Indian Pacing Electrophysiol. J.


   ISSN  0972-6292

Home Page Current Issue List of Editors

Indian Pacing Electrophysiol. J. 2003;3(3):129-142

Review Article


Download PDF 215 KB  

Cardiac Resynchronization Therapy In Heart Failure: Recent Advances And New Insights

Bhatia V, MD*, Bhatia R, MD, Dhindsa S, MD, Virk A, MD, MPH

*Department of Medicine, Mercy Hospital of Buffalo,  Buffalo, NY, 14220,USA.

State University of New York, Buffalo, NY, 14220,USA.

University of Texas, Houston.

Address for correspondence: Dr. Vishal Bhatia, MD, Department of Internal medicine, Mercy Hospital of Buffalo, 565 Abbott road, Buffalo, NY, 14220.
Email: vishalbhatia13@yahoo.com


Abstract

                Newer non-pharmacological therapies for heart failure are being evaluated for patients of congestive heart failure (CHF). Mechanical support with left ventricular assist devices and heart transplantation are reserved for the minority of patients who have severely decompensated heart failure. Despite these therapeutic advances, it is generally accepted that current therapies do not adequately address the clinical need of patients with heart failure, and additional strategies are being developed. Cardiac resynchronization therapy (CRT) is a new modality that involves synchronization of ventricular contraction and has shown a lot of promise in managing symptomatic patients of CHF who are on optimal medical therapy and have interventricular conduction delay (IVCD). It has improved exercise tolerance and NYHA functional class in such patients in sinus rhythm and a recent meta-analysis has also shown mortality benefits in CHF. Recently benefits of CRT have also been observed in CHF patients who do not have wide QRS complexes on electrocardiogram (EKG). It has also been shown to benefit drug refractory angina in CHF. Recent studies have also focused on the combined use of CRT and implantable cardioverter defibrillator (ICD) and it has shown encouraging results. Our aim in this descriptive review is to define practice guidelines and to improve clinicians' knowledge of the available published clinical evidence, concentrating on few randomized controlled trials.        

Introduction

            Approximately 30 percent of patients with cardiomyopathy have IVCD such as left or right bundle-branch block, leading to loss of coordination of ventricular contraction1,2. This dyssynchronous pattern of ventricular contraction is believed to contribute to the pathophysiology of heart failure, reducing the already diminished contractile reserve of the heart3. Specifically, dyssynchronous contraction exacerbates inefficient use of energy by the heart (a process termed mechanoenergetic-uncoupling4). The finding of IVCD has been associated with clinical instability and an increased risk of death in patients with heart failure5,6,7,8.
           
Accordingly, the idea that cardiac-pacing technology might be used to restore the synchrony of ventricular contraction has been of theoretical interest for over a decade. Pacing modalities that utilize biventricular (BiV) or left ventricular (LV) stimulation to optimize cardiac pump function through synchronization of ventricular contraction are referred to as resynchronization or ventricular resynchronization therapies2. Resynchronization therapies can be present in a single device, in a device equipped with bradycardia pacing support, or incorporated into an ICD9.

CHF and IVCD

            The most common causes for an IVCD in patients with heart failure are delayed left ventricular activation and left bundle branch block (LBBB). Impaired left ventricular function is also seen in otherwise normal subjects with isolated LBBB10. Approximately 20 to 30 percent of patients with symptomatic heart failure have an IVCD.2 In a study done by Farewell et al11 patients with a hospital diagnosis of "heart failure" were investigated. These patients did not undergo cardiac catherterization. The criteria for inclusion were severe heart failure (NYHA Class III or IV), heart failure due to dilated cardiomyopathy, QRS duration > 120 ms, or the presence of LBBB or RBBB. Using these criteria, approximately 10 percent of an unselected group of heart failure patients who are admitted to a typical district general hospital in United Kingdom during a calendar year would be candidates for biventricular pacing. A recent study done by Erdogan et al12 estimated that biventricular pacing might be considered as an adjunct to standard heart failure therapy in 5-10 patients per year per 100,000 residents in industrial countries.
In Europe Resynchronization therapy is approved for symptomatic heart failure that occurs in the setting of IVCD or BBB. This approval was granted on the basis of several studies of acute resynchronization therapy and data compiled in approximately 150 patients receiving BiV or LV stimulation for three months as part of two controlled studies (InSync 13,14 and PATH-CHF15). In the United States, resynchronization therapy with or without an ICD is approved for patients with NYHA class III-IV heart failure on the basis of the chronic studies described below, which were all performed with a control group randomly assigned to no resynchronization therapy16,17,18,19,20,21,22.
            There is another setting in which resynchronization might be important. It is estimated that approximately 8 to 15 percent of patients with advanced heart failure have pacemakers implanted for symptomatic bradycardia. Such patients have an increased risk of mortality or urgent transplantation due to progressive pump dysfunction; in one series, the risk at one year was 49 versus 15 percent in patients without a pacemaker).23 This difference may be due in part to the dyssynchronous contraction caused by right ventricular (RV) based pacing.
            Whether such patients would derive long-term benefit from "upgrading" these devices to resynchronization therapies by the addition of a LV lead is currently under investigation. Initial data in patients with severe heart failure, prior atrio-ventricular (AV) junction ablation for rate control of AF, and chronic RV pacing has shown that there are significant benefits by upgrading from RV to BiV pacing.24

