- By sahlhealth
- May 18, 2021
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Brugada (brew-GAH-dah) syndrome is a potentially life-threatening heart rhythm disorder that is sometimes inherited. People with Brugada syndrome have an increased risk of abnormal heart rhythms from the lower chambers of the heart (ventricular arrhythmias).
Many people who have Brugada syndrome don't have any symptoms, and so they're unaware of their condition. A telltale abnormality — called a type 1 Brugada ECG pattern — is detected by an electrocardiogram (ECG) test. Brugada syndrome is much more common in men than women.
Brugada syndrome is treatable with preventive measures such as avoiding aggravating medications, reducing fever and, when necessary, using a medical device called an implantable cardioverter-defibrillator (ICD).
Many people who have Brugada syndrome are undiagnosed because the condition often doesn't cause any noticeable symptoms.
The most important sign of Brugada syndrome is an abnormal pattern on an electrocardiogram (ECG) called a type 1 Brugada ECG pattern. You can't feel a Brugada sign — it's only detected on an ECG.
It's possible to have a Brugada sign, or pattern, without having Brugada syndrome. However, signs and symptoms that could mean you have Brugada syndrome include:
Gasping, labored breathing, particularly at night
Irregular heartbeats or palpitations
Extremely fast and chaotic heartbeat (sudden cardiac arrest)
Brugada syndrome signs and symptoms are similar to some other heart rhythm problems, so it's essential that you see your doctor find out if Brugada syndrome or another heart rhythm problem is causing your symptoms.
When to see a doctor
If you have heart palpitations or an irregular heartbeat (arrhythmia), make an appointment to see your doctor. Your problem could be caused by a heart rhythm problem, but tests can determine if the underlying cause of your heart problem is Brugada syndrome.
If you faint and you suspect it may be because of a heart condition, seek emergency medical attention.
If your parent, sibling or child has been diagnosed with Brugada syndrome, you may want to make an appointment with your doctor. He or she can discuss whether you should have genetic testing to see if you're at risk of Brugada syndrome.
Aside from a typical physical examination, listening to your heart with a stethoscope and the standard 12-lead ECG, other tests to see if you have Brugada syndrome include:
Electrocardiogram (ECG) with medication. In this noninvasive test, a technician places probes on your chest that record the electrical impulses that make your heart beat. An ECG records these electrical signals and can help your doctor detect irregularities in your heart's rhythm and structure.
However, because your heart rhythm can change, an electrocardiogram by itself may not detect an abnormal heart rhythm. Your doctor may give you certain medications — including some types of anti-anginals, antidepressants, antipsychotics or antihistamines — that can unmask the type 1 Brugada ECG pattern in people who have Brugada syndrome. The medication is usually injected by an intravenous (IV) line.
Electrophysiology (EP) test. If your ECG suggests that you have Brugada syndrome, or if you have experienced symptoms such as sudden cardiac arrest, your doctor may also recommend an EP test in an effort to see how easy it is to get the heart to go into the abnormal Brugada rhythm.
In an EP test, a catheter is threaded through a vein in your groin to your heart, similar to cardiac catheterization. Electrodes are then passed through the catheter to different points in your heart. The electrodes then map out any irregular heartbeats. The electrodes don't shock your heart — they just detect the electrical signals running through your heart.
Genetic testing. While genetic testing isn't required to diagnose Brugada syndrome, your doctor may recommend genetic testing to help determine whether other family members are affected if you're diagnosed with Brugada syndrome.
Brugada syndrome treatment depends on the risk of an abnormal heartbeat (arrhythmia). Those considered at high risk have:
A personal history of serious heart rhythm problems
A personal history of fainting spells
A personal history of survived sudden cardiac arrest
Because of the nature of the heart rhythm abnormality, medications usually aren't used to treat Brugada syndrome. A medical device called an implantable cardioverter-defibrillator is the main treatment.
Implantable cardioverter-defibrillator (ICD). For high-risk individuals, treatment may include an implantable cardioverter-defibrillator (ICD). This small device continuously monitors your heart rhythm and delivers electrical shocks when needed to control abnormal heartbeats.
A family, a flexible, insulated wire (lead) is inserted into a major vein under or near your collarbone and guided, with the help of X-ray images, to your heart.
The ends of the leads are secured to your heart's bottom pumping chambers (ventricles), while the other ends are attached to the shock generator, which is usually implanted under the skin beneath your collarbone. The procedure to implant an ICD usually requires overnight hospitalization following the procedure.
ICDs may cause complications, some life-threatening, so it's important to weigh the benefits and the risks. People who have an ICD implanted as a treatment for Brugada syndrome have reported receiving unnecessary shocks from their ICD even when their heartbeat was not life-threatening.
Your doctor will program your ICD to reduce this risk. If you have an ICD implanted as part of your Brugada syndrome treatment, talk to your doctor about ways to avoid inappropriate shocks.
