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&nbsp;<div class="noeditbox">Welcome to [[Pathophysiology of Complex Patient Problems|PT 635 Pathophysiology of Complex Patient Problems]] This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!</div><div class="editorbox">
&nbsp;
<div class="noeditbox">Welcome to [[Pathophysiology of Complex Patient Problems|PT 635 Pathophysiology of Complex Patient Problems]] This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!</div><div class="editorbox">
'''Original Editors '''- [[Pathophysiology of Complex Patient Problems|Students from Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  
'''Original Editors '''- [[Pathophysiology of Complex Patient Problems|Students from Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  


'''Top Contributors''' - {{Special:Contributors/{{FULLPAGENAME}}}} &nbsp;
'''Top Contributors''' - {{Special:Contributors/{{FULLPAGENAME}}}} &nbsp;  
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== Definition/Description  ==
== Definition/Description  ==


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Atrial Fibrillations can occur independently or may be associated with underlying causes.&nbsp;AF not associated with an underlying cause is known as "lone AF". AF can manifest itself suddenly as in "paroxysmal AF" which terminates spontaneously or with intervention within 7 days of onset. If sustained longer than seven days it is known as "persistent AF". When it occurs continuously for longer than twelve months it is known as "long-standing persistent AF". The term "permanent AF" is used when the patient and clinician make a joint decision to stop further attempts to restore or maintain sinus rhythm. Acceptance of permanent AF represents a therapeutic attitude on the part of the patient and clinician rather than an inherent pathophysiological attribute of AF. Acceptance of AF may change as symptoms, efficacy of therapeutic interventions, and patient and clinician preferences evolve. &nbsp;Further, the term "nonvalvular AF" is a term used to describe when there is the absence of rheumatic mitral stenosis, a mechanical or bioprosthetic heart valve, or mitral valve repair. <sup>2</sup>  
Atrial Fibrillations can occur independently or may be associated with underlying causes.&nbsp;AF not associated with an underlying cause is known as "lone AF". AF can manifest itself suddenly as in "paroxysmal AF" which terminates spontaneously or with intervention within 7 days of onset. If sustained longer than seven days it is known as "persistent AF". When it occurs continuously for longer than twelve months it is known as "long-standing persistent AF". The term "permanent AF" is used when the patient and clinician make a joint decision to stop further attempts to restore or maintain sinus rhythm. Acceptance of permanent AF represents a therapeutic attitude on the part of the patient and clinician rather than an inherent pathophysiological attribute of AF. Acceptance of AF may change as symptoms, efficacy of therapeutic interventions, and patient and clinician preferences evolve. &nbsp;Further, the term "nonvalvular AF" is a term used to describe when there is the absence of rheumatic mitral stenosis, a mechanical or bioprosthetic heart valve, or mitral valve repair. <sup>2</sup>  


AF may occur in the elderly without underlying heart disease as well. However changes in cardiac structure and function that accompany the aging process, such as increased myocardial stiffness, may be associated with AF<sup>.3</sup>
AF may occur in the elderly without underlying heart disease as well. However changes in cardiac structure and function that accompany the aging process, such as increased myocardial stiffness, may be associated with AF<sup>.3</sup>  


AF with associated heart disease: specific cardiovascular conditions associated with AF include valvular heart disease (most often mitral valve disease), heart failure (HF), coronary artery disease, and hypertension, particularly when LV hypertrophy is present. In addition, AF may be associated with HCM, dilated cardiomyopathy, or congenital heart disease, especially atrial septal defect in adults. Potential etiologies also include restrictive cardiomyopathies (e.g., amyloidosis, hemochromatosis, and endomyocardial fibrosis), cardiac tumors, and constrictive pericarditis. Other heart diseases, such as mitral valve prolapse with or without mitral regurgitation, calcification of the mitral annulus, cor pulmonale, and idiopathic dilation of the right atrium, have been associated with a high incidence of atrial fibrillation.<sup>3</sup>
AF with associated heart disease: specific cardiovascular conditions associated with AF include valvular heart disease (most often mitral valve disease), heart failure (HF), coronary artery disease, and hypertension, particularly when LV hypertrophy is present. In addition, AF may be associated with HCM, dilated cardiomyopathy, or congenital heart disease, especially atrial septal defect in adults. Potential etiologies also include restrictive cardiomyopathies (e.g., amyloidosis, hemochromatosis, and endomyocardial fibrosis), cardiac tumors, and constrictive pericarditis. Other heart diseases, such as mitral valve prolapse with or without mitral regurgitation, calcification of the mitral annulus, cor pulmonale, and idiopathic dilation of the right atrium, have been associated with a high incidence of atrial fibrillation.<sup>3</sup>  


