System to monitor and manage patient hydration via plethysmograph variablity index in response to the passive leg raising

A patient monitoring device for determining fluid responsiveness of a patient, the patient monitoring device comprising:

• one or more of non-invasive physiological sensors configured to obtain physiological information from the patient, and further configured to emit light towards a tissue site of a patient, and detect the light after it has interacted with the tissue site, and generate a sensor signal based at least in part on the detected light;
• a sensor interface configured to receive the sensor signal from the one or more non-invasive physiological sensors;
• and
• a processor in communication with the sensor interface and configured to:
• automatically determine a plethysmograph variability parameter associated with a plethysmograph waveform corresponding to the sensor signal, wherein the plethysmograph waveform comprises a plurality of pulses corresponding to pulsatile blood flow within the tissue site, wherein the plethysmograph variability parameter corresponds to a value associated with a pleth variability index (PVI) and quantifies variations in the plethysmograph waveform,
• determine a first prediction of fluid responsiveness based at least in part on the plethysmograph variability parameter,
• determine a first confidence value associated with the first prediction of fluid responsiveness based on a value of the plethysmograph variability parameter,
• send a control signal to cause a bed of the patient to move in order to cause a change in elevation of one or more limbs of the patient,
• determine a second prediction of fluid responsiveness based at least in part on a fluid responsiveness parameter that is associated with an elevation of the one or more limbs of the patient that is associated with a passive leg raising (PLR) test,
• determine a second confidence value associated with the second prediction of fluid responsiveness based on a change in the fluid responsiveness parameter,
• output an indication of fluid responsiveness of the patient based at least in part on the first confidence value, the second confidence value, the first prediction of fluid responsiveness, and the second prediction of fluid responsiveness, and
• cause an action, based on the fluid responsiveness of the patient, related to administration of fluid to the patient.