WO2003022131A2 - Method and apparatus for external heart stabilization - Google Patents
Method and apparatus for external heart stabilization Download PDFInfo
- Publication number
- WO2003022131A2 WO2003022131A2 PCT/US2002/028372 US0228372W WO03022131A2 WO 2003022131 A2 WO2003022131 A2 WO 2003022131A2 US 0228372 W US0228372 W US 0228372W WO 03022131 A2 WO03022131 A2 WO 03022131A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heart
- base
- mitral
- cardiac
- ventricular
- Prior art date
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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
- A61F2/2478—Passive devices for improving the function of the heart muscle, i.e. devices for reshaping the external surface of the heart, e.g. bags, strips or bands
- A61F2/2481—Devices outside the heart wall, e.g. bags, strips or bands
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/39—Markers, e.g. radio-opaque or breast lesions markers
- A61B2090/3966—Radiopaque markers visible in an X-ray image
Definitions
- the present invention relates to devices and methods for treating dilatation of the valves at the base of the heart by external stabilization of the base of the heart, which subtend the atrio-ventricular valves of the heart.
- Dilatation of the base of the heart occurs with various diseases of the heart and often is a causative mechanism of heart failure.
- the dilatation may be localized to one portion of the base of the heart (e.g., mitral insufficiency as a consequence of a heart attack affecting the inferior and basal wall of the left ventricle of the heart), thereby affecting the valve in that region.
- the condition may be global affecting more of the heart and its base, causing leakage of particularly the mitral and tricuspid valves.
- mitral valve annulus is reinforced internally by a variety of prosthetic rings (Duran Ring, Medtronic Inc) or bands (Cosgrove- Edwards Annuloplasty Band, Edwards Lifesciences Inc).
- the present paradigm of mitral valve reconstruction is therefore repair from inside the heart, with the annulus being buttressed or reinforced by the implantation of a prosthetic band or ring.
- Levine and co-workers have suggested localized pressure or support of the bulging scar of the inferior wall of the heart from the outside.
- ventricular • containment with a custom made polyester mesh, or cardiac support device U.S. Patent Nos. 6077218 and 6123662. These devices are designed to provide a passive constraint around both ventricles of the heart, and constrain diastolic expansion of the heart.
- Other devices include ventricular assist devices that provide cardiac assistance during systole and dynamic ventricular reduction devices that actively reduce the size of the heart.
- this technique does not specifically address valve leakage using a device that reinforces the base of the heart in all phases of the cardiac cycle. Accordingly, there is a need to provide a less invasive, simple technique of repairing, reinforcing, reducing or stabilizing the base of the heart and its underlying valves (mitral and tricuspid valves) from the outside.
- the present invention addresses the problems discussed above by providing a device for the treatment of certain heart disorders, in particular mitral and/or tricuspid valve insufficiency.
- the device aims to reduce the size of the base of the heart that contains these valvular structures.
- the present invention can be used to address progressive dilatation of any localized area of the heart, such as the atrial or ventricular myocardium, or the cardiac base. It does so by providing external re-enforcement or remodeling of the cardiac base.
- the surgical procedure for implanting the device is referred to as ibasal annuloplasty of the cardia " externally (“BACE”) and the device is referred to as the external cardiac basal annuloplasty system ("ECBAS”) or BASE System.
- a customized or specially constructed biocompatible strip is implanted along the base of the heart at the level of the atrio-ventricular groove.
- the strip or mesh is between 2 and 5 cms wide and is secured by 2 rows of clips or sutures, one on the atrial side and the other on the ventricular side of the atrio-ventricular groove.
- Specific care is taken to avoid injury to the circumflex and right coronary arteries and the coronary sinus. This procedure may be performed either as a stand-alone procedure or as an adjunct to other cardiac surgery. Additionally, it may be performed with or without the aid of cardio-pulmonary bypass.
- Another embodiment of this approach is a device or strip, which once implanted at a certain size, can be tightened over time either by inflation of an attached chamber or programmed to return to a pre-formed size (based on elasticity or pre-existing memory) of the material used.
- Another embodiment of this device while externally stabilizing the base of the heart, also provides a localized increase in contraction along any segment of the base to improve contractile function. This may be accomplished by the aid of contractile metal or modified muscle or other cells.
- Variations of the device include a complete stabilization of the base of the heart, or a partial stabilization around the expansile portions of the mitral and tricuspid valves by a biocompatible strip.
- Another variation seeks to use ports along the device that will facilitate delivery of specialized drugs, gene therapeutic agents, growth factors, etc.
- a specific variation incorporates the use of epicardial bi-ventricular pacing electrodes implanted along with the BACE-Sys, where multi-site pacing might be indicated.
- the invention also provides a method of implantation, which may be through a conventional full median sternotomy with the strip being secured by sutures, or a minimally invasive approach whereby the device/strip may be implanted by a specialized implantation system using adhesives, self-firing clips, sutures, etc.
- Another modification of this technique is the local application of prosthetic material to stabilize scars of the heart to prevent their expansion (local ventricular stabilization).
- the device incorporates additional strips to be used in concert or as an extension to provide localized support to areas of ventricular reconstruction or areas of fresh infarction or old scar.
- Figure 1 depicts a cross-section of the heart, showing the approximate location of a representative embodiment of the device of the present invention by dashed lines.
- Figure 2 depicts a cross-section of the base of the heart between the dotted lines depicted in Figure 1.
- Figure 4 depicts a traditional method of repairing MV and TV with bands inside the heart.
- Figure 5 depicts basal angioplasty of the cardia externally.
- Figure 6 depicts a representative embodiment of the device of the present invention.
