Document Detail

Different effect of exercise on left ventricular diastolic time and interventricular dyssynchrony in heart failure patients with and without left bundle branch block.
Jump to Full Text
MedLine Citation:
PMID:  19002270     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: In patients with idiopathic dilated cardiomyopathy (IDCM) a prolongation of left ventricular (LV) systole at the expense of diastolic time was demonstrated. Our study was aimed to evaluate the effect of exercise on heart rate corrected diastolic time in controls, IDCM with and without LBBB, and patients with LBBB and normal LV function.
METHODS: 47 patients with IDCM, 30 without LBBB, and 17 with LBBB as well as 11 with isolated LBBB were studied during exercise using a combined hemodynamic-radionuclide angiographic approach. The phases of the cardiac cycle were derived with high temporal resolution from the ventricular time-activity curve. The loss of diastolic time per beat (LDT) was quantified using a regression equation obtained from a control group (n=24).
RESULTS: A significant LDT was demonstrated at rest and during peak exercise in IDCM patients with LBBB (39.1+/-32 and 37.3+/-30 ms; p < 0.001). In IDCM patients with normal activation LDT was unaffected at baseline, but elevated during peak exercise. This response was paralleled by an increase in interventricular mechanical dyssynchrony.
CONCLUSION: During exercise an abnormal shortening of LV diastolic time is a common characteristic of heart failure patients which can be explained by the high prevalence of mechanical dyssynchrony.
Gunnar Plehn; Julia Vormbrock; Thomas Butz; Martin Christ; Hans-Joachim Trappe; Axel Meissner
Publication Detail:
Type:  Controlled Clinical Trial; Journal Article     Date:  2008-11-04
Journal Detail:
Title:  International journal of medical sciences     Volume:  5     ISSN:  1449-1907     ISO Abbreviation:  Int J Med Sci     Publication Date:  2008  
Date Detail:
Created Date:  2008-11-12     Completed Date:  2009-02-27     Revised Date:  2013-06-04    
Medline Journal Info:
Nlm Unique ID:  101213954     Medline TA:  Int J Med Sci     Country:  Australia    
Other Details:
Languages:  eng     Pagination:  333-40     Citation Subset:  IM    
Department of Cardiology and Angiology, Marienhospital Herne, University of Bochum, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Bundle-Branch Block / physiopathology*
Diastole / physiology*
Exercise / physiology*
Heart Failure / physiopathology*
Middle Aged
Time Factors
Ventricular Function, Left / physiology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): Int J Med Sci
Journal ID (publisher-id): ijms
ISSN: 1449-1907
Publisher: Ivyspring International Publisher, Sydney
Article Information
Download PDF
? Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License ( Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
Received Day: 1 Month: 10 Year: 2008
Accepted Day: 3 Month: 11 Year: 2008
collection publication date: Year: 2008
Electronic publication date: Day: 4 Month: 11 Year: 2008
Volume: 5 Issue: 6
First Page: 333 Last Page: 340
ID: 2581821
Publisher Id: ijmsv05p0333
PubMed Id: 19002270

Different effect of exercise on left ventricular diastolic time and interventricular dyssynchrony in heart failure patients with and without left bundle branch block
Gunnar Plehn?
Julia Vormbrock
Thomas Butz
Martin Christ
Hans-Joachim Trappe
Axel Meissner
Department of Cardiology and Angiology, Marienhospital Herne, University of Bochum, Germany
Correspondence: ? Correspondence to: Gunnar Plehn, MD, Department of Cardiology and Angiology, Marienhospital Herne, University of Bochum, H?lkeskampring 40, 44625 Herne, Germany. Tel.: (0049)-2323-4995617; Fax: (0049)-2323-499301; Email:
[conflict] Conflict of Interest: The authors have declared that no conflict of interest exists.


