Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06517628

The Heart Outcomes in Pregnancy Expectations for Mom and Baby Study

This is a prospective, observational study which is evaluating the obstetrical, neonatal, and cardiovascular outcomes of 1000 pregnant people with known heart disease to define how best to structure cardio-obstetrics care to optimize outcomes.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

About this study

The US is the only industrialized nation to experience a rise in maternal mortality over the last decade. Despite the Healthy People 2030 agenda target of reducing maternal mortality by 10%, rates in the United States are predicted to increase. Furthermore, maternal mortality disproportionately impacts Black, Hispanic, American Indian/Alaskan Native (AIAN), and Asian/Pacific Islander birthing people, who die at a rate that far greater than their White counterparts. Black birthing people are twice as likely to experience severe maternal morbidity (SMM) and 3-4X more likely to die, even after adjusting for demographic and hospital factors. Unfortunately, this gap is widening, with a 20% increase in death for Blacks as compared with a 5% rise in Whites over the last decade. Understanding contributors to adverse outcomes for marginalized birthing populations cannot solely be determined from retrospective chart adjudication and requires prospective evaluation to better understand patient and treatment factors contributing to maternal morbidity and mortality.

Despite affecting only 2-4% of pregnancies, cardiovascular disease (CVD) accounts for >30% of maternal deaths, making it a leading cause of maternal mortality for all birthing people and the number one cause in the Black population. Pregnant people with acquired and congenital heart disease experience the majority of CV-related morbidity and mortality, of which over three quarters have been deemed preventable. The prevalence of CVD is expected to grow as risk factors for CV-related death (obesity, advanced maternal age, hypertensive disorders, and preexisting heart disease) are rising dramatically in pregnant people, which disproportionately burdens marginalized populations. Provider-based factors are a leading cause of preventable morbidity, yet the lack of evidence-based guidelines, means of risk-stratifying pregnant people with CVD, or insight into how best to structure care limits the ability to improve maternal outcomes.

Mortality is not the only important outcome for pregnant people with CVD. For every maternal death, it is estimated that 100 people - 50,000 per year - will suffer severe maternal morbidity (SMM) during delivery, with significant costs to both their families and the economy. Adverse pregnancy outcomes (APOs) and neonatal adverse clinical events (NACEs), including pre-eclampsia, preterm delivery, fetal growth restriction, stillbirth and maternal hemorrhage, are all significantly more common in those with heart disease. Pregnant people who survive these events are more likely to suffer post-traumatic stress and depression, which can adversely impact mother-child bonding and long-term health. Importantly, there are no studies in this population evaluating quality of life, which cannot be measured using retrospective data.

To address the critical need for reversing the US trend in maternal morbidity and mortality, the Heart Outcomes in Pregnancy Expectations (HOPE) study will focus on the highest risk population, pregnant people with CVD. It will provide deeper insights into maternal risk factors, their association with care, and the influence of alternative structures of cardio-obstetric care with APO, MACE, and NACE outcomes. It is a multi-site, multidisciplinary prospective study at >30 cardio-obstetrics clinics throughout the US with a key secondary goal of better understanding racial disparities in care and outcomes. Not only will traditional APOs, MACE, and NACE events from presentation to 1-year after delivery be collected, generic and disease-specific quality of life will be measured as a way to evaluate their independent impact on outcomes.

Preliminary insights through our pilot program highlight the importance of better structures of care as a means of improving outcomes, which has previously been established in other clinical settings, but not in cardio-obstetrics care. The investigators have identified 6 key structures of care that have been variably adopted through the US and for which additional data to define their independent association with outcomes is needed.

These include:

  • multidisciplinary (OB/maternal-fetal medicine [MFM], cardiology, anesthesia, critical care, etc.) care teams;
  • a COB care coordinator;
  • coordinated inter-disciplinary patient evaluation;
  • team debriefing
  • the ability to perform high-risk deliveries in the ICU and
  • formalized warm hand offs to primary or sub-specialty care after delivery.

After adjusting for extensive patient factors associated with adverse outcomes, the independent association of these structures of care with outcomes will be estimated as a foundation for testing and disseminating those that are most effective.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion:

Must have one or more condition(s) within the 6 following categories - Repaired or Unrepaired

  • Congenital or structural heart disease
  • Aortopathies
  • Arrhythmias
  • Cardiomyopathies and Heart Failure
  • Coronary disease
  • Other (Current endocarditis or history of endocarditis, Pericarditis, Pericardial effusion - Moderate or Large, Pericardial constriction, Pulmonary hypertension (all types) defined as mean pulmonary artery systolic pressure of >20 mmHg by right heart catheterization or pulmonary hypertension estimated in the severe range by echo)

Exclusion criteria

  • Unable to participate in telephone follow-up
  • Too hard of hearing to do follow-up by telephone or deaf
  • Incarcerated prisoner
  • History of dementia.
  • Subjects without a way for contact by telephone for follow-up
  • Refused participation in the study
  • Unable to consent for self
  • Traumatic Aortic Disease
  • Peripartum cardiomyopathy diagnosed in current pregnancy

Treatment and study plan

Purely observational study on the care and outcomes of participants with cardiovascular disease in pregnancy.

Other

The primary exposure variable is the organization of cardio-obstetrics care which will be defined by annual site surveys and its association with outcomes will be defined by hierarchical models adjusting for patient characteristics.

