Sinoatrial Nodal Reentrant Tachycardia
- Article Author:
- Yamama Hafeez
- Article Editor:
- Shamai Grossman
- Updated:
- 7/10/2020 1:45:02 AM
- For CME on this topic:
- Sinoatrial Nodal Reentrant Tachycardia CME
- PubMed Link:
- Sinoatrial Nodal Reentrant Tachycardia
Introduction
The sinoatrial node (SA) is crescent in shape and is located subepicardially. It is 13.5 millimeters in length and is innervated by the vagus and sympathetic nerves in an average adult. The sinoatrial nodal artery supplies blood to the sinoatrial node, it branches off the right coronary artery in 60% of cases, whereas in 40% of cases, it comes from the left circumflex coronary artery. The SA node is a crucial component of the heart's conduction system and is its default pacemaker.[1][2][3]
Sinoatrial nodal reentrant tachycardia is a rare form of paroxysmal supraventricular tachycardia that has the following electrocardiogram features:
- Heart rate usually between 100 to 150 beats per minute (bpm)
- Similar P wave morphology to sinus tachycardia
- A frequent premature atrial complex at the initiation or termination of the tachycardia
- Abrupt onset and termination
The American College of Cardiology/American Heart Association Task Force on clinical practice guidelines and the heart rhythm society has defined sinoatrial nodal reentrant tachycardia as a focal atrial tachycardia from micro-reentry arising from the sinus node.
Etiology
The exact mechanism of sinoatrial nodal reentrant tachycardia remains controversial. Three distinct mechanisms are possible.
- The reentry circuit is existing primarily inside the sinoatrial node.
- The reentry circuit involves the sinoatrial node as a refractory center.
- The reentry circuit involves both the sinoatrial node and the perinodal tissue.
Most evidence suggests that the reentry circuit usually involves either just the sinoatrial node or both the sinoatrial node and the perinodal tissue. The theory of the sinoatrial node as a refractory center seems to lack much evidence.
Epidemiology
Although common in children and adults who have structural heart disease, SANRT is considered an uncommon tachyarrhythmia with very rare symptomatic presentations. In an electrophysiologic study on patients with paroxysmal supraventricular tachycardia incidence of SANRT was found to be within 2% to 17%. The exact prevalence of SANRT is difficult to determine both in the United States and globally as patients with this arrhythmia do not usually have symptoms and therefore do not present for electrophysiology study. Also, since SANRT is very similar to sinus tachycardia on the electrocardiogram, it is underdiagnosed.[4][5]
Pathophysiology
SANRT, as discussed, is prevalent among patients who have structural heart disease. The exact structure of the reentry circuit is controversial but is mostly believed to exist just within the SA node itself or to involve the perinodal tissue together with the SA node for the manifestation of this tachyarrhythmia. No extrinsic factors are known to cause SANRT.
Histopathology
Histopathological features of the reentrant circuit in humans are yet to be studied, although one study in dogs showed that increased intranodal fibrosis post-myocardial infarction provided an increased substrate for SANRT.
History and Physical
Patients with SANRT are usually asymptomatic. In rare cases, patients might present with symptoms of intermittent palpitations secondary to abrupt onset and cessation of the rhythm. Other symptoms patients might present with include dizziness, shortness of breath, pain/discomfort in the neck, pain/discomfort in the chest, anxiety, and polyuria secondary atrial natriuretic factor secreted mainly by the heart atria in response to atrial stretch. Although, uncommon patients with SANRT and a known history of coronary artery disease may present with a myocardial infarction secondary to the stress on the heart. Patients with SANRT and known history of heart failure may come in with acute exacerbation with possibly reduced ejection fraction secondary to tachycardia-induced cardiomyopathy.[6][7][8]
Patients with SANRT usually present with a heart rate within the range of 100 to 150 bpm. If a patient has known heart failure or coronary artery disease, he may complain of chest pain and may also have symptoms of heart failure such as wheezing or swelling in the lower extremities and tachypnea on physical exam. In rare instances, patients with SANRT might present with complaints of syncope secondary to tachycardia-induced reduced ventricular filling as less filling of the ventricles leads to the reduction in the cardiac output, which leads to decreased perfusion of the brain. Tachycardia-induced depression of the sinoatrial node may also contribute to syncopal symptoms. Hypotension secondary to decrease ventricular filling may be a significant physical exam finding in patients presenting with SANRT.