Effect on Contractile Function

            Hemodynamic data acquired in patients with heart failure and bundle branch block (BBB) during acute or chronic BiV or LV stimulation have consistently shown improvements in measures of contractile response, such as force of contraction, cardiac output, left ventricular ejection fraction (LVEF), and pulmonary artery pressure, when compared to normal sinus rhythm or RV pacing25,26,27,28,29,30,31,32. CRT has been shown to decrease the functional mitral regurgitation in advanced systolic heart failure33,34. In contrast to other therapies that increase myocardial contractility, BiV and LV stimulation appear to modestly reduce myocardial energy demands and myocardial oxygen consumption3. The magnitude of acute systolic improvement by CRT is mainly due to resynchronization rather than due to change in myocyte function. An increased mechanical efficiency without increase in oxygen demand can be effective in drug refractory angina in CHF. A study done by Gasparini et al35 showed the beneficial effects of CRT, during a mean follow-up of 9 months, in increasing the angina threshold in severely symptomatic patients with CHF and coronary artery disease (CAD) not amenable to cardiac revascularization. This study suggested that CRT increases the ischemic threshold in CHF patients on the long term, by markedly reducing the incidence of drug refractory anginal episodes, and by increasing a previously profoundly reduced exercise capacity. In another series of 18 patients with dilated cardiomyopathy (DCM) and an IVCD, aortic and LV pressures, dp/dt, and pressure-volume measurements were obtained during stimulation at single RV endocardial sites, at single LV epicardial sites, or during BiV pacing36. There was an improvement in systolic pressures with LV free wall or BiV stimulation, primarily due to an improvement in systolic function; there was no benefit on diastolic filling pressure or relaxation and RV apical or septal stimulation did not produce any hemodynamic changes. The markers of sympathetic activation, such as serum norepinephrine and heart rate variability, often vary directly with the severity of heart failure, these markers have not predictably changed in patients in whom resynchronization therapy appears to improve contractile function37,38,39,40. The improvement in mechanical synchrony appears to be the mechanism for reverse remodeling41.


Reverse Remodeling

            Based upon echocardiography, preliminary data from the MIRACLE trial16 suggested that BiV pacing is associated with reverse remodeling in patients with heart failure. BiV pacing produced an improvement in cardiac structure and function with a significant reduction in mitral regurgitation jet area and left ventricular mass, both signs of reverse remodeling42. Reverse remodeling was also observed in the CONTAK CD, PATH-CHF, and VIGOR CHF trials, in which BiV produced a significant reduction in left ventricular end-systolic and end-diastolic dimensions on echocardiography38,43. In the PATH-CHF trial, baseline left ventricular end-diastolic volumes were significantly smaller in those who exhibited reverse remodeling with BiV pacing compared to those who did not have a reduction in left ventricular volume43.


Clinical Trials

            There are a number of trials evaluating the role of resynchronization therapy in patients with heart failure due to systolic dysfunction. The usual inclusion criteria include symptomatic heart failure that is stable on medical therapy, New York Heart Association (NYHA) class II to IV, left ventricular ejection fraction (LVEF) <35 percent, QRS duration >120 to 140 ms, and, in some trials, an indication for an ICD.


MIRACLE Trial

            In this trial16 453 patients with moderate-to-severe symptoms of heart failure associated with an LVEF of 35 percent or less and a QRS interval of 130 ms or more were studied. They were randomly assigned to a cardiac-resynchronization group (228 patients) or to a control group (225 patients) for six months, while conventional therapy for heart failure was maintained. The primary end points were the NYHA functional class, quality of life, and the distance walked in six-minutes. As compared with the control group, patients assigned to cardiac resynchronization experienced an improvement in the distance walked in six-minutes (+39 vs. +10 m, P=0.005), functional class (P<0.001), quality of life (–18.0 vs. –9.0 points, P= 0.001), time on the treadmill during exercise testing (+81 vs. +19 sec, P=0.001), and ejection fraction (+4.6 percent vs. –0.2 percent, P<0.001). In addition, fewer patients in the group assigned to cardiac resynchronization than control patients required hospitalization (8 percent vs. 15 percent) or intravenous medications (7 percent vs. 15 percent) for the treatment of heart failure (P<0.05 for both comparisons). Implantation of the device was unsuccessful in 8 percent of patients and was complicated by refractory hypotension, bradycardia, or asystole in four patients (two of whom died) and by perforation of the coronary sinus requiring pericardiocentesis in two others.


