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Cory Newman Thesis 5-2021 Signed.Pdf (1.303Mb)
DocuSign Envelope ID: 4851A328-CF63-4770-A833-B4246E7E5D23 Simulating Homonymous Hemianopsia for the Care Team by Cory Newman May 2021 Presented to the Division of Science, Information Arts, and Technologies University of Baltimore In Partial Fulfillment of the Requirements for the Degree of Master of Science 5/25/2021 Approved by: ________________________________ [name, Thesis Advisor] ________________________________5/25/2021 [name, Committee Member] i DocuSign Envelope ID: 4851A328-CF63-4770-A833-B4246E7E5D23 Abstract Homonymous hemianopsia is a visual impairment that involves the bilateral loss of a complete visual field. While research has been done to ascertain the details of cause and prognosis of homonymous hemianopsia, an obvious disparity arose in the research on how to educate the supporting care team of a person with homonymous hemianopsia to maximize the creation of educational and rehabilitation plans. This research presents two studies focused on closing that gap by providing an alternative method of understanding. In the initial study 16 participants with a confirmed caregiver relationship to one or more persons with homonymous hemianopsia were surveyed on their personal knowledge of the visual impairment. These participants were asked to express any visual obstacles they have encountered, and to ascertain the availability of a device or program that could provide an interactive interpretation of how their homonymous hemianopsia patient views their surroundings. Survey results confirmed the need for a program that could easily simulate homonymous hemianopsia for the care provider. An additional usability study was completed by eight of the 16 previous participants on a mobile homonymous hemianopsia simulation application prototype. User tests showed that participants gained a significant increase in understanding of how those with a homonymous hemianopsia visual impairment view the environment. -
Homonymous Hemianopsia
Source: CLEVELAND CLINIC OHIO USA FACTSHEET Homonymous Hemianopsia Homonymous hemianopsia is a condition in which a person sees only one side - right or left of the visual world of each eye; results from a problem in brain function rather than a disorder of the eyes themselves. This can happen after a head or brain injury. What is homonymous hemianopsia? Homonymous hemianopsia is a condition in which a person sees only one side―right or left―of the visual world of each eye. The person may not be aware that the vision loss is happening in both eyes, not just one. Under normal circumstances, the left half of the brain processes visual information from both eyes about the right side of the world. The right side of the brain processes visual information from both eyes about the left side of the world. A visual world of someone with normal vision A visual world of someone with homonymous hemianopsia In homonymous hemianopsia, an injury to the left part of the brain results in the loss of the right half of the visual world of each eye. An injury to the right part of the brain produces loss of the left side of the visual world of each eye. This condition is created by a problem in brain function rather than a disorder of the eyes themselves. What causes homonymous hemianopsia? The most common cause of this type of vision loss is stroke. However, any disorder that affects the brain—including tumours, inflammation, and injuries--can be a cause. Source: CLEVELAND CLINIC OHIO USA It is estimated that 70% of the injuries leading to hemianopsias are due to an obstruction (blockage) of the blood supply (stroke). -
Neuroophthalmology
