Síndrome de Wolff-Parkinson-White
Revisado por Dr Adrian Bonsall, MBBSÚltima atualização por Dr Colin Tidy, MRCGPLast updated 1 Aug 2017
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Wolff-Parkinson-White syndrome is not common but can cause a fast heart rate or other heart rhythm abnormalities from time to time. Treatment can be given for the fast heart rate and also to prevent any further episodes.
At a glance
Wolff-Parkinson-White (WPW) syndrome is an extra electrical connection in the heart present from birth.
It can cause episodes of a very fast heart rate (tachycardia) and other heart rhythm problems.
Symptoms include palpitations, dizziness, and chest pain.
Diagnosis often involves an electrocardiogram (ECG).
Treatment options include medication, radiofrequency ablation, or, rarely, heart surgery.
If symptoms are severe or last a long time, seek medical help.
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What is Wolff-Parkinson-White syndrome?
In Wolff-Parkinson-White (WPW) syndrome there is an extra connection (an accessory pathway) between the atria and ventricles. This means that as well as electrical impulses passing normally between the atria and the ventricles at the AV node, electrical impulses can also pass abnormally along the accessory pathway.
The accessory pathway in WPW syndrome is known as the bundle of Kent. It is a congenital problem which means that it is present from birth. The majority of people with WPW syndrome have no other heart abnormalities.
An electrical impulse that passes along the accessory pathway can arrive at the ventricles more quickly than normal. There is not the usual impulse delay that occurs at the AV node and no limiting of the electrical impulses that pass through. This can cause the heart rate to speed up. The accessory pathway can also sometimes transmit electrical impulses backwards from the ventricles to the atria.
So, in WPW syndrome, the normal electrical activity of the heart is disrupted. There is a risk of developing a fast heart rate (a tachycardia) from time to time and other heart rhythm disturbances (arrhythmias). WPW syndrome can lead to what is called a supraventricular tachycardia. Tachycardia is a heart rate over 100 beats per minute (bpm). 'Supra' means above and because the atria are above the ventricles, the tachycardia is supraventricular.
The common arrhythmia that occurs in WPW syndrome is a paroxysmal (intermittent) supraventricular tachycardia (SVT). Other arrhythmias that can also occur include fibrilação atrial (FA), atrial flutter and atrioventricular re-entrant tachycardia (AVRT). Rarely, another arrhythmia called ventricular fibrillation can develop.
How common is Wolff-Parkinson-White syndrome?
Voltar ao conteúdoWPW syndrome probably affects somewhere between 1-3 in 1,000 people. It is more common in men. There does seem to be some genetic basis, as WPW syndrome can run in families. However, most cases of WPW syndrome occur in people with no known family history.
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Sintomas
Voltar ao conteúdoSymptoms are caused by the episodes of rapid heart rate (tachycardia). How often these episodes occur can vary from person to person. They can include:
In some people, symptoms can be more severe. An episode of a very rapid heart rate (up to about 250 bpm) can cause:
Your blood pressure to drop and lead to collapse (blackout).
A build-up of fluid in your lungs and falta de ar.
Your heart can stop beating altogether (a cardiac arrest). However, this is rare.
In some people, the rapid heart rate only ever occurs once or twice. In others, it can occur a few times per week. Each episode of tachycardia may last from less than a minute to a few hours. An episode of tachycardia may even last for a few days but this is rare.
Many people are not aware that they have WPW syndrome because their symptoms are mild or don't occur very often.
How is Wolff-Parkinson-White syndrome diagnosed?
Voltar ao conteúdoIt may be diagnosed by doing a rastreamento cardíaco (eletrocardiograma, ou ECG). There are classic changes on the ECG that can be seen in some people with WPW syndrome.
Sometimes an ECG ambulatorial may be suggested.
Special tests called electrophysiology studies may be carried out in some people. They can help to find the precise area in the heart where the accessory pathway is located.
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Tratamento
Voltar ao conteúdoTreating an episode of rapid heart rate
Many episodes of SVT soon stop on their own and no treatment is needed.
Simple measures, including drinking a cold glass of water, holding your breath or putting your face into cold water.
If an episode of SVT lasts a long time or is severe, you may need to be admitted to hospital.
Medicines can be used to stop an episode of SVT - eg, adenosine.
Electric shock treatment (cardioversion) is sometimes used.
Prevention of episodes of rapid heart rate
If you have no symptoms and are at low risk of complications you may need no treatment.
