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Flow Appearance

The baseline is placed in the middle of the spectral image. Filling of the left atrium and auricle during ventricular systole is displayed above the baseline (Figure 3.64). An electrocardiogram (ECG) helps identify this systolic flow. Negative flow is displayed during atrial emptying late in diastole. Sometimes there are other positive and negative flows on this spectral image so an ECG identifies the correct flow profiles to use.

Figure 3.64 Filling of the left atrium and auricle during ventricular systole is seen above the baseline (2) and coincides with the QRS complex of the electrocardiogram. Negative flow (1) is displayed during atrial emptying late in diastole coinciding with the P wave of the electrocardiogram.

Tissue Doppler Imaging

Introduction

Returning echoes are constantly bombarding the computer in the ultrasound machine. Until recently filters were in place to eliminate low frequency high amplitude information received from myocardial reflection of sound. Reflection of sound from blood is high frequency and low amplitude. Normal blood flow is typically less than 200 cm/sec while myocardial velocity of motion is usually less than 20 cm/sec. Tissue Doppler imaging (TDI) utilizes this low frequency high amplitude sound to record myocardial velocity during systole and diastole. Pulsed-wave TDI can be obtained in real time by placing a gate over a portion of myocardium and recording positive and negative frequency shifts (65– 74).

Color TDI is obtained by placing a sector of color over the myocardium and saving a video loop of information for off line analysis. After retrieving the color TDI study from computer memory, a gate is placed anywhere color was superimposed over the myocardium, and its corresponding systolic and diastolic movements are displayed. The advantage of color TDI is that the myocardial motion from the entire area of myocardium under the color sector color can be analyzed from one stored loop of video. Gates simply need to be placed over different areas of myocardium under the color sector, and motion information is displayed (Figure 3.65). Information can be displayed simultaneously from

different parts of the ventricle at the same point in the cardiac cycle.

Figure 3.65 (A) Color TDI is obtained by placing a sector of color over the myocardium and saving a video loop of information for off line analysis. This is a systolic frame with red color indicating upward movement. (B) After retrieving the color TDI study from computer memory a gate is placed anywhere color was superimposed over the myocardium and its corresponding systolic and diastolic movements are displayed. Here two gates are placed over the lateral wall of the left ventricle, and myocardial motion is displayed simultaneously from both locations on the right side of the image. (C) Two gates are placed over the lateral wall of the left ventricle on a transverse view, and myocardial motion is displayed simultaneously from both locations on the right side of the image. LV = left ventricle, RV = right ventricle, RA = right atrium, LA = left atrium, S′ = systolic motion, E′ = early diastolic motion, A′ = late diastolic motion.

Pulsed-wave TDI provides information only from one gate location in real time, and the gate must be moved to another location to interrogate any other area of the myocardium (Figure 3.66). Myocardial velocity obtained from PW TDI is usually higher than the velocities obtained off line with color TDI. This is because of better temporal resolution resulting in higher quality velocity

information.

Figure 3.66 Pulsed-wave TDI provides information from one gate location only in real time, and the gate must be moved to another location to interrogate any other area of the myocardium. Here the PW TDI gate is placed at the mitral annulus on an apical four-chamber view. Myocardial motion is displayed to the right. LV = left ventricle, LA = left atrium, S′ = systole, E′ = early diastolic motion, A′ = late diastolic motion.

Imaging Plane Used

Tissue Doppler information can be obtained from a variety of imaging planes. Longitudinal myocardial velocity is obtained from apical four-chamber views of the heart. The lateral walls of the left and right ventricular chamber or the interventricular septum are positioned on the image so that the color sector or Doppler cursor line up parallel with the length of the wall or septum (Figures 3.65, 3.66, 3.67). The loop is stored if using color TDI, and the gate can be place anywhere under the color sector at a later time. PW TDI is immediately obtained by placing the Doppler gate at any point along the wall or septum. Circumferential radial myocardial velocity can be obtained from right parasternal transverse or sagittal imaging planes (Figure 3.67).

Figure 3.67 The lateral walls of the left and right ventricular chamber or the interventricular septum are positioned on the sector so that the color sector or Doppler cursor line up parallel with the length of the wall or septum. Here the color sector is aligned with the right ventricular wall, and a PW TDI display is obtained. RV = right ventricle, RA = right atrium, LA = left atrium, S′ = systolic motion, E′ = early diastolic motion, A′ = late diastolic motion.

Tissue Doppler imaging is an option that can be added to ultrasound equipment. Theoretically, however, by manipulating the filters and changing the pulse repetition frequency, PW tissue velocity information can be obtained from equipment with-out the added option. Turn down the filter settings while in spectral Doppler mode and change the PRF (velocity range) to display low velocity flow of 20 to 30 cm/sec. Place the pulsed-wave gate over the myocardium and press the spectral display button to see the spectral image of myocardial motion under the gate.

