13 www.nature.com/eye 1 2 1 2 REVIEW A review of central DD Varma , S Cugati , AW Lee and CS Chen retinal artery occlusion: clinical presentation and management Abstract Central retinal artery occlusion (CRAO) is an that in turn place an individual at risk of future ophthalmic emergency and the ocular ana- cerebral stroke and ischaemic heart disease. logue of cerebral stroke. Best evidence reflects Although analogous to a cerebral stroke, there that over three-quarters of patients suffer is currently no guideline-endorsed evidence for profound acute visual loss with a visual acuity treatment. Current options for therapy include of 20/400 or worse. This results in a reduced the so-called ‘standard’ therapies, such as functional capacity and quality of life. There is sublingual isosorbide dinitrate, systemic also an increased risk of subsequent cerebral pentoxifylline or inhalation of a carbogen, stroke and ischaemic heart disease. There are hyperbaric oxygen, ocular massage, globe no current guideline-endorsed therapies, compression, intravenous acetazolamide and although the use of tissue plasminogen acti- mannitol, anterior chamber paracentesis, and vator (tPA) has been investigated in two methylprednisolone. None of these therapies randomized controlled trials. This review will has been shown to be better than placebo.5 describe the pathophysiology, epidemiology, There has been recent interest in the use of and clinical features of CRAO, and discuss tissue plasminogen activator (tPA) with two current and future treatments, including the recent randomized controlled trials on the 1Flinders Comprehensive use of tPA in further clinical trials. -
Clinical Findings and Management of Posterior Vitreous Detachment
American Academy of Optometry: Case Report 5 Clinical Findings and Management of Posterior Vitreous Detachment Candidate’s Name, O.D. Candidate’s Address Candidate’s Phone number Candidate’s email Abstract: A posterior vitreous detachment is a degenerative process associated with aging that affects the vitreous when the posterior vitreous cortex separates from the internal limiting membrane of the retina. The composition of the vitreous gel can degenerate two collective ways, including synchysis or liquefaction, and syneresis or shrinking. Commonly, this process of separation occurs with the posterior hyaloid resulting in a Weiss ring overlying the optic nerve. Complications of a posterior vitreous detachment may include retinal breaks or detachments, retinal or vitreous hemorrhages, or vitreomacular traction. This case presentation summarizes the etiology of this ocular condition as well as treatment and management approaches. Key Words: Posterior Vitreous Detachment, Weiss Ring, Vitreous Degeneration, Scleral Depression, Nd:YAG Laser 1 Introduction The vitreous humor encompasses the posterior segment of the eye and fills approximately three quarters of the ocular space.1 The vitreous is a transparent, hydrophilic, “gel-like” substance that is described as a dilute solution of collagen, and hyaluronic acid.2,3,4 It is composed of 98% to 99.7% water.4 As the eye matures, changes may occur regarding the structure and composition of the vitreous. The vitreous functions to provide support to the retina against the choroid, to store nutrients and metabolites for the retina and lens, to protect the retinal tissue by acting as a “shock absorber,” to transmit and refract light, and to help regulate eye growth during fetal development.3,4 Case Report Initial Visit (03/23/2018) A 59-year-old Asian female presented as a new patient for examination with a complaint of a new onset of floaters and flashes of light in her right eye. -
Floaters-Survey-Ophthalmol-2016.Pdf
