FAQ

About Brugada Syndrome

Brugada Syndrome is a condition that affects the heart and can cause problems with the way it beats. Imagine your heart as a pump that sends blood all around your body, providing it with oxygen and nutrients it needs to function properly. Normally, the heart beats in a regular pattern, but in people with Brugada Syndrome the heart beat may be disrupted with very fast and irregular rhythms.

The Electrical System: Your heart has an electrical system that controls its rhythm. In Brugada Syndrome, there can be glitches in this system, causing the heart to beat too fast or too slow.

Risk of Sudden Problems: People with Brugada Syndrome have a higher risk of sudden heart problems, like irregular heartbeats, syncope or even sudden cardiac arrest. This means that sometimes the heart can stop beating suddenly, which can be very serious and even life-threatening.

Symptoms May Vary: Some people with Brugada Syndrome don’t have any symptoms at all, while others may experience fainting, dizziness, or even seizures. It’s important to remember that not everyone with Brugada Syndrome will have the same symptoms or severity.

Brugada Syndrome is usually diagnosed through special tests, like an electrocardiogram (ECG) or a genetic test. These tests help doctors see if there are any irregularities in your heart’s rhythm or if there are specific gene changes related to Brugada Syndrome.

While there is no cure for Brugada Syndrome, there are ways to manage and reduce the risk of complications. Treatment may include medications to control the heart’s rhythm, and in some cases, a device called an implantable cardioverter-defibrillator (ICD) may be implanted to help regulate the heart’s rhythm and prevent sudden cardiac arrest.

Living with Brugada Syndrome means taking certain precautions to keep your heart healthy and reduce the risk of problems. It’s important to follow your doctor’s recommendations, take prescribed medications regularly, avoid triggers that may worsen symptoms (such as certain medications or extreme temperatures), and be aware of any changes in your body or symptoms you may experience.

Brugada Syndrome can be a serious condition, but with proper management and care, many people with Brugada Syndrome can live full and active lives. It’s important to work closely with your healthcare team, stay informed about your condition, and take steps to protect your heart health.

Remember, you’re not alone in this journey. There are resources, support groups, and healthcare professionals who are here to help you navigate through living with Brugada Syndrome.Top of Form

About the Registry

The Pediatric Brugada Registry is like a big book where doctors and researchers keep important information about children who have Brugada Syndrome. Here’s what you need to know about it:

Collects Information: The registry gathers details about children and families who have been diagnosed with Brugada Syndrome. This includes things like their age, symptoms they may have, and how their hearts are doing.

By putting all this information together, doctors can better understand Brugada Syndrome in children. They can see patterns and learn more about how it affects different kids

The registry helps doctors and researchers find better ways to take care of children with Brugada Syndrome. They can learn which treatments work best and how to keep kids with Brugada Syndrome healthy

Sharing Information: Hospitals and doctors from different places of the world share information about children with Brugada Syndrome. This helps create a big picture of the condition and how it affects kids around the world.

Better Treatment: By studying lots of cases, doctors can find new treatments or ways to manage Brugada Syndrome in children. This means kids can get better care and have a higher chance of staying healthy.

Families of children with Brugada Syndrome can feel supported knowing that doctors and researchers are working hard to understand and improve care for their loved ones.

Building Knowledge: Every child added to the registry helps build knowledge about Brugada Syndrome. This means that future generations of children might have even better treatments and care because of what’s learned from the registry