Delivery Device for Medical Implant and Medical Procedure

Abstract

A catheter (4) based medical system (1) and medical procedure for reducing cardiac valve regurgitation are disclosed. The system comprises a resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation having resilient anchoring elements (300), and a delivery device (2) for said annuloplasty implant (3) having a distal curvilinear shaped portion (200) that is hollow to mount said annuloplasty implant (3) and has an annular opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve. A plurality of suction units allows for a atrial approach and symmetric implantation of said implant.

Claims

1. A catheter (4) based medical system (1), including a retractable delivery device (2) for delivery of a medical implant, such as an annuloplasty implant (3) for reducing cardiac valve regurgitation, having a distal portion for releasably holding said implant, and for apposition against a target tissue for said implant, such as an annulus (18) of a cardiac valve, wherein said distal portion comprises a plurality of suction units for providing and/or determining a desired apposition of said distal portion at said target tissue prior to releasing said medical implant to said tissue and retracting said delivery device.

2. The system of claim 1, wherein said suction units are provideable with a negative pressure for suction to said tissue, and wherein said medical implant is not releasable before all suction units are confirmed in apposition with said tissue.

3. The system of claim 1, wherein said plurality of suction units are distributed along a periphery of said distal portion.

4. The system of claims 1-3, wherein a firm seat at said tissue is confirmed by an absence of a reflow of blood from said suction units.

5. The system of claims 1-4, wherein said suction units are arranged to provide for a symmetric delivery of said implant when release to said tissue.

6. The system of claims 1-5, wherein said tissue is a cardiac valve annulus and said implant is an annuloplasty implant, such that said distal portion is arrangeable for a synchronous and simultaneous reshaping procedure of said annulus by said implant.

7. The system of any of the preceding claims 1 to 6, wherein apposition of said suction units is measurable based on a signal for a pressure in said suction unit an energy consumption of a flow generator generating said pressure.

8. The system of any of the preceding claims 1 to 7, wherein said distal portion has arranged thereon a plurality of sensors for indicating contact with said annulus tissue, such as piezo transducers.

9. The system of any of the preceding claims 1 to 8, wherein said cardiac valve is a mitral valve, and wherein said system is adapted for transseptal percutaneous delivery into the left atrium to said atrial side of said mitral valve, and wherein a delivery portion (202) of said delivery device (2) is distally connected to said distal portion (200) and has a distal curvature to allow access from a septal opening towards said mitral valve.

10. The system of any of the preceding claims 1 to 8, wherein said cardiac valve is a tricuspid valve, and wherein said system is adapted for percutaneous delivery into the right atrium to said atrial side of said tricuspid valve, and wherein a delivery portion (202) of said delivery device (2) is distally connected to said distal portion (200) and has a distal curvature to allow suitable access towards said tricuspid valve.

11. The system of claims 1-10, wherein said implant is a resilient curvilinear shaped annuloplasty implant (3) that has a tissue engaging conformation based on a desired downsized shape where said regurgitation of said valve is reduced, and said distal portion (200) has a delivery conformation based on a shape of said dilated valve annulus shape, wherein said delivery conformation has a dimension that is larger than said tissue engaging conformation of said annuloplasty implant (3), such that said annuloplasty implant (3) is resiliently kept in said delivery conformation before release from said distal portion.

12. The system of any of the preceding claims 1 to 11, wherein said distal portion (200) has at least one fiducial marker, wherein said fiducial marker is preferably arranged at a periphery of said distal portion (200); and/or wherein one of said fiducial markers is an annular fiducial marker arranged along said periphery; and/or having a plurality of fiducial markers distributed along said distal curvilinear shaped portion (200) for identifying said distal curvilinear shaped portion (200) inside a body of a patient having said cardiac valve.

