Device for fixing and positioning a heart pump
The heart pump device addresses cellular colonization issues by using a titanium-coated, endothelial cell-adhesive surface and a smooth crown to maintain clear suction ports and stable positioning, ensuring effective and safe heart pump operation.
Patent Information
- Application Number
- FR2021011957
- Authority / Receiving Office
- FR · FR
- Patent Type
- Patents
- Current Assignee / Owner
- Filing Date
- 2021-11-10
- Publication Date
- 2024-12-13
- Estimated Expiration
- 2041-11-10
AI Technical Summary
State-of-the-art implantable heart pumps experience cellular colonization of the insert, leading to obstruction of blood suction orifices, reducing pump performance and posing health risks.
A device with a hollow main body featuring a titanium or titanium alloy coating with controlled surface roughness and protrusions/hollows for endothelial cell adhesion, a smooth crown to prevent cellular colonization, and a clamping mechanism for stable positioning and orientation relative to the aortic valve.
Prevents cellular colonization, maintains clear blood suction ports, ensures proper orientation and stability of the heart pump, and enhances tissue integration and anchoring, thereby preventing blockages and bacterial attacks.
Smart Images

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Abstract
Description
Title of the invention: Device for fixing and positioning a heart pump Technical field
[0001] This document relates to the field of cardiac assist pumps.
[0002] It relates more particularly to a medical device for fixing a heart pump in an opening in a ventricular wall of a beating heart. Prior art
[0003] Heart failure is a condition in which a patient's heart is unable to provide sufficient blood flow to meet the body's metabolic needs.
[0004] Cardiac assist pumps are conventionally used to assist a left ventricle of a heart. This is called an artificial heart pump. This artificial and mechanical pump does not replace the heart, which continues to function, but provides assistance to the weakened ventricle in order to increase blood flow in a manner adapted to the individual's needs.
[0005] In the event that a graft transplantation is not possible, this heart pump is implanted long-term.
[0006] As illustrated in [Fig.l], state-of-the-art implantable heart pumps typically comprise an intraventricular part 2 and an extraventricular part 4. In the extraventricular part 4, a state-of-the-art heart pump medical device comprises from upstream (AM) to downstream (AV): an assembly flange 6, a connector 8, a removable sheath with a non-return valve 10 and a power cable 12. In the intraventricular part 2, this medical device comprises a heart pump 14 and an insert 16 made of polyetheretherketone (PEEK), the latter making it possible to receive, support and orient said heart pump 14 relative to the aortic valve. The upstream and downstream parts are here identified relative to the ventricular wall of the beating heart.
[0007] However, with such a medical device, cellular colonization of the insert 16 is observed, which extends to the projecting part of the body of the heart pump 14. An obstruction of the blood suction orifices of the heart pump 14 thus appears over time, leading to reduced performance of the heart pump, which can have serious consequences for the health of the patient.
[0008] There is therefore a pressing need for an insert that overcomes the drawbacks of the prior art. Subject of the invention
[0009] The present invention aims to overcome the drawbacks of the prior art by proposing a device for fixing a heart pump in an opening in a ventricular wall of a beating heart, simple in its design, making it possible to avoid obstruction of the blood suction orifices of the heart pump, to maintain the latter in the ventricular cavity in a desired orientation and to allow the positioning of the ejection orifice of the heart pump at a controlled distance from the aortic valve.
[0010] Another object of the present invention is a coating whose properties make it possible to facilitate tissue covering and to stiffen an anchoring of the main body of said fixing device.
[0011] Another object of the present invention is the use of a smooth crown preventing any protein, cellular or molecular aggregation, preventing colonization of the pump body by a covering cellular tissue within the ventricle. Presentation of the invention
[0012] The present document relates to a device for fixing a heart pump in an opening in a ventricular wall of a beating heart, comprising
[0013] - a hollow main body of generally cylindrical shape having a surface external,
[0014] - this hollow main body comprising a proximal end and an end distal between which said external surface extends, said distal end being intended to form a projection of said ventricular wall inside the corresponding ventricular cavity of the beating heart,
[0015] - at least a portion of the external surface of said main body intended to be placed inside said ventricular cavity when the proximal end of this fixing device is fixed on said ventricular wall, excluding its distal end, has a surface relief provided with protrusions and hollows made of a material allowing the adhesion and growth of endothelial cells, at least said external surface portion comprising a coating covering a surface of titanium or titanium alloy,
[0016] - the distal end of said hollow main body forms a smooth crown having a arithmetic mean roughness Rmax less than or equal to 1 pm to stop the colonization of said fixation device by endothelial cells.
