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Parents of babies born with heart disease are likely to benefit from routine cardiac genetic counselling to reduce risk, prevent future disease and improve treatment outcomes, according to world-first research led by UNSW Sydney, University of Technology Sydney (UTS) and the Sydney Children’s Hospitals Network.
In a study of one hundred parents of children with congenital heart disease who had surgery between 2000 and 2009, almost all parents showed clear preference for a single genetics appointment with both a specialised clinical geneticist and genetic counsellor, offered as soon as possible after diagnosis.
Lead author UNSW Associate Professor Nadine Kasparian, and co-authors Dr Richard De Abreu Lourenco and Professor Rosalie Viney from the UTS Centre for Health Economics Research and Evaluation, said the study, published in Genetics in Medicine, showed that meeting a specialised clinical geneticist and cardiac genetic counsellor, supported by online health resources, was a high priority for parents of children with heart disease.
“This study highlights an important gap between what parents feel they need and what is currently available,” says Associate Professor Kasparian.
“Specialised paediatric cardiac genetics services can provide information about genetic and other risk factors associated with a child’s heart condition, as well as offer emotional support to alleviate the feelings of guilt, fear and sadness parents so often feel.”
Every day in Australia, eight babies are born with congenital heart disease, which includes malformations of the heart, heart valves or major blood vessels. Worldwide there are about 1.35 million babies diagnosed with congenital heart disease each year. It is a leading cause of infant death and one of the most common reasons babies are admitted to intensive care.
After diagnosis of congenital heart disease, paediatric cardiologists usually discuss the possible genetic implications with parents, however referrals to a cardiac genetics service are less common. Funding of additional resources would allow more referrals to properly structured congenital heart genetics clinics.
Associate Professor Kasparian says the great majority of parents of babies with congenital heart disease would like to be offered this service, with 93% of parents in the study indicating they would attend an appointment with a specialised clinical geneticist and counsellor, if offered within two weeks of referral.
“In order to plan services, we need to understand the needs of the people the service is supposed to help”, says co-author and clinical geneticist UNSW Conjoint Professor Edwin Kirk. “In this study, we heard from parents about their ideal service. We may not always be able to reach the ideal, but this gives us a clear goal to aim for.”
The study showed the presence of a genetic counsellor in addition to a geneticist made it even more likely for parents to attend the appointment.
“The genetics landscape is rapidly evolving, and we are learning more about the genetics of childhood heart disease every day,” says UNSW Associate Professor Kasparian. “This study shows the need for greater resources and new models of care. There are important discoveries being made at molecular level and our services need to be ready for when these discoveries are translated into clinical care.”
More resources, funding and workforce training are needed before the model of care preferred by parents could be implemented, says Associate Professor Kasparian.
“The growing demands for paediatric cardiac genetics services means genetic counsellors, working with cardiac teams, could play a greater role in the care of children with heart disease and their families,” says Associate Professor Kasparian.
The study comes as Health Minister Greg Hunt announced on February 14 the first National Action Plan to discover treatments for thousands of Australians affected by childhood heart disease. It will be important that we extend that action to the delivery of services that better meet the needs of parents of children with heart disease.