Familial associated AF: familial AF, defined as lone AF running in a family, is more common than previously recognized but should be distinguished from AF secondary to other genetic diseases like familial cardiomyopathies. The likelihood of developing AF is increased among the offspring of parents with AF, suggesting a familial susceptibility to the arrhythmia, but the mechanisms associated with transmission are not necessarily electrical, because the relationship has also been seen in patients with a family history of hypertension, diabetes, or HF.<sup>3</sup><sup></sup>  
Familial associated AF: familial AF, defined as lone AF running in a family, is more common than previously recognized but should be distinguished from AF secondary to other genetic diseases like familial cardiomyopathies. The likelihood of developing AF is increased among the offspring of parents with AF, suggesting a familial susceptibility to the arrhythmia, but the mechanisms associated with transmission are not necessarily electrical, because the relationship has also been seen in patients with a family history of hypertension, diabetes, or HF.<sup>3</sup><sup></sup>  


Autonomic Influence in AF: in general, vagally mediated AF occurs at night or after meals, while adrenergically induced AF typically occurs during the daytime. Beta blockers are initial drug of choice for adrenergic dominated AF.<sup>3</sup>
Autonomic Influence in AF: in general, vagally mediated AF occurs at night or after meals, while adrenergically induced AF typically occurs during the daytime. Beta blockers are initial drug of choice for adrenergic dominated AF.<sup>3</sup>  


== Prevalence  ==
== Prevalence  ==
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Atrial fibrillation (AF) is associated with significant morbidity and mortality, affecting more than 3 million people in the United States and 1-2% of the population worldwide. Its estimated prevalence is expected to double within the next 50 years.&nbsp;  
Atrial fibrillation (AF) is associated with significant morbidity and mortality, affecting more than 3 million people in the United States and 1-2% of the population worldwide. Its estimated prevalence is expected to double within the next 50 years.&nbsp;  


AF without associated heart disease: Approximately 30% to 45% of cases of paroxysmal AF and 20% to 25% of cases of persistent AF occur in young patients without demonstrable underlying disease. This is considered lone AF although, over the course of time, an underlying disease that may be causing the atrial fibrillation may appear.<sup><span style="font-size: 11px;">4</span></sup>
AF without associated heart disease: Approximately 30% to 45% of cases of paroxysmal AF and 20% to 25% of cases of persistent AF occur in young patients without demonstrable underlying disease. This is considered lone AF although, over the course of time, an underlying disease that may be causing the atrial fibrillation may appear.<sup><span style="font-size: 11px;">4</span></sup>  


<sup></sup><br>  
<sup></sup><br>  
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<br>"African Americans are less likely than those of European descent to have AFib.<sup>5</sup>"  
<br>"African Americans are less likely than those of European descent to have AFib.<sup>5</sup>"  


