Abstract
Cardiac resynchronization therapy (CRT) is an accepted treatment for patients with heart failure (HF), impaired left ventricular (LV) function, and a wide QRS complex. However, more than 30% of eligible patients fail to benefit from CRT. It is clearly necessary to define the characteristics of the best candidates for this therapy. To this end, surface ECG and echocardiography have been tested. Unfortunately, however, neither of these examinations has proved sufficiently able to identify the best patients. A tailored approach based on the evaluation of both electrical and mechanical delay to guide LV lead placement seems to be the most reasonable strategy in order to increase the efficacy of CRT therapy. The good preliminary data that have been published suggest that using intracardiac echocardiography to define the mechanical delay could be an interesting option. Moreover, at present it is the only option available that can enable intraprocedural evaluation of the mechanical activation sequence. Naturally, further randomized studies with larger populations should be performed in order to ascertain the real benefit of this approach and to evaluate whether it will outweigh the additional cost of this technology.
Keywords: Atrial Fibrillation, Remodeling, Cardiac Resynchronization Therapy, Left Ventricular
Introduction
Cardiac resynchronization therapy (CRT) is an accepted treatment for patients with heart failure (HF), impaired left ventricular (LV) function, and a wide QRS complex. The paradigm for CRT is based on the evidence that conduction disturbances, in particular left bundle branch block (LBBB), lead to LV dysfunction.[1] In 1983, it was first reported that simultaneous septal and LV free wall contraction was hemodynamically superior to dyssynchronous contraction and that the best hemodynamic effect arose from fusion between intrinsic LBBB conduction and the LV pacing stimulus.[2] In accordance with this concept, and on the basis of the benefit observed in early hemodynamic studies[3-4] and the observation that delayed segments predominate at these sites, the conventional approach to resynchronization has involved directing the LV lead to the lateral and posterior walls.
In the last 20 years, several large randomized multicenter trials have shown the clinical benefits of CRT therapy on symptoms, exercise capacity, mortality and HF re-hospitalization.[5-11] In the CARE HF[10] and REVERSE[12] studies, substantial improvements in LV size and function, LVEF, RV function, LA size and mitral regurgitation severity were observed in patients treated with CRT in comparison with ICD only. These results provide consistent evidence of a substantial, progressive and sustained reverse remodeling effect conferred by CRT in the responder population.
The Dark Side: Non-Responder Population
However, more than 30% of eligible patients fail to benefit from CRT. The reasons for the high percentage of non-responders include inappropriate candidate selection, device programming and LV lead placement.[13] In general, the response to CRT is greatest when biventricular pacing serves to synchronize left ventricular contraction as much as possible. The two criteria for pacing sites that are generally held to optimize CRT response are: (1) pacing at areas of live, non-scarred myocardium, and (2) pacing at the area of the most delayed mechanical contraction or electrical activation. Echocardiography and MRI reveal both the regions of latest mechanical activation and areas of scarred, non-contractile myocardium.[14-15] By contrast, ECG excels in determining the regions of latest electrical activation; it also has some ability to distinguish areas of scarring, but is generally unable to guide lead placement.[16-17]
First Mission: Choose the Right Patient
It is clearly necessary to define the characteristics of the best candidates for this therapy. To this end, surface ECG and echocardiography have been tested. Unfortunately, however, neither of these examinations has proved sufficiently able to identify the best patients. Indeed, in candidate selection, electrocardiographic evidence of intraventricular conduction delay has been tested as a surrogate marker for mechanical interventricular and intraventricular dyssynchrony.[6,18] In patients with severe CHF symptoms, LBBB morphology and QRS width > 150ms have been shown to predict a greater likelihood of CRT benefit. On the other hand, in patients with mild heart failure, non-LBBB morphology has been shown to predict minimal CRT benefit, and potentially even harm due to LV pacing. However, a significant proportion of CRT patients fail to respond symptomatically, and an even a larger proportion do not display objective evidence of benefit.[7,10] Moreover, the utility of many echocardiographic measures of mechanical dyssynchrony that once held promise as predictors of response to CRT in single-center studies was tested by the PROSPECT (Predictors of Response to CRT) trial.[19] Even after validation by blinded core laboratories, no echocardiographic measure of dyssynchrony could reliably predict the response to CRT. Negative evidence also comes from the recent Echo CRT study, which failed to show a benefit from CRT-D in patients with QRS duration <130 ms and dyssynchrony assessed echocardiographically.[20] These results seem to suggest that the battle to select patients has been lost, a conviction that is underlined by the simpler CRT indications reported in the latest guidelines.[21] For this reason, research on LV lead placement has attracted considerable interest.