13. The system of claim 12, wherein said fiducial markers include an air inclusion for detection by ultrasound.

14. A medical procedure (8) for reducing cardiac valve regurgitation including the steps of: measuring (80) the geometry of a dilated cardiac valve of a patient including the shape and size of a dilated annulus thereof; determining (82) the downsized shape and size of said annulus; selecting (84) a resilient annuloplasty implant having in a tissue engaging conformation a shape and size to be arranged at said downsized annulus based on said determined downsized shape and size of said annulus; introducing (86) said annuloplasty implant in a delivery device in a compressed state via a catheter to said cardiac valve; releasing (88) an aggregate of a distal portion of said delivery device and said annuloplasty implant in a stretched state in said delivery device from said catheter such that implant assumes an expanded shape; positioning (90) said aggregate at said annulus; fixation said distal portion to said annulus, e.g. by activating suction of suction units; providing and/or verifying a desired apposition of said distal portion at said annulus prior to releasing said implant; releasing (92) and anchoring said annuloplasty implant into said annulus; reducing (94) the size of said delivery device and/or annuloplasty implant for reshaping said annulus to said downsized shape; optionally determining (96) a reduction of said cardiac valve regurgitation, and removing (98) said delivery device and catheter if the reduction is satisfactory, or removing (99) said annuloplasty implant together with said delivery device when said reduction is determined as not being satisfactory.

15. The procedure of claim 14, including ultrasonic measurement for said measuring (80) the geometry of said dilated cardiac valve, and/or said determining (96) a reduction of said cardiac valve regurgitation.

16. The procedure of claim 14, including applying a catheter (4) based medical system (1) for reducing said cardiac valve regurgitation, having said resilient curvilinear shaped annuloplasty implant (3) for reducing the size of a dilated annulus (18) of said valve for reducing said regurgitation, and a delivery device (2) for said annuloplasty implant (3) having a distal portion (200) receiving said annuloplasty implant (3) and has an opening (201) arranged to be in apposition against an annulus (18) of said cardiac valve; said procedure including releasably mounting said annuloplasty implant (3) in said hollow with said resilient anchoring elements (300) arranged in a restrained spring loaded delivery conformation in said hollow, for said introducing (86); positioning (90) said aggregate at said annulus; fixation said distal portion to said annulus, e.g. by activating suction of suction units; providing and/or verifying a desired apposition of said distal portion at said annulus prior to releasing said implant; releasing (92) and anchoring said annuloplasty implant into said annulus.

17. The procedure of any of the preceding claims 14 to 16, including restraining said annuloplasty implant (3) in said hollow of said distal portion (200) with a second restraining unit (221), and releasing said annuloplasty implant (3) from said hollow upon releasing said second restraining unit, wherein said second restraining unit preferably is only released when a correct position of said annuloplasty implant is confirmed, allowing for removing said annuloplasty implant from said annulus if the correct positioning of said annuloplasty implant is not confirmed, and avoiding undesired embolization of said annuloplasty implant.

18. The procedure of any of the preceding claims 14 to 17, including making a transseptal puncture in said heart; wherein said cardiac valve is a mitral valve, and wherein said introducing (86) is a transseptal percutaneous delivery into the left atrium to said atrial side of said mitral valve, and wherein a delivery portion (202) of said delivery device (2) is distally connected to said distal curvilinear shaped portion (200) and has a distal curvature to allow access from a septal opening towards said mitral valve.

19. The procedure of any of preceding claims 14 to 18, including making a transseptal puncture in said heart; wherein said cardiac valve is tricuspid valve, and wherein said system is adapted for percutaneous delivery into the right atrium to said atrial side of said tricuspid valve, and wherein a delivery portion (202) of said delivery device (2) is distally connected to said distal curvilinear shaped portion (200) and has a distal curvature to allow suitable access towards said tricuspid valve.

20. The procedure of any of the preceding claims 14 to 19, including generating a negative pressure in suction units of said distal portion (200) for suction of said distal portion to said annulus.

21. The procedure of claim 20, including measuring said negative pressure and determining a contact of said suction units(s) with said annulus tissue from said measured pressure or an energy consumption of a flow generator generating said pressure.

22. The procedure of any of the preceding claims 14 to 21, including indicating contact with said annulus tissue with a sensor arranged on said distal portion (200), such as based on sound waves emitted and received from a piezo transducer, such as an ultrasonic transducer.