Neuroophthalmology MAREK MICHALEC, MD PHD Clinic of Ophthalmology Faculty Hospital Brno and Masaryk University Version 12/2019 Content • Visual pathway affection • Diseases and affections of optic nerve • Optic chiasm pathology • Pathology of retrochiasmic part • Eye movement disorders • Binocular diplopia • Pupillary reaction abnormalities • Anisocoria • Combined disorders Examination - part I • Medical history • subjective (visual loss, diplopia) • When it started/ how long lasts it? • Does it change in time/ during the day? • Any progression? • What about the fellow eye? • Other signs? • Personal medical history? • Pharmacological history? • objective (pupillary dysfunction, eye movement disorders, ptosis of upper eyelid, red eye) Examination - part II • Visual acuity • Without and with correction • Monocular vision / binocular vision • Basic ophthalmological examination • Anterior segment (by slit lamp) • Posterior segment - arteficial mydriasis is essential (indirect ophthalmoscopy) • Visual field examination (static / kinetic perimetry) Examination - part III • Basic examination (GP) • Neurological examination • Intracranial conditions (including MRI) • neurological signs • Endocrinology • Thyroid associated orbitopathy / ophthalmopathy • Pituitary dysfunction Examination - part IV • Imaging techniques • Ultrasonography (eye bulb, orbit) • X-ray of skull (orbit, paranasal cavities) • Computerised Tomography of head (brain, skull bones, orbital bones) • MRI of head (brain, orbital structures) Optic nerve disorders Clinical signs • -
Oct Institute
Low Vision, Visual Dysfunction and TBI – Treatment, Considerations, Adaptations Andrea Hubbard, OTD, OTR/L, LDE Objectives • In this course, participants will: 1. Learn about interventions involving specialized equipment to adapt an environment for clients with low vision. 2. Learn about the most typical low vision presentations/conditions. 3. Gain increased knowledge of eye anatomy and the visual pathway. Overview of TBI Reference: Centers for Disease Control and Prevention Overview of TBI Risk Factors for TBI Among non-fatal TBI-related injuries for 2006–2010: • Men had higher rates of TBI hospitalizations and ED visits than women. • Hospitalization rates were highest among persons aged 65 years and older. • Rates of ED visits were highest for children aged 0-4 years. • Falls were the leading cause of TBI-related ED visits for all but one age group. – Assaults were the leading cause of TBI-related ED visits for persons 15 to 24 years of age. • The leading cause of TBI-related hospitalizations varied by age: – Falls were the leading cause among children ages 0-14 and adults 45 years and older. – Motor vehicle crashes were the leading cause of hospitalizations for adolescents and persons ages 15-44 years. Reference: Centers for Disease Control and Prevention Overview of TBI Risk Factors for TBI Among TBI-related deaths in 2006–2010: • Men were nearly three times as likely to die as women. • Rates were highest for persons 65 years and older. • The leading cause of TBI-related death varied by age. – Falls were the leading cause of death for persons 65 years or older. -
Neuroanatomy Crash Course
Neuroanatomy Crash Course Jens Vikse ∙ Bendik Myhre ∙ Danielle Mellis Nilsson ∙ Karoline Hanevik Illustrated by: Peder Olai Skjeflo Holman Second edition October 2015 The autonomic nervous system ● Division of the autonomic nervous system …………....……………………………..………….…………... 2 ● Effects of parasympathetic and sympathetic stimulation…………………………...……...……………….. 2 ● Parasympathetic ganglia ……………………………………………………………...…………....………….. 4 Cranial nerves ● Cranial nerve reflexes ………………………………………………………………….…………..…………... 7 ● Olfactory nerve (CN I) ………………………………………………………………….…………..…………... 7 ● Optic nerve (CN II) ……………………………………………………………………..…………...………….. 7 ● Pupillary light reflex …………………………………………………………………….…………...………….. 7 ● Visual field defects ……………………………………………...................................…………..………….. 8 ● Eye dynamics …………………………………………………………………………...…………...………….. 8 ● Oculomotor nerve (CN III) ……………………………………………………………...…………..………….. 9 ● Trochlear nerve (CN IV) ………………………………………………………………..…………..………….. 9 ● Trigeminal nerve (CN V) ……………………………………………………................…………..………….. 9 ● Abducens nerve (CN VI) ………………………………………………………………..…………..………….. 9 ● Facial nerve (CN VII) …………………………………………………………………...…………..………….. 10 ● Vestibulocochlear nerve (CN VIII) …………………………………………………….…………...…………. 10 ● Glossopharyngeal nerve (CN IX) …………………………………………….……….…………...………….. 10 ● Vagus nerve (CN X) …………………………………………………………..………..…………...………….. 10 ● Accessory nerve (CN XI) ……………………………………………………...………..…………..………….. 11 ● Hypoglossal nerve (CN XII) …………………………………………………..………..…………...…………. -
