| CPC A61M 60/50 (2021.01) [A61B 5/00 (2013.01); A61M 60/135 (2021.01); A61M 60/139 (2021.01); A61M 60/178 (2021.01); A61M 60/216 (2021.01); A61M 60/422 (2021.01); A61M 60/531 (2021.01); A61M 60/538 (2021.01); A61M 60/585 (2021.01); A61M 60/816 (2021.01); A61M 60/857 (2021.01); G16H 20/17 (2018.01); G16H 20/40 (2018.01); G16H 50/00 (2018.01); G16H 50/20 (2018.01); A61M 60/148 (2021.01); A61M 60/205 (2021.01); A61M 2205/04 (2013.01); A61M 2205/18 (2013.01); A61M 2205/3303 (2013.01); A61M 2205/3365 (2013.01); A61M 2205/50 (2013.01); A61M 2205/502 (2013.01); A61M 2205/52 (2013.01); A61M 2205/584 (2013.01); A61M 2230/06 (2013.01); A61M 2230/20 (2013.01); A61M 2230/208 (2013.01); A61M 2230/30 (2013.01); A61M 2230/43 (2013.01); G06N 5/045 (2013.01); G06N 20/00 (2019.01)] | 20 Claims |

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1. A method comprising:
acquiring, from an intravascular heart pump system, first data related to time-varying parameters of the heart pump system;
extracting an average left ventricular pressure (LVP) maximum level and an average placement level from the first data, wherein the average placement level is an average aortic pressure or an average differential pressure;
determining, using a prediction model and based on the average LVP maximum level and the average placement level, a prediction value of patient outcome; and
operating the intravascular heart pump system based on the determined prediction value of patient outcome.
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