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On average eight young sportspeople die every
year from an undiagnosed heart defect. We look at what is being done
by the John Ibbotson Memorial Fund to promote awareness of this.
In October 2005, John Ibbotson died suddenly at
the age of 27. He was a talented all-rounder who turned pro at 20 and
raced in Belgium and Italy before finding his true metier as a coach,
with his own business called Fit-For. The cause of his death was a
heart abnormality that simply caused it to stop beating.
Ibbotson had no symptoms of the abnormality before
his death, but it could have been detected with a simple test. When
his mother and fiancé set up a fund in John's name to support young cyclists
who shared 'Ibbo's' ambition as a young rider, to reach the top level of
road racing, they were determined to include cardiac screening as part of
their package of support.
On their way
Now the fund has enough money to support two young
riders for a year, racing with two French clubs, in 2008. They are Mat
Green and Tom Copeland, both from John's home county, Surrey. John's
friend, and a man closely involved with the fund, Russell Clarke, explained
the selection process to us and more importantly the screening the riders
went through:
"We were looking for two riders to benefit from
the legacy of what John was trying to do before he started his coaching
business. Keith Butler from the Surrey Cycle Racing League helped us
to pick the riders and we settled on Matt Green, who has ridded the Ras in
Ireland, and Tom Copeland, who is being coached by Sean Yates. Sean
seems to think that Tom has some potential.
"Tony Mills, who used to own one of our local bike
Shops, Dauphin Sport, and now lives in Brittany, sorted our places for Matt
and Tom is two Breton clubs. We've got enough money to support them
for a year, but before they went we wanted to give them a full MOT on their
hearts."
The Ibbotson Fund turned to a UK charity called
CRY for this. CRY stands for Cardiac Risk in the Young, and it was
formed by Alison Cox, the wife of British pro tennis player Mark Cox, whose
son went to America to pursue his tennis career and was found, by an athlete
screening process they had there, to have an undiagnosed and potentially
life-threatening heart defect.
At the time, although it was known that there were
a number of unexplained sudden deaths among young athletes, no such
screening processes were easily available in Britain, so Mrs Cox set up CRY
in 1995, to increase awareness of Sudden Adult Death Syndrome (SADS).
The charity has grown and recently it launched a
far-reaching study into the problem, called Save Our Athletes. It is
funding a screening programme using the latest equipment available and
headed by Professor Grey Whyte who, as well as holding a number of other key
positions, is the director of science and research at the English Institute
of Sport.
Support
At the launch, which was attended by athletes from
many sports, including Olympic medallist Rob Hayles, Professor Whyte said:
"The Save Our Athletes project will be world
leading, enabling CRY to research the role of cardio-vascular screening, and
allowing us to fully identify disorders capable of causing sudden cardiac
death."
Under Whyte's auspices, the charity opened a
centre for sports cardiology at the Olympic Medical Institute at Northwick
Park Hospital in Harrow. So, when the Ibbotson fund heard that CRY
were offering subsidised screening using the latest equipment from Royal
Philips Electronics at the centre, they applied to have Green and Copeland
tested there.
"We heard that it was where the British Olympic
Association were doing a lot of their screening" says Clarke. "The
test was a full MOT on their hearts. They had an ECG and an ultrasound
test, and they were both given a complete all clear.
"Since John's death I've become really aware of
heart problems in athletes and how they might have been undiagnosed in the
past. Just in my own area, we've had Sean Yates with his problem, and
another top rider, Russell Fenton raced for years at a high level and has
only recently found out that he had a problem.
"When you think about it, there have always been
stories of riders just dropping dead. It's often been put down to
drugs, but it has made me think now that the problem is much more common."
Yates, whose heart problem emerged after his pro
career was over, says. "Testing is common sense. The two of them will
probably get more when they get to their clubs in France."
The Ibbotson Fund has pledged to support CRY in
its current campaign to introduce screening for teenagers in secondary
schools, as well as Olympic-level athletes, and promoting their subsidised
screening programme at Harrow, Colchester and in Northern Ireland. CRY
also has a mobile unit that visits sports clubs, schools and local
communities.
It makes sense at any time of life to have a
complete physical check-up if you are involved in sport. Some national
cycling bodies already make it a condition of their issuing a racing
licence, although British Cycling doesn't at the moment.
One day, CRY hopes to make the screening of young
sportspeople a routine precaution that everyone goes through.
CRY testing
The tests on Matt Green and Tom Copeland were
carried out a Northwick Park by cardiac screener Clare Farrell. She
explained the process.
