'My' p6 Searchterm 'My' found in 42 articles 5 terms [ • ] - 37 definitions [• ] Result Pages : •
From Philips Medical Systems; 'The HDI 4000 system brings the track record of our patented High Definition Imaging to your lab, along with 4D imaging technology and new, innovative data management tools. Premium features create images of exceptional clarity, aiding in the visualization of subtle anatomy and pathology. This blend of features never before offered on a system in this price range, combined with superb image quality, makes the HDI 4000 the best choice in its category.' Specifications for this system will be available soon. •
Harmonic B-mode imaging takes advantage of the non-linear oscillation
of microbubbles. During harmonic imaging, the sound signal is transmitted at a frequency of around 1.5 to 2.0 MHz and received at twice this frequency. The microbubbles also reflect waves with wavelengths different from the transmitted one, the detectors can be set to receive only the latter ones and create only images of the contrast agent. Using bandpass filters the transmitted frequency is separated from the received signal to get improved visualization of vessels containing ultrasound contrast agents (USCAs). The signal to noise ratio during the presence of microbubbles in tissue is four- to fivefold higher at the harmonic compared with the basic frequency. Using harmonic B-mode imaging, harmonic frequencies produced by the ultrasound propagation through tissue have to be taken into account. The tissue reflection produces only a small amount harmonic energy compared to USCAs, but has to be removed by background subtraction for quantitative evaluation of myocardial perfusion. See also Non-linear Propagation. •
The earliest introduction of vascular ultrasound contrast agents (USCA) was by Gramiak and Shah in 1968, when they injected agitated saline into the ascending aorta and cardiac chambers during echocardiographic to opacify the left heart chamber. Strong echoes were produced within the heart, due to the acoustic mismatch between free air microbubbles in the saline and the surrounding blood. The disadvantage of this microbubbles produced by agitation, was that the air quickly leak from the thin bubble shell into the blood, where it dissolved. In addition, the small bubbles that were capable of traversing the capillary bed did not survive long enough for imaging because the air quickly dissipated into the blood. Aside from agitated saline, also hydrogen peroxide, indocyanine green dye, and iodinated contrast has been tested. The commercial development of contrast agents began in the 1980s with greatest effort to the stabilization of small microbubbles. The development generations by now:
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first generation USCA = non-transpulmonary vascular;;
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second generation USCA = transpulmonary vascular, with short half-life (less than 5 min);
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third generation USCA = transpulmonary vascular, with longer half-life (greater than 5 min).
To pass through the lung capillaries and enter into the systemic circulation, microspheres should be less than 10 μm in diameter. Air bubbles in that size range persist in solution for only a short time; too short for systemic vascular use. The first developed agent was Echovist (1982), which enabled the enhancement of the right heart. The second generation of echogenic agents, sonicated 5% human albumin-containing air bubbles (Albunex), were capable of transpulmonary passage but often failed to produce adequate imaging of the left heart. Both Albunex and Levovist utilize air as the gas component of the microbubble. In the 1990s newer developed agents with fluorocarbon gases and albumin, surfactant, lipid, or polymer shells have an increased persistence of the microspheres. This smaller, more stable microbubble agents, and improvements in ultrasound technology, have resulted in a wider range of application including myocardial perfusion. See also First Generation USCA, Second Generation USCA, and Third Generation USCA. Further Reading: Basics:
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M-mode (Motion-mode) ultrasound shows the motion of cardiac structures. M-mode echocardiography records the amplitude and rate of motion of a moving structure in real time by repeatedly measuring the distance of the object from the single transducer at a given moment. The single sound beam is transmitted and reflected signals are displayed as dots of varying intensities, creating lines across the screen. It yields a one-dimensional image, sometimes called an 'ice pick' view of the heart. M-mode echocardiography is used to detect valvulopathies (calcifications, etc.) and cardiomyopathies (dyskinesis, aneurysm, etc.). See also Bicycle Stress Echocardiography, Transthoracic Echocardiography, and Transesophageal Echocardiography. Further Reading: News & More: •
MRX 115 is a liposome based microbubble formulation and has been demonstrated as effective for cardiac blood pool imaging, Doppler enhancement and potentially myocardial perfusion imaging. MRX 115 is based upon the demand for a stable, robust blood pool ultrasound contrast agents, also called DMP 115 or Aerosomes™ (ImaRx LLC) and now Definity®. Result Pages : |