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Each year millions of people experience abnormal heart rhythms [arrhythmias], which are common as we age. For most, a normal resting heart rate is 60 to 100 beats per minute [bpm]. For athletic individuals, a normal resting heart rate may be as low as 40 to 60 bpm. Abnormal heart rhythms can be described as a heart beating too fast [above 100 bpm] or slow [below 60 bpm], a fluttering sensation in the chest area or the skipping of a heart beat. When electrical impulses in the heart become too fast, too slow, or irregular they cause the heart to beat irregularly.
Abnormal heart rhythms may cause the heart to pump blood inefficiently causing poor blood circulation in the body. As a result, less oxygen reaches other parts of the body and can cause organ damage. In most cases, abnormal heart rhythms are harmless, however, some cases may cause uncomfortable symptoms like dizziness, palpitations, pounding in the chest, fainting, shortness of breath, weakness, or fatigue. If some types of abnormal heart rhythms are left untreated, they may even cause sudden cardiac death.
Types
Main types of arrhythmia include:
Bradycardia – The heart beats too slow, below 60 bpm. For athletic individuals, a normal resting heart rate can be below 60 bpm, and not cause problems. Bradycardia is caused by a disruption of the electrical impulses conducted by the heart. Aging, hypothermia, damage from a heart attack or heart disease, and other factors can contribute to the disruption of impulses.
Tachycardia – The heart beats too fast, above 100 bpm. Tachycardia is caused by a disruption of the electrical impulses conducted by the heart. Damage from a heart attack or heart disease, congenital heart disease, high blood pressure, smoking and other factors can contribute the disruption of impulses.
- Atrial or Supraventricular Tachycardias – Occurs either in the upper chambers [atria] or the middle region.
- Sinus Tachycardia – A correctly functioning heart with a faster heart rate.
- Ventricular Tachycardias – Occurs in the lower chambers of the heart [ventricles], can be life-threatening.
Fibrillation – The heart quivers.
- Atrial Fibrillation – A manageable condition, a common abnormal heart rhythm.
- Ventricular Fibrillation – A life-threatening condition.
Premature Contraction – early heart beat.
- Premature Atrial Contractions [PACs] – Occurs in the upper chambers of the heart [atria].
- Premature Ventricular Contractions [PVCs] – Occurs in the lower chambers of the heart [ventricles].
Symptoms
Abnormal heart rhythms can cause a wide-range of symptoms. Symptoms may include:
- Fatigue
- Dizziness
- Lightheadedness
- Fainting
- Rapid heartbeat
- Shortness of breath
- Chest pain
- Sudden cardiac arrest, in severe cases
Follow Up Care
Lifestyle Changes
- If you smoke, quit.
- Limit alcohol and caffeine use.
We offer classes and support groups that focus on the how to care for your heart and vascular system.
Medications
Antiarrhythmic drugs can help correct an irregular or abnormal heartbeat. There are a wide variety of medications available for treatment. Our cardiologists have extensive experience in the use of drug therapy in the treatment of abnormal heart rhythms and can prescribe an appropriate medication. In many cases, abnormal heart rhythms cannot be cured with medication, but can be controlled. Your cardiologist and primary care physician play an important role in the regulation of this medication.
Follow Up Care
MemorialCare's experienced staff provides follow-up care for abnormal heart rhythms. Follow up care may include:
- Pacemaker and Arrhythmia Clinic
Locations Treating Abnormal Heart Rhythms [Arrhythmias]
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Related Services
Heart & Vascular Care
MemorialCare Heart and Vascular Institute specializes in minimally invasive heart procedures. With these innovative techniques, patients benefit from fewer complications, less scarring, greater comfort and faster recoveries. Distinguished as a leading heart and vascular institute.
Continuing Education Activity
The sinoatrial node is the natural cardiac pacemaker located in the upper right atrium. The atrioventricular node is a separate cardiac pacemaker located in the inferior-posterior right atrium. The His bundle is a separate cardiac pacemaker located at the inferior end of the atria and ventricle. A junctional rhythm is an abnormal heart rhythm that originates from the AV node or His bundle. This activity reviews the evaluation and management of junctional rhythm and highlights the role of the interprofessional team in educating patients about their prognosis.
Objectives:
Outline the risk factors of developing a junctional rhythm.
Review the pathophysiology of junctional rhythms.
Explain the differential diagnosis of junctional rhythm.
