- #1
HeartEcho
- 2
- 0
Hi all,
I work as a cardiac sonographer. I've been struggling to understand a concept as dictated in ultrasound textbooks and it regards the Nyquist limit.
During my work I observed that when I increased my ultrasound transducer frequency (e.g. from 1.7 MHz to 3.0 MHz) when using pulsed wave Doppler at a given depth, the maximal detectable velocity (i.e. Doppler shift) decreased; and vice versa.
The textbooks state that the maximal Doppler shift that can accurately be determined is based on the Nyquist limit (i.e. half the sample rate of a discrete signal processing system). I understand this concept. What I do not understand is why, in the case of pulse wave Doppler ultrasound, the Nyquist limit is determined by the PRF (pulsed repetition frequency): the Nyquist limit is half the PRF.
Why can't the ultrasound machine simply generate an initial pulse, followed by a time delay to estimate depth, and then very rapidly sample the returning pulse (i.e. pizoelectric crystal voltage changes). Would this not be independent of the pulse transmit/recieve frequency (i.e. PRF). Can some one please highlight what I am missing here? Any help would be greatly appreciated. thanks
I work as a cardiac sonographer. I've been struggling to understand a concept as dictated in ultrasound textbooks and it regards the Nyquist limit.
During my work I observed that when I increased my ultrasound transducer frequency (e.g. from 1.7 MHz to 3.0 MHz) when using pulsed wave Doppler at a given depth, the maximal detectable velocity (i.e. Doppler shift) decreased; and vice versa.
The textbooks state that the maximal Doppler shift that can accurately be determined is based on the Nyquist limit (i.e. half the sample rate of a discrete signal processing system). I understand this concept. What I do not understand is why, in the case of pulse wave Doppler ultrasound, the Nyquist limit is determined by the PRF (pulsed repetition frequency): the Nyquist limit is half the PRF.
Why can't the ultrasound machine simply generate an initial pulse, followed by a time delay to estimate depth, and then very rapidly sample the returning pulse (i.e. pizoelectric crystal voltage changes). Would this not be independent of the pulse transmit/recieve frequency (i.e. PRF). Can some one please highlight what I am missing here? Any help would be greatly appreciated. thanks
Last edited by a moderator: