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Echocardiographic “smoke” is produced by an interaction of erythrocytes and plasma proteins modulated by shear forces FREE

Alvaro Merino, MD, PhD; Paul Hauptman, MD; Lina Badimon, PhD; Juan Jose Badimon, PhD; Marc Cohen, MD, FACC; Valentin Fuster, MD, PhD, FACC; Martin Goldman, MD, FACC
[+] Author Information

Dr. Merino is the recipient of a NIH-Fogarty International Fellowship Award from the National Institutes of Health, Bethesda, Maryland.

Dr. Badimon is an Investigator of the Consejo Superior de Investigaciones Cientificas (National Research Council of Spain, Madrid, Spain).

This study was supported in part by Grant HL39840 from the National Heart, Lung, and Blood Institute, National Institutes of Health. It was presented in part at the 64th Annual Scientific Session of the American Heart Association, Anaheim, California, November 1991.Address for correspondence: Alvaro Merino, MD, Division of Cardiology, Box 1030, The Mount Sinai Medical Center, One Gustave L. Levy Place, New York, New York 10029.

J Am Coll Cardiol. 1992;20(7):1661-1668. doi:10.1016/0735-1097(92)90463-W
Published online

  Objectives. This study was designed to determine the blood elements responsible for spontaneous echocardiographic contrast.Background. Spontaneous contrast or “smoke” is an echocardiographic image usually found in low flow conditions. Two blood elements, erythrocytes and platelets, have been related to the generation of smoke.Methods. The echogenicity of percine blood products was assessed in static and flow conditions and was graded on a digitized videodensity computer program that assigned a score of 0 for black and 100 for white images. Blood elements were circulated from a small tube (4-mm diameter) into a larger cylindric chamber (30-mm diameter) under controlled flow rate conditions. The following blood products were studied: whole blood, platelet-depleted blood, platelet-rich plasma, platelet-poor plasma, erythrocytes suspended in saline solution, adenosine dipbosphate (ADP) added to platelet-rich plasma, and saline solution as a control medium.Results. As blood flow was increased in 30 ml/min increments from 0 to 180 ml/min, whole blood echo videodensity (scale 0 to 100) progressively decreased in the larger tube from 38 and 42 to 20, 12, 14, 16 and 14, respectively. When flow increased from 0 to 30 ml/min in the smaller tube, corresponding to a wall shear rate of 0 to 80 s−1, the blood entering the chamber was completely echolucent. The echogenicity of blood products in the larger tube was for static flow (0 ml/min) and high flow (180 ml/min), respectively: platelet-depleted blood = 36 and 14; platelet-rich plasma = 2 and 2; platelet-poor plasma = 0 and 0; erythrocytes in saline solution = 8 and 12; ADP added to platelet-rich plasma = 0 and 15; saline solution = 0 and 0. Because platelets alone were nonechogenic but platetet-depleted blood produced a flow-dependent echogenicity similar to that produced by whole blood, platelets may not be involved in the production of smoke. However, when platelets were aggregated by ADP, they were echogenic but in dense clumps and in a flow-independent pattern not typical of the smokelike images. Erythrocytes suspended in saline solution had an intermediate density image.Conclusions. Echogenic smoke appears to be due primarily to the interection of red blood cells and plasma proteins at low flow and low shear rate conditions.