Summarize the interprofessional team's strategies for improving care coordination and communication regarding the management of patients with junctional rhythm.
Access free multiple choice questions on this topic.
Introduction
The sinoatrial node [SA] is the default pacemaker and is located subepicardially and is crescent in shape. The atrioventricular node [AV] is a subendocardial structure situated in the inferior-posterior right atrium. It sits within an anatomic region bordered posteriorly by the coronary sinus ostium, superiorly by the tendon of Todaro, and anteriorly by the septal tricuspid valve annulus. This anatomic region is also commonly referred to as the triangle of Koch. 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 blood supply to the AV node is from the AV nodal branch of the right coronary artery [90%] or the left circumflex artery [10%] depending on the right or left dominant blood supply to the heart. The first septal perforator of the left anterior descending artery also supplies blood to the AV node. A junctional rhythm is where the heartbeat originates from the AV node or His bundle, which lies within the tissue at the junction of the atria and the ventricle. Generally, in sinus rhythm, a heartbeat is originated at the SA node. This electrical activity then travels through the atria to the AV node from where it reaches the Bundle of His from where the electrical signals travel to the ventricles through the Purkinje fibers.[1][2][3][4][5][6]
The terminology used to identify the type junctional rhythm depends on its rate and is as follows:
Junctional bradycardia: rate below 40 beats per minute
Junction escape rhythm: rate 40 to 60 beats per minute
Accelerated junctional rhythm: rate of 60 to 100 beats per minute
Junctional tachycardia: rate above 100 beats per minute
Etiology
When the electrical activity of the SA node is blocked or is less than the automaticity of the AV node/His bundle, a junctional rhythm originates. Numerous conditions and medications can lead to a diseased SA node and lead to the AV node/His bundle taking over due to the higher automaticity of the ectopic pacemaker.[7][8][9]
Some of these conditions and medications are listed below.
Chest trauma
Sick sinus syndrome
Radiation therapy
Collagen vascular disease
Myocarditis
Clonidine
Reserpine
Adenosine
Cimetidine
Antiarrhythmics class I to IV
Lithium
Amitriptyline
Neuromuscular disorder
X-linked muscular dystrophy
Familial disorder
Vasovagal simulation [endotracheal suctioning]
Carotid sinus hypersensitivity
Beta-blockers
Calcium channel blockers
Digoxin
Ivabradine
Opioids
Cannabinoids
Isoproterenol infusion
Hypothyroidism
Sleep apnea
Hypoxia
Intracranial hypertension
-
Hyperkalemia
Anorexia nervosa
Amyloidosis
Pericarditis
Lyme disease
Rheumatic fever
Ischemic heart disease
Acute myocardial infarction
Acute and chronic coronary artery disease
Repair of congenital heart disease
Inherited channelopathy
Other than the above-listed causes of severe SA node disease, which can result in junctional rhythm, a high-grade second-degree heart block and a third-degree heart block can also result in a junctional rhythm. Digoxin toxicity can also lead to an accelerated junctional rhythm.
Epidemiology
Junctional rhythm is typical among individuals who have a sinus node dysfunction [SND], and 1 in every 600 cardiac patients above the age of 65 within the United States has SND. Patients with sick sinus syndrome, young children, and athletes who have increased vagal tone may also intermittently exhibit junctional rhythm, especially during sleep. Junctional rhythm is reported equally among males and females.[10]
Pathophysiology
A heart has numerous pacemaker sites within its conduction system, which are independently able to keep the heart beating. And the rate of a heartbeat depends upon the pacemaker site, and as we go down its conduction system, the rate of spontaneous depolarization at pacemaker sites decreases. [1][2][3]
Pacemaker sites and their depolarization rates are listed below:
Sinoatrial node: 60 to 100 beats per minute
Atria: less than 60 beats per minute
Atrioventricular node: 40 to 60 beats per minute
Ventricles: 20 to 40 beats per minute
Histopathology
Histopathology of a disease SA node that can contribute to the AV node/His bundle taking over as a pacemaker secondary to their intrinsic automaticity includes SA node fibrosis, atrophy, hypoplasia, or amyloidosis. A normal SA node histopathology does not rule out reduced SA node automaticity contributing to a junctional rhythm.[11][12]
History and Physical
