Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2412—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body with soft flexible valve members, e.g. tissue valves shaped like natural valves
  • A61F2/2418—Scaffolds therefor, e.g. support stents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B17/064—Surgical staples, i.e. penetrating the tissue
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
  • A61B17/064—Surgical staples, i.e. penetrating the tissue
  • A61B2017/0649—Coils or spirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2220/0008—Fixation appliances for connecting prostheses to the body
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2220/0008—Fixation appliances for connecting prostheses to the body
  • A61F2220/0016—Fixation appliances for connecting prostheses to the body with sharp anchoring protrusions, e.g. barbs, pins, spikes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2230/00—Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2230/0063—Three-dimensional shapes
  • A61F2230/0091—Three-dimensional shapes helically-coiled or spirally-coiled, i.e. having a 2-D spiral cross-section

Definitions

• the application relates generally to a heart valve replacement system and transcatheter implantation of prosthetic heart valves, e.g., for replacing diseased mitral and/or tricuspid valves in humans or animals. More particularly, embodiments of the subject matter relate to a tissue-based valve leaflet replacement system and methods to operatively deliver and secure the leaflet replacement valve in its target position.
• the mitral valve sits between the left atrium (LA) and the left ventricle (LV) of a human heart and normally consists of a mitral annulus (MA), two leaflets, chordae tendineae (“chords”), two papillary muscles, and the left ventricular myocardium.
• the mitral annulus is subdivided into an anterior portion and a posterior portion.
• Mitral regurgitation is dysfunction of the MV that causes an abnormal leakage of blood from the LV back into the left atrium during systole (i.e., the expulsion phase of the heart cycle in which blood moves from the LV into the aorta).
• the current treatments for MV diseases include surgical repair and replacement of the MV, and more recently, transcatheter repair and replacement of the MV.
• the noted challenges to an efficacious MV replacement device generally include operative delivery challenges; positioning and fixation challenges; seal and paravalvular leakage challenges; and hemodynamic function challenges such as left ventricle outflow tract (LVOT) obstruction.
• LVOT left ventricle outflow tract
• a prosthetic mitral valve may have a large overhanging atrial portion or flare which can prevent leakage, but, problematically, it also requires a large valve size at the ventricular level so that the prosthesis can be tightly fitted in the native MV.
• a prosthetic mitral valve is smaller than the diseased native valve and additional material is added around the prosthetic valve to compensate for the large native mitral annulus. Undesirably, adding more material to a prosthetic valve increases the size of the delivery system and may cause valve thrombosis.
• Some of the current transcatheter delivery systems utilize folding structures of the replacement valve stent to capture and grab the native leaflets and annulus to anchor the replacement valve. Such methods frequently suffer from the dislodgement of the device due to either insufficient interactive force between the implant and the native tissue, or excess interactive force that leads to native tissue damage (e.g ., tearing) and/or remodeling (e.g., elongation, reshaping), which causes the instability and/or migration of the implant.
• native tissue damage e.g ., tearing
• remodeling e.g., elongation, reshaping
• a heart valve leaflet replacement system that includes a heart valve leaflet replacement device (e.g., a prosthetic mitral valve replacement device) and a multi-stage, multi-lumen (MSML) heart valve delivery and implantation system for guiding and fixation of the heart valve leaflet replacement device to one or more of the native annuli.
• a heart valve leaflet replacement device e.g., a prosthetic mitral valve replacement device
• MSML multi-stage, multi-lumen
• the MSML heart valve delivery and implantation system can be configured to guide and fix the mitral valve replacement device to the native mitral annulus.
• the MSML heart valve delivery and implantation system can be configured to guide and fix the prosthetic tricuspid valve replacement device to the native tricuspid annulus.
• valve leaflet replacement devices for the treatment of functional and degenerative mitral regurgitation
• the valve leaflet replacement device, the MSML delivery and implantation system and the associated methods can be used or otherwise configured to be used to treat other valve disease conditions and replace other valves of the human heart, or could be used or otherwise configured to be used in other mammals or animals suffering from valve deficiencies as well.
• the heart valve leaflet replacement system can comprise a heart valve leaflet replacement device, or prosthesis, that is configurable or otherwise sizable to fit in the MSML delivery and implantation system and to subsequently be selectively expanded to an operative size and position once removed from the MSML delivery and implantation system within the heart.
• at least a portion of the prosthesis can comprise a stent with an upper atrial flared portion and a lower ventricular portion.
• the atrial flared portion can be configured to couple with a plurality of dual guiding and fixation (DGF) members to guide and fix the stent on the annulus, which can help prevent paravalvular leakage and dislodgement of the prosthesis after implantation.
• DGF dual guiding and fixation
• the lower ventricular portion of the prosthesis can displace a portion of native leaflets out of the blood flow tract and houses at least one prosthetic leaflet.
• the heart valve leaflet replacement device can comprise a lining skirt that can be coupled to at least a portion of the inner and/or outer surfaces of the stent.
• the outer surfaces of the stent can be configured with additional skirt material to prevent paravalvular leakage.
• at least one prosthetic leaflet can be mounted on the inner lumen of the stent and/or on at least a portion of the outer side of the stent, which can function in place of at least one native leaflet to restore normal valve function, e.g., to prevent mitral regurgitation.
• the MSML delivery system can be configured to implant the heart valve leaflet replacement system in a two-step procedure.
• step 1 a plurality of DGF members are implanted into the native annulus of the diseased valve.
• step 2 a prosthetic heart valve leaflet replacement device is implanted and secured in position at the implanted DGF members.
• the delivery of the prosthesis can be conducted using several desired delivery access approaches, such as, for example and not meant to be limiting, a minimally invasive surgical, a trans-septal, or a trans-atrial approach.
• the trans-septal approach can comprise creating an opening in the internal jugular or femoral vein for the subsequent minimally invasive delivery of portions of the heart valve leaflet replacement device, or a prosthetic device, through the superior or inferior vena cava, which flow into the right atrium of the heart.
• the access path of the trans-septal approach crosses the atrial septum of the heart, and once achieved, the components of the heart valve leaflet replacement device can operatively be positioned in the left atrium, the native mitral valve, and the left ventricle.
• the MSML delivery and implantation system can comprise a main docking/guiding system, a DGF member delivery system and a valve housing, positioning, and locking system (VHPL).
• VHPL positioning, and locking system
• the VHPL can comprise a guide sheath, a plurality of locking catheters, a stent holder sheath, and a valve chamber sheath.
• a main docking sheath can be placed within the access path to allow desired components of the heart valve leaflet replacement system to be operatively positioned with the left atrium without complications.
• one component of the heart valve leaflet replacement device can comprise DGF members which can be operatively positioned and implanted at desired locations in the native annulus prior to the delivery of the prosthesis.
