This document provides a brief history and overview of optical coherence tomography (OCT). It discusses that OCT was first used to image the retina in 1991 with a resolution of 17 μm. Commercially available OCT systems emerged in 1996 and provided cross-sectional retinal images with 10 μm resolution. The document then outlines the development and advantages of newer spectral domain OCT technology, which offers higher resolution, faster scanning speeds, and 3D imaging capabilities compared to earlier time domain OCT. A variety of clinical applications of OCT are also reviewed.
OPTICAL COHERENCE TOMOGRAPHY (SKIN OCT)....
Optical coherence tomography (OCT) is an established medical imaging technique that uses light to capture micrometer-resolution, three dimensional images from within optical scattering media (e.g., biological tissue). Optical coherence media (e.g., biological tissue). Optical coherence tomography is based on low coherence interferometry, typically employing near-infrared light. The use of relative long wavelength light allows it to penetrate into the scattering medium. Confocal microscopy, another optical technique, typically penetrates less deeply into the sample but with higher resolution.
OCT is a great technology,Many ophthalmologist find very difficult to understand it ,SO I have tired to simplify it as much as possible .Hope everyone can understand now onwards the basic about OCT .
Every feedback s most welcomed sothat i can improve further in coming days
Please email your feedback to me in the following address
yourgyanu@gmail.com
Flexible fiberoptic catheter used for light delivery
OCT enhances imaging resolution that may permit the evaluation of clinical (e.g., luminal measurements during PCI) and research (e.g., fibrous cap thickness and strut levelanalysis) parameters for the interventional cardiologist.
This presentation is mainly focused on the clinical diagnosis and interpretation of oct macula.This is presented on 4th year optometry as topic presentation.
OPTICAL COHERENCE TOMOGRAPHY (SKIN OCT)....
Optical coherence tomography (OCT) is an established medical imaging technique that uses light to capture micrometer-resolution, three dimensional images from within optical scattering media (e.g., biological tissue). Optical coherence media (e.g., biological tissue). Optical coherence tomography is based on low coherence interferometry, typically employing near-infrared light. The use of relative long wavelength light allows it to penetrate into the scattering medium. Confocal microscopy, another optical technique, typically penetrates less deeply into the sample but with higher resolution.
OCT is a great technology,Many ophthalmologist find very difficult to understand it ,SO I have tired to simplify it as much as possible .Hope everyone can understand now onwards the basic about OCT .
Every feedback s most welcomed sothat i can improve further in coming days
Please email your feedback to me in the following address
yourgyanu@gmail.com
Flexible fiberoptic catheter used for light delivery
OCT enhances imaging resolution that may permit the evaluation of clinical (e.g., luminal measurements during PCI) and research (e.g., fibrous cap thickness and strut levelanalysis) parameters for the interventional cardiologist.
This presentation is mainly focused on the clinical diagnosis and interpretation of oct macula.This is presented on 4th year optometry as topic presentation.
DR WANI'S TALK ON Optical coherence tomography of posterior segment FOR KLE ...vbwani
This presentation gives info about 1) History of OCT
2)basics of OCT
3) how it differs from USB scan
4) generations of OCT
5)how the posterior segment OCT is captured
6)normal retina and its layers on the OCT,
7) what abnormalities to look for OCT
8) common retinal diseases and their OCT appearance
this slide sharer contents are basic principle of CT fluoroscopy , software and hardware parts of equipment and image aqua cation and radiation dose comparison and videos related to equipment .
Optical coherence tomography (OCT) uses near-infrared light to generate high-resolution images of coronary arteries in vivo.
The near-infrared light with a wavelength of about 1.3 μm is invisible to the human eye.
To generate cross-sectional images, OCT uses low-coherence interferometry by measuring the echo time delay and intensity of the light reflected from internal structures in tissue.
Review of the imaging modalities in Glaucoma. Structural loss precedes functional loss. Presentation includes a review of OCT, HRT and GDxVcc for posterior segment as well as AS-OCT and UBM for anterior segment.
