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Peripartum Cardiomyopathy Support Network |
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about ppcm |
NY PPCM Study Group
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Send a Letter Download this informational letter (provided by James D. Fett, MD) and mail it to your OBGYN or PCP. If you have a few extra stamps left over, please mail this to as many doctors in your local area as you see fit.
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Help Us Establish a PPCM Registry At this time there
is no database of Peripartum Cardiomyopathy patients in North America. A
registry established to provide a population base to describe the
epidemiologic features and clinical course of PPCM would promote the
development of etiology specific treatments, and help us to understand
regional, ethnic, and age differences in PPCM. It will also help to
determine whether certain baseline factors at diagnosis, or trends over
time, can predict outcomes for mortality, late abnormalities of
ventricular structure and function, congestive heart failure and listing
for heart transplantation or receiving a heart transplantation, as well
as help to predict which patients may be at least or greatest risk of a
reoccurrence or worsening of PPCM in subsequent pregnancies. |
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