(Circulation. 2005;111:2146-2150.)
© 2005 American Heart Association, Inc.
AHA Science Advisory |
| Abstract |
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Key Words: AHA Science Advisories heart failure pacing arrhythmias therapy
| Introduction |
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| Mechanism of Action for CRT |
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Compared with the delayed activation that occurs in the setting of an interventricular conduction delay, CRT depolarizes the left ventricle earlier. CRT is believed to reverse the deleterious effects of dyssynchronous ventricular activation by decreasing the electromechanical delay associated with an interventricular conduction delay and providing near-simultaneous contraction of the ventricular septum and the left ventricular free wall. Numerous clinical investigations have demonstrated that in selected patients CRT significantly improves cardiac output, systolic pressure, maximal rate of pressure rise, the magnitude of wall contraction, mitral regurgitation, and left atrial pressure. Furthermore, these acute hemodynamic benefits are achieved while reducing myocardial energy consumption.7,8
To a much lesser degree than biventricular pacing, optimization of the atrioventricular interval for patients in sinus rhythm may improve cardiac hemodynamics by coordinating the timing of atrial systole relative to ventricular filling.
| Benefits of CRT |
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| Patient Selection for CRT |
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On the basis of the inclusion criteria and the results of these studies, a high level of evidence supports CRT in patients with systolic dysfunction and heart failure resulting from either ischemic or nonischemic cardiomyopathy who have a left ventricular ejection fraction (LVEF)
0.35, are in NYHA functional class III or IV, are on maximal medical therapy, have a QRS complex duration >120 ms, and are in sinus rhythm (Table 4).
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| Uncertainties of CRT |
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0.35, a QRS complex duration >120 ms, or sinus rhythm.16 Some trials suggest that CRT may be of benefit for other clinical scenarios in addition to this patient profile. Recently, 2 randomized multicenter trials assessed the benefit of CRT in patients with NYHA functional class II symptoms despite medical therapy, a depressed LVEF, a wide QRS duration, and an indication for implantable defibrillator therapy.5,10 In these studies, CRT demonstrated functional improvement as well as left ventricular remodeling. At present, however, the use of CRT in patients with minimal heart failure symptoms is not universally recommended and is the focus of ongoing clinical trials.
The majority of patients enrolled in CRT trials had a wide QRS complex on the basis of a left bundle-branch block16; however, the relative therapeutic benefit among patients with a left versus a right bundle-branch block is unclear. Nonetheless, the current recommendation for CRT is based on QRS duration, not on QRS morphology.
The role of CRT in other groups of patients with heart failure resulting from systolic dysfunction, including patients with atrial fibrillation or a wide QRS morphology on the basis of right ventricular pacing, is unclear. Preliminary data from a large study and results from a few small studies suggest that in patients with atrial fibrillation and complete atrioventricular block, CRT may provide functional improvement when compared with right ventricular pacing.1114 Among patients with a cardiomyopathy, sinus rhythm, and an indication for an implantable defibrillator but not permanent pacing, right ventricular pacing precipitates and has a negative impact on heart failure.15 The results of this study15 suggest that right ventricular pacing is not optimal in this group of patients and that biventricular pacing may be better; however, there are no prospective data to support this approach.
The published randomized CRT studies have used QRS complex duration as a surrogate marker for dyssynchrony.16 In the future, we may be able to identify patients with ventricular dyssynchrony and who will respond to CRT with the use of tissue Doppler or other echocardiographic or visualization techniques.16
Three other unresolved issues with regard to CRT are (1) the risks and benefits of left ventricular pacing without a right ventricular lead, (2) the risks and benefits of a surgically placed left ventricular pacing lead versus a nonthoracotomy approach, and (3) the use of CRT in patients with NYHA class IV symptoms who are nonambulatory and dependent on intravenous inotropes for hemodynamic support.
| Risks and Complications of CRT |
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1%); infection (
1%); hematoma (
1%); pneumothorax (
1%); pericardial effusion with or without tamponade (
1%); and myocardial infarction, stroke, and death (
1/500). Transvenous implantation of a left ventricular lead for CRT is accomplished via the coronary sinus and its tributaries. The specific risks associated with implantation of a left ventricular lead for CRT include coronary sinus dissection and perforation (
1%), lead dislodgment (
5%), extracardiac stimulation (
5%), and the risks associated with intravenous contrast, including acute renal failure (<1%).16 Limited data suggest that ventricular proarrhythmia may be a rare but potential risk of CRT.17 | Conclusions |
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0.35, a QRS complex >120 ms, and sinus rhythm, and are NYHA functional class III or IV despite maximal medical therapy for heart failure. In general, these patients are treated with a CRT device that also has defibrillation capabilities. A variety of unresolved issues include the role of CRT for patients with NYHA functional class II symptoms or with atrial fibrillation, prospective identification of responders to CRT, and the role of CRT in other categories of patients.
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| Footnotes |
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This statement was approved by the American Heart Association Science Advisory and Coordinating Committee on January 7, 2005. A single reprint is available by calling 800-242-8721 (US only) or writing the American Heart Association, Public Information, 7272 Greenville Ave, Dallas, TX 75231-4596. Ask for reprint No. 71-0319. To purchase additional reprints: up to 999 copies, call 800-611-6083 (US only) or fax 413-665-2671; 1000 or more copies, call 410-528-4121, fax 410-528-4264, or e-mail kgray@lww.com. To make photocopies for personal or educational use, call the Copyright Clearance Center, 978-750-8400.
