Accelerated idioventricular rhythm
Accelerated idioventricular rhythm | |
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Accelerated idioventricular rhythm (AIVR) at a rate of 55/min presumably originating from the left ventricle (LV). Note the typical QRS morphology in lead V1 characteristic of ventricular ectopy from the LV. Monophasic R-wave with smooth upstroke and notching on the downstroke (i.e., the so-called taller left peak or "rabbit-ear".) | |
Specialty | Cardiology ![]() |
Accelerated idioventricular rhythm is a ventricular rhythm with a rate of between 40 and 120 beats per minute. Idioventricular means “relating to or affecting the cardiac ventricle alone” and refers to any ectopic ventricular arrhythmia.[1] Accelerated idioventricular arrhythmias are distinguished from ventricular rhythms with rates less than 40 (ventricular escape) and those faster than 120 (ventricular tachycardia).[2] Though some other references limit to between 60 and 100 beats per minute.[3] It is also referred to as AIVR and "slow ventricular tachycardia."
It can be present at birth.[4] However, it is more commonly associated with reperfusion after myocardial injury.[2] AIVR is generally considered to be a benign abnormal heart rhythm. It is typically temporary and does not require treatment.
Pathophysiology
The accelerated idioventricular rhythm occurs when depolarization rate of a normally suppressed focus increases to above that of the "higher order" focuses (the sinoatrial node and the atrioventricular node). This most commonly occurs in the setting of a sinus bradycardia.[5]
Accelerated idioventricular rhythm is the most common reperfusion arrhythmia in humans. However, ventricular tachycardia and ventricular fibrillation remain the most important causes of sudden death following spontaneous restoration of antegrade flow.[6] Prior to the modern practice of percutaneous coronary intervention for acute coronary syndrome, pharmacologic thrombolysis was more common and accelerated idioventricular rhythms were used as a sign of successful reperfusion.[7] It is considered a benign arrhythmia especially in the setting of STEMI(where it is conventionally thought to be an indicator of reperfusion) that does not require intervention, though atrioventricular dyssynchrony can cause hemodynamic instability, which can be treated through overdrive pacing or atropine.[2]
Diagnosis
Differential diagnosis
AIVR appears similar to ventricular tachycardia with wide QRS complexes (QRS >0.12s) and a regular rhythm. It can most easily be distinguished from VT in that the rate is less than 120 and usually less than 100 bpm. There may or may not be AV dissociation depending on whether it is due to ventricular escape or AV block.[8]
References
- ^ Norris, RM; Mercer, CJ (Mar–Apr 1974). "Significance of idioventricular rhythms in acute myocardial infarction". Progress in Cardiovascular Diseases. 16 (5): 455–68. doi:10.1016/0033-0620(74)90006-1. PMID 4590952.
- ^ a b c Fuster V, Walsh RA, Harrington RA, eds. (2011). Hurst's the Heart (13th ed.). New York: McGraw-Hill Medical. ISBN 9780071636469.
- ^ Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J, eds. (2012). Harrison's Principles of Internal Medicine (18th ed.). New York: McGraw-Hill. ISBN 978-0071748896.
- ^ Freire G, Dubrow I (March 2008). "Accelerated idioventricular rhythm in newborns: a worrisome but benign entity with or without congenital heart disease". Pediatr Cardiol. 29 (2): 457–62. doi:10.1007/s00246-007-9024-z. PMID 17687587. S2CID 28730649.
- ^ "Accelerated Idioventricular Rhythm: Overview - eMedicine". Retrieved 2008-12-21.
- ^ Moens, A.L.; Claeys, M.J.; Timmermans, J.P.; Vrints, C.J. (April 2005). "Myocardial ischemia/reperfusion-injury, a clinical view on a complex pathophysiological process". International Journal of Cardiology. 100 (2): 179–190. doi:10.1016/j.ijcard.2004.04.013. PMID 15823623.
- ^ Bonnemeier, H; Ortak, J; Wiegand, UK; Eberhardt, F; Bode, F; Schunkert, H; Katus, HA; Richardt, G (Apr 2005). "Accelerated idioventricular rhythm in the post-thrombolytic era: incidence, prognostic implications, and modulating mechanisms after direct percutaneous coronary intervention". Annals of Noninvasive Electrocardiology. 10 (2): 179–87. doi:10.1111/j.1542-474X.2005.05624.x. PMC 6931919. PMID 15842430.
- ^ Papadakis MA, McPhee SJ, eds. (2013). Current Medical Diagnosis & Treatment 2014 (53rd ed.). New York: McGraw-Hill Medical. ISBN 978-0071806336.