Cardiac disease in pregnancy and peripartum cardiomyopathy
Cardiac disease in pregnancy Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview
Peripartum cardiomyopathy is defined as:
- Heart failure within last month of pregnancy or five months postpartum
- Absence of prior heart disease
- No determinable cause
- Strict echocardiographic indication of left ventricular dysfunction:
- Ejection fraction <45% and/or
- Fractional shortening <30%
- End-diastolic dimension >2.7 cm/m2 BSA (body surface area)
Common Mimickers
- Accelerated HTN
- Infection/sepsis
- Diastolic dysfunction
- High output state of pregnancy
Demographics
- Estimates of incidence 1/1300-15000
- Previous studies likely overestimated
- More common in women with:
- Multiple pregnancies
- African decent
- h/o toxemia
- Long-term tocolytic use
- Age>30
- Twin Pregnancy
- Etiology remains unknown
- Signs and sxs similar to those of nl pregnancy
Hemodynamic Findings
Chamber | Normal Pregnancy | Peripartum cardiomyopathy |
---|---|---|
RA | 2 | 11 (2-34) |
PA | 11 | 39 (18-62) |
PCW | 6 | 18 (5-32) |
CO (L/min) | 7 | 6 (5-9) |
HR | 83 | 104 (76-142) |
Treatment of Peripartum Cardiomyopathy
- Digoxin and diuretics are Class C
- ACE inhibitors absolutely contraindicated prepartum (hydralazine drug of choice)
- Anticoagulation recommended (Heparin prepartum and coumadin postpartum)
Outcome of Peripartum Cardiomyopathy
- Mortality 25-50% (half deaths in first 3 months)
- Remainder stable/recover within 6 months
- Can recur with subsequent pregnancies
- Favorable outcomes with cardiac transplantation