HVAD flushing through non-uniform thrust bearing clearances

文档序号:143638 发布日期:2021-10-22 浏览:38次 中文

阅读说明:本技术 通过非均匀推力轴承间隙进行hvad冲洗 (HVAD flushing through non-uniform thrust bearing clearances ) 是由 C·雷耶斯 J·沃尔曼 于 2020-02-10 设计创作,主要内容包括:一种血泵,其具有包括入口元件的壳体。所述入口元件具有近端部分,所述近端部分被设定尺寸以用于容纳在患者心脏的至少一部分内并限定主纵向轴线。转子被配置成围绕所述主纵向轴线在所述壳体内旋转并促使血液从心脏流出。至少一个定子安置在所述壳体内,并且定位在所述壳体内,位于所述转子的上游和下游这两种情况中的至少一个。在所述血泵的操作过程中,所述转子相对于所述主纵向轴线保持斜角。(A blood pump has a housing including an inlet element. The inlet element has a proximal end portion sized for receipt within at least a portion of a patient's heart and defining a major longitudinal axis. A rotor is configured to rotate within the housing about the major longitudinal axis and urge blood out of the heart. At least one stator is disposed within the housing and positioned within the housing at least one of upstream and downstream of the rotor. During operation of the blood pump, the rotor is held at an oblique angle relative to the main longitudinal axis.)

1. A blood pump, comprising:

a housing including an inlet element having a proximal end portion sized for receipt within at least a portion of a patient's heart and defining a major longitudinal axis;

a rotor configured to rotate within the housing about the major longitudinal axis and to urge blood out of the heart;

at least one stator disposed within the housing and positioned within the housing at least one of upstream and downstream of the rotor; and

during operation of the blood pump, the rotor is held at an oblique angle relative to the main longitudinal axis.

2. The pump of claim 1, wherein the oblique angle is between 1-30 degrees relative to a longitudinal axis transverse to the major longitudinal axis.

3. The pump of claim 1, wherein the at least one stator includes a first stator downstream of the rotor and a second stator upstream of the rotor.

4. The pump of claim 3, further comprising a first non-ferromagnetic disk disposed between the first stator and the rotor and a second non-ferromagnetic disk disposed between the second stator and the rotor.

5. The pump of claim 4, wherein the first stator comprises a first back iron and the second stator comprises a second back iron, and wherein at least one of the group consisting of the first back iron and the second back iron is disposed at an oblique angle relative to a respective one of the first non-ferromagnetic disk and the second ferromagnetic disk.

6. The pump of claim 5, wherein the first back iron is disposed at an oblique angle relative to the first non-ferromagnetic disk and the second back iron is disposed at an oblique angle relative to the second ferromagnetic disk.

7. The pump of claim 6, wherein the bevel angle of the first back iron is the same as the bevel angle of the second back iron.

8. The pump of claim 5, wherein the rotor is an impeller, and wherein the impeller defines a plurality of hydrodynamic thrust bearings, and wherein the plurality of hydrodynamic thrust bearings face the second non-ferromagnetic disk.

9. The pump of claim 1, wherein the housing includes a center post, and wherein the rotor defines an opening sized to receive the center post, and wherein the rotor rotates about the center post.

10. The pump of claim 9, wherein the center post comprises a plurality of inner bearing magnets, and wherein the rotor comprises a plurality of outer bearing magnets, and wherein the plurality of inner bearing magnets and the plurality of outer bearing magnets are configured to space the rotor a distance from the center post, and wherein the plurality of inner bearing magnets are disposed at the oblique angle relative to the plurality of outer bearing magnets such that the rotor is tilted at an oblique angle relative to the main longitudinal axis.

11. The pump of claim 9, wherein the center post is symmetric about the major longitudinal axis.

12. A blood pump, comprising:

a housing including an inlet element having a proximal end portion sized for receipt within at least a portion of a patient's heart and defining a major longitudinal axis;

a rotor configured to rotate within the housing about the major longitudinal axis and to urge blood out of the heart;

a first stator disposed within the housing downstream of the rotor and a second stator disposed within the housing upstream of the rotor;

a first non-ferromagnetic disk disposed between the first stator and the rotor; and

during operation of the blood pump, the rotor is maintained at a predetermined and constant non-uniform distance from the first non-ferromagnetic disk.

Technical Field

The present technology relates generally to implantable blood pumps.