The introduction of cardiac resynchronization therapy has recently renewed the clinical interest in the analysis of specific phases of the cardiac cycle and their temporal relationship 1. In heart failure patients two major abnormalities of the gross time course of cardiac contraction were demonstrated: a prolongation of total isovolumic time (t-IVT) which represents the time wasted within the cardiac cycle and a disproportionate shortening of left ventricular (LV) diastolic time which suggests an impaired temporal relation between LV systole and diastole 2,3,4. Whether left bundle branch block (LBBB) has a similar, consistent effect on the systolic-diastolic phase proportion at rest and during stress has not been thoroughly investigated. Therefore, our study sought to separate the effects of LBBB and ventricular disease on the relative duration of LV systole and diastole in heart failure patients during peak incremental exercise.


All NYHA class III patients undergoing invasive hemodynamic exercise testing for clinical reasons were consecutively screened as potential candidates. Inclusion criteria were: idiopathic dilated cardiomyopathy (IDCM) diagnosed on the basis of the exclusion of other causes of LV dysfunction, such as of evidence of myocarditis in endomyocardial biopsy, significant coronary artery stenoses revealed by angiography, valvular heart disease except of functional mitral regurgitation. Only patients with an echocardiographic ejection fraction (EF) < 40% were included. Patients with atrial fibrillation, QRS prolongation with non-LBBB pattern and disorders other than cardiac disease that limit exercise performance were excluded.

According to QRS duration the selected patients (n =47) were divided into two groups: 30 patients with normal QRS duration (< 120 ms; IDCM-na) and 17 patients with prolonged QRS duration (? 120 ms) and LBBB activation pattern (IDCM-LBBB).

Additional 11 patients with isolated LBBB were retrospectively selected from a larger cohort of patients evaluated in our hemodynamic laboratory. All of these patients had a normal left ventricular cavity size and baseline ejection fraction as evaluated by radionuclide angiography. Coronary artery disease was excluded by angiography. All of these patients had a limited exercise tolerance classified as NYHA II.

The control group consisted of 24 patients referred for ventricular function assessment with radionuclide angiography before cardiotoxic cancer treatment. None of these patients had a history of cardiac disease, diabetes or hypertension.

All patients included in the overall study gave their written informed consent prior to the examination.

Exercise hemodynamics

The patients performed supine bicycle exercise beginning at a load of 25 watt with increases of 25 watt every 5 min until the development of fatigue or limiting dyspnoea. Rest and exercise hemodynamics were measured with a pulmonary artery balloon flotation right heart catheter. Resting measurements were obtained twice, once 15 min before and again immediately before the exercise. Peak and mean pulmonary arterial pressure (MPA) as well as mean pulmonary arterial wedge (PCWP) pressure were recorded. Right atrial pressure was measured at baseline and immediately after cessation of exercise. The brachial arterial systolic and diastolic pressures were measured by sphygmomanometer. Forward cardiac output was measured by the thermodilution technique both at rest and during exercise immediately after the pressure measurements. Between three and five thermodilution cardiac output measurements were carried out at each exercise stage for calculation of the mean value. Cardiac index (CI), stroke volume index (SVI) and systemic vascular resistance (SVR) were calculated according to standard formulae. LV end-diastolic volumes (EDVI) was calculated by dividing thermodilution stroke volume index by the respective ejection fraction.


Two-dimensional echocardiography was performed in all patients using an ultrasonic device equipped with a 2.5-MHz transducer. The left ventricular diastolic and systolic dimensions were measured in the parasternal long-axis view according to the standard recommendations 5. The left ventricular ejection fraction was calculated according to the formula established by Quinones et al. 6

Radionuclide angiography

Simultaneously with hemodynamic measurements, equilibrium radionuclide angiography was performed using a high sensitivity, low-energy parallel hole collimator interfaced to a computer system (Sopha-DS7-gammacamera) as previously described 7. Acquisition was carried out at LAO 20?-30? angulation and 15? caudal tilting to achieve a precise separation of the interventricular septum. Data were registered in a 64 x 64 matrix at 32 frames per cardiac cycle at rest and during exercise and time-activity curves were constructed. As usual, the R-wave of the electrocardiograph was used to identify the onset of each new cardiac cycle. A dynamic filtration acquisition mode was used, with rejection of cardiac cycles beyond ?10% of the mean R-R interval. The data were further processed and analyzed by a semi-automated computer routine 8. Right- and left-ventricular regions of interest were traced simultaneously on diastolic images and functional images obtained by Fourier amplitude and phase analysis to provide a clear definition of the septum and the atrio-ventricular junction. Left ventricular ejection fraction (LVEF) was calculated as (end-diastolic counts-end-systolic counts)/end-diasto?lic counts.

