For people with heart defects, mental health support is essential to care at every age
Congenital heart defects (CHD) occur when people are born with structural abnormalities of the heart or blood vessels involving the heart. Surgery and catheter interventions are often required to address these issues. Most people with CHD survive through adulthood, with adults now outnumbering children among more than 2.4 million living with CHD in the United States. A surgical intervention, however, does not cure CHD. People may need multiple operations, and specialty heart care is required throughout their lives, especially if they were born with complex heart problems.
“Decades of research describes the psychological and social stressors and challenges that can present across the lifespan for people with CHD,” said Adrienne H. Kovacs, Ph.D., chair of the writing committee for the scientific statement and a clinical psychologist who specializes in working with people who have CHD. “It’s long overdue that we move beyond awareness to action and providing more resources and expert mental health care for people living with CHD.”
An American Heart Association scientific statement is an expert analysis of current research and may inform future guidelines. The Association’s 2011 scientific statement on a related topic addressed developmental delays and other neurodevelopmental outcomes in children with CHD. However, this is the first statement to summarize the psychological and social challenges from childhood through adulthood and to review age-appropriate mental health interventions to improve quality of life.
According to the new statement, children with more complex CHDs have a 5-times higher rate of receiving an anxiety diagnosis in their lifetime compared to children without CHD. Despite the evidence of emotional, social and behavioral difficulties, only a small fraction of children with CHD are offered or participate in mental health assessment or treatment. For adults with CHD, the rate of experiencing a mood or anxiety disorder in their lifetime is about 50%, compared to about 30% for adults in the general population.
The statement summarizes the psychosocial impact of CHD during various stages of life:
“It’s completely understandable to have a psychological reaction to living with a congenital heart defect. The condition presents numerous challenges throughout the lifespan and may include unexpected news — such as a person realizing they can no longer physically manage the demands of their job, or learning that there are significant risks to pregnancy,” said Kovacs. “Many people with CHD have tremendous resilience in the face of these challenges. At the same time, we want to normalize psychological reactions and increase the prevalence of care for psychological well-being to help people with CHD experience a full and healthy life.”
According to the statement, approaches to mental health care may encompass self-care strategies, such as relaxation techniques and hospital-based or online support groups; psychotherapy such as talk therapies for individuals, couples, families or groups; and medication therapy where a medical team can determine appropriate, heart-safe medications for depression or anxiety.
The statement strongly advocates for the integration of mental health professionals within CHD specialty care teams. Integrated mental health care normalizes emotional reactions to health challenges, reduces stigma, improves timely access as soon as health challenges arise, and provides coordinated care across the multidisciplinary health care team.
“The goal of this statement is to foster psychologically informed care that empowers people with CHD and their families and provides emotional support,” said Kovacs. “We would like mental health assessment and support to be part of comprehensive care for all people with CHD rather than a special service that is offered only in some places or special circumstances.”
In addition, the statement highlights priority areas for research to better understand and improve psychological outcomes for people with CHD, including:
This statement follows two other scientific statements from the Association addressing care for people with CHD: a March 2022 scientific statement on support for the transition from pediatric to adult health care; and an April 2022 scientific statement addressing the impact of social determinants of health on CHD care throughout life.
This scientific statement was prepared by the volunteer writing group on behalf of the American Heart Association’s Council on Lifelong Congenital Heart Disease and Heart Health in the Young (Young Hearts) and the Stroke Council. The writing group included a diverse, interdisciplinary group of experts with a long-standing commitment to the psychological care of individuals with CHD including two authors with CHD.
American Heart Association scientific statements promote greater awareness about cardiovascular diseases and stroke issues and help facilitate informed health care decisions. Scientific statements outline what is currently known about a topic, and what areas need additional research. While scientific statements inform the development of guidelines, they do not make treatment recommendations. American Heart Association guidelines provide the Association’s official clinical practice recommendations.
Co-authors are Vice Chair Lazaros K. Kochilas, M.D., M.S., FAHA; Judith Brouillette, M.D., Ph.D.; Patricia Ibeziako, M.D.; Jamie L. Jackson, Ph.D.; Nadine A. Kasparian, Ph.D.; Yuli Y. Kim, M.D.; Tracy Livecchi, L.C.S.W.; and Christina Sillman, M.S.N. Authors’ disclosures are listed in the manuscript.