System for cardiac procedures

Claim 2

An endovascular device for partitioning a human patient's ascending aorta between a coronary ostium and a brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a preshaped distal portion configured to conform generally to the patient's aortic arch; a straightening element for straightening the distal portion of the shaft to facilitate introducing the shaft into an artery downstream of the patient's ascending aorta; and an occluding member near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough without occluding either the coronary ostia or the brachiocephalic artery.

Claim 3

The endovascular device of claim 1 wherein the preshaped distal portion of the shaft is generally U-shaped in an unstressed condition to facilitate positioning the shaft from an arterial location downstream of the patient's aortic arch.

Claim 4

The endovascular device of claim 2 Wherein the preshaped distal portion has a distal segment for positioning in the ascending aorta and a proximal segment for positioning in the descending aorta, the distal segment being non-coplanar with a plane containing the proximal segment.

Claim 5

The endovascular device of claim 1 wherein the preshaped distal portion of the shaft has a radius of curvature in the range of 20 to 80 mm.

Claim 6

The endovascular device of claim 1 wherein the straightening element comprises a stylet slidably disposed in the first inner lumen of the shaft and having a bending stiffness greater than the bending stiffness of the shaft.

Claim 7

The endovascular device of claim 1 wherein the shaft has a bending stiffness selected to maintain the position of the occluding member within the patient's ascending aorta against systolic blood flow from the patient's heart when the occluding member is expanded.

Claim 8

The endovascular device of claim 1 wherein the shaft has a bending modulus in a range of 70 to 100 kpsi.

Claim 9

The endovascular device of claim 1 wherein the occluding member has a collapsed profile for insertion into an artery of the patient and an expanded profile for occluding the ascending aorta, the expanded profile diameter being about 5 to 10 times the collapsed profile diameter.

Claim 10

The endovascular device of claim 8 wherein the occluding member comprises an inflatable balloon.

Claim 11

The endovascular device of claim 9 wherein the balloon has a blow-up ratio in a range of 200-400%.

Claim 12

The endovascular device of claim 10 wherein the balloon has at least one pleat or fold when deflated.

Claim 13

The endovascular device of claim 1 wherein the occluding member has a working surface for contacting a wall of the aorta with an axial length in a range of about 3 cm to no more than about 7 cm.

Claim 14

The endovascular device of claim 1 wherein the shaft has a length of at least 80 cm. to facilitate transluminal positioning from a femoral artery to the ascending aorta.

Claim 15

The endovascular device of claim 1 wherein the first inner lumen has a diameter of at least about 5 mm to facilitate positioning a surgical instrument therethrough.

Claim 16

The endovascular device of claim 1 further comprising a pressure monitoring device in communication with the exterior of the shaft distal to the occluding member for monitoring pressure in the ascending aorta between the occluding member and the aortic valve.

Claim 17

The endovascular device of claim 1 wherein the shaft has a pressure port distal to the occluding member and a pressure lumen extending from the proximal end of the shaft to the pressure port.

Claim 18

The endovascular device of claim 1 wherein the first inner lumen is configured to permit cardioplegic fluid flow therethrough at a rate of at least about 250 ml/min and a pressure of at most about 300 mmHg.

Claim 19

The endovascular device of claim 1 wherein the first inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 20

The endovascular device of claim 1 wherein the occluding member is elastically expandable to a range of diameters so as to completely occlude aortas of various sizes.

Claim 21

An endovascular device for partitioning a human patient's ascending aorta between the coronary ostia and the brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a shaped distal portion configured to conform generally to at least a portion of the patient's aortic arch; and an occluding member near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough without occluding either the coronary ostia or the brachiocephalic artery.

Claim 22

An endovascular device for partitioning a human patient's ascending aorta between the coronary ostia and the brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a shaped distal portion configured to conform generally to at least a portion of the patient's aortic arch; and an occluding member near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough without occluding either the coronary ostia or the brachiocephalic artery.

Claim 23

The endovascular device of claim 20 wherein the shaped distal portion is preshaped to have a configuration in an unstressed condition suitable for positioning in at least a portion of the aortic arch.

Claim 24

The endovascular device of claim 21 wherein the shaped distal portion is generally U-shaped in an unstressed condition to facilitate positioning the shaft from an arterial location downstream of the patient's aortic arch.

Claim 25

The endovascular device of claim 22 wherein the shaped distal portion has a radius of curvature in the range of 20-80 min.