References

Black  IW, Hopkins  AP, Lee  LCL, Walsh  WF; Left atrial spontaneous echo contrast: a clinical and echocardiographical analysis. J Am Coll Cardiol. 18 1991:398-404.
CrossRef | PubMed
Beppu  S, Nimura  Y, Sakakihara  H, Negata  S, Park  Y, Izami  S; Smoke-like echo in the left atrial cavity in mitral valve disease: its features and significance. J Am Coll Cardiol. 6 1985:744-749.
CrossRef | PubMed
Iliceto  S, Antonelli  G, Sorino  M, Biasco  G, Rizzon  P; Dynamic intracavitary left atrial echoes in mitral stenosis. Am J Cardiol. 55 1985:603-606.
CrossRef | PubMed
Daniel  WG, Nellessen  U, Schroeder  E; Left atrial spontaneous echo contrast in mitral valve disease: an indicator for an increased thomboembolic risk. J Am Coll Cardiol. 11 1988:1204-1211.
CrossRef | PubMed
Castello  R, Pearson  AC, Labovitz  AJ; Prevalence and clinical implications of atrial spontaneous contrast in patients undergoing transesophageal echocardiography. Am J Cardiol. 65 1990:1149-1153.
CrossRef | PubMed
Asinger  RW, Mikell  FL, Elsperger  J, Hodges  M; Incidence of left-ventricular thrombosis after acute transmural myocardial infarction. Serial evaluation by two-dimensional echocardiography. N Engl J Med. 305 1981:297-302.
CrossRef | PubMed
Mikell  FL, Asinger  RW, Elsperger  KJ, Anderson  WR, Hodges  M; Regional stasis of blood in the dysfunctional left ventricle: echocardiographic detection and differentiation from early thrombosis. Circulation. 66 1982:755-763.
CrossRef | PubMed
Wolverson  ME, Nouri  S, Joist  JH, Sundaram  M, Heiberg  F; The direct visualization of blood flow by real time ultrasound: clinical observations and underlying mechanisms. Radiology. 140 1981:443-448.
PubMed
Sigel  B, Coelho  JCU, Spigos  DG; Ultrasonography of blood during stasis and coagulation. Invest Radiol. 16 1981:71-76.
CrossRef | PubMed
Mahony  C, Sublett  KL, Harrison  MR; Resolution of spontaneous contrast with platelet disaggregatory therapy (trifluoperazine). Am J Cardiol. 63 1989:1009-1010.
CrossRef | PubMed
Mahony  C, Evans  JM, Spain  C; Spontaneous contrast and circulating placelets (abstr). Circulation. 80 (suppl II) 1990:II-1.
Pollick  C, Taylor  D; Assessment of left atrial appendage function by transesophegeal echocardiography. Implications for the development of thrombus. Circulation. 84 1991:223-231.
CrossRef | PubMed
Filly  RA, Sommer  FG, Minton  MJ; Characterization of biological fluids by ultrasound and computed tomography. Radiology. 134 1980:167-171.
PubMed
Loeb  WF, Bannerman  RM, Rininger  BF, Johnson  AJ; Hematologic Disorders.Benirschke  K, Garner  FM, Jones  TC; Pathology of Laboratory Animals. 1978 Springer Verlag New York:889-1032.
Wickham  LL, Bauersachs  RM, Wenby  RB, Sowemimo-Coker  S, Meisclman  HJ, Elsner  R; Red cell aggregation and viscoelasticity of blood from seals, swine and man. Biorheology. 27 1990:191-204.
PubMed
Merrill  EW; Rheology of blood. Physiol Rev. 49 1969:863-868.
PubMed
Levich  VG; Physiocochemical Hydrodynamics. 1962 Prentice-Hall Englewood Cliffs, NJ
Bird  RB, Steward  WE, Lightfoot  EN; Transport Phenomena. 1960 John Wiley & Sons New York:42-47.
Sigel  B, Machi  J, Beitler  JC, Justin  JR, Coelho  JC; Variable ultrasound echogenicity in flowing blood. Science. 218 1982:1321-1323.
CrossRef | PubMed
Yuan  YW, Shung  KK; Ultrasonic back scatter from flowing whole blood. I: Dependence on shear rate and hematocrit. J Acoust Soc Am. 84 1988:52-58.
CrossRef | PubMed
Chien  S, Dormendy  J, Ernst  E, Matroi  A; Rheology of Blood Cells.Chien  S; Clinical Hemorheology. 1987 Martinus Nijhoff Dordrecht, The Netherlands:87-91.
Fabry  TL; Mechanism of erythrocyte aggregation and sedimentation. Blood. 70 1987:1572-1576.
PubMed
Yuan  YW, Shung  KK; Ultrasonic back scatter from flowing whole blood. II: Dependence on frequency and fibrinogen concentration. J Acoust Soc Am. 84 1988:1195-1200.
CrossRef | PubMed

