Blood pump

Patent metadata

Field	Value
Publication number	US-2025381385-A1
Application number	US-202519243838-A
Country	US
Kind code	A1
Filing date	Jun 20, 2025
Priority date	Jun 23, 2015
Publication date	Dec 18, 2025
Grant date	—

Abstract

A blood pump comprises a pump casing having a blood flow inlet and a blood flow outlet, and an impeller arranged in said pump casing so as to be rotatable about an axis of rotation. The impeller has blades sized and shaped for conveying blood from the blood flow inlet to the blood flow outlet. The blood pump also has an outflow cannula having an upstream end portion, a downstream end portion and an intermediate portion extending between the upstream end portion and the downstream end portion. The upstream end portion of the outflow cannula is connected to the pump casing such that blood is conveyed from the blood flow outlet of the pump casing into and through the intermediate portion of the outflow cannula towards the downstream end portion of the outflow cannula, wherein the downstream end portion has a blood flow outlet through which blood can exit the outflow cannula. At least a portion of the intermediate portion of the outflow cannula has an outer diameter that is larger than an outer diameter of the pump casing.

First claim

1 . A blood pump ( 1 ; 201 ; 301 ), comprising:
a pump casing ( 2 ; 202 ; 302 ) having a blood flow inlet ( 21 ; 221 ; 321 ) and a blood flow outlet ( 22 ; 222 ; 322 ), an impeller ( 3 ; 203 ; 303 ) arranged in said pump casing ( 2 ; 202 ; 302 ) so as to be rotatable about an axis of rotation for conveying blood from the blood flow inlet ( 21 ; 221 ; 321 ) to the blood flow outlet ( 22 ; 222 ; 322 ), and an outflow cannula ( 4 ; 204 ; 304 ) having an upstream end portion ( 41 ; 241 ; 341 ), a downstream end portion ( 43 ; 243 ; 343 ) and an intermediate portion ( 42 ; 242 ; 343 ) extending between the upstream end portion ( 41 ; 241 ; 341 ) and the downstream end portion ( 43 ; 243 ; 343 ), the upstream end portion ( 41 ; 241 ; 341 ) of the outflow cannula ( 4 ; 204 ; 304 ) being connected to the pump casing ( 2 ; 202 ; 302 ) such that blood is conveyed from the blood flow outlet ( 22 ; 222 ; 322 ) of the pump casing ( 2 ; 202 ; 302 ) into and through the intermediate portion ( 42 ; 242 ; 342 ) of the outflow cannula ( 4 ; 204 ; 304 ) towards the downstream end portion ( 43 ; 243 ; 343 ) of the outflow cannula ( 4 ; 204 ; 304 ), wherein the downstream end portion ( 43 ; 243 ; 343 ) has a blood flow outlet ( 44 ; 244 ; 344 ) through which blood can exit the outflow cannula ( 4 ; 204 ; 304 ) and which is arranged at least partially radially inwards relative to an outermost circumference of the outflow cannula's intermediate portion ( 42 ; 242 ; 342 ), wherein at least a portion of the intermediate portion ( 42 ; 242 ; 342 ) of the outflow cannula ( 4 ; 204 ; 304 ) has an outer diameter that is larger than an outer diameter of the pump casing ( 2 ; 202 ; 302 ), wherein at least the outflow cannula's intermediate portion ( 42 ; 242 ; 342 ) is sized and shaped to contact an inner wall of a patient's vessel ( 104 ; 108 ) in which the blood pump ( 1 ; 201 ; 301 ) is placed during operation of the blood pump ( 1 ; 201 ; 301 ) in order to occlude the vessel ( 104 ; 108 ) during operation of the blood pump ( 1 ).

2 . The blood pump of claim 1 , wherein the blood flow outlet ( 44 ; 244 ; 344 ) is disposed in the downstream end portion ( 43 ; 243 ; 343 ), such that blood can exit the outflow cannula ( 4 ; 204 ; 304 ) at least partially in an axial direction.

3 . The blood pump of claim 1 or 2 , wherein a cross-sectional area of the blood flow outlet ( 44 ; 244 ; 344 ) of the outflow cannula's downstream end portion ( 43 ; 243 ; 343 ) is smaller than a largest cross-sectional area of the outflow cannula's intermediate portion ( 42 ; 242 ; 342 ), wherein the cross-sectional area of the blood flow outlet ( 44 ; 244 ; 344 ) of the outflow cannula's downstream end portion ( 43 ; 243 ; 343 ) is preferably less than 50%, preferably less than 40%, more preferably less than 30%, of the cross-sectional area of the outflow cannula's intermediate portion ( 42 ; 242 ; 342 ), and/or
wherein the blood flow outlet ( 44 ; 244 ; 344 ) of the outflow cannula's downstream end portion ( 43 ; 243 ; 343 ) comprises at least two openings, preferably three openings, more preferably four openings.

4 . The blood pump of any one of claims 1 to 3 , wherein the diameter of the outflow cannula's intermediate portion ( 42 ; 242 ; 342 ) is at least 1.5 times as large as the diameter of the pump casing ( 2 ; 202 ; 302 ), preferably twice, more preferably three times, still more preferably four times as large.

