to point you at www.examintelligence.com, where the new
blog and website are being maintained!
See you there!
Being an attempt to gather thoughts on passing the Final FRCA, and other random matter associated with not studying for it when one should be...
See you there!
The SAQ paper was set on February 28th 2008. At this meeting the members of the SAQ group noted
that some of the repeat questions continued to be poorly answered, and that questions relating to
issues of public interest and patient safety were poorly done. Although matters relating to patient
safety are not textbook knowledge, they will continue to be part of the syllabus and candidates can
expect that the examiners will emphasise this important aspect of the College’s work.
Firstly, an adiabatic change is one in which NO HEAT is TRANSFERRED TO or FROM a fluid (gas/liquid) doing work, or having work done on it. Normally this occurs when there is a change in pressure in a gas.
In other words, as a gas is compressed, it’s temperature will increase. Have you ever pumped up your bicycle tyre, and the nozzle or barrel of the pump has got really hot, almost too hot to touch by the time you’ve finished pumping the last bit of air in? That’s because of adiabatic HEATING. Diesel engines work on the same process of compression generating enough heat to cause ignition. There is no external source of heat, but the temperature has still increased. This must all have come from the act of pumping, i.e. pressurising, the air. The energy of the pumping has been converted to heat energy (internal energy) of the compressed gas.
Conversely, if a gas is suddenly allowed to expand, it will cool. A CO2 fire extinguisher (They used to be solid black, didn’t they? Now we’ve just got those EU compliant red things with different labels on. How the hell are you supposed to recognise the difference in a hurry now?? – Ed.)…when it is used, or any gas cylinder opened and allowed to vent suddenly will rapidly cool. In fact, if you are using a CO2 extinguisher, don’t put your hand on the funnel, because it might freeze to it. Why does this happen? As the gas expands, it does work on the surrounding air, pushing it out of the way. Since energy cannot be created or destroyed, merely converted from one form to another, the energy has to come from somewhere, and it comes from the internal energy of the gas doing the expanding, which we conveniently refer to as temperature.
So, as a gas is compressed or expands rapidly, it’s temperature changes, but no HEAT energy has been transferred into or out of the system. If heat is added to or lost from the surroundings, this is NOT a-diabatic. So for example a gas expanding as a result of being heated is not adiabatic, and a gas contracting as a result of being cooled is not adiabatic either. These processes involve a transfer of heat energy.
Eventually, after the sudden compression or expansion, there will be a transfer of heat energy, but at the time of the expansion or compression, there is not.
And that, in a nutshell, is adiabatic changes.
(It also happens with magnets, apparently, and they’re not fluids…- Ed.) Okay, yes it does happen with magnets, but don’t try and complicate the issue. (If you want to know more, see Adiabatic Demagnetisation on Wikipedia, but make sure you have your maths head on. You have been warned!)
where:
The last question we can tell you about, as intelligence
received has run thin in the last 24 hours, was a
pharmacology question which came up about the use of
NSAIDs, including the pathway and enzymes they act on and
the implications of their use and the controversy of COX-2
selective inhibitors and why increased cardiovascular
deaths occurred.
EI is going to take a (quite frankly well deserved) break
for a few days, before starting to home in on further
tips, tricks and techniques for studying, learning,
remembering and most importantly passing the Final
Examination.
Please keep visiting, as there is something new on the
horizon which is going to be developed behind the scenes,
and will initially be released in bits and pieces before
coming together in one fell swoop.
Congratulations to all those who passed, and our
comiserations for those of you that didn't. Stick with EI
and we will try to bring you information to maximise your
chances of success.
Secondly, for those doing the Final FRCA in the
future....the grapevine has told us that The Clinical
Anaesthesia Viva book is going to reach us in a second
incarnation sometime soon, so keep your eyes peeled for
that one....
If you have any information you want to share, please pass
it on to examintelligence"AT"googlemail.com .
Good luck to anyone still awaiting their viva!
Just to cover the further questions...
The remaining question in the morning was about epidural
abscess:
-Why do people get them? Predisposing factors?
Looking for usual: cleaning, asepsis, repeated attempts,
duration of catheter in situ, diabetes, pre-existing
infection
-How do you recognise it?
Signs and symptoms.
-How do you diagnose it?
-Investigations?
Make sure you get in that it is an emergency.
In the afternoon: "Here comes the science bit..."
-What is the anatomy of the pleura?
-What is the clinical significance to the anaesthetist?
-What is its function?
-What are the problems associated with eg.
pleurodesis/pleuradhesis (pick your spelling!)?