MUSTIC Trial

            The MUSTIC (Multisite Stimulation in Cardiomyopathies) trial is a single-blind randomized, controlled crossover study involving 131 patients who were divided into two groups based upon their underlying rhythm17,18,19. Group one included 67 patients with NYHA class III heart failure, QRS duration >150 ms with stable sinus rhythm and no conventional indications for pacemaker therapy17. The patients were randomly assigned to BiV pacing or no BiV pacing for three months, after which the pacing modes were switched; a total of 48 patients completed both phases of the study (MUSTIC SR). Exercise tolerance, as measured by the six-minute walk distance, increased by 23 percent after BiV pacing (399 versus 326 m, p<0.001). Other significant improvements included a 32 percent increase in quality of life, an 8 percent increase in peak oxygen consumption, and a two-thirds reduction in hospitalizations. Furthermore, BiV pacing was preferred by 85 percent of patients. At the end of the six-month crossover phase, the patients were programmed to the phase they preferred or, if there was no preference, according to the physician's judgment; almost all patients ended up with BiV pacing. The benefits with BiV pacing compared to baseline were maintained at 12 months19. Group two included 59 patients with heart failure and chronic atrial fibrillation (AF) with a wide QRS complex that required a permanent pacemaker because of a slow ventricular rate (MUSTIC AF). These patients were randomly assigned to either single site RV pacing or BiV pacing in the same fashion as in group one18,19. Only 37 patients completed the six-month crossover trial, which limits any conclusions that can be drawn18. Using an intention-to-treat analysis, there were no significant differences in exercise tolerance or peak oxygen consumption. In contrast, when only the 37 patients who completed the study were evaluated, biventricular pacing was associated with a significant increase in six-minute walking distance (9.3 percent, 32 meters) and peak oxygen consumption (13 percent, 1.7 mL/kg per min). At the end of the six-month crossover phase, 33 of 37 patients (89 percent) preferred BiV pacing. Among 33 patients followed at one year, significant improvements persisted in both six-minute walking distance and peak oxygen consumption.

CRT and Implantable Cardioverter Defibrillator (ICD) Therapy

            Recently there has been some trials evaluating the combined use of CRT and ICD in patients of heart failure.

I.     InSync trial44 demonstrated the efficacy and safety of implanting a combined device in 362 patients with class III and IV heart failure who also required an ICD. Patients were randomly assigned to have BiV pacing turned on or off; the ICD was active in all patients. InSync ICD Italian Registry45 studied InSync ICD model 7272, a dual chamber ICD combined with CRT. In this registry, CRT combined with ICD implantation has been feasible with few device or left pacing lead related complications and this was found to be concordant with previous reports9. The clinical benefits match those obtained in recipients of biventricular pacemakers, both in LVEF and NYHA functional class16.

II.     VENTAK CHF/CONTAK CD22 enrolled 581 patients with heart failure, most of whom had an ischemic cardiomyopathy, who also had an indication for an ICD. The majority of patients were male, had NYHA class II to IV heart failure, and a QRS duration >120 ms. The study utilized an ICD system designed to provide BiV pacing. All patients had an ICD and either BiV pacing or no pacing, each for six months.

III.     The COMPANION trial46 is a study of resynchronization therapy with and without an ICD in patients with NYHA class III-IV heart failure who had a hospitalization for heart failure within the year prior to enrollment. Nearly half of all patients enrolled had a non-ischemic etiology of heart failure. Patients were randomly assigned to optimal medical therapy, resynchronization alone, or resynchronization with an ICD. The trial was discontinued in November 2002 due to a significant benefit in the combined end point of total hospitalizations and mortality among the device treated patients.


Effects Of CRT and ICD Therapy on Arrhythmic Burden

            Preliminary reports suggest that BiV pacing has an anti-arrhythmic effect43,47. The anti-arrhythmic effect has been attributed to improved hemodynamics. A low mean number of ventricular arrhythmic episodes were observed in the whole population and in the patients without Class I indications in InSync Italian registry45. It was found that the patients without standard ICD indications sustained serious arrhythmic events, confirming their high risk of death.


Pacing Sites

            Short-term studies have suggested that the lateral wall is a preferred site of LV stimulation to achieve effective CRT3,25. However, this choice may be limited by technical difficulties like high capture threshold from the presence of scar or fibrosis, particularly in patients with CAD, determining high LV pacing threshold, unfavorable coronary venous anatomy with narrow and tortuous coronary sinus tributary (CST), phrenic nerve stimulation or pacing lead instability. Gasparini et al48 conducted a study to evaluate the effects of different pacing sites in patients treated with CRT. The data from this study revealed that, during long term follow-up, the most important clinical and echocardiographic parameters improved significantly in the patients, independently of the stimulation site. This was the case when considering each CST separately, or when dividing patients between “lateral” and “septal” sites, in the entire population and in the subgroups of patients without CAD. Hence in the presence of major technical difficulties preventing stimulation of the lateral LV, alternative-pacing sites, particularly the basal anterior LV wall, may be suitable to offer effective CRT to these patients. Tissue Doppler echocardiography has also been used to determine the optimal pacing site for BiV pacing47 and to document an improvement in LV function, manifest by an increase in LV and interventricular synchrony, a shortened isovolumic contraction time, and an increased diastolic filling time41,50.