23. The procedure of any of the preceding claims 14 to 22, including identifying said distal portion (200) inside a body of a patient having said cardiac valve by means of detecting at least one fiducial marker of said delivery device, such as a plurality of fiducial markers distributed along said distal portion (200) for said identifying and/or a fiducial marker that is arranged at a periphery of said distal portion (200), and/or wherein one of said fiducial markers is an annular fiducial marker arranged along said periphery.

24. A method of virtually planning an annuloplasty implantation, such as for a medical procedure of claims 14-23, comprising, in a computer environment, image based, such as ultrasonic based, measuring a geometry of a dilated cardiac valve from patient image data, and determining a reduction of a regurgitation of said valve when downsizing the annulus of said dilated valve; selecting a patient adapted shape and size of a catheter (4) based medical system, such as of any of claims 1-13, including a resilient annuloplasty implant for a tissue engaging conformation to be arranged at the downsized annulus based on the determined downsized shape and size of the annulus; and providing production data for said device and/or a delivery system thereof.

25. The method of claim 24, wherein said measuring (80) the geometry of a dilated cardiac valve of a patient including the shape and size of a dilated annulus thereof, and said determining (82) the downsized shape and size of said annulus are made in a computer based, virtual environment.

26. A method of producing a medical device from production data obtained by the virtual planning of claim 24.

27. A computer based system for virtually planning an annuloplasty implantation, such as in a simulated medical procedure of claims 14-23, comprising, in a computer environment, image based, such as ultrasonic based, measuring a geometry of a dilated cardiac valve from patient image data, and computer based determining a reduction of a regurgitation of said valve when downsizing the annulus of said dilated valve is made; selecting a patient adapted shape and size of a catheter (4) based medical system, such as of any of claims 1-13, including a resilient annuloplasty implant for a tissue engaging conformation to be arranged at the downsized annulus based on the determined downsized shape and size of the annulus; and providing production data for said device and/or a delivery system thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0072] These and other aspects, features and advantages of which embodiments of the invention are capable of will be apparent and elucidated from the following description of embodiments of the present invention, reference being made to the accompanying drawings, in which

[0073] FIG. 1 is a schematic illustration of a portion of a heart 10 including a left ventricle 14, a left atrium 12 and a mitral valve 15;

[0074] FIG. 2 is a schematic illustration of a mitral valve 15 having an anterior valve leaflet 17 and a posterior valve leaflet 16;

[0075] FIG. 3 is a schematic illustration of a portion of a heart 10 including right atrium 11, a catheter 4 and a medical system 1;

[0076] FIG. 4 is a schematic illustration of a delivery device 2 arranged and pushed down on a mitral valve annulus 18, wherein the valve is dilated as seen at the opening 19 between the leaflets 16, 17;

[0077] FIG. 5 is a schematic illustration of an aggregate of a delivery device 2 and the annuloplasty curvilinear shaped structure 3;

[0078] FIGS. 6A-6D are a elevated, partly cross sectional vie (6A), and sectional views, FIGS. 6C and 6D at A (in FIG. 5) and FIG. 6B at B, of a distal portion of the aggregate of FIG. 5, respectively;

[0079] FIGS. 7A-7C illustrate the example of delivery of an annuloplasty curvilinear shaped structure 2 by means of a delivery device 3 to a mitral valve and downsizing of the valve; and

[0080] FIG. 8 is a flowchart illustrating a medical procedure.

DESCRIPTION OF EMBODIMENTS

[0081] Specific embodiments of the invention now will be described with reference to the accompanying drawings. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. The terminology used in the detailed description of the embodiments illustrated in the accompanying drawings is not intended to be limiting of the invention. In the drawings, like numbers refer to like elements.

[0082] In an embodiment of the invention according to the Figures, a catheter 4 based medical system 1 for reducing cardiac valve regurgitation is shown. The system 1 has a resilient and/or elastic curvilinear shaped structure annuloplasty implant 3 for reducing the size of a dilated annulus 18 of the valve for reducing the regurgitation having resilient anchoring elements 300. The anchoring elements 300 may be provided as barbs or hooks.

