AFIB Flashcards

(60 cards)

1
Q

Compare AFib vs A flutter

A
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2
Q

Most common cardiac arrythmia

A

AFIB

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3
Q

What is AFIB

A

A supraventricular arrhythmia (above the ventricles) which results from continuous and chaotic atrial activity

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4
Q

Risks of AFIB

A

Rarely life-threatening;

increases the risk of stroke (most severe)

left ventricular dysfunction (loss of ventricular ejection –> fatigue, exercise intolerance, light headed, palpitations)

Non-anticoagulated patients have 3-5 fold increased risk of stroke (generally severe)

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5
Q

W\hat is lost on an EKG during Afib?

A

P- wave is lost

Distance between p waves should be the same

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6
Q

What is afib classified as:

A

an irregularly, irregular rhythm

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7
Q

Prevalence Afib

A

Prevalence increases with age

The age adjusted prevalence is greater in men

10-30% of heart failure patients have AF (lost the atrial kick)

Common and undiagnosed

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8
Q

Sx Afib

A

Fatigue
Palpitations
Chest Pain
dyspnea
Dizziness

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9
Q

afib pathophys

A

ectopic foci that generate electrical impulses

Atria experience rapid irregular and uncoordinated contractions

Because electrical impulses reach the AV node erratically, the ventricular rhythm is irregular

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10
Q

Initiating event of AFIB

A

Factors which destabilize the myocardium such as electrolyte disturbances, ischemic and excessive sympathetic stimulation can contribute to the initiating event

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11
Q

How can afib be classified based on structural disease?

A

Valvular (Warfarin) –> Very significant valve disease (rheumatic fever, valve replacement, or mitral valve repair)

Non-Valvular (DOACS here only)
Absence of rheumatic mitral valve disease, a prosthetic heart valve, or mitral valve repair

“Lone” AF  Young, no heart or pulmonary disease
Absence of clinical or echocardiographic findings of:
Other CVD (including hypertension)
Related pulmonary disease
Cardiac abnormalities; ex/ enlargement of the left atrium
Age under 60 years

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12
Q

Paraoxysmal AFib

A

lasting longer than 30 seconds and self-terminating within 7 days of recognized onset (jump in and jump out)

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13
Q

Persistent Afib

A

continuous AF episode lasting longer than 7 days but less than 1 year

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14
Q

Longstanding Afib

A

continuous AF equal or greater than 1 year in who rhythm control management is being pursued

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15
Q

Permenant Afib

A

continuous AF for which a therapeutic decision has been made not to pursue sinus rhythm restoration

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16
Q

What is a substrate?

A

a pre-existing condition that forms a prerequisite for the induction of an arrhythmia

Examples:

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17
Q

triggers

A

Stimulants
Alcohol
Sleep Depreivation
Emotional STress
Physical Exertiom
Sleep
Digestive

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18
Q

Risk factors

A

HTN
DM

Tobacco
Alcohol

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19
Q

Investigating AFib

A

12-lead ECG

Echocardiogram

LAb Investigations

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20
Q

Goals of tx and anticipated outcomes

A

Prevent stroke or systemic thromboembolism

Cardiovascular risk reduction

Improve symptoms, functional capacity and quality of life

Prevent complications (eg. LV dysfunction and falls)

Outcomes:

Improvement in survival
Reduction in healthcare utilization (ED visits or hospitalization)

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21
Q

Afib Diagnosus Scheme

A

Rate –> Let you be in AFIB but slow down the ventricular rhythym

Rhythym –> Put you back into sinus rhythym

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22
Q

CHad 65 Scores

A
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23
Q

Stroke Prevention ChadS 65

A

Anticoagulate AF in the presence of:

“Valvular AF”
–> Any mechanical heart valve
–> Moderate to severe mitral stenosis (rheumatic or non-rheumatic)
Hypertrophic cardiomyopathy
Hyperthyroidism
Amyloid cardiomyopathy
Non-Valvular AF

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24
Q

Stroke Prevention Obese

A

Higher BMI may be associated with lower stroke rates; higher bleeding rates (obesity paradox)

