how to demontrate gonioscopy to the external from start to finish step by step

Reading File
Finding Sources
Finding Sources
Searching PubMed

gonioscopy AND examination

Searching the Web

gonioscopy examination technique steps patient positioning indentation grading angle structures

Reading File
Reading File
Reading File
Searching Images

gonioscopy angle anatomy Schwalbe line trabecular meshwork scleral spur ciliary body band diagram

Gonioscopy demonstration for an external examiner

Equipment: slit lamp, clean/disinfected goniolens, topical anaesthetic, coupling gel if using a Goldmann lens, tissue/cotton tip.

1. Introduction and preparation

  1. Wash hands and introduce yourself.
  2. Confirm the patient’s identity and explain:
    “I need to examine the drainage angle of your eye using a special contact lens. I will put in an anaesthetic drop first. The lens may feel like pressure, but it should not be painful.”
  3. Obtain consent. Ask about allergy to topical anaesthetic or previous relevant ocular problems.
  4. Ensure the goniolens has been disinfected and is clean.
  5. Perform this before pupillary dilatation, particularly when angle closure is suspected.
  6. Dim the room lights. Bright light and pupillary constriction can artificially open a narrow angle.
  7. Set the slit lamp to a narrow, short beam at the lowest illumination that still permits viewing. Avoid shining the beam through the pupil.
  8. Seat the patient correctly, with forehead firmly against the headband and chin on the chin rest. Ask them to keep both eyes open and look straight ahead.

2. Anaesthesia and lens placement

  1. Instil one drop of topical anaesthetic into the eye being examined.
  2. Select the lens:
  • Goldmann single/three-mirror lens: needs coupling gel.
  • Zeiss/Posner/Sussman four-mirror lens: usually no coupling gel and permits indentation gonioscopy.
  1. If using Goldmann, put a small amount of coupling gel on the contact surface, avoiding air bubbles.
  2. Ask the patient to look up.
  3. Gently retract the lower lid if necessary and place the inferior edge of the lens onto the inferior cornea.
  4. Rotate/bring the lens onto the cornea smoothly, then ask the patient to look straight ahead. Avoid pressing on the globe.

3. Explain the image orientation

Say to the examiner:
“With an indirect goniolens, I see the angle opposite the mirror. Therefore, to examine the inferior angle, I place the mirror superiorly.”
This is a common viva/OSCE point.

4. Examine the angle systematically

  1. Begin with the inferior angle, because it is generally widest and trabecular pigmentation is often easiest to identify.
  2. Then examine all four quadrants in a consistent order:
  • Inferior
  • Nasal
  • Superior
  • Temporal
For each quadrant, identify structures from anterior to posterior:
  1. Schwalbe’s line
  2. Anterior non-pigmented trabecular meshwork
  3. Posterior pigmented trabecular meshwork
  4. Scleral spur
  5. Ciliary body band
  6. Iris root/recess
A useful spoken sequence is:
“I identify Schwalbe’s line, then the trabecular meshwork, followed by the scleral spur and ciliary body band. The most posterior structure visible indicates the degree of angle opening.”
Gonioscopy is necessary because the angle cannot be directly seen through the intact cornea due to total internal reflection at the tear film-air interface. A goniolens removes this optical limitation. Kanski’s Clinical Ophthalmology, 10th ed., p. 46.

5. Assess and describe what you see

In every quadrant, comment on:
  • Angle width
  • Most posterior structure visible
  • Iris configuration: flat, convex, plateau-like, concave
  • Trabecular meshwork pigmentation
  • Peripheral anterior synechiae (PAS)
  • Any abnormality such as:
    • Neovascularisation
    • Angle recession
    • Excess pigment
    • Pseudoexfoliative material
    • Blood in Schlemm canal
    • Tumour/cyst/foreign material

6. Grade the angle: Shaffer system

Use the narrowest quadrant for the overall grade.
Shaffer gradeApproximate angleStructures/meaning
435-45°Wide open, ciliary body band usually visible
325-35°Open, scleral spur visible
2About 20°Narrow, trabecular meshwork visible, possible closure risk
1About 10°Extremely narrow, high closure risk
00°Closed, no angle structures visible
A practical report:
“The angle is open to the ciliary body band inferiorly and temporally, and to scleral spur superiorly and nasally, with moderate trabecular pigmentation and no PAS.”