[0083] The system further has a delivery device 2 for the annuloplasty implant 3 having a distal curvilinear shaped portion 200 that is hollow to Mount the annuloplasty implant 3 and has an annular opening 201 arranged to be in apposition against an annulus 18 of the cardiac valve. The annuloplasty implant 3 is mounted to be releasable in the hollow and has the resilient anchoring elements 300 arranged in a restrained spring loaded delivery conformation in the hollow, and wherein the resilient anchoring elements 300 when unrestrained, are arranged in a tissue engaging conformation protruding out of the opening.

[0084] The number of anchoring elements, depth of anchoring elements, etc. may be chosen to effectively treat the valve leakage and reliably anchor the annuloplasty implant to the surrounding tissue. The length of an anchoring element is not limited by other anchoring elements. Thus, relatively long anchoring elements may be provided resulting in a deep tissue anchoring of the implant.

[0085] Anchoring elements 300 may be formed integrally with the annuloplasty implant 3. The implant 3 and the anchoring elements 300 may be formed as a monolithic structure. Alternatively the anchoring elements 300 may be affixed to the annuloplasty implant 3, e.g. by welding, gluing etc. Some of the anchoring elements 300 may be part of a collar (not shown) surrounding the annuloplasty implant 3. The collar may be a fabric collar to improve sealing and/or ingrowth of the implant when implanted. The collar may also provide for an effective assembly of the annuloplasty implant 3 and the anchoring elements 300 by means of the collar. Alternatively, the anchoring elements may protrude radially through the collar at their positions along the implant. In the latter case, such anchoring elements may be positioned outside of the collar element, originating from the annuloplasty implant 3 arranged therein.

[0086] Thus, in embodiments, medical devices are provided for reducing cardiac valve regurgitation. The device includes an elongate resilient curvilinear shaped annuloplasty implant 3 for reducing the size of a dilated annulus of the valve for reducing the regurgitation. The annuloplasty implant has resilient anchoring elements 300 protruding radially outwards from the annuloplasty implant 3. The anchoring elements are arrangeable in a spring loaded first radial direction for delivery, and when released from the delivery position anchor the annuloplasty implant to tissue at the annulus in a second radial direction, different from the first radial direction. This is illustrated in FIGS. 5 and 6A-6D.

[0087] Multiple of the anchoring elements may be arranged at different radial positions around the cross section of the annuloplasty implant. In the Figures it is illustrated that the anchoring elements 301, 302 are arranged as pairs opposite each other. Multiple anchoring elements are shown arranged at the same longitudinal position on the annuloplasty implant. Alternatively or in addition, the anchoring elements may be arranged at different radial positions as single elements at different longitudinal positions (not shown). This allows for flexibility and a reliable anchoring of the annuloplasty implant, e.g. in dependence of anatomical structures that should be avoided to be penetrated by anchoring elements, such as blood vessels.

[0088] The system is minimally invasive deliverable via a transluminal catheter 4, as shown in FIG. 3.

[0089] The resilient curvilinear shaped annuloplasty implant 3 has a tissue engaging conformation based on a desired downsized shape where the regurgitation of the valve is reduced, and the distal curvilinear shaped portion 200 has a delivery conformation based on a shape of the dilated valve annulus shape, wherein the delivery shape has a dimension that is larger than the tissue engaging conformation of the annuloplasty implant 3, such that the annuloplasty implant 3 is resiliently kept in the hollow 201 in the delivery conformation before demounting from the hollow.

[0090] In some embodiments the delivery device may a sizing actuator (not shown), and wherein the distal curvilinear shaped portion 200 is reducible from the delivery conformation by the actuator. In this manner, the delivery device 3 or tool may be affixed to the annuloplasty curvilinear shaped structure 2 during the downsizing step before releasing the curvilinear shaped structure 3 from the tool, and after affixing the curvilinear shaped structure 3 to the annulus tissue by means of the attachment units 300. In this manner, the curvilinear shaped structure 3 is readily retrievable from the cardiac valve in case the positioning thereof is not satisfactory, e.g. as detected via ultrasound based examination of the positioning result.