Claim 26

The endovascular device of claim 22 wherein the shaped distal portion has a distal segment for positioning in the ascending aorta and a proximal segment for positioning in the descending aorta, the distal segment being non-coplanar with a plane containing the proximal segment.

Claim 27

The endovascular device of claim 21 further comprising means in the shaft for straightening the shaped distal portion.

Claim 28

The endovascular device of claim 25 wherein the straightening means comprises a straightening element slidably disposed in the first inner lumen having a bending stiffness greater than the shaped distal portion.

Claim 29

The endovascular device of claim 26 wherein the straightening element comprises a relatively stiff portion of a flexible guidewire extending through the first inner lumen.

Claim 30

The endovascular device of claim 26 wherein the straightening element comprises a stylet having a passage therethrough for receiving a movable guidewire.

Claim 31

The endovascular device of claim 20 wherein the shaft has a bending stiffness selected to maintain the position of the occluding member within the patient's ascending aorta against systolic blood flow from the patient's heart when the occluding member is expanded.

Claim 32

The endovascular device of claim 25 wherein the shaft has a bending modulus in a range of 70 to 100 kpsi.

Claim 33

The endovascular device of claim 20 wherein the occluding member has a collapsed profile for insertion into an artery of the patient and an expanded profile for occluding the ascending aorta, the expanded profile diameter being about 5 to 10 times the collapsed profile diameter.

Claim 34

The endovascular device of claim 20 wherein the occluding member comprises an inflatable balloon with an interior for receiving an inflation fluid for the inflation thereof.

Claim 35

The endovascular device of claim 32 wherein the balloon has a blow-up ratio in a range of 200-400%.

Claim 36

The endovascular device of claim 33 wherein the balloon has at least one pleat or fold when deflated.

Claim 37

The endovascular device of claim 32 further comprising an inflation lumen extending through the shaft from the proximal end to the interior of the balloon.

Claim 38

The endovascular device of claim 35 further comprising means connected to the proximal end of the shaft in fluid communication with the inflation lumen for delivering an inflation fluid to the balloon interior.

Claim 39

The endovascular device of claim 20 wherein the occluding member has a working surface for contacting a wall of the aorta with an axial length in a range of about 3 cm to no more than about 7 cm.

Claim 40

The endovascular device of claim 20 further comprising an additional opening in the shaft distal to the occluding member, and an additional lumen extending from the proximal end to the additional opening.

Claim 41

The endovascular device of claim 38 further comprising a pressure monitoring device in fluid communication with the additional lumen for sensing pressure at the distal end of the shaft.

Claim 42

The endovascular device of claim 20 wherein the shaft has a length of at least about 80 cm to allow transluminal positioning of the shaft from a femoral artery to the ascending aorta.

Claim 43

The endovascular device of claim 20 wherein the first inner lumen has a diameter of at least about 5 mm to facilitate positioning a surgical instrument therethrough.

Claim 44

The endovascular device of claim 20 wherein the first inner lumen is configured to permit cardioplegic fluid flow therethrough at a rate of at least about 250 ml/min and a pressure of at most about 300 mmHg.

Claim 45

The endovascular device of claim 20 wherein the first inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 46

The endovascular device of claim 20 wherein the occluding member is elastically expandable to a range of diameters so as to completely occlude aortas of various sizes.

Claim 49

The system of claim 45 wherein the preshaped distal portion is generally U-shaped in an unstressed condition to facilitate positioning the shaft from an arterial location downstream of the patient's aortic arch.

Claim 50

The system of claim 45 further comprising a cardiopulmonary bypass system having a venous cannula for withdrawing blood from a venous location upstream of the heart, an oxygenator for oxygenating the withdrawn blood, and an arterial cannula for directing the oxygenated blood to an arterial location downstream of the occluding member.

Claim 51

The system of claim 45 further comprising a pressure monitoring device in communication with the exterior of the shaft distal to the occluding member for monitoring pressure in the ascending aorta between the occluding member and the aortic valve.

Claim 52

The system of claim 45 wherein the shaft comprises a pressure monitoring port distal to the occluding member and a pressure lumen extending from the pressure monitoring port to the proximal end of the shaft.

Claim 53

The system of claim 45 wherein the first inner lumen is configured to permit cardioplegic fluid flow therethrough at a rate of at least about 250 ml/min and a pressure of at most about 300 mmHg.