QRS Duration And Dyssynchrony

            Wide QRS duration, possibly with LBBB, has been proposed as an independent predictor of total mortality in CHF patients51,52,53. In addition it has been considered a key criteria for selecting CHF patients for CRT, as wide QRS has been suggested to be associated with marked RV to LV and intra-LV dyssynchrony10,25,54. However, the correlation between the QRS width and regional electromechanical LV dyssynchrony has not been completely clarified47,55,56 and a high prevalence of left ventricular systolic and diastolic asynchrony has been found in patients with congestive heart failure and normal QRS duration57. Hence for a given QRS width there is a considerable scatter in response to CRT responsive patients with narrow complexes and less responsive ones with wide complexes exist 32. A study was done by Gasparini et al58 to assess in a large cohort of patients the role of baseline QRS width (<150 / >150 ms) on clinical and echocardiographic parameters, hospitalization rates, and survival after CRT. In this study 158 CHF patients (121 men, mean age 65 years, mean LVEF 0.29, mean QRS width 174 ms) underwent successful BiV implantation and were then followed for a mean time of 11.2 months. According to the basal QRS duration, patients were divided in two groups with wide QRS group (>150 ms, 128 patients, 81 percent) and the narrow QRS (<10 ms, 30 patients, 19 percent).

In the wide QRS group, following results were noted:
1. LVEF improved from 20 percent to 39 percent (P < 0.0001)
2. Six–minute walk test from 311 to 463 m (P<0.0001)
3. NYHA Class III-IV patients decreased from 86 percent to 8 percent (P<0.0001).

In the narrow QRS group, following were the results:
1. LVEF improved from 30 percent to 38 percent (P<0.0001).
2. Six-minute walk test 370 to 506 m (P<0.0001).
4. NYHA Class III-IV patients decreased from 60 percent to zero percent (P<0.0001).

            The data showed that in wide and narrow QRS patients, BiV pacing significantly improved clinical parameters (NYHA lass, six-minute walk test, quality of life, and hospitalization rate) and main echocardiographic indicators. Furthermore, narrow QRS patients had a better survival rate, rapidly regained left ventricular function, and only a few patients remained in a higher NYHA class during follow-up. These patients should not be excluded "a priori" from CRT.
            This study highlights the important point at what level a QRS has to be considered "wide enough" to be proposed to benefit from CRT. For example this was >150 ms for the MUSTIC study17, >130 ms in the MIRACLE study16, and >120 ms in Comparison of medical therapy, pacing, and defibrillation in chronic heart failure (COMPANION) trial46. It is evident from these differences in opinion that there is still no consensus on just how "wide" QRS should be for an efficacious CRT. Moreover the duration of QRS alone no longer seems to be defining parameter for patients with either inter-or-intraventricular dyssynchrony, given that recent studies have shown that even patients with a QRS<150 ms or without LBBB can suffer from significant dyssynchrony53,54.


Are There Any New Markers of Asynchrony?

           
The results of the recent investigations have prompted a reappraisal of the apparent correlation between conduction disorders and cardiac dyssynchronization. In a tissue Doppler study of 104 patients with BBB, Garrigue et al56 observed that 35 percent of patients with LBBB had no interventricular dyssynchronization, and 20 percent had no left ventricular dyssynchronization. Despite fulfilling the "classic" criteria of wide QRS and LBBB, these patients are hardly candidates for CRT. Conversely, a sizable number of patients with right bundle branch block (RBBB) may present with mechanical anomalies, which may be corrected by CRT. Therefore, new markers of asynchrony are desirable, more directly related to cardiac mechanical function than the EKG. Among several methods available, angioscintigraphy with phase analysis of the contraction isochrones was the first, though its cumbersome implementation, high cost, and limited availability in routine clinical practice have prevented its widespread application59,60.
            A recent study done by Cazeau S et al61 explored the value of an echocardiographic model to identify cardiac electromechanical dyssynchrony parameters (EDP) in candidates for CRT and their potential correction after implantation. The study included 66 CRT recipients of CRT NYHA functional class III or IV who had one or more AV, interventricular or intra-ventricular dyssynchrony criteria. An immediate improvement was observed in 85 percent of the population with partial or total correction of their EDP. However the modification in EDP differed considerably between recipients of de novo CRT systems and patients with previously implanted standard pacing systems upgraded with the implantation of a left ventricular lead. EDP measurements appear to identify candidates for CRT and to confirm the success of system implantation. This is the first report of a selection of candidates for CRT based on mechanical instead of electrical criteria. An overlap certainly exists between patients presenting with a wide QRS and patients with disorders of cardiac synchronization. However the echocardiographic method, which distinguishes three different types of synchronization offers a finer analysis of the anomalies amenable to resynchronization.