[0091] As e.g. shown in FIGS. 5, 6A, 6B and 6C, the delivery device 2 has a first restraining unit 321 for restraining the anchoring elements 300 in the restrained spring loaded delivery conformation. The first restraining unit 321 may be a wire against which the anchoring elements 300 are spring loaded, as illustrated. The wire may alternatively be guided through loops 320 inside the hollow (FIG. 6A).

[0092] The delivery device 2 has a second restraining unit 221 for restraining the annuloplasty implant 3 in the hollow of the distal curvilinear shaped portion 200. The second restraining device is shown as a tethered line holding the curvilinear shaped structure 3 in the hollow against loop eyes 220. In this manner, additional security is provided as the implant may be retracted when it is still restrained to the delivery device by means of the second restraining unit 221. Thus e.g. embolization of the device is avoided, which otherwise would make a surgical retrieval procedure necessary, likely including open chest surgery with all its disadvantages.

[0093] In the illustrated embodiment the delivery device 2 further has a third restraining unit 210 for keeping the annuloplasty implant 3 in the hollow of the distal curvilinear shaped portion 200. The third restraining unit 210 has two arms 210, 212 that hold the curvilinear shaped structure 3 in the hollow. The second restraining device may be omitted. When the curvilinear shaped structure has anchoring elements 300 deployed in the annulus, the third restraining units are provided with such a holding force, that a retraction of the delivery device 2 will release the latter from the curvilinear shaped structure 3.

[0094] In the embodiment having the first, second and third restraining units, the third restraining unit 210 is arranged to release the annuloplasty implant 3 by withdrawing the delivery device 2 when the first restraining unit has released the anchoring elements 300 from the restrained spring loaded delivery conformation and anchored the anchoring elements 300 into the annulus tissue.

[0095] In the illustrated embodiment the cardiac valve is a mitral valve 15, and the system is facilitating transseptal percutaneous delivery into the left atrium to the atrial side of the mitral valve. A delivery portion 202 of the delivery device 2 is distally connected to the distal curvilinear shaped portion 200 and has a distal curvature to allow access from a septal opening towards the mitral valve. The transition may be provided as shown. Alternatively, several arms may be provided at the transition to the hollow. The delivery portion 202 may be tubular hollow

[0096] In some embodiments the cardiac valve is the tricuspid valve, and the system is adapted for percutaneous delivery into the right atrium to the atrial side of the tricuspid valve, and a delivery portion 202 of the delivery device 2 is distally connected to the distal curvilinear shaped portion 200 and has a distal curvature to allow suitable access towards the tricuspid valve.

[0097] Access of catheter 4 or a similar guide is provided to the left atrium, and is e.g. achieved by positioning the catheter 4 in central or peripheral veins, thereby achieving access to the right atrium. In such a situation, the tricuspid valve (not shown) may be accessed from above the valve. The tricuspid valve is alternatively accesses via other vessels, e.g. the jugular vein, for access from above. Then a standard atrial trans-septal approach may be utilized to access the left atrium by creation of an iatrogenic atrial septal defect (ASD). In such a situation, the mitral valve may be accessed from above the valve, see e.g. FIG. 3 and FIG. 4.

[0098] In some embodiments the hollow of the distal curvilinear shaped portion 200 is provided with a negative pressure for suction of the hollow to the annulus. The pressure may e.g. be provided through the hollow delivery portion 202 when the latter has a lumen distally connected to the hollow at the junction thereof. Alternatively, or in addition, separate lumen may be provided for fluid communication with the hollow. A pressure generator is in these embodiments arranged proximally, outside the patient. The pressure in the hollow may be measured. Thus a contact with the annulus tissue is determinable from the measured pressure or an energy consumption of a flow generator generating the pressure. This improves reliability, patient safety, and user acceptance of the system and procedure considerably.

[0099] In some embodiments, alternatively or additional to the entire hollow of the curvilinear shaped portion 200 being provided with a negative pressure for suction of the hollow to the annulus, discrete suction units (not shown in the figures) are provided at that portion 200.

[0100] The distal portion may thus comprise a plurality of suction units for providing and/or determining a desired apposition of the distal portion at the target tissue prior to releasing the medical implant to the tissue and retracting the delivery device.

[0101] In some embodiments, the suction units are provideable with a negative pressure for suction to the tissue, and wherein the medical implant is not releasable before all suction units are confirmed in apposition with the tissue.

