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(Circulation. 2009;119:e235-e240.)
© 2009 American Heart Association, Inc.
AHA/ACCF/HRS Scientific Statement |
Key Words: AHA Scientific Statements electrocardiography electrophysiology conduction IVCD
| Introduction |
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The term intraventricular conduction disturbances refers to abnormalities in the intraventricular propagation of supraventricular impulses that give rise to changes in the shape and/or duration of the QRS complex. These changes in intraventricular conduction may be fixed and present at all heart rates, or they may be intermittent and be tachycardia or bradycardia dependent. They may be caused by structural abnormalities in the His-Purkinje conduction system or ventricular myocardium that result from necrosis, fibrosis, calcification, infiltrative lesions, or impaired vascular supply. Alternatively, they may be functional and due to the arrival of a supraventricular impulse during the relative refractory period in a portion of the conducting system, in which case the term aberrant ventricular conduction is applied. They may also be due to abnormal atrioventricular connections, which bypass the atrioventricular node, resulting in ventricular preexcitation.
In 1985, the electrocardiography (ECG) criteria for intraventricular conduction disturbances and ventricular preexcitation were reviewed by an ad hoc working group established by the World Health Organization and the International Society and Federation of Cardiology. Recommendations were made for the diagnosis of complete and incomplete left and right bundle-branch blocks (LBBB and RBBB), left anterior and left posterior fascicular blocks, nonspecific intraventricular blocks, and ventricular preexcitation.3 The purpose of the present report is to define the normal QRS duration, review the recommendations made in 1985, recommend alterations and additions to those recommendations, and provide recommendations for children and adolescents.
| Normal QRS Duration |
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Because global data and data detailing the effects of age, gender, and race are still evolving,7–10 the committee recommends that for the present, a QRS duration of greater than 110 ms in subjects older than 16 years of age be regarded as abnormal. The data for both children and adults may have to be revised in the near future.
| Review of Prior Recommendations With Revisions Proposed by the Committee |
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Mean Frontal Plane Axis
The mean frontal plane electrical axis, determined by the vector of the maximal (dominant) QRS deflection, depends on age and body habitus (Table). It shifts to the left with increasing age. In adults, the normal QRS axis is considered to be within –30° and 90°. Left-axis deviation is –30° and beyond. Moderate left-axis deviation is between –30° and –45°. Marked left-axis deviation is from –45° to –90° and is often associated with left anterior fascicular block. Moderate right-axis deviation in adults is from 90° to 120°, and marked right-axis deviation, which is often associated with left posterior fascicular block, is between 120° and 180°. In the absence of a dominant QRS deflection, as in an equiphasic QRS complex, the axis is said to be indeterminate.
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In children, there is normally a rightward QRS axis at birth that shifts gradually leftward throughout childhood. In the neonate, the mean electrical axis in the frontal plane is between 60° and 190° and is termed "extreme right axis" when it is between –90° and 190°. Normally, the axis then shifts to the left, and by ages 1 to 5 years, it is generally between 10° and 110°.4 Between 5 and 8 years of age, the normal QRS axis may extend to 140°, and between ages 8 and 16 years, the range of QRS axis extends to 120°. Leftward QRS-axis shifts are present in congenital defects with underdevelopment of the right ventricle, such as tricuspid atresia, and with abnormal location of the conduction system, such as complete atrioventricular septal defect.
Complete RBBB
Of the above criteria, the first 3 should be present to make the diagnosis. When a pure dominant R wave with or without a notch is present in V1, criterion 4 should be satisfied.
Incomplete RBBB
Incomplete RBBB is defined by QRS duration between 110 and 120 ms in adults, between 90 and 100 ms in children between 4 and 16 years of age, and between 86 and 90 ms in children less than 8 years of age. Other criteria are the same as for complete RBBB. In children, incomplete RBBB may be diagnosed when the terminal rightward deflection is less than 40 ms but greater than or equal to 20 ms. The ECG pattern of incomplete RBBB may be present in the absence of heart disease, particularly when the V1 lead is recorded higher than or to the right of normal position and r' is less than 20 ms.
The terms rsr' and normal rsr' are not recommended to describe such patterns, because their meaning can be variously interpreted. In children, an rsr' pattern in V1 and V2 with a normal QRS duration is a normal variant.