survey of ophthalmology 61 (2016) 211e227 Available online at www.sciencedirect.com ScienceDirect journal homepage: www.elsevier.com/locate/survophthal Major review Vitreous floaters: Etiology, diagnostics, and management Rebecca Milston, MOptoma, Michele C. Madigan, PhDb,c, J. Sebag, MD, FACS, FRCOphth, FARVOd,* a Centre for Eye Health, University of New South Wales, Sydney, New South Wales, Australia b School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, Australia c Save Sight Institute and Discipline of Clinical Ophthalmology, Sydney Medical School, University of Sydney, New South Wales, Australia d VMR Institute for Vitreous Macula Retina, Huntington Beach, California, USA article info abstract Article history: Vitreous is a hydrated extracellular matrix comprised primarily of water, collagens, and Received 3 July 2015 hyaluronan organized into a homogeneously transparent gel. Gel liquefaction results from Received in revised form 25 molecular alterations with dissociation of collagen from hyaluronan and aggregation of November 2015 collagen fibrils forming fibers that cause light scattering and hence symptomatic floaters, Accepted 25 November 2015 especially in myopia. With aging, gel liquefaction and weakened vitreoretinal adhesion Available online 8 December 2015 result in posterior vitreous detachment, the most common cause of primary symptomatic floaters arising from the dense collagen matrix of the posterior vitreous cortex. Recent Keywords: studies indicate that symptomatic floaters are not only more prevalent, but also have a vitreous negative impact on the quality of life that is greater than previously appreciated. We review collagen the literature concerning management of symptomatic vitreous floaters, currently either myopia with observation, vitrectomy, or Nd:YAG laser. -
Acute Visual Loss 5 Cédric Lamirel , Nancy J
Acute Visual Loss 5 Cédric Lamirel , Nancy J. Newman , and Valérie Biousse Abstract Visual loss is a common symptom in neurologic emergencies. Although ocular causes of visual loss are usually identifi ed by eye care specialists, many patients appear in an emergency department or a neurologist’s offi ce when the ocular examination is normal or when it suggests a neurologic disorder. Indeed, many causes of monocular or binocular acute visual loss may reveal or precede a neurologic process. In this situation, a quick and simple clinical examination done at bedside in the emergency department allows the neurologist to localize the lesion and determine whether an urgent neurologic workup or further ophthalmologic consultation is necessary. Keywords Central retinal artery occlusion • Funduscopic examination • Optic neuropathy • Retinal emboli • Visual fi eld • Visual loss Acute vision changes typically precipitate emer- gency consultation. Although ocular causes are usually identifi ed by eye care specialists, many patients appear in an emergency department or a C. Lamirel , MD neurologist’s offi ce when the ocular examination Service d’ophtalmologie , Fondation Ophtalmologique is normal or when it suggests a neurologic disor- Adolphe Rothschild , Paris , France der. Indeed, many causes of monocular or binoc- e-mail: [email protected] ular acute visual loss may reveal or precede a N. J. Newman , MD • V. Biousse, MD () neurologic process. In this situation, a quick and Neuro-Ophthalmology Unit , simple clinical examination done at bedside in Emory University School of Medicine , Atlanta , GA , USA the emergency department allows the neurologist e-mail: [email protected]; [email protected] to localize the lesion and determine whether an K.L. -
Approach to Acute Visual Loss
APPROACH TO ACUTE VISUAL LOSS 11 : 2 Satish Khadilkar, Pramod Dhonde, Mumbai INTRODUCTION Acute visual loss is common in clinical practice. The symptom is very disturbing to patients and requires rapid clinical analysis and therapy, as it can be associated with significant morbidity. Etiologies of acute visual impairment range from retina to the occipital cortex, resulting in a plethora of presentations. For example in a case of retinal disease patient may feel as if a curtain is rising or dropping and in cases of occipital lesions, patients may give history of bumping into the objects without realization. Also, patients tend to mistake diplopia for visual loss, which needs careful analysis. Acute visual loss could either be monocular or binocular. Monocular loss is often related to local eye pathologies as glaucoma, uveitis, retinitis or neurological diseases like optic neuritis (ON) and anterior ischemic optic neuropathy (AION). Binocular diseases are usually associated with lesions affecting