Aortic flow meter and pump for partial-aortic occlusion
Systems and methods for partial aortic occlusion are provided. The system may include a catheter having an expandable aortic blood flow regulation device disposed on the distal end of the catheter for placement within an aorta of a patient, and a catheter controller unit that causes the device to expand and contract to restrict blood flow through the aorta. The system also may include sensors for measuring blood pressure distal and proximal to the expandable device. The system further may include non-transitory computer readable media having instructions stored thereon, wherein the instructions, when executed by a processor coupled to the sensors, cause the processor to estimate aortic blood flow based on the measured blood pressures and corresponding waveforms, compare the estimated aortic blood flow with a target aortic blood flow range, generate an alert if the estimated aortic blood flow falls outside the target aortic blood flow range, and cause the catheter controller unit to adjust expansion and contraction of the expandable device to adjust an amount of blood flow through the aorta if the estimated aortic blood flow falls outside the target aortic blood flow range.
1. A controller unit for automating expansion and contraction of an expandable blood flow regulation device, the expandable blood flow regulation device disposed at a distal region of a catheter, the controller unit comprising:
a pump in fluid communication with the expandable blood flow regulation device via the catheter, the pump configured to expand and contract the expandable blood flow regulation device;
a processor operatively coupled to one or more sensors and configured to:
receive physiological information from the one or more sensors;
compare the physiological information from the one or more sensors with a target physiological range;
calculate a dynamic scaling factor;
calculate a bolus volume based at least in part on the dynamic scaling factor; and
cause the pump to adjust expansion or contraction of the expandable blood flow regulation device by the bolus volume to adjust an amount of blood flow through a vessel if the physiological information from at least one of the one or more sensors falls outside the target physiological range.
2. The controller unit of claim 1 , wherein the expandable blood flow regulation device comprises a balloon configured to be inflated to expand to restrict blood flow through the vessel, and wherein the pump is configured to inflate or deflate the balloon to adjust the amount of blood flow through the vessel if the physiological information from at least one of the one or more sensors falls outside the target physiological range.
3. The controller unit of claim 2 , wherein the pump is configured to inflate or deflate the balloon by delivering bolus volumes as small as 1 microliters.
4. The controller unit of claim 2 , wherein the pump is configured to inflate or deflate the balloon by delivering bolus volumes between 1 and 50 microliters.
5. The controller unit of claim 2 , wherein the pump is configured to inflate or deflate the balloon via a stepper motor coupled to the processor.
6. The controller unit of claim 5 , wherein the pump is a syringe pump.
7. The controller unit of claim 1 , wherein the pump is configured to automatically adjust expansion or contraction of the expandable blood flow regulation device to adjust the amount of blood flow through the vessel if the physiological information from at least one of the one or more sensors falls outside the target physiological range.
8. The controller unit of claim 1 , wherein the pump is configured to adjust expansion or contraction of the expandable blood flow regulation device to adjust the amount of blood flow through the vessel if the physiological information from at least one of the one or more sensors falls outside the target physiological range based on user input.
9. The controller unit of claim 1 , further comprising a graphical user interface configured to display information indicative of the comparison.
10. The controller unit of claim 9 , wherein the graphical user interface is further configured to communicate decision support audibly based on the comparison such that a user may provide user input based on the decision support.
11. The controller unit of claim 1 , wherein the processor generates an alert if the physiological information from at least one of the one or more sensors falls outside the target physiological range.
12. The controller unit of claim 1 , wherein the one or more sensors comprises a proximal sensor positioned proximal to the expandable blood flow regulation device.
13. The controller unit of claim 1 , wherein the one or more sensors comprises a distal sensor positioned distal to the expandable blood flow regulation device.
14. The controller unit of claim 1 , wherein the one or more sensors comprises one or more blood pressure sensors.
15. The controller unit of claim 1 , wherein the physiological information includes blood pressure waveforms.
16. The controller unit of claim 1 , wherein the processor is further configured to:
prior to calculating the dynamic scaling factor, cause the pump to adjust expansion or contraction of the expandable blood flow regulation device a first time.
17. The controller unit of claim 1 , wherein the processor is further configured to:
determine that a time delay has elapsed;
after causing the pump to adjust expansion or contraction of the expandable blood flow regulation device by the bolus volume and in response to determining that the time delay has elapsed, receive subsequent physiological information from the one or more sensors; and
calculate a difference between the subsequent physiological information from at least one of the one or more sensors and the target physiological range.
18. The controller unit of claim 17 , wherein the bolus volume is a first bolus volume, and wherein the processor is further configured to:
modify the dynamic scaling factor based on the difference; and
calculate a second bolus volume based on the modified dynamic scaling factor.
19. The controller unit of claim 17 , wherein the time delay is based on the difference.
20. A system for partial-aortic occlusion comprising:
the controller unit of claim 1 ; and
the expandable blood flow regulation device disposed at the distal region of the catheter; and
the one or more sensors.
21. The system of claim 20 , further comprising one or more additional sensors operatively coupled to the processor and configured to measure at least one of pressure within the expandable blood flow regulation device, heart rate, respiratory rate, blood temperature, cardiac output of a patient, carotid blood flow, pulmonary pressures, peripheral vascular resistance, or intracranial pressure.
22. The system of claim 20 , further comprising an external central processing unit operatively coupled to the controller unit and the one or more sensors, the external central processing unit comprising the processor and configured to transmit information indicative of whether the physiological information from at least one of the one or more sensors falls outside the target physiological range to the controller unit.
23. The system of claim 22 , wherein the external central processing unit transmits the information to the controller unit via at least one of WiFi, Bluetooth, Wixel-based communication, cellular communication, or other form of communication.
24. A method for blood flow regulation comprising:
advancing a catheter comprising an expandable blood flow regulation device into a vessel of a patient;
expanding the expandable blood flow regulation device to restrict blood flow through the vessel via a catheter controller unit coupled to the catheter;
measuring physiological information via one or more sensors coupled to the catheter;
comparing the measured physiological information from the one or more sensors with a target physiological range;
calculating a dynamic scaling factor;
calculating a bolus volume based at least in part on the dynamic scaling factor; and
adjusting expansion or contraction of the expandable blood flow regulation device by the bolus volume if the measured physiological information from at least one of the one or more sensors falls outside the target physiological range.