Ophthalmoscopy
A clinical examination of the posterior segment by the means of an ophthalmoscope.
It is primarily done to assess the state of fundus and detect the opacities of ocular media.
Ophthalmoscope
An instrument that allows the ophthalmologist to look inside a person’s eye and see the details of the living retina
Scleral lens is a large rigid contact lens with a diameter range of 15mm to 25mm. Its resting point is beyond the
corneal borders, and are believed to be among the best vision correction options for irregular corneas. Wearing scleral lens also can postpone or even prevent surgical intervention as well as decrease the risk of corneal scarring.
Scleral lens is a large rigid contact lens with a diameter range of 15mm to 25mm. Its resting point is beyond the
corneal borders, and are believed to be among the best vision correction options for irregular corneas. Wearing scleral lens also can postpone or even prevent surgical intervention as well as decrease the risk of corneal scarring.
Presenters :
Jenil Shelsiya
Sisira PS
Gopika Jyothirmayan
Special Thanks To Sushma Shrestha
and Mentor Deepak Rai (Optometrist).
If any query,Viewers are requested to refer to book for detailed explanation or can ask me question directly in the comment box. Answers will be given from Presenter's side.
Presenters :
Jenil Shelsiya
Sisira PS
Gopika Jyothirmayan
Special Thanks To Sushma Shrestha
and Mentor Deepak Rai (Optometrist).
If any query,Viewers are requested to refer to book for detailed explanation or can ask me question directly in the comment box. Answers will be given from Presenter's side.
Retinoscope is an objective refraction instrument used to
determine the spherocylindrical refractive error, as well as
observe optical aberrations, irregularities, and opacities.
The technique is called Retinoscopy/Skiascopy/Shadow Test
. Introduction Biomicroscope derives its name from the fact that it enables the practitioner to observe the living tissue of eye under magnification. It not only provides magnified view of every part of eye but also allows quantitative measurements and photography of every part for documentation.
3. • The lamp facilitates an examination which looks at anterior segment, or frontal structures, of the human eye, which includes the –Eyelid –Cornea –Sclera –Conjunctiva –Iris –Aqueous –Natural crystalline lens and –Anterior vitreous.
4. Important historical landmarks De Wecker 1863 devised a portable ophthalmomicroscope . Albert and Greenough 1891,developed a binocular microscope which provided stereoscopic view. Gullstrand ,1911 introduced the illumination system which had for the first time a slit diapharm in it Therefore Gullstrand is credited with the invention of slit lamp.
These lectures has prepared for postgraduate student (Ophthalmology) according to the curriculum of Bangladesh College of Physician and Surgeons (BCPS) and Bangabondhu Sheikh Mujib Medical University (BSMMU) Bangladesh
these slides explain the objective refraction in optometry , and describes its types and its measurement , and it gives you in details the types of Retinoscopy.
A Classroom presentation, showing the various types of slit-lamps, their parts, and other accessory instruments that can be used with it for enhanced optometric clinical examination.
