Arrhythmias



Arrhythmias





7.1 Supraventricular Arrhythmias

Nejm 2004;338:1369; 2001;344:1067; J Am Coll Cardiol 2003;42: 1493; Circ 2003;107:1096; 2002;106:649

Cause: Mechanisms include increased automaticity of ectopic atrial focus (APC), triggered activity associated with disorders of repolarization, and reentrant arrhythmias involving accessory pathways between atria and ventricles (35-40%), within the AV node (60-65%), or within the SA node for SVT or in RA for Aflut, and macro-reentrant circuits within the atria. Afib may also be due to single, rapidly discharging focus, in which case elimination of the focus by radio-frequency ablation also eliminates the arrhythmia (Circ 1997;95:562).

Multifocal atrial tachycardia is typically seen in elderlypts with severe illnesses, most commonly COPD. The mechanism may be delayed after depolarization, leading to triggered activity (Chest 1998;113:203).

Epidem: Prevalence of PSVT is 225/1000 persons; incidence is 35/100,000 person-yr. Other CVD is present in 90% of malepts and 48% of femalepts. 90% ofpts have AV or AV node reentrant tachycardia (J Am Coll Cardiol 1998;31:150).

The lifetime risk of Afib is 1 in 4 for subjects > 40 yr old (Circ 2004;110:1042). Inpts > 65 yr, overall incidence of Afib is 192/1000 person-years (age 65-74: men, 176 and women, 101; age 75-84: men, 427 and women, 216). Use of diuretics, h/o
valvular heart disease, CAD, advancing age, higher systolic BP, glucose, and LA size are all associated with increased risk of Afib (Jama 2001;285:2370; Circ 1997;96:2455).

SV arrhythmias occur in 76% ofpts undergoing noncardiac surgery. Correlates include male sex, age > 70 yr, significant valvular disease, h/o asthma, CHF, APC on pre-op EKG, and abdominal, vascular, and intrathoracic surgery (Ann IM 1998;129:279). Up to 33% ofpts will develop Afib after CABG. Predictors include age > 70 yr, male sex, HT, need for IABP, post-op pneumonia, mechanical ventilation > 24 hr, and h/o Afib or CHF (Circ 1996;94:390; Jama 1996;276:300). Post-op atrial pacing in conjunction with β-blockade reduces the incidence of Afib following CV surgery (J Am Coll Cardiol 2000;35:1411).

Up to 25% ofpts with ablation of Aflut develop Afib over 2 yr. The risk is 10% forpts with neither h/o Afib nor EF < 50%; 20% with either of these; and 74% with both (Circ 1998; 98:315).

Pathophys:

PSVT: In 90% ofpts with AV node reentrant tachycardia, anterograde conduction occurs over the slow atrioventricular nodal pathway and retrograde conduction over the fast pathway. In mostpts, posterior atrionodal input to the AV node serves as the anterograde limb of the reentry circuit, and anterior atrionodal inputs serve as the retrograde limb (Nejm 1995;332:162; 1999;340:534).

Aflut: Due to macro-reentry involving counterclockwise reentrant activation of RA. The critical element of the reentrant circuit is the isthmus between the IVC and tricuspid valve annulus.

Afib: Pts with AMI are prone to Afib. Predictors are 3-vessel CAD, advanced age, higher peak CK levels, worse Killip class (IV vs I), and increased heart rate. The unadjusted mortality rate is higher at 30 d (14.3% vs 6.2%) and at 1 yr
(21.5% vs 8.6%) in patients with Afib (GUSTO-I; J Am Coll Cardiol 1997;30:406).

After cardioversion of chronic Afib to NSR, there is a gradual increase of 56% in CO over 4 wk, due to return and increasing strength of LA mechanical activity. CO decreases transiently after cardioversion of Afib in > 1/3 ofpts; the decrease may last 1 wk (Arch IM 1997;157:1070).

Sx: Palpitations; may be associated with lightheadedness, dyspnea, and nausea. Pts treated with radio-frequency ablation report an improvement in sx (Circ 1996;94:1585).

Si: Irregular heartbeat; tachycardia

Crs: In the Framingham Heart Study, Afib was associated with a 15-to 19-fold higher mortality risk after adjustment for preexisting CV conditions (Circ 1998;98:946).