[0102] In some embodiments, the plurality of suction units are distributed along a periphery of the distal portion.

[0103] In some embodiments, a firm seat at the tissue is confirmed by an absence of a reflow of blood from the suction units.

[0104] In some embodiments, the suction units are arranged to provide for a symmetric delivery of the implant when release to the tissue.

[0105] In some embodiments, the tissue is a cardiac valve annulus and the implant is an annuloplasty implant, such that the distal portion is arrangeable for a synchronous and simultaneous reshaping procedure of the annulus by the implant.

[0106] In some embodiments the distal curvilinear shaped portion 200 has arranged thereon a sensor (not shown) for indicating contact with the annulus tissue, such as a piezo transducer. The senor is preferably integrated into the edge of the distal curvilinear shaped portion 200, oriented towards the annulus. In this manner, a clear difference can be identified between blood and valve tissue. This improves reliability, patient safety, and user acceptance of the system and procedure considerably. In addition, the correct seating and positioning of the curvilinear shaped structure 3 and the delivery device may be checked with other measurements, e.g. ultrasonic imaging based measurements.

[0107] In some embodiments the distal curvilinear shaped portion 200 has at least one fiducial marker. The fiducial marker may be arranged at a periphery of the distal curvilinear shaped portion 200; and/or wherein one of the fiducial markers is an annular fiducial marker arranged along the periphery. A plurality of fiducial markers may be distributed along the distal curvilinear shaped portion 200 for identifying the distal curvilinear shaped portion 200 inside a body of a patient having the cardiac valve. The fiducial markers may e.g. be air filled gaps in the wall of the distal curvilinear shaped portion 200. The fiducial markers may be made integrally with the distal curvilinear shaped portion 200.

[0108] As illustrated in FIG. 8 a medical procedure 8 for reducing cardiac valve regurgitation is now described. The procedure comprises the steps described hereinafter.

[0109] The geometry of a dilated cardiac valve of a patient including the shape and size of a dilated annulus thereof is measured 80.

[0110] Then a downsized shape and size of the annulus is determined. The procedure continues with selecting 84 a resilient annuloplasty implant having in a tissue engaging conformation a shape and size to be arranged at the downsized annulus based on the determined downsized shape and size of the annulus. This may be done in a virtual environment, planning the delivery of a patient adapted annuloplasty curvilinear shaped structure 3. The patient adapted annuloplasty curvilinear shaped structure 3 may be produced from manufacturing data output from the virtual planning. Alternatively, an annuloplasty curvilinear shaped structure 3 may be chosen from a library of pre-manufactured curvilinear shaped structures 3. In more detail, a method of virtually planning an annuloplasty implantation for a medical procedure may comprise, performing in a computer environment, an image based, such as ultrasonic based, measuring of a geometry of a dilated cardiac valve. This is based on patient image data. Further, the virtual planning may comprise determining a reduction of a regurgitation of the valve when downsizing the annulus of the dilated valve. The determining may be based on a simulation algorithm emulating the patient tissue performance in the computer environment. Moreover, the planning includes selecting a patient adapted shape and size of a resilient annuloplasty implant 3 for a tissue engaging conformation to be arranged at the downsized annulus based on the determined downsized shape and size of the annulus. From this planning, production data may be provided for the annuloplasty implant 3, components thereof, and/or a delivery system thereof. In a method of producing a medical device the production data obtained by the virtual planning may be used for producing the element(s). Production may be done my rapid prototyping techniques, or other manufacturing methods that the skilled person will be aware of in the present context.

[0111] The procedure then continues with introducing 86 the annuloplasty implant in a delivery device 3 in a compressed state via a catheter to the cardiac valve. The annuloplasty curvilinear Shaped structure may e.g. be stretched into an elongate configuration to fit into catheter 4 for delivery.

[0112] When the distal end of the catheter is at the release site at the valve, the procedure continues with releasing 88 an aggregate of a distal portion of the delivery device and the annuloplasty implant in a stretched state in the delivery device from the catheter such that implant resumes an expanded shape. The expanded shape is determined by the delivery device shape and size, and the annuloplasty curvilinear shaped structure 3 is expanded in relation to its tissue engaging conformation. The expanded shape corresponds to the shape of the dilated cardiac valve, allowing for easy positioning of the aggregate.