Background

Implantable blood pumps are commonly used to assist the pumping action of a failing heart. Typically, implantable blood pumps are surgically implanted in a patient and include a housing having an inlet and an outlet, and having a rotor mounted within the housing. The inlet of the housing is connected to a chamber of the patient's heart, typically the left ventricle, and the outlet is connected to an artery such as the aorta. Rotation of the pump rotor drives blood from the inlet to the outlet, thereby facilitating blood flow from the heart chamber into the artery.

Some implantable blood pumps are provided with non-contact bearings so that in operation, the rotor floats within the housing. With non-contact bearings, there is no solid-solid contact between the rotor and the housing, and therefore no mechanical wear during operation. One form of non-contact bearing is a hydrodynamic bearing. In hydrodynamic bearings, the pumped liquid passes between the surfaces of the gap between the surface of the rotor and the surface of the hydrodynamic bearing, the gap being many times larger than the size of the blood cells. However, in some cases, the blood passing through the pump may contain thrombus particles, solid or semi-solid deposits that are generated in the patient. Thrombus can become lodged on the surface of the hydrodynamic bearing and interfere with its operation. The surfaces are configured such that as the rotor rotates, fluid disposed between the surfaces exerts pressure on the rotor surfaces that holds the rotor away from the housing.

Disclosure of Invention

The technology of the present disclosure relates generally to implantable centrifugal blood pumps having non-uniform thrust bearing clearances.

In one aspect, the present disclosure provides a blood pump having a housing including an inlet element. The inlet member has a proximal end portion sized for receipt within at least a portion of a patient's heart and defining a major longitudinal axis. A rotor configured to rotate within the housing about a main longitudinal axis and to urge blood out of the heart. At least one stator is disposed within the housing and is positioned within the housing at least one of upstream and downstream of the rotor. During operation of the blood pump, the rotor is held at an oblique angle relative to the main longitudinal axis.

In another aspect, the oblique angle to a longitudinal axis transverse to the major longitudinal axis is between 1-30 degrees.

In another aspect, the at least one stator includes a first stator downstream of the rotor and a second stator upstream of the rotor.

In another aspect, a first non-ferromagnetic disk is disposed between the first stator and the rotor and a second non-ferromagnetic disk is disposed between the second stator and the rotor.

In another aspect, the first stator comprises a first back iron and the second stator comprises a second back iron, and wherein at least one of the group consisting of the first back iron and the second back iron is disposed at an oblique angle relative to a respective one of the first non-ferromagnetic disk and the second ferromagnetic disk.

In another aspect, the first back iron is positioned at an oblique angle relative to the first non-ferromagnetic disk and the second back iron is positioned at an oblique angle relative to the second ferromagnetic disk.

In another aspect, the bevel angle of the first back iron is the same as the bevel angle of the second back iron.

In another aspect, the rotor is an impeller, and wherein the impeller defines a plurality of hydrodynamic thrust bearings, and wherein the plurality of hydrodynamic thrust bearings face the second non-ferromagnetic disk.

In another aspect, the housing includes a center post, and wherein the rotor defines an opening sized to receive the center post, and wherein the rotor rotates about the center post.

In another aspect, the central column comprises a plurality of inner bearing magnets, and wherein the rotor comprises a plurality of outer bearing magnets, and wherein the plurality of inner bearing magnets and the plurality of outer bearing magnets are configured to space the rotor a distance from the central column, and wherein the plurality of inner bearing magnets are disposed at an oblique angle relative to the plurality of outer bearing magnets to tilt the rotor at an oblique angle relative to the major longitudinal axis.

In another aspect, the central column is symmetrical about the major longitudinal axis.

In one aspect, the present disclosure provides a method of operating an implantable blood pump. An implantable blood pump includes an inflow cannula defining a main longitudinal axis and a rotor configured to rotate about the main longitudinal axis and to urge blood downstream from the inflow cannula to an outlet downstream of the rotor. The method includes maintaining the impeller at a predetermined oblique angle relative to the main longitudinal axis as the impeller rotates about the main longitudinal axis.

In another aspect, the implantable blood pump is a centrifugal blood pump.

In another aspect, the oblique angle is between 1-30 degrees.

In another aspect, an implantable blood pump includes a stator having a back iron, and wherein the back iron is disposed at an oblique angle relative to a main longitudinal axis.

In another aspect, an implantable blood pump includes a central column, and wherein the central column is disposed at an oblique angle relative to a major longitudinal axis.

In another aspect, an implantable blood pump includes a central column, and wherein the central column includes a plurality of internal bearing magnets, and wherein the internal bearing magnets are disposed at an oblique angle relative to a main longitudinal axis.