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References

Black  IW, Hopkins  AP, Lee  LCL, Walsh  WF; Left atrial spontaneous echo contrast: a clinical and echocardiographical analysis. J Am Coll Cardiol. 18 1991:398-404.
CrossRef | PubMed
Beppu  S, Nimura  Y, Sakakihara  H, Negata  S, Park  Y, Izami  S; Smoke-like echo in the left atrial cavity in mitral valve disease: its features and significance. J Am Coll Cardiol. 6 1985:744-749.
CrossRef | PubMed
Iliceto  S, Antonelli  G, Sorino  M, Biasco  G, Rizzon  P; Dynamic intracavitary left atrial echoes in mitral stenosis. Am J Cardiol. 55 1985:603-606.
CrossRef | PubMed
Daniel  WG, Nellessen  U, Schroeder  E; Left atrial spontaneous echo contrast in mitral valve disease: an indicator for an increased thomboembolic risk. J Am Coll Cardiol. 11 1988:1204-1211.
CrossRef | PubMed
Castello  R, Pearson  AC, Labovitz  AJ; Prevalence and clinical implications of atrial spontaneous contrast in patients undergoing transesophageal echocardiography. Am J Cardiol. 65 1990:1149-1153.
CrossRef | PubMed
Asinger  RW, Mikell  FL, Elsperger  J, Hodges  M; Incidence of left-ventricular thrombosis after acute transmural myocardial infarction. Serial evaluation by two-dimensional echocardiography. N Engl J Med. 305 1981:297-302.
CrossRef | PubMed
Mikell  FL, Asinger  RW, Elsperger  KJ, Anderson  WR, Hodges  M; Regional stasis of blood in the dysfunctional left ventricle: echocardiographic detection and differentiation from early thrombosis. Circulation. 66 1982:755-763.
CrossRef | PubMed
Wolverson  ME, Nouri  S, Joist  JH, Sundaram  M, Heiberg  F; The direct visualization of blood flow by real time ultrasound: clinical observations and underlying mechanisms. Radiology. 140 1981:443-448.
PubMed
Sigel  B, Coelho  JCU, Spigos  DG; Ultrasonography of blood during stasis and coagulation. Invest Radiol. 16 1981:71-76.
CrossRef | PubMed
Mahony  C, Sublett  KL, Harrison  MR; Resolution of spontaneous contrast with platelet disaggregatory therapy (trifluoperazine). Am J Cardiol. 63 1989:1009-1010.
CrossRef | PubMed
Mahony  C, Evans  JM, Spain  C; Spontaneous contrast and circulating placelets (abstr). Circulation. 80 (suppl II) 1990:II-1.
Pollick  C, Taylor  D; Assessment of left atrial appendage function by transesophegeal echocardiography. Implications for the development of thrombus. Circulation. 84 1991:223-231.
CrossRef | PubMed
Filly  RA, Sommer  FG, Minton  MJ; Characterization of biological fluids by ultrasound and computed tomography. Radiology. 134 1980:167-171.
PubMed
Loeb  WF, Bannerman  RM, Rininger  BF, Johnson  AJ; Hematologic Disorders.Benirschke  K, Garner  FM, Jones  TC; Pathology of Laboratory Animals. 1978 Springer Verlag New York:889-1032.
Wickham  LL, Bauersachs  RM, Wenby  RB, Sowemimo-Coker  S, Meisclman  HJ, Elsner  R; Red cell aggregation and viscoelasticity of blood from seals, swine and man. Biorheology. 27 1990:191-204.
PubMed
Merrill  EW; Rheology of blood. Physiol Rev. 49 1969:863-868.
PubMed
Levich  VG; Physiocochemical Hydrodynamics. 1962 Prentice-Hall Englewood Cliffs, NJ
Bird  RB, Steward  WE, Lightfoot  EN; Transport Phenomena. 1960 John Wiley & Sons New York:42-47.
Sigel  B, Machi  J, Beitler  JC, Justin  JR, Coelho  JC; Variable ultrasound echogenicity in flowing blood. Science. 218 1982:1321-1323.
CrossRef | PubMed
Yuan  YW, Shung  KK; Ultrasonic back scatter from flowing whole blood. I: Dependence on shear rate and hematocrit. J Acoust Soc Am. 84 1988:52-58.
CrossRef | PubMed
Chien  S, Dormendy  J, Ernst  E, Matroi  A; Rheology of Blood Cells.Chien  S; Clinical Hemorheology. 1987 Martinus Nijhoff Dordrecht, The Netherlands:87-91.
Fabry  TL; Mechanism of erythrocyte aggregation and sedimentation. Blood. 70 1987:1572-1576.
PubMed
Yuan  YW, Shung  KK; Ultrasonic back scatter from flowing whole blood. II: Dependence on frequency and fibrinogen concentration. J Acoust Soc Am. 84 1988:1195-1200.
CrossRef | PubMed

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