[0017] The smooth crown thus makes it possible to create a barrier to colonization, generating a space free of any natural tissue. As a result, the openings of the heart pump are no longer obstructed and therefore the heart pump is no longer blocked.
[0018] Endothelization of the main body coating is controlled by the surface condition of said coating. Endothelization means colonization by a tissue natural cellular. The coating of the main body, thanks to a surface relief provided with outgrowths and hollows, promotes this endothelization. This is even more favored if the coating is made of titanium or a titanium alloy. Indeed, by this technique, cellular adhesion is improved.
[0019] Such endothelization has the advantage of guaranteeing anchoring and good orientation of a main body - heart pump assembly. Indeed, this endothelization makes it possible to exert pressure on the main body - heart pump assembly. This notion of orientation of the body of the heart pump is very important because it not only allows the heart pump to be held in place, but also to be well arranged and kept stable with respect to the aortic valve. The pump is thus blocked at the desired depth in the ventricle.
[0020] Thanks to this endothelization, the coating of the main body is also protected from possible bacterial attacks. The quantity of cellular tissue agglomerating on the coating is optimized according to the geometry of the heart, depending on whether this heart has an obtuse or oblique apex.
[0021] Said hollow main body may comprise a first hollow cylindrical body made entirely of titanium or titanium alloy, said first cylindrical body comprising on at least part of its external surface said surface coating, a second hollow cylindrical body having an external collar at one end, said second cylindrical body being inserted into said first hollow cylindrical body so that its end is placed in the extension of said external surface of the first cylindrical body forming a surface continuity therewith, said end of the second cylindrical body defining the distal end of said main body.
[0022] This arrangement not only allows the heart pump to be held securely in place, but also allows it to be properly arranged and kept stable in relation to the aortic valve.
[0023] Said distal end or external collar may have a longitudinal dimension of between 10 mm and 20 mm.
[0024] The amount of cellular tissue agglomerating on the coating is optimized according to the geometry of the core. Thanks to this longitudinal dimension, the case of an obtuse core is covered.
[0025] The distal end or external collar may have a longitudinal dimension of between 2 mm and 10 mm.
[0026] The amount of cellular tissue agglomerating on the coating is optimized according to the geometry of the core. Thanks to this longitudinal dimension, the case of an oblique core is covered.
[0027] Said second cylindrical body can be smooth and made entirely of ceramic or PEEK (polyetheretherketone).
[0028] When the second body is made of PEEK, it is advantageously hydrophobic and inert. This second body is all the more hydrophobic and inert as its surface is smooth. This second body does not support cell adhesion.
[0029] An arithmetic mean roughness of the coating covering the external surface of titanium or a titanium alloy may be between 100 pm and 300 pm.
[0030] The coating of the main body, thanks to the increase in the contact area or more precisely to the high arithmetic mean roughness, promotes endothelization.
[0031] The proximal end of said main body may comprise a flared shape delimiting a housing for receiving a clamping ring, the function of which is to annularly clamp the body of the heart pump, the inner wall of said proximal end further having a first internal thread for screwing a serrated nut.
[0032] This clamping ring provides sealing and maintenance of the serrated nut.
[0033] An outer wall of the proximal end may comprise a second external thread for receiving a ring comprising at least one ear, preferably four (4), each comprising an orifice for receiving the end of a tightening tool.
[0034] Advantageously, this ring facilitates the tightening of the serrated nut for the operator. The tightening tool comprising an imprint intended to cooperate with the serrated nut, such as teeth complementary to the teeth of the serrated nut, the free end of this tightening tool can be inserted into the opening of an ear so that its imprint is engaged with teeth of the serrated nut for tightening this nut.
[0035] Furthermore, the distal end of said main body may be chamfered to ensure pinching of the body of the heart pump inserted into said device when said at least one portion of the external surface of the main body has been colonized by endothelial cells. The pump body is thus held firmly in position.
[0036] The geometry of this chamfered distal end makes it possible to adapt to the geometry of the beating heart and to allow better orientation of the cardiac pump.
[0037] The coating may be formed solely from titanium microspheres.
[0038] These titanium microspheres facilitate tissue coverage and solidify or stiffen the anchoring of the main body.
[0039] The titanium microspheres may each have an average diameter of between 100 μm and 300 μm.