Eyelid laceration repair with defects.pptxSHAYRI PILLAI
PRINCIPLES OF EYELID REPAIR
Wounds should be copiously irrigated and explored, with the removal of any foreign material after local anesthesia
Reconstruction should be done in layers as per correct anatomical orientation
Wounds should not be extended to explore structures unless the exploration is for suspected foreign body
The orbital septum if damaged should never be repaired-result incompromised eyelid excursion and even lagophthalmos
Vernal keratoconjunctivitis (VKC) is a chronic, bilateral, at times asymmetrical, seasonally exacerbated, allergic inflammation of the ocular surface, involving tarsal and⁄or bulbar conjunctiva
More common in children and young adults
Has an atopic background
First mentioned in the ophthalmic literature as conjunctiva lymphatica more than 150 years ago
More common in the summers than in the winters
Pseudoexfoliative material is a grey-white fibrillary substance
Age related multifactorial, progressive disorder
Material is deposited on various ocular structures includes-
- Lens capsule
- Zonular fibres
- Iris
- Trabeculum
- Conjunctiva
Deposits in blood vessels,skin, gall bladder, kidneys,lungs,heart and meninges
Ocular surface squamous neoplasia (OSSN) includes spectrum of disease from mild dysplasia to carcinoma in situ to invasive squamous cell carcinoma
Involving conjunctiva and cornea
Usually in the interpalpebral area, mostly at the limbus
Uvea consists of the middle, pigmented, vascular structures of the eye and includes the iris, ciliary body, and choroid
Uveitis is broadly defined as inflammation (ie, -itis)of the uvea (from the Latin uva, meaning "grape")
It emphasizes the close relationship between the anatomically distinct parts of the uveal tract, for inflammatory processes tend to involve the uvea as a whole and are generally not limited to a single region
PCR- breach in the posterior capsule of the crystalline lens during cataract surgery
Common complication
Lead to sub-optimal visual outcomes if not recognized early or managed appropriately
Complication varies with the stage at which it occurred or was recognized
Consequent Vitreous loss -major determinant of post-operative outcomes
TASS
Toxic solution enters the anterior chamber
Produce severe intraocular inflammation as well as corneal edema
Form of sterile, noninfectious endophthalmitis
Endophthalmitis
Present in an acute form or in a more indolent or chronic form the latter is associated with organisms of lower pathogenicity
Since de Wecker first described the “filtering cicatrix”, as a surgical treatment for glaucoma in 1882
Glaucoma filtering surgery (GFS) differs from most surgical procedures in that inhibition of wound healing is desirable to achieve surgical success
Testing colour vision requires elaborate apparatus for scientific investigation. There are two objectives in testing for colour blindness
(i) the exact nature of the defect and
(ii) whether the subject is likely to be a source of danger to the community.
After the tunnel has been dissected with crescent knife
Entry is made into the anterior chamber at 10 O’ Clock
position with MVR/V-Lance 20G blade
Viscoelastic is injected to make the eyeball hypertensive
A special property of the cone system is color vision.
Perceiving color allows humans (and many other animals) to discriminate objects on the basis of the distribution of the wavelengths of light that they reflect to the eye.
The perception of color is a response to electromagnetic energy at wavelengths between 400 and 700 nm, which is absorbed by cone outer segment visual pigments.
The degree to which a beam of light is deflected as it
passes through the lens depends on the focal and prismatic power of the lens and the distance from its optical centre.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- 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
5. Ophthalmoscopy
A clinical examination of the posterior segment by the
means of an ophthalmoscope.
It is primarily done to assess the state of fundus and
detect the opacities of ocular media.
Ophthalmoscope
An instrument that allows the ophthalmologist to look
inside a person’s eye and see the details of the living
retina.
6. TECHNIQUES OF USED FOR FUNDUS EXAMINATION
Three methods of examination used in Ophthalmoscopy
are:
Distant direct ophthalmoscopy
Direct ophthalmoscopy
Indirect ophthalmoscopy
7. Slit-lamp biomicroscopic examination of the fundus by:
Indirect slit-lamp biomiscroscopy
Hruby lens biomicroscopy
Contact lens biomicroscopy
8. HISTORY
1848- Babbage invented ophthalmoscope
1850- Helmoltz direct ophthalmoscope
1852- Reute 1st mono ocular indirect ophthalmoscope
1864- Nagel indirect ophthalmoscope
1946- Charles Schepens modern binocular indirect
ophthalmoscope
10. OPTICS:
An internal relay lens system re inverts the initially inverted
image to a real erect one, which is then magnified.
This image is focusable using the focusing lever.
12. PARTS:
It consists of-
Illumination rheostat at its base.
Focusing lever for image refinement.
Filter dial with red free and yellow filters.
Forehead rest for proper observer head positioning.
Iris diaphragm lever to adjust the illumination beam
diameter.
13. ADVANTAGE:
Field of view similar to IO.
