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DIAGNOSING MS
"Is it easy to diagnose MS?"
Diagnosing multiple sclerosis is anything but easy. There is no specific
test for multiple sclerosis and, anyway, it is not even certain that it is
only one disease. To an extent, getting an MS diagnosis (dx) is a process of
eliminating all other possibilities. Typically, people who have finally been
diagnosed with definite MS will have been through several diagnostic stages
which I shall try to deal with in this section. This process is often drawn
out over months or years. This can be a very unsettling and frightening
period for the PwMS - the uncertainty can be very difficult to deal with.
Inevitably, I draw heavily on personal experience here - the fears,
insecurities and other emotions that I went through may not apply to
everyone and I certainly don't intend to shoehorn everyone with MS into my
own stereotype.
"So what are the stages in getting a diagnosis?"
Usually, the first thing anyone does when they notice strange neurological
symptoms is to go to see their family doctor. "It's nothing to worry about"
- "It's a pinched nerve" - "It's the side effect of a virus" - "It's all in
your head" - "It's a temporary side effect of a migraine" - "It's Conversion
Disorder". These and many other labels are used to dismiss what are very
real symptoms. I've even heard of, "You're an alcoholic in denial", being
used to dismiss one poor woman suffering with MS vertigo.
Provided that they aren't dismissive of the patient, I don't blame the
Primary Care Physicians - MS is a very varied disease with a score of
different manifestations. It is common medical practice to assume the most
likely outcome rather than the more malign possibilities. Additionally, MS
has a score of differential diagnoses (conditions that present with one
of more of the same symptoms as MS). PCPs aren't neurologists and they can't
be expected to perform neurological examinations with the same level of
expertise as neurologists can, nor are they as skilled at interpreting them.
This is understandable - a General Practitioner will usually have between
zero and six patients with MS on their books and, even then, rely heavily on
the patient's neurologist for diagnosis and treatment. I had four
neurological examinations in two months - one by my General Practitioner,
one by a casualty Senior House Officer and two by neurologists. The
difference in skill level was immediately apparent and, although the PCPs
detected the more obvious clinical symptoms, both neurologists were able to
detect very many more subtle deficits.
"Is this a difficult time for the PwMS?"
Unfortunately, yes. The process of misdiagnosis causes a lot of anxiety. We
know that something is wrong - often we fear a plethora of malignant
outcomes, including MS, which we generally do not understand at all well at
this point in time. We certainly don't need to be told that we are making it
all up. I was terrified during this stage - more so than when I finally got
a diagnosis and had something to understand and come to terms with.
During this phase, the PwMS may be referred to specialists in completely the
wrong field or sent off for tests for completely different conditions. This
just compounds the uncertainty. The majority of PwMS first present with relapsing/remitting MS and have often completely recovered
from the presenting symptoms within as little as six weeks or less. I was
worried about a number of possible outcomes but wanted there to be nothing
the matter. Nobody wants to have multiple sclerosis. A combination of my
health care professionals' denial and my own enabled me to disregard the
disease for many years. Each relapse was entirely different in nature to
those that had gone before. Each time I was terrified and each time I
apparently recovered completely. During this period, I moved location
frequently and was never seen by the same GP twice which must have prevented
each from building up a case history. Often times, the PwMS will start to
doubt their own perceptions and to believe that they are indeed a
hypochondriac. I know I did - it didn't do too much for my state of mind
but, in a way, I'm grateful for those years of false freedom from the
disease.
"So when do you get to see a neurologist?"
Sooner or later we wind up with a referral to a neurologist. For most people
it is sooner than it was for me. Now come a battery of tests designed to
eliminate the various differential diagnoses. The first thing a neurologist
will do is go through the patient's medical history and that of their
family. It may well be that the patient has had previous symptoms consistent
with multiple sclerosis or have relatives with the disease. This makes MS
more likely. They will then ask the patient to describe their current
symptoms. The patient's description of his/her symptoms is an important
indicator.
The neurologist will then go through a thorough neurological examination,
testing reflexes with hammers, sticking you with pins, tickling the bottom
of your feet, examining you with opthalmoscopes and testing your senses with
tuning forks. You are made to stand still with your eyes closed, walk
heel-to-toe and your muscle strength is tested. The neurologist will be
looking for specific deficits and testing for certain signs.
"What are these deficits and signs?"
There are many different neurological tests and the ones your neurologist
chooses to perform will depend, in part, on the symptoms that you present
with. Here are some of the more common ones.
Romberg's sign: This is a test for ataxia (incoordination or clumsiness of movement that is
not the result of muscular weakness) and involves standing with your feet
together with your eyes closed. Ataxics have great problems standing still
under these conditions.
Gait and coordination: The neurologist evaluates ataxia in various parts of the body by observing
the patient walking normally, walking heel-to-toe and finger-to-nose tests.
The neurologist will also be looking for intention tremor (shaking when
performing small motor movements) as well as ataxia in this last test.
