Cover test at distance and near: 8Δ left hypertropia at distance, 10Δ left hypertropia at near
Maddox rod: 8Δ left hypertropia at distance, 10Δ left hypertropia at near
Version: Full OU
Case 1: Left hypertropia increasing at near. Likely thyroid eye disease. Start with Fresnel prism to alleviate diplopia. Consider referral to endocrinologist for further workup and management.
Optics of Contact lenses by Ankit Varshney. If you understand optics properly you can prescribe contact lenses scientifically. Comparison between spectacles and contact lenses.
The presentation I have made and uploaded provides you with an in-depth insight into the patterns the strabismus may take following anomalies of extraocular muscles, deformities of the orbital structures,innnervational disturbances.
The author does not assume responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work.
No copyright infringement, or plagiarism intended.
Amrit Pokharel
Optics of Contact lenses by Ankit Varshney. If you understand optics properly you can prescribe contact lenses scientifically. Comparison between spectacles and contact lenses.
The presentation I have made and uploaded provides you with an in-depth insight into the patterns the strabismus may take following anomalies of extraocular muscles, deformities of the orbital structures,innnervational disturbances.
The author does not assume responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work.
No copyright infringement, or plagiarism intended.
Amrit Pokharel
Contact lens for congenital aphakia and other eye conditions for infants and toddlers. The slide presentation encompasses indications for CL fitting in paediatric, contact lens options, fitting techniques, challenges and contact lens as myopia control.
Current Trend in Management of Amblyopia (Amblyopia Therapy)/ Amblyopia Treat...Bikash Sapkota
DIRECT DOWNLOAD LINK ❤❤https://healthkura.com/lazy-eye-amblyopia/❤❤
Dear viewers, to download this presentation visit___ https://healthkura.com/lazy-eye-amblyopia/
Current Trend in Management of Amblyopia. Latest as well as old methods of amblyopia management which include active and passive therapies. Amblyopia Therapy/ Amblyopia Treatment
What would be the perfect amblyopia therapy?
Effective
Good compliance
Acceptable to pts. and parent
Quick
Safe
Easy to administer
Cost effective
Well maintained
..............
Summary
Amblyopia occurs due to abnormal visual experience early in life
Proper optical correction alone is necessary for short period of time (6-8 weeks)
before initiation of other therapy
Part time occlusion of better eye is mainstay of treatment since 18th century to till
now
For severe and moderate amblyopia, 6 hrs and 2 hrs of patching is advised
respectively
Atropine is also used in children with poor compliance
Trial of patching can be given in patients as old as 17 yrs
Perceptual learning and pharmacological manipulation have shown areas of
amblyopia treatment beyond the critical period of visual development
Binocular stimulation, software based treatments and other methods do not have
promising result to replace the patching therapy till date
Most of the active therapy methods have good results when used together with
patching therapy
Contact lens for congenital aphakia and other eye conditions for infants and toddlers. The slide presentation encompasses indications for CL fitting in paediatric, contact lens options, fitting techniques, challenges and contact lens as myopia control.
Current Trend in Management of Amblyopia (Amblyopia Therapy)/ Amblyopia Treat...Bikash Sapkota
DIRECT DOWNLOAD LINK ❤❤https://healthkura.com/lazy-eye-amblyopia/❤❤
Dear viewers, to download this presentation visit___ https://healthkura.com/lazy-eye-amblyopia/
Current Trend in Management of Amblyopia. Latest as well as old methods of amblyopia management which include active and passive therapies. Amblyopia Therapy/ Amblyopia Treatment
What would be the perfect amblyopia therapy?
Effective
Good compliance
Acceptable to pts. and parent
Quick
Safe
Easy to administer
Cost effective
Well maintained
..............