Erect real image similar to DO.
DISADVANTAGE:
Lack of stereopsis
Limited illumination
Fixed magnification.
15. INTRODUCTION
The binocular indirect ophthalmoscope or indirect
ophthalmoscope, is an optical instrument worn on the
examiner’s head and sometimes attached to spectacles,
that is used to inspect the fundus or back of the eye.
It produces an stereoscopic image.
16. Applicable to all refractive errors.
Beam penetrates opacities in most media.
There is a reduced image size.
A wide view of the retina and its defects can be
obtained.
17. OPTICAL PRINCIPLE
The principle of IO is to make the eye highly myopic by
placing a strong convex lens in front of patient’s eye so that
the emergent rays from an area of the fundus are brought
to focus as a real, inverted image between the lens and the
observer’s eye.
An aerial image is formed.
20. In the indirect method of ophthalmoscopy a powerful
convex lens (called the condensing lens) is held in front
of the patient's eye. The usual powers used are +20 D
and +13 D.
The illuminating light beam passes the condensing lens
into the eye and light reflected from the retina is
refracted by the condensing lens to form a real image
between the condensing lens and the observer.
The observer studies this real image of the patient's
retina
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-174
21. Image formed by indirect ophthalmoscope
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-174
22. PREREQUISITES:
Darkroom
Source of light and concave mirror or self
illuminated indirect ophthalmoscope.
Convex lens (now-a-days commonly employed
lens is of +20 D)
Pupils of the patient should be dilated.
24. Illumination is usually provided by an electric lamp
mounted on the observer's head.
Light from this source is rendered convergent by the
condensing lens.
A convergent beam enters the patient's eye and is
brought to a focus within the vitreous by the eye's
refractive system.
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-174
25. The light then diverges to strike the retina.
The illumination is therefore bright and even, as it
comes from the real image of the light source within
the patient's eye.
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-174
27. The condensing lens is held in front of the patient's eye
at such a distance that the patient's pupil and the
observer's pupil are conjugate foci.
Light arising from a point in the subject's pupillary plane
is brought to a focus by the condensing lens in the
observer's pupillary plane.
Conjugacy of pupil
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-175
29. A reduced image of the observer's pupil is formed in
the subject's pupillary plane (the image of a 4 mm pupil
is approximately 0.7 mm).
The observer's pupil is the 'sight-hole' of the system
and its size influences the field of view.
Construction of the reduced image
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-175
30. The field of view is also limited by the aperture or size
of the condensing lens.
Only those rays which leave the subject's eye via the
image of the observer's pupil and which then pass
through the condensing lens will be seen by the
observer.
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-175
32. Light emerging from the patient's eye is refracted by the
condensing lens to form a real image of the retina
between the condensing lens and the observer.
The image is both vertically and laterally inverted (upside
down and back to front).
It is situated at or near the second principal focus of the
condensing lens, i.e. approximately 8 cm in front of a
+13 D lens .
Elkington A.R.et.al Clinical Optics 3rd EditionU.K. P-177
PROCEDURE
33. The observer holds the condensing lens at arm's
length and thus views the image from a distance of
40–50 cm.
To see the image clearly the observer must
accommodate or use a presbyopic correction.
The binocular indirect opthalmoscopes have +2.0 D
lenses incorporated in the binocular prismatic
eyepieces so that the observer does not need to
accommodate.
Elkington A.R.et.al Clinical Optics 3rd Edition U.K. P-177
34. Examiner stand opposite the clock hour position to be
examined, e.g., to examine inferior quadrant (around 6
O’clock meridian)or the examiner stands towards
patient’s head (12 O’clock meridian) and so on.
By asking the patient to look in extreme gaze, and using
of scleral indenter, the whole peripheral retina up to ora
serrata can be examined.
36. A retinal indenter will both increase the peripheral view
and throw some retinal lesions into relief (for example,
retinal tears) so they are more easily seen.
