Key result
Cardiomyopathy during pregnancy carries significant maternal and fetal risks requiring specialized assessment and intrapartum care.
This review outlines the types, risks, and management principles of cardiomyopathy during pregnancy, emphasizing intrapartum care and hemodynamic monitoring.
Supports heightened vigilance for peripartum cardiomyopathy; leaves open optimal protocols pending prospective trials.
Cardiomyopathy is an acquired cardiac disorder that, although rare, accounts for a rising proportion of reported pregnancy-related deaths in the United States. During pregnancy, cardiomyopathy may be divided into 2 groups. The first group is peripartum cardiomyopathy; the second group is stratified according to 3 classically defined pathophysiologic presentations: hypertrophic, dilated, or restrictive. Within this second group, the cardiomyopathy can be either idiopathic or due to a specific identified cause. This disorder poses significant risks of morbidity and/or mortality to the pregnant woman and fetus/neonate. This article describes types of cardiomyopathy during pregnancy, perinatal risks, and general management principles with a focus on intrapartum care. Hemodynamic and oxygen transport data are presented to illustrate interpretation of patient assessment findings and the effects of interventions for abnormal maternal and fetal findings.
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Nan H. Troiano (2015) conducted a review in Cardiomyopathy during pregnancy. Cardiomyopathy during pregnancy poses significant risks of maternal and fetal morbidity and mortality, requiring specialized assessment and intrapartum care.
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