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.
| References |
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3. Abraham WT, Fisher WG, Smith AL, Delurgio DB, Leon AR, Loh E, Kocovic DZ, Packer M, Clavell AL, Hayes DL, Ellestad M, Trupp RJ, Underwood J, Pickering F, Truex C, McAtee P, Messenger J; MIRACLE Study Group. Multicenter InSync Randomized Clinical Evaluation. Cardiac resynchronization in chronic heart failure. N Engl J Med. 2002; 346: 18451853.
4. Young JB, Abraham WT, Smith AL, Leon AR, Lieberman R, Wilkoff B, Canby RC, Schroeder JS, Liem LB, Hall S, Wheelan K; Multicenter InSync ICD Randomized Clinical Evaluation (MIRACLE ICD) Trial Investigators. Combined cardiac resynchronization and implantable cardioversion defibrillation in advanced chronic heart failure: the MIRACLE ICD Trial. JAMA. 2003; 289: 26852694.
5. Higgins SL, Hummel JD, Niazi IK, Giudici MC, Worley SJ, Saxon LA, Boehmer JP, Higginbotham MB, De Marco T, Foster E, Yong PG. Cardiac resynchronization therapy for the treatment of heart failure in patients with intraventricular conduction delay and malignant ventricular tachyarrhythmias. J Am Coll Cardiol. 2003; 42: 14541459.
6. Bristow MR, Saxon LA, Boehmer J, Krueger S, Kass DA, De Marco T, Carson P, DiCarlo L, DeMets D, White BG, DeVries DW, Feldman AM; Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure (COMPANION) Investigators. Cardiac-resynchronization therapy with or without an implantable defibrillator in advanced chronic heart failure. N Engl J Med. 2004; 350: 21402150.
7. Nelson GS, Curry CW, Wyman BT, Kramer A, Declerck J, Talbot M, Douglas MR, Berger RD, McVeigh ER, Kass DA. Predictors of systolic augmentation from left ventricular preexcitation in patients with dilated cardiomyopathy and intraventricular conduction delay. Circulation. 2000; 101: 27032709.
8. Nelson GS, Berger RD, Fetics BJ, Talbot M, Spinelli JC, Hare JM, Kass DA. Left ventricular or biventricular pacing improves cardiac function at diminished energy cost in patients with dilated cardiomyopathy and left bundle-branch block. Circulation. 2000; 102: 30533059.
9. Bradley DJ, Bradley EA, Baughman KL, Berger RD, Calkins H, Goodman SN, Kass DA, Powe NR. Cardiac resynchronization and death from progressive heart failure: a meta-analysis of randomized controlled trials. JAMA. 2003; 289: 730740.
10. Abraham WT, Young JB, Leon AR, Adler S, Bank AJ, Hall SA, Lieberman R, Liem LB, OConnell JB, Schroeder JS, Wheelan KR; Multicenter InSync ICD II Study Group. Effects of cardiac resynchronization on disease progression in patients with left ventricular systolic dysfunction, an indication for an implantable cardioverter-defibrillator, and mildly symptomatic chronic heart failure. Circulation. 2004; 110: 28642868.
11. Leclercq C, Walker S, Linde C, Clementy J, Marshall AJ, Ritter P, Djiane P, Mabo P, Levy T, Gadler F, Bailleul C, Daubert JC. Comparative effects of permanent biventricular and right-univentricular pacing in heart failure patients with chronic atrial fibrillation. Eur Heart J. 2002; 23: 17801787.
12. Leon AR, Greenberg JM, Kanuru N, Baker CM, Mera FV, Smith AL, Langberg JJ, DeLurgio DB. Cardiac resynchronization in patients with congestive heart failure and chronic atrial fibrillation: effect of upgrading to biventricular pacing after chronic right ventricular pacing. J Am Coll Cardiol. 2002; 39: 12581263.
13. Linde C, Leclercq C, Rex S, Garrigue S, Lavergne T, Cazeau S, McKenna W, Fitzgerald M, Deharo JC, Alonso C, Walker S, Braunschweig F, Bailleul C, Daubert JC. Long-term benefits of biventricular pacing in congestive heart failure: results from the MUltisite STimulation in cardiomyopathy (MUSTIC) study. J Am Coll Cardiol. 2002; 40: 111118.
14. Doshi R, Daoud E, Fellows C, Turk K, Duran A, Hamden M, and the investigators of the PAVE study. Mortality and congestive heart failure in the PAVE study. Europace. 2004; 6 (suppl 1): 92. Abstract 115/1.
15. Wilkoff BL, Cook JR, Epstein AE, Greene HL, Hallstrom AP, Hsia H, Kutalek SP, Sharma A; Dual Chamber and VVI Implantable Defibrillator Trial Investigators. Dual-chamber pacing or ventricular backup pacing in patients with an implantable defibrillator: the Dual Chamber and VVI Implantable Defibrillator (DAVID) Trial. JAMA. 2002; 288: 31153123.
16. Bax JJ, Ansalone G, Breithardt OA, Derumeaux G, Leclercq C, Schalij MJ, Sogaard P, St. John Sutton M, Nihoyannopoulos P. Echocardiographic evaluation of cardiac resynchronization therapy: ready for routine clinical use? A critical appraisal. J Am Coll Cardiol. 2004; 44: 19.
17. Medina-Ravell VA, Lankipalli RS, Yan GX, Antzelevitch C, Medina-Malpica NA, Medina-Malpica OA, Droogan C, Kowey PR. Effect of epicardial or biventricular pacing to prolong QT interval and increase transmural dispersion of repolarization: does resynchronization therapy pose a risk for patients predisposed to long QT or torsade de pointes? Circulation. 2003; 107: 740746.
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