# US 11,896,813 B2 · Expandable mechanical hemodynamic support systems, devices, and methods > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 11,896,813 B2 - Document ID: US11896813B2 - Status: Granted - Kind: B2 - Application number: 18/108,450 - Filed: 2023-02-10 - Published: 2023-08-17 - Granted: 2024-02-13 - Earliest claimed: 2022-02-14 - Assignees: Narwhal Medical LLC - Applicants: Narwhal Medical LLC - Inventors: Loïc Van Horne - Web page: https://patentgrep.com/patent/US11896813B2 ## CPC - A61M 60/178: drawing blood from a ventricle and returning the blood to the arterial system via a cannula external to the ventricle, e.g. left or right ventricular assist devices - A61M 60/13: by means of a catheter allowing explantation, e.g. catheter pumps temporarily introduced via the vascular system - A61M 60/174: discharging the blood to the ventricle or arterial system via a cannula internal to the ventricle or arterial system - A61M 60/216: including a rotating member acting on the blood, e.g. impeller - A61M 60/226: the blood flow through the rotating member having mainly radial components - A61M 60/414: transmitted by a rotating cable, e.g. for blood pumps mounted on a catheter - A61M 60/416: transmitted directly by the motor rotor drive shaft - A61M 60/538: Regulation using real-time blood pump operational parameter data, e.g. motor current - A61M 60/585: User interfaces - A61M 60/808: specially adapted for deformable impellers, e.g. expandable impellers - A61M 60/81: Pump housings - A61M 60/824: Hydrodynamic or fluid film bearings - A61M 60/841: of balloon pumps for circulatory assistance - 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 Some embodiments of percutaneous ventricular assist devices have a two-part design that includes a housing component and a separately deployable rotatable inner catheter component. The housing component can include an expandable pump housing. The inner catheter can include an expandable pump impeller and an associated flexible drive shaft. The drive shaft can be coupled to a motor located external to the patient. The motor can rotate the drive shaft to spin the pump impeller inside of the pump housing, causing blood to be pumped within the patient. In some embodiments, the pump impeller is inflatable or self-expandable. The two-part percutaneous ventricular assist devices with inflatable or self-expandable pump impellers are designed to have very small delivery profiles. Accordingly, various deployment modalities, including radial artery deployment, are practicable using the two-part percutaneous ventricular assist devices described herein. ## Claims ### Claim 1 A method for deploying a percutaneous blood flow assist device to a target location within a patient, the method comprising: advancing, through an incision of the patient, an elongate delivery sheath device, the delivery sheath device defining a sheath lumen that contains a housing component slidably disposed in the sheath lumen, the housing component comprising: an elongate drive shaft housing defining a housing lumen; a pump housing disposed at a distal end portion of the drive shaft housing; and an inlet cannula extending distally from the pump housing, wherein the pump housing and the inlet cannula are radially reconfigurable between: (i) low-profile configurations when radially constrained in the sheath lumen and (ii) radially expanded configurations when unconstrained by the delivery sheath device; retracting, when the pump housing is at the target location, the delivery sheath device relative to the housing component to express the inlet cannula and the pump housing out from the sheath lumen; inserting a rotatable inner catheter into the housing lumen of the drive shaft housing, wherein the inner catheter comprises: an elongate flexible drive shaft; and a pump impeller disposed at a distal end of the drive shaft, wherein the pump impeller is in a radially collapsed configuration when within the housing lumen; advancing the inner catheter relative to the housing component to position the pump impeller within the pump housing; and expanding the pump impeller to a radially expanded operable configuration while the pump impeller is within the pump housing. ### Claim 2 (depends on 1) The method of claim 1, further comprising rotating, while the pump impeller is in the radially expanded operable configuration and within the pump housing, the drive shaft using a motor positioned external to the patient. ### Claim 3 (depends on 2) The method of claim 2, wherein the rotating the drive shaft causes the pump impeller to rotate relative to the pump housing, and wherein the pump impeller self-centers relative to the pump housing while rotating relative to the pump housing. ### Claim 4 (depends on 3) The method of claim 3, wherein the delivery sheath device and the drive shaft housing each define one or more openings, and wherein the one or more openings of the delivery sheath device at least partially align with the one or more openings of the drive shaft housing when the pump impeller is positioned in the pump housing. ### Claim 5 (depends on 4) The method of claim 4, wherein blood flows through the aligned one or more openings of the delivery sheath device and the drive shaft housing and distally toward the pump impeller to provide a hydrodynamic bearing between the pump impeller and the pump housing. ### Claim 6 (depends on 2) The method of claim 2, wherein the motor and a system controller are portable and mobile with the patient such that the patient is freely ambulatory while receiving circulatory support from the percutaneous blood flow assist device. ### Claim 7 (depends on 1) The method of claim 1, wherein the pump impeller is expanded by supplying an inflation fluid to the pump impeller via an inflation lumen of the drive shaft to inflate the pump impeller. ### Claim 8 (depends on 7) The method of claim 7, wherein the inflation fluid is radiopaque. ### Claim 9 (depends on 1) The method of claim 1, wherein the incision provides access to a femoral artery of the patient and the delivery sheath device is advanced to the target location via the femoral artery. ### Claim 10 (depends on 1) The method of claim 1, wherein the incision provides access to a radial artery of the patient and the delivery sheath device is advanced to the target location via the radial artery. ### Claim 11 (depends on 1) The method of claim 1, wherein the incision provides access to a thoracic cavity of the patient and the delivery sheath device is advanced to the target location via the thoracic cavity. ### Claim 12 (depends on 1) The method of claim 1, wherein the target location is an aortic valve region of the patient. ### Claim 13 (depends on 1) The method of claim 1, wherein the incision is created using standard percutaneous blood vessel access techniques. ### Claim 14 (depends on 1) The method of claim 1, wherein the pump impeller is movable relative to the pump housing in response to retraction or advancement of the drive shaft relative to the drive shaft housing. ### Claim 15 (depends on 1) The method of claim 1, wherein the delivery sheath device, the housing component, and the inner catheter all include radiopaque markers to allow identification and correct placement relative to the patient's anatomy and relative to each other. ### Claim 16 (depends on 1) The method of claim 1, wherein the target location is a pulmonary valve region of the patient. ### Claim 17 (depends on 1) The method of claim 1, wherein the target location is in a descending aorta at a renal artery level to provide additional blood flow to the patient's kidneys. ### Claim 18 (depends on 1) The method of claim 1, wherein the inlet cannula extends into a left ventricle while the pump housing is in an aorta.