Heel/Shin test: This is a test for ataxia and cerebellar dysfunction. You have to bring the
ball of your heel onto the knee of your other leg and then move it down the
shin.
L'Hermittes sign: This is a test for lesions on the spinal cord in the neck. The neurologist
will ask you to lower your head towards your chest. A positive L'Hermittes
will generate buzzing, tingling or electrical shock sensations in one or
more parts of the body.
Optic Neuritis: This is a condition of the eye caused by inflammation and demyelination of
the Optic Nerve and is perhaps the most commonly presenting symptom in MS.
The tests involve the ubiquitous reading of letters from a board and a test
for colour vision using an "Ishihara" colour chart. An examination with an
opthalmoscope will reveal pallor of the optic nerve in old optic neurites.
Hearing Loss: This is done by lightly clicking the fingers next to each ear and asking the
patient which ear the click was done next to.
Muscle Strength: This involves resisting the neurologist with various muscle groups.
Differences in strength between left and right sides are easier to evaluate
than symmetrical loss unless the weakness is severe.
Reflexes: This is done with both ends of the hammer. The reflexes can be normal,
brisk, i.e. too easily evoked, or non-existent.
Babinski's sign: A test for signs of disease process in the motor neurons of the pyramidal
tract. The test involves drawing a semi-sharp object along the bottom of the
foot. The normal response in adults and children is for the toes to reflex
downwards (flexor response). In babies and people with neurological problems
of the corticospinal tract, the big toe moves upwards (extensor response).
Chaddock's Sign: Similar to Babinsky's but testing for lesions in the corticospinal tract.
The neurologist touches the skin at the outside of the ankle. A positive
response in upwards fanning of the big toe just like in Babinski's test.
Hoffman's sign: This is also similar to Babinski's but involves the hands rather than the
feet. Again it tests for problems in the corticospinal tract. The test
involves tapping the nail on the third or forth finger. A positive response
is seen in flexion of terminal phalanx of thumb.
Doll's Eye Sign: The neurologist is looking for dissociation between movement of the eyes and
of the head. A positive response is when the eyes moves up and head moves
down.
Sensory:
This is done with tuning forks and pins and tests the level of sensory
perception in certain parts of your body.
"Can you get a definite diagnosis from the neurological examination?"
It is very rare to get a definite diagnosis at this stage. Certain signs and
symptoms are more indicative of multiple sclerosis than others, but,
assuming that you do have the disease, the most definitive dx you will get
will be "probable MS". You are much more likely to get a dx of "possible
MS".
The neurologist will probably book you in for several tests including MRI
scans, spinal taps and evoked potential tests.
It is important to note that whatever the results of these tests or the
neurological exam, it is not possible to diagnose definite MS from a single
episode. There are a number of demyelinating conditions of unknown aetiology
which are self-limiting and strike only once. In order to diagnose MS, there
must be at least two episodes separated by at least one month and the
location of the lesions must be in a least two distinct sites in the central
nervous system. This means that the PwMS will, by definition, have to wait
at least the period of time that separate the first two relapses that cause
clinical symptoms. This could be as little as one month but is more likely
to be several months or even years. Often people want a definite diagnosis,
but they certainly don't want to have to have another relapse to prove it.
Catch-22.
Magnetic Resonance Imaging (MRI)
Along with the neurological exam, this is by far and away the most useful
and definitive of diagnostic tools. MRI is a branch of Nuclear Magnetic
Resonance (NMR) a procedure that involves detecting how molecules spin in
powerful magnetic fields. MRI was first used in medicine in 1977 and, though
expensive, it is unparalleled at detecting changes and abnormalities inside
soft bodily tissue. Water molecules, which are present in all soft tissue,
carry a small electromagnetic polarity and, as a result, act like minuscule
magnets. MRI scanners exert enormously powerful magnetic fields around the
patient who lies in a tube in the middle of the scanner. This causes all the
water molecules to wobble and this is detected and imaged on a computer,
from which it can be printed onto a negative.
MRI is completely harmless provided that you do not have any magnetic metals
around your person during the scan. For more details on MRI and safety
procedures, follow this link: Magnetic Resonance Imaging.
MRI scans give detailed high resolution images of cross sections of the
brain and to a lesser extent, the spinal cord. Multiple Sclerosis lesions
show up as paler areas on those images. From an MRI, the neurologist can not
only identify that there have been probable demyelination events but can
also see where those lesions are and use them to explain both present and
potential signs and symptoms.
Surprisingly perhaps, and despite its accuracy, an MRI scan alone cannot be
used to make a definite diagnosis of MS. Clinical symptoms are usually
necessary and, because there are a number of other demyelinating conditions,
these must be ruled out. As already mentioned, the clinician will also want
evidence that there has been at least two identified demyelinating episodes
separated by at least one month in at least two different locations in the
CNS.
Nor do MRI scans always pick up MS lesions. There is evidence that some
older lesions remyelinate sufficiently to be undetectable with MRI scans.
Having said this, the vast majority of people with a definite dx of MS will
show evidence of disease activity on MRI scans.