structures such as optic chiasma, lateral geniculate body, occipital radiations and occipital cortex. Pain is an important association of visual loss. Painful visual impairment is seen in ON, Tolosa Hunt Syndrome, orbital apex syndrome, pituitary apoplexy and glaucoma. On the other hand, diseases of the optic tracts, radiations, occipital cortex and AION tend to be painless. The natural history of the visual impairment is helpful in the differential diagnosis. Transient visual deficit is seen in vascular diseases, demyelinations, raised intracranial tension and hyper coagulable states. Lasting deficits are seen with, strokes, tumors and AION. Following cases will illustrate various clinical situations of acute visual impairment, encountered by clinicians. -
And Pneumatic Displacement of Submacular Hemorrhage
5. Ross R, Gitter K, Cohen G, Schomaker K. Idiopathic polypoi- subretinal blood through a retinotomy.4 To move the dal choroidal vasculopathy associated with retinal arterial blood out of the central macula without the need for a pars macroaneurysm and hypertensive retinopathy. Retina 1996; plana vitrectomy and retinotomy, Heriot (American 16:105–111. Academy of Ophthalmology Annual Vitreoretinal Update presentations, 1996–1997, unpublished data) reported the use of an intravitreal injection of tissue plasminogen Vitreous Hemorrhage After activator and gas with postoperative face down positioning Intravitreal Tissue Plasminogen to lyse the blood clot and then displace the blood periph- Activator (t-PA) and Pneumatic erally from the submacular space. Intravitreal injection of tissue plasminogen activator and gas was performed in two Displacement of Submacular cases of sudden submacular hemorrhage associated with Hemorrhage retinal arterial macroaneurysm. Dense vitreous hemor- Gregg T. Kokame, MD rhage was noted after intravitreal injection of tissue plas- minogen activator and intraocular gas. PURPOSE: To report the immediate complication of dense ● vitreous hemorrhage after intravitreal injection of tissue CASE 1: A 92-year-old man developed sudden vision plasminogen activator and gas for treatment of two cases loss in his left pseudophakic eye for 1 day before of sudden submacular hemorrhage associated with retinal presentation. His visual acuity was RE: 20/20, LE: arterial macroaneurysm. 20/400. A thick subfoveal hemorrhage and subinternal METHODS: Case reports. limiting membrane hemorrhage in the central macula RESULTS: Two patients, a 67-year-old woman and a were noted. Two days after symptom onset, an intra- 92-year-old man, presented with sudden vision loss vitreal 50- g injection of tissue plasminogen activator related to submacular hemorrhage from a retinal macro- and 0.55 ml of sulfur hexafluoride (SF6) gas were given aneurysm. -
Branch Retinal Vein Occlusion with Vitreous
International Journal of Retina (IJRETINA) 2018, Volume 1, Number 1. P-ISSN. 2614-8684, E-ISSN.2614-8536 BRANCH RETINAL VEIN OCCLUSION WITH VITREOUS HEMORRHAGE IDENTIFIED DURING INTRAOPERATIVE VITRECTOMY Nafila Mahida Sukmono1, Ramzi Amin1,2 1Ophthalmology Department, Universitas Sriwijaya 2Mohammad Hoesin Hospital Palembang ABSTRACT Introduction Retinal vein occlusion is the largest group of retinal blood vessels after diabetic retinopathy. Occlusion occurring in the retinal vein is divided into central retinal vein occlusion (CRVO) occlusion and branch retinal vein occlusion (BRVO) occlusion. The Beijing Eye Study, reported a higher incidence of BRVO than CRVO, where 10-year incidents for BRVO were 1.6 per 100 subjects, and CRVO was only 0.3% 100 subjects.1 To report a case of Branch Retinal Vein Occlusion with vitreous hemorrhage identified during intraoperative vitrectomy Method: A 49-year-old woman with a history of 15 years of hypertension had right eye vision complaints, increasingly blurred since last 2 months. The right eye visual acuity 2/60 cannot be corrected and left eye 6/30 cannot be corrected. The posterior segment on right eye is difficult to assess. USG B-Scan right eye found vitreous echospike appearance of vitreous bleeding. We manage with vitrectomy and during intraoperative we identified bleeding and ghost vessel in superotemporal area. Bleeding in the superotemporal quadrant is done by photocoagulation laser action. Results: First day postoperative there was increased in visual acuity to 6/60 with a posterior segment that could be assessed, obtained tortous blood vessels, slight bleeding and ghost vessel in the superotemporal area with laser injury. Conclusion: In this case report, patients with BRVO with complications of vitreous hemorrhage performed vitrectomy with additional endolaser in the ischemic area. -