Etiology of CHF and CRT

            The mechanisms of CHF in patients with DCM are complex and multiple. A study done by Gasparini et al61 examined the importance of underlying cardiac pathology on the outcome of CRT, hypothesizing that myocardial infarction scar and the non-contractile segment represent limitations to the ability to resynchronize cardiac contraction in patients with CHF associated with DCM. The results of this study showed that the functional capacity improved significantly during CRT in CAD and non-CAD patients. LVEF and NYHA class in non-CAD patience showed a significantly greater improvement. However, changes in quality-of-life were similar in both groups. The mechanisms of slow myocardial conduction associated with asynergic contraction in patients with DCM vary with the underlying pathology5,62,63. In patients with DCM not due to CAD, ventricular asynergy may be associated with interventricular or intra-ventricular conduction delays. Interventricular asynergy is most often associated with LBBB. A progressive remodeling of myocardial collagen matrix well documented in familial cardiomyopathies may impair intraventricular conduction. Disruption of collagen network, by altering the cellular architecture, impairs intraventricular conduction and the coordinated mechanical response of the ventricles. The consequences are QRS prolongation and waste of mechanical work. In patients with CAD, beside ventricular remodeling, ventricular asynergy may be associated with segmental wall- motion abnormalities as result of myocardial infarction scars, or of ischemic non-contractile segments. Segmental wall motion abnormalities affect intraventricular conduction and the coordinated mechanical response of the ventricles. CRT may correct conduction delay in remodeled dilated myocardial segments, but has no effect on extensive myocardial scars or ischemic segments. CRT can only recruit and coordinate a fraction of the myocardial mass to increase ventricular mechanical work in patients with CAD. Although significant benefits were observed in both groups after CRT, myocardial infarction scars limit the mechanical benefits of QRS narrowing and resynchronization. Hence the benefits of CRT should not be denied to patients with severe CHF on the basis of underlying cardiac pathology including patients with severe LV dysfunction associated with CAD and wide QRS64.

Pacing in AF

            Paroxysmal or persistent AF occurs in up to 30 percent of patients with HF65. Rate control can be achieved with pharmacological therapy. In patients refractory to such therapies these objectives can be achieved with radiofrequency ablation of the AV node and pacemaker therapy with traditional RV-based pacemakers. Initial data regarding "upgrading" from RV to BiV pacing using an LV lead to achieve cardiac resynchronization in heart failure patients with chronic AF who have undergone radiofrequency AV nodal ablation followed by standard RV pacing is promising.24


Recommendations

            BiV pacing is an effective approach to the therapy of patients with heart failure and IVCD and studies suggest that BiV pacing can improve exercise tolerance and NYHA functional class in such patients in sinus rhythm. A meta-analysis was done by Bradley et al66 of the available studies to determine the effect of CRT on mortality in CHF. 11 reports of 4 randomized trials with 1634 total patients were included in this meta-analysis. It was found that cardiac resynchronization reduces mortality from progressive heart failure in patients with symptomatic left ventricular dysfunction. This finding suggests that cardiac resynchronization may have a substantial impact on the most common mechanism of death among patients with advanced heart failure. Cardiac resynchronization also reduces heart failure hospitalization and shows a trend toward reducing all-cause mortality.
            More data on effect of CRT on mortality in CHF is still awaited. Although suggestive, the data are insufficient to prove efficacy in patients in AF18. As a result of the MIRACLE trial, the FDA has approved BiV pacing as a treatment for moderate to severe heart failure. Potential concerns include the small risk of serious complications during implantation as noted in MIRACLE16 and lack of data concerning the long-term effects of cardiac resynchronization as noted by the 2001 Task Force of the ACC/AHA67.
            At present, it seems reasonable to consider BiV pacing in patients with a low LVEF and prolonged QRS duration who remain symptomatic (NYHA class III or IV HF) despite optimal medical therapy68. The 2002 task force of the ACC/AHA/NASPE gave a class IIa recommendation (weight of evidence in favor of efficacy) to BiV pacing in medically refractory, symptomatic NYHA class III or IV patients with idiopathic dilated or ischemic cardiomyopathy, prolonged QRS interval (130 ms), LV end-diastolic diameter greater than or equal to 55 mm and ejection fraction less than or equal to 30 percent.
            It is not known if these devices should routinely incorporate a defibrillator. The MADIT II trial showed a significant survival benefit from ICD placement in patients who have had a previous myocardial infarction and have an LVEF 30 percent69. Combination therapy with an ICD and BiV might therefore be beneficial in such patients who have QRS prolongation.

References

1. Rose EA, Gelijns AC, Moskowitz AJ, Heitjan DF, Stevenson LW, Dembitsky W, Long JW, Ascheim DD, Tierney AR, Levitan RG, Watson JT, Meier P, Ronan NS, Shapiro PA, Lazar RM, Miller LW, Gupta L, Frazier OH, Desvigne-Nickens P, Oz MC, Poirier VL. Long-term mechanical left ventricular assistance for end-stage heart failure. N Engl J Med. 2001;345:1435-43.

2.  Leclercq C, Kass DA. Retiming the failing heart: principles and current clinical status of cardiac resynchronization. J Am Coll Cardiol. 2002;39:194-201.

3. 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;102:3053-9.

4.  Cappola TP, Kass DA, Nelson GS, Berger RD, Rosas GO, Kobeissi ZA, Marban E, Hare JM. Allopurinol improves myocardial efficiency in patients with idiopathic dilated cardiomyopathy. Circulation. 2001;104:2407-11.

5.  Xiao HB, Roy C, Fujimoto S, Gibson DG. Natural history of abnormal conduction and its relation to prognosis in patients with dilated cardiomyopathy. Int J Cardiol. 1996;53:163-70.

6. Unverferth DV, Magorien RD, Moeschberger ML, Baker PB, Fetters JK, Leier CV. Factors influencing the one-year mortality of dilated cardiomyopathy. Am J Cardiol. 1984;54:147-52.