<br><br>
<br><br>  


== Characteristics/Clinical Presentation == Symptoms vary on the functional state of the heart, the location of the fibrillation, and may exist without symptoms.<sup>1,6</sup>&nbsp;Individuals are usually aware of the irregular heart action and may report feeling palpitations or sensations of fluttering, skipping and pounding. Other symptoms experienced can be inadequate blood flow which can cause feelings of dizziness, chest pain, fainting, dyspnea, pallor, fatigue, nervousness, and cyanosis. More than six palpitations occurring in a minute or prolonged repeated palpitations should be reported to the physician.<sup><span style="font-size: 13.8333px;">6</span></sup> <sup></sup> Over time, palpitation may disappear as the arrhythmia becomes permanent, it may become asymptomatic- this is particularly common among the elderly. Some patients experience symptoms only during paroxysmal AF, or only intermittently during sustained AF. An initial appearance of AF may be caused by an embolic complication or an exacerbation of HF. Most patients complain of palpitations, chest pain, dyspnea, fatigue, lightheadedness, or syncope. Further, frequent urination (Polyuria) may be associated with the release of atrial natriuretic peptide, particularly as episodes of AF begin or terminate. <sup><span style="font-size: 13.8333px;">3</span></sup> <sup></sup>An irregular pulse should raise the suspicion for AF. Patients may present initially with TIA or ischemic stroke. Most patients experience asymptomatic episodes of arrhythmias before being diagnosed. Patients with mitral valve disease and heart failure often have higher incidence of AF. Intermittent episodes of AF may progress in duration and frequency and over time many patients will develop sustained AF. For a newly diagnosed patient of AF, reversible causes such as pulmonary embolism, hyperthyroidism, pericarditis and MI should be investigated.<sup>7</sup> <br> <sup></sup>Pathophysiology <br>Atrial factors: Any kind of structural heart disease may trigger remodeling of the heart. Structural remodeling such as atrial fibrosis and loss of muscle mass are the most frequent histopathological changes in AF which facilitates initiation and perpetuation of AF. Electrical remodeling occurs, which results in changes in the action potential and contributes to maintenance of AF. AF reduces left atrial flow velocities and causes delayed emptying from atria.<sup>7</sup><sup>, 8&nbsp;</sup>This can increase the risk of stroke.<sup>1&nbsp;</sup>Prolonged AF makes restoration and maintenance of sinus rhythm more difficult.<sup>7</sup>
== Characteristics/Clinical Presentation == Symptoms vary on the functional state of the heart, the location of the fibrillation, and may exist without symptoms.<sup>1,6</sup>&nbsp;Individuals are usually aware of the irregular heart action and may report feeling palpitations or sensations of fluttering, skipping and pounding. Other symptoms experienced can be inadequate blood flow which can cause feelings of dizziness, chest pain, fainting, dyspnea, pallor, fatigue, nervousness, and cyanosis. More than six palpitations occurring in a minute or prolonged repeated palpitations should be reported to the physician.<sup><span style="font-size: 13.8333px;">6</span></sup> <sup></sup> Over time, palpitation may disappear as the arrhythmia becomes permanent, it may become asymptomatic- this is particularly common among the elderly. Some patients experience symptoms only during paroxysmal AF, or only intermittently during sustained AF. An initial appearance of AF may be caused by an embolic complication or an exacerbation of HF. Most patients complain of palpitations, chest pain, dyspnea, fatigue, lightheadedness, or syncope. Further, frequent urination (Polyuria) may be associated with the release of atrial natriuretic peptide, particularly as episodes of AF begin or terminate. <sup><span style="font-size: 13.8333px;">3</span></sup> <sup></sup>An irregular pulse should raise the suspicion for AF. Patients may present initially with TIA or ischemic stroke. Most patients experience asymptomatic episodes of arrhythmias before being diagnosed. Patients with mitral valve disease and heart failure often have higher incidence of AF. Intermittent episodes of AF may progress in duration and frequency and over time many patients will develop sustained AF. For a newly diagnosed patient of AF, reversible causes such as pulmonary embolism, hyperthyroidism, pericarditis and MI should be investigated.<sup>7</sup> <br> <sup></sup>Pathophysiology <br>Atrial factors: Any kind of structural heart disease may trigger remodeling of the heart. Structural remodeling such as atrial fibrosis and loss of muscle mass are the most frequent histopathological changes in AF which facilitates initiation and perpetuation of AF. Electrical remodeling occurs, which results in changes in the action potential and contributes to maintenance of AF. AF reduces left atrial flow velocities and causes delayed emptying from atria.<sup>7</sup><sup>, 8&nbsp;</sup>This can increase the risk of stroke.<sup>1&nbsp;</sup>Prolonged AF makes restoration and maintenance of sinus rhythm more difficult.<sup>7</sup>  