Standard DOAC dose is reasonable for BMI <40 kg/m2

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25
DOAC Use Obese Guidelines
26
Dose Warfarin And DOACS
27
Apixaban when:
Consider Apixaban 2.5 mg po bid if 2 of 1) age 80 years or older, 2) body weight 60 kg or less 3) serum creatinine 133 𝜇mol/L or more;
28
DOAC D.I.
29
DOAC antidote
30
Dosing DOAC differences
31
Dual Tx Doses
1 antiplatlet (P12Y or ASA)
32
Triple Therapy
ASA + P12Y +
33
Do Not use DOACS if:
Mechanical heart valves and significant mitral valve stenosis Use of strong P-gp and 3A4 inhibitors or inducers* (check current product monographs) Pregnancy and lactation (no safety – more heparin product here) Expert bodies indicate need for clinical judgement in extremes of body weight (<50kg; >120kg)** Pediatrics Caution when combined with dual antiplatelets – triple therapy**
34
Monitoring of anticoag
Adherence Frequency of adverse effects (affects adherence) Signs and symptoms of bleeding and bleeding risk factors Regular SCr, CrCl, Hgb
35
Acute Management
Determine if AF is the primary concern or secondary to another acute medical illness Consider hemodynamic stability (blood pressure) Determine whether rate vs rhythm control is appropriate In newly diagnosed AF – rhythm control has been associated with reduced CV death and stroke Determine need for hospitalization Determine need for OAC – start as soon as possible (in ED) if required – CCS algorithm Early follow up
36
Define Rate Control
allow the patient to remain in Atrial Fibrillation, however ensure that the ventricular rate is slowed sufficiently to minimize negative outcomes
37
Benefit of Rhthym COntrol
used in stable patients with recent-onset AF with the decision made on the basis of patient symptoms and goals of care, recognizing that early rhythm control has been associated with a lower risk of stroke and CV death
38
Rhythym control in who:
Recently diagnosed (<1 year) Highly asymptomatic Multiple recurrences Difficulty to achieve rate control Arrthymia-induced cardiomyopathy (Rhythym has more anti death)
39
Acute rate control:
40
Goal of rate control
Reduction in HR of greater than 20% with control of symptoms
41
ND-CCB Examples
Verapamil Diltazem
42
Targets of Rate Control
Resting heart rate < 100 bpm at rest B-blockers or ND-CCBs first line agents Selection of BB vs CCB should be on the basis of patient comorbidities, contraindications and side effects Achieved goal at rest/exercise
43
Ventricular Rate control Choice
Hemodynamic instability --> Digoxin is a poor choice – delayed onset AF associated with exercise, thyrotoxicosis, fever etc. --> ß-blockers are first line --> CCBs are more effective than digoxin Age CCB preferentially used in the young
44
Long term RAte Control
45
Cardioversion and AFIB ANticoagulation
AFIB for more than 48 hours --> need to anticoagulated for 3 weeks before put back into sinus rhthym Do not want to push the clot to the brain Transesophageal ECHO  see if blood clot in atria
46
Risky Rhythym Control
increased the risk of systemic embolism, it is important to start appropriate anticoagulation as time allows for all patients
47
Rhythym COntrol Objectives
Relief of symptoms such as palpitations, fatigue and dyspnea Improve CO and exercise tolerance Prevention of tachycardia-induced myocardial remodeling and heart failure Hemodynamic improvements may take days to weeks
48
Ways to achieve Sinus Rhthym
Rate Control & Await Spontaneous Conversion Electrical (Direct Current) Cardioversion --> Treatment of choice with ventricular rate >150 bpm who are hemodynamically unstable or have serious signs/symptoms i.e., chest pain, pulmonary edema Chemical (pharmacologic) Cardioversion
49
Cardioversion Risk
Must anticoagulate if AF>48 hours (therapeutic INR for 3 weeks before and 4 weeks post conversion to NSR)
50
Patients most likelky to maintain normal sinus rhthym after cardioversion?
Short duration of AF and absence of left atrial dilation
51
Patients who NSR should be attempted?
Recent onset of AF Heart failure Angina Hypotension
52
Cardioversion benefit and risk vs Pharm Conversion
Electrical cardioversion is more effective than pharmacologic cardioversion especially for more prolonged AF episode durations Pharmacologic has the advantage of being immediately feasible in a nonfasting patient as well as avoiding the delays and risks associated with procedural sedation
53
Treatment Indications
54
Before and after cardioversion
OAC for 3 weeks before and 4 weeks after for patients with valvular AF or NVAF >48h
55
Cardioversion acute management Guide
56
Drugs used for pharmacological conversion
Sodium Channel Blockers (Class I agents) and amiodarone are superior to placebo in acute and chronic AF Digoxin, ß-Blockers or CCBs are NOT effective for the conversion of AF to sinus rhythm (Not effective)
57
Side effects pharmacologic conversion
GI related Left Ventricular Depression Negative inotropic effects with many agents Pro-Arrhythmia (life-threatening) ~1-2% Accelerated ventricular response can be seen if converted to atrial flutter Slowing of atrial rate & vagolytic effects of some agents can lead to 1:1 AV conduction
58
Recommendation managing s/e
Concurrent rate control agent
59
Drugs used for Achieveing sinus rhthym
In Paris, friends party
60
Long Term Rhthym Control