Ministry of Public Health of Ukraine Ukrainian Medical Stomatological Academy
Ministry of Public Health of Ukraine Ukrainian Medical Stomatological Academy Approved At the meeting of the department of neurological diseases with neurosurgery and medical genetic "__"__ ____________20___ Protocol №________ Head of department _______________ prof. Delva M.Yu. METHODICAL INSTRUCTIONS FOR THE INDEPENDENT WORK OF STUDENTS FOR PREPARATION TO PRACTICAL CLASSES AND DURING PRACTICAL CLASSES Academic subject Neurology The module № 1 General neurology Topic Syndromes of defeat oculomotor nerves. Pathology of olfactory and visual analyzers. Year of study IV Faculty Foreign Students Training (Medicine) Poltava 20___ 1.Relevance of the topic: the olfactory and visual analyzers play a role in receptor function of the nervous system. With the functions of these disorders analyzers, as well as with oculomotor disturbances faced by doctors of different specialties - neurologists, ophthalmologists, neurosurgeons, pediatricians, phthisiatricians, endocrinologists, internists. Violations of the functions of these analyzers is observed in a variety of inflammatory, demyelinating processes, tumors, trauma, endocrine disorders. The correct methodological approach to the study of functions, pathological changes of the olfactory and visual analyzers, oculomotor nerves makes it possible to deliver topical and clinical diagnosis and treatment in a timely manner. 2. Specific Objectives: To investigate the function of I, II, III, IV, VI pairs of cranial nerves, identify signs of a lesion of the nerve disorder Examine the identification functions -
Central Serous Choroidopathy
Br J Ophthalmol: first published as 10.1136/bjo.66.4.240 on 1 April 1982. Downloaded from British Journal ofOphthalmology, 1982, 66, 240-241 Visual disturbances during pregnancy caused by central serous choroidopathy J. R. M. CRUYSBERG AND A. F. DEUTMAN From the Institute of Ophthalmology, University of Nijmegen, Nijmegen, The Netherlands SUMMARY Three patients had during pregnancy visual disturbances caused by central serous choroidopathy. One of them had a central scotoma in her first and second pregnancy. The 2 other patients had a central scotoma in their first pregnancy. Symptoms disappeared spontaneously after delivery. Except for the ocular abnormalities the pregnancies were without complications. The complaints can be misinterpreted as pregnancy-related optic neuritis or compressive optic neuropathy, but careful biomicroscopy of the ocular fundus should avoid superfluous diagnostic and therapeutic measures. Central serous choroidopathy (previously called lamp biomicroscopy of the fundus with a Goldmann central serous retinopathy) is a spontaneous serous contact lens showed a serous detachment of the detachment of the sensory retina due to focal leakage neurosensory retina in the macular region of the from the choriocapillaris, causing serous fluid affected left eye. Fluorescein angiography was not accumulation between the retina and pigment performed because of pregnancy. In her first epithelium. This benign disorder occurs in healthy pregnancy the patient had consulted an ophthal- adults between 20 and 45 years of age, who present mologist on 13 June 1977 for exactly the same with symptoms of diminished visual acuity, relative symptoms, which had disappeared spontaneously http://bjo.bmj.com/ central scotoma, metamorphopsia, and micropsia. after delivery. -
Neuroimaging in Ophthalmology
