Key result
PH in pregnant cardiac patients is linked to more low-birth-weight infants but similar maternal mortality.
Why the study?
Does coexisting pulmonary hypertension worsen maternal and fetal outcomes in pregnant women with cardiac disease?
Cohort (n=40)
Does coexisting pulmonary hypertension worsen maternal and fetal outcomes in pregnant women with cardiac disease?
Coexisting pulmonary hypertension in pregnant women with cardiac disease (excluding Eisenmenger's syndrome) generally has a favorable outcome for both mother and fetus, without significant increases in maternal mortality or morbidity.
May support fetal growth monitoring in this group; leaves open confirmation of maternal safety in larger prospective studies.
OBJECTIVE: To ascertain the significance of coexisting pulmonary hypertension in cardiac disease in pregnancy. METHODS: Over a 3-year period a group of pregnant women with cardiac disease was followed until 6 weeks postpartum. Twenty women with pulmonary hypertension were compared with 20 controls without pulmonary hypertension with particular reference to maternal and fetal outcome. Analysis of data was carried out using Fisher's exact test and Student's t-test. RESULTS: Except for Eisenmenger's syndrome, there were no differences in maternal morbidity and mortality between the two groups. There were more low birth weight babies but no significant differences in premature delivery rate, mode of delivery or perinatal mortality. CONCLUSION: Except for Eisenmenger's syndrome, coexisting pulmonary hypertension complicating cardiac disease in pregnancy generally has a favorable outcome for both mother and fetus.
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Haris Bin Tahir (1995) conducted a cohort in Cardiac disease in pregnancy (n=40). Pulmonary hypertension vs. No pulmonary hypertension was evaluated on Maternal and fetal outcome. Coexisting pulmonary hypertension in pregnant women with cardiac disease (excluding Eisenmenger's syndrome) was associated with more low birth weight babies but no differences in maternal mortality.
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