Fetal Growth and Pregnancy Complications Among Women With Heart Disease

Overview

An increasing proportion of women with heart disease now go through pregnancy and childbirth. More knowledge about the risk of complications and adverse outcomes for the mother and the baby is needed to guide clinical care in this diverse patient group. The purpose of this study is to, in a cohort of pregnant women with heart disease; – determine fetal growth, and risk of fetal growth restriction and preterm birth – determine whether maternal blood biomarkers are associated with development of preeclampsia, the time of delivery and maternal and perinatal adverse outcomes – determine the risk of hypertensive pregnancy complications The expected outcome of the project is to increase the knowledge of optimal diagnosis and treatment of women with heart disease that go through pregnancy to be able to improve clinical care and the outcomes for mother and baby.

Full Title of Study: “Fetal Growth and Pregnancy Complications Among Women With Heart Disease in Norway: a Cohort Study”

Study Type

  • Study Type: Observational [Patient Registry]
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: April 30, 2020

Detailed Description

Heart disease is about to become the most important cause of maternal deaths in industrialized countries. In addition, heart disease in pregnancy is associated to an increased rate of fetal growth restriction, premature birth, preeclampsia and other pregnancy complications for the mother and the baby. As many women with congenital or acquired heart disease now go through pregnancy and childbirth, more knowledge about the risk of complications and adverse outcomes for the mother and the baby is needed to guide clinical care in this diverse patient group. The National Unit for Pregnancy and Heart Disease is located at Oslo University Hospital, Rikshospitalet, and receive moderate and high risk pregnant women as referrals from hospitals nationwide for follow-up and treatment. The unit has established Oslo University Hospital Register for Pregnancy and Heart disease; a quality register for maternal and fetal outcome in women with heart disease. The purpose of this study was therefore to, in a cohort of pregnant women with heart disease; – determine fetal growth, and risk of fetal growth restriction and preterm birth – determine whether maternal blood biomarkers are associated with development of preeclampsia, the time of delivery and maternal and perinatal adverse outcomes – determine the risk of hypertensive pregnancy complications By the next two years, 150 patients will be included in two prospective longitudinal studies. In the first study fetal growth and utero-placental-fetal blood flow will be assessed by serial measurements at specific gestational ages. The mother's cardiac function will also be measured. Primary outcome is fetal growth curve and wellbeing at birth. In the second study, biomarkers in maternal serum will be measured during the last half of pregnancy to assess if angiogenetic factors are prognostic for the risk of hypertensive complications. In the last study the researchers will use retrospective data from the Oslo University Hospital Register for Pregnancy and Heart disease to determine the association between heart disease and hypertensive complications in a retrospective cohort of approximately 800 patients. The expected outcome of the project is to increase the knowledge of optimal diagnosis and treatment of women with heart disease that go through pregnancy to be able to improve clinical care and the outcomes for mother and baby.

Arms, Groups and Cohorts

  • Fetal growth cohort
    • Longitudinal measurements of fetal growth, fetal circulation and maternal circulation
  • Hypertensive cohort
    • Retrospective cohort of women with heart disease that underwent oregnancy and childbirth

Clinical Trial Outcome Measures

Primary Measures

  • Fetal growth
    • Time Frame: From gestational week 12 until time of birth of baby
    • Serial measurements of fetal biometry
  • Occurrence of hypertension/preeclampsia in pregnancy or postpartum
    • Time Frame: From time of study inclusion until time of discharge from maternity unit after birth of baby
    • Diagnosis in index pregnancy or postpartum until discharge from maternity unit
  • Fetoplacental circulation
    • Time Frame: From gestational week 12 until time of birth of baby
    • Serial measurements of fetoplacental circulation

Participating in This Clinical Trial

Inclusion Criteria

  • Pregnant women diagnosed with heart disease before or during pregnancy classified as maternal WHO risk class 2-4 Exclusion Criteria:

  • Non-consent

Gender Eligibility: All

Minimum Age: 16 Years

Maximum Age: 65 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Oslo University Hospital
  • Provider of Information About this Clinical Study
    • Principal Investigator: Ingvil Krarup Sørbye, Consultant OBGYN, MD PhD – Oslo University Hospital
  • Overall Official(s)
    • Mette E Estensen, PhD, MD, Study Director, Oslo University Hospital, Dep. of Cardiology
  • Overall Contact(s)
    • Ingvil K Sørbye, PhD, MD, +4723070000, isorbye@ous-hf.no

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