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C Veyrat

Publications and source records attributed to C Veyrat.

At least 19 recordsLinked to original sources

New insights into septal anterior wall motion velocities at end-systole in normal and hypertrophied left ventricles.

AIMS: It was two-fold (1) to define tissue Doppler echocardiographic characteristics of the end-systolic septal anterior motion: passive due to heart translation, or active motion free of translational effects, substantiated by a myocardial velocity gradient. (2) to specify the temporal features of this septal anterior motion on normal and hypertrophied left ventricles since it occurs while the posterior wall contracts during late ejection. METHODS AND RESULTS: Myocardial velocity gradient was calculated during the anterior motion in simultaneously colour M-mode imaged septal and posterior walls of 21 controls (49+/-12 years) and 17 patients (49+/-13 years) with left ventricle hypertrophy. Timings of septal motion were compared with flow and posterior wall motion. In controls, septal anterior motion started prior to, and overlapped the end of subaortic flow and that of the posterior wall anterior motion. Myocardial velocity gradient was found, exceeding that at the posterior wall (2.5+/-1.6 vs 0.9+/-0.5s(-1), P=0.001). In patients, septal myocardial velocity gradient was lower than in controls (1.2+/-1.04 s(-1)P=0.006). The anterior motion had a longer duration than in controls (75+/-37 vs 50+/-17ms, P=0.003). Myocardial velocity gradient and duration were correlated with septal thickness (P=<0.01). CONCLUSIONS: The septal anterior motion was active. Patients showed a decreased myocardial velocity gradient, while wall asynchrony increased. Unusual higher septal than posterior wall systolic velocities at tissue Doppler echocardiography may suggest a relaxation pattern, in spite of its end-systolic onset.

Adult↗

Tissue Doppler, strain, and strain rate echocardiography for the assessment of left and right systolic ventricular function.

Tissue Doppler (TDE), strain, and strain rate echocardiography are emerging real time ultrasound techniques that provide a measure of wall motion. They offer an objective means to quantify global and regional left and right ventricular function and to improve the accuracy and reproducibility of conventional echocardiography studies. Radial and longitudinal ventricular function can be assessed by the analysis of myocardial wall velocity and displacement indices, or by the analysis of wall deformation using the rate of deformation of a myocardial segment (strain rate) and its deformation over time (strain). A quick and easy assessment of left ventricular ejection fraction is obtained by mitral annular velocity measurement during a routine study, especially in patients with poor endocardial definition or abnormal septal motion. Strain rate and strain are less affected by passive myocardial motion and tend to be uniform throughout the left ventricle in normal subjects. This paper reviews the underlying principles of TDE, strain, and strain rate echocardiography and discusses currently available quantification tools and clinical applications.

Echocardiography, Doppler, Color↗

[Doppler tissue imaging in the assessment of dilated cardiomyopathy].

Doppler myocardial tissue imaging is a recent technique of objective assessment of wall motion by real time measurement of intra-myocardial velocities. This technique is being evaluated in patients with dilated cardiomyopathy. Doppler myocardial tissue imaging has been used for the quantification of dobutamine stress echocardiography, for the detection of an ischaemic aetiology in patients with dilated cardiomyopathy and for non-invasive estimation of left ventricular filling pressures. At the present time, the recordings have to be analysed a posteriori and only a small number of centres have acquired expertise of these techniques at rest or during stress. Standardisation of a posteriori procedures of image processing and validation of pertinent parameters have yet to be established in this pathology.

Cardiomyopathy, Dilated↗

Those who faced turbulence and launched the era of flow dynamic concepts for cardiac investigation.

This paper puts emphasis on pioneers who developed cardiac flow dynamics concepts during the second half of the 20th century at a period where pressure measurements were the rule. Thinking flow instead of pressure dynamics corresponded to in-depth conceptual changes: whereas blood pressure generally has a single positive sign and a similar pattern at all points of a cardiac chamber or a vessel, flow fluctuates around the zero line and its pattern changes within a given cardiac chamber or vessel level. These specific changes and fluctuations were the exciting tools needed to renew our pathophysiological insights, just in time with the take off of Doppler ultrasound making noninvasive investigation of fluid dynamics easily available. Each decade was marked by a specific historical contribution to evolving concepts. Instead of a merely phenomenological approach to flow dynamics, pioneers assigned a value of paradigms to basic flow patterns. They generated a system of heuristical hypotheses which turned out to underlay a modernistic understanding of flow dynamics in normal and diseased hearts. So far, flow investigation had definitely gained acceptance completing pressure data at the middle of the 1980s, widely opening a breakthrough for future pathophysiological insights.