[0040] This diameter size distribution is calculated to increase as much as possible the arithmetic mean roughness of the coating.
[0041] The covering may alternatively comprise an openwork fabric formed from a plurality of polyester filaments.
[0042] The coating may be of the Spondycoat type - T317A.
[0043] The external surface of the coating may still have a stripped surface condition. The term "stripped surface condition" means a surface condition in which a layer of material from the external surface is removed, leaving a substrate visible. For example, the condition of this surface could be that resulting from sandblasting the external surface of the coating. During this sandblasting, an abrasive is projected at high speed using compressed air through a nozzle onto the external surface to be stripped.
[0044] The coating may include protrusions and hollows with a random distribution. Brief description of the drawings
[0045] Other characteristics, details and advantages will appear on reading the detailed description below, and on analyzing the attached drawings, in which: Fig.l
[0046] [Fig.l] shows a heart pump according to the prior art. Fig. 2
[0047] [Fig.2] shows a first view of an assembly of a fixing device according to the invention. Fig. 3
[0048] [Fig.3] shows a second view of a partially assembled assembly of the device fixing illustrated in [Fig.2], according to the invention. Fig. 4
[0049] [Fig.4] shows a view from a ring and a serrated nut of the fixing device, according to the invention. Fig. 5
[0050] [Fig.5] shows a view according to [Fig.4] of the fixing device showing a posi operation of a clamping ring, according to the invention. Fig. 6
[0051] [Fig.6] shows a downstream view of the fixing device with the serrated nut mounted in said fixing device, according to the invention. Fig. 7
[0052] [Fig.7] shows a side view of the fixing device. Fig. 8
[0053] [Fig.8] shows a sectional and schematic view of the fixing device. Fig. 9
[0054] [Fig.9] shows a mounting of the serrated nut against the ring of the fixing device. Fig. 10
[0055] [Fig. 10] shows a first embodiment of a coating of a fixing tube, according to the invention. Fig. 11
[0056] [Fig. 11] shows a second embodiment of a coating of a fixing tube, according to the invention. Fig. 12
[0057] [Fig. 12] shows a third embodiment of a coating of a fixing tube, according to the invention. Fig. 13
[0058] [Fig. 13] shows a fourth embodiment of a coating of a fixing tube, according to the invention. Fig. 14
[0059] [Fig. 14] shows a heart pump according to the invention. Detailed description
[0060] The drawings and the description below contain, for the most part, elements of a certain character. They may therefore not only serve to better understand the present invention, but also contribute to its definition, where appropriate. It should be noted that the figures are not to scale.
[0061] The present document relates to a device 18 for fixing a heart pump in an opening in a ventricular wall of a beating heart.
[0062] As illustrated in Figures 2 to 8, the fixing device 18 comprises a hollow main body 20 of generally cylindrical shape. This main body 20 comprises a distal end 22 and a proximal end 24. By distal end 22 is meant the end of the hollow main body 20 furthest from the ventricular wall of the beating heart. Conversely, by proximal end 24 is meant the end of the hollow main body 20 closest to the ventricular wall of the beating heart. The hollow main body 20 comprises a first hollow cylindrical body 26 and a second hollow cylindrical body 28. The first hollow cylindrical body 26 is made of titanium or a titanium alloy. The second hollow cylindrical body 28 is made entirely of ceramic or PEEK (polyetheretherketone).
[0063] The first cylindrical body 26 of the main body 20 comprises, at the proximal end 24, a flared shape delimiting an interior housing. The flared shape may, for example, be conical in shape. The housing delimits a space inside the first cylindrical body 26 of the main body 20 capable of receiving a ring of clamping 30. This clamping ring 30 is capable of deforming to fit an inner wall of the first cylindrical body 26 of the main body 20 near said proximal end 24.
[0064] The first cylindrical body 26 comprises at the proximal end 24 a first internal thread 32 and a second external thread 34. The first internal thread 32 of the first cylindrical body 26 is configured to receive a serrated nut 36 capable of being screwed into said first internal thread 32 and of coming into contact with one end 38 of the clamping ring 30. The second external thread 34 of the first cylindrical body 26 is configured to receive a ring 40. This ring 40 is capable of being screwed along said second external thread 34. The ring 40 comprises four lugs 42. These lugs 42 each comprise a receiving orifice 44 for a clamping tool 46. As illustrated in [Fig.8], the clamping tool 46 comprises a free end 48 cooperating with the serrated nut 36.