Drug therapy. Sometimes, medications such as quinidine are used to prevent the heart from going into its potentially dangerous rhythm. It may also be helpful as supplemental therapy for people who already have an ICD.
However, if a person with Brugada syndrome is at high risk because of a prior cardiac arrest or a concerning fainting episode, the main treatment is ICD implantation.
Coping and support
Finding out you have Brugada syndrome can be difficult. You may worry about whether your treatment will work or if other family members could be at risk. There are ways to cope with your feelings about your condition, including:
Support groups. Finding out that you or a loved one has heart disease can be unnerving. Turning to friends and family for support is essential, but if you find you need more help, talk to your doctor about joining a support group. You may find that talking about your concerns with others who are experiencing the same difficulties can help.
Continued medical checkups. If you have Brugada syndrome, it's a good idea to regularly check in with your doctor to make sure you're properly managing your heart condition. Regular checkups can help your doctor decide if you need to change your treatment and may help catch any new problems early.
Preparing for your appointment
If your doctor thinks you have Brugada syndrome, you'll likely need several appointments to confirm the diagnosis and figure out how serious your condition is. Your doctor should give you instructions before each appointment on specific preparations.
Here's some information to help you get ready for your appointment, and to know what to expect from your doctor.
What you can do
Be aware of any pre-appointment restrictions. At the time you make the appointment, be sure to ask if there's anything you need to do in advance. For example, if you're having a test to look at your heart's electrical activity (electrophysiology study), you'll need to fast for eight to 12 hours before your test.
Write down any symptoms you're experiencing, including any that may seem unrelated to Brugada syndrome.
Write down key personal information, especially any family history of sudden death, cardiac arrest or heart conditions, and any personal history of fainting or heart arrhythmias.
Make a list of all medications, vitamins or supplements you're taking.
Take a family member or friend along, if possible. Someone who accompanies you may remember something that you missed or forgot.
Write down questions for your doctor.
Preparing a list of questions will help you make the most of your time with your doctor. For Brugada syndrome, some basic questions to ask your doctor include:
What is likely causing my symptoms or condition?
What are other possible causes for my symptoms or condition?
What kinds of tests will I need?
Will I need treatment for Brugada syndrome?
What's the best treatment?
What's an appropriate level of physical activity?
How often do I need follow-up visits to monitor my condition?
I have other health conditions. How can I best manage them together?
Are there any restrictions that I need to follow?
Should I see a specialist?
Are there brochures or other printed material I can take home with me? What websites do you recommend?
Should my family be screened?
Don't hesitate to ask any other questions you have.
What to expect from your doctor
Your doctor is likely to ask you a number of questions, such as:
Do you have a family history of Brugada syndrome or other heart rhythm problems?
When did your symptoms start?
Have your symptoms been continuous or occasional?
How often do you have symptoms, such as fainting?
Brugada syndrome is a heart rhythm disorder. Each beat of your heart is triggered by an electrical impulse generated by special cells in the right upper chamber of your heart. Tiny pores, called channels, on each of these cells direct this electrical activity, which makes your heart beat.
In Brugada syndrome, a defect in these channels can cause your heart to beat abnormally and spin electrically out of control in an abnormally fast and dangerous rhythm (ventricular fibrillation).
As a result, your heart doesn't pump effectively and not enough blood travels to the rest of your body. This will cause fainting if that rhythm lasts for only a short time or sudden cardiac death if the heart remains in that bad rhythm.
Brugada syndrome is often inherited, but it may also result from a hard-to-detect structural abnormality in your heart, imbalances in chemicals that help transmit electrical signals through your body (electrolytes), or the effects of certain prescription medications or cocaine use.
Brugada syndrome usually is diagnosed in adults and, sometimes, in adolescents. It's rarely diagnosed in young children.
Risk factors for Brugada syndrome include:
Family history of Brugada syndrome. If other family members have had Brugada syndrome, you're at an increased risk of having the condition.
Being male. Adult men are more frequently diagnosed than are women. In young children and adolescents, however, boys and girls are diagnosed at about the same rate.
Race. Brugada syndrome occurs more frequently in Asians than in other races.
Fever. While having a fever doesn't cause Brugada syndrome by itself, a fever can irritate the heart and stimulate a Brugada-triggered faint or sudden cardiac arrest, especially in children.
Complications of Brugada syndrome require emergency medical care. They include:
Sudden cardiac arrest. If not treated immediately, this sudden loss of heart function, breathing, and consciousness, which often occurs while sleeping, is fatal. With fast, appropriate medical care, survival is possible.
Administering cardiopulmonary resuscitation (CPR) — rapid compressions to the chest — and an external shock from an automatic external defibrillator (AED) can improve the chances of survival until emergency personnel arrives.
Fainting (syncope). If you have Brugada syndrome and you faint, seek emergency medical attention.