Summary
Amblyopia occurs due to abnormal visual experience early in life
Proper optical correction alone is necessary for short period of time (6-8 weeks)
before initiation of other therapy
Part time occlusion of better eye is mainstay of treatment since 18th century to till
now
For severe and moderate amblyopia, 6 hrs and 2 hrs of patching is advised
respectively
Atropine is also used in children with poor compliance
Trial of patching can be given in patients as old as 17 yrs
Perceptual learning and pharmacological manipulation have shown areas of
amblyopia treatment beyond the critical period of visual development
Binocular stimulation, software based treatments and other methods do not have
promising result to replace the patching therapy till date
Most of the active therapy methods have good results when used together with
patching therapy
Gives a very brief review of how to evaluate a case of squint in day to day clinical practice. How to diagnose a basic abnormality of the movement of eye.
This presentation is a detailed description of how a patient should be examined in an oprthoptic clinic. it lists down all the investigations sequentially. the order of investigations mentioned is the best way to investigate a squint case.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...
Prism for-diplopia cybersight
1. Prescribing Prism for
Diplopia in Neuro-
Ophthalmic Disorders
KELSEY MOODY MILESKI, OD, FAAO
EMORY EYE CENTER
ASSISTANT PROFESSOR OF OPHTHALMOLOGY
SECTION OF OPTOMETRY
4. Double vision
Seeing 2 images of the same object
Monocular
Refractive error
Cornea
Lens
Retina
5. Double vision
Seeing 2 images of the same object
Monocular
Refractive error
Cornea
Lens
Retina
Binocular
Not bifoveal
6. Double vision evaluation
History is KEY
BINOCULAR symptom
Direction
Duration
Location
Associated symptoms
History of eye turn or abnormal head position
10. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Unilateral – direction and duration
Alternating – magnitude and pattern
11. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Unilateral – direction and duration
Alternating – magnitude and pattern
When eye is covered, it will move to resting position
ESOTROPIA - EYE RESTS IN
EXOTROPIA – EYE RESTS OUT
HYPERTROPIA – EYE RESTS UP
HYPOTROPIA – EYE RESTS DOWN
17. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Unilateral – tells you direction and duration
Left hypertropia
19. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Unilateral – tells you direction and duration
Left hypotropia or
Right HYPERtropia
23. Examination Tools/Techniques
Prism
Refracting surface that bends light
Used in patients with diplopia to move image to the eye
IMAGE MOVES TOWARDS THE APEX
TO MEASURE:
PUT APEX TO WHERE THE EYE IS
30. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Unilateral – direction and duration
Alternating – magnitude and pattern
31. Examination Tools/Techniques
Sensory
Motor
Ductions/Versions
Cover testing or Maddox rod
Subjective response from patient
Exo and hyper’s are crossed
Eso and hypo are uncrossed
Biousse V, Newman NJ Neuro-ophthalmology Illustrated 2nd ed New York : Thieme; 2016:349-
350
32. Examination Tools/Techniques
Sensory
Worth 4-dot
Randot
Motor
Ductions/Version
Cover test or Maddox rod
Exophthalmometry
Lid evaluation
Double Maddox rod
33. Treating Double Vision
Rule out pathologic cause
Neuro-imaging
Bloodwork
Nonsurgical
Surgical
35. Treating Double Vision
Prism
Goal is binocular vision in primary gaze