[0065] An external surface 52 of the first cylindrical body 26, excluding the distal end 22 of this first cylindrical body 26, comprises a coating 54. This coating 54 has a surface relief provided with a random distribution of protrusions and hollows. This coating covering the external surface 52 of the first cylindrical body 26 with the exception of the distal end 22 has an arithmetic mean roughness parameter of between 100 qm and 300 qm.
[0066] In a particular embodiment illustrated in [Fig. 10], this coating 54 may comprise a plurality of layers of titanium microspheres 56. These titanium microspheres 56 have an average diameter of between 100 qm and 300 qm. This coating 54 has a surface relief characterized by an arithmetic mean roughness of between 100 and 300 qm. These microspheres 56 are projected onto the external surface 52 of the first cylindrical body 26 excluding the distal end. The microspheres 56 are bonded to the external surface 52 by heating to a temperature close to the melting temperature of titanium. No binder is used to hold the microspheres 56 together.
[0067] In a particular embodiment illustrated in [Fig. 11], this covering 54 may comprise an openwork fabric 58 formed from a plurality of polyester filaments. The filaments have an average diameter of between 250 qm and 350 qm. This fabric comprises openings 60 with an average diameter of between 50 qm and 100 qm.
[0068] In a particular embodiment illustrated in [Fig. 12], the coating 54 may comprise a stripped surface state 62. This stripping results in a granularity being present on the surface, increasing the contact area between said coating and blood circulating in the left ventricle of the heart. This granularity can be quantified in terms of arithmetic mean roughness. The arithmetic mean roughness of said coating is between 100 and 300 qm. This stripping is obtained by sandblasting.
[0069] In a particular embodiment illustrated in [Fig. 13], the external surface has received a surface treatment. The coating is made of PEEK having received a plasma projection. Conventionally, plasma is a partially ionized gas composed of atoms, molecules, ions and excited free radicals, following stimulation by radio frequencies, microwaves or an electron discharge. This plasma projection is configured to influence a hydrophilic / hydrophobic character, a charge and a surface roughness. The coating can be of the Spondycoat 64 - T317A type.
[0070] The second cylindrical body 28 is capable of being inserted inside the first hollow cylindrical body 26 so that a first portion 66 is in contact with an internal surface of the second hollow cylindrical body 26 and a second portion 68 projects from a distal end 66 of the first hollow cylindrical body 26, this distal end 70 of the first cylindrical body 26 being on the side opposite the second external thread 34. This second portion 68 of the second cylindrical body 28 forms the distal end 22 of the main body 20. This second portion 68 comprises an external collar 72. This external collar 72 comprises a smooth crown 74. This smooth crown 74 has an arithmetic mean roughness Rmax less than or equal to 1 μm to stop the colonization of said fixation device 18 by endothelial cells. The distal end 22 of the main body 20 and therefore the smooth crown 74 is chamfered.This chamfered smooth crown 74 is configured to pinch the heart pump 76. As illustrated in [Fig. 14], the heart pump 76 is inserted from the side of the serrated nut 36, passes inside the main body 20 and comes out from the side of the smooth crown 74.
[0071] A longitudinal dimension over which the smooth crown 74 extends depends on a span of the core and a thickness of a wall of said core. By longitudinal dimension, we mean a spacing between the distal end 70 of the first cylindrical body 26 and a distal end 76 of the smooth crown 74. We can also speak of a depth of the smooth crown 74.
[0072] The depth of the smooth crown is between 2 and 10 mm, if the heart has a very obtuse apex at the end of contraction. Indeed, during contraction, there is then very little contact between the smooth crown and the wall of the heart.
[0073] On the other hand, the depth of the smooth crown 74 is between 10 and 20 mm, if the heart has a very acute apex at the end of contraction. Indeed, the increase in the depth of the smooth crown 74 is configured to prevent the walls of the heart from being in contact with this smooth crown 74. There is thus no deposition of cells on said smooth crown 74.
[0074] In operation, the smooth crown 74 makes it possible to create a barrier to colonization generating a spacing free of any natural tissue. Indeed, the smooth crown 74 in PEEK is hydrophobic and inert. This smooth crown 74 is all the more hydrophobic and inert as its surface is polished, the distal end of the smooth crown 74 will not support cell adhesion. As a result, openings 78 of the heart pump 76 are no longer obstructed and therefore the heart pump 76 is no longer blocked.