Second Mission: Choose the Right Vein
The standard technique of CRT implantation has remained substantially unchanged since it was first described in the 1990s.[22] A posterolateral position with acceptable pacing parameters and no diaphragmatic stimulation is usually considered a good angiographic result. However, several studies have reported a correlation between LV lead position and CRT outcome and mortality.[23-25] Derval and colleagues showed that the pacing site is the primary determinant of the hemodynamic response to LV pacing in patients with non-ischemic, dilated cardiomyopathy,[26] pacing at the best LV site being associated acutely with fewer non-responders. In another study, Duckett et al. reported that the acute hemodynamic response seemed to predict reverse remodeling both in ischemic and dilated cardiomyopathy.[27] In a smaller but significant group of patients, Spragg and colleagues assessed the greatest percentage rise in LV-dP/dtmax in a target other than the posterolateral and lateral veins. They reported that, in their institutional experience, 8 of 11 patients who underwent intraoperative hemodynamic measurements while being paced at various endocardial surfaces were found to have an optimal pacing site that was not at locations traditionally used for LV pacing.[28]
These data confirm the idea that even when the LV lead is deployed in a “good” fluoroscopic position, the response is variable. Thus, a concept has evolved according to which targeting segments of latest LV “activation” improves response. The ways of defining the optimal LV segment to pace are different.
Pacing at the Site of Latest Mechanical Activation
Dyssynchrony imaging, which plays a small role in patient selection, may be useful in LV lead deployment. In a prospective study, Ypenburg et al. found that pacing at the site of latest mechanical activation, as determined by speckle-tracking radial strain analysis, resulted in a superior echocardiographic response after 6 months of CRT and better prognosis during long-term follow-up.[29] In the TARGET randomized study, the authors showed that a targeted approach to LV lead placement based on the definition of the latest segment activated, as identified by speckle-tracking echocardiography, resulted in significant benefit in terms of LV reverse remodeling, clinical status and the long-term endpoint of combined death and heart failure-related hospitalization, in comparison with a standard approach.[30] The main limitation of that study was that speckle-tracking echocardiography could not be performed in all the patients. Secondly, despite targeting, the constraints of coronary venous anatomy appear to have restricted concordance to only two thirds of patients, and in 8% of all patients the LV lead was still placed at areas of scarring. Several data have suggested that the viability of the paced LV segment can influence the outcome of CRT. In this regard, pacing areas of scarring is associated with a worse response[31,32] than pacing viable myocardium. Increasing scar transmurality31 and scar density[14] also portend a worse response. Another recent randomized study evaluated the impact of echocardiography-guided left ventricular lead placement with the aid of speckle-tracking echocardiography at the site of latest mechanical activation on the rate of freedom from appropriate CRT-D therapy for ventricular arrhythmias. The authors reported a higher percentage of CRT response in the echo-guided LV lead placement group (72% vs 48%, p = 0.006) with a consequent improved therapy-free survival rate.[33] When the trans-thoracic echocardiography approach is used, the best LV lead site is identified and implantation is performed at different times; it is therefore impossible to adjust the lead position if placement is suboptimal.
