Systems and methods for selective occlusion of the peripheral venous vasculature to unload the heart
Systems and methods for intermittently occluding a patient's venous vasculature to unload the heart while increasing cardiac output and improving perfusion to the patient's heart is provided. The system may include first and second balloon catheters that may be selectively actuated to intermittently occlude first and second veins for increasing venous vascular resistance in the patient's lower and upper extremities, respectively, to thereby selectively reduce arterial blood flow to the lower and upper extremities, while maintaining arterial vascular resistance of the patient's heart and central organs and increasing perfusion to the patient's heart and central organs.
1 . A system for unloading a heart of a patient to improve cardiac performance, the system comprising:
a first flow limiting element configured to be selectively actuated to occlude a superior vena cava (SVC) in fluid communication with a first extremity of the patient;
a second flow limiting element configured to be selectively actuated to occlude an inferior vena cava (IVC) in fluid communication with a second extremity of the patient;
a controller operatively coupled to the first and second flow limiting elements, the controller configured to cause the first and/or second flow limiting elements to expand according to a predetermined actuation regimen to selectively occlude the SVC and/or IVC to reduce cardiac preload and increase mean arterial pressure to thereby selectively increase arterial vascular resistance of the patient's extremities, while maintaining arterial vascular resistance of the patient's heart and end organs and increasing perfusion to the patient's heart and end organs.
2 . The system of claim 1 , further comprising:
a catheter operatively coupled to the controller,
wherein the first and second flow limiting elements are disposed on a distal region of the catheter.
3 . The system of claim 1 , wherein the predetermined actuation regimen is programmed to:
cause only the first flow limiting element to expand for a first time period;
cause the first and second flow limiting elements to expand for a second time period after the first time period;
cause only the second flow limiting element to expand for a third time period after the second time period; and
cause the first and second flow limiting elements to expand for a fourth time period after the third time period.
4 . The system of claim 1 , wherein the predetermined actuation regimen is programmed to cause at least 70% occlusion of the SVC and IVC during a treatment period.
5 . The system of claim 1 , wherein the predetermined actuation regimen is programmed in the controller such that the first flow limiting element or the second flow limiting element, or both, maintains occlusion throughout a treatment session.
6 . The system of claim 1 , further comprising one or more sensors configured to measure one or more parameters and to generate one or more signals indicative of the one or more measured parameters.
7 . The system of claim 6 , wherein a first sensor of the one or more sensors is disposed proximal to the first flow limiting element and a second sensor of the one or more sensors is disposed proximal to the second flow limiting element.
8 . The system of claim 6 , wherein the controller is configured to adjust the predetermined actuation regimen to selectively occlude the SVC and/or IVC responsive to the one or more signals indicative of the one or more measured parameters.
9 . A system for unloading a heart of a patient to improve cardiac performance, the system comprising:
a first flow limiting element configured to be selectively actuated to occlude a first vein in fluid communication with a first extremity of the patient;
a second flow limiting element configured to be selectively actuated to occlude a second vein in fluid communication with a second extremity of the patient;
a controller operatively coupled to the first and second flow limiting elements, the controller configured to cause the first and/or second flow limiting elements to expand according to a predetermined actuation regimen to selectively occlude the first and/or second veins to reduce cardiac preload and increase mean arterial pressure to thereby selectively increase arterial vascular resistance of the patient's extremities, while maintaining arterial vascular resistance of the patient's heart and end organs and increasing perfusion to the patient's heart and end organs,
wherein each occlusion period during a treatment session is at least one minute.
10 . The system of claim 9 , wherein the first vein is a contralateral iliac vein and the second vein is an ipsilateral iliac vein.
11 . The system of claim 10 , further comprising a mechanical circulatory support (MCS) device.
12 . The system of claim 10 , further comprising:
a third flow limiting element operatively coupled to the controller, and configured to be selectively actuated to occlude a superior vena cava (SVC) of the patient,
wherein the controller is configured to cause the third flow limiting element to expand according to a second predetermined actuation regimen to occlude the SVC and reduce cardiac preload.
13 . The system of claim 12 , further comprising a mechanical circulatory support (MCS) device.