NW2012 Intraocular Lens Design and Effects on VisionNawat Watanachai
some information about intraocular lens materials, designs; and their effect on surgery and visual function.
I'm sorry that i one i previously uploaded was the wrong file.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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
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
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
- 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
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
1. A brief history of OCT
Nawat Watanachai
Sir Charles Gairdner Hospital
October 2007
2.
3. OCT : Optical Coherence Tomography
1st OCT image of the retina
Resolution: 17 μm
depth ~1.5 mm into the
tissue
• Huang, Hee, Fujimoto, Puliafito 1991
• 1st in vivo retinal images at the MIT in 1993
• Commercially available in 1996
• Optical B-scans (Cross-sections)
• Resolution ~ 10 microns
5. Clinical Applications
Visualization of vitreoretinal interface
Cross-sectional visualization retinal pathology
Nerve fiber layer analysis for glaucoma
Optic nerve head analysis for glaucoma
Other jobs eg. Anterior segment
6. Does OCT make a difference?
Clinical Diagnosis/
Decision Making
Medical Record/
Documentation
Patient Education/
Satisfaction
7. Medical Proof
OCT provides objective evidence for treatment
decisions, both to treat or not to treat, and of
response to treatment
Examples:
CNV and AMD
cystoid macular oedema
Macular hole
retinal vein occlusion
PMF
diabetic maculopathy
Others eg fleck diseases
8. Time domain OCT
Current clinical OCT devices utilize time domain
technology ---> limit in signal acquisition time
700-900 nm*
Samples tissue with 1024 data points
over 2mm depth
Z Dimension:
Takes a sample every 5-60 microns
apart, 128-512 scans
X-Y Dimension:
9. Time domain OCT : problems
1 detector, Each A-scan requires the movement of
several mechanical parts
Excellent image quality…if device and patient are
not moving
10. Time domain OCT : problems
~400 A-scan per sec
take time to catch the image
Can give poor image resolution
No image registration --> not easily reproduce
Error in both quantitative and qualitative
measurement in some situations
11. So, what are we looking for in the newer OCTs?
•
•
•
•
Higher resolution
Higher imaging speed
Image registration
Quantitative information
extraction
12. Newer OCTs
1. Spectral domain OCT -- available
2. Other OCTs
2.1 Ultrahigh resolution OCT
2.2 Adaptive optic OCT
2.3 Hybrid machines eg OCT/SLO, HRA/OCT
3. OCT for anterior segment
14. 1. Spectral domain OCT
High speed high resolution OCT
Frequency swept light source at around 850-1040 nm
Improved axial image resolutions (<6 microns axial
resolution appears possible)
15. 1. Spectral domain OCT
The output is measured with
the use of a spectrometer
(may be > 2,000 detector
elements), doesn’t need
moving part during scanning
16,000-75,000 scan/sec
(TD-OCT ~400)
16. 1. Spectral domain OCT
Real time display and data streaming capabilities
enable video-rate imaging at more than 30fps
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
17. 1. Spectral domain OCT
Can produce 3-D projection image which can be aligned
with the actual fundus image to provide pixel-to-pixel
registration
3-D imaging produces layers of information
Isolation of retinal layers makes image analysis possible
in a broad fashion
3-D thickness map
QuickTime™ and a
Microsoft Video 1 decompressor
are needed to see this picture.
18. 1. Spectral domain OCT
Pixel-to-pixel registration
Precise scan location
Image reproducibility
Some machines can
generate fundus imaging
and register the spatial
location of each OCT
section image
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
19. 1. Spectral domain OCT
Pros
Higher resolution/ 3D imaging
Enhanced imaging speed
Pinpoint registration
Cons
Signal strength and depth resolution is dependent on the
path difference between the retina and the reference mirror
--> the greater the distance (myopic eye), the weaker the
signal and the lower the resolution
Yes………it’s price!