Pacing at the Site of Latest Electrical Activation
Another approach to identifying the right vein to pace is based on the evaluation of local ecg delay. The measurements of the QLV interval in each of the CS tributaries is the most used method to define the area of most delayed ventricular electrical activation. The QLV interval is defined as the time that elapses between the beginning of the QRS complex on surface ECG and the onset of the sensed electrogram at the LV lead. Placement of the CS lead at the site of the longest QLV interval is correlated with improved hemodynamics, including higher maximum dP/dT.[34] Moreover, a substudy of the SMART-AV trial showed that the length of the QLV interval was associated to a better outcome of CRT in patients with greater electrical dyssynchrony.[35] Similar results were observed also in the MADIT trial.[24]
This approach has the advantages of requiring minimal additional procedural time and it does not require the implementation of additional tests as echocardiography o cardiac MRI.
Another strategy was described in 2012 by Del Greco and colleagues, who demonstrated the ability of an electroanatomic navigation system (NavX system) to guide CRT–ICD implantation. The authors concluded that this approach was feasible and safe and reduced X-ray exposure both for patients and physicians. A further benefit was that the system provided more detailed information and accuracy during CS lead placement, in terms of both 3D visualization of anatomy and ventricular activation time, which optimize the pacing site choice.[36]
Currently, several additional studies are underway to correlate the QLV interval, as measured at the CS lead, and the clinical and echocardiographic response to CRT.
Intracardiac Echocardiography
In an early study conducted on dogs, Jiang et al. reported the feasibility and ability of intracardiac echocardiography in visualizing the left ventricle from the right ventricle and monitoring LV function.[37] Some years later, Saksena and colleagues proposed a clinical technique using intraoperative ICE to guide LV lead positioning and CRT device optimization. In their study, ICE was used in 23 patients to assess baseline LV function and LVEF in the B-mode and/or M-mode view and to evaluate the stroke volume indirectly by means of aortic flow spectra from Doppler analysis. The final LV position was selected according to the greatest changes in LVEF and/or aortic flow parameters measured in each possible vein during CRT stimulation.[38] The same approach was also used for AV and VV optimization. Intracardiac echocardiographic visualization of LV function was achieved in all the patients. On using this approach, the authors reported a significant improvement in LVEF compared with the baseline evaluation (24±9% to 43±13%) and only one patient experienced worsening of heart failure during a follow-up of 11±5 months. On the other hand, ICE evaluation prolonged the procedure time by 45 minutes. The main limitations of that study were the small patient population and the inability to confirm the real benefit of ICE, owing to the study design.
In another study, Bai et al. proposed using ICE coupled with vector velocity imaging to evaluate LV dyssynchrony and to guide LV lead placement at the time of CRT implantation. Starting from a manual endocardial perimeter tracing of each B-mode LV image, the vector velocity imaging software creates 6-segment radial/longitudinal strain curves that enable LV dyssynchrony to be detected.[39] This analysis was performed in the basal condition, during LV only or during CRT pacing in at least 2 veins in the first 50 patients. These data were compared with those from the following 54 patients, in whom standard CRT implantation was performed. Reverse remodeling was observed in both groups, but the percentage of responders in the ICE group was significantly higher than in the standard group (82% vs 63%). In the ICE group, all the responders displayed optimal visual resynchronization on vector velocity imaging. The authors concluded that ICE-VVI analysis could be easily and safely performed during CRT implantation, and that its use was associated with a better outcome on CRT therapy during follow-up. Moreover, ICE guidance enablesthe final LV lead position to be chosed from among all candidate veins by means of “real-time” synchrony analysis. Alternatively, if optimal resynchronization cannot be achieved in the procedure, the patient may not be a suitable candidate for transvenous CRT.
Conclusions
Cardiac resynchronization therapy is the most powerful weapon to reduce morbidity and mortality in patients with symptomatic severe heart failure and ECG evidence of interventricular conduction delay. A tailored approach based on the evaluation of both electrical and mechanical delay to guide LV lead placement seems to be the most reasonable strategy in order to increase the efficacy of CRT therapy. The good preliminary data that have been published suggest that using intracardiac echocardiography to define the mechanical delay could be an interesting option. Moreover, at present it is the only option available that can enable intraprocedural evaluation of the mechanical activation sequence. Naturally, further randomized studies with larger populations should be performed in order to ascertain the real benefit of this approach and to evaluate whether it will outweigh the additional cost of this technology.
