Diagnosis

To diagnose long QT syndrome, your doctor will review your symptoms, your medical and family history, and conduct a physical examination. If your doctor thinks you may have long QT syndrome, you might need several tests to confirm the diagnosis. These include:

  • Electrocardiogram (ECG). During an ECG, doctors attach sensors to your chest (electrodes) that can detect the electrical activity of your heart. An ECG measures the timing and duration of each electrical phase in your heartbeat.

    You might have this test while at rest or during an exercise stress test, in which doctors monitor your heart activity as you exercise on a treadmill or a stationary bicycle. Your doctor may also suggest your family members have ECGs.

  • Holter monitor. This portable ECG device can be worn for a day or more to record your heart's activity as you go about your routine.
  • Event monitor. This portable ECG device is attached to your body to monitor your heart activity over a few weeks to a few months. When you have symptoms, you press a button. This allows your doctor to check your heart rhythm at the time of your symptoms.

In some people with suspected long QT syndrome, the ECG doesn't show an abnormally prolonged QT interval. You may need other tests, such as:

  • A nonexercise (medication) stress test. This is an ECG test done while you're given a medication such as epinephrine (Adrenalin) that stimulates your heart in a way similar to exercise. Doctors then monitor the effects of the medication on the way your heart recharges.

    This test can help doctors diagnose people with suspected long QT syndrome and may help determine which genes are associated with the condition. It may also be used to diagnose people with long QT syndrome who have a gene associated with long QT syndrome but who have a normal QT interval (recharging time) at rest.

  • Genetic testing. A genetic test for long QT syndrome is available and may be covered by some private and governmental insurance plans. Genetic tests for long QT syndrome can generally find the genetic cause for about 3 out of every 4 cases of inherited long QT syndrome. However, genetic tests can't detect all cases of long QT syndrome.

    If your genetic cause of long QT syndrome is discovered through a positive genetic test, your doctor may recommend that your family members also be tested to determine whether they inherited the same genetic mutation.

  • A second opinion. You might want to seek a second opinion before proceeding with treatment if your doctor diagnoses you with long QT syndrome. People can sometimes be misdiagnosed as having long QT syndrome when it's not actually present.

Treatment

Treatment for inherited long QT syndrome involves some simple preventive measures. It can also involve medications, as well as left cardiac sympathetic denervation surgery or implanting medical devices such as a defibrillator (ICD), or both.

The goal of treatment is either to prevent the long QT heart from ever beating out of control or to prevent sudden death. Your doctor will discuss with you the most appropriate treatment options for your condition based on your symptoms, your type of long QT syndrome, and your risk of fainting or sudden cardiac arrest.

For acquired long QT syndrome, treating the cause of the condition may eliminate it. Doctors will also treat heart rhythm disorders (arrhythmias) as needed.

If you are diagnosed with acquired long QT syndrome due to certain medications, your doctor may recommend that you stop taking the medication causing the condition and switching medications. Some people might need additional treatment.

Medications

Medications used to treat long QT syndrome may include:

  • Beta blockers. These heart drugs include nadolol (Corgard) and propranolol (Inderal LA, InnoPran XL). They slow the heart rate and make the rhythm associated with long QT syndrome less likely. Beta blockers work by blunting the way your heart reacts to adrenaline.
  • Mexiletine. Taking this anti-arrhythmic drug in combination with beta blockers might help shorten the QT interval and decrease the likelihood of a long QT syndrome-triggered faint, seizure or sudden death.

    This medication is often used for the third-most common subtype of inherited long QT syndrome, LQT3. However, it may also be used for the two most common subtypes, LQT1 and LQT2.

  • Spironolactone and potassium. For certain forms of long QT syndrome, spironolactone (Aldactone), a medication used to help the body hold on to potassium, or potassium supplements, or both, might improve the heart's recharging system.
  • Fish oil. In general, current evidence does not support supplementation with heart-healthy fish oil (omega-3 fatty acid) or eating fish high in omega-3 fatty acids to decrease the risk of cardiac events or death from abnormal heart rhythms. However, if you have inherited long QT syndrome, fish oil may be a reasonable complementary alternative medication to take in addition to other therapies. Talk to your doctor before starting fish oil or any other supplements or medications.