== Associated Co-morbidities  ==
== Associated Co-morbidities  ==


Obesity - Obesity and the magnitude of nocturnal oxygen desaturation, which is an important pathophysiological consequence of OSA, are independent risk factors for incident AF in individuals &lt;65 years of age.<sup>9</sup><br>Obesity is an important risk factor for the development of AF (103). After adjustment for clinical risk factors, the excess risk of AF appears related to LA dilation. There is a graded increase in LA size as body mass index increases from normal to the overweight and obese categories, and weight has been linked to regression of LA enlargement (104). These findings suggest a physiological link between obesity, AF, and stroke and raise the intriguing possibility that weight reduction may decrease the risk associated with AF.<sup>3</sup><br>Diabetes<br>May cause CHF<br>Mitral valve disease<br>Heart failure<br>Coronary artery disease<br>Hypertension associated with left ventricular hypertrophy<br>Hypertrophic obstructive cardiomyopathy<br>Dilated cardiomyopathy<br>Atrial septal defect<br>A persistently elevated ventricular rate during AF (usually &gt; 120 beats/min) for prolonged time periods may also result in increased mitral regurgitation, eventually leading to a dilated ventricular cardiomyopathy (tachycardia-induced cardiomyopathy).<sup>8</sup><br><br>
Obesity - Obesity and the magnitude of nocturnal oxygen desaturation, which is an important pathophysiological consequence of OSA, are independent risk factors for incident AF in individuals &lt;65 years of age.<sup>9</sup><br>Obesity is an important risk factor for the development of AF (103). After adjustment for clinical risk factors, the excess risk of AF appears related to LA dilation. There is a graded increase in LA size as body mass index increases from normal to the overweight and obese categories, and weight has been linked to regression of LA enlargement (104). These findings suggest a physiological link between obesity, AF, and stroke and raise the intriguing possibility that weight reduction may decrease the risk associated with AF.<sup>3</sup><br>Diabetes<br>May cause CHF<br>Mitral valve disease<br>Heart failure<br>Coronary artery disease<br>Hypertension associated with left ventricular hypertrophy<br>Hypertrophic obstructive cardiomyopathy<br>Dilated cardiomyopathy<br>Atrial septal defect<br>A persistently elevated ventricular rate during AF (usually &gt; 120 beats/min) for prolonged time periods may also result in increased mitral regurgitation, eventually leading to a dilated ventricular cardiomyopathy (tachycardia-induced cardiomyopathy).<sup>8</sup><br><br>  


== Medications  ==
== Medications  ==
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Rhythm control (Antiarrhythmics)<br>Amiodarone(Cordarone)<br>Flecainide (Tambocor)<br>Propafenone(Rythmol)<br>Sotalol(Betapace)  
Rhythm control (Antiarrhythmics)<br>Amiodarone(Cordarone)<br>Flecainide (Tambocor)<br>Propafenone(Rythmol)<br>Sotalol(Betapace)  


Meds such as anticoagulants can cause brain hemorrhage. Benefits must be closely monitored. <sup>7</sup><br>
Meds such as anticoagulants can cause brain hemorrhage. Benefits must be closely monitored. <sup>7</sup><br>  


== Diagnostic Tests/Lab Tests/Lab Values  ==
== Diagnostic Tests/Lab Tests/Lab Values  ==


12 lead EKG<sup>6</sup><br> Several characteristic electrocardiogram (ECG) changes define AF: 1. Presence of low-amplitude fibrillatory waves on ECG without defined P-waves 2. Irregularly irregular ventricular rhythm 3. Fibrillatory waves typically have a rate of &gt; 300 beats per minute 4. Ventricular rate is typically between 100 and 160 beats per minute. <sup>8</sup><br>Holter monitor<sup>7</sup><br>Event recorder<sup>7</sup><br>Blood test<sup>7</sup><br>Stress tests<sup>7</sup><br>Chest X-ray<sup>7</sup><br>LV Hypertrophy<sup>3</sup><br>6 minute walk test<sup>3</sup><br>Physical Exam: Irregular pulse, irregular jugular venous pulsations, variation in intensity of first heart sound.<sup>4</sup><br><br>
12 lead EKG<sup>6</sup><br> Several characteristic electrocardiogram (ECG) changes define AF: 1. Presence of low-amplitude fibrillatory waves on ECG without defined P-waves 2. Irregularly irregular ventricular rhythm 3. Fibrillatory waves typically have a rate of &gt; 300 beats per minute 4. Ventricular rate is typically between 100 and 160 beats per minute. <sup>8</sup><br>Holter monitor<sup>7</sup><br>Event recorder<sup>7</sup><br>Blood test<sup>7</sup><br>Stress tests<sup>7</sup><br>Chest X-ray<sup>7</sup><br>LV Hypertrophy<sup>3</sup><br>6 minute walk test<sup>3</sup><br>Physical Exam: Irregular pulse, irregular jugular venous pulsations, variation in intensity of first heart sound.<sup>4</sup><br><br>  


== Etiology/Causes  ==
== Etiology/Causes  ==
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AF is a common early postoperative complication of cardiac and thoracic surgery. (other sources (Surgery (intrathoracic) - common as an early post op complication of thoracic surgery including cardiac surgery. )<br>Alcohol use (Holiday syndrome)<br>Caffeine*<br>High fevers*severe infection/ pneumonia<br>Presence of helicobacter pylori in stomach is associated with persistent AF*<br>Emotional stress* BOOK  
AF is a common early postoperative complication of cardiac and thoracic surgery. (other sources (Surgery (intrathoracic) - common as an early post op complication of thoracic surgery including cardiac surgery. )<br>Alcohol use (Holiday syndrome)<br>Caffeine*<br>High fevers*severe infection/ pneumonia<br>Presence of helicobacter pylori in stomach is associated with persistent AF*<br>Emotional stress* BOOK  