Inpts with CHF and Afib, amiodarone produced conversion to NSR in 31% and reduced incidence of recurrent Afib. Pts who converted to NSR had a lower mortality rate than those who did not (Circ 1998;98:257).

Cmplc: 15% ofpts presenting with Afib will have atrial thrombi identified by TEE. Pts with Afib have an annual stroke rate of 45%; the rate is 14% for anticoagulatedpts. The risk of stroke in Afibpts is 15% for age 50-59 vs 23.5% for age 80-89 (Framingham). Pts with previous TIA, CVA, or systemic embolism; age > 75 yr; HT; poor LV function; prosthetic heart valve (mechanical or tissue valve); or rheumatic mitral valvular disease have an increased risk. Diabetes, CAD, age 65-75 yr, or thyrotoxicosis may also increase this risk (Chest 1998;114:S579).

Forpts with Afib clinically estimated to have lasted < 48 hr, the likelihood of cardioversion-related clinical thromboembolism is 0.1%. Approximately 67% will convert spontaneously (Ann IM 1997;126:615).

Inpts with Afib for < 2 wk before cardioversion, normal atrial mechanical function returns within 24 hr of cardioversion.
Pts with Afib present for 2-6 wk require up to 1 wk, and those with Afib for < 6 wk require up to 3 wk for full recovery of atrial mechanical function (Circ 1998;98:479). Overall, effective mechanical atrial function is recovered by 68% ofpts by 3 and by 76% by 7 after cardioversion. Electrical cardioversion produces a greater degree and longer duration of mechanical atrial dysfunction than those who convert pharmacologically or spontaneously (J Am Coll Cardiol 1997;30:481).

Pts with Aflut are also at risk for thromboembolus postcardioversion (J Am Coll Cardiol 1997;29:582). In one series, TEE showed LA thrombus in 11% ofpts with Aflut for 4 ± 9 wk (Circ 1997; 95:962).

Lab: Thyroid function, electrolytes

EKG: (See Chapter 3 for EKG diagnostic criteria.) Wolff-Parkinson-White syndrome—ventricular depolarization through AV node and accessory pathways, with reentrant tachyarrhythmias and characteristic short PR interval and delta wave

TEE: Features independently associated with increased thromboembolic risk in Afib include LA appendage thrombi, dense spontaneous echo contrast, LA appendage peak flow velocity < 220 cm/sec, and complex aortic plaque. Pts with h/o HT have an increased incidence of atrial appendage thrombi on TEE. The presence of complex aortic plaque also distinguishespts with Afib at high risk from those at moderate risk of thromboembolism (J Am Coll Cardiol 1998;31:1622; Ann IM 1998;128:639).

Rx: See Tables 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9 and 7.10.

PSVT: More than 90% of tachycardias due to AV or AV nodal reentry are terminated by a 12-mg dose of adenosine. Adenosine also frequently terminates sinus-node reentrant tachycardia and occasionally terminates unifocal atrial tachycardia (Nejm 1995;332:162).









Table 7.1 Acute Management of Stable Regulator Tachycardias
























EKG Finding


First Choice


Second Choice


Narrow complex SVT


Vagal maneuvers, adenosine, verapamil, diltiazem


β-Blockers, amiodarone, digoxin


Wide Complex Tachycardias


SVT with BBB


Vagal maneuvers, adenosine, verapamil, diltiazem


β-Blockers, amiodarone, digoxin


Pre-excitation


Flecanide, ibutilide, procainamide, DC cardioversion


Wide complex tachycardia of unknown origin


Procainamide, sotalol, amiodarone, DC cardioversion


Lidocaine, adenosine









Table 7.2 Management of Focal Atrial Tachycardias



























Clinical Situation


First Choice


Second Choice


Acute Conversion


DC cardioversion


Adenosine, β-blockers, verapamil, diltiazem, procainamide, flecanide, propafenone


