TY - JOUR
T1 - Pregnancy outcomes in correlation with placental histopathology in subsequent pregnancies complicated by preeclampsia
AU - Levy, Michal
AU - Kovo, Michal
AU - Schreiber, Letizia
AU - Kleiner, Ilia
AU - Koren, Liron
AU - Barda, Giulia
AU - Volpert, Eldar
AU - Bar, Jacob
AU - Weiner, Eran
N1 - Publisher Copyright:
© 2019 International Society for the Study of Hypertension in Pregnancy
PY - 2019/10
Y1 - 2019/10
N2 - Objective: In attempt to deepen our understanding of the etiopathogenesis of preeclampsia we aimed to study the placental component and pregnancy outcomes in two consecutive pregnancies complicated by preeclampsia in the same patient. Study design: Pregnancy and placental reports of all pregnancies complicated by preeclampsia between 2008 and 2018 were reviewed. Included were only cases with recurrent preeclampsia in two consecutive pregnancies Neonatal outcomes and placental histopathology were compared between the first preeclampsia delivery (first preeclampsia group) and the subsequent preeclampsia delivery (subsequent preeclampsia group), thus each subject served as her own control in two consecutive pregnancies. Placental lesions were classified according to the current “Amsterdam” criteria. Adverse neonatal outcome was defined as ≥1 early neonatal complication. Results: Included in the study a total of 83 cases with recurrent preeclampsia. The first preeclampsia group delivered at an earlier gestational age (35.7 ± 3.7 vs. 36.8 ± 3.1 weeks, p = 0.03) and had higher rates of severe features (44.6% vs. 25.3%, p = 0.03), placental weight <10th percentile (44.5% vs. 26.5%, p = 0.02), maternal vascular malperfusion (MVM) lesions (84.3% vs. 62.6%, p = 0.002), SGA (44.5% vs. 33.7%, p = 0.03), and adverse neonatal outcome (55.4% vs. 34.9%,p = 0.01), compared to the subsequent preeclampsia group. Using multivariate logistic regression analysis, severe features (aOR = 1.36, 95%CI = 1.12–2.36), MVM lesions (aOR = 1.12, 95%CI = 1.04–1.87) and adverse neonatal outcome (aOR = 1.26 95%CI = 1.14–2.23) were found to be independently associated with the first preeclampsia group. Conclusion: The first event of preeclampsia is characterized by an earlier, more severe presentation, as well as a higher rate of MVM lesions, SGA, and adverse neonatal outcome, compared to preeclampsia in a subsequent pregnancy.
AB - Objective: In attempt to deepen our understanding of the etiopathogenesis of preeclampsia we aimed to study the placental component and pregnancy outcomes in two consecutive pregnancies complicated by preeclampsia in the same patient. Study design: Pregnancy and placental reports of all pregnancies complicated by preeclampsia between 2008 and 2018 were reviewed. Included were only cases with recurrent preeclampsia in two consecutive pregnancies Neonatal outcomes and placental histopathology were compared between the first preeclampsia delivery (first preeclampsia group) and the subsequent preeclampsia delivery (subsequent preeclampsia group), thus each subject served as her own control in two consecutive pregnancies. Placental lesions were classified according to the current “Amsterdam” criteria. Adverse neonatal outcome was defined as ≥1 early neonatal complication. Results: Included in the study a total of 83 cases with recurrent preeclampsia. The first preeclampsia group delivered at an earlier gestational age (35.7 ± 3.7 vs. 36.8 ± 3.1 weeks, p = 0.03) and had higher rates of severe features (44.6% vs. 25.3%, p = 0.03), placental weight <10th percentile (44.5% vs. 26.5%, p = 0.02), maternal vascular malperfusion (MVM) lesions (84.3% vs. 62.6%, p = 0.002), SGA (44.5% vs. 33.7%, p = 0.03), and adverse neonatal outcome (55.4% vs. 34.9%,p = 0.01), compared to the subsequent preeclampsia group. Using multivariate logistic regression analysis, severe features (aOR = 1.36, 95%CI = 1.12–2.36), MVM lesions (aOR = 1.12, 95%CI = 1.04–1.87) and adverse neonatal outcome (aOR = 1.26 95%CI = 1.14–2.23) were found to be independently associated with the first preeclampsia group. Conclusion: The first event of preeclampsia is characterized by an earlier, more severe presentation, as well as a higher rate of MVM lesions, SGA, and adverse neonatal outcome, compared to preeclampsia in a subsequent pregnancy.
KW - Maternal malperfusion lesions
KW - Neonatal outcome
KW - Placental pathology
KW - Preeclampsia
KW - Preeclampsia recurrence
UR - http://www.scopus.com/inward/record.url?scp=85073630071&partnerID=8YFLogxK
U2 - 10.1016/j.preghy.2019.09.021
DO - 10.1016/j.preghy.2019.09.021
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C2 - 31648156
AN - SCOPUS:85073630071
SN - 2210-7789
VL - 18
SP - 163
EP - 168
JO - Pregnancy Hypertension
JF - Pregnancy Hypertension
ER -