Saudi Journal of Ophthalmology (2012) 26, 401–407 Oculoplastic Imaging Update Neuroimaging in ophthalmology ⇑ James D. Kim, MD, MS b; Nafiseh Hashemi, MD a; Rachel Gelman, BA c; Andrew G. Lee, MD a,b,c,d,e, Abstract In the past three decades, there have been countless advances in imaging modalities that have revolutionized evaluation, manage- ment, and treatment of neuro-ophthalmic disorders. Non-invasive approaches for early detection and monitoring of treatments have decreased morbidity and mortality. Understanding of basic methods of imaging techniques and choice of imaging modalities in cases encountered in neuro-ophthalmology clinic is critical for proper evaluation of patients. Two main imaging modalities that are often used are computed tomography (CT) and magnetic resonance imaging (MRI). However, variations of these modalities and appropriate location of imaging must be considered in each clinical scenario. In this article, we review and summarize the best neuroimaging studies for specific neuro-ophthalmic indications and the diagnostic radiographic findings for important clinical entities. Keywords: Neuroophthalmology, Imaging, Magnetic resonance imaging, Computed tomography Ó 2012 Saudi Ophthalmological Society, King Saud University. All rights reserved. http://dx.doi.org/10.1016/j.sjopt.2012.07.001 Introduction Computed tomography Advances in neuroimaging have revolutionized the evalua- The computed tomography (CT) scan obtains image by tion, management, and treatment of neuro-ophthalmic disor- conventional X-ray technology. The CT X-ray source moves ders. Despite the ever-increasing resolution ability of modern around the patient and the X-ray detectors located on the neuroimaging technology, it remains critical that both the opposite side of the X-ray source measure the amount of ordering eye physician and the interpreting radiologist com- attenuation. -
Eleventh Edition
SUPPLEMENT TO April 15, 2009 A JOBSON PUBLICATION www.revoptom.com Eleventh Edition Joseph W. Sowka, O.D., FAAO, Dipl. Andrew S. Gurwood, O.D., FAAO, Dipl. Alan G. Kabat, O.D., FAAO Supported by an unrestricted grant from Alcon, Inc. 001_ro0409_handbook 4/2/09 9:42 AM Page 4 TABLE OF CONTENTS Eyelids & Adnexa Conjunctiva & Sclera Cornea Uvea & Glaucoma Viitreous & Retiina Neuro-Ophthalmic Disease Oculosystemic Disease EYELIDS & ADNEXA VITREOUS & RETINA Blow-Out Fracture................................................ 6 Asteroid Hyalosis ................................................33 Acquired Ptosis ................................................... 7 Retinal Arterial Macroaneurysm............................34 Acquired Entropion ............................................. 9 Retinal Emboli.....................................................36 Verruca & Papilloma............................................11 Hypertensive Retinopathy.....................................37 Idiopathic Juxtafoveal Retinal Telangiectasia...........39 CONJUNCTIVA & SCLERA Ocular Ischemic Syndrome...................................40 Scleral Melt ........................................................13 Retinal Artery Occlusion ......................................42 Giant Papillary Conjunctivitis................................14 Conjunctival Lymphoma .......................................15 NEURO-OPHTHALMIC DISEASE Blue Sclera .........................................................17 Dorsal Midbrain Syndrome ..................................45 -
Intracranial Mass Lesion in a Patient Being Followed up for Amblyopia
DOI: 10.4274/tjo.galenos.2020.36360 Turk J Ophthalmol 2020;50:317-320 Case Report Intracranial Mass Lesion in a Patient Being Followed up for Amblyopia Ali Mert Koçer, Bayazıt İlhan, Anıl Güngör Ulucanlar Ophthalmology Trainig and Research Hospital, Clinic of Ophthalmology, Ankara, Turkey Abstract A 12-year-old boy being followed up for amblyopia presented to our hospital with visual disturbance in the left eye. The patient’s best corrected visual acuity on Snellen chart was 1.0 in the right eye and 0.3 in the left eye. Increased horizontal cup-to-disc ratio was detected on dilated fundus examination. Retinal nerve fiber layer measurement showed diffuse nerve fiber loss and visual field test showed bitemporal hemianopsia. Magnetic resonance imaging revealed a lesion that filled and widened the sella and suprasellar cistern and compressed the optic chiasm. The patient was operated with transcranial approach. The pathologic examination revealed craniopharyngioma. Keywords: Amblyopia, craniopharyngioma, hemianopsia Introduction cylindrical refractive errors of 1.5-2 diopters (D) or more and is more common in hyperopic eyes than in myopia.2 Amblyopia is poor best corrected visual acuity (BCVA) in one Craniopharyngioma is a benign tumor that develops from or both eyes due to low vision or abnormal binocular interaction the remnant of Rathke’s pouch and is located in the sellar/ without any detectable structural defect in the eye or visual parasellar region.3 It shows a bimodal age distribution, with pathways. Amblyopic vision loss can be corrected if treated at patients usually diagnosed between the ages of 5 and 14 or after an early age. -