• the DGF members can guide the subsequent precise positioning and fixation of the prosthesis.
• the plurality of DGF members can help prevent leakage of blood between the operatively positioned prosthesis and the native mitral annulus.
• the DGF member can be configured with removable and permanent components, where removable components can aid in guiding the heart valve leaflet replacement device to the operable position, and then be removed from the patient’s body after fixing the prosthesis, and permanent components remain in the patient’s body to keep the heart valve leaflet replacement device secured to the native annulus.
• the DGF members can comprise multiple sections, such as a head member, a body member and a tail member.
• the DGF head member can be operatively inserted and embedded in the annular tissue.
• the DGF body member can be configured with a DGF locking member to fix the heart valve leaflet replacement device to the native mitral annulus.
• the DGF body member can be configured so that it can be engaged to a catheter, drill the DGF head member into the tissue, and disengage from the catheter to leave the entire DGF member permanently implanted in the annulus.
• the DGF members are designed to be removable and repositionable.
• the DGF tail member can be configured as a flexible component that extends from the proximal portion of the DGF body to the proximal end of the MSML system.
• the DGF tail can be configured to be selectively removable, such that it can be removed from the body at the completion of the heart valve leaflet replacement system implantation procedure.
• the DGF head member can be configured with a stabilizer member, e.g., a concentric needle within the DGF head member, that acts to stabilize the DGF member and the DGF member delivery mechanism during DGF member implantation.
• the stabilizer member can be configured with other mechanisms that can engage and/or disengage the tissue, such as vacuum suction, clamping and release, or other mechanisms due to changes induced by electromagnetic or thermal fields.
• the DGF body member can be configured with a prosthetic valve fixation mechanism including a plurality of DGF locking members.
• the DGF locking members can be configured to engage the prosthetic valve to fix it in the operative position.
• the DGF locking member can be configured to attach to the DGF body member via a flexible component.
• the DGF locking member can be configured to engage the DGF tail member.
• the prosthesis can be configured to engage the DGF locking member via a plurality of through-holes in the atrial flared portion of the stent frame.
• the DGF tail member can be a tether that is configured so that one end of the tether is attached to the DGF body member and the other end of the tether can exit the body. Subsequently, the tether can be inserted through the hole on the atrial flared portion of the stent, such that prosthesis can be delivered over the DGF tail members and the atrial flared portion of the stent can be precisely delivered to the DGF body members embedded in the annulus.
• the positioning of such DGF members is not random.
• the spacing of the DGF members on the annulus should be closely matched to the spacing of the through-holes on the prosthetic stent to ensure accurate positioning and placements of the prosthesis within the posterior annulus.
• two sets of DGF members can be deployed separately.
• the initial set of DGF members can be implanted at the proximity of the commissures of the native valve and the middle of the posterior annulus. This set of DGF members will guide the precise positioning and deployment of the prosthesis.
• a second set of DGF members can be implanted directly on the top of the deployed prosthesis.
• the second set of DGF members can be deployed on top of the flare section of the prosthetic stent.
• the DGF locking member can be configured such that it can selectively be compressed to a diameter smaller than the diameter of the hole on the atrial flared portion of the stent, such that it can pass through the hole, and subsequently be selectively re-expanded to its original size, larger than the diameter of the hole on the flared portion of the stent to prevent backward motion of the DGF locking member through the hole.
• the DGF locking member can be configured with a plurality of radially compressible legs, e.g., forming a cone shape where the proximal tip of the cone shape has a smaller diameter than the hole on the atrial flare of the stent, and the distal base of the cone shape has a larger diameter than the hole on the atrial flare of the stent.
• the DGF tails can be tensioned to pull the proximal tips of the DGF locking members into the holes on the atrial flared portion of the stent, and as the locking member legs come into contact with the edges of the holes, will compress radially to allow the DGF locking member to be pulled completely through the holes.
• the DGF locking member legs can re-expand to full size to prevent backward motion of the DGF locking member through the holes in the atrial stent flare.
• the VHPL system can comprise a guide sheath that fits within the lumen of the docking sheath and can house all the other VHPL system components.
• the guide sheath can be configured with a separator at the distal tip, which organizes all the inner tubes and prevents tangling or overlapping of the DGF tails and locking catheters.
• the entire guide sheath could be configured with multiple lumens to organize the inner tubes.
• the separator can have four lumens: one central lumen surrounded by three outer lumens. The stent holder sheath can go through the center lumen of the separator, and a locking catheter can go through each of the three outer lumens.
• the VHPL can comprise a valve chamber.
• the heart valve leaflet replacement device can be crimped down to fit within a valve chamber on the distal end of the VHPL system, and subsequently be selectively expanded to an operative size and positioned once removed from the valve chamber in the VHPL system.
• a stent holder can be configured to fit within the lumen of the valve chamber and to facilitate prosthesis valve release.
• the stent holder can be configured to attach to the distal tip of a stent holder sheath that extends to the proximal side of the VHPL system, such that the stent holder position within the valve chamber can be controlled by manipulating the stent holder sheath on the proximal side of the VHPL system.
• valve chamber sheath can be configured, steerable or non-steerable, to fit within the lumen of the stent holder sheath.
• the valve chamber sheath can be optionally configured as a tube or solid rod.
• the stent can be crimped over the stent holder sheath proximal to the stent holder and loaded into the valve chamber.
• the prosthesis can then be subsequently released from the valve chamber by advancing the valve chamber sheath distally while keeping the stent holder position fixed.
• the stent holder will prevent distal motion of the prosthesis, and as the valve chamber is moved distally, the prosthetic valve will be released from the valve chamber beginning with the proximal side of the prosthetic valve and ending with the distal side of the prosthetic valve.
• three DGF head members can be implanted in the annulus first: one at the medial commissure, one at the lateral commissure, and one in the center of the posterior annulus.
• the slits on the valve chamber will align with the holes on the medial edge, lateral edge, and the center of the atrial flared portion of the crimped prosthetic valve respectively, such that the trailing DGF tails can easily be fed through the corresponding atrial flare holes, and then through the corresponding locking catheter in the valve housing, positioning, and locking system.
• the VHPL system can be inserted into the patient’s body and the DGF tails can be tensioned to guide the valve chamber, and thus the prosthetic valve, to the operative position at the previously implanted DGF head members. Once in position at the mitral annulus, the valve chamber sheath can be advanced to release the prosthetic valve starting with the atrial flared portion and continuing until the entire ventricular portion of the prosthetic valve has been released.
• one or more sheaths within the MSML delivery system can be configured to be deflectable and/or steerable.
• the heart valve leaflet replacement system can be implanted in the mitral annulus through a transfemoral, trans-septal procedure.
• the docking sheath can be inserted into the femoral vein, advanced to the inferior vena cava and then can be articulated to bend the distal tip from the inferior vena cava through the trans-septal puncture site at the fossa ovalis to gain access to the left atrium.