7. Indentation gonioscopy, if the angle appears narrow or closed

Use a four-mirror lens.
  1. First document the static view in dim light, primary gaze, without indentation.
  2. Then gently press the lens posteriorly against the central cornea, without excessive force.
  3. Observe the effect:
  • If the angle opens, this indicates appositional closure.
  • If it does not open, this supports peripheral anterior synechiae (PAS).
Say:
“On indentation, the angle opens, suggesting appositional iridotrabecular contact rather than PAS.”
or:
“The area remains closed on indentation, consistent with PAS.”
Indentation moves aqueous toward the angle and pushes the peripheral iris posteriorly. An appositionally closed angle opens, whereas an angle closed by PAS remains closed. Kanski’s Clinical Ophthalmology, 10th ed., p. 47. The basic technique review also stresses grading in dim light, primary gaze, and before indentation.

8. Finish the examination

  1. Remove the lens gently, usually by asking the patient to look up and breaking the inferior seal.
  2. Wipe excess gel from lids and lashes.
  3. Check that the patient is comfortable.
  4. Repeat in the other eye.
  5. Clean/disinfect the lens according to local infection-control policy.
  6. Thank the patient and document findings.

Example of a complete OSCE-style presentation

“Gonioscopy was performed in a dim room using topical anaesthetic and a four-mirror goniolens. The patient maintained primary gaze, and static gonioscopy was performed before indentation. All four quadrants were examined. In the right eye, the angle was open to the scleral spur in all quadrants, with moderate trabecular pigmentation, a flat iris configuration, and no peripheral anterior synechiae or neovascularisation. Indentation did not reveal any additional abnormality. The left eye was examined similarly.”

High-yield errors to avoid

  • Doing gonioscopy in a bright room.
  • Directing the slit beam through the pupil.
  • Pressing too hard with a non-indentation lens, causing corneal folds or artificial angle distortion.
  • Forgetting that the mirror shows the opposite quadrant.
  • Calling an angle open after asking the patient to look too far toward the mirror.
  • Performing indentation before recording the true static angle.
  • Failing to compare all four quadrants and both eyes.

apllanation tonometry demonstation and viva points and disinfection

Reading File
Finding Sources
Finding Sources
Searching PubMed

Goldmann applanation tonometry AND disinfection

Searching the Web

Goldmann applanation tonometry technique fluorescein disinfection guidance prism 2025

Reading File
Reading File

Goldmann applanation tonometry: OSCE demonstration

Equipment

  • Slit lamp with Goldmann applanation tonometer
  • Disinfected prism or disposable cap
  • Topical anaesthetic
  • Fluorescein strip/drop
  • Cobalt-blue filter
  • Tissue/cotton wool

Step-by-step demonstration

1. Introduction and safety

  1. Wash hands. Introduce yourself and confirm patient identity.
  2. Explain the procedure:
    “I will measure the pressure inside your eye using a blue light and a small contact prism. I will first put in an anaesthetic and yellow dye drop. It should not hurt, although you may feel gentle contact.”
  3. Obtain consent.
  4. Ask about:
    • Allergy to local anaesthetic
    • Active red eye, discharge, suspected conjunctivitis or corneal infection
    • Recent corneal trauma or epithelial defect
  5. Inspect the prism. It must be clean, intact, and free of cracks or residue. Ensure it has been disinfected or attach a disposable tip.
  6. Check tonometer calibration according to local policy, ideally before the clinical session.

2. Prepare the patient

  1. Seat the patient comfortably at the slit lamp.
  2. Adjust chin rest and headband. Ensure the forehead is firmly against the headrest.
  3. Ask the patient to keep both eyes open, look straight ahead, relax, and breathe normally.
  4. Instil topical anaesthetic followed by a small amount of fluorescein into the lower conjunctival fornix. Avoid excessive fluorescein.
  5. Ask the patient to blink gently to distribute the drops.

3. Set up the slit lamp and tonometer

  1. Set the Goldmann tonometer dial initially to 1.0, equivalent to 10 mmHg.
  2. Use the cobalt-blue filter.
  3. Set the slit beam to maximum brightness and direct it at approximately 60 degrees to the prism.
  4. Position the prism in front of the corneal apex.