The patient is asked initially to look up or down to
facilitate placement of the indenter through the lower
or upper lid respectively.
Indentation
37. The patient then looks towards the indenter and the
examiner gently presses on the indenter; a small
indentation should be seen in the peripheral retina.
The indenter is gently moved round the eye, and
again the examiner needs to move around the patient
to maximise the view.
40. Linear Magnification= ab/AB
Angle aCF = angle ANB because Ca and AN are parallel
Tan aCF= ab/CF =tan ANB =AB/BN
Therefore
ab/AB = CF/BN
CF is the focal length of the condensing lens. BN is the
distance between the nodal point and the retina of the
subject's eye.
Elkington A.R.et.al Clinical Optics 3rd Edition U.K. P-178
41. The exact values depend on the distance from which the
observer views the real image of the subject's retina, and
upon the distance between the condensing lens and the
subject's eye if this is ametropic .
Elkington A.R.et.al Clinical Optics 3rd Edition U.K. P-178
42. The refractive state of the patient's eye affects the size
and position of the real image formed by the condensing
lens.
Indirect ophthalmoscope. Relative positions of the image
Elkington A.R.et.al Clinical Optics 3rd Edition U.K. P-179
43. All rays emerging from an emmetropic eye are parallel.
Rays emerging from a hypermetropic eye are divergent,
and the real image is therefore formed outside the
second principal focus of the condensing lens.
Emergent rays from a myopic eye are convergent, and
the real image is therefore always within the second
focal length of the lens.
Elkington A.R.et.al Clinical Optics 3rd Edition U.K. P-178
45. Comparison of view within the same fundus using the indirect
ophthalmoscope and the direct ophthalmoscope in DR
46. Biomicroscopic examination of the fundus can be
performed after full mydriasis using a slit-lamp and any
one of the following lenses:
Indirect slit-lamp biomicroscopy- +78 D, +90 D small
diameter lenses is presently the most commonly employed
technique for biomicroscopic examination of the fundus.
Hruby lens biomicroscopy- Hruby lens is a
planoconcave lens with dioptric power 58.6D. This lens
provides a small field with low magnification and cannot
visualize the fundus beyond equator.
47. Contant lens biomicroscopy can be performed by
following lenses:
Posterior fundus contact lens is a modified
Koeppe’lens.The image produced by it is virtual and erect.
Goldmann’s three-mirror contact lens
consists central contact lens and three mirrors placed in
the cone, each with different angles of inclination .
With this the central as well as peripheral parts of the
fundus can be visualized.
48. A, +78D or +90D, small diameter lens. B, Hruby lens; C, Posterior
fundus contact lens (modified Koeppe’s lens); D, Goldmann’s three-
mirror contact lens.
49. VOLK DOUBLE ASPHERIC LENSES
HISTORY
In 1956,aspheric ophthalmic lenses for subnormal vision
were developed by Dr. David Volk. He found that an
aspheric surface corrected the aberrations present in more
common spherical lenses.
Several developments ocurred up to 1982 when all Volk
lens for indirect ophthalmoscopy were redesigned with both
surfaces aspheric, providing substantial improvement in
image quality.
50. INTRODUCTION
Volk’s 60D,78D and 90d fundus lenses have establishes
slit lamp indirect ophthalmoscopy as comprehensive
fundus evalution.
Examination of the retina by Slit lamp and Volk double
aspheric lenses is called a Bio microscopic Indirect
Ophthalmoscope BIO.
51. Characteristics
Stereoscopic,3 dimensional view of the retina.
Binocular viewing through the slit lamp.
Better image achieved when viewing through
media opacities like cataract.
Allows for manipulation of the image.
Slit lamp magnification filters.
Image size less affected by patient refractive error.
52. Slit-lamp-based indirect lenses
90 D lens
Used to carry out indirect ophthalmoscopy using the
slit lamp as a light source.
Gives more magnification than with a conventional
indirect ophthalmoscope, but may not give such ready
access to the retinal periphery.