• the VHPL system can be inserted through the docking sheath and advanced to the left atrium.
• the stent holder and valve chamber sheaths can be advanced, and the stent holder sheath can be articulated to bend the stent holder sheath tip towards the left ventricle and position the valve chamber in the center of the mitral annular orifice.
• the prosthesis can be fixed in position at one or more implanted DGF head members prior to full release of the crimped prosthesis from the valve chamber by tensioning the respective DGF tail and engaging the corresponding DGF locking device with the prosthesis.
• the VHPL system can be configured with a suture tensioning mechanism that can be operated to individually tension the DGF tails, or optionally a plurality of DGF tails simultaneously, to guide heart valve replacement system positioning and locking.
• the plurality of locking catheters can be advanced distally against the atrial flared portion of the stent while tensioning the DGF tails to engage the DGF locking mechanism with the prosthesis.
• the locking catheters are configured to be flexible and can bend together with the other steerable sheaths during locking of the prosthesis.
• the distal tip of the locking catheters has a larger inner diameter than the DGF locking members such that they can pass over the DGF locking members. In this aspect, the locking catheters will be pushed against the atrial flared portion of the prosthesis until the DGF locking members are pulled through the atrial flare holes.
• the lower ventricular portion of the stent can be configured with a mechanism to selectively engage the VHPL system such that the prosthesis can be guided, positioned, and fixed in place in a highly controlled manner.
• the stent holder can be configured with a recess with a complimentary shape to a tab on the lower ventricular portion of the stent frame, such that the tab fits inside the recess of the stent holder and the recess acts to hold the tab of the stent frame against the valve chamber inner wall until the valve chamber has been advanced distally enough to reveal the tab recess.
• the lower ventricular portion of the stent frame can be configured with a tab on the tip of an extended member that is longer than the rest of the stent, such that, in operation, the tab is the lowest point of the stent.
• the stent frame can be configured similar to a stingray in shape where the extended member resembles the stingray tail that can be extended longer than the body of the stent frame, and the tip of the extended member can be configured to engage with the stent holder.
• the lower ventricular portion of the stent frame can be configured with a plurality of tabs or holes, or other engagement members on the tips of a plurality of extended members that are longer than the rest of the stent.
• the engagement members can be operatively engaged with complementary engagement members such as recesses or protrusions on the stent holder or the stent holder sheath.
• the prosthesis can be released from the valve chamber leaving only the extended member tab engaged in the stent holder such that the prosthesis can expand fully in the mitral annulus.
• the locking catheters can be advanced and the DGF tails tensioned to lock the prosthesis in position at the implanted DGF members, while keeping the stent tab engaged in the stent holder.
• the blood pressure in the left ventricle can cause the prosthesis to migrate undesirably.
• This mechanism can be realized by a variety of different engagement members that can engage and disengage the prosthetic valve device with a portion of the VHPL system during the prosthetic valve deployment process.
• a plurality of additional DGF members can be deployed on top of the prosthetic leaflet device with the DGF delivery system, such that each DGF head member of the additional DGF members is driven through the skirt material on the atrial flared portion of the prosthesis and embedded into the muscular annulus tissue until the body portion of the DGF body member lies flush against the atrial flared portion of the prosthesis.
• no additional fixation mechanism i.e., locking member, is required on the DGF body member.
• FIGS. 1 A-1D illustrate different schematic views of the prosthetic valve.
• FIG. 1 A illustrates the front view of the stent frame of the prosthetic valve, showing the atrial flared portion featuring a plurality of through-holes, and a lower ventricular portion featuring an elongated member with a tab.
• FIG. IB illustrates the side view of the stent frame of the prosthetic valve.
• FIG. 1C illustrates the front view of the prosthetic valve, showing the three leaflets.
• FIG. ID illustrates the side view of the leaflet attachment to the prosthetic valve stent, showing the prong structures of the middle leaflet attachment to the interior stent surface.
• FIGS. 2A-2C show an exemplary aspect of a DGF member.
• FIG. 2A illustrates each component of the DGF member.
• FIG. 2B illustrates the top view of the DGF head member.
• FIG. 2C illustrates the DGF locking member and its components.
• FIGS. 3 A and 3B are schematic views of the stent fixed in position by a plurality of DGF members.
• FIG. 3 A is the side view showing the atrial flared portion of the stent being sandwiched between the DGF head and the DGF locking member.
• FIG. 3B illustrates the locations of the three DGF members along the flared portion of the prosthetic valve stent.
• FIG. 4 is a schematic view depicting one aspect where additional DGF members without the DGF locking members are implanted in the atrial flared portion of the stent.
• FIG. 5 is a schematic of a docking system and valve housing, positioning, and locking system mounted on an angled base.
• FIG. 6 is a schematic of the valve housing, positioning, and locking system catheters with the valve chamber attached to the distal section, follow by the stent holder mounted on the steerable stent holder sheath, and a plurality of locking catheters; all reside within the guide sheath and separated by a separator.
• FIG. 7 is a perspective view of the valve chamber attached to the distal end of the valve chamber sheath.
• FIGS. 8A-8D illustrate a heart valve leaflet replacement system and steps for loading, releasing, and locking a prosthetic valve.
• FIG. 8A shows the prosthetic valve (stent only for clear visual) is loaded into the valve chamber.
• FIG. 8B shows the release of the prosthetic valve by advancing the valve chamber distally.
• FIG. 8C shows the prosthetic valve stabilized during locking by a mechanism in the valve chamber, and the locking catheters being guided by DGF member tails (not shown) to the DGF members (not shown) on the prosthetic valve flared section, and locking the prosthetic valve in place.
• FIG. 8D shows that the prosthesis is fixed at the first three DGF members, and the entire valve housing, positioning, and locking system can be removed.
• Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another aspect includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.
• prosthetic valve and “prosthesis” and “valve stent” and “heart valve leaflet replacement device” and “valve device” are used interchangeably and is contemplated as a heart valve replacement device described herein.
• distal indicates an apparatus portion distant from, or a direction away from the operator and “proximal” indicates an apparatus portion near to, or a direction towards the operator.
• the heart valve replacement system described herein may be utilized with any heart valve replacement devices or prostheses. It is contemplated that the heart valve replacement system described herein comprises a series of systems that can be used concurrently to deliver a prosthetic valve 2 into a subject’s heart.
• the heart valve replacement system includes a multi-stage, multi-lumen (MSML) delivery system that can be configured to deliver the heart valve replacement device, or prosthesis 2, to the implanted site, or the native mitral annulus.
• MSML multi-stage, multi-lumen
• Such system may include a dual-guiding-and-fixation (DGF) delivery system and a valve housing, positioning, and locking (VHPL) system.