Disclosures
None.
References
- 1.Wiggers C. The muscular reactions of the mammalian ventricles to artificial surface stimuli. Am J Physiol. 1925;13:346–78. [Google Scholar]
- 2.An even more physiological pacing: changing the sequence of ventricular activation. In: Steinbach K, Laskovics A, editors. Proceedings of the 7th World Symposium on Cardiac Pacing. Darmstadt, Germany: Steinkopff-Verlag. 1983;0:395–401. [Google Scholar]
- 3.Leclercq C, Gras D, Le Helloco A, Nicol L, Mabo P, Daubert C. Hemodynamic importance of preserving the normal sequence of ventricular activation in permanent cardiac pacing. Am. Heart J. 1995 Jun;129 (6):1133–41. doi: 10.1016/0002-8703(95)90394-1. [DOI] [PubMed] [Google Scholar]
- 4.Auricchio A, Klein H, Tockman B, Sack S, Stellbrink C, Neuzner J, Kramer A, Ding J, Pochet T, Maarse A, Spinelli J. Transvenous biventricular pacing for heart failure: can the obstacles be overcome? Am. J. Cardiol. 1999 Mar 11;83 (5B):136D–142D. doi: 10.1016/s0002-9149(98)01015-7. [DOI] [PubMed] [Google Scholar]
- 5.Cazeau S, Leclercq C, Lavergne T, Walker S, Varma C, Linde C, Garrigue S, Kappenberger L, Haywood G A, Santini M, Bailleul C, Daubert J C. Effects of multisite biventricular pacing in patients with heart failure and intraventricular conduction delay. N. Engl. J. Med. 2001 Mar 22;344 (12):873–80. doi: 10.1056/NEJM200103223441202. [DOI] [PubMed] [Google Scholar]
- 6.Auricchio Angelo, Stellbrink Christoph, Sack Stefan, Block Michael, Vogt Jürgen, Bakker Patricia, Huth Christof, Schöndube Friedrich, Wolfhard Ulrich, Böcker Dirk, Krahnefeld Olaf, Kirkels Hans. Long-term clinical effect of hemodynamically optimized cardiac resynchronization therapy in patients with heart failure and ventricular conduction delay. J. Am. Coll. Cardiol. 2002 Jun 19;39 (12):2026–33. doi: 10.1016/s0735-1097(02)01895-8. [DOI] [PubMed] [Google Scholar]
- 7.Abraham William T, Fisher Westby G, Smith Andrew L, Delurgio David B, Leon Angel R, Loh Evan, Kocovic Dusan Z, Packer Milton, Clavell Alfredo L, Hayes David L, Ellestad Myrvin, Trupp Robin J, Underwood Jackie, Pickering Faith, Truex Cindy, McAtee Peggy, Messenger John. Cardiac resynchronization in chronic heart failure. N. Engl. J. Med. 2002 Jun 13;346 (24):1845–53. doi: 10.1056/NEJMoa013168. [DOI] [PubMed] [Google Scholar]
- 8.Young James B, Abraham William T, Smith Andrew L, Leon Angel R, Lieberman Randy, Wilkoff Bruce, Canby Robert C, Schroeder John S, Liem L Bing, Hall Shelley, Wheelan Kevin. Combined cardiac resynchronization and implantable cardioversion defibrillation in advanced chronic heart failure: the MIRACLE ICD Trial. JAMA. 2003 May 28;289 (20):2685–94. doi: 10.1001/jama.289.20.2685. [DOI] [PubMed] [Google Scholar]
- 9.Bristow Michael R, Saxon Leslie A, Boehmer John, Krueger Steven, Kass David A, De Marco Teresa, Carson Peter, DiCarlo Lorenzo, DeMets David, White Bill G, DeVries Dale W, Feldman Arthur M. Cardiac-resynchronization therapy with or without an implantable defibrillator in advanced chronic heart failure. N. Engl. J. Med. 2004 May 20;350 (21):2140–50. doi: 10.1056/NEJMoa032423. [DOI] [PubMed] [Google Scholar]