Cardiology↗

Cardiovascular applications of the Doppler technique: A long way from birth to scientific acceptance.

Analysis of the early developments of cardiac Doppler illustrates a gap, frequently encountered in science, between initial concepts and final acceptance. Acceptance may only emerge as a result of multidisciplinary collaboration and fruitful dialogue between physicians, physiologists, physicists, and engineers. By 1980, after a good deal of trial and error and a long period of incremental improvement, the majority of the theoretic and scientific issues had been defined. The explosive development of Doppler techniques can now intervene to sweep aside the medical community's scepticism.

Echocardiography, Doppler↗

Comparison of 2 myocardial velocity gradient assessment methods during dobutamine infusion with Doppler myocardial imaging.

Myocardial velocity gradient (MVG) has been shown to be the best quantitative parameter for the detection of ischemic myocardium during dobutamine infusion with the use of Doppler myocardial imaging. MVG has been previously assessed by velocity measurements across the thickness of the myocardium at the time of visually selected maximal color brightness (thickness-velocity plot method). We hypothesized that MVG could be assessed by velocity measurements throughout the cardiac cycle in the subendocardium parallel to the endocardial boundary to the left ventricular cavity and in the subepicardium parallel to the epicardial boundary (time-velocity plot method). This study was designed to compare MVG obtained from the thickness-velocity plot method and from the time-velocity plot method in quantifying dobutamine-induced changes in myocardial wall motion in 8 phases of the cardiac cycle on color M-mode Doppler myocardial imaging recordings of the left ventricular posterior wall performed in 8 conscious dogs at baseline and at steady state during dobutamine infusion (10 microg/kg per minute). For both methods, MVG was considered present if its mean value was significantly different from zero and if endocardial and epicardial velocities were significantly different. There was close agreement between the 2 methods. MVG was present during the preejection period, systole, rapid ventricular filling, and atrial contraction. Dobutamine induced a significant increase in MVG during the preejection period (from 2.64 +/- 0.83 to 4.05 +/- 0.81 seconds-1 ), systole (from 2.14 +/- 0.59 to 6.08 +/- 2.20 seconds-1 in early systole, from 1.90 +/- 1.06 to 5.31 +/- 2.95 seconds-1 in mid systole, from 1.37 +/- 0.57 to 2.44 +/- 0.53 seconds-1 in end systole), and rapid ventricular filling (from 3.06 +/- 1.12 to 7.82 +/- 2.58 seconds-1 ), related to a greater rise in endocardial than in epicardial velocities. The time-velocity plot method showed that ejection and diastole were 11% and 28% decreased during dobutamine infusion, respectively, as heart rate was 31% increased. Thus according to our quantitative criteria, both MVG assessment procedures enabled objective interpretation of dobutamine effects on left ventricular wall motion. In addition, the time-velocity plot method provided automatic detection of peak velocity, timing, and duration of wall velocity changes over time.

Animals↗

Concordance between dobutamine Doppler tissue imaging echocardiography and rest reinjection thallium-201 tomography in dysfunctional hypoperfused myocardium.

OBJECTIVE: To evaluate the efficiency of the new technique colour Doppler tissue imaging (DTI) by studying the concordance between dobutamine DTI, standard grey scale echocardiography (SE), and rest-reinjection TI-201 tomography (TI) in dysfunctional myocardium. PATIENTS: 23 patients with chronic wall motion abnormalities and proven coronary artery disease (> 70% diameter stenosis of at least one major coronary artery at angiogram). METHODS: The contractile reserve and the resting perfusion characteristics of dysfunctional myocardial segments were assessed with low dose dobutamine SE and/or DTI (2.5 up to 20 gamma/kg/min) and TI on a semiquantitative basis. The DTI or SE data were separately compared with TI, on the basis of a 13 segment ventricular model. The resulting score of combined DTI and SE was also compared with TI. Finally the results obtained from DTI were compared with SE. RESULTS: A total of 142 severely hypokinetic or akinetic segments were visualised. The viability study was feasible in 127 (89%) and 121 (85%) segments with DTI and SE, respectively. TI detected viability more frequently than DTI (84 v 61, p < 0.001) and SE (80 v 50, p < 0.001). However, as many viable segments were detected with combined DTI and SE as with TI (78 v 84, NS). The kappa values between TI and SE, DTI or combined SE and DTI were 0.38, 0.45, and 0.57, respectively, and increased to 0.52 and 0.76, respectively, for SE and DTI versus TI when mid-anterior and mid-inferior segments only were considered. The kappa value between SE and DTI was 0.34. CONCLUSIONS: DTI is a helpful adjunct to SE, when using low dose dobutamine. This combination revealed as many viable segments as TI and showed a better agreement than DTI or SE alone for the assessment of myocardial viable segments evidenced by TI.