• DGF dual-guiding-and-fixation
• VHPL valve housing, positioning, and locking
• the DGF delivery system described herein is configured to implant a plurality of DGF members in the native annulus and to aid in guiding and fixing a prosthetic valve to the targeted implanted location.
• the novel VHPL system can be configured to house and organize a plurality of DGF member tails, crimped prosthetic valve, and can be designed to incrementally release a crimped prosthetic valve and to fix the prosthetic valve at the implanted DGF members via a DGF body fixation mechanism.
• the MSML delivery system can access the mitral valve via the inferior vena cava, enters the right atrium, crosses the atrial septum to the left atrium then articulates downward to the native mitral annulus. It is contemplated that the MSML delivery system could also be navigated to the implantation site via the superior vena cava and follows the same previously described pathway towards the native mitral annulus.
• a crescent shaped stent 3 of the MSML delivery system can comprise an atrial flared portion 4, a ventricular portion 5, and a neck portion 6.
• the atrial flared portion 4, ventricular portion 5, and neck portion 6 are continuously attached to form a single body.
• At least a portion of the atrial flared portion 4 and/or a portion of the ventricular portion 5 can be formed to be self-expandable or balloon expandable to the desired operative position.
• the stent 3 can be conventionally laser cut or woven into a desired shape that can be radially collapsible and expandable.
• the stent 3 can comprise a plurality of operatively linked components to form an expandable meshed or non-meshed body that can be made of a metal, or polymeric material, or biologically-made material, including but not limited to, cobalt chromium, stainless steel; or a metal having inherent shape memory properties, including but not limited to, Nitinol.
• the stent 3 can comprise a plurality of vertical stiff structures that are connected by compliant materials such as biological tissue, synthetic materials such as polymers and the like. The stent 3 can be configured to permit the natural dynamic motion of any remaining native leaflet(s) to coapt with prosthetic leaflet(s) 10.
• the atrial flared portion 4 of the stent 3 when implanted, it is contemplated that the atrial flared portion 4 of the stent 3 can be configured to be positioned on and/or above the native annulus. In this aspect, the atrial flared portion 4 of the stent 3 can be configured to facilitate fixation and sealing of the prosthesis 2, which can assist in preventing paravalvular leakage and dislodgement post implantation.
• the mitral valve annulus is asymmetrical.
• the atrial flared portion 4 of the prosthesis 2 can be configured to cover or overlay the posterior portion of the mitral annulus, which is divided into three scallops, namely PI, P2 and P3.
• the atrial flared portion 41 can span the two commissures, i.e., the AC-anterior commissure and the PC-posterior commissure.
• the atrial flared portion 4 can comprise an anterior atrial flared portion as well as a posterior atrial flared portion, such that it covers the entire circumference of the mitral valve when operatively positioned.
• the bend can be an upward curl away from the heart chamber wall to prevent over expansion of the heart chamber that could result in deep penetration of the heart tissue.
• the upward curl portion is oriented between about ninety and one hundred twenty degrees (90-120°) from the atrial flared portion 4.
• this bend 14 is only at the cell struts of the atrial flared portion 4, thus, does not interfere or distort the circular shape of the through-holes 9 in the atrial flared portion 4.
• At least a portion of the atrial flared portion 4 is configured to have a plurality of through-holes 9 to selectively engage the DGF members 101.
• the through-holes 9 can be designed with a circular shape, connecting the cell struts and forming a bridge connection with the neighboring cells.
• the through- holes 9 can be designed at every bridge connection of the atrial flared portion 4.
• the through-holes 9 can be designed at fewer locations than the total number of bridge connections of the atrial flared portion 4.
• the entire circumference of the ventricular portion 5 of the stent can be bent towards the left ventricle wall.
• the bending angle 15 can be between sixty and one hundred twenty degrees (60-120°) with respect to the atrial flared portion 4 of the stent 3.
• the stent 3 is configured with an extending member 7.
• the extending member 7 can be configured as a straight segment.
• the extending member 7 can be configured with a short extension length and a tab 8 at a distal end that is continuously connected to the straight segment.
• the tab 8 can be configured to have a larger width than the rest of the extending member 7.
• At least one extending member 7 can be designed at the center of the distal portion of the ventricular portion 5 of stent.
• the extending member 7 in the operative position, is the longest section of the stent 3 that extends the furthest into the left ventricle.
• the extending member 7 is about two to seven millimeters (2-7 mm) longer than the other parts of the stent 3.
• the extending member 7 can be configured to curve inward radially to avoid interference with the posterior wall of the ventricle in operation.
• the extending member 7 can be located at other sections along the circumference of the ventricular portion 5 of the stent. In an exemplary aspect, referring to FIG. 1 A, the extending member 7 can extend from one or more lower cells of the ventricular portion 5 of the stent 3.
• the tab 8 of the extending member 7 is configured to hold the prosthesis during release from the VHPL system to prevent it from migrating unexpectedly before the DGF fixation mechanism can be engaged.
• the (VHPL) system 1 is selectively designed to attach to the tab 8 of the extending member 7 until the prosthesis is secured to the targeted implanted location. Once the prosthesis 2 is fully fixed in the implanted position, the tab 8 could be selectively released from the (VHPL) system 1 to disengage the prosthesis 2 from the (VHPL) system 1.
• the tab 8 is configured with a dome, circular, square, rectangular, triangular, or irregular shape. In another aspect, the tab 8 is configured with at least one-through hole.
• At least one prosthetic leaflet 10 is mounted on an inner surface of the ventricular portion 5 of the stent 3, as depicted in FIGS. 1C and ID.
• at least one prosthetic leaflet 10 of the plurality of prosthetic leaflets has a different shape.
• at least one prong structure 11 of the at least one prosthetic leaflet 10 comprises a plurality of prong structures 11. It is contemplated that at least one prong structure 11 is coupled to the leaflet free edge.
• the prosthetic leaflets 10 can be configured similarly in shape to the native posterior mitral leaflets.
• the at least one prosthetic leaflet 10 and at least one prong structure 11 can be configured with one single, flat piece of flexible material such as biological tissue, polymeric material, or fabric, and can be attached to the stent 3 in such a way that it creates a 3D dome-like structure billowing radially inwards from the stent attachment points.
• the prosthetic leaflet 10 can be configured to be mobile during the cardiac cycle, where the prosthetic leaflet 10 moves closer to the inner surface of the stent during diastole, and further away from the inner surface of the stent in systole.
• the at least one prosthetic leaflet 10 can comprise three leaflets: two smaller lateral leaflets, and one large central leaflet, which form three distinct dome-like structures extending radially from the inner surface of the ventricular portion 5 of the stent 3.
• the three leaflets can be configured to span the circumference of the lower ventricular portion of the stent.
• the prosthetic leaflets 10 can be mounted closely together on the inner surface of the stent 3 in order to prevent transvalvular leakage in operation.