Claim 54

The system of claim 45 wherein the first inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 55

The system of claim 45 wherein the occluding member is elastically expandable to a range of diameters so as to completely occlude aortas of various sizes.

Claim 56

A closed-chest cardiopulmonary bypass (CPB) system comprising: an arterial cannula having a distal end configured for percutaneous introduction into a peripheral artery, a proximal end, an inner lumen extending therebetween, and an outflow port at the distal end in fluid communication with the inner lumen; a venous cannula having a distal end configured for percutaneous introduction into a peripheral vein, a proximal end, an inner lumen extending therebetween, and an inflow port at the distal end in fluid communication with the inner lumen; an aortic catheter having a distal end configured for percutaneous introduction into a peripheral artery downstream of the aortic arch, a proximal end, an inner lumen extending therebetween, a distal port at the distal end in fluid communication with the inner lumen, the aortic catheter having a length selected to facilitate transluminal positioning of the distal port from the peripheral artery to an ascending aortic location downstream of the aortic valve, and an occluding member proximal to the distal port configured to occlude the ascending aorta between the coronary ostia and the brachiocephalic artery to block substantially all blood flow therethrough without occluding either the coronary ostia or the brachiocephalic artery when the distal port is in the ascending aortic location; a cardioplegic fluid supply in communication with the inner lumen of the aortic catheter for delivering cardioplegic fluid through the inner lumen into the ascending aorta distal to the occluding member so as to arrest the heart; means at the proximal end of the venous cannula in fluid communication with the inner lumen of the venous cannula for receiving deoxygenated blood from the patient's venous system; an oxygenator for oxygenating the deoxygenated blood; means at the proximal end of the aortic catheter in fluid communication with the inner lumen thereof for receiving blood from the aortic root and delivering the blood to the oxygenator; and means connecting the oxygenator to the inner lumen of the arterial cannula for delivering oxygenated blood into the patient's arterial system.

Claim 57

A closed-chest cardiopulmonary bypass (CPB) system comprising: an arterial cannula having a distal end configured for percutaneous introduction into a peripheral artery, a proximal end, an inner lumen extending therebetween, and an outflow port at the distal end in fluid communication with the inner lumen; a venous cannula having a distal end configured for percutaneous introduction into a peripheral vein, a proximal end, an inner lumen extending therebetween, and an inflow port at the distal end in fluid communication with the inner lumen; an aortic catheter having a distal end configured for percutaneous introduction into a peripheral artery downstream of the aortic arch, a proximal end, an inner lumen extending therebetween, a distal port at the distal end in fluid communication with the inner lumen, the aortic catheter having a length selected to facilitate transluminal positioning of the distal port from the peripheral artery to an ascending aortic location downstream of the aortic valve, and an occluding member proximal to the distal port configured to occlude the ascending aorta between the coronary ostia and the brachiocephalic artery to block substantially all blood flow therethrough without occluding either the coronary ostia or the brachiocephalic artery when the distal port is in the ascending aortic location; a cardioplegic fluid supply in communication with the inner lumen of the aortic catheter for delivering cardioplegic fluid through the inner lumen into the ascending aorta distal to the occluding member so as to arrest the heart; means at the proximal end of the venous cannula in fluid communication with the inner lumen of the venous cannula for receiving deoxygenated blood from the patient's venous system; an oxygenator for oxygenating the deoxygenated blood; means at the proximal end of the aortic catheter in fluid communication with the inner lumen thereof for receiving blood from the aortic root and delivering the blood to the oxygenator; and means connecting the oxygenator to the inner lumen of the arterial cannula for delivering oxygenated blood into the patient's arterial system.

Claim 58

The CPB system of claim 53 further comprising valve means connected to the inner lumen of the aortic catheter for switching between the cardioplegic fluid supply and the means for receiving blood from the aortic root.

Claim 59

The CPB system of claim 53 wherein the occluding member comprises a balloon, the aortic catheter further comprising an inflation lumen for delivering an inflation fluid into the balloon.

Claim 60

The CPB system of claim 53 further comprising a pressure monitoring device in communication with the ascending aorta distal to the occluding member.

Claim 61

The CPB system of claim 53 wherein the aortic catheter comprises a pressure monitoring port in the shaft distal to the occluding member, and a pressure lumen extending from the pressure monitoring port to the proximal end of the aortic catheter.

