Assessment of Fetal Cardiac Function in Mild Preeclampsia

dc.contributor.author Balli, Sevket
dc.contributor.author Kibar, Ayse Esin
dc.contributor.author Ece, Ibrahim
dc.contributor.author Oflaz, Mehmet Burhan
dc.contributor.author Yilmaz, Ozcan
dc.date.accessioned 2025-05-10T17:22:30Z
dc.date.available 2025-05-10T17:22:30Z
dc.date.issued 2013
dc.description Oflaz, Mehmet Burhan/0000-0003-1515-4654 en_US
dc.description.abstract This study investigated cardiac function in 65 fetuses of mildly preeclamptic mothers and 55 fetuses of healthy mothers at 26-40 weeks of gestation. Fetuses with intrauterine growth restriction were excluded. Cardiac functions were evaluated by M-mode, pulsed-wave, and tissue Doppler echocardiography. The two groups were similar in terms of maternal age, gravidity, parity, and gestational age. Peak systolic aortic and pulmonary artery velocities were significantly lower in the fetuses of the preeclamptic mothers than in the fetuses of the healthy mothers. The two groups did not differ significantly in terms of shortening fraction or with regard to mitral or tricuspid annular plane systolic excursion. Pulsed-wave Doppler-derived E/A ratios in the mitral and tricuspid valves were similar in the two groups. The deceleration time of early mitral inflow was prolonged in the fetuses of the preeclamptic mothers. The Ea, Aa, and Ea/Aa ratios in the interventricular septum, left ventricle posterior wall, and right ventricle free wall were lower in the preeclampsia group than in the control group. The E/Ea ratio was higher in the preeclampsia group than in the control group. The isovolumic relaxation time and the right and left myocardial performance indices were higher in the fetuses of the preeclamptic mothers than in the fetuses of the healthy mothers. An increased ductus venosus pulsatility index (PI) and a decreased middle cerebral artery (MCA) PI were found in the fetuses of the preeclamptic mothers. All the fetuses were asymptomatic. The results suggest that the increase in fetal cardiac afterload in mild preeclampsia may have caused early subclinical changes in fetal systolic and diastolic cardiac function. In addition, the decrease in MCA-PI may have been caused by redistribution of fetal cardiac output in favor of the left ventricle, secondary to increased placental vascular resistance. en_US
dc.identifier.doi 10.1007/s00246-013-0702-8
dc.identifier.issn 0172-0643
dc.identifier.issn 1432-1971
dc.identifier.scopus 2-s2.0-84885389546
dc.identifier.uri https://doi.org/10.1007/s00246-013-0702-8
dc.identifier.uri https://hdl.handle.net/20.500.14720/10604
dc.language.iso en en_US
dc.publisher Springer en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cardiac Dysfunction en_US
dc.subject Fetal Echocardiography en_US
dc.subject Preeclampsia en_US
dc.title Assessment of Fetal Cardiac Function in Mild Preeclampsia en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Oflaz, Mehmet Burhan/0000-0003-1515-4654
gdc.author.scopusid 35290695100
gdc.author.scopusid 16417157900
gdc.author.scopusid 36637236400
gdc.author.scopusid 35290933200
gdc.author.scopusid 7103213350
gdc.author.wosid Oflaz, Mehmet Burhan/L-5566-2019
gdc.author.wosid Ballı, Sevket/Aak-7541-2021
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Balli, Sevket] Balikesir Ataturk Hosp, Dept Pediat Cardiol, Balikesir, Turkey; [Kibar, Ayse Esin] Mersin Childrens Hosp, Dept Pediat Cardiol, Mersin, Turkey; [Ece, Ibrahim] Yuzuncu Yil Univ, Dept Pediat Cardiol, Fac Med, Van, Turkey; [Oflaz, Mehmet Burhan] Cumhuriyet Univ, Dept Pediat Cardiol, Fac Med, Sivas, Turkey; [Yilmaz, Ozcan] Balikesir Ataturk Hosp, Dept Obstet & Gynecol, Balikesir, Turkey en_US
gdc.description.endpage 1679 en_US
gdc.description.issue 7 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 1674 en_US
gdc.description.volume 34 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.pmid 23591803
gdc.identifier.wos WOS:000324638500019
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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