The Heart of a Child Fund

What is Hypoplastic Left Heart Syndrome

Hypoplastic Left Heart Syndrome (HLHS) is one of the most complex cardiac defects seen in the newborn and remains probably the most challenging to manage of all congenital heart defects. It is one of a group of cardiac anomalies that can be grouped together under the description single ventricle defects.

 

Image of a normal heart.

Example of a normal heart

Image of a heart with Hypoplastic Left Heart Syndrome.

Example of Hypoplastic Left
Heart Syndrome

  1. Hypoplastic ascending aorta and aortic arch. 
  2. Hypoplastic left ventricle.
  3. Large patent ductus arteriosus supplying the only source of blood flow to the body.
  4. Atrial septal defect allowing blood returning from lungs to reach the single ventricle.

In a child with Hypoplastic Left Heart Syndrome, all of the structures on the left side of the heart (the side which receives oxygen-rich blood from the lungs and pumps it out to the body) are severely underdeveloped.

The baby often seems normal at birth, but will come to medical attention within a few days of birth as the ductus closes. Babies with this syndrome become ashen, have rapid and difficult breathing and have difficulty feeding. This heart defect is usually fatal within the first days or months or life unless it's treated.

Although this defect is not correctable, some babies can be treated with a series of operations, or a heart transplantation. Until an operation is performed, the ductus is kept open by intravenous medication. Because these operations are complex and need to be individualized for each patient, it's necessary to discuss all the medical and surgical options with your child's doctor. Your doctor will help you decide which is best for your baby.

If you and your child's doctor agree that surgery should be performed, it will be done in several stages. The first stage, referred to as the Norwood procedure, allows the right ventricle to pump blood to both the lungs and the body. It must be performed soon after birth. The final stage(s) has many names, including bi-directional Glenn, Fontan operation and lateral tunnel. These operations create a connection between the veins returning blue blood to the heart and the pulmonary artery. The overall goal of the operation is to allow the right ventricle to pump only oxygenated blood to the body and to prevent or reduce mixing of the red and blue blood. Some infants require several intermediate operations to achieve the final goal.

Some doctors will recommend heart transplantation to treat this problem. Although it does provide the infant with a heart that has normal structure, the infant will require life-long medications to prevent rejection. Many other transplant-related problems can develop, and these should be discussed with your doctor.

Children with hypoplastic left heart syndrome require lifelong follow-up by a cardiologist for repeated checks of how their heart is working. Virtually all the children will require heart medicines. They also risk infection on the heart's valves (endocarditis) and will need antibiotics such as amoxicillin before dental work and certain surgeries to help prevent endocarditis. Good dental hygiene also lowers the risk of endocarditis. For more information about dental hygiene and preventing endocarditis, ask your pediatric cardiologist.

Hypoplastic Left Heart Syndrome appears to be on the increase, but stillill inadeqaute services to help diagnoise this often fatal disease is not available in Ireland. The Heart of a Child Fund will be looking further into this in the coming months, with the aim to provide as much detailed information and research into Womens Ante- Natal Care in Ireland.

We are looking to follow a variety of women here through their pregnancy with the view to helping improve the service in this area and the area of adequate up to date scanning of women who are pregnant in Ireland

Baby Ben's death should never have happened, but it did, he died sadly while breast feeding. Dawn thought he was asleep. She cant change what happened to Ben, but she can help work towards giving all babies a better chance of survival in Ireland. Dawn's following two children where born in Northern Ireland where more up to date Scanning is available for all Women.

If you feel you can assist us in our research please dont hesitate to contact us at heartofachildfund@gmail.com


 

 

Join as a Member Now

Current News

We are delighted to announce the launch of our HLHS Support Group.

This space was created to allow Parents, family and friends of HLHS Kids join and be part of a group of courageous people that share a common experience.

Parents and Family who have also sadly lost a Child to HLHS can join also and share tribute pictures and stories.

This Site also allows you to chat directly with our Team and with each other.

We will be hosting regular on line coffee mornings where our staff will offer support where they can.

Join us Here

http://hypoplastichearts.ning.com/


This Month also saw the creation of our New Awareness Campaign Video 

The Video is a Wonderful Way of Helping Us Promote the New Chat Site and highlight the affects of HLHS.

Please feel free to use the link to share it where you feel its relevant for you.

Its Viewable Here

http://www.youtube.com/watch?v=Ba0n_u73BRk


We are currently gathering information for our first HLHS Booklet

and after obtaining a vast amount of information on HLHS we are now building our Report .

To date we have collected 1063 Signatures for our petition.


A big thank you to all who have signed and supported us.

In TRUTH our LIGHT shines,

Together we are Making a Difference!



Up Coming Events

We Are Currently Structuring some Fundraising Events


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