53. It is a useful technique for the examination of the optic
disc posterior pole and relatively peripheral retina.
An advantage is that examination of the central fundus
can also take place with minimal or no dilation of the
pupil, although a more accurate examination is always
achieved with a dilated pupil.
Other commonly used non-contact lenses are variants
of the 90 D such as the 60 D, the superfield NC
(non-contact) and the 70 D lens.
54. Procedure
The slit beam is positioned vertically and centrally in
front of the patient’s pupil.
The short mirror should be in place.
The lens is held in parallel to the patient’s cornea and
close to it. The examiner’s fingers can be used to
support the eyelids.
The slit beam thus passes through the lens and pupil
to the retina.
55. The slit lamp is then slowly drawn backwards and
towards the examiner whilst the examiner maintains
a view through the binocular eyepieces until the
inverted retinal image comes into focus.
The slit beam is manipulated to vary the area of
retina being illuminated and the patient asked to look
in the relevant direction to view different areas of the
retina.
56. The lens is tilted to look at various parts of the
peripheral fundus .
Adjustment to the focus also allows the vitreous to be
seen.
The system of examination is similar to that outlined for
the direct ophthalmoscope.
59. Indications
Useful method of examination for patients in a general
clinic to obtain a view of the fundus, even when the
pupil is not dilated.
Gives a reasonably magnified image and a good field
of view.
The optic disc is well seen and the stereoscopic view
is useful in analysing the neuroretinal rim.
It is also a useful method for delivering laser energy to
the fundus, for it does not disturb the corneal surface,
giving a clear image.
There are two types of Indirect ophthalmoscope: Monocular indirect ophthalmoscope and binocular indirect ophthalmoscope
The binocular indirect ophthalmoscope or indirect
ophthalmoscope, is an
optical instrument worn on the examiner’s head and sometimes attached to spectacles, that is used to inspect the fundus or back of the eye.
applicable to all refractive errors as its beam penetrates opacities in most media and there is a reduced image size, it is possible to obtain a wide view of the retina and its defects
The principle of indirect ophthalmoscopy is to make the eye highly myopic by placing a strong convex lens in front of patient’s eye so that the emergent rays from an area of the fundus are brought to focus as a real, inverted image between the lens and the observer’s eye.
In the indirect method of ophthalmoscopy a powerful convex lens (hereafter called the condensing lens) is held in front of the patient's eye. The usual powers used are +20 D and +13 D. The illuminating light beam passes through the condensing lens into the eye and light reflected from the retina is refracted by the condensing lens to form a real image between the condensing lens and the observer. The observer studies this real image of the patient's retina
, In indirect ophthalmoscopy, the observer’s pupil (O) and patient’s pupil (P) are conjugate to avoid “wasting” light. B, If the condensing lens is too close to the patient’s eye, the peripheral retina will not be illuminated. C, If the condensing lens is too far from the patient’s eye, light from the patient’s peripheral retina will not reach the observer’s eye.
Indirect ophthalmoscope. The field of view is limited by the image of the observer's pupil O1 in the subject's pupil S and by the aperture of the condensing lens. (a) When a large aperture condensing lens is used, the field of view is limited only by the observer's pupil O1. (b) When a small aperture condensing lens is used, it is the lens aperture that limits the field of view.
If this distance BN is taken to be 15 mm, the linear magnification is equal to the focal length of the lens (in mm) divided by 15. Thus, the linear magnification of a +13 D lens (f = 75 mm) is approximately × 5, while the linear magnification of a +20 D (f = 50 mm) lens is approximately × 3. The angular magnification also can be calculated, and once again a +13 D lens magnifies approximately × 5 while a +20 D lens magnifies approximately × 3. The exact values depend on the distance from which the observer views the real image of the subject's retina, and upon the distance between the condensing lens and the subject's eye if this is ametropic .
The image of the retina of an emmetropic eye is always located at the second principal focus of the condensing lens, regardless of the position of the lens relative to the eye.