"The electrocardiogram was a resting, non-invasive
look at the electrical activity of their hearts. The reason it is done
is to compare the reading against normal heart reading. By comparing
measurements of the trace the heart produces, looking at things like the QT
interval, against a normal trace, you can detect any abnormalities in the
structure of the heart, such as HCM.
"The ultrasound gives you a picture of the heart
in action. From that you can check the various dimensions of the heart
and you can see the blood flowing into and out of it. This shows any
abnormalities or restrictions that might be present and will require further
investigation by a consultant cardiologist.
Heart defects that cause sudden death in young
people
We look at the main two causes, both of which can
be detected by screening.
Heart-related sudden death in older people is
usually due to coronary heart disease (blocked arteries n the heart), but
sudden death in people who are less than 35 years old is usually due to
hereditary conditions. The most common is Hypertrophic Cardiomyopathy
(HCM), followed by Arrhythmogenic Right Ventricular Cardiomyopathy
(ARC).
HCM
This is sometimes called chunky heart disorder.
It is uncommon, although as many as 10,000 people might have it in the UK.
Heart muscle in a normal heart is arranged in an ordered way and, although
it may become thickened as a result of athletic training, it keeps its
ordered shape and doesn't interfere with blood flow. It may also
become thickened due to height blood pressure.
However, in Hypertrophic Cardiomyopathy cases, the
heart muscle fibres are arranged haphazardly and become thickened for no
apparent reason, making the heart vulnerable to potentially fatal heart
rhythms.
HCM is caused by abnormalities in the genes that
make the proteins responsible for the heart contraction. The condition
affects either sex and all ethnic groups, and abnormal growth can even begin
the in the foetal heart."
The symptoms and severity of HCM vary - many
sufferers do not even show any symptoms at all and suspicions are raised
when another family member is screened or diagnosed. It is also quite
common for nothing to be know until unexplained sudden death occurs.
However, any shortness of breath, chest pains, palpitations or light
headedness and blackouts should be checked by a GP as soon as possible.
Diagnosis is by investigation of the heart's
electrical signal by an electrocardiogram (ECG), but the gold standard test
is by looking at the heart while it's working by using ultrasound
techniques. Clinics supported by CRY carry out both of these tests.
ARVC
This disorder results in the progressive
replacement of normal right ventricular muscle tissue by fibrous tissue and
fat. The problem can also spread to other heart chambers. It's
not known why this happens but the condition is believed to be genetic.
Again, it affects both sexes and all ethnic groups, but there is a larger
than average distribution of this disease in northern Italy and a lot of the
research work has been done there. The children of an affected person
have a 50 per cent chance of inheriting this disease.
Symptoms include bouts of rapid heartbeat,
associated with light headedness or fainting. Unusually for a heart
complaint, shortness of breath and chest pains are rare. Diagnosis of
the disease is very difficult as its presence may not show on ECG's and
techniques have to be combined to investigate it thoroughly. If
routine screening has revealed any suggestion that this disorder may be
present, patients are referred for further investigation using more
specialised techniques.
The Subjects
We asked the two Ibbotson-funded riders what the
tests they underwent were like, and what difference the results have made to
them.
Matt Green
How old are you Matt?
19
Tell us what the ECG was like
"It was no problem if you don't mind taking your
shirt off with people watching. They just stick a load of electrodes
on your chest and you lie still. There was no discomfort at all.
Where will you be based in 2008 and how long
will you be there?
I'll be living in Rennes and riding for a club
called VCR Point P. The fund is supporting me in France from February
until September.
How much training are you doing at the moment?
I'm full-time, so about 25 hours a week and it's
soon to go up.
You got an all-clear after both tests, is that
a useful thing to know, bearing in mind how much work you are doing?
Yes. A heart problem is something I've never
thought about, so to be prompted to go and be checked out was good. I
suppose it gives you the peach of mind to get on with your training.
Tom Copeland
How old are you Tom?
18
What was having the ultrasound heart test like?
They rub gel all over your chest and just move a
sensor around on it. You don't see anything while this is happening.
Then later they put all the pictures together and
you see a video of your heart working. I thought it was a good thing
to see, because not many people will see their own hearts.
Have the tests made a difference to you?
Yes, it's good to know that you've got back-up
like that. It's good to know that you are OK and that you've got
nothing physically to worry about.
Where will you be based in 2008 and what club
will you ride for?
In Quimper in Brittany. I'll be riding for
VS Quimper.
How much training are you doing at the moment?
About 20 hours.
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