Spectral Appearance

Place the baseline in the middle of the spectral display. Systolic contraction (S′ or Sm) (sometimes labeled Sa if the gate is placed at the annulus of an AV valve) results in a positive frequency shift. Diastolic motion of the myocardium is negative and has two phases: early diastolic motion (E′ or Em) (sometimes labeled Ea if the gate is placed at the AV annulus) and late diastolic motion secondary to the atrial contraction (A′ or Am) (sometimes labeled Aa if the gate is placed at the AV annulus) (Figures 3.65, 3.66, 3.67). Between the diastolic and systolic waves, isovolumic contraction and relaxation times can be identified. These systolic and diastolic waves are similar in appearance with slight changes in velocity whether the motion is recorded from longitudinal or circumferential fibers. Fast heart rates, just as with transmitral and trans tricuspid flows will result in superimposed E′ and A′ (Figure 3.68).

Figure 3.68 Fast heart rates, just as with transmitral and trans tricuspid flows, will result in superimposed E′ and A′ myocardial motion. S′ = systolic motion, EA′ = summated early diastolic and late diastolic motion.

References

1.Pipers F, Hamlin R. Echocardiography in the horse. JAVMA 1977;170:815–819.

2.Franklin T, Weyman A, Egenes K. A closed-chest model for cross-sectional echocardiographic study. Am J Physiol Heart Circ Physiol 1977;233:H417–H419.

3.Kerber R, Abboud F. Echocardiographic detection of regional myocardial infarction: an experimental study. Circ 1973;47:997–1005.

4.Kerber R, Abboud F, Marcus M, et al. Effect of inotropic agents on the localized dyskinesis of acutely ischemic myocardium: an experimental ultrasound study. Circ 1974;49:1038–1046.

5.Landiano S, Yellen E, Kotler M, et al. A study of the dynamic relations between the mitral valve echogram and phasic mitral flow. Circ 1975;51:104–113.

6.Bishop V, Horwitz H, Stone H, et al. Left ventricular internal diameter and cardiac function in conscious dogs. J Appl Physiol 1969;27:619–623.

7.Baylen B, Garner D, Laks M, et al. Improved echocardiographic evaluation of the closed-chest canine: methods and anatomic observations. J Clin Ultra 1980;8:335–340.

8.Mashiro I, Nelson R, Cohn J, et al. Ventricular dimensions measured noninvasively by echocardiography in the awake dog. J App Physiol 1976;41:953–959.

9.Stefan G, Bing R. Echocardiographic findings in experimental myocardial infarction of the posterior left ventricular wall. Am J Cardiol 1972;30:629–639.

10.Wyatt H, Heng M, Meerbaum S. Cross sectional echocardiography. I. Analysis of mathematical models for quantifying mass of the left ventricle in dogs. Circ 1979;60:1104–1113.

11.Dennis M, Nealeigh R, Pyle R, et al. Echocardiographic assessment of normal and abnormal valvular function in Beagle dogs. Am J Vet Res 1978;39:1591–1598.

12.Pipers F, Bonagura J, Hamlin R, et al. Echocardiographic abnormalities of the mitral valve associated with left-sided heart diseases in the dog. JAVMA 1981;179: 580–586.

13.Bonagura J, Pipers F. Echocardiographic features of pericardial effusion in dogs. JAVMA

1981;179:49–56.

14.Bonagura J, Pipers F. Echocardiographic features of aortic valve endocarditis in a dog, a cow, and a horse. JAVMA 1983;182:595–599.

15.Pipers F, Rings D, Hull B, et al. Echocardiographic diagnosis of endocarditis in a bull. JAVMA 1978;172: 1313–1316.

16.Lacuata A, Yamada H, Nakamura Y, et al. Electrocardiographic and echocardiographic findings in four cases of bovine endocarditis. JAVMA 1980;176:1355–1365.

17.Pipers F, Hamlin R, Reef V. Echocardiographic detection of cardiovascular lesions in the horse. J Eq Med Surg 1979;3:68–77.

18.Wingfield W, Miller C, Voss J, et al. Echocardiography in assessing mitral valve motion in three horses with atrial fibrillation. Eq Vet J Suppl 1980;12:181–184.

19.Okamoto Y, Hasegawa A. Studies on canine echocardiography. I. Normal pattern of echocardiogram. J Jap Vet Med Assoc 1977;30:588–594.

20.Yamada E. A basic study on echocardiography of the dog. I anatomical relationship between the heart and the direction of ultrasonic beams transmitted from the body surface. Bul Azabu Vet Coll 1978;3:225–234.

