General fitness, health and nutrition · Public discussion

QUESTION: Implanted Pacemaker AND Implanted Defribulator(two seperate units) OR the Combination Unit

Started by Raymond A. Mill · · Last activity · 5 posts · 1,965 views

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General fitness, health and nutrition
Published
13 June 2004
Last activity
13 June 2004
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Raymond A. Mill
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  1. Hello, Caucasian male, age 52, non smoker, non drinker, not
    overweight. Then the negatives: Dilated cardiomyopathy
    (diagnosed around 1991), Sarcoidosis *Lungs involved and
    possibly liver* (diagnosed in 1994). Losing strength,
    easily short of breath, current ejection factor is almost
    17%, The heart condition is likely a genetic issue as it
    killed my sister at age 22 in 1966, killed my mother at age
    70 in 1999 and nearly took our oldest sons' life at age 15
    in 1995 (Thank God he had a cardiologist that I would
    compare to a real life Marcus Welby, MD! And finally my
    level of stress has been sky-high since January 2000 due to
    circomstances beyond my control> My cardiologist has
    determined that I need a pacemaker and a defribulator. He
    spoke of the two individual devices, suggesting I wait
    until the defribulator - pacemaker single unit is approved.
    I came away a bit confused and thought I'd jump in here to
    ask a question or two.
    1. Am I correct that there are pacemakers and defribulators
    (as indivual units) available now? I may be misinformed.
    2. The doctor is saying he can put in a pacemaker now and
    the defribulator down a few months. He indicated that it
    is more problematic to go this way and believes I should
    wait. I would think that at least the pacemaker would
    ease the load on my heart and limit further damage.

    If anyone here has any thoughts, ideas, experiences then I'd
    sure be one very grateful person.

    Sincerely & God Bless Ray Miller [email hidden]

  2. Raymond A. Miller said:


    Hello, Caucasian male, age 52, non smoker, non drinker, not
    overweight. Then the negatives: Dilated cardiomyopathy
    (diagnosed around 1991), Sarcoidosis *Lungs involved and
    possibly liver* (diagnosed in 1994). Losing strength,
    easily short of breath, current ejection factor is almost
    17%, The heart condition is likely a genetic issue as it
    killed my sister at age 22 in 1966, killed my mother at age
    70 in 1999 and nearly took our oldest sons' life at age 15
    in 1995 (Thank God he had a cardiologist that I would
    compare to a real life Marcus Welby, MD! And finally my
    level of stress has been sky-high since January 2000 due to
    circomstances beyond my control> My cardiologist has
    determined that I need a pacemaker and a defribulator. He
    spoke of the two individual devices, suggesting I wait
    until the defribulator - pacemaker single unit is approved.
    I came away a bit confused and thought I'd jump in here to
    ask a question or two.
    1. Am I correct that there are pacemakers and defribulators
    (as indivual units) available now? I may be misinformed.

    I am sure you are right. I have a pacemaker with a wire to
    both the left atrium and left ventricle. To the best of my
    knowledge a defibrillator deals with ventricular tachycardia
    but someone will correct me if I have it wrong. They are
    both available now.

    Quoted message said:

    2. The doctor is saying he can put in a pacemaker now and
    the defribulator down a few months. He indicated that it
    is more problematic to go this way and believes I should
    wait. I would think that at least the pacemaker would
    ease the load on my heart and limit further damage.

    Did the doctor indicate how long it might be before this
    dual appliance comes to the market? Diana

    Quoted message said:


    If anyone here has any thoughts, ideas, experiences then
    I'd sure be one very grateful person.

    Sincerely & God Bless Ray Miller [email hidden]

  3. Raymond A. Miller said:

    Hello, Caucasian male, age 52, non smoker, non drinker,
    not overweight. Then the negatives: Dilated cardiomyopathy
    (diagnosed around 1991), Sarcoidosis *Lungs involved and
    possibly liver* (diagnosed in 1994). Losing strength,
    easily short of breath, current ejection factor is almost
    17%, The heart condition is likely a genetic issue as it
    killed my sister at age 22 in 1966, killed my mother at
    age 70 in 1999 and nearly took our oldest sons' life at
    age 15 in 1995 (Thank God he had a cardiologist that I
    would compare to a real life Marcus Welby, MD! And finally
    my level of stress has been sky-high since January 2000
    due to circomstances beyond my control>

    Could be cardiac sarcoidosis.

    Quoted message said:


    My cardiologist has determined that I need a pacemaker and
    a defribulator. He spoke of the two individual devices,
    suggesting I wait until the defribulator - pacemaker
    single unit is approved. I came away a bit confused and
    thought I'd jump in here to ask a question or two.
    1. Am I correct that there are pacemakers and
    defribulators (as indivual units) available now? I may
    be misinformed.