Complete LBBB
Incomplete LBBB
Nonspecific or Unspecified Intraventricular Conduction Disturbance
QRS duration greater than 110 ms in adults, greater than 90 ms in children 8 to 16 years of age, and greater than 80 ms in children less than 8 years of age without criteria for RBBB or LBBB. The definition may also be applied to a pattern with RBBB criteria in the precordial leads and LBBB criteria in the limb leads, and vice versa.
Left Anterior Fascicular Block
These criteria do not apply to patients with congenital heart disease in whom left-axis deviation is present in infancy.
Left Posterior Fascicular Block
Ventricular Preexcitation of Wolff-Parkinson-White Type
Whether preexcitation is full or not cannot be determined from the body surface ECG, but the following criteria are suggestive of full preexcitation:
Terms Not Recommended
The term Mahaim-type preexcitation is not recommended because the diagnosis cannot be made with certainty on the basis of the surface ECG. The terms atypical LBBB, bilateral bundle-branch block, bifascicular block, and trifascicular block are not recommended because of the great variation in anatomy and pathology producing such patterns. The committee recommends that each conduction defect be described separately in terms of the structure or structures involved instead of as bifascicular, trifascicular, or multifascicular block.
The term Brugada pattern to describe a pattern that simulates incomplete RBBB in lead V1 with ST-segment changes is not recommended for incorporation into automated interpretative algorithms because there are 3 different types of ST-segment changes15,16 and because the pattern is not specific for the Brugada syndrome. The use of this term should be left to the discretion of the overreader.
The term left septal fascicular block is not recommended because of the lack of universally accepted criteria.
Additional Terms
Peri-infarction block17,18: The term possible peri-infarction block is recommended when, in the presence of an abnormal Q wave generated by a myocardial infarction in the inferior or lateral leads, the terminal portion of the QRS complex is wide and directed opposite to the Q wave (ie, a QR complex in the inferior or lateral leads).
Peri-ischemic block19,20: This term is recommended when a transient increase in QRS duration accompanies the ST- segment deviation seen with acute injury.
| Acknowledgments |
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| Footnotes |
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The American Heart Association, the American College of Cardiology, and the Heart Rhythm Society make every effort to avoid any actual or potential conflicts of interest that may arise as a result of an outside relationship or a personal, professional, or business interest of a member of the writing panel. Specifically, all members of the writing group are required to complete and submit a Disclosure Questionnaire showing all such relationships that might be perceived as real or potential conflicts of interest.
Parts I and II of this series, "Recommendations for the Standardization and Interpretation of the Electrocardiogram," were published in the March 13, 2007, issue of Circulation (Circulation. 2007;115:1306–1324 and 1325–1332). They are available online at http://circ.ahajournals.org/content/vol115/issue10/
Parts III, IV, V, and VI of this series are available online at http://circ.ahajournals.org/content/vol119/issue10/ (Circulation. 2009;119:e235–e240; e241–e250; e251–e261; and e262–e270). They also published ahead of print February 19, 2009.
This statement was approved by the American Heart Association Science Advisory and Coordinating Committee on August 7, 2008, by the American College of Cardiology Board of Trustees on May 16, 2008, and by the Heart Rhythm Society on June 18, 2008.
The American Heart Association requests that this document be cited as follows: Surawicz B, Childers R, Deal BJ, Gettes LS. AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram, part III: intraventricular conduction disturbances: a scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. Circulation. 2009;119:e235–e240.
This article has been copublished in the Journal of the American College of Cardiology.
Copies: This document is available on the World Wide Web sites of the American Heart Association (my.americanheart.org), the American College of Cardiology (www.acc.org), and the Heart Rhythm Society (www.hrsonline.org). A copy of the document is also available at http://www. americanheart.org/presenter.jhtml?identifier=3003999 by selecting either the "topic list" link or the "chronological list" link (No. LS-1886). To purchase additional reprints, call 843-216-2533 or e-mail kelle.ramsay@wolterskluwer.com.
Expert peer review of AHA Scientific Statements is conducted at the AHA National Center. For more on AHA statements and guidelines development, visit http://www.americanheart.org/presenter.jhtml?identifier=3023366.
Permissions: Multiple copies, modification, alteration, enhancement, and/or distribution of this document are not permitted without the express permission of the American Heart Association. Instructions for obtaining permission are located at http://www.americanheart.org/presenter.jhtml?identifier=4431. A link to the "Permissions Request Form" appears on the right side of the page.
| References |
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2. Mason JW, Hancock EW, Gettes L, et al. Recommendations for the standardization and interpretation of the electrocardiogram, part II: electrocardiography diagnostic statement list: a scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. Circulation. 2007; 115: 1325–32.