Duration of left ventricular systole and diastole (method of calculation)

The absolute duration of left ventricular systole was defined as the time interval between the onset of the R-wave and the minimal volume on the time-activity curve (end-systole). The relative duration of left ventricular systole was derived as the product of absolute systolic time and heart rate and expressed in seconds per minute. Diastolic time was calculated as the cardiac length (RR interval) minus the duration of systole. To define diastolic duration during exercise more precisely, diastolic time in IDCM patients was compared with its predicted value obtained from putting each heart rate of IDCM patients into a regression equation obtained from the control group. The loss of diastolic time per beat (LDT) was defined as the difference between and calculated and individually observed diastolic time values.

Interventricular mechanical dyssynchrony (method of calculation)

Phase image analysis was applied to the scintigraphic data using the above mentioned computer routine. The phase program assigns a phase angle to each pixel of the phase image, derived from the first Fourier harmonic of time. The phase angle corresponds to the relative sequence and pattern of ventricular contraction during the cardiac cycle. The mean phase angles were computed for right ventricular (RV) and LV blood pools as the arithmetic mean phase angle for all pixels in the ventricular region of interest. Interventricular mechanical dyssynchrony was evaluated as the difference between LV and RV mean phase angles (RV-LV-delay). Phase data were expressed in degrees between 0? and 360?.

Statistical analysis

All data are given in terms of the mean ? SD. Differences in group means were analyzed with the two tailed unpaired t-test. For comparison of the individually observed and predicted time values and for comparison of within-group changes a repeated measures analysis of variance was used. If analysis of variance showed an overall difference, pairwise comparison was performed with a paired t-test. Correlation was performed by linear regression analysis. Analyses were performed using the software package ?SPSS for Windows 12.0.1?.

Systolic and diastolic time intervals

The clinical characteristics and time interval details of the patient groups and the control group are presented in Table 1. Medical treatment was similar in both patient groups with IDCM. In those with normal activation, 27 of 30 were receiving a beta-blocking agent, 30 an angiotensinconverting enzyme inhibitor or angiotensin receptor blocker, and 19 a diuretic. In patients with conduction disturbance, 13 of 17 patients were receiving a beta-blocking agent, 15 an angiotensinconverting enzyme inhibitor or angiotensin receptor blocker, and 10 a diuretic. 8 of 11 patients with isolated LBBB had beta-blocker therapy. All groups had similar baseline heart rates. During peak exercise heart rates were slightly lower in all three patient groups. To better separate the effect of heart rate from cardiac function time intervals diastolic time was plotted against the corresponding heart rate of each exercise stage and regression analysis was performed. An inverse, nonlinear relation between heart rate and LV diastolic time was found in either normal subjects and both patient groups with IDCM. The equations were: diastolic time = 101905xHR-1.23; r = 0.97, p < 0.001 for normal subjects, 187663xHR-1.38; r = 0.92 for IDCM-na patients; p < 0.001 and 174925xHR-1.38; r = 0.90 for IDCM-LBBB patients; p < 0.001. The regression equation obtained from the control group was used to quantify the loss of diastolic time per beat in all three patient groups. When predicted and observed values of diastolic time were compared a significant LDT was demonstrated at rest (20.1?29 ms; p = 0.003) and during peak exercise (21.8?16 ms; p < 0.001) in patients with isolated LBBB. In IDCM-LBBB patients the alteration was even more pronounced (39.1?32 ms at rest and 37.3?30 ms at peak exercise; p < 0.001). In IDCM-na patients LDT was not significant at baseline (5.4?31 ms; ns), however during exercise a significant LDT was observed (28.1 ? 36 ms; p = 0.03). Within this subgroup of patients a significant exercise-related increase in LDT was demonstrated (5.4 ? 31 ms vs. 28.1 ? 36 ms; p = 0.02) (Figure 1).