Claim 62

The CPB system of claim 53 wherein the inner lumen is configured to permit cardioplegic fluid flow therethrough at a rate of at least about 250 ml/min and a pressure of at most about 300 mmHg.

Claim 63

The CPB system of claim 53 wherein the first inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 64

The CPB system of claim 53 wherein the occluding member is elastically expandable to a range of diameters so as to completely occlude aortas of various sizes.

Claim 67

An endovascular system for accessing a patient's heart having a left ventricle, an aorta having an aortic lumen therein leading away from the left ventricle to a peripheral artery, a coronary artery branching from the aorta at a first location, and a brachiocephalic artery branching from the aorta at a second location downstream of the first location, the system comprising: a) an elongated intra-aortic catheter having proximal and distal ends, a port at the distal end, an inner lumen extending from the proximal end to the port, and an expandable member on a distal portion thereof proximal to the port, the intra-aortic catheter having a length to allow the port and the expandable member to be positioned in an ascending aortic location in the aortic lumen between the first and second locations with the proximal end extending intraluminally to the peripheral artery, the expandable member being configured to expand into sealing engagement with an inner wall of the aorta to occlude the aortic lumen to prevent the passage of blood therethrough without blocking the coronary artery or the brachiocephalic artery; b) a fluid receiving device at the proximal end of the catheter in communication with the inner lumen for receiving fluid withdrawn from within the aortic lumen through the port; and c) a cardiopulmonary by-pass system including a venous cannula to withdraw blood from a venous system of the patient, an oxygenator to oxygenate the blood withdrawn from the venous system, and an arterial cannula positionable in an artery downstream of the expandable member to direct oxygenated blood into the artery.

Claim 68

An endovascular system for accessing a patient's heart having a left ventricle, an aorta having an aortic lumen therein leading away from the left ventricle to a peripheral artery, a coronary artery branching from the aorta at a first location, and a brachiocephalic artery branching from the aorta at a second location downstream of the first location, the system comprising: a) an elongated intra-aortic catheter having proximal and distal ends, a port at the distal end, an inner lumen extending from the proximal end to the port, and an expandable member on a distal portion thereof proximal to the port, the intra-aortic catheter having a length to allow the port and the expandable member to be positioned in an ascending aortic location in the aortic lumen between the first and second locations with the proximal end extending intraluminally to the peripheral artery, the expandable member being configured to expand into sealing engagement with an inner wall of the aorta to occlude the aortic lumen to prevent the passage of blood therethrough without blocking the coronary artery or the brachiocephalic artery; b) a fluid receiving device at the proximal end of the catheter in communication with the inner lumen for receiving fluid withdrawn from within the aortic lumen through the port; and c) a cardiopulmonary by-pass system including a venous cannula to withdraw blood from a venous system of the patient, an oxygenator to oxygenate the blood withdrawn from the venous system, and an arterial cannula positionable in an artery downstream of the expandable member to direct oxygenated blood into the artery.

Claim 69

The system of claim 62 including a fluid directing device to direct cardioplegic fluid through coronary blood vessels in the patient's heart.

Claim 70

The system of claim 63 wherein the fluid directing device is adapted to deliver the cardioplegic fluid through the inner lumen of the intra-aortic catheter and out of the port into the aortic lumen distal to the expandable member.

Claim 71

The system of claim 64 further comprising a valve for selectively connecting the inner lumen to either the fluid receiving device or the fluid directing device.

Claim 72

The system of claim 62 further comprising an adaptor having at least three access ports attached to the proximal end of the intra-aortic catheter, at least one of the access ports being in communication with the inner lumen and in communication with the fluid receiving device.

Claim 73

The system of claim 62 wherein the inner lumen of the elongated intra-aortic catheter has a diameter of sufficient size to facilitate passage therethrough of instruments for performing a cardiac procedure.

Claim 74

The system of claim 62 wherein the expandable member on the elongated intra-aortic catheter is an inflatable member, the intra-aortic catheter further comprising an inflation lumen in communication with the inflatable member and extending to the proximal end.

Claim 75

The system of claim 62 wherein the fluid receiving device for receiving fluid from the inner lumen is adapted to direct the fluid to an extracorporeal treatment system.

Claim 76

The system of claim 69 including a fluid return device to return treated fluid from the extracorporeal treatment system to an artery of the patient.

Claim 79

The method of claim 71 further comprising paralyzing the patient's heart while the occluding member is occluding the aortic lumen.