In another aspect, an implantable blood pump includes a stator having a back iron and a non-ferromagnetic disk disposed between the rotor and the stator, the back iron being spaced apart from and disposed at an oblique angle relative to the non-ferromagnetic disk.

In another aspect, an implantable blood pump includes a second stator having a second back iron spaced apart from and disposed at an oblique angle relative to a second non-ferromagnetic disk and the second non-ferromagnetic disk disposed between the rotor and the second stator.

In one aspect, the present disclosure provides a blood pump. The blood pump includes a housing including an inlet element having a proximal end portion sized for receipt within at least a portion of a patient's heart and defining a major longitudinal axis. A rotor configured to rotate within the housing about a main longitudinal axis and to urge blood out of the heart. The first stator is disposed in the housing downstream of the rotor and the second stator is disposed in the housing upstream of the rotor. A first non-ferromagnetic disk is disposed between the first stator and the rotor. During operation of the blood pump, the rotor is maintained at a predetermined and constant non-uniform distance from the first non-ferromagnetic disk.

The details of one or more aspects of the disclosure are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the techniques described in the disclosure will be apparent from the description and drawings, and from the claims.

Drawings

A more complete understanding of the present invention and the attendant advantages and features thereof will be more readily understood by reference to the following detailed description when considered in conjunction with the accompanying drawings wherein:

FIG. 1 is an exploded view of an implantable blood pump constructed in accordance with the principles of the present application;

FIG. 2 is an assembled cross-sectional view of the implantable blood pump shown in FIG. 1, showing the poles of the inner and outer bearings of the implantable blood pump, and showing a second back iron that is angled;

FIG. 3 is a cross-sectional view of an impeller, first and second non-ferromagnetic disks, and first and second back irons of the implantable blood pump of FIG. 2;

FIG. 4 is an impeller, first and second non-ferromagnetic disks, and first and second back irons of the implantable blood pump of FIG. 3, wherein the first and second back irons are inclined at an oblique angle; and

FIG. 5 is a cross-sectional view of an alternative embodiment of the inner and outer bearings shown in FIG. 2, wherein the inner bearing is tilted at an oblique angle.

Detailed Description

It should be understood that the various aspects disclosed herein may be combined in different combinations than those specifically presented in the description and drawings. It will also be understood that, depending on the example, certain acts or events of any of the processes or methods described herein may be performed in a different sequence, may be added, merged, or omitted altogether (e.g., all described acts or events may not be necessary for performing these techniques), and further, for clarity purposes, while certain aspects of the disclosure are described as being performed by a single module or unit, it should be understood that the techniques of this disclosure may be performed by a unit or combination of modules associated with, for example, a medical device.

In one or more examples, the described techniques may be implemented in hardware, software, firmware, or any combination thereof. If implemented in software, the functions may be stored on a computer-readable medium in the form of one or more instructions or code and may be executed by a hardware-based processing unit. The computer-readable medium may include a non-transitory computer-readable medium corresponding to a tangible medium such as a data storage medium (e.g., RAM, ROM, EEPROM, flash memory, or any other medium that can be used to store desired program code in the form of instructions or data structures and that can be accessed by a computer).

The instructions may be executed by one or more processors, such as one or more Digital Signal Processors (DSPs), general purpose microprocessors, Application Specific Integrated Circuits (ASICs), field programmable logic arrays (FPGAs), or other equivalent integrated or discrete logic circuitry. Thus, the term "processor," as used herein may refer to any of the foregoing structure or any other physical structure suitable for implementing the described techniques. Also, the techniques may be fully implemented in one or more circuits or logic elements.

Referring now to the drawings in which like reference designators refer to like elements, there is shown in fig. 1-2 an exemplary blood pump constructed in accordance with the principles of the present application and designated generally as "10". The blood pump 10 according to one embodiment of the present disclosure includes a static structure or housing 12 that houses components of the blood pump 10. In one configuration, the housing 12 includes a lower housing or first portion 14, an upper housing or second portion 16, and an inlet element or inflow sleeve 18 that includes an outer tube 18a and an inner tube 18 b. The first and second portions 14, 16 cooperatively define a volute chamber 20 having a major longitudinal axis 22 extending through the first portion and the inflow cannula 18. The chamber 20 defines a radius that gradually increases about the axis 22 to an exit location on the perimeter of the chamber 20. The first portion 14 and the second portion 16 define an outlet 24 in communication with the chamber 20. The first and second portions 14, 16 also define an isolation chamber (not shown) separated from the volute chamber 20 by a magnetically permeable wall.

