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Cardiac Arrhythmias and Conduction Abnormalities Andrew P. Wilper, MD
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Goals and Objectives Diagnose common cardiac arrhythmias Discuss importance of, and indications for anticoagulation in atrial fibrillation Diagnose common cardiac conduction abnormalities
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PART 1 We Are a Part of the Rhythm Nation
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You are seeing a 61-year-old man in urgent care. He complains of light headedness. He denies chest pain and dyspnea. ATRIAL FIBRILLATION Irregularly irregular & undulating baseline
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ATRIAL FIBRILLATION Rule #1 Narrow and irregularly irregular is atrial fibrillation until proven otherwise. Why did it occur? MI? PE? Hyperthyroidism? ETOH? Valvular Disease? Treatment Rate control: diltiazem, beta blocker, digoxin, ablation Rhythm control? Generally no unless very poor output Anticoagulation Embolic risk ~ 5%/year CHADS2 points score NNT CHF10417Review VASc RF HTN11125Anticoagulation Age > 751281Anticoagulation DM1333Anticoagulation Secondary (TIA, CVA)2427 Anticoagulation 5/644Anticoagulation
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What about CHADS2=0? Consider use of additional risks in form of CHA2DS2-VASc – Gives two points for age 75 years and older – An additional point for age 65-74 – An additional point for females – An additional point for vascular dz (CAD, PVD) – Better identifies risk among CHADS2=0 patients
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Skanes. Can Jour Cardiol. 2012. 28, 125-136
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RE-LY. NEJM. 2009
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You are seeing a 44 yo female with a complaint of palpitations.
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What was the rhythm? What was the treatment? What is the problem? Supraventricular tachycardia Adenosine IV Wolff-Parkinson-White Rate 180 QRS Morphology when in sinus rhythm
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SUPRAVENTRICULAR TACHYCARDIA (SVT) RATE 150-250 (typically ~ 180) Why did it occur? Accessory pathway? ETOH? Stimulants? Caffeine? Treatment Vagal Maneuvers Adenosine (temporary A-V blockade) Cardiovert if unstable EPS w/ablation for WPW
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Common SVT Characteristics Sinus tachycardia EATMATAfibAflutterWPW Rate>100100-180>100Variable (can be fast or slow) Vent rate: 125-175 140+ RegularityRegular Irregularly irregular Usually regular Irregular or regular P waveEctopic focus different At least 3 different morphologies NoneSawtoothedBuried P:QRS ratio 1:1 NoneMost commonly 2:1, others are 3:1 and 4:1 1:1 if you can see it PR intervalNormal to slightly shortened Ectopic focus with different interval VariableNoneVariableVery shortened; QRS is also typically wide
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You are seeing a patient in the ED with a complaint of palpitations. Recent history of pericarditis.
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Rate 150 ATRIAL FLUTTER Flutter waves
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ATRIAL FLUTTER Rule #2 Narrow, regular, and 150 is atrial flutter until proven otherwise. Why did it occur? CHF? COPD? Pericartidis? Recent Cardiac Surgery? Treatment -Usually goes away or converts to A-fib -Anticoagulation-similar approach to atrial fibrillation -Radiofrequency ablation of reentrant circuit
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FAST, NARROW RHYTHMS Irregularly irregular (Rule #1) A-FIB Rate > Rhythm ControlCHADS2 (Remember MAT) Regular at ~ 150 (Rule #2) A-FLUTTER Adenosine for diagnosis Regular > 150 SVTAccessory pathway (ablation) Stimulants Adenosine for treatment
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You are seeing a 61-year-old man in urgent care. He complains of light headedness. He denies chest pain and dyspnea. V – TACH 1. Abnormal and wide qrs (>120 ms) with secondary st and t wave changes, qrs concordance in V1-V6 2. Rate 140-200 3. Regular or slightly irregular 4. Abrupt onset and termination 5. AV dissociation 6. Capture beats-regular qrs from atrial p wave 7. Fusion Beats-partial depolarization by atrial and ventricular impulse
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You are called to the bedside of a patient with a history of drug-induced long QT syndrome.
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Diagnosis?