• the leaflets can be configured to billow inward radially from the stent 3 such that they are positioned in the blood flow track in operation and can close the mitral orifice under systolic blood pressure.
• the smaller lateral leaflets can be asymmetric with a shorter length on the lateral edges corresponding to the shape of the lower ventricular portion 5 of the stent 3.
• the larger central leaflet can have a symmetric shape and two prong structures 11 extending from the leaflet free edge.
• the free ends of the prongs 11 can attach to portions of the stent 3, for instance, by sewing the ends of the prongs 11 to the stent via the through- holes 12 in the lower ventricular portion 5 of the stent 3.
• the prong structures 11 prevent excessive billowing and prolapse of the large central leaflet and also help to evenly distribute stress in the prosthetic leaflet 10 which is important for durability.
• one or more prong structures 11 can be added to the lateral leaflets.
• the MSML delivery and implantation system can comprise a docking system 326, a DGF member delivery system, and a VHPL system 1, which can be mounted on a handle platform 301 to facilitate the delivery process.
• the handle platform 301 is mounted on a base 324.
• the base 324 features a mechanism that allows for adjustment of the angle of the MSML system to optimally enter the access site of the body.
• the base 324 can be made of, but is not limited to, rigid materials such as metals, plastics, and others of the like.
• the docking system 326 includes a docking sheath 327 and a docking handle.
• the docking sheath 327 may first enter the body through an introducer sheath.
• the docking sheath 327 can be configured to be deflectable in order to access the implantation site.
• the distal end of the docking sheath 327 can be configured to bend up to one hundred eighty degrees (180°) with respect to the proximal end of the sheath.
• the DGF system can be introduced.
• a plurality of DGF members 101 e.g., as shown in FIG. 2, can be sequentially or simultaneously delivered and implanted at the desired locations on the annulus.
• a method of implanting DGF members 101 can be implemented prior to the delivery of the prosthesis 2.
• the DGF member 101 can comprise a DGF head member 102, a DGF body member 103, a DGF locking member 105, and a tether 114, which are intended to be permanently implanted in the mitral annulus.
• implanting additional DGF members 101A can be implemented after the delivery and fixation of the prosthesis 2.
• the DGF members 101 A can be configured with a DGF head member 102, a DGF body member 103 and a DGF tether 114 forming a loop.
• the DGF member 101 is configured with a head portion 102 which engages the tissue on or around the annulus, and a body portion 103 with an engager 109 that engages a DGF delivery catheter.
• the DGF head member 102 can be configured to implant into the native annulus tissue and to resist separation after implantation.
• the DGF head member 102 can have, but is not limited to, a spiral shape, a coil shape, a pronged shape, a screw shape, and a barbed hook shape that engages the annular tissues.
• the DGF head member 102 can be formed of, but is not limited to, Nitinol, stainless steel, cobalt chromium, polymer, and the like.
• the DGF head member 102 is configured with a coil 108 with a length between about four and ten millimeters (4-10 mm), and a diameter between about two and five millimeters (2-5 mm), formed with wire with a diameter between 0.25 and one millimeter (0.25-1.0 mm).
• the DGF head member 102 can be configured with a stabilization member 111 to facilitate controlled implantation of the DGF head member 102 into the annular tissue via the DGF delivery system in operation.
• the stabilization member 111 is configured as a straight wire with a diameter between about 0.25 and one millimeter (0.25-1.0 mm) extending axially through the center of the spiral with a sharpened tip extending between about one and three millimeters (1-3 mm) beyond the end of the spiral.
• the stabilization member 111 could be configured as a needle with a sharpened distal tip 112 that extends axially beyond the DGF head member coil 108 by about one to five millimeters (1-5 mm).
• the stabilization member 111 can be used to engage the annular tissue prior to screwing in the DGF head member 102 into the tissue, which will help to prevent undesired motion of the DGF delivery system, so the DGF head member 102 can be easily implanted at the desired position along the annulus. It can be appreciated that such stabilization member 111 can be used to engage the tissue with the DGF member at the preferable implantation site and prevent the DGF member from moving from the target location during implantation.
• the tip 119 of the coil 108 of the DGF head member 102 can be shaped and configured to facilitate easy penetration into the annular tissue.
• the tip 119 of the coil 108 is sharpened and curved to the same pitch as the remainder of the coil 108.
• the tip 119 can be straight.
• the tip 119 can have an arc length between about one and three millimeters (1-3 mm).
• the DGF body member 103 comprises a base and an extruded section 109 that is configured for engaging the DGF delivery catheter.
• the base and the extruded section can be one piece.
• the extruded section 109 has a smaller dimension than the outer diameter of the base so that the DGF delivery catheter can engage it.
• the extruded section 109 comprises three through holes, with two of the holes 110 configured for attachment of the DGF locking member 105 via the tether 114.
• the distal section of the tether 114 is fixed to the DGF body via the two attachment holes 110, the middle portion of the tether 114 is configured to loop through the DGF locking member 105 in such a way that constrains the DGF locking member 105 from moving along the tether 114, and the proximal section of the tether 114 at the proximal side of the DGF locking member 105 is configured with a loop.
• the DGF body member 103 comprising the DGF locking member is configured for attaching a DGF tail member 104 via the loop at the proximal side of the tether 114.
• the tether 114 can be straight, curved, single, or double or multiple lines.
• the distance between the DGF body member 103 and the DGF locking member 105 can be between about 0.4 and one millimeter (0.4-1.0 mm) such that the atrial flared portion 4 of the stent 3 can fit snugly between DGF body member 103 and the DGF locking member 105 in the operative position.
• each DGF body member 103 can include a plurality of DGF locking members 105, where the spacing between adjacent DGF locking members 105 can be between about 0.4 and two millimeters (0.4-2.0 mm).
• the DGF body member 103 and DGF locking members 105 can be separated on the tether 114 by, for example, tying a plurality of knots on the tether 114.
• the tether 114 is made of metal or plastic of the like, small protrusions can be welded, molded, or adhered to the flexible component to maintain the spacing.
• the tether 114 containing the DGF locking member 105 can be formed of a tether made from suture, string, wire, or polymeric material.
• the DGF head member 103 and DGF body member 103 can be formed as a single component or optionally, by joining distinct parts by one or more of welding, bonding, adhesives, and the like that can resist separation during in vivo loading. Further, in this aspect, the DGF head member 103 and DGF body member 103 may be formed with strong and biocompatible materials such that they can be permanently implanted in the human body and resist damage, for example, but not limited to, stainless steel, cobalt chromium, nitinol, non-absorbable polymer, biological material and the like.
• the DGF locking members 105 can be configured to allow passage of a portion of the atrial flared portion 4 of the stent 3, guided by the DGF tail member 104, in one direction only, and to resist the subsequent movement of the atrial flared portion 4 of the stent 3 in the opposite direction.