Evaluation
The most significant component of the assessment for a patient who presents with signs and symptoms of sinoatrial nodal reentrant tachycardia is history and physical exam. These should include vital signs (respiratory rate, blood pressure, temperature, and heart rate) and an electrocardiogram. A patient presenting with SANRT should undergo evaluation for any unknown underlying coronary artery disease or heart failure. During an assessment, it should be established whether the patient is hemodynamically stable based mainly on his blood pressure, mental status, and respiratory rate. Initial evaluation of patients with SANRT can include testing to access the patient's thyroid and pulmonary function, together with routine blood work. Since there is a frequent association between SANRT and structural heart disease, part of patients evaluation might also include echocardiography.
Treatment / Management
Most patients with SANRT do not need medical intervention as a heart of 100 to 150 bpm rarely induces any symptoms. In rare cases, patients with frequent SANRT might develop symptoms and require medical management. These patients might also benefit from treatment to avoid long-term adverse effects such as tachycardia-induced cardiomyopathy.
Medical management of patients presenting with SANRT begins with an initial evaluation of their hemodynamically stability. Hemodynamically unstable patients present with tachycardia associated with hypotension, ischemic chest pain, altered mental status, respiratory failure, or shock, and these patients need their SANRT terminated electrically with an urgent electrical cardioversion. Hemodynamically stable patients should be treated first with a carotid massage or other such vagal maneuvers to cease the rhythm acutely. If such methods are ineffective or inappropriate, intravenous adenosine is the next best step in the absence of contraindications to adenosine.[9][10]
Currently, there is a lack of large pharmacological studies in patients who present with SANRT due to the rarity of the rhythm and its less frequent complications. For chronic suppression of recurrent SANRT radiofrequency catheter ablation is recommended rather than suppressive medical therapy due to higher success rates of ablations together with short and long-term side effects of the medications. However, in patients who require prolonged suppressive medical therapy, verapamil, digoxin, or amiodarone can be used.
Differential Diagnosis
- Junctional ectopic tachycardia
- Nonparoxysmal junctional tachycardia
- Atrial flutter with variable block
- Atrial fibrillation
- Intraatrial reentrant tachycardia
- Atrial tachycardia
- Multifocal atrial tachycardia (MAT)
- Sinus tachycardia
- Inappropriate sinus tachycardia
- Atrial flutter
- Atrioventricular nodal reentrant tachycardia
- Atrioventricular reciprocating (reentrant) tachycardia
Pearls and Other Issues
As a result of extensive autonomic innervation of the sinus node, Valsalva maneuvers tend to terminate SANRT abruptly in contrast to sinus tachycardia where Valsalva maneuvers result in gradual slowing and then a gradual acceleration of the rhythm upon stopping of such maneuvers.
Enhancing Healthcare Team Outcomes
SANRT is a rare arrhythmia but can be confused with other atrial arrhythmias. Healthcare workers, including the nurse practitioner, should carefully examine these patients and rule out other reversible causes. Patients should be referred to a cardiologist if there is any echocardiographic evidence of structural heart disease. Most patients with SANRT do not need medical intervention as a heart of 100 to 150 bpm rarely induces any symptoms. Emergency department and cardiac nurses are responsible for monitoring patients and notify the interprofessional team if there are issues. In rare cases, patients with frequent SANRT might develop symptoms and require medical management. These patients might also benefit from treatment to avoid long-term adverse effects such as tachycardia-induced cardiomyopathy.
Currently, there is a lack of large pharmacological studies in patients who present with SANRT due to the rarity of the rhythm and its less frequent complications. For chronic suppression of recurrent SANRT radiofrequency catheter ablation is recommended rather than suppressive medical therapy due to higher success rates of ablations together with short and long-term side effects of the medications. However, in patients who require prolonged suppressive medical therapy, verapamil, digoxin, or amiodarone can be used. Pharmacists review prescribed medications for doses and interactions, as well as, providing patient education. [Level 5]