- 10.Cleland John G F, Daubert Jean-Claude, Erdmann Erland, Freemantle Nick, Gras Daniel, Kappenberger Lukas, Tavazzi Luigi. The effect of cardiac resynchronization on morbidity and mortality in heart failure. N. Engl. J. Med. 2005 Apr 14;352 (15):1539–49. doi: 10.1056/NEJMoa050496. [DOI] [PubMed] [Google Scholar]
- 11.Moss Arthur J, Hall W Jackson, Cannom David S, Klein Helmut, Brown Mary W, Daubert James P, Estes N A Mark, Foster Elyse, Greenberg Henry, Higgins Steven L, Pfeffer Marc A, Solomon Scott D, Wilber David, Zareba Wojciech. Cardiac-resynchronization therapy for the prevention of heart-failure events. N. Engl. J. Med. 2009 Oct 1;361 (14):1329–38. doi: 10.1056/NEJMoa0906431. [DOI] [PubMed] [Google Scholar]
- 12.Linde Cecilia, Abraham William T, Gold Michael R, St John Sutton Martin, Ghio Stefano, Daubert Claude. Randomized trial of cardiac resynchronization in mildly symptomatic heart failure patients and in asymptomatic patients with left ventricular dysfunction and previous heart failure symptoms. J. Am. Coll. Cardiol. 2008 Dec 2;52 (23):1834–43. doi: 10.1016/j.jacc.2008.08.027. [DOI] [PubMed] [Google Scholar]
- 13.Zacà Valerio, Mondillo Sergio, Gaddi Rosaria, Favilli Roberto. Profiling cardiac resynchronization therapy patients: responders, non-responders and those who cannot respond--the good, the bad and the ugly? Int J Cardiovasc Imaging. 2011 Jan;27 (1):51–7. doi: 10.1007/s10554-010-9651-y. [DOI] [PubMed] [Google Scholar]
- 14.Adelstein Evan C, Saba Samir. Scar burden by myocardial perfusion imaging predicts echocardiographic response to cardiac resynchronization therapy in ischemic cardiomyopathy. Am. Heart J. 2007 Jan;153 (1):105–12. doi: 10.1016/j.ahj.2006.10.015. [DOI] [PubMed] [Google Scholar]
- 15.Chalil Shajil, Foley Paul W X, Muyhaldeen Sarkaw A, Patel Kiran C R, Yousef Zaheer R, Smith Russell E A, Frenneaux Michael P, Leyva Francisco. Late gadolinium enhancement-cardiovascular magnetic resonance as a predictor of response to cardiac resynchronization therapy in patients with ischaemic cardiomyopathy. Europace. 2007 Nov;9 (11):1031–7. doi: 10.1093/europace/eum133. [DOI] [PubMed] [Google Scholar]
- 16.Varma Niraj. Left ventricular conduction delays and relation to QRS configuration in patients with left ventricular dysfunction. Am. J. Cardiol. 2009 Jun 1;103 (11):1578–85. doi: 10.1016/j.amjcard.2009.01.379. [DOI] [PubMed] [Google Scholar]
- 17.Ploux Sylvain, Lumens Joost, Whinnett Zachary, Montaudon Michel, Strom Maria, Ramanathan Charu, Derval Nicolas, Zemmoura Adlane, Denis Arnaud, De Guillebon Maxime, Shah Ashok, Hocini Mélèze, Jaïs Pierre, Ritter Philippe, Haïssaguerre Michel, Wilkoff Bruce L, Bordachar Pierre. Noninvasive electrocardiographic mapping to improve patient selection for cardiac resynchronization therapy: beyond QRS duration and left bundle branch block morphology. J. Am. Coll. Cardiol. 2013 Jun 18;61 (24):2435–43. doi: 10.1016/j.jacc.2013.01.093. [DOI] [PubMed] [Google Scholar]