• the DGF locking member 105 can be configured such that it can selectively be compressed to a diameter smaller than the diameter of the through- hole 9 on the atrial flared portion 4 of the stent 3, such that it can pass through the hole, and subsequently be selectively re-expanded to its original size, larger than the diameter of the through-hole 9 to prevent backward motion of the DGF locking member 105 through the hole.
• the DGF locking member [115] In one exemplary aspect, referring to FIG. 2C, the DGF locking member
• the locking member 105 can be configured with proximal 107 and distal 106 portions.
• the locking member 105 can have a total length between about 1.5 and 3.5 millimeters.
• the length of the proximal portion 107 can be between about 0.5 and 1.5 millimeters.
• the length of the distal portion 106 can be between about one and two millimeters (1.0- 2.0 mm).
• the proximal portion 106 comprises a tubular shape with an outer diameter ranging between about 0.5 and 1.5 millimeters and an inner diameter ranging between about 0.4 and 1.2 millimeters.
• the distal portion 106 of the DGF member 101 comprises a plurality of radially compressible legs forming a cone shape in its original state.
• the outer diameter of the proximal portion of the locking member is smaller than the inner diameter of the through-hole 9 on the atrial flare 4 of the stent 3.
• the distal tip 107 of the DGF locking member 105 can be configured with a maximum fully-expanded outer diameter that is larger than the inner diameter of the through-hole 9 on the atrial flare 4 of the stent 3 such that it cannot pass through the through-hole 9.
• portions of the DGF locking member 105 can be connected and continuous.
• the DGF member tails 104 can be tensioned to pull the proximal portion 107 of the DGF locking member 105 into the through-holes 9, and as the distal portion 106 of the DGF locking member comes into contact with the edges of the through-hole 9, it will collapse radially, such that its outer diameter is less than the inner diameter of the through-hole 9, which will allow the DGF locking member 105 to pass through the through-holes 9.
• the DGF distal portion 106 can re-expand to its original size to prevent backward motion of the DGF locking member 105 through the through-holes 9.
• the DGF locking member 105 can be manufactured, for example, by laser cutting a plurality of slits from a tube, then deforming the legs by bending these legs outwards radially.
• the slit may be between about 0.3 to 0.6 millimeters wide and between about 0.6 to 1.5 millimeters long.
• a heat-treatment process can be done to form the final flared cone shape geometry.
• the legs are designed so that they can be selectively compressed to pass through the through-holes 9, and then re-expand and return to their original shape once fully passed through the through-holes 9.
• the one or more DGF locking members 105 can be formed of, but are not limited to polymers, polytetrafluoroethylene (PTFE), stainless steel, Nitinol, and metal-like materials, or a combination of these materials.
• the extruded section 109 of the DGF body member 103 can be configured as a protrusion which is shaped to fit snugly in a complimentary recess within the distal tip of the DGF delivery catheter, such that, when the protrusion is engaged with the distal DGF delivery catheter, rotation of the DGF delivery catheter in one direction will engage the DGF head member 102 with the tissue and rotation of the DGF delivery catheter in another direction will result in disengaging the DGF head member 102 from the tissue.
• the extruded section 109 of the DGF body member 103 can have a rounded rectangular shape which is raised about 0.5 to two millimeters (0.5-2 mm) from the base of the DGF body member 103.
• the loop on the tether 114 can be configured to engage the DGF tail member 104.
• one end of the DGF member tail 104 can be inserted through the loop on the tether 114, and both free ends of the DGF member tail 104 can extend through and out of the proximal side of the MSML delivery system.
• the DGF member tail 104 links the DGF delivery system and the VHPL system 1.
• the DGF member tail 104 acts as a bridging element to guide the VHPL system 1 from the access site to the implantation site.
• the two free ends of the DGF member tails 104 can be inserted through the atrial flared through-holes 9 of the prosthesis 2.
• both free ends of the DGF member tails 104 can also be inserted into the VHPL system 1, such that when an operator pulls on the exiting free ends of the DGF member tails 104 away from the body, the DGF member tails 104 can be tensioned and guide the VHPL system components towards the DGF members 101 implanted in the annulus. Further tensioning of the DGF tail members 104 will aid in fixing the prosthesis to the annulus via the DGF locking members 105 on the DGF member 101. Following device implantation, DGF member tails 104 can be removed from the VHPL system and from the body by pulling one free end of DGF member tails 104.
• one end of the DGF tail members 104 can be tied to the loop and the other end can extend out of the body to the proximal side of the MSML delivery system.
• the trailing DGF tails can be cut by traditional cutting methods or a transcatheter suture cutting device.
• the DGF tail member 104 can be configured to fit within the inner catheters of the MSML delivery system and be long enough to extend from the DGF body member 103 and exit the MSML delivery system.
• the DGF tail member 104 can have a diameter of about 0.1 to 0.5 millimeters and can be at least about 2.5 meters in length.
• the atrial flared portion 4 of the prosthesis 2 will be sandwiched between the DGF locking member 105 and the DGF body member 103. It can be appreciated that the spacing between the DGF locking member 105 and the DGF body member 103 is optimized so that there is limited motion of the prosthesis 2 after implantation.
• At least three DGF members 101 are implanted, with two DGF members 101 implanted at the lateral portions and one at the center of the atrial flared portion 4 of the stent 3.
• At least three DGF members 101 are implanted in the annulus prior to the implantation of the prosthesis 2 via the VHPL system 1. Once the prosthesis 2 is implanted, at least one additional DGF member 101 A—without the DGF locking member 105 — will be implanted over the atrial flared portion 4 of the prosthesis 2.
• the DGF members 101 A can penetrate the skirt material of the prosthesis and anchor into the tissue.
• the DGF members 101 A can be configured to go through the through-hole 9 of the atrial flared portion 4. Referring to FIG. 4, as illustrated, three DGF members 101 can be implanted at the lateral sides (PI and P3) of the atrial flared portion 4, one DGF member 101 can be implanted at the center (P2) of the atrial flared portion 4.
• Additional DGF members 101 A can be implanted between the DGF members 101 at PI and P2, as well as P2 and P3 locations. By implanting additional DGF members 101 A, as one skilled in the art will appreciate, paravalvular leakage between the prosthesis 2 and the annulus can be eliminated, and dislodgement of the prosthesis 2 can be prevented, thus allowing normal coaptation between the prosthetic leaflets and the native leaflet.
• VHPL system 1 design for successfully delivering and fixing the prosthesis.
• the shape and designs of the outer compartments, constructions and assembly of the VHPL system 1 controls may change as long as they can perform the same general functions, i.e., translation or restricted motion of a sheath, tensioning of a wire or tether, etc.