21.Boon J, Wingfield W, Miller C. Echocardiographic indices in the normal dog. Vet Rad Ultra 1983;24:214–221.

22.Pipers F, Andrysco R, Hamlin R. A totally noninvasive method for obtaining systolic time intervals in the dog. AM J Vet Res 1978;39:1822–1826.

23.Jacobs G, Mahjoob K. Multiple regression analysis, using body size and cardiac cycle length, in predicting echocardiographic variables in dogs. Am J Vet Res 1988;49: 1290–1294.

24.Lombard C. Normal values of the canine m-mode echocardiogram. Am J Vet Res 1984;45:2015– 2018.

25.Soderberg S, Boon J, Wingfield W, et al. M-mode echocardiography as a diagnostic aid for feline cardiomyopathy. Vet Rad Ultra 1983;24:66–73.

26.Allen D. Echocardiographic study of the anesthetized cat. Can J Comp Med 1982;46:115–122.

27.Allen D, Downey R. Echocardiographic assessment of cats anesthetized with xylazine-sodium pentobarbital. Can J Comp Med 1983;47:281–283.

28.Allen D, Nymeyer D. A preliminary investigation on the use of thermodilution and echocardiography as an assessment of cardiac function in the cat. Can J Comp Med 1983;47:112–117.

29.Pipers F, Hamlin R. Clinical use of echocardiography in the domestic cat. JAVMA 1980;176:57–

30.Pipers F, Reef V, Hamlin R. Echocardiography in the domestic cat. Am J Vet Res 1979;40:882–

31.Fox P, Bond B, Peterson M. Echocardiographic reference values in healthy cats sedated with ketamine hydrochloride. Am J Vet Res 1985;46:1479–1484.

32.Jacobs G, Knight D. M-mode echocardiographic measurements in nonanesthetized healthy cats: Effects of body weight, heart rate, and other variables. Am J Vet Res 1985;46:1705–1711.

33.Jacobs G, Knight D. Change in m-mode echocardiographic values in cats given ketamine. Am J Vet Res 1985;46:1712–1713.

34.O’Callaghan M. Comparison of echocardiographic and autopsy measurements of cardiac dimensions in the horse. Eq Vet J Suppl 1985;17:361–368.

35.Lombard C, Evans M, Martin L, et al. Blood Pressure, electrocardiogram and echocardiogram measurements in the growing pony foal. Equine Vet J Suppl 1984;16: 342–347.

36.Stewart J, Rose R, Barko A. Echocardiography in foals from birth to three months old. Eq Vet J Suppl 1984;16: 332–341.

37.Lescure F, Tamazali Y. Valeurs de reference en echocardiographie TM chez le cheval de sport. Rev Med Vet 1984;135:405–418.

38.Lescure F, Tamazali Y. L’echocardiographie TM le cheval: la technique. Le Point Vet 1983;15:37–

39.Pipers F, Reef V, Hamlin R, et al. Echocardiography in the bovine animal. Bov Prac 1978;13:114–

40.Pipers F, Muir W, Hamlin R. Echocardiography in swine. Am J Vet Res 1978;39:707–710.

41.Long K, Bonagura J, Darke P. Standardized imaging technique for guided m-mode and Doppler echocardiography in the horse. Eq Vet J 1992;24:226–235.

42.Stadler P, Weinberger T, Deegen E. Pulsed Doppler echocardiography in healthy warm blooded horses. J Vet Med A 1993;40:757–778.

43.Reef V, Lalezari K, De Boo J, et al. Pulsed-wave Doppler evaluation of intracardiac blood flow in

30clinically normal Standardbred horses. Am J Vet Res 1989;50:75–83.

44.Long K. Doppler echocardiography in the horse. Eq Vet Ed 1990;2:15–17.

45.Brown D, Knight D, King R. Use of pulsed-wave Doppler echocardiography to determine aortic and pulmonary velocity and flow variables in clinically normal dogs. Am J Vet Res 1991;52:543–550.

46.Yuill C, O’Grady M. Doppler-derived velocity of blood flow across the cardiac valves in the normal dog. Can J Vet Res 1991;55:185–192.

47.Darke P, Bonagura J, Miller M. Transducer orientation for Doppler echocardiography in dogs. J Sm An Prac 1993;34:2–8.

48.Gaber C. Normal pulsed wave Doppler flow velocities in adult dogs. Proc 5th ACVIM 1987:923.

49.Kirberger R, Bland-van den Berg P, Darazs B. Doppler echocardiography in the normal dog: Part I, Velocity findings and flow patterns. Vet Rad Ultra 1992;33:370–379.