Apex of prism is where the eye is
Exotropia: base in prism
Esotropia: base out prism
Right hypertropia: base down prism
Right hypotropia: base up prism
May need 2 pairs of glasses if deviation is different at distance and near
36. Treating Double Vision
Fresnel prism
Press-on lens for alleviation
of diplopia
Can use initially to
determine if patient can
adapt to prism
Good to use if etiology is still
under investigation or
alignment may change
Advantages
Can be put on glasses
immediately in clinic for
relief
Easy to change
Lightweight
Can be prescribed up to 40
PD! – Ideal for large
deviations
Inexpensive
Disadvantages
Blur
Only use in front of one
eye
Visible
Hard (but possible) to
correct both horizontal and
vertical deviations
simultaneously
38. Treating Double Vision
Ground-in prism
Prism built into glasses
prescription
Good to use when
deviation is stable
Advantages
Two clear lenses
Can be split between
right and left eye to
make lenses symmetric
Not easily visible
Easily corrects vertical
and horizontal
Disadvantages
Can only make up to 20
PD total
Time to be made
Expensive
May need multiple
changes
39. Treating Double Vision
Occlusion
Goal is monocular
vision to alleviate
diplopia
Advantages
Diplopia resolves in
all positions of gaze
No additional
glasses needed
Immediate relief
Inexpensive
Disadvantages
Cosmesis
Lack of binocular
vision
43. Double Vision Differential: Brain
Dinkin M. Diagnostic Approach to Diplopia. Continuum (Minneap Minn)
2014;20(4):942-965
44. Double Vision Differential
Brain
Internuclear ophthalmoplegia
Gaze palsy
Skew deviation
Dorsal midbrain syndrome
Neurodegenerative disease
Nerve
CN III
CN IV
CN VI
Neuromuscular junction
Myasthenia gravis
Muscle
Thyroid eye disease
Orbital fracture
Orbital mass
Inflammation
45. Treating Neurologic Conditions with
Prism
Assuming etiology is known or under investigation…
1. Update refraction at distance and near
2. Cover test/Maddox rod without Rx in all positions of gaze at distance
3. Cover test/Maddox rod at distance and near with Rx
4. Trial prism at distance and near
46. Horizontal prism
1. Start with ½ objective measurement and move bar up until fusion
1. Can be placed over either eye
1. Needs to be placed over the paretic eye only if need to move the image to be able
to fixate on it
2. Move bar up and down by 2 PD until fusion breaks – median point is end point
3. Recheck fusion
47. Vertical prism
1. Start with objective measurement and move bar up until fusion
1. Can be placed over either eye
1. Needs to be placed over the paretic eye only if need to move the image to be able
to fixate on it
2. Move bar up and down by 1-2 PD until fusion breaks – median point is end point
3. Recheck fusion
48. Horizontal + Vertical Prism
1. Neutralize larger deviation first (will still be diplopic)
1. Goal: Move image until they are lined up vertically or horizontally
2. Add in second prism over fellow eye
3. If end point is difficult, trial frame Rx and prism and make small changes (1
PD)
4. Can be challenging and time consuming but obtainable
49. Treating Neurologic Conditions with
Prism
Start with Fresnel first
Etiology unknown
Deviation may change
Consider ground-in prism
If any deficit remains
Once deficit is stable
Consider referral for surgical intervention
50. Treating Neurologic Conditions with
Prism
When to refer for surgery
Constant diplopia
Cover testing has been stable for ~1 year
Unlikely to progress
Not undergoing treatment, etc.