[0075] An endothelization of the coating 54 of the first cylindrical body 26 is controlled by the surface condition of said coating 54. By endothelization, we mean a colonization by a natural cellular tissue. The coating 54 of the first cylindrical body 26, thanks to the increase in the contact area or more precisely to the high arithmetic mean roughness, promotes endothelization. Indeed, by this technique, cellular adhesion is improved. This endothelization has the advantage of reinforcing the good orientation of a main body 20 - heart pump 76 system. Indeed, this endothelization makes it possible to exert pressure on the main body 20 - heart pump 76 assembly. This notion of orientation of the body of the heart pump 76 is very important because it makes it possible not only to keep the heart pump 76 in place, but also to arrange it well and keep it stable opposite an aortic valve.Thanks to this endothelization, the coating 54 of the first cylindrical body 26 is preserved from possible bacterial attacks. The quantity of cellular tissue agglomerating on the coating 54 is optimized according to the geometry of the heart, depending on whether this heart has an obtuse or oblique apex.
[0076] The use of the second cylindrical body 28 makes it possible to avoid scratching the heart pump 76 by using a softer material.
Claims
Claims
1. Device (18) for fixing a heart pump (76) in an opening of a ventricular wall of a beating heart, comprising - a hollow main body (20) of generally cylindrical shape having an external surface (52), - this hollow main body (20) comprising a proximal end (24) and a distal end (22) between which said external surface (52) extends, said distal end (22) being intended to form a projection of said ventricular wall inside the corresponding ventricular cavity of the beating heart, - at least a portion of the external surface (52) of said main body (20) intended to be placed inside said ventricular cavity, excluding its distal end (22), has a surface relief provided with protrusions and hollows made of a material allowing the adhesion and growth of endothelial cells,at least said external surface portion (52) comprising a coating (54) covering a titanium or titanium alloy surface, - the distal end (22) of said hollow main body forms a smooth crown (74) having an arithmetic mean roughness Rmax less than or equal to 1 pm to stop the colonization of said fixation device by endothelial cells, and - the distal end (22) of said main body is chamfered to pinch the body of the heart pump (76) inserted into said device when said at least a portion of the external surface (52) of the main body (20) has been colonized by endothelial cells.,
2. Device according to claim 1, wherein said hollow main body (20) comprises a first hollow cylindrical body (26) made entirely of titanium or titanium alloy, said first cylindrical body (26) comprising on at least a portion of its external surface (52) said surface coating (54), a second hollow cylindrical body (28) having an external collar (72) at its end, said second cylindrical body (28) being inserted into said first hollow cylindrical body (26) so that its end is placed in the extension of said external surface (52) of the first cylindrical body (26) forming a surface continuity therewith, said end of the second cylindrical body (28) defining the distal end (22) of said main body (20).
3. Device according to one of the preceding claims, in which said distal end (22) or external collar (72) has a longitudinal dimension of between 10 mm and 20 mm.
4. Device according to one of the preceding claims, in which the distal end (22) or external collar (72) has a longitudinal dimension of between 2 mm and 10 mm.
5. Device according to one of the preceding claims, in which said second cylindrical body (28) is smooth and made entirely of ceramic or PEEK (polyetheretherketone).
6. Device according to one of the preceding claims, in which an arithmetic mean roughness of the coating (54) covering the external surface (52) of titanium or a titanium alloy is between 100 qm and 300 qm.
7. Device according to one of the preceding claims, in which the proximal end (24) of said main body (20) has a flared shape delimiting a housing for receiving a clamping ring (30) for annularly pinching the body of the heart pump (76), the inner wall of said proximal end (24) having a first internal thread (32) for screwing a serrated nut (36).
8. Device according to one of the preceding claims, in which an outer wall of the proximal end (24) comprises a second external thread (34) for receiving a ring (40) comprising at least one ear (42) comprising an orifice (44) for receiving the end of a tightening tool (46).
9. Device according to one of the preceding claims, in which the coating (54) is formed solely of titanium microspheres (56).
10. Device according to claim 9, in which the titanium microspheres (56) each have an average diameter of between 100 qm and 300 qm.
11. Device according to one of claims 1 to 8, in which the covering (54) comprises an openwork fabric (58) formed from a plurality of polyester filaments.
12. Device according to one of claims 1 to 8, in which the coating (54) is of the Spondycoat (64) - T317A type.
13. Device according to one of claims 1 to 8, in which the external surface of the coating (54) has a stripped surface state (62).
14. Device according to one of the preceding claims, in which the coating (54) comprises protrusions and hollows with a re- random partition.
