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Abstract
Peripartum cardiomyopathy (PPCM) is a relatively rare form of acute heart failure.
Onset is from the last trimester of pregnancy to 5 months postpartum. Diagnosis is
made by excluding other causes of acute heart failure, such as infections or toxins,
and by determining that the patient does not have an underlying cardiac problem that
has been unmasked by pregnancy. Diagnosis in the last trimester is complicated by
the fact that the early symptoms of this disorder may mimic the symptoms of normal
pregnancy. PPCM must be considered in any patient who presents with new onset peripheral
edema, dyspnea on exertion, or paroxysmal nocturnal dyspnea during late pregnancy
or up to 5 months postpartum. Limited studies suggest that early and aggressive therapy
is associated with a better outcome. Therapy is directed toward decreasing preload
and improving cardiac function. Return of cardiac size to normal is associated with
a better prognosis than continued cardiomegaly.
Keywords
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Article info
Publication history
Accepted:
September 17,
1991
Received in revised form:
September 3,
1991
Received:
January 14,
1991
Identification
Copyright
© 1992 Published by Elsevier Inc.