7. Shamim W, Francis DP, Yousufuddin M, Varney S, Pieopli MF, Anker SD, Coats AJ. Intraventricular conduction delay: a prognostic marker in chronic heart failure. Int J Cardiol. 1999;70:171-8

8. Brophy JM, Deslauriers G, Rouleau JL. Long-term prognosis of patients presenting to the emergency room with decompensated congestive heart failure. Can J Cardiol. 1994;10:543-7.

9.  Kuhlkamp V. Initial experience with an implantable cardioverter-defibrillator incorporating cardiac resynchronization therapy. J Am Coll Cardiol. 2002;39:790-7.

10.  Grines CL, Bashore TM, Boudoulas H, Olson S, Shafer P, Wooley CF. Functional abnormalities in isolated left bundle branch block. The effect of interventricular asynchrony. Circulation. 1989;79:845-53.

11.  Farwell D, Patel NR, Hall A, Ralph S, Sulke AN. How many people with heart failure are appropriate for biventricular resynchronization? Eur Heart J. 2000;21:1246-50.

12.  Erdogan A, Rueckleben S, Tillmanns HH, Waldecker B. Proportion of candidates for cardiac resynchronization therapy. Pacing Clin Electrophysiol. 2003;26:152-4.

13.  Gras D, Cazeau S, Mabo P. Long-term benefit of cardiac resynchronization in heart failure patients: the 12 month results of the InSync trial (abstract). J Am Coll Cardiol. 2000;35:230A.

14.  Gras D, Mabo P, Bucknall C. Responders and nonresponders to cardiac resynchronization therapy: Results from the InSync trial (abstract). J Am Coll Cardiol. 2000;35:230A.

15. Auricchio A, Stellbrink C, Sack S. Chronic benefit as a result of pacing in congestive heart failure: Results of the PATH CHF trial (abstract). J Card Fail. 1999;5 (3 Suppl 1):78.

16.  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. Cardiac resynchronization in chronic heart failure. N Engl J Med. 2002;346:1845-53.

17.  Cazeau S, Leclercq C, Lavergne T, Walker S, Varma C, Linde C, Garrigue S, Kappenberger L, Haywood GA, Santini M, Bailleul C, Daubert JC. Effects of multisite biventricular pacing in patients with heart failure and intraventricular conduction delay. N Engl J Med. 2001;344:873-80.

18. 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;23:1780-7.

19. 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;40:111-8.

20. Williams ES, JM. M. Results from late-breaking clinical trial sessions at the American College of Cardiology 51st Annual Scientific Session. J Am Coll Cardiol. 2002;40. (abstract)

21. Daoud E, Hummel J, Higgins S, et al. Does ventricular resynchronization therapy influence total survival? North American Society of Pacing and Electrophysiology 22nd Annual Scientific Sessions; May 2-5, 2001; Boston, Massachusetts. Abstract Session 1, Number 4.

22.  Leclercq C, Alonso C, Revault D'allonnes F, Pavin D, Mabo P. Is the long-term benefit of biventricular
pacing in patients with advanced heart failure influenced by the baseline QRS duration? North American Society of Pacing and Electrophysiology 22nd Annual Scientific Sessions; May 2-5, 2001; Boston, Massachusetts. Abstract Session 1, Number 6.

23. Saxon LA, Stevenson WG, Middlekauff HR, Stevenson LW. Increased risk of progressive hemodynamic deterioration in advanced heart failure patients requiring permanent pacemakers. Am Heart J. 1993;125:1306-10.

24. 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;39:1258-63.

25. Auricchio A, Stellbrink C, Block M, Sack S, Vogt J, Bakker P, Klein H, Kramer A, Ding J, Salo R, Tockman B, Pochet T, Spinelli J. Effect of pacing chamber and atrioventricular delay on acute systolic function of paced patients with congestive heart failure. The Pacing Therapies for Congestive Heart Failure Study Group. The Guidant Congestive Heart Failure Research Group. Circulation. 1999;99:2993-3001.

26. Saxon LA, Kerwin WF, Cahalan MK, Kalman JM, Olgin JE, Foster E, Schiller NB, Shinbane JS, Lesh MD, Merrick SH. Acute effects of intraoperative multisite ventricular pacing on left ventricular function and activation/contraction sequence in patients with depressed ventricular function. J Cardiovasc Electrophysiol. 1998;9:13-21.

27. Leclercq C, Cazeau S, Le Breton H, Ritter P, Mabo P, Gras D, Pavin D, Lazarus A, Daubert JC. Acute hemodynamic effects of biventricular DDD pacing in patients with end-stage heart failure. J Am Coll Cardiol. 1998;32:1825-31.

28.  Cazeau S, Ritter P, Bakdach S, Lazarus A, Limousin M, Henao L, Mundler O, Daubert JC, Mugica J. Four chamber pacing in dilated cardiomyopathy. Pacing Clin Electrophysiol. 1994;17:1974-9.

29. Blanc JJ, Etienne Y, Gilard M, Mansourati J, Munier S, Boschat J, Benditt DG, Lurie KG. Evaluation of different ventricular pacing sites in patients with severe heart failure: results of an acute hemodynamic study. Circulation. 1997;96:3273-7.