• the illustrations displayed herein are for a better description and clarification but not limited to a specific design of any components.
• the VHPL system 1 can comprise an outer sheath 306 that houses a plurality of catheters and tubes that function to deliver a prosthesis.
• the outer sheath 306 can be a guide sheath.
• the guide sheath 306 may house a stent holder sheath 206 that is attached to a valve chamber, 201 which houses a prosthetic valve in a crimped stage.
• the stent holder sheath 206 can deflect to guide and position the valve chamber 201 from the access site to the left ventricle.
• the valve chamber 201 is connected to a valve chamber sheath 203 that can slide along the inner lumen of the stent holder sheath 206.
• the sliding of the valve chamber sheath 203 is the mechanism to release the prosthetic valve.
• the outer sheath 306 may house a plurality of locking catheters 317.
• the locking catheters 317 and the stent holder sheath 206 can be organized with a multi-lumen guide sheath 306, all of which can be inserted into the body through a larger diameter docking sheath 327.
• the prosthetic valve 2 is guided to a plurality of previously implanted DGF members 101 by tracking over the DGF tails 104, which are loaded through the atrial flare holes 9 of the crimped prosthetic valve 2 and through the corresponding locking catheters 317 to the proximal end of the VHPL system 1.
• valve chamber sheath 203, stent holder sheath 206, locking catheters 317, and guide sheath 306 are configured to move independently of the docking sheath 327 to gain proper positioning. Further, the valve chamber sheath 203 and stent holder sheath 206 are configured to move together and independently of the locking catheters 317 and guide sheath 306.
• the valve chamber sheath 203 can be advanced relative to the stent holder sheath 206.
• the DGF member tails 104 must be tensioned individually while each locking catheter 317 is individually advanced. Once the prosthesis 2 is fully released and fixed in place, all the sheaths can be retracted together, out of the patient’s body.
• the VHPL system can be mounted on a handle platform 301, e.g., as shown in FIG. 5.
• the handle platform 301 sits proximal to the docking system 326 on base 324.
• the outermost guide sheath 306 and the associated inner sheaths, on the handle platform 301, are inserted into the docking sheath 327.
• the handle platform 301 is configured such that it allows the guide sheath 306, the stent holder sheath 206, and valve chamber sheath 203 to slide simultaneously along the base 324 at specified distances.
• the handle platform 301 is designed to prevent rotation of the guide sheath 306 throughout the valve delivery process.
• the handle platform 301 can be made of any rigid and durable material, such as metals, plastics, and the like.
• the guide sheath 306 is composed of a distal and proximal portion.
• the distal portion of the guide sheath 306 may be made of a composition of materials that are flexible and conforms to the sharp curvature of the deployment pathway in the native heart chambers, one of which including from the inferior vena cava to the septum; and the proximal portion of the guide sheath 306 may be made of a composition of materials that are more rigid than the distal portion for the purpose of preventing buckling during the delivery process.
• the distal end of the guide sheath 306 can be configured with a separator 307.
• the separator 307 of the guide sheath 306 acts as an organizer to separate the internal sheaths within the guide sheath 306 to avoid tangling throughout the prosthetic valve delivery process.
• the separator 307 of the guide sheath 306 is a separate component that is fixed to the distal portion of the guide sheath 306.
• the separator 307 may be a cylinder component that has at a plurality of lumen.
• the separator 307 can have multiple lumens, e.g., four lumens, with one center lumen and three outer lumens surrounding the center lumen.
• the separator 307 organizes the internal sheaths within the guide sheath 306 to avoid tangling throughout the prosthetic valve 2 delivery process.
• the guide sheath 306 can be configured as a multi-lumen tube throughout its entire length with no additional separator 307.
• the multi-lumen guide sheath can have four lumens, one in the center and three in the peripheral, and all lumens are separated by the walls.
• the stent holder sheath 206 can deflect and translate along the handle platform.
• the stent holder sheath 206 can be mounted on a handle system 309, 301 that allows the operator to deflect the distal portion of the stent holder sheath 206.
• the stent holder sheath 206 can be mounted on a handle system that can slide.
• the deflectable stent holder sheath 206 can be at the center lumen of the guide sheath separator 307.
• the deflectable stent holder sheath 206 can be configured as a composite sheath comprising portions of varying stiffness and flexibility, among other notable characteristics such as pushability and kink-resistance. These characteristics allow the stent holder sheath 206 to deflect from 0° to 180° while maintaining its integrity and ability to deflect the sheathes contained within.
• deflectable stent holder sheath 206 can comprise three sections, i.e., the distal, middle and proximal sections.
• the distal section is a stiff straight section in which the prosthetic valve 2 is crimped over.
• the middle section of the deflectable stent holder sheath 206 is a soft, coiled section that has an inherent ability to bend in a tight radius without kinking or causing damage to any sheaths residing within.
• the proximal portion of the deflectable stent holder sheath 206 is a long stiff section that provides stability and rigidity that spans throughout the VHPL 1.
• At least one pull wire is embedded within the walls of the deflectable stent holder sheath 206. By selectively tensioning the at least one pull wire, the deflection of the soft middle section can be controlled.
• the stent holder 207 functions as a safety feature within the delivery system to maintain control and repositionability of the prosthetic valve before it is fully deployed and locked onto the native mitral annulus.
• the tab 8 on the extending member 7 of the stent 3 is released from the stent holder 207 when the valve chamber 201 is translated distally past the stent holder 207, thereby completely freeing the prosthetic valve from the valve chamber 201.
• the distal section of the VHPL system 1 can comprise a valve chamber 201 to house the prosthetic valve 2 within the VHPL system 1.
• the prosthetic valve 2 can be crimped down to fit within a valve chamber 201 on the distal end of the VHPL 1, and subsequently be selectively expanded to an operative size and positioned once released from the valve chamber 201.
• the valve chamber 201 can include a cylinder or conical shape, which is closed on the distal end and has an inner diameter of about six to eight millimeters (6-8 mm), or large enough to house the crimped prosthetic valve 2, and an outer diameter of about seven to nine millimeters (7-9 mm) or small enough to fit within the docking sheath.
• the length of the valve chamber lumen can be configured to be larger than the length of the crimped prosthetic valve 2, such that it can house the entire crimped prosthetic valve 2 inside.
• the length of the valve chamber lumen can be about twenty to fifty millimeters (20-50 mm).
• a smaller diameter valve chamber sheath 203 can be configured to attach to the closed end on the distal end of the valve chamber 201 which extends to the proximal side of the VHPL system 1, such that the valve chamber 201, and thus the prosthetic valve 3, position within the heart can be controlled by manipulating the valve chamber sheath 203 on the proximal side, i.e., the operator’s side, of the VHPL system 1.
• the distal end of the valve chamber 204 and the cylindrical part of the valve chamber 201 can be made from one solid piece of material or optionally from separate pieces and of similar or dissimilar materials that are otherwise attached together.
