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Objectives. Discuss where ventricular arrhythmias originateList characteristics of each ventricular rhythmExplain how to interpret ventricular arrhythmias on an ECG strip. DysrhythmiasVentricular Escape Complexes and RhythmsAccelerated Idioventricular RhythmPremature Ventricular ContractionsV
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1. Ventricular Dysrhythmias, Asystole and Paced Rhythms
2. Objectives Discuss where ventricular arrhythmias originate
List characteristics of each ventricular rhythm
Explain how to interpret ventricular arrhythmias on an ECG strip
3. Dysrhythmias
Ventricular Escape Complexes and Rhythms
Accelerated Idioventricular Rhythm
Premature Ventricular Contractions
Ventricular Tachycardia
Related Dysrhythmia
Ventricular Fibrillation
Asystole
Artificial Pacemaker Rhythm Dysrhythmias Originating in the Ventricles
4. Origin Ventricular arrhythmias originate in the ventricles below the bundle of HIS
They occur when electrical impulses depolarize the myocardium using a different pathway from normal impulses
the atrium does not depolarizes and atrial kick is lost decreasing CO
May be benign but are potentially lethal because they are ultimately responsible for CO
5. Premature Ventricular Contractions
Etiology
Single ectopic impulse resulting from an irritable focus in either ventricle.
Causes may include myocardial ischemia, increased sympathetic tone, hypoxia, idiopathic causes, acid–base disturbances, electrolyte imbalances, or as a normal variation of the ECG.
May occur in patterns
Bigeminy, trigeminy, or quadrigeminy.
Couplets and triplets. Dysrhythmias Originating in the Ventricles
6. Premature Ventricular Contractions
Clinical Significance
Malignant PVCs
More than 6/minute, R on T phenomenon, couplets or runs of ventricular tachycardia, multifocal PVCs, or PVCs associated with chest pain.
Ventricles do not adequately fill, causing decreased cardiac output. Dysrhythmias Originating in the Ventricles
7. Premature Ventricular Contractions
Treatment
Non-malignant PVCs do not usually require treatment in patients without a cardiac history.
Cardiac patient with nonmalignant PVCs .
Administer oxygen and establish IV access
Malignant PVCs:
Lidocaine 1.0 –1.5 mg/kg IV bolus.
If PVCs are not suppressed, repeat doses of 0.5-0.75 mg/kg to max dose of 3.0 mg/kg.
If PVCs are suppressed, administer lidocaine drip 2–4 mg/min.
Reduce the dose in patients with decreased output or decreased hepatic function and patients > 70 years old. Dysrhythmias Originating in the Ventricles
8. Dysrhythmias Originating in the Ventricles