Radiofrequency destruction (ablation) is the treatment of choice but other options are available.
Radiofrequency ablation
A thin tube called a catheter is inserted into an artery near your groin. The tube is passed up to your heart.
The small area in your heart that causes the fast heart rate (the accessory pathway) is destroyed using a type of energy called radiofrequency.
Radiofrequency ablation can have very good results and can cure the condition in most people.
Medication treatment
Long-term treatment with a medicine may be advised if you don't want to have radiofrequency ablation, or if this has failed. One medicine used is called amiodarona.
Heart surgery
Heart surgery is still used in some cases - eg, if radiofrequency ablation has failed and you don't want to take medication for the rest of your life. Open heart surgery aims to find and destroy the accessory pathway that causes the fast heart rate.
Qual é a perspectiva?
Voltar ao conteúdoWPW syndrome can be life-threatening during an acute episode of SVT but the outlook (prognosis) is otherwise very good. Catheter ablation usually cures WPW syndrome but some people with WPW aren't suitable for this treatment.
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Perguntas frequentes
Can Wolff-Parkinson-White syndrome only be found in people with a family history of heart conditions?
No, while there does seem to be a genetic basis for WPW syndrome and it can run in families, most cases occur in people where there is no known family history of the condition. It is a congenital problem, meaning it is present from birth.
What is the 'bundle of Kent' mentioned in the article?
The 'bundle of Kent' is the name for the extra connection, or accessory pathway, between the upper and lower chambers of the heart in people with Wolff-Parkinson-White syndrome. It allows electrical impulses to bypass the normal pathway, which can lead to a faster heart rate.
I have WPW syndrome but don't experience symptoms very often. Is this normal?
Yes, many people with WPW syndrome are not aware they have it because their symptoms are mild or do not occur very often. The frequency of rapid heart rate episodes can vary greatly from person to person.
If I have an episode of a rapid heart rate, what simple things can I try to stop it?
If you experience an episode of rapid heart rate, simple measures like drinking a cold glass of water, holding your breath, or putting your face into cold water may help to stop it. Many episodes resolve on their own without further treatment.
Are there any situations where radiofrequency ablation might not be the best treatment for WPW syndrome?
Yes, radiofrequency ablation is considered the treatment of choice and can often cure the condition. However, if you prefer not to have this procedure, or if it has been unsuccessful, long-term medication treatment might be advised. In some cases, heart surgery may also be considered if ablation fails and medication is not preferred for life.
What is the overall long-term outlook for someone diagnosed with Wolff-Parkinson-White syndrome?
The overall long-term outlook for people with Wolff-Parkinson-White syndrome is generally very good. Although it can be life-threatening during an acute, severe episode of a rapid heart rate, treatments like catheter ablation usually cure the condition for most individuals. However, some people may not be suitable for this specific treatment.
Leitura adicional e referências
- Symptoms, Diagnosis and Monitoring of Arrhythmias; American Heart Association, 2009
- Kireyev D, Fernandez SF, Gupta V, et al; Targeting tachycardia: diagnostic tips and tools. J Fam Pract. 2012 May;61(5):258-63.
- Camm AJ; Arritmias cardíacas--desafios e tribulações. Lancet. 27 de outubro de 2012;380(9852):1448-51. doi: 10.1016/S0140-6736(12)61773-5.
- Raviele A, Giada F, Bergfeldt L, et al; Gestão de pacientes com palpitações: um documento de posição da Associação Europeia de Ritmo Cardíaco. Europace. 2011 Jul;13(7):920-34. doi: 10.1093/europace/eur130.
- Verificando seu pulso; Fundação Britânica do Coração
- Sohinki D, Obel OA; Current trends in supraventricular tachycardia management. Ochsner J. 2014 Winter;14(4):586-95.
- Albert CM, Stevenson WG; O Futuro das Arritmias e da Eletrofisiologia. Circulation. 21 de junho de 2016; 133(25): 2687-96. doi: 10.1161/CIRCULATIONAHA.116.023519.
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About the authorView full bio

Dr Colin Tidy, MRCGP
Médico Generalista, Autor Médico
MBBS, MRCGP, MRCP (Paediatrics), DCH
Dr Colin Tidy é um médico do NHS, baseado em Oxfordshire.
About the reviewerView full bio

Dr Adrian Bonsall, MBBS
Autor Médico
MA (Química), MBBS (Hons), DCH
Desde 2000, Adrian trabalha em pediatria de emergência e cuidados críticos em Sydney, com interesses particulares em toxicologia, trauma e ressuscitação.
Histórico do artigo
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1 Aug 2017 | Última versão

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