30. Kass DA, Chen CH, Curry C, Talbot M, Berger R, Fetics B, Nevo E. Improved left ventricular mechanics from acute VDD pacing in patients with dilated cardiomyopathy and ventricular conduction delay. Circulation. 1999;99:1567-73.

31. Kerwin WF, Botvinick EH, O'Connell JW, Merrick SH, DeMarco T, Chatterjee K, Scheibly K, Saxon LA. Ventricular contraction abnormalities in dilated cardiomyopathy: effect of biventricular pacing to correct interventricular dyssynchrony. J Am Coll Cardiol. 2000;35:1221-7.

32. Kerwin WF FE, Paccanaro M, et al. Effect of chronic biventricular pacing on doppler measures of myocardial performance correlate with doppler measures of systolic function (abstract). Pacing Clin Electrophysiol;. 1999;22(Suppl):732

33. St John Sutton MG, Plappert T, Abraham WT, Smith AL, DeLurgio DB, Leon AR et al. Effect of Cardiac Resynchronization Therapy on Left Ventricular Size and Function in Chronic Heart Failure. Circulation 2003 Mar 31; [epub ahead of print].

34.. Breithardt OA, Sinha AM, Schwammenthal E, Bidaoui N, Markus KU, Franke A et al. Acute effects of cardiac resynchronization therapy on functional mitral regurgitation in advanced systolic heart failure. J Am Coll Cardiol 2003 Mar 5;41(5):765-70

35. Gasparini M, Mantica M, Galimberti P, Ceriotti C, Simonini S, Mangiavacchi M, Gronda E. Relief of drug refractory angina by biventricular pacing in heart failure. Pacing Clin Electrophysiol. 2003;26:181-4.

36. Kass DA CC, Curry C, et al. Improved left ventricular mechanics from acute vdd pacing in patients with dilated cardiomyopathy and ventricular conduction delay. Circulation. 1999;99:1567.

37. Auricchio A, Spinelli J. Cardiac resynchronization for heart failure: present status. Congest Heart Fail. 2000;6:325-329.

38. Saxon LA, De Marco T, Schafer J, Chatterjee K, Kumar UN, Foster E. Effects of long-term biventricular stimulation for resynchronization on echocardiographic measures of remodeling. Circulation. 2002;105:1304-10.

39.  Saxon LA DT, Chatterjee K, et al. The magnitude of sympathoneural activation in advanced heart failure is altered with chronic biventricular pacing (abstract). Pacing Clin Electrophysiol. 1998;;21(Part II): 499.

40.  Dibs SR KW, Godin G, et al. Chronic biventricular pacing does not worsen autonomic imbalance in heart failure (abstract). Pacing Clin Electrophysiol. 2000.

41.   Yu CM, Chau E, Sanderson JE, Fan K, Tang MO, Fung WH, Lin H, Kong SL, Lam YM, Hill MR, Lau CP. Tissue Doppler echocardiographic evidence of reverse remodeling and improved synchronicity by simultaneously delaying regional contraction after biventricular pacing therapy in heart failure. Circulation. 2002;105:438-45.

42.  Abraham WT. Data from Multicenter InSync Randomized Clinical Evaluation (MIRACLE) presented at the American College of Cardiology 50th Annual Scientific Session, Orlando, Florida, 2001.

43.  Stellbrink C, Breithardt OA, Franke A, Sack S, Bakker P, Auricchio A, Pochet T, Salo R, Kramer A, Spinelli J. Impact of cardiac resynchronization therapy using hemodynamically optimized pacing on left ventricular remodeling in patients with congestive heart failure and ventricular conduction disturbances. J Am Coll Cardiol. 2001;38:1957-65.

44.  Williams ES, Miller JM. Results from late-breaking clinical trial sessions at the American College of Cardiology 51st Annual Scientific Session. J Am Coll Cardiol. 2002;40:1-18.

45.  Gasparini M, Lunati M, Bocchiardo M, Mantica M, Gronda E, Frigerio M, Caponi D, Carboni A, Boriani G, Zanotto G, Ravazzi PA, Curnis A, Puglisi A, Klersy C, Vicini I, Cavaglia S. Cardiac resynchronization and implantable cardioverter defibrillator therapy: preliminary results from the InSync implantable cardioverter defibrillator italian registry. Pacing Clin Electrophysiol. 2003;26:148-51.

46.  Bristow MR, Feldman AM, Saxon LA. Heart failure management using implantable devices for ventricular resynchronization: Comparison of Medical Therapy, Pacing, and Defibrillation in Chronic Heart Failure (COMPANION) trial. COMPANION Steering Committee and COMPANION Clinical Investigators. J Card Fail. 2000;6:276-85.

47.  Higgins SL, Yong P, Sheck D, McDaniel M, Bollinger F, Vadecha M, Desai S, Meyer DB. Biventricular pacing diminishes the need for implantable cardioverter defibrillator therapy. Ventak CHF Investigators. J Am Coll Cardiol. 2000;36:824-7.

48. Gasparini M, Mantica M, Galimberti P, Bocciolone M, Genovese L, Mangiavacchi M, Marchesina UL, Faletra F, Klersy C, Coates R, Gronda E. Is the left ventricular lateral wall the best lead implantation site for cardiac resynchronization therapy? Pacing Clin Electrophysiol. 2003;26:162-8.