3. Willems JL, Robles de Medina EO, Bernard R, et al. Criteria for intraventricular conduction disturbances and pre-excitation: World Health Organization/International Society and Federation for Cardiology Task Force Ad Hoc. J Am Coll Cardiol. 1985; 5: 1261–75.[Abstract]
4. Davignon A, Rautaharju P, Boisselle E, et al. Normal ECG standards for infants and children. Pediatr Cardiol. 1980; 1: 123–31.[CrossRef]
5. Lepeschkin E, Surawicz B. The measurement of the duration of the QRS interval. Am Heart J. 1952; 44: 80–8.[CrossRef][Medline] [Order article via Infotrieve]
6. MacFarlane PW, Lawrie TDV. The normal electrocardiogram and vector cardiogram. In: Macfarlane PW, Lawrie TDV, eds. Comprehensive Electrocardiology: Theory and Practice in Health Disease. New York, NY: Pergamon Press; 1989: 424–49.
7. Matthes T, Gottsch G, Zywietz C. Interactive analysis of statistical ECG diagnosis on an intelligent electrocardiograph: an expert system approach. In: Willems JL, van Bemmel JH, Zywietz C, eds. Computer ECG Analysis: Towards Standardization. New York, NY: Elsevier; 1986: 215–20.
8. Wu J, Kors JA, Rijnbeek PR, et al. Normal limits of the electrocardiogram in Chinese subjects. Int J Cardiol. 2003; 87: 37–51.[CrossRef][Medline] [Order article via Infotrieve]
9. Macfarlane PW, McLaughlin SC, Devine B, Yang TF. Effects of age, sex, and race on ECG interval measurements. J Electrocardiol. 1994; 27 (suppl): 14–9.[CrossRef][Medline] [Order article via Infotrieve]
10. Rijnbeek PR, Witsenburg M, Schrama E, et al. New normal limits for the paediatric electrocardiogram. Eur Heart J. 2001; 22: 702–11.
11. Sgarbossa EB, Pinski SL, Barbagelata A, et al; GUSTO-1 (Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries) Investigators. Electrocardiographic diagnosis of evolving acute myocardial infarction in the presence of left bundle-branch block [published correction appears in N Engl J Med. 1996;334:931]. N Engl J Med. 1996; 334: 481–7.
12. Gunnarsson G, Eriksson P, Dellborg M. ECG criteria in diagnosis of acute myocardial infarction in the presence of left bundle branch block. Int J Cardiol. 2001; 78: 167–72.[CrossRef][Medline] [Order article via Infotrieve]
13. Swiryn S, Abben R, Denes P, Rosen KM. Electrocardiographic determinants of axis during left bundle branch block: study in patients with intermittent left bundle branch block. Am J Cardiol. 1980; 46: 53–8.[CrossRef][Medline] [Order article via Infotrieve]
14. Childers R, Lupovich S, Sochanski M, Konarzewska H. Left bundle branch block and right axis deviation: a report of 36 cases. J Electrocardiol. 2000; 33 (suppl): 93–102.[Medline] [Order article via Infotrieve]
15. Alings M, Wilde A. "Brugada" syndrome: clinical data and suggested pathophysiological mechanism. Circulation. 1999; 99: 666–73.
16. Eckardt L, Probst V, Smits JP, et al. Long term prognosis of individuals with right precordial ST-segment–elevation Brugada syndrome. Circulation. 2005; 111: 257–63.
17. Grant RP. Peri-infarction block. Prog Cardiovasc Dis. 1959; 2: 237–47.[CrossRef][Medline] [Order article via Infotrieve]
18. Vassallo JA, Cassidy DM, Marchlinski FE, et al. Abnormalities of endocardial activation pattern in patients with previous healed myocardial infarction and ventricular tachycardia. Am J Cardiol. 1986; 58: 479–84.[CrossRef][Medline] [Order article via Infotrieve]
19. Wagner NB, Sevilla DC, Krucoff MW, et al. Transient alterations of the QRS complex and ST segment during percutaneous transluminal balloon angioplasty of the left anterior descending coronary artery. Am J Cardiol. 1988; 62: 1038–142.[CrossRef][Medline] [Order article via Infotrieve]
20. Surawicz B. Reversible QRS changes during acute myocardial ischemia. J Electrocardiol. 1998; 31: 209–20.[CrossRef][Medline] [Order article via Infotrieve]
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