# US 8,540,615 B2 · Left and right side heart support > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 8,540,615 B2 - Document ID: US8540615B2 - Status: Granted - Kind: B2 - Application number: 12/846,366 - Filed: 2010-07-29 - Published: 2011-01-27 - Granted: 2013-09-24 - Earliest claimed: 1998-12-23 - Assignees: Maquet Cardiovascular LLC - Applicants: Walid Najib Aboul-Hosn; William R. Kanz; Jodi Akin; Michael Guidera; Robert G. Matheny - Inventors: Walid Najib Aboul-Hosn; William R. Kanz; Jodi Akin; Michael Guidera; Robert G. Matheny - Web page: https://patentgrep.com/patent/US8540615B2 ## CPC - A61M 1/3621: {Extra-corporeal blood circuits (single-needle circuits A61M1/30)} - A61M 1/3613: {Reperfusion, e.g. of the coronary vessels, e.g. retroperfusion} - A61M 60/148: in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices - A61M 60/17: inside a ventricle, e.g. intraventricular balloon pumps - A61M 60/183: drawing blood from both ventricles, e.g. bi-ventricular assist devices [BiVAD] - A61M 60/232: Centrifugal pumps - A61M 60/237: the blood flow through the rotating member having mainly axial components, e.g. axial flow pumps - A61M 60/279: Peristaltic pumps, e.g. roller pumps - A61M 1/3663: {Flow rate transducers; Flow integrators} - A61M 60/894: Passive valves, i.e. valves actuated by the blood - A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)} ## Abstract A cannulation system for cardiac support uses an inner cannula disposed within an outer cannula. The outer cannula includes a fluid inlet for placement within the right atrium of a heart. The inner cannula includes a fluid inlet extending through the fluid inlet of the outer cannula and the atrial septum for placement within at least one of the left atrium and left ventricle of the heart. The cannulation system also employs a pumping assembly coupled to the inner and outer cannulas to withdraw blood from the right atrium for delivery to the pulmonary artery to provide right heart support, or to withdraw blood from at least one of the left atrium and left ventricle for delivery into the aorta to provide left heart support, or both. ## Claims ### Claim 1 A cannulation system for cardiac support comprising: an inflow cannula including a fluid inlet sized and configured to extend through an atrial septum for accessing at least one of a left atrium and a left ventricle of a heart and a lumen extending proximally of the fluid inlet; said inflow cannula being configured to couple to a pump to withdraw blood from the left side of the heart through the lumen; an outflow cannula configured to couple to the pump and adapted to extend into the arterial system for delivering the withdrawn blood into the arterial system to provide left heart support; and at least one radially extending member adjacent to the fluid inlet and configured for securing the cannula system in position through the atrial septum. ### Claim 2 (depends on 1) The cannulation system of claim 1, further comprising a dilator member disposed proximally of the fluid inlet adapted to facilitate passing the fluid inlet of the cannula through the atrial septum for positioning within the left side of the heart, wherein the radially extending member is coupled with the dilator member and comprises an inflatable cuff assembly adapted for securing the dilator member in position through the atrial septum. ### Claim 3 (depends on 2) The cannulation system of claim 2, wherein the inflatable cuff assembly includes a first inflation member and a second inflation member which, in use, are adapted to be deployed on either side of the atrial septum. ### Claim 4 (depends on 3) The cannulation system of claim 3, wherein the inflation members are selectively deployable through the use of a fluid source coupled to the interior of the inflation members. ### Claim 5 (depends on 4) The cannulation system of claim 4, wherein the cannula is equipped with at least one lumen formed in the wall thereof to pass fluid from the fluid source to the interior of the inflation members to selectively inflate and deflate the inflation members. ### Claim 6 (depends on 1) The cannulation system of claim 1, wherein at least one radially extending member is configured to seal an aperture formed in the atrial septum through which the cannula can be disposed. ### Claim 7 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises a first member and a second member disposed distally of the first member. ### Claim 8 (depends on 7) The cannulation system of claim 7, further comprising a dilating structure disposed distally of the first member. ### Claim 9 (depends on 8) The cannulation system of claim 8, wherein the dilating structure is separate from and positioned distally of the second member. ### Claim 10 (depends on 8) The cannulation system of claim 8, wherein the cannula is adapted to be moveable relative to the dilating structure such that the dilating structure can be positioned before the cannula is positioned. ### Claim 11 (depends on 7) The cannulation system of claim 7, wherein the first and second members comprises inflation members. ### Claim 12 (depends on 7) The cannulation system of claim 7, wherein the first and second members are configured to sandwich the patient's atrial septum tissue therebetween. ### Claim 13 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises a member adapted to be positioned distal of the atrial septum to prevent the inlet of the cannula from being pushed proximally out of the left side of the patient's heart. ### Claim 14 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises a member adapted to be positioned proximal of the atrial septum to prevent the fluid inlet of the inflow cannula from being pushed distally within the left side of the patient's heart. ### Claim 15 