The inflow sleeve 18 is generally cylindrical and extends from the second portion 16 generally along an axis 22. The inflow cannula 18 has an upstream or proximal end 26 distal to the second portion 16 and a downstream or distal end 28 proximal to the chamber 20. The components of the housing 12 described above are fixedly connected to one another such that the housing 12 as a whole defines a continuous closed flow path. The flow path extends from an upstream end 26 at an upstream end of the flow path to an outlet 24 at a downstream end of the flow path. The upstream and downstream directions along the flow path are represented in fig. 1 by arrows U and D, respectively. The center post 30 is mounted to the first portion 14 symmetrically along the axis 22 and about the axis 22. A generally disc-shaped ferromagnetic rotor or impeller 32 having a central bore 34 is mounted within the chamber 20 for rotation about the axis 22. The rotor 32 includes permanent magnets and flow channels for transferring blood from near the center of the rotor 32 to the periphery of the rotor 32. In the assembled state, the post 30 is received in a central bore of the rotor 32. A first stator 36 having at least two coils and a first back iron 37 may be disposed within the first section 14 downstream of the rotor 32. The first stator 36 may be axially aligned with the rotor along the axis 22 such that when current is applied to the coils in the first stator 36, the electromagnetic force generated by the first stator 36 rotates the rotor 32 and pumps blood. A second stator 38 including a second back iron 39 may be disposed within the second portion 16 upstream of the rotor 32. The second stator 38 may be configured to operate in conjunction with or independent of the first stator 36 to rotate the rotor 32.

Electrical connectors 41 and 43 are disposed on the first and second portions 14 and 16, respectively, for connecting the coils to a power source, such as a controller (not shown). The controller is arranged to apply electrical power to the coils of the pump to generate a rotating magnetic field that rotates the rotor 32 about the axis 22 in a predetermined first rotational direction, for example in the direction R indicated by the arrow in figure 1, i.e. counter-clockwise as viewed from the upstream end of the inflow sleeve 18. In other configurations of the blood pump 10, the first direction may be a clockwise direction. Rotation of the rotor 32 causes the blood to flow downstream along the flow path such that the blood moves along the flow path in the downstream direction D and exits through the outlet 24. A first non-ferromagnetic disk 40, such as a ceramic disk, may be disposed within the first portion 14 downstream of the rotor 32 between the first stator 36 and the rotor 32. A second non-ferromagnetic disk 42 may be positioned within the second portion 16 upstream of the rotor 32 between the second stator 38 and the rotor 32. The first and second disks 40 and 42 may be constructed of a ceramic material that is attached to the first portion 14 or the second portion 16 of the housing 12. During rotation, the fluid dynamic bearing 44 and the plurality of internal magnetic bearings 46 and the plurality of external magnetic bearings 48 support the rotor 32 and maintain the rotor 32 out of contact with the inner surfaces of the first and second non-ferromagnetic disks 40, 42. In other words, the operation of the rotor 32 is contactless in that it does not contact any component of the pump 10 other than the fluid flowing through the pump 10. The general arrangement of the above components may be similar to that of HeartWare corporation, the assignee of the present application, under the nameA blood pump 10 is sold. In U.S. patent No. 6,688,861; 7,575,423, respectively; 7,976,271, respectively; and 8,419,609, the arrangement of components used in such pumps, such as magnets, electromagnetic coils, and fluid dynamic bearings, and variations of the overall design.

Referring now to fig. 2-3, in one configuration, the rotor 32 is held at an oblique angle relative to the main longitudinal axis 22 during operation of the pump 10. For example, the rotor 32 may be tilted relative to the main longitudinal axis 22 such that a gap between at least one of the group consisting of the first non-ferromagnetic disk 40 and the second non-ferromagnetic disk 42 is maintained at a predetermined non-uniform distance. In particular, as shown in fig. 3, the rotor 32 has a small gap between the first non-ferromagnetic disk 42 facing the first hemisphere 50 of the first non-ferromagnetic disk 42 and the second hemisphere 52 facing the first non-ferromagnetic disk 42 opposite the first hemisphere 50. This gap is maintained as the rotor 32 rotates about the axis 22, through which thrombus may escape to avoid coagulation or deposition on the rotor 32, as explained in more detail below.

