Systems and methods for selectively occluding the superior vena cava for treating heart conditions
Systems and methods and devices are provided for treating conditions such as heart failure and/or pulmonary hypertension by at least partially occluding flow through the superior vena cava for an interval spanning multiple cardiac cycles. A catheter with an occlusion device is provided along with a controller that actuates a drive mechanism to provide at least partial occlusion of the patient's superior vena cava, which reduces cardiac filling pressures, and induces a favorable shift in the patient's Frank-Starling curve towards healthy heart functionality and improved cardiac performance. The occlusion device may include a lumen obstructed by a relief valve that may permit fluid flow through the occlusion device to release an excessive build-up of pressure.
1. A system for unloading of cardiac preload and afterload, the system comprising:
a cardiac assist device configured to pump blood within a patient to reduce cardiac afterload;
a flow limiting element configured to be positioned at a superior vena cava (SVC) of the patient; and
a controller configured to be coupled to the flow limiting element, the controller configured to cause the flow limiting element to fully occlude the SVC over multiple cardiac cycles to reduce cardiac preload.
2. The system of claim 1 , wherein the flow limiting element is disposed on a catheter configured to be intravascularly positioned within the SVC, and
wherein the controller is configured to fully occlude the SVC by expanding the flow limiting element.
3. The system of claim 1 , wherein the controller is configured to cause the flow limiting element to expand and contract within the SVC to reduce the cardiac preload.
4. The system of claim 3 , wherein the controller is configured to cause the flow limiting element to repeat the expansion and the contraction over a course of a treatment.
5. The system of claim 4 , wherein the controller is configured to cause the flow limiting element to expand to fully occlude the SVC for a first predetermined time interval and to contract for a second predetermined time interval over multiple cardiac cycles.
6. The system of claim 5 , wherein the first predetermined time interval is at least five times greater than the second predetermined time interval.
7. The system of claim 5 , wherein the first predetermined time interval is 5-20 minutes and the second predetermined time interval is 10-100 seconds.
8. The system of claim 1 , wherein the controller is configured to cause the flow limiting element to fully occlude the SVC for more than a minute during expansion.
9. The system of claim 1 , wherein the cardiac assist device comprises a catheter.
10. The system of claim 9 , wherein the cardiac assist device comprises an impeller pump disposed at a distal portion of the catheter.
11. The system of claim 9 , wherein the cardiac assist device is a left ventricular assist device (LVAD).
12. The system of claim 1 , wherein the cardiac assist device is a percutaneous left ventricular assist device (LVAD).
13. The system of claim 1 , wherein the cardiac assist device is an intra-aortic balloon pump (IABP).
14. The system of claim 1 , wherein the controller is configured to cause the flow limiting element to fully occlude the SVC to reduce the patient's diastolic volume and improve cardiac performance as measured by at least one of: reduced cardiac filling pressures, increased left ventricular relaxation, increased left ventricular capacitance, increased left ventricular stroke volume, increased lusitropy, reduced left ventricular stiffness or reduced cardiac strain.
15. The system of claim 1 , wherein the controller is configured to cause the flow limiting element to fully occlude the SVC to create a negative pressure sink in a right atrium of the patient, accelerating flow from a renal vein, thereby enhancing renal decongestion and promoting blood flow across a kidney of the patient.
16. The system of claim 1 , further comprising a sensor for monitoring pressure differential across the flow limiting element in the SVC indicative of an amount or degree of occlusion in the SVC.
17. The system of claim 1 , further comprising:
a first pressure sensor disposed proximal to the flow limiting element, the first pressure sensor configured to output a first pressure signal; and
a second pressure sensor disposed distal to the flow limiting element, the second pressure sensor configured to output a second pressure signal,
wherein the controller is configured to determine pressure in the SVC based on the first pressure signal or the second pressure signal or both.
18. The system of claim 1 , wherein the cardiac assist device and the flow limiting element utilize coaxial catheters.
19. The system of claim 1 , further comprising a sensor configured to generate a signal corresponding to a physiologic parameter indicative of the patient's hemodynamic state,
wherein the controller is configured to permit adjustment of actuation of the flow limiting element responsive to the signal.
20. The system of claim 1 , wherein the flow limiting element is a balloon.
21. A system for unloading of cardiac preload and afterload, the system comprising:
a percutaneous heart pump configured to pump blood within a patient to reduce cardiac afterload;
a balloon catheter configured to be positioned within a superior vena cava (SVC) of the patient; and
a controller configured to be coupled to the balloon catheter, the controller configured to cause a balloon of the balloon catheter to expand to fully occlude the SVC over multiple cardiac cycles to reduce cardiac preload.
22. The system of claim 21 , wherein the controller is configured to cause the balloon to expand and contract within the SVC over a course of a treatment to reduce the cardiac preload.
23. The system of claim 22 , wherein the controller is configured to cause the balloon to expand to fully occlude the SVC for a first predetermined time interval and to contract for a second predetermined time interval over multiple cardiac cycles.
24. The system of claim 23 , wherein the first predetermined time interval is at least five times greater than the second predetermined time interval.
25. The system of claim 24 , wherein the first predetermined time interval is 5-20 minutes and the second predetermined time interval is 10-100 seconds.