SVR at peak exercise did not correlate with LDT at peak exercise, nor did its exercise related change correlate with the corresponding change in SVR. Although a significant left ventricular chamber dilatation from rest to exercise was evident in IDCM-na and IDCM-LBBB patients (188 ? 57 vs. 211 ? 92 ml/m2; p = 0.04 and 193 ? 39 vs. 225? 88 ml/m2; p = 0.02), no correlations between the absolute values of EDVI at rest or during exercise or the exercise-related increase in EDVI and the corresponding LDT values were found in both IDCM subgroups.

Interventricular mechanical dyssynchrony

At baseline a significant RV-LV delay was demonstrable in LBBB patients, but not in IDCM patients with normal QRS duration. During peak exercise, however, all three subgroup of patients showed a significant RV-LV delay compared to control subjects (Table 1, Figure 2). Within IDCM-na patients a significant increase of RV-LV delay from rest to peak exercise was observed (1.5 ? 6.4 vs. 5.1 ? 7.7?; p < 0.001).

In patients with LBBB no significant correlation between the rest or exercise values of RV-LV delay and the corresponding LDT was found. In addition, there was no significant correlation between the exercise-related change of RV-LV-delay and LDT within these subgroups. In IDCM-na, however, there was a weak correlation between the exercise related change of both parameters (r = 0.34; p = 0.04). Furthermore, a moderate correlation between the exercise-related change in RV-LV delay and LDT at peak exercise was demonstrable (Figure 3).


Our study demonstrated a significant prolongation of LV systole and a consecutively shortened LV diastole in patients with LBBB irrespective of the presence of left ventricular systolic dysfunction. The absolute loss of diastolic time was consistent in these groups whether measurements were taken at rest or during exercise. In contrast, heart failure patients without LBBB exhibited a more dynamic response pattern. At baseline LV diastolic time was within physiological limits. During exercise, however, a significant shortening of LV diastolic time was observed.

These findings strongly suggest that conduction mediated and conduction independent factors did not additively contribute to the derangement of the systolic-diastolic phase proportion during exercise in heart failure patients.

Principally, alterations of the two principal components of the entire systolic phase may have contributed to its prolongation. LV ejection time was generally found to be unchanged or rather reduced in severe systolic heart failure 2,9. However, a few exceptions were noted. During exercise a progressive left ventricular dilatation and a reduced systemic vasodilator capacity may produce sub-optimal afterload conditions resulting in a prolongation of left ventricular ejection and total LV systole 10,11. This effect of loading conditions on the duration of LV systole is a well documented finding in cardiac disease states with considerable afterload-mismatch as aortic stenosis and hypertrophic obstructive cardiomyopathy 12,13. The end-diastolic volume increase during exercise, may bring the failing ventricle onto the descending limb of its function curve. In this situation a prolongation of left ventricular ejection was demonstrated which may be viewed as a compensatory mechanism that serves to maintain left ventricular pump performance 14,15. However, systemic vascular resistance decrease during exercise and the degree of left ventricular enlargement was similar in IDCM patients with and without LBBB. Hence, these mechanisms may equally be operative in both subgroups and may not have contributed to the observed differences in temporal characteristics induced by exercise.

On the other hand, there is consistent evidence that isovolumic contraction time as the other major component of LV systolic duration is increased in patients with dilated cardiomyopathy. A disturbed electromechanical activation leading to intraventricular dyssynchrony is typically present in patients with LBBB but also common in patients without LBBB 16. As a result of the heterogeneous onset of LV contraction and its heterogeneous termination LV isovolumic time intervals were found to be increased at the expense of LV diastolic time in heart failure patients 17,18.