- 18.Rouleau F, Merheb M, Geffroy S, Berthelot J, Chaleil D, Dupuis J M, Victor J, Geslin P. Echocardiographic assessment of the interventricular delay of activation and correlation to the QRS width in dilated cardiomyopathy. Pacing Clin Electrophysiol. 2001 Oct;24 (10):1500–6. doi: 10.1046/j.1460-9592.2001.01500.x. [DOI] [PubMed] [Google Scholar]
- 19.Chung Eugene S, Leon Angel R, Tavazzi Luigi, Sun Jing-Ping, Nihoyannopoulos Petros, Merlino John, Abraham William T, Ghio Stefano, Leclercq Christophe, Bax Jeroen J, Yu Cheuk-Man, Gorcsan John, St John Sutton Martin, De Sutter Johan, Murillo Jaime. Results of the Predictors of Response to CRT (PROSPECT) trial. Circulation. 2008 May 20;117 (20):2608–16. doi: 10.1161/CIRCULATIONAHA.107.743120. [DOI] [PubMed] [Google Scholar]
- 20.Ruschitzka Frank, Abraham William T, Singh Jagmeet P, Bax Jeroen J, Borer Jeffrey S, Brugada Josep, Dickstein Kenneth, Ford Ian, Gorcsan John, Gras Daniel, Krum Henry, Sogaard Peter, Holzmeister Johannes. Cardiac-resynchronization therapy in heart failure with a narrow QRS complex. N. Engl. J. Med. 2013 Oct 10;369 (15):1395–405. doi: 10.1056/NEJMoa1306687. [DOI] [PubMed] [Google Scholar]
- 21.Priori Silvia G, Blomström-Lundqvist Carina, Mazzanti Andrea, Blom Nico, Borggrefe Martin, Camm John, Elliott Perry Mark, Fitzsimons Donna, Hatala Robert, Hindricks Gerhard, Kirchhof Paulus, Kjeldsen Keld, Kuck Karl-Heinz, Hernandez-Madrid Antonio, Nikolaou Nikolaos, Norekvål Tone M, Spaulding Christian, Van Veldhuisen Dirk J. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC). Eur. Heart J. 2015 Nov 1;36 (41):2793–867. doi: 10.1093/eurheartj/ehv316. [DOI] [PubMed] [Google Scholar]
- 22.Daubert J C, Ritter P, Le Breton H, Gras D, Leclercq C, Lazarus A, Mugica J, Mabo P, Cazeau S. Permanent left ventricular pacing with transvenous leads inserted into the coronary veins. Pacing Clin Electrophysiol. 1998 Jan;21 (1 Pt 2):239–45. doi: 10.1111/j.1540-8159.1998.tb01096.x. [DOI] [PubMed] [Google Scholar]
- 23.Kronborg Mads Brix, Albertsen Andi Eie, Nielsen Jens Cosedis, Mortensen Peter Thomas. Long-term clinical outcome and left ventricular lead position in cardiac resynchronization therapy. Europace. 2009 Sep;11 (9):1177–82. doi: 10.1093/europace/eup202. [DOI] [PubMed] [Google Scholar]
- 24.Singh Jagmeet P, Klein Helmut U, Huang David T, Reek Sven, Kuniss Malte, Quesada Aurelio, Barsheshet Alon, Cannom David, Goldenberg Ilan, McNitt Scott, Daubert James P, Zareba Wojciech, Moss Arthur J. Left ventricular lead position and clinical outcome in the multicenter automatic defibrillator implantation trial-cardiac resynchronization therapy (MADIT-CRT) trial. Circulation. 2011 Mar 22;123 (11):1159–66. doi: 10.1161/CIRCULATIONAHA.110.000646. [DOI] [PubMed] [Google Scholar]
- 25.Rossillo Antonio, Verma Atul, Saad Eduardo B, Corrado Andrea, Gasparini Gianni, Marrouche Nassir F, Golshayan Ali Reza, McCurdy Richard, Bhargava Mandeep, Khaykin Yaariv, Burkhardt J David, Martin David O, Wilkoff Bruce L, Saliba Walid I, Schweikert Robert A, Raviele Antonio, Natale Andrea. Impact of coronary sinus lead position on biventricular pacing: mortality and echocardiographic evaluation during long-term follow-up. J. Cardiovasc. Electrophysiol. 2004 Oct;15 (10):1120–5. doi: 10.1046/j.1540-8167.2004.04089.x. [DOI] [PubMed] [Google Scholar]