VISUAL FIELD Pathway Extends from the „Front‟ to the „Back‟ of the RETINA Brain
NOTE: To change the image on this slide, select the picture and delete it. Then click the Pictures icon in the placeholde r to insert your own image. Visual Pathway Disorders Amr Hassan, MD, FEBN Associate professor of Neurology - Cairo University Optic nerve • Anatomy of visual pathway • How to examine • Visual pathway disorders • Quiz 2 Optic nerve • Anatomy of visual pathway • How to examine • Visual pathway disorders • Quiz 3 Optic nerve The Visual Pathway VISUAL FIELD Pathway extends from the „front‟ to the „back‟ of the RETINA brain. ON OC OT LGN OPTIC RADIATIONS ON = Optic Nerve OC = Optic Chiasm OT = Optic Tract LGN = Lateral Geniculate Nucleus of Thalamus VISUAL CORTEX 5 The Visual Pathway Eyes & Retina Light >> lens >> retina (inverted and reversed image). Eyes & Retina Eyes & Retina • Macula: oval region approximately 3-5 mm that surrounds the fovea, also has high visual acuity. • Fovea: central fixation point of each eye// region of the retina with highest visual acuity. Eyes & Retina • Optic disc: region where axons leaving the retina gather to form the Optic nerve. Eyes & Retina • Blind spot located 15° lateral and inferior to central fixation point of each eye. Object to be seen Peripheral Retina Central Retina (fovea in the macula lutea) 12 Photoreceptors © Stephen E. Palmer, 2002 Photoreceptors Cones • Cone-shaped • Less sensitive • Operate in high light • Color vision • Less numerous • Highly represented in the fovea >> have high spatial & temporal resolution >> they detect colors. © Stephen E. Palmer, 2002 Photoreceptors Rods • Rod-shaped • Highly sensitive • Operate at night • Gray-scale vision • More numerous than cons- 20:1, have poor spatial & temporal resolution of visual stimuli, do not detect colors >> vision in low level lighting conditions © Stephen E. -
1- Orientation, History Taking, and Examination (Part II)
432 Ophthalmology Team #1- Orientation, History Taking, and Examination (Part II) Done by: Shaikha Aldossari Revised by: Alanoud Alyousef Doctor's note Team's note Not important Important 431 teamwork in a yellow box 432 Ophthalmology Team Objectives of The Comprehensive Ophthalmic Evaluation: 1. Obtain an ocular and systemic history. 2. Determine the optical and health status of the eye and visual system. 3. Identify risk factors for ocular and systemic disease. 4. Detect and diagnose ocular diseases. 5. Establish and document the presence or absence of ocular symptoms and signs of systemic disease. 6. Discuss the nature of the findings and the implications with the patient. 7. Initiate an appropriate response. (e.g. further diagnostic tests, treatment, or referral). History Taking & Physical Examination HISTORY • It is a gathering information process from the patient guided by an educated and active mind. • It is a selective guided and progressive elicitation and recognition of significant information • History by skilled person can arrive at the proper diagnosis in 90% of patients. • It gives vital guidance for: o Physical examination o Laboratory work o Therapy • Failure to take history can lead to missing vision or life threatening conditions. Chief complaint: ’’The patient’s own words’’ ‘’She cannot see with the right eye’’ You should not come to conclusion that her problem is nearsightedness and write down “Myopia of RE”. 432 Ophthalmology Team • The patient needs will not be satisfied until he/she has received an acceptable explanation of the meaning of the chief complaint and its proper management. History of the Present Illness: • Detailed description of the chief complaint to understand the symptoms and course of the disorder.