49. Ansalone G, Giannantoni P, Ricci R, Trambaiolo P, Fedele F, Santini M. Doppler myocardial imaging to evaluate the effectiveness of pacing sites in patients receiving biventricular pacing. J Am Coll Cardiol. 2002;39:489-99.

50. Ansalone G, Giannantoni P, Ricci R, Trambaiolo P, Laurenti A, Fedele F, Santini M. Doppler myocardial imaging in patients with heart failure receiving biventricular pacing treatment. Am Heart J. 2001;142:881-96.

51. Wilensky RL, Yudelman P, Cohen AI, Fletcher RD, Atkinson J, Virmani R, Roberts WC. Serial electrocardiographic changes in idiopathic dilated cardiomyopathy confirmed at necropsy. Am J Cardiol. 1988;62:276-83.

52. Baldasseroni S, Opasich C, Gorini M, Lucci D, Marchionni N, Marini M, Campana C, Perini G, Deorsola A, Masotti G, Tavazzi L, Maggioni AP. Left bundle-branch block is associated with increased 1-year sudden and total mortality rate in 5517 outpatients with congestive heart failure: a report from the Italian network on congestive heart failure. Am Heart J. 2002;143:398-405.

53. Gottipati V, Kralis S, Lu F. The Resting Electrocardiogram Provides a Sensitive and Inexpensive Marker of Prognosis in Patients with Chronic Congestive Heart Failure. (Abstract). J Am Coll Cardiol. 1999;33:145 A.

54. 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;101:2703-9.

55. Aneslme F SI. Is QRS duration a good predictor of right to left ventricular asynchrony? Comparison with conventional Doppler and tissue Doppler imaging criteria. (abstract). PACE. 2002;25:528.

56. Garrigue S BH, Reuter S. QRS duration and morphology are not reliable parameters to identify heart failure patients with left ventricular dyssynchrony. An Echocardiographic Doppler Tissue Imaging Study. (abstract). PACE. 2002;25:547 A.

57. Yu CM, Lin H, Zhang Q. High prevalence of left ventricular systolic and diastolic asynchrony in patients with congestive heart failure and normal QRS duration. Heart 2003 Jan;89(1):54-60

58. Gasparini M, Galimberti P, Marconi M, Genovese L, Faltera F et al. Beneficial Effects of Biventricular Pacing in Patients with a Narrow QRS. PACE. 2003;26[pt.II]:169-174.

59. Cazeau S RP. Multisite pacing for end-stage heart failure: early experience. Pacing Clin Electrophysiol. 1996;Nov;19(11 Pt 2):1748-57.

60. Botvinick EH FM. An accurate means of detecting and characterizing abnormal patterns of ventricular activation by phase image analysis. Am J Cardiol. 1982;Aug;50(2):289-98.

61. Cazeau S, Bordachar P, Jauvert G, Lazarus A, Alonso C, Vandrell MC, Mugica J, Ritter P. Echocardiographic modeling of cardiac dyssynchrony before and during multisite stimulation: a prospective study. Pacing Clin Electrophysiol. 2003;26:137-43.

62. Burch GE, Giles TD, Colcolough HL. Ischemic cardiomyopathy. Am Heart J. 1970;79:291-2.

63. Littmann L, Symanski JD. Hemodynamic implications of left bundle branch block. J Electrocardiol. 2000;33 Suppl:115-21.

64. Gasparini M MM, Galimberti P, Genovese L, Pini D, Faletra F. Is the outcome of cardiac resynchronization therapy related to the underlying etiology. PACE. 2003;26[Pt. II]:175-180.

65. Saxon LA. Atrial fibrillation and dilated cardiomyopathy: therapeutic strategies when sinus rhythm cannot be maintained. Pacing Clin Electrophysiol. 1997;20:720-5.

66. Bradley DJ, Bradley EA, Baughman KL, Berger RD, Calkins H, Goodman SN et al. Cardiac resynchronization and death from progressive heart failure: a meta-analysis of randomized controlled trials. JAMA 2003 Feb 12;289(6):730-40.

67. Hunt SA, Baker DW, Chin MH, Cinquegrani MP, Feldman AM, Francis GS, Ganiats TG, Goldstein S, Gregoratos G, Jessup ML, Noble RJ, Packer M, Silver MA, Stevenson LW, Gibbons RJ, Antman EM, Alpert JS, Faxon DP, Fuster V, Jacobs AK, Hiratzka LF, Russell RO, Smith SC, Jr. ACC/AHA guidelines for the evaluation and management of chronic heart failure in the adult: executive summary. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to revise the 1995 Guidelines for the Evaluation and Management of Heart Failure). J Am Coll Cardiol. 2001;38:2101-13.

68. Hare JM. Cardiac-resynchronization therapy for heart failure. N Engl J Med. 2002;346:1902-5.

69. Moss AJ, Zareba W, Hall WJ, Klein H, Wilber DJ, Cannom DS, Daubert JP, Higgins SL, Brown MW, Andrews ML. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction. N Engl J Med. 2002;346:877-83.

Home Page Current Issue List of Editors