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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: Clinical 3D stack-of-spirals PRFS thermometry enables feasible volumetric and spatial estimation during hepatic MWA, though residual deviations remain. Central slices approach clinically relevant precision despite susceptibility effects. Targeted correction strategies and faster reconstruction may enable reliable real-time thermometry for guiding and validating thermal therapies in the abdomen.
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CONCLUSION: FLORET-UTE enables quantitative 3-D MR thermometry of frozen tissue with < 20 s temporal resolution and < 2°C accuracy, overcoming the speed limitations of earlier UTE methods. The technique is a promising candidate for real-time MR-guided cryoablation and warrants in vivo evaluation.
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CONCLUSION: FLORET-UTE enables quantitative 3-D MR thermometry of frozen tissue with < 20 s temporal resolution and < 2°C accuracy, overcoming the speed limitations of earlier UTE methods. The technique is a promising candidate for real-time MR-guided cryoablation and warrants in vivo evaluation.
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CONCLUSION: FLORET-UTE enables quantitative 3-D MR thermometry of frozen tissue with < 20 s temporal resolution and < 2°C accuracy, overcoming the speed limitations of earlier UTE methods. The technique is a promising candidate for real-time MR-guided cryoablation and warrants in vivo evaluation.