Blood pump

Patent metadata

Field	Value
Publication number	US-2024024656-A1
Application number	US-202318215373-A
Country	US
Kind code	A1
Filing date	Jun 28, 2023
Priority date	Jun 23, 2015
Publication date	Jan 25, 2024
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 - 17 . (canceled)

18 . A blood pump configured to be placed in a renal vein of a patient to pump blood from a kidney of the patient towards an inferior vena cava of the patient, the blood pump comprising:
a pump casing having a blood flow inlet and a first blood flow outlet; an impeller arranged in the blood pump casing so as to be rotatable about an axis of rotation for conveying blood from the blood flow inlet to the first blood flow outlet; 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; and a drug eluting device at least partially surrounding the intermediate portion of the outflow cannula, the drug eluting device being configured to deliver a pharmaceutical substance to a target area in a patient, wherein the upstream end portion of the outflow cannula is connected to the pump casing such that blood is conveyed from the first blood flow outlet into and through the intermediate portion of the outflow cannula towards the downstream end portion of the outflow cannula, wherein the downstream end portion of the outflow cannula has a second blood flow outlet through which blood can exit the outflow cannula and which is arranged at least partially radially inwards relative to an outermost circumference of the intermediate portion of the outflow cannula, wherein 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, and wherein at least the intermediate portion of the outflow cannula is sized and shaped to contact an inner wall of the renal vein of the patient in which the blood pump is placed during operation of the blood pump in order to occlude the renal vein during operation of the blood pump.

19 . The blood pump of claim 18 , wherein the second blood flow outlet is disposed in the downstream end portion, such that blood can exit the outflow cannula at least partially in an axial direction.

20 . The blood pump of claim 18 , wherein a cross-sectional area of the second blood flow outlet is smaller than a largest cross-sectional area of the intermediate portion of the outflow cannula.

21 . The blood pump of claim 18 , wherein the outer diameter of the intermediate portion of the outflow cannula is at least 1.5 times as large as the outer diameter of the pump casing.

22 . The blood pump of claim 18 , wherein a largest diameter of the intermediate portion of the outflow cannula is between about 5 mm and 2 cm.

23 . The blood pump of claim 18 , wherein a longitudinal length of the intermediate portion of the outflow cannula is less than 5 cm.

24 . The blood pump of claim 18 , wherein the outflow cannula comprises a material that is softer than a material of the pump casing.

25 . The blood pump of claim 18 , wherein at least one of the upstream end portion of the outflow cannula and the downstream end portion of the outflow cannula is tapered.

26 . The blood pump of claim 18 , wherein a minimum inner diameter of the upstream end portion of the outflow cannula corresponds to the outer diameter of the pump casing and the outflow cannula is sealingly connected to the pump casing.

27 . The blood pump of claim 18 , wherein the drug eluting device comprises a reservoir that is connected to an access lumen for at least one of injecting and removing the pharmaceutical substance to or from the reservoir.

28 . The blood pump of claim 18 , wherein the drug eluting device is at least one of a substantially cylindrical and a substantially conical pad.

29 . The blood pump of claim 18 , comprising a support structure that is arranged around at least a portion of the intermediate portion of the outflow cannula, wherein the support structure is at least one of a substantially cylindrical and a substantially conical pad.

30 . The blood pump of claim 29 , wherein the support structure comprises the pharmaceutical substance.

31 . The blood pump of claim 29 , wherein the support structure is configured to conform to shape of the renal vein.

32 . The blood pump of claim 29 , wherein the support structure is configured to improve occlusion of the renal vein by the pump.

33 . The blood pump of claim 18 , wherein the blood pump is connected to a catheter that extends from the pump casing through the outflow cannula, or wherein the blood pump is connected to a catheter that extends from the pump casing in a direction away from the outflow cannula.

34 . The blood pump of claim 18 , wherein the blood pump is one of an axial blood pump, a centrifugal blood pump and a mixed-type blood pump.

35 . The blood pump of claim 20 , wherein the cross-sectional area of the second blood flow outlet is less than 50% of the cross-sectional area of the intermediate portion of the outflow cannula.

36 . The blood pump of claim 22 , wherein the largest diameter of the intermediate portion of the outflow cannula is between about 1 and 1.5 cm.

37 . The blood pump of claim 23 , wherein the longitudinal length of the intermediate portion of the outflow cannula is less than 3 cm.

Assignees

• Abiomed Europe Gmbh

Inventors

• Siess Thorsten
• Aboulhosn Walid

Classifications

• A61M60/135 Primary

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

• A61M60/812

  Vanes or blades, e.g. static flow guides · CPC title

• A61M60/81

  Pump housings · CPC title

• A61M60/861

  Connections or anchorings for connecting or anchoring pumps or pumping devices to parts of the patient's body · CPC title

• A61M60/33

  of kidneys · CPC title