Spinal Tap
A spinal tap (also known as a lumbar puncture) is a procedure whereby a
sample of cerebrospinal fluid (CSF) is taken from close to the
spinal cord. At the same time a blood sample is taken usually from the arm
and a quantity of blood serum is isolated. Both of these samples are then
processed using a technique called electrophoresis. A positive spinal tap will produce oligoclonal bands in the CSF but not in the blood serum. These
bands indicate a type of immune system activity. Although uncomfortable, the
spinal tap itself is often not too painful, whereas in the period following
the tap, the patient may experience dizziness, nausea, vomiting and severe
headaches, occasionally for as much as a week. There are a few rare but
serious side-effects of spinal taps.
95% of people with a definite diagnosis of MS exhibit oligoclonal bands on a
spinal tap. This may sound impressive but so do 90% of people with Sub-Acute
Sclerosing Panencephalitis and 100% of people with Herpes Simplex
Encephalitis among other conditions. Positive spinal taps are indicative of
an immunological response but they are not diagnostic for a particular
condition. That 5% of PwMS do not exhibit oligoclonal banding means that
spinal taps neither rule-in nor rule-out MS.
The primary purpose of CSF analysis should be to rule out other conditions
than multiple sclerosis. Although they can be highly suggestive of MS, they
do not, in themselves, provide definitive disgnosis. Indeed, I myself, was
given a definite diagnosis based on medical history, clinical examination,
MRI and evoked potential tests - I declined to have a spinal tap.
Before MRI, electrophoresis of spinal fluid played a major role in
supporting diagnoses, the Medical Profession now use a scale called the
McDonalds Criteria to assimulate a diagnoses.
In April, 2001, an international panel in association with the NMSS of
America recommended revised diagnostic criteria for multiple sclerosis.
These new criteria have become known as the McDonald criteria after their
lead author. They make use of advances in MRI imaging techniques and are intended to replace the Poser Criteria and the older Schumacher Criteria. The new revised criteria are as
follows:
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However, CSF analysis technology is still advancing and researchers continue
to look for definitive molecular markers of MS. Should they find such a
marker, spinal taps will reassume their importance. Other researchers are
looking into urine and blood for markers and we can hope that they are
successful and spinal taps become completely unnecessary to the diagnosis of
multiple sclerosis.
Evoked Potential (EP) tests
Evoked Potential tests are procedures for measuring the speed of impulses
along neurons. Responses can be measured using EEG readings from electrodes attached to the scalp and
occasionally other areas of the skin. Although this may sound like something
from Frankenstein, they are in fact completely painless and entirely
harmless. Based on input signals to the particular sense being measured, the
time taken for that response to register can be accurately measured and
compared to normal readings. The results are then analysed on a computer and
average speeds recorded.
Demyelinated neurons transmit nerve signals slower than non-demyelinated
ones and this can be detected with EP tests. Although they may appear to
function perfectly, even remyelinated neurons are slower than normal nerves
and so historical lesions can be detected in this way.
There are three main types of evoked potential test:
Visually Evoked Potential (VEP)
This test measures the speed of the optic nerve. The patient has to focus on
the centre of a "TV" screen on which there is a black and white chequered
pattern. Each square in the pattern alternates between black and white at
measured intervals. The patient wears a patch on one eye for a while and
then on the other, so that the speed of both optic nerves can be measured.
85-90% of people with definite MS and 58% of people with probable MS will
have abnormal VEP test results.
Brainstem Auditory Evoked Response (BAER)
The BAER test measures the speed of impulses along the auditory portion of
Cranial Nerve VIII. This nerve arises in the Pons area of the Brainstem and
therefore this test may be indicative of lesions in that area. The patient
lies down in a darkened room to prevent visual signals from interfering with
measurements. A series of clicks and beeps are played back to the patient.
67% of people with definite MS and 41% of people with probable MS will have
abnormal BAER test results.
SomatoSensory Evoked Potential (SSEP)
The SSEP test involves strapping an electrical stimulus around an arm or
leg. The current is switched on for 5 seconds and electrodes on the back and
skull measure the response at particular junctions. The current is very low
indeed and completely painless. The speed of various nerves can be measured
in this way and the points of slow-down (i.e. demyelinated lesions)
approximated to because of the sampling at several places.
77% of people with definite MS and 67% of people with probable MS will have
abnormal SSEP test results.
Slow nerve responses in any of these tests are not necessarily indicative of
MS but can be used in conjunction with a neurological examination, medical
history, an MRI and a spinal tap to deduce some kind of diagnosis.
CT scans
Computed Tomography scans use X-rays to produce images of the brain. CT
scanners look a lot like MRI scanners and are also used to produce
cross-sectional images of internal parts of the body. However, CT scans
detect soft body tissue with far less precision that MRI scans and their use
has largely been replaced by them. Since CT scans use X-rays which are
potentially very harmful, this is no bad thing. Sadly, MRI scanners are much
more expensive than CT scanners and many areas where MS is relatively common
do not have access to them.
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