4. Take the measurement

  1. Without touching or pressing on the globe, gently separate the lids if required by holding them against the orbital rim. Do not exert pressure on the eye.
  2. Advance the prism slowly until it just contacts the centre of the cornea.
  3. Look through the slit-lamp oculars.
  4. Identify the two green fluorescein semicircular mires, one upper and one lower.
  5. Ensure the mires are:
  • Centrally placed
  • Equal in size
  • Correct thickness, about 10% of the diameter of the arc
  1. Rotate the dial until the inner borders of the upper and lower semicircles just touch.
“I adjust the force until the inner margins of the fluorescein semicircles are in contact.”
  1. Read the dial and multiply by 10 to obtain IOP in mmHg.
    Example: dial reading 1.8 = 18 mmHg.
  2. Withdraw the prism gently and repeat once to confirm, especially if the reading is unexpected or the mires were suboptimal.
  3. Repeat on the other eye.

5. Complete the examination

  1. Wipe away excess fluorescein if needed and ensure that the patient is comfortable.
  2. Document the IOP, eye, time, technique, and any factors affecting reliability, such as corneal oedema, marked astigmatism, or poor cooperation.
  3. Disinfect the reusable prism or dispose of the single-use cap.
  4. Wash hands and thank the patient.

Short OSCE presentation

“I measured intraocular pressure by Goldmann applanation tonometry. After confirming consent and excluding suspected ocular infection or corneal injury, I applied topical anaesthetic and fluorescein. With the patient positioned at the slit lamp, I used cobalt-blue illumination at approximately 60 degrees and set the dial initially to 10 mmHg. I gently contacted the central cornea with the prism, avoiding pressure on the globe. I adjusted the dial until the inner edges of the two fluorescein semicircular mires just touched. The dial value multiplied by 10 gives IOP in mmHg. I repeated the measurement and documented the result and its reliability.”

Viva points

1. Principle of Goldmann applanation tonometry

It is based on the Imbert-Fick principle:
P = F/A
Where:
  • P = pressure inside an ideal sphere
  • F = force required to flatten its surface
  • A = area flattened
Goldmann tonometry applanates a corneal diameter of 3.06 mm. At this diameter, the opposing effects of corneal rigidity and surface tension of the tear film approximately cancel each other.
Source: Kanski’s Clinical Ophthalmology, 10th ed., p. 43.

2. Why is fluorescein used?

It stains the tear film and produces visible green semicircular mires under cobalt-blue illumination. The endpoint is reached when their inner borders just touch.

3. What is the normal IOP?

Approximately 10-21 mmHg, but interpretation depends on the optic nerve, visual field, cornea, and overall clinical context. A single “normal” reading does not rule out glaucoma, and an elevated reading alone does not establish glaucoma.

4. Why use cobalt-blue light?

It makes fluorescein fluorescence visible, allowing the examiner to see the mires clearly.

5. Why should the patient not squeeze their eyes?

Eyelid squeezing, breath-holding/Valsalva, or examiner pressure on the globe can produce a falsely high reading.

6. Why must the patient not look down at the prism?

Looking down can alter lid/globe pressure and disturb positioning. The patient should look straight ahead, commonly toward the examiner’s opposite ear.

7. Causes of falsely high GAT readings

  • Thick cornea
  • Excess fluorescein: thick mires
  • Corneal scarring or rigidity
  • Corneal oedema can produce variable readings, although commonly falsely low
  • Pressure on globe by fingers/lids
  • Squeezing eyelids
  • Valsalva/breath-holding
  • Tight extraocular muscles, for example thyroid eye disease
  • Marked astigmatism if not corrected for
  • Incorrect calibration

8. Causes of falsely low GAT readings

  • Thin cornea
  • Insufficient fluorescein: thin mires
  • Post-refractive-surgery cornea
  • Corneal oedema
  • Corneal irregularity
  • Incorrect calibration
GAT assumes a central corneal thickness of about 520 micrometres. A thinner cornea generally underestimates IOP, and a thicker cornea generally overestimates it. Kanski’s Clinical Ophthalmology, 10th ed., p. 43.