    Current FDA-approved defibrillators (AICDs) have pacemaker
    function (not the biventricular kind that your cardiologist
    is probably thinking about)

    Quoted message said:


    2. The doctor is saying he can put in a pacemaker now and
    the defribulator down a few months. He indicated that
    it is more problematic to go this way and believes I
    should wait. I would think that at least the pacemaker
    would ease the load on my heart and limit further
    damage.

    The biventricular pacemaker may improve your heart function
    though it is unlikely to limit further damage (especially
    from sarcoidosis).

    Quoted message said:


    If anyone here has any thoughts, ideas, experiences then
    I'd sure be one very grateful person.

    Sincerely & God Bless Ray Miller [email hidden]

    You are welcome.

    You will be in my prayers to God in Christ's name.

    Servant to the humblest person in the universe,

    Andrew

    --
    Dr. Andrew B. Chung, MD/PhD
    Board-Certified Cardiologist
    heartmdphd.comheartmdphd.com

    **
    Who is the humblest person in the universe?
    makeashorterlink.commakeashorterlink.com

    What is all this about?
    makeashorterlink.commakeashorterlink.com

    Is this spam?
    makeashorterlink.commakeashorterlink.com

  4. "Raymond A. Miller" <[email hidden]> wrote in message news:<[email hidden]>...

    Quoted message said:


    If anyone here has any thoughts, ideas, experiences then
    I'd sure be one very grateful person.

    Sincerely & God Bless Ray Miller [email hidden]

    Hi Ray, glad you're here. First of all, let me reassure you
    that cardiology electrophysiology is rapidly changing daily.
    We constantly work on the genetics of this disease, new drug
    technology, and new assist device technology. It's similar
    to buying a computer... get my point?

    So, where we are at any given time can be fluid.

    What area are you in? (This will help me to know for example
    if you're in the UK with socialized medicine what your
    options may be vs. an insured patient in the U.S. with
    access to private healthcare.)

    What I would do is contact medtronics or Guidant and ask
    them. They have websites and hotline numbers to answer
    questions for people like you. They are proud of their
    devices and want to share them, so YOU contact them and
    find out for yourself and bypass ANY deals your own
    private cardiologist may have struck with the companies
    (he may be waiting on the company that's been wining and
    dining him, etc.).

    Let me just share with you from personal experience...
    pacemaker companies go a long mile to win the loyalties of
    physicians and support staff. I personally have been the
    recipient of Broadway shows, steak dinners, etc. all so a
    pacer company could talk about their latest model!

    YOU do the calling and YOU find out. You don't need a doctor
    to do this for you.

    And, when you find out what you want, TELL your doctor
    what model you want, discuss it with him, and get it put
    in post haste.

    With an ejection fraction of 17% and the other issues you
    describe you need to get something in fast. Get cracking on
    this and get an assist device in in the next few weeks,
    don't paly with this. (And in my opinion, I would rather
    have two devices than wait one day too long and well, have a
    sudden death episode. I personally know people who have two
    and they do just fine) Take care and good luck to you, Sandy

  5. "Dr. Andrew B. Chung, MD/PhD" <[email hidden]> wrote in message news:<[email hidden]>...

    Quoted message said:

    "Raymond A. Miller" wrote:

    Quoted message said:


    The biventricular pacemaker may improve your heart
    function though it is unlikely to limit further damage
    (especially from sarcoidosis).

    Quoted message said:


    If anyone here has any thoughts, ideas, experiences then
    I'd sure be one very grateful person.

    Here is a link that discusses the Guidant bi-ventricular
    pacer/ICD's on the market right now
    guidant.comaicd.shtml and here's one
    from medtronics (a geneal FAQ sheet) medtronics.c-medtronics.c-
    om/servlet/ContentServer?pagename=Medtronic/Website/Stag-
    eArticle&ConditionName=Sudden+Cardiac+Arrest&Stage=Treat-
    ment&Article=tachy_art_how_defibrillation_works

    Guidant is known for having innovative devices well ahead of
    it's time, and Medtronics is known for being the largest
    company in the world with the most financial power (it has
    wanted to buy guidant for years and just may already have?
    Not sure). Don't be afraid to give them both a call, there
    are so many valuable patient resources found through those
    two companies.

    I also believe you would benefit from eating yucca root
    daily because of your sarcoidosis. Just do some reading
    on that South American root, avoid supplements, just
    eat the food.

    As well, did your doc talk about making you pacer dependent
    or giving you a pacer that would only turn on when needed? I
    know a patient who has cardiomyopathy that they went ahead
    and made pacer dependent, it was the only way for him so
    that he could function as his atria was so active it was
    just creating a mess. How is your synchronization?

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