TY - JOUR
T1 - Prevalence of pre-eclampsia and adverse pregnancy outcomes in women with pre-existing cardiomyopathy
T2 - a multi-centre retrospective cohort study
AU - Ormesher, Laura
AU - Vause, Sarah
AU - Higson, Suzanne
AU - Roberts, Anna
AU - Clarke, Bernard
AU - Curtis, Stephanie
AU - Ordonez, Victoria
AU - Ansari, Faiza
AU - Everett, Thomas R.
AU - Hordern, Claire
AU - Mackillop, Lucy
AU - Stern, Victoria
AU - Bonnett, Tessa
AU - Reid, Alice
AU - Wallace, Suzanne
AU - Oyekan, Ebruba
AU - Douglas, Hannah
AU - Cauldwell, Matthew
AU - Reddy, Maya
AU - Palmer, Kirsten
AU - Simpson, Maggie
AU - Brennand, Janet
AU - Minns, Laura
AU - Freeman, Leisa
AU - Murray, Sarah
AU - Mary, Nirmala
AU - Castleman, James
AU - Morris, Katie R.
AU - Haslett, Elizabeth
AU - Cassidy, Christopher
AU - Johnstone, Edward D.
AU - Myers, Jenny E.
N1 - Funding Information:
We thank Dr Cathy Head for facilitating collaborations through UK Maternal Cardiac Society, Lizzy Cottrell and Andy Trafford for supervision and Omar Asghar for assistance with cardiological classifications.
Funding Information:
LM is supported by the NIHR Oxford Biomedical Research Centre and part-time employee of Sensyne Health plc. The remaining authors declare no competing interests.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Pre-eclampsia is associated with postnatal cardiac dysfunction; however, the nature of this relationship remains uncertain. This multicentre retrospective cohort study aimed to determine the prevalence of pre-eclampsia in women with pre-existing cardiac dysfunction (left ventricular ejection fraction < 55%) and explore the relationship between pregnancy outcome and pre-pregnancy cardiac phenotype. In this cohort of 282 pregnancies, pre-eclampsia prevalence was not significantly increased (4.6% [95% C.I 2.2–7.0%] vs. population prevalence of 4.6% [95% C.I. 2.7–8.2], p = 0.99); 12/13 women had concurrent obstetric/medical risk factors for pre-eclampsia. The prevalence of preterm pre-eclampsia (< 37 weeks) and fetal growth restriction (FGR) was increased (1.8% vs. 0.7%, p = 0.03; 15.2% vs. 5.5%, p < 0.001, respectively). Neither systolic nor diastolic function correlated with pregnancy outcome. Antenatal ß blockers (n = 116) were associated with lower birthweight Z score (adjusted difference − 0.31 [95% C.I. − 0.61 to − 0.01], p = 0.04). To conclude, this study demonstrated a modest increase in preterm pre-eclampsia and significant increase in FGR in women with pre-existing cardiac dysfunction. Our results do not necessarily support a causal relationship between cardiac dysfunction and pre-eclampsia, especially given the population’s background risk status. The mechanism underpinning the relationship between cardiac dysfunction and FGR merits further research but could be influenced by concomitant ß blocker use.
AB - Pre-eclampsia is associated with postnatal cardiac dysfunction; however, the nature of this relationship remains uncertain. This multicentre retrospective cohort study aimed to determine the prevalence of pre-eclampsia in women with pre-existing cardiac dysfunction (left ventricular ejection fraction < 55%) and explore the relationship between pregnancy outcome and pre-pregnancy cardiac phenotype. In this cohort of 282 pregnancies, pre-eclampsia prevalence was not significantly increased (4.6% [95% C.I 2.2–7.0%] vs. population prevalence of 4.6% [95% C.I. 2.7–8.2], p = 0.99); 12/13 women had concurrent obstetric/medical risk factors for pre-eclampsia. The prevalence of preterm pre-eclampsia (< 37 weeks) and fetal growth restriction (FGR) was increased (1.8% vs. 0.7%, p = 0.03; 15.2% vs. 5.5%, p < 0.001, respectively). Neither systolic nor diastolic function correlated with pregnancy outcome. Antenatal ß blockers (n = 116) were associated with lower birthweight Z score (adjusted difference − 0.31 [95% C.I. − 0.61 to − 0.01], p = 0.04). To conclude, this study demonstrated a modest increase in preterm pre-eclampsia and significant increase in FGR in women with pre-existing cardiac dysfunction. Our results do not necessarily support a causal relationship between cardiac dysfunction and pre-eclampsia, especially given the population’s background risk status. The mechanism underpinning the relationship between cardiac dysfunction and FGR merits further research but could be influenced by concomitant ß blocker use.
UR - https://www.scopus.com/pages/publications/85145515810
U2 - 10.1038/s41598-022-26606-z
DO - 10.1038/s41598-022-26606-z
M3 - Article
C2 - 36599871
AN - SCOPUS:85145515810
SN - 2045-2322
VL - 13
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 153
ER -