Acute Rate Control


β-Blockers, verapamil, diltiazem


Digoxin


Prophylaxis



Recurrent symptomatic AT


Catheter ablation, β-blockers, verapamil, diltiazem


Disopyramide, flecanide, propafenone, sotalol, amiodarone



Incessant AT


Catheter ablation











Table 7.3 Long-Term Rx of Recurrent AVNRT


























Clinical Situation


First Choice


Second Choice


Hemodynamically unstable AV node reentrant tachycardia


Catheter ablation


β-Blockers, verapamil, diltiazem, sotalol, amiodarone


Recurrent symptomatic AVNRT


Catheter ablation, β-blockers, verapamil, diltiazem


Digoxin


Recurrent AVNRT unresponsive to β-or Ca++-channel blockers


Flecanide, propafenone, sotalol


Amiodarone


PSVT with only dual AV node pathways


β-Blockers, verapamil, diltiazem, flecanide, propafenone


Infrequent well-tolerated AVNRT


Nothing, vagal maneuvers, “pill in pocket,” β-blockers, verapamil, diltiazem, catheter ablation










Table 7.4 Rx of Junctional Tachycardia














Arrhythmia


First Choice


Second Choice


Focal junctional tachycardia


β-Blockers, flecanide, propafenone, sotalol, amiodarone, catheter ablation


Nonparoxysmal junctional tachycardia


Correct hypokalemia or digitalis toxicity, treat ischemia


β- or Ca++-channel blockers










Table 7.5 Acute Rx of Atrial Flutter






























Clinical Status/Aim


First Choice


Second Choice


Poorly Tolerated



Conversion


DC cardioversion



Rate control


β-Blockers, verapamil, diltiazem


Digoxin, amiodarone


Stable



Conversion


Atrial/transesophageal pacing, DC cardioversion


Ibutilide, flecanide, propafenone, sotalol, procainamide, amiodarone



Rate control


β-Blockers, verapamil, diltiazem


Digoxin, amiodarone









Table 7.6 Long-Term Management of Afib






















Clinical Status/Aim


First Choice


Second Choice


Well tolerated, first episode


DC cardioversion


Catheter ablation


Well tolerated, recurrent


Catheter ablation, dofetilide


Amiodarone, sotalol, flecanide, propafenone, procainamide, disopyramide, quinidine


Poorly tolerated


Catheter ablation


Aflut after use of amiodarone or IC agents


Catheter ablation












Table 7.7 Drugs for Conversion of Afib and Maintenance of NSR1

























































Drug


Conversion Dose


Maintenance Dose


Comments


Flecainide


300 mg orally (2 mg/kg of body weight iv)


50-150 mg bid


Iv formulation not available in U.S. Approved only for paroxysmal Afib with structurally normal heart.


Propafenone


600 mg orally (2 mg/kg iv)


150-300 mg bid


Same limitations as flecainide.


Procainamide


100 mg iv every 5 min to maximum of 1000 mg


Slow-release formulation, 1000-2000 mg bid


Long-term use associated with lupus. Not FDA approved for Afib.


Quinidine


200 mg sulfate orally, followed 1-2 hr later by 400 mg


200-400 mg sulfate qid, or 324-648 mg gluconate tid


Approved for Afib but risk of death increased during long-term therapy.


Disopyramide


200 mg orally every 4 hr to maximum of 800 mg


100-150 mg qid or 200-300 mg controlled-release formulation bid


Not FDA approved for Afib. Strong negative inotropic effect.


Sotalol


Not recommended (conversion rate is low)


120-160 mg bid


Poor conversion efficacy. Approved for maintenance of sinus rhythm. Hospitalization for initiation is mandatory.


Dofetilide


0.5 mg bid orally (adjust dose downward for patients with renal disease)


0.5 mg bid (adjust dose downward for patients with renal disease)


FDA approved for conversion and maintenance. Hospitalization for initiation is mandatory.


Amiodarone


1200 mg iv in 24 hr


600 mg/day for 2 wk, then 200-400 mg qd (lower dose is preferable)


iv amiodarone moderately effective for conversion, but onset is slow. Good rate slowing in Afib. Not FDA approved for this indication.


Ibutilide


1 mg iv over 10 min in patients weighing ≥ 60 kg, or 0.01 mg/kg over 10 min in patients weighing < 60 kg; may be repeated once if arrhythmia does not end within 10 min after end of initial infusion


Not available for maintenance (iv formulation only)


Do not use in patients with hypokalemia, a prolonged QT interval, or torsades de pointes.


1. Iv flecainide and propafenone (the doses of which are given in parentheses) are not available in the United States.


Source: Reprinted with permission, Falk, Medical Progress. Atrial Fibrillation 2001;344:1067-1078, New England Journal of Medicine.

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Jul 21, 2016 | Posted by in CARDIOLOGY | Comments Off on Arrhythmias

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