Adrenergic beta-Agonists↗

Pre-ejectional left ventricular wall motions studied on conscious dogs using Doppler myocardial imaging: relationships with indices of left ventricular function.

Duration of the pre-ejection period is a sensitive index of myocardial function. Our purpose was to document normal pre-ejectional left ventricular (LV) wall motions at rest and under dobutamine using Doppler myocardial imaging (DMI), and to correlate posterior wall velocities with indices of LV systolic function. M-mode recordings of both walls were imaged on eight conscious dogs chronically instrumented. Subendocardial pre-ejectional velocities were digitized and measured every 3.8 ms. DMI analysis consisted of sign recognition, velocity measurement, duration and timing from the Q wave of the electrocardiogram. Isovolumic contraction time (Ict) was represented by the time interval from onset to peak of the first derivative of LV pressure. Conventional Doppler labelling of velocity signs, positive toward and negative away from the transducer, was applied to the direction of encoded wall motions. For physiological understanding, wall motions of both walls were also labelled inward and outward with respect to the left ventricular cavity center. In each wall, PEP was shown as several colored strips, each strip representing the period of time that the wall was moving in one direction. Changes in velocity sign corresponding to changes in direction of motion were opposed in each wall (p < 0.001), featuring successive inward and outward wall motions. There was a markedly sustained inward motion during Ict. Its velocity amplitude increased with dobutamine. There was a positive correlation between velocities of the inward motion contemporaneous of Ict and ejection fraction (r = 0.72, p < 0.003). Values of Ict respectively drawn from DMI and from hemodynamics were also significantly correlated (r = 0.85, p < 0.007). Thus, the inward motion evidenced by DMI during Ict appears promising to assess myocardial function and effect of drugs.

Animals↗

[Doppler tissue imaging of pre-ejection left ventricular wall dynamics in normal subjects].

Pre-ejectional left ventricular wall motion has been demonstrated clinically by angiography. Intramyocardial wall velocities generated by cardiac contraction may be measured by Doppler tissue imaging. The aim of this study was to detect pre-ejectional wall motion and to analyse its sequencer. A long axis M Mode with simultaneous septal and posterior wall imaging was performed in 11 normal subjects (age 37 +/- 15 years) with velocity analysis between the electrocardiographic Q wave and the onset of ejection by digitised analysis between the electrocardiographic Q wave and the onset of ejection by digitised images with automatic velocity extraction (3.8 ms) along a horizontal subendocardial line. The total duration of the pre-ejectional periods in conventional and Doppler tissue imaging are compared. Oscillatory velocimetric appearances with alternate colours of adjacent bands in each wall and a mirror image between walls was observed. The mean and peak velocities of the first four bands were significantly different between the walls (p < 0.001) as were the absolute values between bands 2 (p < 0.02) and 3 (p < 0.006). The duration of band 2, related to motion mainly towards the center of the ventricular chamber exceeded that of the adjacent bands (septum p < 0.02, posterior wall p < 0.001). The correlation coefficient for total duration of the pre-ejectional period between Doppler tissue imaging and conventional Doppler was 0.83, p < 0.05 for the interventricular septum and 0.76, p < 0.04 for the posterior was. The authors conclude that regional pre-ejectional wall motion can be recorded. During isovolumic contraction, there is motion predominantly towards the center of the left ventricular chamber of the two walls, confirming previous angiographic findings. Its timing suggests that wall motion proceeds the increase in ventricular pressure.

Adult↗

[Contribution of doppler imaging of the myocardium to the study of cardiomyopathies].

Colour Doppler imaging (CDI) is a recent method of evaluation of cardiomyopathy based on intra-myocardial abnormalities. CDI provides quantitative assessment of myocardial wall motion both circumferential by studying the movements of the myocardium and longitudinal by studying the movements of the mitral annulus. The harmonious decrease in velocity between the endocardium and epicardium disappears in pathological conditions, showing disorganisation of wall motion within the myocardium. The decrease in the early diastolic transmural velocity gradient in patients with cardiomyopathy indicates diastolic dysfunction independent of the left ventricular systolic function. In addition, CDI is more sensitive than conventional Doppler echocardiography with grey scale because it enables earlier detection of changes induced by low-dose dobutamine, allowing distinction between trained athletes and patients with hypertrophic cardiomyopathy. The velocities of the mitral annulus help to prevent errors of interpretation of mitral blood flow as they are relatively independent on the left ventricular preload.