9. What if astigmatism exceeds 3 dioptres?

Significant astigmatism distorts the mires and may cause error. Align the red mark on the prism holder with the negative axis of the spectacle prescription, or take measurements with the prism 90 degrees apart and use the average. Kanski’s Clinical Ophthalmology, 10th ed., p. 43.

10. Contraindications or situations to defer contact GAT

  • Suspected infectious conjunctivitis or keratitis, especially adenoviral disease
  • Corneal epithelial defect, ulcer, or significant trauma
  • Recent ocular surgery, depending on surgeon guidance
  • Severe patient distress or inability to cooperate
In these situations, use a non-contact or alternative method only if clinically appropriate and consistent with local practice.

11. Alternatives to Goldmann tonometry

  • Perkins handheld applanation tonometer
  • Tono-Pen
  • iCare rebound tonometry
  • Non-contact air-puff tonometry
  • Dynamic contour tonometry
  • Pneumotonometry
Goldmann applanation is often considered the clinical reference standard, but readings must be interpreted in relation to corneal thickness and biomechanics.

Disinfection of the Goldmann prism

Between patients

  1. Wear gloves if indicated by local infection-control policy.
  2. Remove visible fluorescein, tears, mucus, and debris first.
  3. Use the manufacturer-approved protocol and local hospital infection-control policy. Do not assume every prism tolerates every disinfectant.
  4. A commonly cited method for a reusable prism is immersion in 2% sodium hypochlorite for at least 5 minutes, followed by a thorough sterile-water or sterile-saline rinse and complete air-drying before reuse.
  5. Inspect the prism after cleaning. Do not use it if there is cracking, clouding, swelling, roughness, or residual disinfectant.
  6. Consider disposable single-use prisms/caps where available, especially in high-volume settings or where infection risk is a concern.
Kanski notes that 2% sodium hypochlorite is effective against adenovirus and herpes simplex virus. However, repeated disinfectant exposure can swell or crack a reusable tip, and residual disinfectant can cause corneal abrasion. Kanski’s Clinical Ophthalmology, 10th ed., p. 43.
The AAO disinfection guidance cites soaking in 10% household bleach for 5 minutes as an effective protocol. This wording can be confusing because “10% bleach” may refer to a dilution of household bleach, rather than 10% sodium hypochlorite. Follow your specific manufacturer and hospital protocol for the product concentration, soak time, rinsing, and storage.

Important viva statement

“I would not rely on a 70% isopropyl alcohol wipe alone for a reusable Goldmann prism, because it may not provide adequate protection against viral transmission. I would follow the manufacturer-approved and local infection-control disinfection protocol, rinse thoroughly, dry completely, and inspect the prism before reuse.”

Post-exposure / high-risk patient

If there is known or suspected viral conjunctivitis, keratitis, blood/body-fluid contamination, or a prion-risk issue, stop and follow local infection-control escalation and device-manufacturer guidance. Do not use a potentially contaminated reusable prism on another patient.

indirect ophthalmoscopy funsus examination

Reading File
Finding Sources
Finding Sources
Searching PubMed

indirect ophthalmoscopy AND examination

Searching the Web

binocular indirect ophthalmoscopy examination technique systematic peripheral fundus examination

Searching Images

normal fundus examination optic disc macula retinal vessels labelled image

Reading File
Reading File

Binocular indirect ophthalmoscopy (BIO): fundus examination demonstration

Aim: to examine the vitreous, optic disc, macula, retinal vessels, and especially the peripheral retina. It provides a wide, stereoscopic view and is helpful even with some media opacity.

Equipment

  • Head-mounted binocular indirect ophthalmoscope
  • Condensing lens, usually 20 D
  • Dilating drops, if appropriate
  • Tissue
  • Optional scleral depressor/cotton-tipped applicator for peripheral examination

OSCE step-by-step method

1. Introduction, consent and safety

  1. Wash hands, introduce yourself, confirm identity.
  2. Explain:
“I will examine the back of your eye with a head-mounted light and a hand-held lens. The light is bright but the test should not be painful. Your vision may be blurred and light-sensitive if dilating drops are used.”
  1. Obtain consent.
  2. Ask about:
    • Previous adverse reaction to dilating drops
    • History/symptoms of angle closure glaucoma
    • Current red painful eye or acute visual loss
    • Whether they need to drive after dilation
  3. Check visual acuity, pupils, and anterior segment first.
  4. Dilate the pupil unless contraindicated or unsafe. If there is concern for narrow angles, assess the angle before dilatation.
  5. Allow adequate time for dilation, usually 15-30 minutes depending on the agents used.
  6. Advise the patient not to drive until their near vision and glare sensitivity have returned to normal.