• the distal end of the valve chamber 201 can be configured with a central lumen to facilitate attachment to the valve chamber sheath 203 and rounded edges to prevent damage to surrounding tissues in operation.
• the valve chamber sheath 203 can be optionally configured as a tube or solid rod.
• the valve chamber sheath 203 can be configured with multiple sections with varied stiffness along its length.
• the valve chamber sheath 203 can be configured with a stiff distal section within the valve chamber 201, followed by a compliant middle section to allow for bending and facilitate maneuvering of the VHPL system 1 within the patient’s body, followed by another stiff section at the proximal end to provide pushability.
• a stent holder 207 can be configured to fit within the lumen of the valve chamber 201 with the same outer diameter as the crimped prosthesis 2.
• the stent holder 207 can be configured to attach to the distal tip of a smaller diameter stent holder sheath 206 that extends to the proximal side of the VHPL system 1, such that the stent holder 207 position within the valve chamber 201 can be controlled by manipulating the stent holder sheath 206 on the proximal side of the VHPL system 1.
• the stent holder 207 in operation, can be positioned distal to the crimped prosthesis 2 within the valve chamber 201.
• the valve chamber lumen can be configured with a length that is longer than the lengths of the stent holder 207 and crimped prosthesis 2 added together.
• the prosthetic valve 2 can be crimped over (around) the stent holder sheath 206 proximal to the stent holder 207 and loaded into the valve chamber 201.
• the valve stent 2 can then be subsequently released from the valve chamber 201 by advancing the valve chamber sheath 203 distally with respect to the stent holder 207.
• the stent holder 207 will prevent distal motion of the prosthesis 2, and as the valve chamber 201 is moved distally, the prosthesis 2 will be released from the valve chamber 201 beginning with the proximal side of the valve stent 2 and ending with the distal side of the prosthesis 2.
• the stent holder 207 can comprise a recess 208 which is configured to house a tab 8 on the extended member 7 of the prosthetic valve stent frame 3.
• the tab 8 on the extended member 7 of the stent 3 would be inserted into the recess 208 on the stent holder 207, and the stent holder 207 would be advanced into the valve chamber 201 to sandwich the tab 8 between the recess 208 and the inner wall of the valve chamber 201.
• the prosthesis 2 would be crimped around the stent holder sheath 206, and the stent holder 207 would be advanced to the distal end of the valve chamber 201 to load the crimped prosthesis 2 into the valve chamber 201.
• valve chamber sheath 203 would be advanced distally while keeping the stent holder 207 position fixed.
• the tab 8 would be engaged with the stent holder 207 until the valve chamber 201 had been advanced enough to reveal the recess 208 in the stent holder 207.
• this recess 208 thus acts as a safety mechanism to fix the prosthesis 2 to the VHPL system 1 such that it can be positioned and maneuvered within the heart using the VHPL system 1 controls until it is selectively released.
• the valve chamber 201 can have a plurality of slits 205 extending axially from the proximal end of the valve chamber 201 that are about one to five millimeters (1-5 mm) long.
• the slits 205 can be positioned on the valve chamber 201 to align with holes on the flared portion 9 of the crimped stent 3, such that following DGF member 101 implantation, the trailing DGF member tails 104 can be inserted through the slits 205 of the valve chamber 201 can be designed to correspond to the number and location of the implanted DGF members 101.
• three DGF head members 102 can be implanted in the annulus first: one at the medial commissure representing the P3 location, one at the lateral commissure representing the PI location, and one in the center of the posterior annulus representing the P2 location.
• the slits 205 will be positioned along the circumference of the valve chamber 201 to align with the holes 9 on the medial edge, lateral edge, and the center of the flared portion of the crimped prosthesis 2 respectively when the crimped prosthesis 2 is loaded into the valve chamber 201, such that the trailing DGF tails 104 can easily be fed through the slits 205 and into the corresponding flare holes 9, and then through the corresponding locking catheter 317 in the VHPL system 1.
• the VHPL system 1 can be inserted into the patient’s body and the DGF member tails 104 can be tensioned to guide the valve chamber 201, and thus the valve stent, to the operative position at the previously implanted DGF members 101 once in position at the mitral annulus, the valve chamber sheath 203 can be advanced to release the prosthesis starting with the atrial flared portion 4 and continuing until the entire ventricular portion 5 of the prosthesis 2 has been released.
• a plurality of locking catheters 317 are used to prevent proximal motion of the prosthesis 2 while the plurality of DGF member tails 104 are tensioned, in order to pull the locking member 105 on the DGF member 101 through the atrial flare hole 9 of the prosthesis 2, thereby locking the prosthesis 2 into place on the native mitral annulus.
• the locking catheter 317 is a composite sheath consisting, in one exemplary aspect, of three distinct sections that facilitate the fixation of the prosthesis 2.
• the proximal section of the locking catheter 318 can include, but not limited to, a long, rigid metal tube.
• the metal tube 318 can span the majority of the delivery system and can function as the control to translate the locking catheter 317 through the valve housing, positioning, and locking system handle 1.
• the middle portion of the locking catheter 319 can include a flexible material that conforms to the sharp curvature of the deployment pathway.
• the flexible portion 319 of the locking catheter 317 is able to bend equal or greater than about ninety degrees (90°) with a small bend radius to ensure locking is achievable along all parts of the annulus.
• the flexible portion 319 can be made of, but is not limited to, metallic, polymeric, or rubber materials of the like, and optionally can feature a coiled structure to allow for low bending rigidity and prevent the inner lumen from collapsing.
• the distal section of the locking catheter 320 can include a metal locking insert that engages with the locking member 105 and the atrial flared portion 4 of the prosthetic valve 2 to aid in fixing the prosthetic valve 2 at the DGF body member 103.
• the locking catheters 317 can attach to a handle to enable an operator to grab and ease the locking process.
• a suture tensioning mechanism can be configured to allow each of the DGF locking members 105 to be locked into place on the top of the atrial flared portion of the valve 4 independently.
• the DGF tail tension mechanism includes an assembly of ratcheting gears and a turn knob.
• a ratcheting gear includes a round gear with teeth that can be pivoting.
• a spring-loaded finger component engages the teeth of the gear.
• the gear teeth are uniform and both slopes on the teeth are symmetrical, allowing the teeth to move in both forward and backward directions. The stiffness of the spring- loaded finger and the slope on the gear teeth will allow for controlled incremental turning of the gear and thus controlled incremental tensioning of the DGF member tail 104.
• the gear can be configured with an asymmetrical slope to allow one directional turning, thus, preventing the DGF tail member 104 from loosening during the procedure.

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• 2021
  • 2021-03-10 CN CN202180031063.1A patent/CN115461016A/zh active Pending
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