Investigation of a pulse compression technique for medical ultrasound : a simulation study

Pulse compression techniques that are capable of producing a large signal-to-noise (SNR) enhancement, have been used successfully in many different fields. For medical applications, frequency-dependent attenuation in soft tissue can limit the usefulness of this method. In the paper, this issue is ex...

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Veröffentlicht in:Medical & biological engineering & computing 1994-03, Vol.32 (2), p.181-188
1. Verfasser: RAO, N. A. H. K
Format: Artikel
Sprache:eng
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Zusammenfassung:Pulse compression techniques that are capable of producing a large signal-to-noise (SNR) enhancement, have been used successfully in many different fields. For medical applications, frequency-dependent attenuation in soft tissue can limit the usefulness of this method. In the paper, this issue is examined through model-simulation studies. Frequency-modulation (FM) chirp, considered in the study, is just one form of pulse coding technique. Pulse propagation effects in soft tissue are modelled as a linear zero phase filter. A method to perform simulations and estimate the effective time-bandwidth product K is outlined. K describes the SNR enhancement attainable under limitations imposed by the soft-tissue medium. An effective time-bandwidth product is evaluated as a function of soft-tissue linear attenuation coefficient alpha o, scatterer depth z and the bandwidth of the interrogating FM pulse, under realistic conditions. Results indicate that, under certain conditions, K can be significantly lower than its expected value in a non-attenuating medium. It is argued that although limitations exist, pulse compression techniques can still be used to improve resolution or increase penetrational depth. The real advantage over conventional short-pulse imaging comes from the possibility that these improvements can be accomplished without increasing the peak intensity of the interrogating pulse above any threshold levels set by possible bio-effect considerations.
ISSN:0140-0118
1741-0444
DOI:10.1007/bf02518916