- 26.Daubert Claude, Gold Michael R, Abraham William T, Ghio Stefano, Hassager Christian, Goode Grahame, Szili-Török Tamás, Linde Cecilia. Prevention of disease progression by cardiac resynchronization therapy in patients with asymptomatic or mildly symptomatic left ventricular dysfunction: insights from the European cohort of the REVERSE (Resynchronization Reverses Remodeling in Systolic Left Ventricular Dysfunction) trial. J. Am. Coll. Cardiol. 2009 Nov 10;54 (20):1837–46. doi: 10.1016/j.jacc.2009.08.011. [DOI] [PubMed] [Google Scholar]
- 27.Duckett Simon G, Ginks Matthew, Shetty Anoop K, Bostock Julian, Gill Jaswinder S, Hamid Shoaib, Kapetanakis Stam, Cunliffe Eliane, Razavi Reza, Carr-White Gerry, Rinaldi C Aldo. Invasive acute hemodynamic response to guide left ventricular lead implantation predicts chronic remodeling in patients undergoing cardiac resynchronization therapy. J. Am. Coll. Cardiol. 2011 Sep 6;58 (11):1128–36. doi: 10.1016/j.jacc.2011.04.042. [DOI] [PubMed] [Google Scholar]
- 28.Spragg David D, Dong Jun, Fetics Barry J, Helm Robert, Marine Joseph E, Cheng Alan, Henrikson Charles A, Kass David A, Berger Ronald D. Optimal left ventricular endocardial pacing sites for cardiac resynchronization therapy in patients with ischemic cardiomyopathy. J. Am. Coll. Cardiol. 2010 Aug 31;56 (10):774–81. doi: 10.1016/j.jacc.2010.06.014. [DOI] [PubMed] [Google Scholar]
- 29.Ypenburg Claudia, van Bommel Rutger J, Delgado Victoria, Mollema Sjoerd A, Bleeker Gabe B, Boersma Eric, Schalij Martin J, Bax Jeroen J. Optimal left ventricular lead position predicts reverse remodeling and survival after cardiac resynchronization therapy. J. Am. Coll. Cardiol. 2008 Oct 21;52 (17):1402–9. doi: 10.1016/j.jacc.2008.06.046. [DOI] [PubMed] [Google Scholar]
- 30.Khan Fakhar Z, Virdee Mumohan S, Palmer Christopher R, Pugh Peter J, O'Halloran Denis, Elsik Maros, Read Philip A, Begley David, Fynn Simon P, Dutka David P. Targeted left ventricular lead placement to guide cardiac resynchronization therapy: the TARGET study: a randomized, controlled trial. J. Am. Coll. Cardiol. 2012 Apr 24;59 (17):1509–18. doi: 10.1016/j.jacc.2011.12.030. [DOI] [PubMed] [Google Scholar]
- 31.Wong Jorge A, Yee Raymond, Stirrat John, Scholl David, Krahn Andrew D, Gula Lorne J, Skanes Allan C, Leong-Sit Peter, Klein George J, McCarty David, Fine Nowell, Goela Aashish, Islam Ali, Thompson Terry, Drangova Maria, White James A. Influence of pacing site characteristics on response to cardiac resynchronization therapy. Circ Cardiovasc Imaging. 2013 Jul;6 (4):542–50. doi: 10.1161/CIRCIMAGING.111.000146. [DOI] [PubMed] [Google Scholar]