Able to achieve fusion with prism
Instead of moving the image to the eye, surgery moves the eye to the image
If unable to fuse with prism, likely won’t be able to fuse after surgery
Goal is single vision in primary gaze – may still be diplopic in other gazes
51. Yoked prism?
Goal: move the image out of defect
Hemianopsia
Nystagmus
Abnormal head posture
Generally a 2 D prism shifts the image by 1 degree
Max 20PD in ground-in glasses
Shift the field by only 10 degrees
Higher amounts with Fresnel
Will require 2 in front of each eye which creates blur and distortion
Better to place sectorially
53. Yoked prism?
Visual neglect
Common in right brain stroke
Patients ignore left side
Turn head to right
Extinction phenomenon when presented with simultaneous stimulus
Prism adaption
Yoked prism to right and perform exercises
Overcompensate to the right
With practice, adapt
Remove prism and naturally move into neglected field
54. Prism challenges
Other ocular comorbidities
Maculopathies
Asymmetric visual acuity
Glaucoma and/or other visual field defects
Not wanting to come out of progressive lenses or have separate glasses
>40D of prism needed
Nystagmus
Suppression
56. Case 1
54 year old male with blurred vision and eye fatigue x 2.5 years
Chief Complaint: Blurry vision:
Gradually worsening at distance with driving and looking to the left
Double vision in the evening and when he turns his face to shave
With and without glasses on
Ocular history: myopia
Systemic history: Hypercholesterolemia, depression
Medications: Atorvastatin, duloxetine
Allergies: NKDA
Social history: Current every day smoker x 27 years
57. Case 1
OD OS
BCVA 20/25-1 20/20
Glasses -2.25+0.50x105 ADD: +2.00 -2.50+0.50x007 ADD: +2.00
Refraction -1.75 ADD: +2.25 -2.50+0.50x178 sph ADD: +2.25
Pupils 5.00→4.00mm 5.00→4.00mm
Confrontation fields Full to finger count Full to finger count
IOP 15 mmHg (iCare) 12 mmHg (iCare)
Exophthalmometry 23mm 22mm
Anterior segment Unremarkable; (-)ptosis Unremarkable; (-)ptosis
Posterior segment Unremarkable Unremarkable
59. Case 1
Diagnosis: LEFT ABDUCTION DEFICIT
Differential
CN VI palsy
Brain
Intracranial course
Myasthenia gravis
Thyroid eye disease
Orbital mass
Duane’s retraction
Pertinent Findings
ISOLATED
No other cranial neuropathies
No horner’s syndrome
No papilledema
No proptosis
No ptosis
No fatiguability
GRADUAL CHANGE OVER LAST 2.5 YEARS
60. Case 1: POLL
54 year old male with blurred vision and eye fatigue x 2.5 years
What type of prism would you like to prescribe?
1. Base in Fresnel prism
2. Base out Fresnel prism
3. Base in ground-in prism
4. Base out ground-in prism
61. Case 1
Started with 6 BO prism
Still diplopic
Increased prism to 10 BO to obtain fusion
Improved clarity when increased to 12 BO
Blurrier when increased to 14 BO
62. Case 1
Fit with 12 BO Fresnel prism
Needs temporary fix
Able to tolerate at distance and near
Order MRI of the brain and orbits W/W/O contrast
64. Case 1
4-month F/U visit
Referred to neurosurgery
MRI monitoring vs radiotherapy
Plans to monitor with MRI only
Motility and cover testing stable
Bothered by cosmesis of Fresnel and requests ground in prism
66. Case 1
Fit with 20 BO Fresnel prism OVER GROUND IN PRISM (12 BO)
Needs temporary fix
Able to tolerate at distance. Will remove glasses for reading
Refer to radiation oncology
F/U after treatment
67. Case 1
4 month F/U
Finished radiation 1 month and 10 days ago
Hopeful for ground-in prism.- took off 20 BO Fresnel and still diplopic
68. Case 1
Fit with 12 BO Fresnel prism OVER GROUND IN PRISM (12 BO)
24 BO too much for ground-in prism
Refer for strabismus surgery consult
Educated that surgery will not be recommended for several months
70. Case 2
72 year old male with CC of blurred vision OD and OS
Notes hard time looking up and down
Problems reading small print like the newspaper
Also problems seeing TV controls
He had gone through a few pairs of glasses without improvement
Current glasses are progressives
71. Case 2
Ocular history:
Cataract OD/OS
Dry eye syndrome OD/OS
Ophthalmic meds: none
Systemic history:
Arthritis
Atrial fibrillation
Hypertension
Hypercholesterolemia
Obstructive sleep apnea
Progressive supranuclear palsy
Medications
Allegra
Amlodipine
Carvedilol
Eliquis
Furosemide
Losartan
Lovastatin
Memantine
Allergies:
NKDA
Surgical history:
Joint replacement: hip and
knee
Hernia repair
Family history:
Hypertension: mother and
father
Social history
Social alcohol
Former smoker: Quit 33 years
ago
72. Case 2
OD OS
BCVA 20/30-2 PH: 20/20 20/25 PH: 20/20
Pupils Equal, round, reactive to light; no RAPD
Confrontation Fields Normal Normal
Motility Restricted Restricted
IOP 14 15
NPC Reduced at 20 cm
74. Case 2
OD OS
Eyelids
2+ blepharitis and
vascularization
2+ blepharitis and
vascularization
Cornea
Tear debris
1+ SPK
Tear debris
1+ SPK
Lens 1-2+ NS 1-2+ NS
Optic disc 0.30/0.30 0.35/0.35
Retina Normal Normal
75. Case 2 POLL
Diagnosis: Convergence insufficiency in the setting of Progressive Supranuclear Palsy
Work-up: Not needed
What type of prism would you like to prescribe?