2. Positioning and instrument set-up

  1. Dim the room lights.
  2. Recline the patient in a chair or lie them supine. A reclining position helps examination of the inferior retina.
  3. Set the BIO headband comfortably and adjust the interpupillary distance.
  4. Align and focus the illumination beam centrally in the viewing aperture.
  5. Select a 20 D lens for routine examination. Hold it with the flat surface toward the patient.
  6. Ask the patient to keep both eyes open and look at a distant target.

3. Obtain the red reflex

  1. Start at roughly arm’s length, approximately 30-50 cm from the patient.
  2. Direct the illumination through the pupil and obtain a good red reflex.
  3. Hold the 20 D lens between yourself and the patient, centred in the optical path.
  4. Move closer while maintaining the red reflex.
  5. Move the lens gently forwards or backwards until the retinal image is sharply focused.

4. Important orientation statement for the examiner

“The BIO image is real, inverted, laterally reversed, and stereoscopic. Therefore, if the patient looks up, I examine the inferior retina; if the patient looks right, I examine the left peripheral retina.”

5. Examine the fundus systematically

A practical sequence is:
  1. Peripheral retina first
  2. Posterior pole
  3. Macula last or early if central visual symptoms require it
The peripheral retina is often examined first so the patient can adapt to the bright light. Kanski’s Clinical Ophthalmology, 10th ed., p. 41.

Peripheral fundus

  1. Ask the patient to look in the direction that exposes the area you need:
  • To view superior retina, patient looks down
  • To view inferior retina, patient looks up
  • To view temporal retina, patient looks nasally
  • To view nasal retina, patient looks temporally
  1. Examine each quadrant in a consistent order:
  • Superior
  • Temporal
  • Inferior
  • Nasal
  1. Look for:
  • Retinal tears, holes, lattice degeneration
  • Retinal detachment or subretinal fluid
  • Haemorrhages, exudates, cotton-wool spots
  • Chorioretinal scars
  • Neovascularisation
  • Masses or pigmentary abnormalities
  • Vitreous haemorrhage, cells, pigment, or posterior vitreous detachment

Posterior pole

  1. Examine the optic disc:
  • Colour: pink/orange or pale
  • Margins: sharp or blurred
  • Cup-to-disc ratio
  • Neuroretinal rim
  • Disc haemorrhage
  • Swelling or atrophy
  1. Examine the vessels:
  • Artery-to-vein ratio
  • Arteriolar narrowing
  • Arteriovenous crossing changes
  • Haemorrhages, emboli, sheathing or neovascularisation
  1. Examine the macula and fovea:
  • Ask the patient to look directly at the light briefly.
  • Assess foveal reflex, pigmentation, oedema, haemorrhage, drusen, exudates, or membrane.
  1. Compare the two eyes and document the findings.

6. Completion

  1. Switch off the light, remove the lens, and make the patient comfortable.
  2. Explain that blurred near vision and photophobia can persist for several hours after dilatation.
  3. Document the examination, including whether the view was limited by cataract, vitreous haemorrhage, small pupil, or poor cooperation.

Example OSCE presentation

“I performed a dilated binocular indirect ophthalmoscopic examination using a 20 D condensing lens. The patient was reclined in a darkened room. I obtained the red reflex and focused the inverted, laterally reversed stereoscopic retinal image. I examined all four peripheral quadrants systematically, followed by the optic disc, vessels, macula and fovea. In the right eye, the media were clear, the disc margins were sharp with a cup-to-disc ratio of 0.3, vessels were normal, and the macula and peripheral retina were unremarkable with no retinal break or detachment.”

Scleral depression

Use this only after mastering basic BIO, and where there is an indication to assess the far peripheral retina, such as flashes and floaters, trauma, high myopia, or suspected retinal break.