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Polymorphic Ventricular Tachycardia
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Polymorphic VT 1)Paroxysms of VT with irregular RR interval 2)Ventricular rate 200-250 3)Two or more cycles of qrs complexes with alternating polarity 4)Changing amplitude of qrs complexes in sinusoidal fashion 5)If prolonged QTc=Torsades de pointes
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FAST, WIDE RHYTHMS Ventricular Tachycardia QRS > 0.14 ms QRS concordance in V1-6 Notching in V1 down stroke SVT with LBBB deep S in V1, V2 wide R in I, V6 T-wave opposite terminal QRS SVT with RBBB some R wave in V1 prominent S in V6 T-wave opposite in III, V1-3 WiLLiaM MaRRoW=W in V1 and for M in V6 for LBBB, RBBB opposite
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V tach-fusion beat
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You are seeing a 61-year-old man in urgent care. He complains of light headedness. He denies chest pain and dyspnea. 2 o, Mobitz type I (Wenckeback ) Grouped beating Lengthening P-R interval Dropped beat
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APPROACH TO HEART BLOCK (P = QRS) Are there as many P waves as QRS complexes? NO YES1 o (P-R =) Is the P-R interval always equal?YES 2 o, Mobitz II NO (QRS =) Is the QRS interval always equal?YES 3 o NO 2 o, Mobitz I (Wenckebach)
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0.10 Sinus Node Wenckebach (Sick Sinus) 0.860.82 SA A AV V AV Wenckebach SA A AV V Sinus Wenckebach
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54 year old male with intermittent dizziness
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Unchanging PR with unexpected dropped beats Diagnosis=Mobitz II Block
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When to get help!
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Name the Rhythm
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You review the chart….
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And find this
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Name the Rhythm Paced Rhythm Motion Artifact Aberrantly Conducted Native Beats
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42 year old, screening physical RBBB 1. QRS >0.12 sec (in ANY lead) – look for this first 2. Slurred S wave in I and V6 – look for this second 3. RSR’ pattern in V1 with R’ taller than R (“Rabbit ears”) 4. Should be predominately positive in V1 – look for this only AFTER looking for the previous 2 criteria
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Right Bundle Branch Block Clinical Correlates-RVH, sudden increase in right ventricular pressure with stretch (as in pulmonary embolism), Cor Pulmonale, myocardial ischemia, infarction, or inflammation (myocarditis), hypertension. Caveats: Sometimes you will see a qR’ wave indicating an anteroseptal MI in V1 (floppy eared rabbit). You cannot diagnose RVH in RBBB
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75 yo male presents to establish care, prior history of lymphoma LBBB 1. QRS duration >0.12 sec 2. Broad, monomorphic (meaning all positive or all negative) R waves in I and V6, with no Q waves 3. Broad, monomorphic S waves in V1; may have small r wave
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Left Bundle Branch Block Clinical associations: HTN, CAD, valvular heart disease (rheumatic heart disease), endocarditis, cardiomyopathy, infiltrative diseases of the heart, prior XRT Caveats: You cannot Dx LVH or RVH in patients with LBBB. Infarction is tricky to diagnose in LBBB, but possible
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Delays Intraventricular Conduction Delay (IVCD) Criteria: – QRS duration > 0.12 seconds – Doesn’t qualify for LBBB or RBBB **When this is seen, look for hyperkalemia
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Blocks Hemiblocks (Left Anterior Fascicular Block, Left Posterior Fascicular block) A few words: The Left bundle splits into the left anterior fascicle and the left posterior fascicle
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Blocks Criteria: Left Anterior Hemiblock/Fascicular Block (fairly common) – LAD with axis at –30 to –90 degrees – qR complex or an R wave in lead 1, AvL – An rS complex in lead III and usually in II and aVF – Easy shortcut: LAD? yes, then check lead II – if net vector is negative LAHB
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LAFB ECG Axis?Left QRS duration? <120ms Net Vector in II? Negative
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Causes of LAFB CAD Hypertension Valvular disease Degenerative disease of the conducting system Sclerosis of the left cardiac skeleton Myocardial fibrosis Normal Variant (2-5%)
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Blocks Left Posterior Hemiblock/ Fascicular Block (fairly rare) – RAD with axis 90-180 – S wave in lead I and a q in III – Exclusion of RAE and/or RVH
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Left Posterior Hemiblock Axis? Right QRS? <120 ms rS in I and aVL qR in III and aVF
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Causes of LPFB Similar to LAFB Cardiomyopathies Chagas disease Myocarditis Hyperkalemia Acute cor pulmonale
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Note RBBB+LAFB or RBBB + LPFB commonly referred to as bifascicular blocks
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Practice!
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Normal Sinus Rhythm
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VT A fib w/BBB
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A Fib LBBB
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LVH with strain NSR with PAC Rate related LBBB
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Sinus Tachycardia, A-V dissociation RBBB LAFB NS ST/T abn
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Thank you
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