1. Base in Fresnel prism
2. Base out Fresnel prism
3. Base in ground-in prism
4. Base out ground-in prism
76. Case 2
Updated glasses Rx and trial framed near Rx
Started with 10 BI prism at near
Still diplopic
Increased prism to 14 BI to obtain fusion
Blurrier when increased to 12 BI or decreased to 16 BI
Yoked prism attempted but no benefit
Trialed 2 BI prism at distance and uncomfortable
77. Case 2
72 year old male with blurry vision
Take out of progressive lenses
Fit with 14 BI ground-in prism in NVO
Hold reading material higher
Aids to bring reading material higher
Prescribed DVO without prism
F/U in 4-6 weeks
82. Case 3
Diagnosis: Exotropia and hypertropia OS
Differential
CNIII palsy
CN VI palsy
INO
Skew deviation
Myasthenia gravis
Orbit
Thyroid eye disease
IOIS
GCA
Pertinent Findings
3 mm ptosis, anisocoria and diplopia
No proptosis
Pain
83. Case 3: POLL
55 year old female with double vision and headache
What type of prism would you like to prescribe?
1. Base in Fresnel prism
2. Base out Fresnel prism
3. Base down Fresnel prism
4. Occlusion
84. Case 3
Started with 8 BI rotated clockwise in front of left eye to correct
hypotropia
Still diplopic – diagonal
Increased to 10 BI rotated clockwise in front of left eye
Fusion in primary gaze but diplopic with small eye movements
85. Case 3
55 year old female with double vision and headache
Recommend occlusion
Non-comitant
Unable to fuse with prism
Concern for CN III with pupil involvement
Order CTA head to rule out PCOM aneurysm and MRI brain and orbits W/W/O
contrast
Pending normal imaging consider work-up for MG
Neuro-imaging NORMAL!
88. Clinical Pearls
• Prism can be challenging and time consuming
• Schedule appropriate time slots
• Look for neuro-ophthalmic etiology is patient has not undergone work-
up
• Set patient expectations for prism
• Always bring the patient back for follow-up
• Check to make sure glasses were made correctly
• Don’t be afraid to make changes
• It’s okay to sometimes recommend occlusion
• Eye patch, bangarter or occlusion CL
89. References
Cornblath WT. Diplopia due to ocular motor cranial neuropathies. Continuum (Minneap
Minn) 2014;20(4):966-980
Dinkin M. Diagnostic Approach to Diplopia. Continuum (Minneap Minn) 2014;20(4):942-
965
Eggenberger ER. Supranuclear eye movement abnormalities. Continuum (Minneap Minn)
2014;20(4):981-992
Nerrant E, Tilikete C. Ocular Motor Manifestations of Multiple Sclerosis. J Neuroophthalmol.
2017 Sep;37(3):332-340
Peragallo JH, Newman NJ. Diplopia-An Update. Semin Neurol. 2016 Aug;36(4):357-361
Tamhankar MA, Biouuse V, Gui-Shuang Y, et al. Isolated third, fourth and sixth cranial
nerve palsies from presumed microvascular versus other causes: a prospective study.
Ophthalmology. 2013 Nov; 120(11):1-13