Primary outcomes

  1. Rate of Adverse pregnancy outcomes

    Time frame: up to 6 weeks postpartum

    HELLP, preeclampsia, gestational hypertension, eclampsia, superimposed preeclampsia on chronic hypertension (SIPE), premature preterm rupture of membranes (PPROM), preterm delivery, thrombotic complications, hemorrhage, maternal mortality, placental abruption, Admission ICU delivery

Secondary outcomes

  1. Rate of Maternal Adverse Cardiac Events (MACE)

    Time frame: Up to 1 year postpartum

    A composite outcome including any of the following: cardiovascular death, non-fatal stroke, myocardial infarction, hospitalization for acute coronary syndromes, urgent revascularization procedures, decompensated heart failure, aortic dissection, clinically significant arrhythmia requiring treatment (eg. atrial fibrillation/flutter, SVT, ventricular tachycardia, etc), cardiac transplant

  2. Rate of Neonatal adverse clinical events (NACE)

    Time frame: Through maternal hospital discharge

    A composite outcome including any of the following: APGARS < 8 at 5 minutes, birthweight of < 2500 grams, NICU admission, supplemental oxygen use, neonatal death, fetal death, spontaneous abortion/miscarriage, intrauterine fetal growth restriction

Other outcomes

  1. Changes in Generic Quality of Life as Assessed by the Short Form-36

    Time frame: Through 1 year post partum

    All patients will complete the Short Form-36 on enrollment and changes over time through 1 year after delivery and will be compared by patient characteristics and structures of care.

  2. Changes in Depressive Symptoms, as Assessed by the Edinburgh Postpartum Depression Scale

    Time frame: Through 1 year post partum

    This questionnaire will be completed on enrollment and changes over time through 1 year after delivery and will be compared by patient characteristics and structures of care.

  3. Experiences with pregnancy care and delivery will be assessed with the Childbirth Experience Survey

    Time frame: Third trimester and 6 weeks after delivery

    This questionnaire will be completed during the 3rd trimester and 6 weeks after delivery and will be compared by patient characteristics and structures of care.

  4. Perceived Discrimination will be assessed using the Experience of Depression Scale

    Time frame: Enrollment and 6 and 12 months after delivery

    This questionnaire will be completed on enrollment and at 6 and 12 months after delivery so that cross-sectional and changes over time through 1 year after delivery can be compared by patient characteristics and structures of care.

  5. Self-perceived Health Status will be assessed using a version of the Kansas City Cardiomyopathy Questionnaire Modified for Pregnancy

    Time frame: Enrollment, 3rd Trimester, and 6 weeks, 6 months and 12 months after delivery

    This questionnaire will be completed on enrollment and changes over time through 1 year after delivery will be compared by patient characteristics and structures of care.

  6. Coronary-specific Health Status over Time among Participants with a History of Coronary Disease

    Time frame: Enrollment, 3rd Trimester, and 6 weeks and 12 months after delivery

    This questionnaire will be completed by participants with a history of coronary artery disease (including SCAD) on enrollment and changes over time through 1 year after delivery and will be compared by patient characteristics and structures of care.

  7. Atrial Fibrillation-specific Health Status over Time among Participants with a History of Atrial Fibrillation

    Time frame: Enrollment, 3rd Trimester, and 6 weeks and 12 months after delivery

    This questionnaire will be completed by participants with a history of atrial fibrillation on enrollment and changes over time through 1 year after delivery and will be compared by patient characteristics and structures of care.

  8. Disease-specific Health Status over Time among Participants with a History of Congenital Heart Disease

    Time frame: Enrollment, 3rd Trimester, and 6 weeks and 12 months after delivery

    This questionnaire will be completed by participants with a history of congenital heart disease on enrollment and changes over time through 1 year after delivery and will be compared by patient characteristics and structures of care.

Study contacts

Contact information is provided by the study sponsor or research team.

Anna Grodzinsky, MD, MS

CONTACT

[email protected]

816-932-2000

Karen L Florio, DO, MPH

CONTACT

[email protected]

631-579-1030

Sponsors and collaborators

Lead sponsor

University of Missouri, Kansas City

Other

Collaborators

  • Albert Einstein College of Medicine
  • Baylor College of Medicine
  • Beth Israel Deaconess Medical Center
  • Board of Trustees of the Leland Stanford Junior University
  • Columbia University
  • Henry Ford Hospital
  • Northwell Health
  • Northwestern University
  • Oregon Health and Science University
  • Regents of the University of Michigan
  • Saint Luke's Health System Inc.
  • Tennessee Maternal Fetal Medicine PLC
  • The Board of Trustees of the University of Illinois
  • The Brigham and Women's Hospital, Inc.
  • The Children's Hospital Corporation
  • The Curators of the University of Missouri
  • The General Hospital Corporation d/b/a Massachusetts General Hospital
  • The Johns Hopkins University
  • The Miriam Hospital/Lifespan
  • The Regents of the University of California, Irvine
  • The Regents of the University of California, Los Angeles
  • The Research Foundation for the State University of New York
  • The Trustees of the University of Pennsylvania
  • Trustees of Indiana University
  • University of Kansas Medical Center
  • University of Massachusetts, Worcester
  • University of Mississippi Medical Center
  • University of North Carolina, Chapel Hill
  • University of Pittsburgh
  • University of South Florida
  • University of Texas Southwestern Medical Center
  • University of Washington
  • Weil Medical Colleqe of Cornell University
  • Women and Infants Hospital of Rhode Island

Registry information

Acronym: HOPE

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Jul 24, 2024
Registry last updated
Jan 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.