[0113] Then the procedure includes positioning 90 the aggregate at the annulus, e.g. by pushing against the annulus as shown in FIGS. 4, 6A-6D, and 7A,B.

[0114] The aggragate may be fixated to the annulus by activating suction of suction units. P providing and/or verifying a desired apposition of the distal portion at the annulus prior to releasing the implant

[0115] The anchoring elements 300 of the annuloplasty implant are released and are anchoring the anchoring elements into the annulus (FIGS. 6D, 7B).

[0116] Alternatively, or in addition to the anchoring elements described herein, the implant may be permanently affixed to the tissue by sutures, e.g. using a transcatheter deliverable suturing unit, which does not need to be described in more detail herein.

[0117] Then the shape or size of the delivery device and/or annuloplasty implant is reduced for reshaping the annulus to the downsized shape; determining 96 a reduction of the cardiac valve regurgitation; and removing 98 the delivery device and catheter if the reduction is satisfactory, or removing 99 the annuloplasty implant together with the delivery device when the reduction is determined as not being satisfactory.

[0118] In some embodiments the procedure includes ultrasonic measurement for the measuring 80 a geometry of the dilated cardiac valve, and/or the determining 96 a reduction of the cardiac valve regurgitation.

[0119] In some embodiments the procedure further includes subsequently to the positioning 90 the aggregate at the annulus: determining a position of the delivery device at the annulus, and repositioning the delivery device and annuloplasty implant.

[0120] In some embodiments the procedure includes applying a catheter 4 based medical system 1 for reducing the cardiac valve regurgitation, having the resilient curvilinear shaped annuloplasty implant 3 for reducing the size of a dilated annulus 18 of the valve for reducing the regurgitation having resilient anchoring elements 300, and a delivery device 2 for the annuloplasty implant 3 having a distal curvilinear shaped portion 200 that is hollow in which to mount the annuloplasty implant 3 and has an annular opening 201 arranged to be in apposition against an annulus 18 of the cardiac valve; the procedure comprising arranging the annuloplasty implant 3 to be releasable in the hollow with the resilient anchoring elements 300 arranged in a restrained spring loaded delivery conformation in the hollow, for the introducing 86 and releasing 88;

[0121] The resilient anchoring elements 300 are unrestrained by withdrawing the restraining unit 321. Thus the anchoring elements 300 are moving into the tissue of the adjacent annulus and the resilient anchoring elements 300 are arranged in a tissue engaging conformation protruding out of the opening into the annulus to be released 92. The annulus curvilinear shaped structure 30 is thus anchored to the annulus' 18 tissue of the cardiac valve, but still affixed to the delivery device. The delivery device may then be removed by releasing the second and/or third restraining unit. Alternatively, the aggregate may be retracted if so desired.

[0122] The procedure is a minimally invasive procedure.

[0123] The resilient curvilinear shaped annuloplasty implant 3 has in embodiments a tissue engaging conformation based on the desired downsized shape where the regurgitation of the valve is reduced, and the distal curvilinear shaped portion 200 has a delivery conformation based on a shape of the dilated valve annulus shape, wherein the delivery conformation has a dimension that is larger than the tissue engaging conformation of the annuloplasty implant 3, and mounting the annuloplasty implant 3 resiliently in the hollow 201 in the delivery conformation before releasing from the hollow.

[0124] In some embodiments the delivery device comprises a sizing actuator, and reducing the distal curvilinear shaped portion 200 from the delivery conformation by the actuator.

[0125] In some embodiments the procedure includes restraining the anchoring elements 300 in the restrained spring loaded delivery position with a first restraining unit 321 for, and releasing the anchoring elements 300 by releasing the first restraining unit 321 for mounting the anchoring elements into the annulus.

