I am a ST2/ 2nd year
SHO in ophthalmology and I have just finished part one today. I must thank you
and the contributors for the past questions and information. Again, it proves
that preparation with the mock questions in your question book and the website
was immensely useful (despite the recent change to the style of examination)!
Part A MCQ:
Comparing with the mock questions in the book, the questions in the exam was a
lot easier. There were heavy emphases on anatomy and optics, as well as quite
detail genetics and immunology (e.g. what is PAX gene associated with?).
Fortunately the latter topics were only tested in a handful of questions. Some
of the biochemistry (e.g.
corneal collagens) and instrument (e.g. FFA) questions were almost carbon-copy
of the questions on the website or in the book. Microbiology did not really
involve details of each pathogen.
Part B SAQ:
This is the part that me and my colleagues felt quite tricky. Lot of pathology
and optics that were NOT even in Elkington (!!!). I suppose being ST helps,
because there are quite a few clinical questions. I put down the marks for
each question (as far as I can remember) since I thought it is a good
indicator of how much detail you need to put down. I would also hope that this
feature could be included in your 2nd edition of mock question book.
1. Diagram of orbit and asked to name the
bones + fissures/ foramen (1 mark each)
2. Patient underwent cataract surgery and
developed endophthalmitis. Shown a picture of Bisected globe with ?iris
prolapse, IOL and pus in vitreous
a. name the above mentioned structures (3 marks)
b. describe the sequence of events that might
have led to endophthalmitis (3)
c. name the pathogen leading to endophthalmitis
within 2 days, in 5 - 7 days and in 4 weeks (3)
d. what sample would be useful for culture and
what is likelihood of positive results (1!)
3. Lady with PMH of metastatic bowel Ca.
Picture of bisected globe with vitreous/ ?VH/ subretinal mass & histology of
retina + mass
a. name the above (3)
b. what is the differential of the subretinal
mass (2)
c. histology: name a: retina and b ?mass with
vascular ingrowth (2)
d. what is the most likely diagnosis (1)
e. what is the treatment if the lady presented
earlier, and what is the mode of action (2)
4. Optics of chromatic aberration
a. draw the ray diagram (2)
b. what test is based on this principle and how
it works for myope (2)
c. 4 ways of eye limiting spherical aberration
(4)
d. explain what is oblique astigmatism and coma
(2)
5. Optics of keratometer (bear in mind that
no one has seen one for a long time!!)
a. draw the ray diagram (3)
b. explain how radius could be derived from the
keratometer (3)
c. explain the optical difference in von
Helmholtz and Javal-Schiotz (2)
d. explain, with diagram, how doubling of images
is achieved in either instrument (2)
6. Amsler grid
a. what is the instrument (2?)
b. what visual field does it test (2)
c. explain how the instrument should be used to
test the visual field (4)
d. 2 conditions that is useful (2)
7. Optics (again) of slit lamp - this was
very nasty!!
a. name 4 ways of slit-lamp exam of cornea (2)
b. draw optical diagrams of each of the
examination techniques (2 marks each) - this was NOT in Elkington and most of
us struggled. Would be interesting to see how it turns out. I based my answers
on direct focal/ diffuse/ specular reflection and scleral scatter.
8. Electrophysiology
a. what are the main components of ERG and where
are they derived (4,
very generous!)
b. where are the electrodes for ERG (2)
c. 2 TYPES of conditions in which ERG is
affected (2)
d. what does EOG measure (1)
e. where are the electrodes for EOG (1)
9. Goldmann tonometer with labels & 3
diagrams of menisci
a. what is this and where is it rested on
usually (2)
b. purpose of the prism/ calibration nob/
pressure dial (3)
c. cross section of the instrument (2! ?prism
cross-section only? Or the whole tonometer??)
d. among the diagrams of menisci, which is the
correct applanation (1)
e. which is the one when too much pressure
exerted (1)
f. what would happen with thin corneas (1)
10. OCT of macula with CMO
a. what is the investigation (1)
b. explain the basis of the instrument (4)
c. 2 conditions that could be the cause of this
(2)
d. 3 conditions where OCT is useful (3)
11. Visual field x 2, showing left homonymous
superior quad.
a. how is SITA useful (2)
b. which of the field is more reliable and why
(3)
c. what does it show (1)
d. where could the lesion be (2)
e. 2 conditions in which MD and PSD are
different (2)
12. Statistics: 2 x 2 table of a screening
test
a. Prevalence calculation
b. Yield calculation
c. Positive predictive value calculation
d. Sensitivity calculation
e. Specificity calculation
All 2 marks each, so I believe the maths working
is required. They are straight forward enough not to require any calculators
(so you should know that something is wrong if some funny fraction comes out!)
Overall, I felt the exam was just about
being fair, considering the amount of difficult pathology and optics in part B.