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises a buckling cuff. ### Claim 16 (depends on 15) The cannulation system of claim 15, wherein the buckling cuff comprises first and second cuff members. ### Claim 17 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises an expandable member having a proximal end, a distal end, and an elongate portion extending therebetween, the expandable member adapted such that the proximal and distal ends can be drawn toward each other causing the elongate portion extending therebetween to be expanded radially outward from the cannula to form first and second cuff members, the first and second cuff member being sized larger than the size of an aperture formed in the atrial septum for placement of the inlet on the left side of the heart. ### Claim 18 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member comprises a fabric. ### Claim 19 (depends on 1) The cannulation system of claim 1, wherein the at least one radially extending member is disposed proximally of a dilating structure adapted to facilitate placement of the fluid inlet of the inflow cannula on the left side of the heart. ### Claim 20 (depends on 1) The cannulation system of claim 1, further comprising said pump coupled to said inflow cannula and said outflow cannula. ### Claim 21 A cannulation system for cardiac support comprising: a cannula including a fluid inlet sized and configured for placement within the right atrium of a heart, wherein the cannula is equipped with a plurality of members that extend radially relative to the cannula, and wherein the members are configured to secure an atrial septum therebetween; and wherein said cannula is configured to couple to a pumping assembly. ### Claim 22 (depends on 21) The cannulation system of claim 21, wherein the members are mechanically expandable by moving portions of said members relative to said cannula. ### Claim 23 (depends on 21) The cannulation system of claim 21, further comprising said pump coupled to said cannula. ### Claim 24 A cannulation system for cardiac support comprising: an inflow cannula including a fluid inlet sized and configured to extend through an atrial septum for accessing an atrium or a ventricle of a heart and a lumen extending proximally from the fluid inlet; said inflow cannula being configured to couple to a pump to withdraw blood from the heart through the lumen; an outflow cannula configured to couple to the pump and adapted to extend into fluid communication with the arterial system for delivering the withdrawn blood into the arterial system to provide heart support; and at least one anchor member disposed adjacent the fluid inlet and configured for securing the cannula system in position through the atrial septum. ### Claim 25 (depends on 24) The cannulation system of claim 24, further comprising said pump coupled to said inflow cannula and said outflow cannula. ### Claim 26 A cannulation system for cardiac support comprising: an inflow cannula including a fluid inlet and a lumen extending proximally from the fluid inlet, the inflow cannula configured to extend through a heart wall to place the fluid inlet in fluid communication with an atrium or a ventricle of a heart; said inflow cannula configured to couple to a pump to withdraw blood from the heart through the lumen; an outflow cannula configured to couple to the pump and adapted to extend into fluid communication with the arterial system for delivering the withdrawn blood into the arterial system to provide heart support; and at least one anchor member disposed adjacent the fluid inlet and configured for securing the cannula system in position through the heart wall. ### Claim 27 (depends on 26) The cannulation system of claim 26, wherein the fluid inlet comprises an aperture at the distal end of the cannula. ### Claim 28 (depends on 27) The cannulation system of claim 27, wherein the system is configured such that, in use, a length of the cannula extending proximally from the fluid inlet is advanced into the left side of the heart. ### Claim 29 (depends on 26) The cannulation system of claim 26, further comprising a dilator configured for insertion through the heart wall, a distal portion of the cannula being configured to be passed through the dilator into the left side of the heart. ### Claim 30 (depends on 25) The cannulation system of claim 25, further comprising said pump coupled to said inflow cannula and said outflow cannula. ### Claim 31 A heart assist system for coupling into fluid communication with a chamber of a heart comprising: a blood pump including an inlet; an elongate body including a first end, a second end, and a lumen adapted to be coupled into fluid communication with said inlet, said lumen extending along a longitudinal axis, said first and second ends defining openings into said lumen; a dilating structure disposed about said elongate body and adapted to be positioned proximally of a portion of said second end in a direction toward said first end, and expanding radially outward from said longitudinal axis and in said direction; and a ring member disposed around said elongate body and said longitudinal axis, said ring member being spaced from said dilating structure and being adapted for retaining said elongate body in a position relative to a wall of the chamber of the heart. ### Claim 32 (depends on 31) The heart assist system of claim 31, further comprising a second elongate body, the dilating structure being disposed on said second elongate body. ### Claim 33 (depends on 31) The heart assist system of claim 31, wherein said ring member comprises an inflatable balloon. ### Claim 34 (depends on 33) The heart assist system of claim 33, further comprising a second elongate body, the inflatable balloon being disposed on said second elongate body.