Ventricular fibrillation (VF) is a cause of cardiac arrest and sudden cardiac death. The ventricular muscle fibres contract randomly causing a complete failure of ventricular function. Most cases of ventricular fibrillation occur in patients with pre-existing known heart disease but the precise nature of the underlying cause of VF is not currently known.
- VF is the most commonly identified arrhythmia in cardiac arrest patients.
- The incidence of VF parallels the incidence of ischaemic heart disease, with a peak incidence of VF occurring in people aged 45-75 years.
- VF is most often associated with coronary artery disease and as a terminal event. VF may be due to acute myocardial infarction (MI) or ischaemia, or occur because of a chronic infarction scar.
- When electrocardiogram documentation is available, it often shows that rapid VT precedes VF.
- VF can occur during any of the following conditions or situations:
- Antiarrhythmic drug administration.
- Atrial fibrillation.
- Very rapid ventricular rates in the pre-excitation syndrome.
- Electrical shock administered during cardioversion.
- Electrical shock caused by accidental contact with improperly grounded equipment.
- Competitive ventricular pacing to terminate VT.
- Patients may have a history of chest pain, fatigue, palpitations and other nonspecific complaints.
- There may be known diagnosis or suggestion of pre-existing heart disease - eg, coronary artery disease, cardiomyopathy, valvular heart disease, myocarditis, congenital heart disease, long QT syndrome, Wolff-Parkinson-White (WPW) syndrome or Brugada's syndrome.
- Arrhythmias associated with cardiac arrest are divided into two groups:
- Shockable rhythms: VF and VT.
- Non-shockable rhythms: asystole and pulseless electrical activity (PEA): see the separate article on Adult Cardiopulmonary Arrest.
- Other causes of sudden collapse such as aortic dissection and pulmonary embolism.
- Cardiac enzymes (eg, creatine kinase, myoglobin, troponin).
- Electrolytes, calcium and magnesium. Severe metabolic acidosis, hypokalaemia, hyperkalaemia, hypocalcaemia, and hypomagnesaemia are some of the conditions that can increase the risk for arrhythmia and sudden death.
- Drug levels (eg, tricyclic antidepressants, digoxin). Most of the anti-arrhythmic medications also have a pro-arrhythmic effect.
- Toxicology screen: drugs that can lead to vasospasm-induced ischaemia - eg, cocaine.
- Thyroid-stimulating hormone: hyperthyroidism can lead to tachycardia and tachyarrhythmias.
- ECG:evidence of MI, prolonged QT interval, short PR, WPW pattern or other conditions.
- CXR: signs of left heart failure, pulmonary hypertension.
- Echocardiography: underlying structural abnormalities and cardiac dysfunction.
- Nuclear imaging techniques.
- Resting thallium (Tl) or technetium Tc 99m scintigraphy: assessing myocardial damage after MI.
- Exercise nuclear scintigraphy: very sensitive in detecting the presence, extent and location of myocardial ischaemia.
- Coronary angiography:
- Cardiac catheterisation in patients who survive VF, to assess the state of ventricular function and severity and extent of coronary artery disease.
- Coronary angiography identifies patients who may benefit from revascularisation by percutaneous coronary intervention (angioplasty) or coronary artery bypass grafting (CABG), and can also help identify coronary artery anomalies and other forms of congenital heart disease.
Patients who survive the initial episode of VF require a full evaluation of left ventricular function, myocardial perfusion and electrophysiological stability.
- Careful post-resuscitation care is essential to survival because recurrence rates average at about 50%.
- Treatment of myocardial ischaemia, heart failure and electrolyte disturbances.
- Empirical beta-blockers are often given.
- Most survivors of VF should be treated with implantable cardioverter defibrillators (ICDs).Transvenous ICDs can be placed with minimal morbidity and mortality.
- Radiofrequency ablation: most cases of VF are not amenable to radiofrequency ablation and require ICD placement.
- By itself, CABG only prevents recurrent VF if the ejection fraction is normal and ischaemia was the cause of the arrest. Even in these patients, ICDs are frequently placed after CABG.
- Central nervous system ischaemic injury
- Myocardial injury
- Post-defibrillation arrhythmias
- Aspiration pneumonia
- Defibrillation injury to self or others
- Injuries from CPR and resuscitation
- Skin burns
- Prognosis for survivors of VF strongly depends on the time elapsed between onset and medical intervention (prognosis is poor without intervention by 4-6 minutes after onset of VF) as well as on the particular aetiology for the VF.
- Early defibrillation often makes the difference between long-term disability and functional recovery.If defibrillation is delivered promptly, survival rates as high as 75% have been reported.
- Death and disability after successful resuscitation correlate with the degree of central nervous system damage occurring during the event.
- VF that occurs within the first 48 hours of the onset of acute MI has no bearing on prognosis, but VF that occurs more than 48 hours after acute MI is associated with a high rate of recurrence and a poorer prognosis.
- After resuscitation, the prognosis is largely dependent on haemodynamic stability, early neurological recovery and duration of the resuscitation.
- Education and training of non-healthcare professionals in basic life support and the use of automated external defibrillators in public places probably have the greatest impact on improving survival rates.
- A major adverse outcome from a VF event is anoxic encephalopathy.
Further reading and references
; Resuscitation Council UK, 2010
; NICE Technology Appraisal, January 2006
; Theory and practice of defibrillation: (2) defibrillation for ventricular fibrillation. Heart. 2005 Jan91(1):118
; Resuscitation Council UK (2010)