Method

  1. Explain that you will apply mild pressure on the eyelid/white of the eye to see the far periphery.
  2. Use a sterile scleral depressor or cotton-tipped applicator.
  3. To view the superior ora serrata at 12 o’clock:
    • Ask the patient to look down
    • Place the depressor externally over the upper lid at the tarsal margin
    • Then ask them to look up while gently advancing the depressor tangentially to create an internal retinal “bump”
  4. Direct your view to the bump and inspect the retina around it.
  5. Move gradually around the periphery.

Safety

  • Keep the depressor tangential, not perpendicular, to the globe.
  • Do not perform scleral depression in suspected or confirmed open globe injury.
  • Use caution or avoid it in marked inflammation, severe pain, recent surgery, or very thin sclera.
Scleral depression improves visualisation anterior to the equator and permits dynamic assessment of the vitreoretinal interface. Kanski’s Clinical Ophthalmology, 10th ed., p. 41. The AAO BIO overview also describes indirect ophthalmoscopy with scleral depression as the preferred method for detailed peripheral retinal assessment.

Viva points

1. What is binocular indirect ophthalmoscopy?

A head-mounted ophthalmoscopy technique using a condensing lens to produce a wide-field, stereoscopic view of the retina.

2. What type of image does it produce?

A real, inverted, and laterally reversed image.

3. Main advantage over direct ophthalmoscopy?

  • Wider field of view
  • Stereopsis
  • Better peripheral retinal examination
  • Can see through greater media opacity
  • Allows scleral depression
BIO can visualise the retina through greater media opacity than slit-lamp fundus biomicroscopy and facilitates scleral indentation. Kanski’s Clinical Ophthalmology, 10th ed., p. 40.

4. Disadvantages?

  • Lower magnification than direct ophthalmoscopy
  • Requires pupil dilatation for a full examination
  • More difficult to learn
  • Bright light may be uncomfortable
  • Image is inverted and reversed

5. What lens is commonly used?

20 D lens for routine examination.
It gives approximately 3 times magnification and a field of about 45 degrees in standard BIO use. Kanski’s Clinical Ophthalmology, 10th ed., p. 40.

6. What are the uses of a 28 D lens?

  • Smaller pupil
  • Greater field of view
  • Shorter working distance
  • Often useful in children

7. What about a 40 D lens?

It provides lower magnification but a wide field of view and is particularly useful in small children.

8. How do lens power and magnification relate?

They are inversely related:
  • Lower-power lens: more magnification, narrower field
  • Higher-power lens: less magnification, wider field
Approximate magnification = 60 / lens dioptric power. Thus, a 20 D lens gives approximately ×3 magnification.

9. Why dilate the pupil?

To improve the field of view and permit a proper examination of the peripheral retina. A small pupil restricts the view and increases peripheral lens distortion.

10. Why is the patient reclined?

It permits better access to the superior and especially inferior retinal periphery. An upright patient is harder to examine inferiorly.

11. How do you inspect the superior retina?

Ask the patient to look down.

12. How do you inspect the inferior retina?

Ask the patient to look up.

13. What is scleral depression?

External indentation of the sclera that creates an internal retinal elevation, allowing examination of the far peripheral retina and ora serrata.

14. Indications for scleral depression

  • Symptoms of posterior vitreous detachment: flashes/floaters
  • Suspected retinal tear or detachment
  • Ocular trauma, once open globe injury is excluded
  • Lattice degeneration
  • High myopia
  • Fellow eye of a patient with retinal detachment

15. Contraindication to scleral depression?

The key contraindication is suspected open globe injury. Do not exert pressure on a potentially ruptured globe.

16. What should a normal fundus description include?

“Media are clear. Optic disc is pink with sharp margins, normal neuroretinal rim and cup-to-disc ratio. Retinal vessels are of normal calibre. Macula is flat with a normal foveal reflex. The peripheral retina is flat and attached for 360 degrees, with no tears, holes, haemorrhages, exudates or retinal detachment.”

17. Common examination errors

  • Poor alignment of the BIO illumination and viewing system
  • Failure to obtain a stable red reflex
  • Holding the lens upside down
  • Moving the head and lens independently rather than together
  • Examining only the posterior pole and missing peripheral pathology
  • Forgetting the inverted and laterally reversed image orientation
  • Using scleral depression before basic BIO technique is reliable
This is a shared conversation. Sign in to Orris to start your own chat.