Ronald
Kirson
My name is Ronald Kirson.
I'm 51 years old and work as a
training administrator for a
large utility in New York. I
am married and have two sons -
the older one is 26 years old
and a CPA and my younger son
is studying for his MBA at the
Ohio State University.
My internist first
discovered my condition 18
years ago, when I was 34 years
old. I had been diagnosed with
essential hypertension at age
11 and was placed on blood
pressure medication at age 18
after tests ruled out any
renal involvement. It was at
one of my routine visits that
the internist heard a mild
heart murmur and referred me
to a cardiologist for a
consultation. The cardiologist
performed a physical
examination and confirmed the
diagnosis telling me that I
had mild aortic valve
regurgitation. When asked, I
denied any recollection of
ever having had rheumatic
fever but did recall having
had literally scores of sore
throats while growing up in
the 1950's.
After that initial visit to
the cardiologist, the murmur
was monitored by the internist
several times each year when I
came for my routine blood
pressure checks. Sixteen years
ago, I was sent for a gated
stress test that uses
radioactive isotopes to
measure the degree of aortic
regurgitation. Again, the
diagnosis of aortic
regurgitation was confirmed
along with a trace-to-mild
degree of mitral
regurgitation. Shortly after
that, color-flow
echocardiography became
available and I was monitored
annually using that method. It
became clear as the years
passed that my heart condition
was slowly deteriorating and
that I would be facing an
aortic valve replacement at
some point in my life.
That point came during
Thanksgiving week in 1999 when
I received a call from my
internist's office after my
annual color-flow
echocardiogram. A consultation
was quickly arranged with my
cardiologist who explained
that it was time to replace
the valve even though I was
symptom free. My heart had
enlarged further and the
ejection fraction had dropped.
Although the ejection fraction
was still within the normal
range - just over 50%, the
change indicated that my heart
was beginning to fail. I was
scheduled for a cardiac
catherization that confirmed
the valve condition and also
revealed that my coronary
arteries were clear. We
discussed the valve choices -
tissue versus mechanical and
the anticoagulation therapy I
would need. I opted to have a
bi-leaflet St. Jude Valve
installed. The surgery was
performed by Dr. Alan Hartman,
at the Winthrop University
Hospital in Mineola, New York
in December of 1999.
When I awoke in the cardiac
intensive care unit, I was
told that all had went well
and that in addition to the
aortic valve replacement, a
weakened spot on my ascending
aorta began to leak blood
during my removal from the
heart/lung machine. This
potential aneurysm was
repaired with a Dacron patch.
It was surmised that the
ascending aorta was weakened
by nearly 40 years of
hypertension.
My hospital recovery went
fairly well and uneventfully
until I wound up back in the
intensive care unit after
building up fluids in my body
due to insufficient urine
elimination after my catheter
was removed. Dr. Hartman has a
deservedly great reputation
and he was wonderful. Winthrop
Hospital was fine as well,
with attentive nurses and
care. However, they did fail
to catch the urine build-up in
my body because they were not
monitoring my fluid intake and
output. Even though they
weighed me daily, they ignored
the weight gain which was a
symptom of the coming problem.
I returned home after a
week in the hospital, taking
Coumadin and Toprol-XL. My
recovery was fairly routine -
some sternum pain, weakness,
etc. I began the routine of
INR testing at a local
laboratory, calling the
cardiologists office who
adjusted my Coumadin dosage as
the numbers varied. The
Coumadin monitoring and
medication changes were
initially micromanaged by my
cardiologist's registered PA.
Although very thorough, she
attempted to stabilize my INR
by making far too many
frequent dosing changes. After
approximately 3 months
post-op, the Coumadin
management was turned over to
my internist who had a
completely different approach.
He allowed the numbers to
swing a bit as long as they
stayed within the 2.5 to 3.5
range reasonably well. With
fewer dosing changes, my INR
has been reasonably stable. I
take alternating daily dosage
of 4mg and 5mg of Coumadin and
usually maintain an INR of 2.7
to 3.8. I, like many people am
extremely sensitive to small
changes in Coumadin and the
difference of 1 mg. per week
will cause my INR to swing
widely.
This routine of INR
laboratory testing every 2-3
weeks continued until late
last year when I followed
through on my internist's
suggestion to begin home INR
testing. I was fortunate that
my medical insurance company
has fully covered the unit and
supplies. I received the
ProTime unit in December of
2001 and love it. The process
is virtually painless and the
convenience of getting my
results in 2 minutes cannot be
beat. I test once per week now
and purposely maintain my INR
at the upper end of the range
- approximately 3.2 to 3.8.
I'd rather be high than low.
Since my diet is reasonably
consistent, my INR readings
don't swing widely. I would
recommend the use of home
testing to anyone on this high
level of anticoagulation.
Since my surgery, I have had
several color-flow
echocardiograms. The aortic
valve is doing well and my
heart function has recovered
to its earlier high levels.
They still note a mild mitral
valve regurgitation which
hopefully won't progress to
the point of needing
treatment. I found this web
site on a link from the
ProTime home page and have
enjoyed reading the comments
from the other members. I hope
my story is helpful. If you
need to contact me, I can be
reached at kirsonron@aol.com.
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