[0126] In some embodiments the procedure includes restraining the annuloplasty implant 3 in the hollow of the distal curvilinear shaped portion 200 with a second restraining unit 221, and releasing the annuloplasty implant 3 from the hollow upon releasing the second restraining unit, wherein the second restraining unit preferably is only released when a correct position of the annuloplasty implant is confirmed, allowing for removing the annuloplasty implant from the annulus if correct position of the annuloplasty implant is not confirmed, and avoiding undesired embolization of the annuloplasty implant.

[0127] In some embodiments the procedure includes restraining the annuloplasty implant 3 in the hollow of the distal curvilinear shaped portion 200 with a third restraining unit 210 for keeping the annuloplasty implant 3 in the hollow of the distal curvilinear shaped portion 200, thus preventing an undesired release of the annuloplasty implant 3 from the hollow.

[0128] In some embodiments the procedure includes a system having the first, second and third restraining unit, wherein the third restraining unit 210 is releasing the annuloplasty implant 3 by withdrawing the delivery device 2 when the first restraining unit has released the anchoring elements 300 from the restrained spring loaded delivery conformation and anchored the anchoring elements 300 into the annulus tissue.

[0129] In some embodiments the procedure includes making a transseptal puncture in the heart; wherein the cardiac valve is a mitral valve, and wherein the introducing 86 is a transseptal percutaneous delivery into the left atrium to the atrial side of the mitral valve, and wherein a delivery portion 202 of the delivery device 2 is distally connected to the distal curvilinear shaped portion 200 and has a distal curvature to allow access from a septal opening towards the mitral valve.

[0130] In some embodiments the procedure includes making a transseptal puncture in the heart; wherein the cardiac valve is tricuspid valve, and wherein the system is adapted for percutaneous delivery into the right atrium to the atrial side of the tricuspid valve, and wherein a delivery portion 202 of the delivery device 2 is distally connected to the distal curvilinear shaped portion 200 and has a distal curvature to allow suitable access into the atrium towards the tricuspid valve.

[0131] In some embodiments the procedure includes generating a negative pressure in the hollow of the distal curvilinear shaped portion 200 for suction of the hollow to the annulus. The procedure may include measuring the pressure in the hollow and determining a contact with the annulus tissue from the measured pressure or an energy consumption of a flow generator generating the pressure.

[0132] In some embodiments the procedure includes indicating contact with the annulus tissue with a sensor arranged on the distal curvilinear shaped portion 200, such as based on sound waves emitted and received from a piezo transducer, such as an ultrasonic transducer.

[0133] In some embodiments the procedure includes identifying the distal curvilinear shaped portion 200 inside a body of a patient having the cardiac valve by means of detecting at least one fiducial marker of the delivery device, such as a plurality of fiducial markers distributed along the distal curvilinear shaped portion 200 for the identifying and/or a fiducial marker that is arranged at a periphery of the distal curvilinear shaped portion 200, and/or wherein one of the fiducial marker is an annular fiducial marker arranged along the periphery.

[0134] Some embodiments of the invention provide for an alternative system and method of reducing cardiac valve regurgitation. Some embodiments of the invention provide for catheter based minimally invasive procedure in accordance with clinical procedures for accessing an atrium. Clinical personal has thus not to be trained with completely new access procedures to the atrium and will readily learn to apply the inventive concept described herein.

[0135] By means of an atrial delivery path approach, navigation and fixation of a distal portion of the delivery device, prior to release of the implant, a symmetrical implantation of the implant is provided. A synchronous and simultaneous reshaping procedure is provided.

[0136] This is a major progress in the minimally invasive implantation of annuloplasty implants. A reliable implantation is provided. As reshaping is done synchronous and simultaneous upon release of the implant from the distal portion of the delivery device, any tensions or undesired tissue movements are avoided that would need to be corrected by surgical interventions. As additionally, a patient specific implant may be provided and the procedure may be computer simulated in advance of the real medical procedure, results are improved considerably while the procedure is simplified.

[0137] The present invention has been described above with reference to specific embodiments. However, other embodiments than the above described are equally possible within the scope of the invention. Different method steps than those described above, performing the method by hardware or software, may be provided within the scope of the invention. The different features and steps of the invention may be combined in other combinations than those described. The scope of the invention is only limited by the appended patent claims.