In one configuration, to achieve and maintain the rotor 32 at a bevel angle, which may be, for example, between 0.1-30 degrees or any bevel angle, the second back iron 39 of the second stator 38 may be angled relative to the second non-ferromagnetic disk 42. In the example shown in fig. 3, the second back iron 39 is inclined at a bevel angle, which causes the rotor 32 to be inclined at an opposite bevel angle. In other words, the second back iron 39 is tilted such that it is closer to the second hemisphere 52 of the second non-ferromagnetic disk 42 than the first hemisphere 50. In this configuration, the portion of the second back iron closer to the rotor 32 exhibits a greater pulling force on the rotor 32 than the portion of the back iron 39 further from the rotor 32. During operation, the hydrodynamic thrust bearing 44 pushes the rotor 32 away from the second non-ferromagnetic disk 42 and counteracts the pulling force of the second back iron 39, so the gap between the second non-ferromagnetic disk 42 and the second stator 38 is larger where the second back iron 39 exerts a smaller pulling force, and the gap remains at this non-uniform distance.

In another configuration, as shown in FIG. 4, the second back iron 39 and the first back iron 37 are inclined at the same or substantially the same oblique angle, which may be between 0.1-30 degrees, relative to their respective non-ferromagnetic disks 40 and 42. The effect of the tilting of the two back irons 37 and 39 is to tilt the rotor 32 at the same or substantially the same tilt angle as the back irons 37 and 39. In particular, as with the configuration shown in fig. 3, the second back iron 39 is closer to the second hemisphere 52 of the second non-ferromagnetic disk 42 than the first hemisphere 50 of the second non-ferromagnetic disk 42, while the first back iron 39 is closer to the first hemisphere 50 of the first non-ferromagnetic disk 4 than the second hemisphere 52 of the second non-ferromagnetic disk 42. In this configuration, the tilt of the rotor 32 may also be maintained at such a non-uniform oblique angle during operation.

Referring now to fig. 5, in another configuration, the inner bearing magnets 46 may be arranged or otherwise disposed within the center post 30 at an oblique angle relative to the main longitudinal axis of the pump 10. In this configuration, the central column 30 is aligned and symmetrical with the major longitudinal axis 22. Although not shown to scale in fig. 5, the outer bearing magnets 48 of the rotor 32 may be tilted in the same direction as the tilt of the inner bearing magnets 46 due to the respective magnetic polarities. For example, in the configuration shown in FIG. 5, the outer bearing magnet 48 may be tilted in the same direction as the tilt of the inner bearing magnet 46. The configuration shown in fig. 5 may be combined with the configuration shown in fig. 3 or 4, or alternatively be disposed in a pump having a back iron that is not inclined relative to the main longitudinal axis.

Other embodiments of the present application include:

example 1: a method of operating an implantable blood pump, the implantable blood pump comprising: an inflow cannula defining a major longitudinal axis; and a rotor configured to rotate about the main longitudinal axis and push blood downstream of the inflow cannula to an outlet downstream of the rotor, the method comprising:

maintaining the impeller at a predetermined oblique angle relative to the main longitudinal axis as the impeller rotates about the main longitudinal axis.

Embodiment 2. the method of embodiment 1, wherein the implantable blood pump is a centrifugal blood pump.

Embodiment 3. the method of embodiment 1 or 2, wherein the oblique angle is between 1-30 degrees.

Embodiment 5. the method of any of the above embodiments, wherein the implantable blood pump comprises a stator having a back iron, and wherein the back iron is disposed at an oblique angle relative to the major longitudinal axis.

Embodiment 6. the method of any of the above embodiments, wherein the implantable blood pump comprises a central column, and wherein the central column is disposed at an oblique angle relative to the major longitudinal axis.

Embodiment 7. the method of any of the above embodiments, wherein the implantable blood pump comprises a central column, and wherein the central column comprises a plurality of internal bearing magnets, and wherein the internal bearing magnets are disposed at an oblique angle relative to the main longitudinal axis.

Embodiment 8 the method of any of the above embodiments, wherein the implantable blood pump comprises a stator having a back iron and a non-ferromagnetic disk disposed between the rotor and the stator, the back iron being spaced apart from and disposed at an oblique angle relative to the non-ferromagnetic disk.

Embodiment 9. the method of embodiment 8, wherein the implantable blood pump includes a second stator having a second back iron spaced apart from and disposed at an oblique angle relative to a second non-ferromagnetic disk and the second non-ferromagnetic disk disposed between the rotor and the second stator.

It will be appreciated by persons skilled in the art that the present invention is not limited to what has been particularly shown and described hereinabove. In addition, unless mention was made above to the contrary, it should be noted that all of the accompanying drawings are not to scale. Many modifications and variations are possible in light of the above teaching without departing from the scope and spirit of the invention, which is limited only by the following claims.

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