Guidable intravascular blood pump and related methods

US9561314B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9561314-B2
Application numberUS-201615239574-A
CountryUS
Kind codeB2
Filing dateAug 17, 2016
Priority dateSep 3, 1999
Publication dateFeb 7, 2017
Grant dateFeb 7, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

An improved intravascular blood pump and related methods involving the broad inventive concept of equipping the intravascular blood pump with guiding features such that the intravascular blood pump can be selectively positioned at a predetermined location within the circulatory system of a patient.

First claim

Opening claim text (preview).

What is claimed is: 1. An intravascular blood pump system, comprising: an intravascular blood pump adapted to be guided to a predetermined location within the circulatory system of a patient by a guide wire and the intravascular blood pump configured to provide left-heart support, the intravascular blood pump comprising a rotor having a rotor hub tapering in the distal direction, at least one blade extending radially outward from the rotor hub; a cannula coupled to a distal end of the intravascular blood pump, one or more first ports and one or more second ports establishing fluid communication between a lumen of the cannula and an exterior region of the cannula, wherein at least one first port is located in proximity to the rotor and at least one second port is spaced apart from and located distal to the at least one first port, and wherein the intravascular blood pump is configured to draw blood from the patient's heart into the at least one second port through the cannula lumen and out the at least one first port to provide left-heart support while the cannula is positioned across an aortic valve of the patient, the cannula is configured such that when the intravascular blood pump is positioned in the patient to provide left-heart support the distal end of the cannula and the at least one second port are positioned inside the patient's heart and the proximal end of the cannula and the at least one first port are positioned in the patient's aorta; a catheter connected to a proximal end of the intravascular blood pump, a purge lumen extending through the catheter and operatively arranged to deliver purge fluid towards the intravascular blood pump; an elongate lumen arranged coaxially with at least a portion of the cannula and in series longitudinally with the cannula, and an end of the elongate lumen is adjacent an end of the cannula, the elongate lumen sized to slidably receive the guide wire and having a diameter sized smaller than a diameter of the cannula lumen; a pressure sensing element configured to sense pressure proximate the intravascular blood pump; a housing connected to a proximal end of the catheter; and first and second conduits each connected to the housing, at least one of the first conduit and second conduit in fluid communication with the purge lumen. 2. The intravascular blood pump system of claim 1 wherein the rotor comprises a second blade extending radially from the rotor hub and wherein the hub has a distal end extending distally beyond a most distal portion of the blades. 3. The intravascular blood pump system of claim 1 wherein the housing is configured to have the purge fluid pass through it. 4. The intravascular blood pump system of claim 1 wherein the cannula is reinforced with a spiral wire. 5. The intravascular blood pump system of claim 1 wherein the pressure sensing element comprises at least one of a piezo-electric pressure sensing element and a strain gauge. 6. The intravascular blood pump system of claim 5 wherein the pressure sensing element further comprises a fluid column extending through the catheter. 7. The intravascular blood pump system of claim 1 wherein the pressure sensing element is used to determine a differential pressure. 8. The intravascular blood pump system of claim 1 further comprising a rotor shroud, a portion of the rotor shroud having an outer diameter matching an inner diameter of a proximal portion of the cannula. 9. The intravascular blood pump system of claim 1 further comprising a rotor shroud, motor assembly and a drive cable, the drive cable at least partially disposed within the catheter, wherein the motor assembly and drive cable are configured to drive the rotor, wherein the elongate lumen is proximal to the cannula and the motor assembly is configured to remain external to the patient, and wherein the intravascular blood pump system comprises a dual construction arrangement whereby the rotor is configured to be docked within the rotor shroud. 10. The intravascular blood pump system of claim 1 further comprising a distal tip member at one end, the distal tip member comprising a stem portion, extending distally away from a distal end of the cannula lumen, and a curved tail portion located distal to the stem portion. 11. The intravascular blood pump system of claim 10 wherein the elongate lumen is located proximal to the distal tip member. 12. The intravascular blood pump system of claim 1 further comprising a pigtail shaped distal tip member at one end. 13. The intravascular blood pump system of claim 1 further comprising a J-shaped distal tip member at one end. 14. The intravascular blood pump system of claim 1 further comprising a fluid delivery pump configured to deliver purge fluid through the purge lumen towards the intravascular blood pump. 15. The intravascular blood pump system of claim 14 wherein the fluid delivery pump is configured to deliver the purge fluid at a pressure than is both sufficient to avoid clotting of the patient's blood and that is higher than a blood pressure of the patient adjacent the intravascular blood pump. 16. The intravascular blood pump system of claim 1 further comprising a rotor shroud disposed about the rotor and wherein a proximal end of the cannula is disposed about a distal end of the rotor shroud. 17. The intravascular blood pump system of claim 1 further comprising a rotor shroud having a distal portion with a first outer diameter and a more proximal portion with a second outer diameter larger than the first outer diameter. 18. The intravascular blood pump system of claim 1 further comprising an elongate tubular element defining the elongate lumen. 19. The intravascular blood pump system of claim 1 wherein the purge lumen is a side lumen extending longitudinally through the catheter but offset radially from a central axis of the catheter. 20. An intravascular blood pump system, comprising: an intravascular blood pump adapted to be guided to a predetermined location within the circulatory system of a patient by a guide wire and configured to provide left-heart support, the intravascular blood pump comprising a rotor having a rotor hub tapering in the distal direction and a rotor shroud at least partially disposed about the rotor hub, at least one blade extending radially outward from the rotor hub, a distal end of the hub extending distally beyond a most distal portion of the at least one blade; a cannula coupled to a distal end of the intravascular blood pump, a portion of the rotor shroud having an outer diameter matching an inner diameter of a proximal portion of the cannula, the proximal portion of the cannula disposed about a distal end of the rotor shroud, one or more first ports and one or more second ports establishing fluid communication between a lumen of the cannula and an exterior region of the cannula, wherein at least one first port is located in proximity to the rotor and at least one second port is spaced apart from and located distal to the at least one first port, and wherein the intravascular blood pump is configured to draw blood from the patient's heart into the at least one second port through the cannula lumen and out the at least one first port to provide left-heart support while the cannula is positioned across an aortic valve of the patient, the cannula is configured such that when the intravascular blood pump is positioned in the patient to provide left-heart support the distal end of the cannula and the at least one second port are positioned inside the patient's he

Assignees

Inventors

Classifications

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9561314B2 cover?
An improved intravascular blood pump and related methods involving the broad inventive concept of equipping the intravascular blood pump with guiding features such that the intravascular blood pump can be selectively positioned at a predetermined location within the circulatory system of a patient.
Who is the assignee on this patent?
Maquet Cardiovascular Llc
What technology area does this patent fall under?
Primary CPC classification A61M1/125. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Feb 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).