-What can accumulate in the pleura?
-How do we manage that?
-How would you manage a man with a small pneumothorax
before surgery who requires a GA? (What about RA?)
-Tell me a bit about work of breathing.
Then, next up:
-What are the functions of the placenta?
-Tell me abot diffusion. (What are the principle factors
influencing it?)
-What drugs cross the placenta?
-How?
-What other mechanisms of things crossing the placenta do
you know?
-What drugs cross by facilitated diffusion?
-Tell me about local anaesthetics and the placenta.
-What about neuromuscular blockers?
-What hormones does it produce? (Stumbled a bit over
saying beta-human chorionic
gondaotrophin/gonadotropin...!)
-What are their functions?
-Tell me about oxygen crossing the placenta. (Me: "Ah,
we're talking about the difference between fetal and
maternal/adult haemoglobin now, aren't we...so the thing
here is...." - made the examiner smile!)
Then switched examiners and had standard latex allergy
question, as per Bricker, pretty much, with a little
sideline into types of adverse drug reaction, type 1,2,3,4
allergic reactions and management of anaphylaxis, and
finally onto delivery of oxygen/medical gases to the
operating theatre. For this, make sure you know about
VIE, how it works, where it's located, why, and about N2O
cylinder manifolds and any special considerations to do
with temperature.
Reports from other sources tell me that a question
involving a certain kyphoscoliotic lady for
cholecystectomy (though elective this time) has appeared,
and also questions on management of a child with fractured
tib/fib and head injury (short case)....
Watch this space for developments.
NB: IF YOU ARE TAKING THE FINAL IN THE FUTURE, WATCH THIS
BLOG FOR MORE EXAM INTELLIGENCE RELATED ARTICLES!
Everyone has been asking me what I was asked, so here is a
brief breakdown. Other people got asked slightly
different questions.
Long case: (essentially the same case as in The Clinical
Anaesthesia Viva Book for Rhabdomyolysis).
24 year old male.
Recently been admitted to medical ward, weak and drowsy
(GCS 14).
History of depression, alcohol abuse and ??intravenous
drug use.
Conscious level improved with 200 mcg naloxone - became
agitated
His blood pressure is 80/40 mmHg and he has cool and
clammy peripheries.
He has a heart rate of 56.
Arterial blood gases on air after dose of naloxone:
pH 7.27
pO2 8.2 kPa
pCO2 5.72 kPa
HCO3- 20 mmol/L
SaO2 87.6%
U&E
Na 131 mEq/L
K 7.9 mEq/L
Ur 13.? mmol/L
Cr 331 umol/L
CK 49,960 IU
ECG Charcateristic low flat P waves, Broad Bizarre QRS
and Tall Tented T Waves with HR 56
CXR CVP line in situ in RIJ. Bilateral ?lung base
shadowing (difficult to see on photocopy, but Right
Cardiac Border vague, ?consolidation/collapse) No
pneumothorax seen. Left base ?increased opacity
Questions
(They never asked me to summarise the case)
- He is drowsy, and you've been told his GCS is 14. How
would you assess his GCS?
- What are the components of GCS?
- Can you tell me what makes up the Motor component of
GCS? (What movement gives you what score?)
- What could be causing his depressed GCS?
- What about other metabolic causes? (Looking for BM)
- What do you think of his ABG? Does the PaO2 worry you?
(Yes, he's a young fit healthy guy who should have a much
higher PaO2
- So, how are you going to manage this patient when you
first see him? (ABC, 100% O2, IV access, CaCl2,
Insulin/Dextrose, IV NaCl (avoiding K+)).
- Anything else? (Having established his GCS is 14 and
maintaining own airway).
- What about his airway? What if he was not opening his
eyes, making incomprehensible sounds and flexing to pain?
(Intubate, Thio 375mg, cricoid pressure, Roc 50mg
(assuming no predictors of difficult airway present), size
8.0 COETT and off to ICU).
I made sure I got the point that this was rhabdomyolysis
across, and mentioned I would fluid resuscitate, encourage
urine output to avoid depositions in the kidneys, and
would do CVVHF. They never went into any detail with me
about the management of it though, and never asked the
differences between CVVHF and dialysis (though they did
ask some people).
Next up:
- You're anaesthetising a young, fit healthy chap, you
give him Fentanyl and Propofol and then you are unable to
ventilate him with a facemask.
They were looking for simple airway adjuncts first, I
mentioned an LMA as well (they said they'd come to that
later).
- What's the problem with a nasopharyngeal airway?
Trauma to the nasal mucosa.
- What other things might be stopping you from
ventilating?