MI<br>Pericarditis/pericardial disease/myocarditis <br>Pulmonary Embolism<br>Electrocution<br>Hyperthyroidism (up to 15% of hyperthyroidism pts)<br>Kidney dis/ electrolyte abnormalities/Other metabolic<br>Increasing age<br>Male &gt; Female (source 8 also)<br>mitral valve disease, <br>conduction system disorders, Wolff-Parkinson-White syndrome, <br>Conditions associated with AF:<br>thyrotoxicosis, hypothermia, hypoxia,<br>Digoxin toxicity<br>Lone AF applies to AF in individuals younger than 60 years of age without clinical or echocardiographic evidence of cardiopulmonary disease (including hypertension), Lone AF is favorable in regard to statistics of thromboembolism and mortality.<sup>3</sup><sup>,6,7,8,9</sup><br>
MI<br>Pericarditis/pericardial disease/myocarditis <br>Pulmonary Embolism<br>Electrocution<br>Hyperthyroidism (up to 15% of hyperthyroidism pts)<br>Kidney dis/ electrolyte abnormalities/Other metabolic<br>Increasing age<br>Male &gt; Female (source 8 also)<br>mitral valve disease, <br>conduction system disorders, Wolff-Parkinson-White syndrome, <br>Conditions associated with AF:<br>thyrotoxicosis, hypothermia, hypoxia,<br>Digoxin toxicity<br>Lone AF applies to AF in individuals younger than 60 years of age without clinical or echocardiographic evidence of cardiopulmonary disease (including hypertension), Lone AF is favorable in regard to statistics of thromboembolism and mortality.<sup>3</sup><sup>,6,7,8,9</sup><br>  


== Systemic Involvement  ==
== Systemic Involvement  ==


High concentrations of CRP, which confirm the presence of systemic inflammation are present in people with AF. A potential non-cardiovascular disease that predisposes individuals to AF may be chronic gastritis caused by chronic H. pylori infection.<sup>3&nbsp;</sup><br>
High concentrations of CRP, which confirm the presence of systemic inflammation are present in people with AF. A potential non-cardiovascular disease that predisposes individuals to AF may be chronic gastritis caused by chronic H. pylori infection.<sup>3&nbsp;</sup><br>  


== Medical Management (current best evidence)  ==
== Medical Management (current best evidence)  ==


Rate control and rhythm control through medications<br>Catheter ablation<br>Atrioventricular node ablation<br>Surgical maze procedure<br>Studies have demonstrated that a rate control strategy, with a target resting heart rate between 80 and 100 beats/minute, is recommended over rhythm control in the vast majority of patients. add text here<br>Thromboembolism Prevention<sup>3,6,7</sup>
Rate control and rhythm control through medications<br>Catheter ablation<br>Atrioventricular node ablation<br>Surgical maze procedure<br>Studies have demonstrated that a rate control strategy, with a target resting heart rate between 80 and 100 beats/minute, is recommended over rhythm control in the vast majority of patients. add text here<br>Thromboembolism Prevention<sup>3,6,7</sup>  


== Physical Therapy Management (current best evidence)  ==
== Physical Therapy Management (current best evidence)  ==


Limited research on the effect of traditional physical therapy and Atrial Fibrillation <br>Conflicting information on the use of exercise to reduce the risk of AF
Limited research on the effect of traditional physical therapy and Atrial Fibrillation <br>Conflicting information on the use of exercise to reduce the risk of AF  


== Differential Diagnosis  ==
== Differential Diagnosis  ==


Atrial tachycardia
Atrial tachycardia  


<br>Atrial flutter with variable AV block<br>Frequent atrial ectopiesPulmonary Embolism
<br>Atrial flutter with variable AV block<br>Frequent atrial ectopiesPulmonary Embolism  


Hyperthyroidism
Hyperthyroidism  


Pericarditis
Pericarditis  


&nbsp;MI<br>Antegrade atrioventricular nodal conduction
&nbsp;MI<br>Antegrade atrioventricular nodal conduction  


== Case Reports/ Case Studies  ==
== Case Reports/ Case Studies  ==


add links to case studies here (case studies should be added on new pages using the [[Template:Case Study|case study template]])<br>
add links to case studies here (case studies should be added on new pages using the [[Template:Case Study|case study template]])<br>  


== Resources <br> ==
== Resources <br> ==


add appropriate resources here  
add appropriate resources here  
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<div class="researchbox">
<div class="researchbox">
<rss>addfeedhere|charset=UTF-8|short|max=10</rss>  
<rss>addfeedhere|charset=UTF-8|short|max=10</rss>  
</div>
</div>  
 
== References  ==
== References  ==



Revision as of 01:53, 11 April 2016

 

Welcome to PT 635 Pathophysiology of Complex Patient Problems This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!