50.Kirberger R, Bland-van den Berg P, Grimbeek R. Doppler echocardiography in the normal dog: Part II, Factors influencing blood flow velocities and a comparison between left and right heart blood flow. Vet Rad Ultra 1992;33:380–386.

51.Darke P. An evaluation of transducer sites for measurement of aortic and pulmonary flows by Doppler echocardiography. Proc 9th ACVIM 1991:703–705.

52.Darke P. Two-dimensional imaging for Doppler echocardiography in dogs. Proc 8th ACVIM 1990:261–268.

53.Kirberger R. Pulsed wave Doppler echocardiographic evaluation of intracardiac blood flow in normal sheep. Res Vet Sci 1993;55:189–194.

54.Lusk R, Ettinger S. Echocardiographic techniques in the dog and cat. J Am An Hosp Assoc 1990;26:473–488.

55.Bonagura JD. Echocardiography. J AM Vet Med Assoc 1994;204:516–522.

56.Miller M, Knauer K, Herring D. Echocardiography: principles of interpretation. Seminars Vet Med Surg (Sm Am) 1989;4:58–76.

57.Sisson D, Schaeffer D. Changes in linear dimensions of the heart, relative to body weight, as measured by m-mode echocardiography in growing dogs. Am J Vet Res 1991;52:1591–1596.

58.Reef V. Echocardiographic examination in the horse: the basics. Compendium 1990;12:1312–1320.

59.Gaber C. Normal pulsed Doppler flow velocities in adult dogs. Proc 5th ACVIM 1987:923.

60.Schober KE, Fuentes VL. Effects of age, body weight, and heart rate on transmitral and pulmonary venous flow in clinically normal dogs. American Journal of Veterinary Research 2001;62:1447–1454.

61.Schober KE, Luis Fuentes V, McEwan JD, et al. Pulmonary venous flow characteristics as assessed by transthoracic pulsed Doppler echocardiography in normal dogs. Vet Radiol Ultrasound 1998;39:33–41.

62.Rivas-Gotz C, Khoury DS, Manolios M, et al. Time interval between onset of mitral inflow and onset of early diastolic velocity by tissue Doppler: a novel index of left ventricular relaxation: experimental studies and clinical application. J Am Coll Cardiol 2003;42:1463–1470.

63.Hirota Y. A clinical study of left ventricular relaxation. Circ 1980;62:756–763.

64.Schober KE, Maerz I. Doppler echocardiographic assessment of left atrial appendage flow velocities in normal cats. Journal of Veterinary Cardiology 2005;7:15–25.

65.Chetboul V. Tissue Doppler imaging: a promising technique for quantifying regional myocardial function. J Vet Cardiol 2002;4:7.

66.Chetboul V, Athanassiadis N, Carlos C, et al. Assessment of repeatability, reproducibility, and effect of anesthesia on determination of radial and longitudinal left ventricular velocities via tissue Doppler imaging in dogs. American Journal of Veterinary Research 2004;65: 909–915.

67.Chetboul V, Athanassiadis N, Carlos C, et al. Quantification, repeatability, and reproducibility of feline radial and longitudinal left ventricular velocities by tissue Doppler imaging. Am J Vet Res 2004;65: 566–572.

68.Chetboul V, Gouni V, Sampedrano CC, et al. Assessment of regional systolic and diastolic myocardial function using tissue Doppler and strain imaging in dogs with dilated cardiomyopathy. J Vet Intern Med 2007;21: 719–730.

69.Chetboul V, Sampedrano CC, Concordet D, et al. Use of quantitative two-dimensional color tissue Doppler imaging for assessment of left ventricular radial and longitudinal myocardial velocities in dogs. American Journal of Veterinary Research 2005;66:953–961.

70.Chetboul V, Sampedrano CC, Tissier R, et al. Quantitative assessment of velocities of the annulus of the left atrioventricular valve and left ventricular free wall in healthy cats by use of twodimensional color tissue Doppler imaging. American Journal of Veterinary Research 2006;67: 250–

71.Koffas H, Dukes-McEwan J, Corcoran M, et al. Pulsed tissue Doppler imaging in normal cats and cats with hypertrophic cardiomyopathy. Journal of Veterinary Internal Medicine 2006;20:65–77.

72.Hori Y, Sato S, Hoshi F, et al. Assessment of longitudinal tissue Doppler imaging of the left ventricular septum and free wall as an indicator of left ventricular systolic function in dogs. Am J Vet Res 2007;68: 1051–1057.

73.Sengupta P, Mohan JC, Pandian NG. Tissue Doppler echocardiography. Ind Heart J 2002;54:1.

74. Yu CM, Sanderson JE, Marwick TH, et al. Tissue Doppler imaging a new prognosticator for cardiovascular diseases. J Am Coll Cardiol 2007;49:1903–1914.