20. 2. Other OCTs
2.1 Ultrahigh resolution OCT
2.2 Adaptive optic OCT
2.3 Hybrid machines eg OCT/SLO,
HRA/OCT
21. 2.1 Ultra-high Resolution OCT
First described by Drexler and Fujimoto in 2001
Broad bandwidth, 150nm femtosecond Ti-sapphire
laser source (TD-OCT 10-25 nm)
1-3 microns axial resolution
QuickTime™ and a
decompressor
are needed to see this picture.
22. 2.1 Ultra-high Resolution OCT
Video-rate with up to 25-50 B-scans/sec
3,000 axial pixels and 600 transverse pixels (OCT-3
1,024 and 512 pixels)
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
24. 2.1 Ultra-high Resolution OCT
Pros
Enhanced anatomic
detail
Enhanced
visualization of the
subretinal CNV
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
25. 2.1 Ultra-high Resolution OCT
Cons
Slow acquisition time of 4-5 sec (OCT-3 can do
the job in 1.3 sec)
Require significant technical support for day-today operation
Limited ability to localize scans in relation to
precise fundus landmarks
Alignment of serial scans dependent on fixation is
inaccurate
26. 2.2 Adaptive optic OCT
Use electromagnetic deformable mirror (adaptive
optic) to improve the spatial resolution
Correct chromatic aberration of the eye to get
better light pathway
27. 2.2 Adaptive Optic OCT
Pixel resolution of 3µm x 3µm
Very fine image : able to Imaging the retinal cells
28. 2.2 Adaptive optic OCT
3D video
Voxel resolution of 3µm x 3µm x 3 µm
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
29. 2.3 OCT/SLO : multimodal imaging
Introduced by
Podoleanu and Jackson
in 1998
Employs OCT scan
simultaneous with
confocal SLO images
SLO = surface detail
OCT = internal detail
30. 2.3 OCT/SLO : multimodal imaging
Single illumination source with parallel detector
systems ensures pixel-to-pixel correlation between
views
Overlay capability permits view of internal anatomy
beneath surface landmarks
QuickTime™ and a
Cinepak decompressor
are needed to see this picture.
31. 2.3 OCT/SLO : multimodal imaging
Coronal OCT scans capture details often lost in
fixation-driven B scanning
SLO channel facilitates integration of functional
testing such as angiography, microperimetry, and
mfERG
34. 2.3 OCT/HRA
OCT + laser angiography
Image registration --> precisely define the scan
location -->good for repeat measurement
Record fundus image in the same time
35. 2.3 other multimodaling machines
Ultra-high Resolution OCT/SLO
Combined Spectral Domain/ Time Domain HighResolution OCT/SLO
36. Will you own this machine?
Keeps in mind
OCT has become gold standard for some diseases
eg. PMF, MH
Non invasive
limitation
OCT does NOT provide dynamic information (FA
does)
Depend on operator techniques
Degraded in the presence of media opacity
Computer can do wrong things
37. Which OCT is ‘the one’ for you?
devices
B-scan/ 3D
Axial
resolution
Scanning
speed
Non-OCT
imaging
(TD-OCT)
Yes/no
10
400
Near IR
Heidelberg
Spectralis
HRA/OCT
Yes/yes
7
40,000
SLO, ICG, autoF
Optopol Copernicus
2
Yes/yes
6
25,000
Near IR
Optovue RTVue1001
Yes/yes
5
26,000
Near IR
OTI OCT/SLO1
Yes/yes
5
28,000
SLO, ICG,
microperimetry
Topcon 3D-OCT10002
Yes/yes
6
18,000
Near IR/ color
Carl Zeiss Meditec
Cirrus1
Yes/yes
5
27,000
LSLO
38. Which OCT is ‘the one’ for you?
Time domain OCT (~60,000+ AUD)
Spectral domain OCT (>100,000 AUD)
Researchers
Retinal specialists who can use this
images to help with decision making in
selected difficult cases
OCT brought the ability to regenerate cross-sectional reconstructions from infrared A -scan images reconstructed in a B-scan format by linear scanning.
Supportive evidence for decisions of whether to treat or not; measurable objective evidence of whether disease is present or changing