Definition/Description[edit | edit source]

Atrial fibrillation (AF) is the most common type of heart arrhythmia. During atrial fibrillation the heart can beat too fast, too slow, or with an irregular rhythm.

AF occurs when rapid, disorganized electrical signals cause the heart's two upper chambers known as the atria to fibrillate.  The term "fibrillate" means that a muscle uscle is not performing full contractions. Instead, the cardiac muscle in the atria is quivering at a rapid and irregular pace.

Due to the atrial fibrillations, blood pools in the atria as it is not completely pumped out of the atria into the two lower chambers known as the ventricles.1

Atrial Fibrillations can occur independently or may be associated with underlying causes. AF not associated with an underlying cause is known as "lone AF". AF can manifest itself suddenly as in "paroxysmal AF" which terminates spontaneously or with intervention within 7 days of onset. If sustained longer than seven days it is known as "persistent AF". When it occurs continuously for longer than twelve months it is known as "long-standing persistent AF". The term "permanent AF" is used when the patient and clinician make a joint decision to stop further attempts to restore or maintain sinus rhythm. Acceptance of permanent AF represents a therapeutic attitude on the part of the patient and clinician rather than an inherent pathophysiological attribute of AF. Acceptance of AF may change as symptoms, efficacy of therapeutic interventions, and patient and clinician preferences evolve.  Further, the term "nonvalvular AF" is a term used to describe when there is the absence of rheumatic mitral stenosis, a mechanical or bioprosthetic heart valve, or mitral valve repair. 2

AF may occur in the elderly without underlying heart disease as well. However changes in cardiac structure and function that accompany the aging process, such as increased myocardial stiffness, may be associated with AF.3

AF with associated heart disease: specific cardiovascular conditions associated with AF include valvular heart disease (most often mitral valve disease), heart failure (HF), coronary artery disease, and hypertension, particularly when LV hypertrophy is present. In addition, AF may be associated with HCM, dilated cardiomyopathy, or congenital heart disease, especially atrial septal defect in adults. Potential etiologies also include restrictive cardiomyopathies (e.g., amyloidosis, hemochromatosis, and endomyocardial fibrosis), cardiac tumors, and constrictive pericarditis. Other heart diseases, such as mitral valve prolapse with or without mitral regurgitation, calcification of the mitral annulus, cor pulmonale, and idiopathic dilation of the right atrium, have been associated with a high incidence of atrial fibrillation.3

Familial associated AF: familial AF, defined as lone AF running in a family, is more common than previously recognized but should be distinguished from AF secondary to other genetic diseases like familial cardiomyopathies. The likelihood of developing AF is increased among the offspring of parents with AF, suggesting a familial susceptibility to the arrhythmia, but the mechanisms associated with transmission are not necessarily electrical, because the relationship has also been seen in patients with a family history of hypertension, diabetes, or HF.3

Autonomic Influence in AF: in general, vagally mediated AF occurs at night or after meals, while adrenergically induced AF typically occurs during the daytime. Beta blockers are initial drug of choice for adrenergic dominated AF.3

Prevalence[edit | edit source]

Atrial fibrillation (AF) is associated with significant morbidity and mortality, affecting more than 3 million people in the United States and 1-2% of the population worldwide. Its estimated prevalence is expected to double within the next 50 years. 

AF without associated heart disease: Approximately 30% to 45% of cases of paroxysmal AF and 20% to 25% of cases of persistent AF occur in young patients without demonstrable underlying disease. This is considered lone AF although, over the course of time, an underlying disease that may be causing the atrial fibrillation may appear.4


"An estimated 2.7–6.1 million people in the United States have AFib. With the aging of the U.S. population, this number is expected to increase.5"


"Approximately 2% of people younger than age 65 have AFib, while about 9% of people aged 65 years or older have AFib.5"


"African Americans are less likely than those of European descent to have AFib.5"