Laryngospasm, bronchospasm, chest wall rigidity
(fentanyl), foreign body (unlikely/rare in this instance),
secretions/plugging???
- What about more proximally? Any non-patient factors?
Machine, gas supply, obstruction in circuit.
- How would you deal with that?
(I wouldn't bloody have them because I check my machine!!)
Erm, check each part of the connections of the circuit, if
in any doubt, switch to ventilating with Ambu Bag from
back of machine and oxygen cylinder.
- If you still can't ventilate him, what are you going to
do? What about a laryngoscopy?
Not in a patient with just fentanyl and propofol. I would
consider giving him suxamethonium and then laryngoscopy?!
And if I can't intubate him? That's can't intubate,
can't ventilate, so cricothyroid puncture.
- Could you just let him wake up?
Yes, but in the meantime, he needs to be oxygenated, so I
would do the cricothyroid puncture.
Okay, so then a flexion/extension C-Spine X-ray, which
made my heart sink.
- What is this?
- What are the changes?
- What's this at C1-C2? (Subluxation)
- Where else do you get subluxation? Is it just C1-C2?
Erm....no, it could happen at other places to.
- Where?
C7-T1....? (Didn't really know the answer to that one.
Almost lost the plot at this point and was very gratified
to get a smile from the examiner).
- How would you manage this patient?
Carefully, not too much flexion/extension.
- Are there any ways of predicting difficult airway?
Mallampatti, Sternomental, Thyromental, Wilson.
Combination is better, one alone is poor predictor.
This one the examiner had to prompt me a bit with the
X-ray, pointing things out and asking what the abnormality
was, what this and that were, which was obvious once I saw
it, but was annoying, and was my worst moment in the whole
exam.
(I'm afraid that I will have to stop writing here due to
work commitments, but hopefully that helps a
little....more will follow.....)
No-one is sure how to accurately predict the chances of someone having an MI or sudden cardiac death whilst they are having an anaesthetic. We can make an estimation (for example that 56% I mentioned) based on complex scoring systems (Goldman Cardiac Risk Index for example), but can’t say for certain that one person will have problems, whilst another definitely will not.
So how many scoring systems/assessment methods are there? I can’t tell you. Too many. The most common one is the Goldman Cardiac Risk Index, but there are others such as the Detsky system (a calculator may be found here), Lee’s Revised Cardiac Risk Index and more!
And then the AHA/ACC go and publish another document!
One way of practicing critical thinking and prioritisation
is to try and answer viva questions with only five
critical words (key words). You can try doing this for
either a big topic or a subsection of a question when you
are practicing. Obviously you will need a friend, and an
ideal answer or example of a very good answer laid out in
front of you.
By practicing this Five Word Viva Game, when it comes to
the real thing you will have an advantage. It will help
your exam technique in several ways.
Firstly, when you practice it will make you think very
carefully about anything you DO know about the topic, and
you will formulate an answer which at least gives an
overview. One of the most difficult things to do in the
exam is to get away from waffle. You start answering a
question and then end up using lots of filler words, which
take up time, but don't go anywhere near answering the
question. Suddenly the bell goes, and ooops... By
summarising down to five important key words you have
automatically got the main points in your head, you are
more likely to say those than waffle, and you can get away
with using filler words a bit more (but should still try
and avoid anything which is not relevant).
Secondly, if you don't know anything about the topic when
your...friend...asks you the really difficult question
about immunoglobulins, when you go off and read about it,
and then try and figure out "What are my five key points I
need to get across for answering a viva question on this?"
then you have to process the information you have read.
This makes your brain form associations using that
information. You "intra-integrate", so to speak, the
information within itself, and you also "extra-integrate"
with information you already know and have thought about.
This means that you are more likely to remember it at
another time, and will actually allow you to trigger off
more information at another time.
An example of five words:
Q:Tell me a little bit about the immune system.
A:Innate, acquired, lymphocytes, antibodies, complement.
Q:Tell me a little bit about the innate immune system.
A:Barrier (skin/secretions), non-specific, phagocytosis,
cytotoxic, cytokines
Q:Tell me a little bit about acquired immunity.
A:(Previous) exposure, lymphocytes (B&T), antibodies
(ADGEM), specific, T-helper
So hopefully you see what I mean.
Now obviously it doesn't have to be five words, it could
three or seven, but five is a nice number, and three is
really too few for some of the topics. The point is, that
you aim to slim down to key words. Better yet if you can
associate those key words with key images, but I'll talk
about that another time.