Visual Loss Due to Progressive Multifocal Leukoencephalopathy In
CLINICOPATHOLOGIC REPORTS, CASE REPORTS, AND SMALL CASE SERIES SECTION EDITOR: W. RICHARD GREEN, MD but there was a single nucleotide visible, fine-linear white scarring in Visual Loss Due to substitution (C155T) in exon 1 of this area (Figure 2). In the most se- Progressive Multifocal the WAS gene. verely affected gyri, the cortex was Leukoencephalopathy Six weeks later his vision was bi- also involved and had a darker color, in a Congenital lateral finger counting. A magnetic with apparent expansion and soften- resonance imaging (MRI) scan ing of its affected parts. Immunodeficiency Disorder showed scattered areas of white- Although the individual le- matter foci, predominantly peri- sions were present throughout the A 20-year-old man with Wiskott- pheral and not periventricular, on cerebral hemispheres, they were Aldrich syndrome (WAS) initially de- proton density and T2-weighted most frequent bilaterally in the oc- veloped a mild visual disturbance that scans. He was given intravenous cipital poles, which were also the progressed to blindness, increasing methylprednisolone sodium succi- major site of linear cortico–white- neurological deficits, and death nate because of the possibility of de- matter junction lesions and scar- within 4 months. Wiskott-Aldrich myelination. No improvement oc- ring as well as the regions of diffuse syndrome is an X-linked immuno- curred, and he was registered as blind. cortical involvement. A microsco- deficiency disorder characterized by Reduced sensation and generalized pic examination of the brain sec- thrombocytopenia, eczema, and sus- mild weakness (level 4-5) devel- tions showed small, spherical, white ceptibility to infection.1 This case il- oped in his right-hand side and face. -
Home>>Common Retinal & Ophthalmic Disorders
Common Retinal & Ophthalmic Disorders Cataract Central Serous Retinopathy Cystoid Macular Edema (Retinal Swelling) Diabetic Retinopathy Floaters Glaucoma Macular degeneration Macular Hole Macular Pucker - Epiretinal Membrane Neovascular Glaucoma Nevi and Pigmented Lesions of the Choroid Posterior Vitreous Detachment Proliferative Vitreoretinopathy (PVR) Retinal Tear and Detachment Retinal Artery and Vein Occlusion Retinitis Uveitis (Ocular Inflammation) White Dot Syndromes Anatomy and Function of the Eye (Short course in physiology of vision) Cataract Overview Any lack of clarity in the natural lens of the eye is called a cataract. In time, all of us develop cataracts. One experiences blurred vision in one or both eyes – and this cloudiness cannot be corrected with glasses or contact lens. Cataracts are frequent in seniors and can variably disturb reading and driving. Figure 1: Mature cataract: complete opacification of the lens. Cause Most cataracts are age-related. Diabetes is the most common predisposing condition. Excessive sun exposure also contributes to lens opacity. Less frequent causes include trauma, drugs (eg, systemic steroids), birth defects, neonatal infection and genetic/metabolic abnormalities. Natural History Age-related cataracts generally progress slowly. There is no known eye-drop, vitamin or drug to retard or reverse the condition. Treatment Surgery is the only option. Eye surgeons will perform cataract extraction when there is a functional deficit – some impairment of lifestyle of concern to the patient. Central Serous Retinopathy (CSR) Overview Central serous retinopathy is a condition in which a blister of clear fluid collects beneath the macula to cause acute visual blurring and distortion (Figure 2). Central serous retinochoroidopathy Left: Accumulation of clear fluid beneath the retina.