== Characteristics/Clinical Presentation == Symptoms vary on the functional state of the heart, the location of the fibrillation, and may exist without symptoms.1,6 Individuals are usually aware of the irregular heart action and may report feeling palpitations or sensations of fluttering, skipping and pounding. Other symptoms experienced can be inadequate blood flow which can cause feelings of dizziness, chest pain, fainting, dyspnea, pallor, fatigue, nervousness, and cyanosis. More than six palpitations occurring in a minute or prolonged repeated palpitations should be reported to the physician.6 Over time, palpitation may disappear as the arrhythmia becomes permanent, it may become asymptomatic- this is particularly common among the elderly. Some patients experience symptoms only during paroxysmal AF, or only intermittently during sustained AF. An initial appearance of AF may be caused by an embolic complication or an exacerbation of HF. Most patients complain of palpitations, chest pain, dyspnea, fatigue, lightheadedness, or syncope. Further, frequent urination (Polyuria) may be associated with the release of atrial natriuretic peptide, particularly as episodes of AF begin or terminate. 3 An irregular pulse should raise the suspicion for AF. Patients may present initially with TIA or ischemic stroke. Most patients experience asymptomatic episodes of arrhythmias before being diagnosed. Patients with mitral valve disease and heart failure often have higher incidence of AF. Intermittent episodes of AF may progress in duration and frequency and over time many patients will develop sustained AF. For a newly diagnosed patient of AF, reversible causes such as pulmonary embolism, hyperthyroidism, pericarditis and MI should be investigated.7
Pathophysiology
Atrial factors: Any kind of structural heart disease may trigger remodeling of the heart. Structural remodeling such as atrial fibrosis and loss of muscle mass are the most frequent histopathological changes in AF which facilitates initiation and perpetuation of AF. Electrical remodeling occurs, which results in changes in the action potential and contributes to maintenance of AF. AF reduces left atrial flow velocities and causes delayed emptying from atria.7, 8 This can increase the risk of stroke.Prolonged AF makes restoration and maintenance of sinus rhythm more difficult.7

Associated Co-morbidities[edit | edit source]

Obesity - Obesity and the magnitude of nocturnal oxygen desaturation, which is an important pathophysiological consequence of OSA, are independent risk factors for incident AF in individuals <65 years of age.9
Obesity is an important risk factor for the development of AF (103). After adjustment for clinical risk factors, the excess risk of AF appears related to LA dilation. There is a graded increase in LA size as body mass index increases from normal to the overweight and obese categories, and weight has been linked to regression of LA enlargement (104). These findings suggest a physiological link between obesity, AF, and stroke and raise the intriguing possibility that weight reduction may decrease the risk associated with AF.3
Diabetes
May cause CHF
Mitral valve disease
Heart failure
Coronary artery disease
Hypertension associated with left ventricular hypertrophy
Hypertrophic obstructive cardiomyopathy
Dilated cardiomyopathy
Atrial septal defect
A persistently elevated ventricular rate during AF (usually > 120 beats/min) for prolonged time periods may also result in increased mitral regurgitation, eventually leading to a dilated ventricular cardiomyopathy (tachycardia-induced cardiomyopathy).8

Medications[edit | edit source]

Rate control*
Beta Blocker
Metoprolol CR/XL(Toprol XL)
Bisoprolol (Zebeta)
Atenolol (Tenormin)
Esmolol (Brevibloc)
Propranolol (Inderal)
Carvedilol (Coreg)
Antihypertensive and calcium channel blocker
Verapamil (Calan)
Diltiazem (Cardizem)
Antiarrhythmic and blood pressure support
Digoxin (Lanoxin)
Antiarrhythmic
Amiodarone (Cordarone)
Dronedarone (Multaq)

Rhythm control (Antiarrhythmics)
Amiodarone(Cordarone)
Flecainide (Tambocor)
Propafenone(Rythmol)
Sotalol(Betapace)

Meds such as anticoagulants can cause brain hemorrhage. Benefits must be closely monitored. 7

Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]

12 lead EKG6
Several characteristic electrocardiogram (ECG) changes define AF: 1. Presence of low-amplitude fibrillatory waves on ECG without defined P-waves 2. Irregularly irregular ventricular rhythm 3. Fibrillatory waves typically have a rate of > 300 beats per minute 4. Ventricular rate is typically between 100 and 160 beats per minute. 8
Holter monitor7
Event recorder7
Blood test7
Stress tests7
Chest X-ray7
LV Hypertrophy3
6 minute walk test3
Physical Exam: Irregular pulse, irregular jugular venous pulsations, variation in intensity of first heart sound.4

Etiology/Causes[edit | edit source]