5 . The blood pump of any one of claims 1 to 4 , wherein a largest diameter of the outflow cannula's intermediate portion ( 42 ; 242 ) is between about 5 mm and 2 cm, preferably between about 1 and 1.5 cm, or wherein a largest diameter of the outflow cannula's intermediate portion ( 342 ) is preferably between about 0.5 and 5 mm, more preferably about 2 mm.

6 . The blood pump of any one of claims 1 to 5 , wherein a longitudinal length of the outflow cannula's intermediate portion ( 42 ; 242 ) is less than 5 cm, preferably less than 3 cm, or wherein a longitudinal length of the outflow cannula's intermediate portion ( 342 ) is between about 1 and 3 mm.

7 . The blood pump of any one of claims 1 to 6 , wherein the outflow cannula ( 4 ; 204 ; 304 ) comprises a material that is softer than a material of the pump casing ( 2 ; 202 ; 302 ), wherein preferably the material of the outflow cannula ( 4 ; 204 ; 304 ) is elastic.

8 . The blood pump of any one of claims 1 to 7 , wherein at least one of the outflow cannula's upstream end portion ( 41 ; 241 ; 341 ) and the outflow cannula's downstream end portion ( 43 ; 243 ; 343 ) is tapered.

9 . The blood pump of any one of claims 1 to 8 , wherein a minimum inner diameter of the outflow cannula's upstream end portion ( 41 ; 241 ; 341 ) corresponds to an outer diameter of the pump casing ( 2 ; 202 ; 302 ) and the outflow cannula ( 4 ; 204 ; 304 ) is sealingly connected to the pump casing ( 2 ; 202 ; 302 ).

10 . The blood pump of any one of claims 1 to 9 , comprising a support structure ( 47 ; 47 ′) that is arranged around at least a portion of the outflow cannula's intermediate portion ( 42 ), wherein preferably the support structure ( 47 ; 47 ′) is at least one of a substantially cylindrical and substantially conical pad, the support structure ( 47 ; 47 ′) preferably comprising a pharmaceutical substance.

11 . The blood pump of any one of claims 1 to 9 , comprising a drug eluting device ( 347 ), the drug eluting device ( 347 ) being configured to deliver a pharmaceutical substance to a target area in a patient, wherein preferably the drug eluting device ( 347 ) at least partially surrounds the intermediate portion ( 342 ) of the outflow cannula ( 304 ), wherein more preferably the drug eluting device ( 347 ) is at least one of a substantially cylindrical and substantially conical pad.

12 . The blood pump of claim 11 , wherein the drug eluting device ( 347 ′) comprises a reservoir ( 348 ) that is connected to an access lumen ( 360 ) for at least one of injecting and removing a pharmaceutical substance to or from the reservoir ( 348 ).

13 . The blood pump of any one of claims 1 to 12 , wherein the blood pump ( 1 ; 301 ) is connected to a catheter ( 5 ; 305 ) that extends from the pump casing ( 2 ; 302 ) through the outflow cannula ( 4 ; 304 ), or wherein the blood pump ( 201 ) is connected to a catheter ( 205 ) that extends from the pump casing ( 202 ) in a direction away from the outflow cannula ( 204 ).

14 . The blood pump of any one of claims 1 to 13 , wherein the blood pump ( 1 ; 201 ; 301 ) is an axial blood pump, a centrifugal blood pump or a mixed-type blood pump, and/or wherein the blood pump is configured to be placed in a human patient's renal vein ( 104 ) to pump blood from the patient's kidney ( 105 ) towards the patient's inferior vena cava ( 103 ), or configured to be placed in a human patient's coronary artery ( 108 ).

15 . A method for supporting a blood flow in a patient's blood vessel using a blood pump,
the blood pump ( 1 ; 201 ; 301 ) comprising a pump casing ( 2 ; 202 ; 302 ) having a blood flow inlet ( 21 ; 221 ; 321 ) and a blood flow outlet ( 22 ; 222 ; 322 ), an impeller ( 3 ; 203 ; 303 ) arranged in said pump casing ( 2 ; 202 ; 302 ) so as to be rotatable about an axis of rotation for conveying blood from the blood flow inlet ( 21 ; 221 ; 321 ) to the blood flow outlet ( 22 ; 222 ; 322 ), and an outflow cannula ( 4 ; 204 ; 304 ) having an upstream end portion ( 41 ; 241 ; 341 ), a downstream end portion ( 43 ; 243 ; 343 ) and an intermediate portion ( 42 ; 24

Assignees

• Abiomed Europe Gmbh

Inventors

• Siess Thorsten
• Aboulhosn Walid

Classifications

• A61M60/135 Primary

  inside a blood vessel, e.g. using grafting · CPC title

• A61M60/33

  of kidneys · CPC title

• A61M60/157

  mechanically acting upon the inside of the patient's blood vessel structure, e.g. contractile structures placed inside a vessel · CPC title

• A61M60/13

  by means of a catheter allowing explantation, e.g. catheter pumps temporarily introduced via the vascular system · CPC title

• A61M60/411

  generated by an electromotor · CPC title