- 32.Chalil S, Stegemann B, Muhyaldeen S A, Khadjooi K, Foley P W, Smith R E A, Leyva F. Effect of posterolateral left ventricular scar on mortality and morbidity following cardiac resynchronization therapy. Pacing Clin Electrophysiol. 2007 Oct;30 (10):1201–9. doi: 10.1111/j.1540-8159.2007.00841.x. [DOI] [PubMed] [Google Scholar]
- 33.Adelstein Evan, Alam Mian Bilal, Schwartzman David, Jain Sandeep, Marek Josef, Gorcsan John, Saba Samir. Effect of echocardiography-guided left ventricular lead placement for cardiac resynchronization therapy on mortality and risk of defibrillator therapy for ventricular arrhythmias in heart failure patients (from the Speckle Tracking Assisted Resynchronization Therapy for Electrode Region [STARTER] trial). Am. J. Cardiol. 2014 May 1;113 (9):1518–22. doi: 10.1016/j.amjcard.2014.01.431. [DOI] [PubMed] [Google Scholar]
- 34.Singh Jagmeet P, Fan Dali, Heist E Kevin, Alabiad Chrisfouad R, Taub Cynthia, Reddy Vivek, Mansour Moussa, Picard Michael H, Ruskin Jeremy N, Mela Theofanie. Left ventricular lead electrical delay predicts response to cardiac resynchronization therapy. Heart Rhythm. 2006 Nov;3 (11):1285–92. doi: 10.1016/j.hrthm.2006.07.034. [DOI] [PubMed] [Google Scholar]
- 35.Gold Michael R, Birgersdotter-Green Ulrika, Singh Jagmeet P, Ellenbogen Kenneth A, Yu Yinghong, Meyer Timothy E, Seth Milan, Tchou Patrick J. The relationship between ventricular electrical delay and left ventricular remodelling with cardiac resynchronization therapy. Eur. Heart J. 2011 Oct;32 (20):2516–24. doi: 10.1093/eurheartj/ehr329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Del Greco Maurizio, Marini Massimiliano, Bonmassari Roberto. Implantation of a biventricular implantable cardioverter-defibrillator guided by an electroanatomic mapping system. Europace. 2012 Jan;14 (1):107–11. doi: 10.1093/europace/eur250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Jiang L, Weissman N J, Guerrero J L, He J, Weyman A E, Levine R A, Picard M H. Percutaneous transvenous intracardiac ultrasound imaging in dogs: a new approach to monitor left ventricular function. Heart. 1996 Nov;76 (5):442–8. doi: 10.1136/hrt.76.5.442. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Saksena Sanjeev, Simon Ann Marie, Mathew Philip, Nagarakanti Rangadham. Intracardiac echocardiography-guided cardiac resynchronization therapy: technique and clinical application. Pacing Clin Electrophysiol. 2009 Aug;32 (8):1030–9. doi: 10.1111/j.1540-8159.2009.02435.x. [DOI] [PubMed] [Google Scholar]
- 39.Bai Rong, Di Biase Luigi, Mohanty Prasant, Hesselson Aaron B, De Ruvo Ermenegildo, Gallagher Peter L, Elayi Claude S, Mohanty Sanghamitra, Sanchez Javier E, Burkhardt J David, Horton Rodney, Gallinghouse G Joseph, Bailey Shane M, Zagrodzky Jason D, Canby Robert, Minati Monia, Price Larry D, Hutchins C Lynn, Muir Melody A, Calo' Leonardo, Natale Andrea, Tomassoni Gery F. Positioning of left ventricular pacing lead guided by intracardiac echocardiography with vector velocity imaging during cardiac resynchronization therapy procedure. J. Cardiovasc. Electrophysiol. 2011 Sep;22 (9):1034–41. doi: 10.1111/j.1540-8167.2011.02052.x. [DOI] [PubMed] [Google Scholar]