AF is a common early postoperative complication of cardiac and thoracic surgery. (other sources (Surgery (intrathoracic) - common as an early post op complication of thoracic surgery including cardiac surgery. )
Alcohol use (Holiday syndrome)
Caffeine*
High fevers*severe infection/ pneumonia
Presence of helicobacter pylori in stomach is associated with persistent AF*
Emotional stress* BOOK

MI
Pericarditis/pericardial disease/myocarditis
Pulmonary Embolism
Electrocution
Hyperthyroidism (up to 15% of hyperthyroidism pts)
Kidney dis/ electrolyte abnormalities/Other metabolic
Increasing age
Male > Female (source 8 also)
mitral valve disease,
conduction system disorders, Wolff-Parkinson-White syndrome,
Conditions associated with AF:
thyrotoxicosis, hypothermia, hypoxia,
Digoxin toxicity
Lone AF applies to AF in individuals younger than 60 years of age without clinical or echocardiographic evidence of cardiopulmonary disease (including hypertension), Lone AF is favorable in regard to statistics of thromboembolism and mortality.3,6,7,8,9

Systemic Involvement[edit | edit source]

High concentrations of CRP, which confirm the presence of systemic inflammation are present in people with AF. A potential non-cardiovascular disease that predisposes individuals to AF may be chronic gastritis caused by chronic H. pylori infection.

Medical Management (current best evidence)[edit | edit source]

Rate control and rhythm control through medications
Catheter ablation
Atrioventricular node ablation
Surgical maze procedure
Studies have demonstrated that a rate control strategy, with a target resting heart rate between 80 and 100 beats/minute, is recommended over rhythm control in the vast majority of patients. add text here
Thromboembolism Prevention3,6,7

Physical Therapy Management (current best evidence)[edit | edit source]

Limited research on the effect of traditional physical therapy and Atrial Fibrillation
Conflicting information on the use of exercise to reduce the risk of AF

Differential Diagnosis[edit | edit source]

Atrial tachycardia


Atrial flutter with variable AV block
Frequent atrial ectopiesPulmonary Embolism

Hyperthyroidism

Pericarditis

 MI
Antegrade atrioventricular nodal conduction

Case Reports/ Case Studies[edit | edit source]

add links to case studies here (case studies should be added on new pages using the case study template)

Resources
[edit | edit source]

add appropriate resources here

Recent Related Research (from Pubmed)[edit | edit source]

see tutorial on Adding PubMed Feed

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References[edit | edit source]

1. National Heart, Lung, and Blood Institute [Internet]. [Place Unknown]: U.S. Department of Health and Human Services; Atrial Fibrillation. [updated 2014 September 18; cited 2016 April 2]. Available from: http://www.nhlbi.nih.gov/health/health-topics/topics/af

2. January CT, Wann LS, Alpert JS, Calkins H, Cigarroa JE, Cleveland JC, et al. 2014 ACC/AHA/ESC Guidelines for the Management of Patients with Atrial Fibrillation: Executive Summary. J Am Coll Cardiol. 2014: 64(21) p. 2246-80.

3. Fuster V, Rydén LE, Cannom DS, Crijns HJ, Curtis AB, Ellenbogen KA, et al. ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients With Atrial Fibrillation): Developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. J Am Coll Cardiol. 2006: 114(7): p. 257-354.

4. Amerena JV, Walters TE, Mirzaee S, Kalman JM. Update on the management of atrial fibrillation. Med J Aust. 2013: 199(9): p. 592-7.

5. Atrial Fibrillation Fact Sheet [Internet]. Center for Disease Control and Prevention; 2013 [updated 2015 August 13; cited 2016 April 5] Available from: http://www.cdc.gov/dhdsp/data_statistics/fact_sheets/fs_atrial_fibrillation.htm

6. Goodman CC, Snyder TE. Differential Diagnosis for Physical Therapists, Screening for Referral. 5th ed. St. Louis Saunders; 2012. p. 264-266.

7. Wadke R. Atrial Fibrillation. Disease-a-Month. 2013 March: 59(3): 67-73.

8. Oishi ML, Xing S. Atrial fibrillation: Management strategies in the emergency department. Emerg Med Prac. 2013: 15(2): p. 1-26.

9. Gami AS, Hodge DO, Herges RM, Olson EJ, Nykodym J Kara T, Somers VK. Obstructive Sleep Apnea, Obesity, and the Risk of Incident Atrial Fibrillation. J Am Coll Cardiol [Internet]. 2007 Feb [cited 2016 April 9]; 49(5): 565-571. Available from: http://content.onlinejacc.org/article.aspx?articleid=1188673&...#tab1