Patients with junctional rhythm may present with a varied array of symptoms or may be asymptomatic. Symptoms mostly depend on the underlying cause of the junctional rhythm, for instance, a patient presenting with heart failure exacerbation may present with shortness of breath, wheezing, and lower extremity edema. Patients with rheumatic fever may present with a heart murmur secondary to the damage to the heart valves, fever, joint pain, and a rash with an electrocardiogram showing a junctional rhythm. Some patients might present with generalized complaints such as dizziness, fatigue, syncope/presyncope, and intermittent palpitations. Non-specific physical exam findings include pulsating veins and regular heart rate with the heart rate varying from 20 to over 100 beats per minute.[13][14][15]
Evaluation
A significant component of an assessment for a patient who presents with signs and symptoms of junctional rhythm is history and physical exam. These should include vital signs [respiratory rate, blood pressure, temperature, and heart rate], a review of the patient's medication list, and an electrocardiogram. See the image below. During their evaluation, it should be established if the patient is hemodynamically stable. The patient should be assessed for any underlying ischemic heart disease or heart failure. A healthcare provider should consider thyroid function testing, pulmonary function testing, including routine blood work, and echocardiography as part of their initial evaluation.[13][14][15]
Treatment / Management
Treatment of a junctional rhythm primarily depends on the underlying cause of the rhythm. In circumstances where the junctional rhythm is a result of underlying sinus node dysfunction that is leading to asystole or bradycardia, it should not be terminated, for it is maintaining the heart rate. Therefore, before establishing a management plan for patients presenting with a junctional rhythm, an underlying etiology must be determined first. Otherwise, healthy individuals who have junctional rhythm and are asymptomatic need no medical management as the rhythm is usually a result of their increased vagal tone suppressing the SA node intrinsic automaticity. In the setting of digoxin toxicity, a patient must be treated with atropine and digoxin-specific antibody. If a patient is refractory to these pharmacologic treatments and goes into junctional tachycardia, intravenous phenytoin can be administered in a monitored setting as these patients can develop hypotension. In the pediatric population, persistent symptomatic junctional tachycardia is an indication for percutaneous radiofrequency ablation. In patients with sick sinus syndrome, or complete or high-grade AV block, a permanent pacemaker is indicated.[16][17][18][19][20]
Differential Diagnosis
Digoxin toxicity
Atrioventricular nodal reentrant tachycardia
Atrioventricular reentrant tachycardia
Sinus node dysfunction
High-grade second-degree heart block
Third-degree heart block
Prognosis
Prognosis is good when the rhythm is promptly identified by a healthcare provider.
Complications
If not identified promptly symptomatic complications such as syncope, fatigue, or dizziness can occur.
Deterrence and Patient Education
If available patient education should be provided using resources familiar to the patient including online resources and pamphlets.
Pearls and Other Issues
Always check serum digoxin levels in patients who are on it for comorbidities. Also, check Lyme titers and empirically treat those patients who present with junctional rhythm and have possible exposure to ticks with antibiotics.
Enhancing Healthcare Team Outcomes
Educating patients at risk for this rhythm and making a closed-loop communication between them and their providers can help further improve the management of these rhythms. An interprofessional team best manages this condition. Initial diagnosis is by primary care or emergency providers. Referral to a cardiologist may be indicated. Cardiology and emergency department nurses administer treatment, monitor responses, and report back to the physician or nurse practitioner. Pharmacists should review prescribed medications, check for drug-drug interactions, and educate patients about dosing and side effects. [Level 5]
Review Questions
Figure
Junctional Rhythm. Contributed by Dhaval Desai, MD, MPH
References
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3.Dobrzynski H, Anderson RH, Atkinson A, Borbas Z, D'Souza A, Fraser JF, Inada S, Logantha SJ, Monfredi O, Morris GM, Moorman AF, Nikolaidou T, Schneider H, Szuts V, Temple IP, Yanni J, Boyett MR. Structure, function and clinical relevance of the cardiac conduction system, including the atrioventricular ring and outflow tract tissues. Pharmacol Ther. 2013 Aug;139[2]:260-88. [PubMed: 23612425]
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13.Kim D, Shinohara T, Joung B, Maruyama M, Choi EK, On YK, Han S, Fishbein MC, Lin SF, Chen PS. Calcium dynamics and the mechanisms of atrioventricular junctional rhythm. J Am Coll Cardiol. 2010 Aug 31;56[10]:805-12. [PMC free article: PMC3050609] [PubMed: 20797495]
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