14 . The system of claim 10 , further comprising:
a third flow limiting element operatively coupled to the controller, and configured to be selectively actuated to occlude a contralateral subclavian vein of the patient; and
a fourth flow limiting element operatively coupled to the controller, and configured to be selectively actuated to occlude an ipsilateral subclavian vein of the patient,
wherein the controller is configured to cause the third and/or fourth flow limiting elements to expand according to a second predetermined actuation regimen to selectively occlude the contralateral and/or ipsilateral subclavian veins to reduce cardiac preload and increase mean arterial pressure to thereby selectively increase arterial vascular resistance of the patient's extremities, while maintaining arterial vascular resistance of the patient's heart and end organs and increasing perfusion to the patient's heart and end organs.
15 . The system of claim 14 , further comprising a mechanical circulatory support (MCS) device.
16 . The system of claim 14 , further comprising:
a fifth flow limiting element operatively coupled to the controller, and configured to be selectively actuated to occlude a superior vena cava (SVC) of the patient,
wherein the controller is configured to cause the fifth flow limiting element to expand according to a third predetermined actuation regimen to occlude the SVC and reduce cardiac preload.
17 . The system of claim 16 , further comprising a mechanical circulatory support (MCS) device.
18 . The system of claim 9 , wherein the first vein is a superior vena cava (SVC) and the second vein is an inferior vena cava (IVC).
19 . The system of claim 18 , further comprising a mechanical circulatory support (MCS) device.
20 . The system of claim 18 , further comprising:
a first catheter operatively coupled to the controller; and
a second catheter operatively coupled to the controller,
wherein the first flow limiting element is disposed on a distal region of the first catheter, and the second flow limiting element is disposed on a distal region of the second catheter.
21 . A method for unloading a heart of a patient to improve cardiac performance, the method comprising:
positioning a first flow limiting element within a superior vena cava (SVC) in fluid communication with a first extremity of the patient;
positioning a second flow limiting element within an inferior vena cava (IVC) in fluid communication with a second extremity of the patient; and
causing the first and/or second flow limiting elements to expand according to a predetermined actuation regimen to selectively occlude the SVC and/or IVC to reduce cardiac preload and increase mean arterial pressure to thereby selectively increase arterial vascular resistance of the patient's extremities, while maintaining arterial vascular resistance of the patient's heart and end organs and increasing perfusion to the patient's heart and end organs.
22 . The method of claim 21 , further comprising:
positioning a third flow limiting element within a contralateral iliac vein of the patient, and
positioning a fourth flow limiting element within an ipsilateral iliac vein of the patient.
23 . The method of claim 21 , further comprising:
positioning a third flow limiting element within a contralateral subclavian vein of the patient;
positioning a fourth flow limiting element within an ipsilateral subclavian vein of the patient; and
causing the third and/or fourth flow limiting elements to expand according to a second predetermined actuation regimen to selectively occlude the contralateral and/or ipsilateral subclavian veins to reduce cardiac preload and increase mean arterial pressure to thereby selectively increase arterial vascular resistance of the patient's extremities, while maintaining arterial vascular resistance of the patient's heart and end organs and increasing perfusion to the patient's heart and end organs.
24 . The method of claim 21 , further comprising:
positioning a third flow limiting element within a third vein of the patient; and
intermittently actuating the third flow limiting element according to a second predetermined actuation regimen to occlude the third vein.
25 . The method of claim 21 , further comprising:
positioning a mechanical circulatory support (MCS) device within the patient's heart; and
actuating the MCS device.
26 . The method of claim 21 , wherein causing the first and/or second flow limiting elements to expand according to the predetermined actuation regimen comprises causing the first flow limiting element or the second flow limiting element, or both, to maintain occlusion throughout a treatment session.
27 . The method of claim 21 , where causing the first and/or second flow limiting elements to expand according to the predetermined actuation regimen comprises:
causing only the first flow limiting element to expand for a first time period;
causing the first and second flow limiting elements to expand for a second time period after the first time period;
causing only the second flow limiting element to expand for a third time period after the second time period; and
causing the first and second flow limiting elements to expand for a fourth time period after the third time period.
28 . The method of claim 21 , wherein each occlusion period during a treatment session is at least one minute.