Claim 80

The method of claim 72 wherein the heart has a coronary vasculature in communication with the coronary artery, the step of paralyzing the heart comprising delivering cardioplegic fluid into the coronary vasculature.

Claim 81

The method of claim 73 wherein the step of delivering comprises delivering cardioplegic fluid through the access lumen of the intra-aortic catheter into the aortic lumen upstream of the occluding member, the step of venting being discontinued during the step of delivering.

Claim 82

The method of claim 71 wherein the peripheral artery is a femoral artery.

Claim 83

The method of claim 71 further comprising the step of performing a surgical procedure on the heart while the aorta is occluded.

Claim 84

The method of claim 76 wherein the patient has a rib cage including a sternum and a plurality of ribs, the method further comprising maintaining each of the ribs and sternum intact throughout the surgical procedure.

Claim 85

The method of claim 71 wherein the patient has a rib cage including a sternum and a plurality of ribs, the method further comprising maintaining the sternum and each of the ribs intact during each of the steps of providing, introducing, advancing, expanding, venting, and withdrawing.

Claim 88

The method of claim 79 wherein the patient has a rib cage having a sternum and a plurality of ribs around the heart, the method further comprising maintaining the sternum and each of the ribs substantially intact during each of the steps of maintaining circulation, occluding, delivering and venting.

Claim 89

The method of claim 79 wherein the step of delivering comprises delivering the cardioplegic fluid through an inner lumen in the intra-aortic catheter.

Claim 90

The method of claim 79 wherein the step of venting comprises venting the fluid through an inner lumen in the intra-aortic catheter.

Claim 91

The method of claim 79 wherein the peripheral artery comprises a femoral artery.

Claim 92

The method of claim 79 further comprising the step of performing a surgical procedure on the heart while the aorta is occluded.

Claim 93

The method of claim 84 wherein the patient has a rib cage including a sternum and a plurality of ribs, the method further comprising maintaining each of the ribs and sternum intact throughout the surgical procedure.

Claim 94

An endovascular device for partitioning a human patient's ascending aorta between a coronary ostium and a brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a preshaped distal portion configured to conform generally to the patient's aortic arch, the inner lumen being configured for delivering a cardioplegic fluid into the ascending aorta at a rate sufficient to arrest the heart; a straightener for straightening the distal portion of the shaft to facilitate introducing the shaft into an artery downstream of the patient's ascending aorta; and occluding means near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough.

Claim 95

An endovascular device for partitioning a human patient's ascending aorta between a coronary ostium and a brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a preshaped distal portion configured to conform generally to the patient's aortic arch, the inner lumen being configured for delivering a cardioplegic fluid into the ascending aorta at a rate sufficient to arrest the heart; a straightener for straightening the distal portion of the shaft to facilitate introducing the shaft into an artery downstream of the patient's ascending aorta; and occluding means near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough.

Claim 96

The endovascular device of claim 86 wherein the inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 97

The endovascular device of claim 86 wherein the inner lumen is configured to deliver cardioplegic fluid at a rate of at least about 250 ml/min at a pressure of no more than about 300 mm Hg.

Claim 98

An endovascular device for partitioning a patient's ascending aorta between the coronary ostia and the brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a shaped distal portion configured to conform generally to at least a portion of the patient's aortic arch, the first inner lumen being configured for delivering a cardioplegic fluid into the ascending aorta at a rate sufficient to arrest the heart; and occluding means near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough.

Claim 99

An endovascular device for partitioning a patient's ascending aorta between the coronary ostia and the brachiocephalic artery, comprising: a flexible shaft having a distal end, a proximal end, a first inner lumen extending therebetween, an opening at the distal end in fluid communication with the first inner lumen, and a shaped distal portion configured to conform generally to at least a portion of the patient's aortic arch, the first inner lumen being configured for delivering a cardioplegic fluid into the ascending aorta at a rate sufficient to arrest the heart; and occluding means near the distal end of the shaft proximal to the opening in the first inner lumen configured to sealingly engage an inner wall of the aorta for occluding the ascending aorta between the coronary ostia and the brachiocephalic artery so as to block substantially all blood flow therethrough.

Claim 100

The endovascular device of claim 89 wherein the inner lumen has a cross-sectional area of at least about 4.5 mm 2 .

Claim 101

The endovascular device of claim 89 wherein the inner lumen is configured to deliver cardioplegic fluid at a rate of at least about 250 ml/min at a pressure of no more than about 300 mmHg.