Since our findings and other previous studies suggested that tachycardia acts as a mechanism that aggravates abnormalities of the systolic-diastolic phase proportion in IDCM patients with narrow QRS complex, it is tempting to relate these observation to an exercise induced exacerbation of intra-LV dyssynchrony 3,7. This assumption is supported by recent findings. Lafitte et al. demonstrated that the mean degree of intra LV dyssynchrony did not change with exercise in heart failure patients with predominantly wide QRS duration 19. Similarily, Valzania et al. reported a lack of increase in LV dyssynchrony during dobutamine stress in patients with wide QRS duration 20. In contrast, Kurita et al. reported on an increased mechanical dyssynchrony during pacing-induced tachycardia in patients with normal QRS duration 21. A remarkable increase in intra-LV dyssynchrony was also demonstrated during pharmacological stress in systolic heart failure patients with normal QRS duration. The prevalence of dyssynchrony was low in this patient group at rest, but approached that observed in patients with wide QRS during stress 22. Furthermore, exercise LV dyssynchrony may play a more important role in the pathophysiology of left ventricular remodelling than baseline LV dyssynchrony 23. Probably for that reason additional hemodynamic benefits from cardiac resynchronization were obtained when RV-LV delay was separately optimized during exercise 24.

Our findings are in good concordance with these results and underline the highly dynamic nature of mechanical ventricular dyssynchrony in heart failure patients with normal QRS duration. By characterizing mechanical interventricular dyssynchrony, which was commonly found to be associated with intra-LV dyssynchrony in heart failure patients 16, we were able to demonstrate that the abnormal shortening of the duration of left ventricular diastole is closely related to the phenomenon of mechanical dyssynchrony. These findings may further explain why patients with normal QRS duration may benefit from cardiac resynchronization whether or not they have mechanical dyssynchrony under resting conditions. As demonstrated in patients with left bundle branch block biventricular pacing typically improves the time course of cardiac contraction at rest and during exercise by reducing LV dyssynchrony and thereby liberating a further segment of the RR interval for diastole 24. Considering that direct evaluation of LV dyssynchrony is still complex and time-consuming, the extent of diastolic time loss may represent a simple surrogate measure of the degree of LV dyssynchrony. Furthermore, the shortening of diastolic time is an often overlooked mechanism of cardiac dysfunction. The duration of diastole is a principal determinant of myocardial perfusion and of the blood volume received during diastole. Since both, a reduced myocardial perfusion reserve and diastolic heart failure, are an integral part of systolic heart failure any abnormal shortening of diastolic time, particularly during exercise, should exaggerate these preexisting abnormalities 25,26.


The present study included a relatively small number of subjects. Our results were limited to patients with advanced heart failure and NYHA III functional class and may therefore not be readily generalizable to patients with a milder or a more severer degree of heart failure. Furthermore, all patients with dilated cardiomyopathy were examined under cardioactive medication. Beta-blocker therapy should have significantly contributed to a reduction in peak exercise heart rate in these patients. However, beta-blockers were shown to have no effect on the relationship between heart rate and diastolic time and to reduce rather than aggravate LV dyssynchrony in heart failure 27,28. Although patients with isolated LBBB were of younger age than the other three study groups it would be highly unlikely that the observed abnormalities in this group were due to an age-dependent effect. Basic cardiac time intervals as diastolic filling time were shown to be similar in young and elderly populations 29.


The current study, which evaluated the effect of exercise on heart rate corrected diastolic time in IDCM patients yielded the following findings: LBBB was a major determinant of the duration of LV systole, irrespective of the presence of left ventricular disease. The effect of the electrical conduction defect was independent from heart rate causing a relatively constant loss of diastolic time per beat. Unlike patients with LBBB those with IDCM and normal activation demonstrated a more dynamic response. A prolongation of LV systole and hence shortening of LV diastole was solely evident during exercise probably as a result of an increase in LV mechanical dyssynchrony.

