2016
DOI: 10.1109/tuffc.2015.2502987
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Safety Assessment of Advanced Imaging Sequences I: Measurements

Abstract: Abstract-A method for rapid measurement of intensities (I spta ), mechanical index (MI), and probe surface temperature for any ultrasound scanning sequence is presented. It uses the scanner's sampling capability to give an accurate measurement of the whole imaging sequence for all emissions to yield the true distributions. The method is several orders of magnitude faster than approaches using an oscilloscope, and it also facilitates validating the emitted pressure field and the scanner's emission sequence soft… Show more

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Cited by 24 publications
(18 citation statements)
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“…21 These limits concern the mechanical index, M I ≤ 1.9, the derated spatial-peak-temporal-average intensity, I spta ≤ 720 mW/cm 2 . The measured values using the scheme described by Jensen,22 are M I = 0.62 and a I spta = 106.8 mW/cm 2 , which are both below the FDA limits. The transducer surface temperature was also tested, where the transducer surface did not exceeded an increase of 30…”
Section: In-vivomentioning
confidence: 72%
“…21 These limits concern the mechanical index, M I ≤ 1.9, the derated spatial-peak-temporal-average intensity, I spta ≤ 720 mW/cm 2 . The measured values using the scheme described by Jensen,22 are M I = 0.62 and a I spta = 106.8 mW/cm 2 , which are both below the FDA limits. The transducer surface temperature was also tested, where the transducer surface did not exceeded an increase of 30…”
Section: In-vivomentioning
confidence: 72%
“…The transmit pressure measurements of the lens was carried out using an AIMS III intensity measurement system (Onda Corporation, Sunnyvale, California, USA) connected to the experimental research scanner SARUS [13], [14]. The OptiSon ultrasound beam analyzer (Onda Corporation, Sunnyvale, California, USA) was used to validate the diverging properties of the lens in a water tank.…”
Section: Methodsmentioning
confidence: 99%
“…Content may change prior to final publication. Before starting the clinical trials, measures are conducted to adjust the transmit levels such that intensities and temperature constraints are obeyed [43]- [46]. Once parameters of the two competing methods are fixed, a few in-vivo measurements are obtained to study the preliminary efficacy.…”
Section: A Phase I: Demonstration Of Prototypementioning
confidence: 99%