Your doctor might suggest treatment for long QT syndrome even if you don't often experience signs or symptoms.

If you do need treatment, take the medications your doctor prescribes as directed. While medications won't cure the condition, they provide some protection against possibly fatal disruptions of your heart rhythm. You might need to take a medication such as a beta blocker indefinitely.

Surgical procedures

Depending on your condition, your doctor might consider other treatments for you, including:

  • Left cardiac sympathetic denervation surgery. In this procedure, surgeons remove specific nerves along the left side of your spine in your chest. These nerves are part of the body's sympathetic nervous system, which helps regulate heart rhythm. The surgery significantly reduces the risk of sudden death.

    This surgery is generally reserved for people who are considered at high risk of sudden death and are experiencing appropriate ICD shocks, people who are continuing to experience fainting or seizures while taking their medications, or people unable to tolerate their medications because of side effects.

  • Implantable cardioverter-defibrillator (ICD). This device, which is implanted under the skin of your chest, can stop a potentially fatal arrhythmia. An ICD continuously monitors your heartbeat. If it detects an abnormal heart rhythm, it delivers electrical shocks to reset the heart to a normal rhythm.

    Implanting an ICD is a major procedure and can result in inappropriate shocks and other complications. Therefore, the decision to implant an ICD, especially in children, needs to be carefully considered.

    Most people with inherited long QT syndrome do not need an ICD. Importantly, an ICD should not be implanted solely because of the tragic occurrence of a long QT syndrome-triggered sudden death in a relative.

Potential future treatments

A combination of advances in the field of genetics, computerized clinical decision support systems that alert doctors to drug interactions, and handheld or wearable monitors may help improve treatment for people with both inherited and acquired long QT syndrome.

Lifestyle changes

In addition to medications or surgery, your doctor might recommend lifestyle changes to reduce your chances of a long QT syndrome-related fainting spell or sudden cardiac arrest. These could include:

  • Avoiding medications that could cause prolonged QT intervals
  • Getting plenty of liquids during illnesses that are causing vomiting or diarrhea
  • Lowering your temperature if a fever occurs
  • Reducing your exposure to loud or startling noises
  • Staying away from situations that could make you excited or angry
  • Avoiding strenuous exercise or contact sports, or have a safety plan in place if you continue in competitive sports

Work with your doctor to balance these lifestyle recommendations against the clear, heart-healthy benefits of an active lifestyle. It may be possible to stay fully active in sports, including competitive sports, after carefully reviewing the risks and benefits with your doctor.

If your symptoms are mild or don't occur very often, your doctor might recommend only simple preventive measures or lifestyle changes, and he or she might not prescribe any daily medications for you.

Clinical trials

Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this disease.

Lifestyle and home remedies

Once you've been diagnosed with long QT syndrome, several steps can help you avoid serious consequences, including:

  • Don't overexert yourself. You might not need to give up sports if you have long QT syndrome. Your doctor might permit recreational activities as long as you have a buddy along in case you have a fainting episode. In general, people with long QT syndrome should never swim alone.

    Strenuous exercise might be dangerous and isn't recommended for some people with long QT syndrome. However, others might have a lower risk of complications and may be able to continue strenuous exercise and even competitive sports. Discuss this issue with your doctor in detail.

  • Know your symptoms. Be fully aware of symptoms that can warn you of irregular heart rhythms and decreased blood flow to your brain, such as feeling like you may faint.
  • Inform other people. Make family, friends, teachers, neighbors and anyone else who has regular contact with you aware of your heart condition. Wear a medical alert identification to notify health care providers of your condition.
  • Have plans in case of an emergency cardiac event. Family members may want to learn cardiopulmonary resuscitation (CPR) so they can provide immediate resuscitation if you ever need it. In some situations, it might be appropriate to have or be able to rapidly access an automatic external defibrillator (AED).

    However, if your inherited long QT syndrome has been evaluated and treated carefully, you are generally unlikely to ever need CPR or an AED.

  • Control startling events as much as possible. Turn down the volume on doorbells and turn off the telephone ringer or your cellphone at night.
  • Visit your doctor. Your cardiologist will likely recommend that you have regular follow-up appointments with him or her. Let your doctor know if you have symptoms of long QT syndrome or any changes in your condition. Your doctor may make changes to your treatment plan or suggest additional treatments for you.

Sexual intercourse doesn't appear to increase the risk of long QT syndrome. Pregnancy and delivery aren't associated with an increased risk of symptoms in women with long QT syndrome.

Still, if you have inherited long QT syndrome, your doctor will want to monitor you closely both during your pregnancy and after. Women with long QT syndrome, especially a form called LQT2, are at increased risk during the period following delivery and need careful monitoring.

Coping and support

Long QT syndrome can be a worrisome condition because of its serious potential outcomes. Worrying about possible fatal heart rhythms can obviously be stressful for you and your family.

Families with inherited long QT syndrome might find it helpful to talk to a cardiologist with expertise in long QT syndrome, a genetics counselor and a therapist, as well as other families with the condition.

Preparing for your appointment

If you develop signs and symptoms of long QT syndrome, contact your doctor. After an initial exam, your doctor likely will refer you to a doctor trained in diagnosing and treating heart conditions (cardiologist), a doctor trained in heart rhythm conditions (electrophysiologist) or a cardiologist who specializes in genetic heart conditions (genetic cardiologist) that may predispose people to sudden death.

Here's some information to help you prepare for your appointment, and what to expect from your doctor.

What you can do

  • Write down any signs and symptoms you've had, and for how long.
  • Write down your key medical information, including any other health conditions and the names of all of your medications. It will also be important to share any family history of heart disease or sudden death with your doctor.
  • Find a family member or friend who can come with you to the appointment, if possible. Someone who accompanies you can help remember what the doctor says.
  • Write down the questions you want to be sure to ask your doctor.

Questions to ask the doctor at your initial appointment include:

  • What is likely causing my signs and symptoms?
  • Are there any other possible causes for these signs and symptoms?
  • What tests are needed?
  • Should I consult a specialist?

Questions to ask if you're referred to a cardiologist or electrophysiologist include:

  • Do I have long QT syndrome? What type?
  • What is my risk of complications from this condition?
  • What treatment approach do you recommend?
  • If the first treatment doesn't work, what will you recommend next?
  • If you're recommending medications, what are the possible side effects?

Questions to ask if your doctor recommends surgery include:

  • What type of procedure is most likely to be effective in my case and why?
  • Where should I have my surgery performed?
  • Should I be referred to a long QT syndrome center of excellence?
  • What should I expect from my recovery and rehabilitation after surgery?

Additional questions include:

  • Will I need frequent exams and lifelong treatment for this condition?
  • What emergency signs and symptoms of long QT syndrome should I be aware of?
  • Should I tell my friends, teachers and co-workers that I have this condition?
  • What activity restrictions will I need to follow?
  • Could any dietary changes help me manage this condition?
  • What medicines should I avoid?
  • What is my long-term outlook with treatment?
  • Will it be safe for me to become pregnant in the future?
  • What is the risk that my future children would have this defect?
  • Should I meet with a genetic counselor?

In addition to the questions that you've prepared ahead of time, don't hesitate to ask other questions during your appointment if you don't understand something.