1. Veyrat C,Larrazet F,Pellerin D. Renewed interest in preejectional isovolumic phase: new applications of tissue Doppler indexes: implications to ventricular asynchronyAm J Cardiol 2005;96:1022–30. [pmid: 16188536]
2. Duncan AM,Francis DP,Henein MY. Limitation of cardiac output by total isovolumic time during pharmacologic stress in patients with dilated cardiomyopathy: activation-mediated effects of left bundle branch block and coronary artery diseaseJ Am Coll Cardiol 2003;41:121–8. [pmid: 12570954]
3. Friedberg MK,Silverman NH. Cardiac ventricular diastolic and systolic duration in children with heart failure secondary to idiopathic dilated cardiomyopathyAm J Cardiol 2006;97:101–5. [pmid: 16377292]
4. Plehn G,Vormbrock J,Z?hlke C,Christ M,Perings C,Perings S,Trappe HJ,Meissner A. Disproportionate shortening of left ventricular diastolic duration in patients with dilated cardiomyopathyMed Klin 2007;102:707–13.
5. Schiller NB,Shah PM,Crawford M,DeMaria A,Devereux R,Feigenbaum H,Gutgesell H,Reichek N,Shah D,Schnittger I,Silverman NH,Tajik AJ. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiogram: recommendations for quantitation of the left ventricle by two-dimensional echocardiographyJ Am Soc Echocardiogr 1989;2:358–367. [pmid: 2698218]
6. Quinones MA,Waggoner AD,Reduto LA,Nelson JG,Young JB,Winters WL Jr,Ribeiro LG,Miller RR. A new, simplified and accurate method for determining ejection fraction with two-dimensional echocardiographyCirculation 1981;64:744–753. [pmid: 7273375]
7. Plehn G,Vormbrock J,Perings C,Machnick S,Zuehlke C,Trappe HJ,Meissner A. Loss of diastolic time as a mechanism of exercise-induced diastolic dysfunction in dilated cardiomyopathyAm Heart J 2008;155:1013–9. [pmid: 18513513]
8. Standke R,H?r G,Maul D. Fully automated equilibrium radionuclide ventriculography. - Proposal of a method for routine use: exercise and follow-upEur J Nucl Med 1983;8:77–83. [pmid: 6840128]
9. Zhou Q,Henein M,Coats A,Gibson D. Different effects of abnormal activation and myocardial disease on left ventricular ejection and filling timesHeart 2000;84:272–6. [pmid: 10956289]
10. Hayashida W,Kumada T,Nohara R,Tanio H,Kambayashi M,Ishikawa N,Nakamura Y,Himura Y,Kawai C. Left ventricular regional wall stress in dilated cardiomyopathyCirculation 1990;82:2075–83. [pmid: 2242531]
11. Latham RD,Thornton JW,Mulrow JP. Cardiovascular reserve in idiopathic dilated cardiomyopathy as determined by exercise response during cardiac catheterizationAm J Cardiol 1987;59:1375–9. [pmid: 3591694]
12. Moskowitz RL,Weschler BM. Left ventricular ejection time in aortic and mitral valve diseaseAm Heart J 1961;62:367–78. [pmid: 13784135]
13. Arshad W,Duncan AM,Francis DP,O'Sullivan CA,Gibson DG,Henein MY. Systole-diastole mismatch in hypertrophic cardiomyopathy is caused by stress induced left ventricular outflow tract obstructionAm Heart J 2004;148:903–9. [pmid: 15523325]
14. Braunwald E,Sarnoff SJ,Stainsby WN. Determinants of Duration and Mean Rate of Ventricular EjectionCirc Res 1958;6:319–325. [pmid: 13523814]
15. Siri FM,Malhotra A,Factor SM. Sonnenblick EH, Fein FS. Prolonged ejection duration helps to maintain pump performance of the renal-hypertensive-diabetic rat heart: correlations between isolated papillary muscle function and ventricular performance in situCardiovas Res 1997;34:230–40.
16. Ghio S,Constantin C,Klersy C,Serio A,Fontana A,Campana C,Tavazzi L. Interventricular and intraventricular asynchrony are common in heart failure patients, regardless of QRS durationEur Heart J 2004;25:571–8. [pmid: 15120054]