Cardiomegaly↗

Preejectional left ventricular wall motion in normal subjects using Doppler tissue imaging and correlation with ejection fraction.

Relations have been demonstrated between the preejection period (PEP) and indexes of left ventricular (LV) systolic function. Doppler tissue M-mode imaging has the capability to measure wall velocities and to display as colored strips within the walls velocity reversals representing changes in direction of wall motion. To document LV preejectional wall motions, this procedure was performed on 16 normal subjects with a twofold purpose: to measure septal and posterior preejectional intramyocardial velocities and durations and to correlate preejectional parameters with LV ejection fraction (LVEF). Parasternal M-mode images of simultaneously recorded walls were digitized. Subendocardial wall velocities were measured every 3.8 ms from the Q wave to the onset of ejection. Total duration measured from Doppler tissue and flow traces was compared in 10 subjects. PEP total duration did not differ between both walls or techniques. Several adjacent velocity reversals with mirror signs in opposite walls were substantiated by 2 to 5 colored strips. Colored strips corresponding to the same sign in each wall had a progressively damped velocity amplitude (septum 19 +/- 8, -21 +/- 10, 15 +/- 7, -8 +/- 5, 4 +/- 2 mm/s; posterior wall -13 +/- 16, 11 +/- 7, -8 +/- 5, 9 +/- 6, -2 mm/s). Peak velocity values of opposite signs significantly differed between both walls (p <0.0001). Absolute values differed only for colored strips 2 and 3 (p <0.009). Strip 2 featured a simultaneous early inward motion of both walls toward the LV cavity with significantly prolonged duration (p <0.0001). The only positive correlation with LVEF was found for peak velocities of strip 2 in the posterior wall (r = 0.71, p <0.006). Thus, the posterior wall and its inward motion velocities have potential for future clinical implications.

Adolescent↗

Right and left isovolumic ventricular relaxation time intervals compared in patients by means of a single-pulsed Doppler method.

Right and left isovolumic ventricular relaxation time intervals measurements were obtained as follows: from the peak R wave on the electrocardiogram to either the mitral or the tricuspid pulsed Doppler flow trace onset minus the R to end-ejection zero flow crossing of the subaortic (left side) or pulmonary (right side) D flow trace time interval. A ratio was calculated as a percent difference duration between both isovolumic ventricular relaxation time intervals. The aim was to compare isovolumic ventricular relaxation time interval values in 42 healthy controls and to study the changes induced by heart diseases in 27 patients with (1) controlled hypertension without left ventricular hypertrophy, (2) hypertrophic cardiomyopathy, and (3) Cor pulmonale. Mean values of isovolumic ventricular relaxation time intervals significantly differed at paired and unpaired studies, with right isovolumic ventricular relaxation time intervals shorter than those of the left side in all groups (p < 0.001) except for patients with Cor pulmonale. Isovolumic ventricular relaxation time intervals did not correlate with heart rate and moderately correlated with left ventricular mass and age. No significant difference was found between healthy controls and patients with controlled hypertension. Significant changes were found in patients with hypertrophic cardiomyopathy and Cor pulmonale versus healthy controls for both isovolumic ventricular relaxation time intervals. However, significant changes in the ratio were only found in patients with Cor pulmonale (p < 0.005) because of abnormal similar values for both isovolumic ventricular relaxation time intervals. This Doppler method enabled, for the first time, serial comparison of isovolumic ventricular relaxation time intervals with a homologous method. Both isovolumic ventricular relaxation time intervals significantly lengthened with age and with left ventricular indexed mass, but their ratio remained insignificantly changed except for patients with Cor pulmonale. The concomitant right and left isovolumic ventricular relaxation time intervals lengthening in patients with hypertrophic cardiomyopathy and Cor pulmonale suggests interdependence of both ventricles through the septum. This makes recommendable systematic comparison of both sides. The calculation of a ratio, free from the effect of factors intervening on isovolumic ventricular relaxation time intervals, may, in addition, be of diagnostic help.

Adolescent↗

[Myocardial Doppler tissue imaging: past, present and future].