What to expect from your doctor

A doctor who sees you for possible long QT syndrome might ask a number of questions, including:

  • What are your symptoms?
  • When did you first begin experiencing symptoms?
  • Have your symptoms gotten worse over time?
  • Do strong emotions trigger your symptoms, such as excitement, anger or surprise?
  • Does exercise bring on your symptoms?
  • Does being startled — such as by a doorbell or phone ringing — trigger your symptoms?
  • Do your symptoms include feeling lightheaded or dizzy?
  • Have you ever fainted?
  • Have you ever had a seizure?
  • Do your symptoms include a fluttering sensation in your chest?
  • Do you gasp in your sleep that you're aware of?
  • Have you been diagnosed with any other medical conditions?
  • Are you aware of any history of heart conditions in your family?
  • Have any first-degree relatives — parent, sibling or child — ever died unexpectedly, such as from drowning, or died suddenly without explanation?
  • What medications are you currently taking, including over-the-counter and prescription drugs as well as vitamins and supplements?
  • Have you ever used recreational drugs? If so, which ones?
  • What is your usual daily diet?
  • Do you use caffeine? How much?
  • Do you have any children? Are you planning any future pregnancies?

What you can do in the meantime

While you wait for your appointment, check with your family members to find out if any first-degree relatives (children, siblings, parents), second-degree relatives (aunts, uncles, grandparents), third-degree relatives (great aunts, great uncles, cousins) or any other known relatives have been diagnosed with heart disease or have died suddenly.

Having a first-degree relative who died from an unexpected cause — such as from SIDS, from drowning or while driving — is an important clue for your doctor. In general, knowing as much as possible about your family's health history will help your doctor determine the next steps for your diagnosis and treatment.

A nonprofit advocacy organization called the Sudden Arrhythmia Death Syndromes (SADS) Foundation can help you prepare and understand your family history as it relates to a possible diagnosis of LQTS.

If exercise makes your symptoms worse, avoid exercising until you see your doctor.