17. Hay I,Melenovsky V,Fetics BJ,Judge DP,Kramer A,Spinelli J,Reister C,Kass DA,Berger RD. Short-term effects of right-left heart sequential cardiac resynchronization in patients with heart failure, chronic atrial fibrillation, and atrioventricular nodal blockCirculation 2004;110:3404–10. [pmid: 15557370]
18. Salukhe TV,Francis DP,Morgan M. Mechanism of cardiac output gain from cardiac resynchronization therapy in patients with coronary artery disease or idiopathic dilated cardiomyopathyAm J Cardiol 2006;97:1358–64. [pmid: 16635611]
19. Lafitte S,Bordachar P,Lafitte M,Garrigue S,Reuter S,Reant P,Serri K,Lebouffos V,Berrhouet M,Jais P,Haissaguerre M,Clementy J,Roudaut R,DeMaria AN. Dynamic ventricular asynchrony: an exercise-echocardiography studyJ Am Coll Cardiol 2006;47:2253–9. [pmid: 16750692]
20. Valzania C,Gadler F,Eriksson MJ,Olsson A,Boriani G,Braunschweig F. Electromechanical effects of cardiac resynchronization therapy during rest and stress in patients with heart failureEur J Heart Fail 2007;9:644–50. [pmid: 17347041]
21. Kurita T,Onishi K,Dohi K,Tanabe M,Fujimoto N,Tanigawa T,Setsuda M,Isaka N,Nobori T,Ito M. Impact of heart rate on mechanical asynchrony and left ventricular contractility in patients with heart failure and normal QRS durationEur J Heart Fail 2007;9:637–43. [pmid: 17467334]
22. Chattopadhyay S,Alamgir MF,Nikitin NP,Fraser AG,Clark AL,Cleland JG. The effect of pharmacological stress on intraventricular dyssynchrony in left ventricular systolic dysfunctionEur J Heart Fail 2008;10:412–420. [pmid: 18395672]
23. Kang SJ,Lim HS,Choi BJ,Choi SY,Yoon MH,Hwang GS,Shin JH,Tahk SJ. The Impact of Exercise-induced Changes in Intraventricular Dyssynchrony on Functional Improvement in Patients with Nonischemic CardiomyopathyJ Am Soc Echocardiogr. 2008 [Epub ahead of print]
24. Bordachar P,Lafitte S,Reuter S,Garrigue S,Laborderie J,Reant P,Jais P,Haisaguerre M,Roudaut R,Clementy J. Echocardiographic assessment during exercise of heart failure patients with cardiac resynchronization therapyAm J Card 2006;97:1622–25. [pmid: 16728226]
25. Inoue T,Sakai Y,Morooka S,Hayashi T,Takayanagi K,Yamanaka T,Kakoi H,Takabatake Y. Coronary flow reserve in patients with dilated cardiomyopathyAm Heart J 1993;125:93–8. [pmid: 8417548]
26. Little WC. Diastolic dysfunction beyond distensibility: adverse effects of ventricular dilatationCirculation 2005;112:2888–90. [pmid: 16275877]
27. Boudoulas H,Rittgers SE,Lewis RP,Leier CV,Weissler AM. Changes in diastolic time with various pharmacologic agents: implication for myocardial perfusionCirculation 1979;60:164–9. [pmid: 376175]
28. Takemoto Y,Hozumi T,Sugioka K,Takagi Y,Matsumura Y,Yoshiyama M,Abraham TP,Yoshikawa J. Beta-blocker therapy induces ventricular resynchronization in dilated cardiomyopathy with narrow QRS complexJ Am Coll Cardiol 2007;49:778–83. [pmid: 17306707]
29. Stratton JR,Levy WC,Caldwell JH,Jacobson A,May J,Matsuoka D,Madden K. Effects of aging on cardiovascular responses to parasympathetic withdrawalJ Am Coll Cardiol 2003;41:2077–83. [pmid: 12798585]

Article Categories:
  • Research Paper

Keywords: diastolic time, heart failure, left bundle branch block, exercise test, interventricular dyssynchrony.

Previous Document:  Viscous instabilities in flowing foams: a Cellular Potts Model approach.
Next Document:  XeNA: capecitabine plus docetaxel, with or without trastuzumab, as preoperative therapy for early br...