In the end, we counseled him on PALs that can replace the 3 different pairs of reading glasses with just one pair. I hope he will invest in one.
length of exam: 2.5 hours
Things I learned today:
1. Measure optic disk size by placing the slit of light over the disk and then shrinking the slit until its vertical dimensions are the same as the disk. Then read the gauge above the filter settings, units are in mm.

2. Optic disk typing. It helps to categorize what shape each disk is, as some are harder to measure than others.

3. Parks 3 step tends to over-diagnose superior obliques. Longstanding deviations develop comitancy due to other muscles compensating for the paretic muscle (deviations will appear the same on left and right gaze) Think about replacing P3S with computerized Hess plots.
4. 4 ways to treat any BV problem:
- Do nothing
- Orthoptics
- Prisms
- Refer for surgery
6. What is the pathophysiology behind hydrocephalus and sunset eyes?
7. Reminder: Pencil trick, if px talks too much, drop pencil and "as I was saying....". Don't let px hijack your exams. Px hijacks so far: 2
8. Keep a binder full of documents that you will either refer to constantly, or frequently show pxs.
9. BV pyramid (look into this some more)
- Stereopsis
- Sensory fusion
- Fusional reserves
- Accommodation
- EOM function
- VA
11. Reminder: VA charts with numbers at the end ie.
F Z B D 4 = 20/40 = 6/12
O F L C 3 = 20 / 30 = 6/9
12. Smith's technique on ant. chamber depth
- slit and eyepieces at 60 degrees
- rotate slit to horizontal position
- illuminate the cornea, see the reflection of the light on the cornea and on the lens
- widen/shorten the slit length until the cornea bar touches the lens bar
- read gauge, apply conversion factor
14. Pencil pushups do not work
15. Distributers for lenses for biomicroscopy often talk about magnification and field, but what does it really matter when a) the only field you see is the slit width and b) magnification can be toggled on the slit lamp? Get a lens you're comfortable holding in your hands that allows you room to move around and view periphery as well.
16. The only way you can see periphery in high mag is by doing biomicroscopy in various gazes, BIO will not give you such magnification.
17. When trying to neutralize a difficult cyl on ret, try pushing the collar all the way up. This will turn the cyl reflex into a "with" instead of "against", making it easier to neutralize the axis and power.
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