Long QT syndrome care at Mayo Clinic

Nov. 18, 2017
References
  1. What is long QT syndrome? National Heart, Lung, and Blood Institute. http://www.nhlbi.nih.gov/health/health-topics/topics/qt. Accessed Feb. 18, 2017.
  2. Conduction disorders. American Heart Association. http://www.heart.org/HEARTORG/Conditions/Arrhythmia/AboutArrhythmia/Conduction-Disorders_UCM_302046_Article.jsp#.WLhwehiZOu4. Accessed March 2, 2017.
  3. Seslar SP, et al. Clinical features of congenital long QT syndrome. http://www.uptodate.com/home. Accessed Feb. 15, 2017.
  4. Zimetbaum PJ, et al. Genetics of congenital and acquired long QT syndrome. http://www.uptodate.com/home. Accessed Feb. 15, 2017.
  5. Berul CI, et al. Acquired long QT syndrome. http://www.uptodate.com/home. Accessed Feb. 15, 2017.
  6. AskMayoExpert. Screening (adult). Rochester, Minn.: Mayo Foundation for Medical Education and Research; 2017.
  7. AskMayoExpert. Significance of a long QT interval (adult). Rochester, Minn.: Mayo Foundation for Medical Education and Research; 2017.
  8. What is the heart? National Heart, Lung, and Blood Institute. http://www.nhlbi.nih.gov/health/health-topics/topics/hhw. Accessed Feb. 18, 2017.
  9. AskMayoExpert. Prolonged QT interval: Signs and symptoms (adult). Rochester, Minn.: Mayo Foundation for Medical Education and Research; 2017.
  10. Arrhythmia. National Heart, Lung, and Blood Institute. http://www.nhlbi.nih.gov/health/health-topics/topics/arr/types. Accessed Feb. 18, 2017.
  11. Seslar SP, et al. Diagnosis of congenital long QT syndrome. http://www.uptodate.com/home. Accessed Feb. 18, 2017.
  12. Ferri FF. Prolonged Q-T interval syndrome. In: Ferri's Clinical Advisor 2016. Philadelphia, Pa.: Mosby Elsevier; 2016. https://www.clinicalkey.com. Accessed Feb. 15, 2017.
  13. Zimetbaum PJ, et al. Prognosis and management of congenital long QT syndrome. http://www.uptodate.com/home. Accessed Feb. 15, 2017.
  14. Ackerman JP, et al. The promise and peril of precision medicine: Phenotyping still matters most. Mayo Clinic Proceedings. 2016;91:1606.
  15. Aziz PF, et al. Sports participation in genotype positive children with long QT syndrome. Clinical Electrophysiology. 2015;1:62.
  16. Riggin ER. Allscripts EPSi. Mayo Clinic, Rochester, Minn. Jan. 10, 2017.
  17. Schwartz PJ, et al. Management of survivors of cardiac arrest — The importance of genetic investigation. Nature Reviews: Cardiology. 2016;13:560.
  18. Genetic testing. Sudden Arrhythmia Death Syndromes Foundation. http://www.sads.org/living-with-sads/Insurance/Genetic-Testing#.VfB_G9iFODZ. Accessed Feb. 15, 2017.
  19. Mazzanti A, et al. Gene-specific therapy with mexiletine reduces arrhythmic events in patients with long QT syndrome type 3. Journal of the American College of Cardiology. 2016;67:1053.
  20. Fish Oil. Natural Medicines. https://naturalmedicines.therapeuticresearch.com/databases/food,-herbs-supplements/professional.aspx?productid=993. Accessed Feb. 21, 2017.
  21. Schwartz PJ, et al. Predicting the unpredictable: Drug-induced QT prolongation and torsades de pointes. Journal of the American College of Cardiology. 2016;67:1639.
  22. Loar RW, et al. Sudden cardiac arrest during sex in patients with either catecholaminergic polymorphic ventricular tachycardia or long-QT syndrome: A rare but shocking experience. Journal of Cardiovascular Electrophysiology. 2015;26:300.
  23. Garg L, et al. The influence of pregnancy in patients with congenital long QT syndrome. Cardiology in Review. In press. Accessed Feb. 20, 2017.
  24. Ackerman MJ (expert opinion). Mayo Clinic, Rochester, Minn. Mar. 13, 2017.
  25. Priori SG, et al. HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes. Heart Rhythm. 2013;10:1932.
  26. Priori SG, et al. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death. European Heart Journal. 2015;36:2793.
  27. Ackerman MJ, et al. Beta-blocker therapy for long QT syndrome and catecholaminergic polymorphic ventricular tachycardia: Are all beta-blockers equivalent? Heart Rhythm. 2017;14:e41.
  28. Fernández-Falgueras A, et al. Cardiac channelopathies and sudden death: Recent clinical and genetic advances. Biology. 2017;6:7.
  29. Giudicessi JR, et al. Calcium revisited: New insights into the molecular basis of long-QT syndrome. Circulation: Arrhythmia and Electrophysiology. 2016;9:e002480.
  30. Collura CA, et al. Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgery. Heart Rhythm. 2009;6:752.
  31. Gaba P, et al. Implantable cardioverter-defibrillator explantation for overdiagnosed or overtreated congenital long QT syndrome. Heart Rhythm. 2016;13:879.
  32. Desimone CV, et al. Effects on repolarization using dynamic QT interval monitoring in long-QT patients following left cardiac sympathetic denervation. Journal of Cardiovascular Electrophysiology. 2015;26:434.
  33. Johnson JN, et al. Competitive sports participation in athletes with congenital long QT syndrome. JAMA. 2012;308:765.
  34. Johnson JN, et al. Return to play? Athletes with congenital long QT syndrome. British Journal of Sports Medicine. 2013;47:28.
  35. Antiel RM, et al. Quality of life after videoscopic left cardiac sympathetic denervation in patients with potentially life-threatening cardiac channelopathies/cardiomyopathies. Heart Rhythm. 2016;13:62.
  36. Sriram CS, et al. Malignant bileaflet mitral valve prolapse syndrome in patients with otherwise idiopathic out-of-hospital cardiac arrest. Journal of the American College of Cardiology. 2013;62:222.

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