Do you have any useful tips/tricks/comments to make about
passing Primary or Final FRCA? If so please contact me by
using the comments page.
I mentioned earlier that I like to try and sit down and
decide what I intend to learn from a particular study
session. What I hadn't thought about was that I should
define a period of time I am going to spend on doing the
learning. There appear to be a couple of reasons that
make setting a goal and a time limit a good idea.
Firstly, if we decide on what it is we are intending to
learn, we avoid meandering around a lot and ending up
becoming distracted by concepts or ideas that are not
central or essential to what we want or need to learn. If
you read an article and don't understand a concept, you
can usually read to the end of the article without
understanding the concept, and grasp the central tenet of
the article anyway. If each time you didn't understand
something you went off and looked it up, several things
would happen. You would waste time looking it up, and you
would get distracted from your main theme.
Secondly, there is something called the serial position
effect.
When asked to repeat back a list of things they have just
been told, people will usually (not always) start with the
last thing they were told (called the recency effect),
then more than likely some of the first few things they
were told (the primacy effect) and then those things in
the middle are least well remembered. By working
continuously without interruption for lengthy periods of
time, we don't give ourselves beginnings and endings
(primacy and recency) to recall from, and if we don't set
ourselves a time limit or a "learning limit" or "learning
goal", we are less likely to stop work. (This appears to
me to be a special application of Parkinson's Law, where
work will simply expand to fill the time available, and by
giving ourselves an indefinite time to finish, we could
give ourselves and indefinite and infinite amount of
work).
Thirdly, there is always the "fear of the unknown".
Imaging you want to learn the contents of e.g.
Fundamentals (Pinnock et al) or Miller's Anaesthesia, or
(my favourite) Hutton. How many pages are there in each
of those books? (963, 3376 and 1072, in case you were
wondering). A lot. Imagine sitting down and starting to
read at page ONE, only to read all the way through? Every
time you stop and come back, you still have "1072 pages
less whatever I read so far" to go. Or are you a glass
half-full kind of chap/chapess and think "I've read this
many pages, fantastic"? And how long is it going to take
to read (well you could work it out, I suppose)? This
uncertainty of the amount of time it will take is almost
certainly going to be a millstone around your neck.
So what am I trying to say here?
Well, basically it boils down to: when studying, set
yourself a goal, and set yourself a (realistic) time in
which to achieve that goal. Take a break when you've got
to the end of that goal to allow primacy and recency a
chance to exert their power, and then come back to your
studying. Which is where I'm going now.
The areas of particular interest are cranial nerves,
sympathetic and parasympathetic nervous system, triangles
of the neck, epidural and spinal anatomy, paravertebral,
costal/intercostal/diaphragmatic anatomy, anatomy of the
airway including lungs, femoral triangle, cervical, lumbar
and sacral nerve plexi (or should that be plexuses?),
anywhere where a nerve runs that we can stick a needle,
and of course vascular anatomy...
Erm...quite a lot then.
Quite frankly I personally can't be bothered to go back to
the anatomy books to start from scratch about learning all
this stuff, but we have discovered a former urology
surgeon who now teaches anatomy at Cambridge has
co-authored a book which some of you may have seen at
college. Instant anatomy is a fantastic little book, full of simple
diagrams and lists. Even better than this, though, is the
website, which is cheaper (read free), but also provides
the opportunity to buy a CD-ROM, a snip at £17.99. Full of diagrams, podcasts
and PowerPoint presentations, we've found it an invaluable
aid in our...revision (ahem). Simply pop it in your
computer, get out your popcorn/pizza/wild boar and venison
sausages and chianti/Tamatar Dal (that's Dal with
tomatoes, apparently best done with Urad Dal, which I
haven't tried) and salad, click, sit back and relax as you
absorb the information in your own personal lecture.
PS: Sadly I get no commission for encouraging anyone to
buy it, but it really is a good CD...
I did, however, find this, which seems to be a fairly straightforward, as long as you
recognise that a "tuberculin syringe" (or TB syringe) is
very very similar to what we might call an "insulin
syringe" (see here), that "anode tubes" are reinforced ET tubes, and
remember that Pentothal is the trade name for Sodium
Thiopental.
Another little resource is the SNACC website (Society for
Neurosurgical Anesthesia (sic) and Critical Care), which
has this little guide on it.
In all honesty I think, however, that the questions are
more likely to be asked on principles, such as ICP (and
management) and Cerebral Blood Flow (and that nice graph
with the three lines for MAP, PaCO2 and PaO2 on it plus
effects of anaesthetic drugs). There might be a mention
of air embolism and management in a sitting neuro case...
