IP Library › Granted Patent US 12,364,799
Granted Patent B2
US 12,364,799 · App. 18/420,914 · Granted Jul 22, 2025

Blood pump with flow cannula

Inventors: Thorsten Siess (Aachen, DE); Gerd Spanier (Aachen, DE); Walid Aboulhosn (Aachen, DE)
Assignee: ABIOMED EUROPE GMBH
A61M1/3659A61M60/178A61M60/216A61M60/237A61M60/859A61M2205/04A61M2210/125
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Quick Facts
Patent No.
US 12,364,799
App. No.
18/420,914
Granted
Jul 22, 2025
Kind
B2
Abstract

A blood pump for supporting a patient's heart includes a flow cannula having a distal portion including a distal end and a proximal portion including a proximal end opposite the distal end, the distal end of the flow cannula configured to be connected to the patient's heart or a blood vessel to establish fluid communication between the blood pump and the patient's heart and blood vessel, respectively. The flow cannula further includes an intermediate portion attached to the distal portion and the proximal portion, wherein the intermediate portion allows twisting thereof with a lower force than the distal portion and the proximal portion. The intermediate portion can be fully occluded by twisting it. At least a portion of the intermediate portion either alone or in combination with the distal portion is adapted to be permanently attached to the patient's heart or a blood vessel.

Claims (85)

1. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion comprises an attachment member at a distal end of the intermediate portion, wherein the attachment member is configured to be attached to the heart of the patient permanently and is sutured to the heart of the patient.

2. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion comprises an attachment member at a distal end of the intermediate portion, wherein the attachment member is made of a felt material.

3. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion comprises an attachment member at a distal end of the intermediate portion, wherein the attachment member comprises a disc, a plate, or a sheet.

4. The blood pump of claim 3 , wherein the attachment member comprises a continuous disc, a continuous plate, or a continuous sheet.

5. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion comprises an attachment member at a distal end of the intermediate portion, wherein the attachment member comprises a plurality of sections separated by respective gaps, and wherein the plurality of sections extend radially from the intermediate portion.

6. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion comprises an attachment member at a distal end of the intermediate portion, wherein the attachment member is attached to the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula by at least one security filament.

7. A blood pump for supporting a heart of a patient, the blood pump comprising:

a pump casing including at least a first inlet and a first outlet;

an impeller disposed in the pump casing, the impeller configured to draw blood into the pump casing;

an outflow cannula having a proximal end and a distal end, the proximal end of the outflow cannula coupled to the pump casing at the first outlet, the distal end of the outflow cannula configured to be attached to an aorta of the patient; and

an inflow cannula coupled to the pump casing at the first inlet, the inflow cannula comprising:

a distal end of the inflow cannula;

a proximal end of the inflow cannula opposite the distal end of the inflow cannula along a longitudinal axis of the inflow cannula, the distal end of the inflow cannula configured to be connected to the heart of the patient or a blood vessel of the patient in order to establish a fluid communication between the blood pump and the heart of the patient or between the blood pump and the blood vessel of the patient, respectively;

a distal portion of the inflow cannula including the distal end of the inflow cannula;

a proximal portion of the inflow cannula including the proximal end of the inflow cannula,

wherein the proximal portion of the inflow cannula and distal portion of the inflow cannula are formed as a single piece; and

an intermediate portion placed over the single piece of the distal portion of the inflow cannula and the proximal portion of the inflow cannula, wherein the intermediate portion allows twisting thereof with a lower force than at least one of the distal portion of the inflow cannula and the proximal portion of the inflow cannula,

wherein the intermediate portion is configured to be fully occluded by twisting thereof,

wherein at least a portion of the intermediate portion is configured to be permanently attached to the heart of the patient or the blood vessel of the patient, and

wherein the intermediate portion is attached to the proximal portion of the inflow cannula by a friction fit.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2024
From: SIESS, THORSTEN; SPANIER, GERD; ABOULHOSN, WALID
To: ABIOMED EUROPE GMBH
Reel/Frame 066365/0783 →
Priority Claims (1)
EP 16186860 · Sep 1, 2016 · regional
Continuity (4)
Continuation 18096038 · Jan 12, 2023
Continuation 17556638 · Dec 20, 2021
Division 16329252
Related Publication 20240252733A1 · Aug 1, 2024
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