The first Doppler spectral and pulsed tissue recordings in 1992 have given way to a new generation of machines which enable cardiologists to study mechanical events of the myocardium during the cardiac cycle by Doppler tissue imaging. This technique provides valuable information about regional function with quantitative analysis of the velocities within the myocardial wall as opposed to the global qualitative or semi-quantitative character of usual echocardiographic data. The velocity mode is the most commonly used in its three different presentations: two-dimensional, M mode and, more traditionally, pulsed spectral modes. Two-dimensional imaging gives a global view of the different myocardial segments and allows a rapid approximation of the differences of velocities between these segments and of myocardial wall thickness; however, it lacks the temporal resolution of pulsed Doppler and M mode. In addition, M mode with automatic programmes of velocity analysis has the advantage of providing a continuous spatio-temporal recording of the velocities within the myocardial wall, layer by layer. There is a physiological gradient of velocities highest at the endocardium and lowest at the epicardium. Despite the present limitations related to the Doppler principle itself, the technology, and the complexity of myocardial architecture, Doppler tissue imaging is a useful complement to information already available concerning pressures, flow and cardiac structures. The future is promising and should exceed this simple complementarity to existing ultrasound methods. Progress in the fields of ultrasound physics, technology, computerisation for acquisition of two- and three-dimensional imaging should provide a new physiopathological approach to the understanding of wall motion changes during cardiac disease.

Animals↗

Colour doppler valvar and subvalvar flow diameter imaging versus echo score in mitral stenosis: comparison with type of surgery.

OBJECTIVE: To compare the value of echo score with that of Doppler subvalvar flow broadening in deciding the type of mitral stenosis surgery. PATIENTS: 30 patients, mean age 47 years, with severe stenosis undergoing surgery were divided into two groups according to type of surgery: open heart commissurotomy (group 1, n = 12), or prosthesis (group 2, n = 18). A control group of 10 patients with prosthesis served as reference, representing mild stenosis without subvalvar connection. METHODS: For echo, the score proposed by Wilkins for cross sectional imaging was used. For Doppler, the flow diameters were measured in cm by an independent examiner from the long axis view in early diastole at two levels: (1) at the level of the stenosis (origin flow diameter), and (2) 1.5 cm downstream from the stenosis in the left ventricle (subvalvar flow diameter) with calculation of a Doppler ratio relating these two measurements, expressed as a percentage of broadening. Diagnostic value was compared for both procedures. RESULTS: There was no significant difference in age, mitral valve areas, or haemodynamics for the two groups. Mean values (SD) were: echo score: group 1, 9.83 (1.26) v group 2, 10.8 (8.1), NS; Doppler ratio %: group 1, 44 (24) v group 2, 12 (21) (P < 0.001); control group: 69 (15). The per cent diagnostic value for an open heart commissurotomy of respective cut off points was: Doppler ratio > 25% (range 71% to 87%); echo score < 10 (range 50% to 75%). CONCLUSIONS: The new Doppler ratio diagnostic value agreed better with surgical management, repair or prosthesis, in this study. Thus, it appears to better reflect the subvalvar involvement and changes in kinetics than the echo score alone. This easy Doppler method might become a routine examination for follow up of patients with open heart commissurotomy, to avoid performing repeated transoesophageal echocardiography.

Adolescent↗

Critical influence of resistance to streptogramin B-type antibiotics on activity of RP 59500 (quinupristin-dalfopristin) in experimental endocarditis due to Staphylococcus aureus.

In order to determine the microbiological and pharmacokinetic parameters that best predicted the in vivo antistaphylococcal activity of the streptogramin RP 59500 (quinupristin-dalfopristin), we evaluated the activity in rabbit aortic endocarditis of three regimens of quinupristin-dalfopristin against five strains of Staphylococcus aureus with various streptogramin B-type antibiotic resistance phenotypes and susceptible to streptogramin A-type antibiotics. Quinupristin-dalfopristin was as active as vancomycin against three strains that were susceptible to its streptogramin B component quinupristin, including one strain that was inducibly resistant to erythromycin, but had a significantly decreased activity against two strains that were resistant to quinupristin, for all quinupristin-dalfopristin regimens tested (P < 0.05). The area under the concentration-time curve for quinupristin-dalfopristin in plasma divided by the MIC of quinupristin was the only parameter retained by multilinear regression that predicted the in vivo activity of quinupristin-dalfopristin (P = 0.0001), emphasizing the importance of determining the susceptibility to quinupristin in order to predict the in vivo activity of quinupristin-dalfopristin against S. aureus.

Animals↗