- Figure 7 depicts a schematic drawing of a heart with a representative device in place.
- the present invention is directed to external support of the base of the heart.
- the support functions to decrease, and/or prevent increases in, the dimensions of the base, and in particular the atrio-ventricular junction, beyond a pre-determined size.
- the device is designed to reduce the size of the cardiac base in a manner similar to an internal annuloplasty band or ring.
- This invention is particularly suited for use in regurgitation of the mitral and tricuspid valves.
- the device may also be used prophylactically in heart failure surgery to prevent further cardiac basal dilation or expansion even if the underlying mitral and tricuspid valves are competent.
- the device may be used in moderate or advanced heart failure to prevent progression of basal dilatation or reduce the size of the dilated base.
- cardiac base refers to the junction between the atrial and ventricular chambers of the heart, also known as the atrio-ventricular junction marked externally by the atrio-ventricular groove. This is easily identified in the change of appearance of the cardiac muscle and also the presence of arteries and veins.
- the heart is enclosed within a double walled sac known as the pericardium.
- the inner layer of the pericardial sac is the visceral pericardium or epicardium.
- the outer layer of the pericardial sac is the parietal pericardium.
- endocardial surface refers to the inner walls of the heart.
- epicardial surface refers to the outer walls of the heart.
- Mitral regurgitation is a condition whereby blood leaks back through the mitral valve into the left atrium. Over time, this creates a damming of blood in the lungs causing symptoms of shortness of breath.
- the left heart particularly the left ventricle has to pump a greater volume of blood as a result causing greater strain on this chamber.
- FIG. 2 is an anatomic diagram of the base of the heart, showing the valves and the structures in contact with them.
- Figure 3 is a schematic representation of the valves at the cardiac base.
- Mitral valve repair or replacement at present is always performed from inside the heart with the aid of cardiopulmonary bypass. Rings are implanted along the inner surfaces of the entire or expansile portions of the mitral and tricuspid annuli ( Figure 4). Alternatively, when mitral valve malfunction is severe, replacement of the valve with a prosthetic valve may be indicated.
- the basal ventricular stabilization of the present invention works by using a prosthetic material such as polyester mesh anchored or sutured to the base of the heart at the level of the atrio-ventricular groove. This serves to stabilize the mitral and tricuspid annuli from the outside ( Figure 5).
- This technique reduces the complexity of the procedure and minimizes the invasive nature and complications from work on the valve.
- This technique is of particular benefit in patients that have morphologically normal valves with annular dilatation.
- the device can be applied and anchored to the cardiac base, with the heart beating, without the aid of cardio-pulmonary bypass. Many patients with moderate degrees of mitral regurgitation are not treated surgically, because the risks of surgery outweigh the potential benefits in this group of patients.
- the device of the present invention can be constructed of any suitable implantable material.
- suitable implantable material examples include, e.g., synthetic polymers such as polyester, polytetrafluoroethylene, polypropylene, teflon felt, etc., as well as metallic materials such as stainless steel.
- Such metals may provide "memory", such that they return to a specific shape after deformation, and in this manner provide an element of dynamic contraction, h yet another embodiment, the device may be constructed either partially or completely by natural materials, such as polyglycolic acid or compressed and/or crosslinked collagen, which may or may not be reinforced with synthetic polymers or other means.
- the preferred device is in a "strip" configuration and comprised of two edge members and a center portion, each of which may be constructed by the same or different material. In one embodiment (not shown), there is no distinction between the edge members and the center portion and the device is completely uniform from top to bottom.
- the center portion of the device may be in the form of a solid single or multilayer sheet, but is preferably of an open mesh, porous or woven design, such that the exterior of the heart is not completely covered and therefore remains exposed to the surrounding tissue.
- the size of the openings in the mesh can vary, for example from 2 mm to 2 cm, and can take any shape, such as circular, square, octagonal, triangular, or irregular.
- the center portion of the device is a mesh as depicted in Figure 6.
- the center portion may also be adapted for the delivery of various therapeutic agents, such as growth factors or plasma proteins.
- various therapeutic agents such as growth factors or plasma proteins.
- it may be adapted to facilitate cellular growth, which in turn may facilitate anchorage of the device.
- the device may be designed to completely circle the base of the heart, or it may be a "C" shape, in which case it is specifically designed and implanted so as to not impede blood flow through the aorta and pulmonary artery.
- the biomaterial from which the device is constructed may also be radiolucent , radio-opaque or have radio-opaque markers at present intervals to monitor the movement of the cardiac base in real-time using fluoroscopy and to facilitate implantation.
- the device may be completely rigid prior to implantation, or may have regions of varying rigidity. However, it is important that the device is sufficiently flexible to move with the expansion and contraction of the heart without impairing its function. It should, however, be designed to prevent expansion of the cardiac base during diastolic filling of the heart to a predetermined size. Since the size expansion parameters of a beating heart are well known, this can be accomplished by testing the device in vitro by applying forces that mimic heart expansion.
- edges of the device may be constructed of a more rigid material, such as carbon fiber tubing, hi addition, means of making the device, or portions thereof, such as one or both edges and/or the center portion, more or less rigid post-implantation are also within the present invention.
- the center portion may be constructed of a partially biodegradable material and may become more flexible after implantation when the biodegradable material is hydrolyzed by the surrounding tissues and fluids.
- the edges may be provided with means for making them more rigid or flaccid prior to implantation, such as by inflating/deflating closed chambers. Many alternate means for adjusting the rigidity/flexibility of the device, or portions thereof, would be easily adapted from other mechanisms known in the surgical arts.
- the device may be attached to the outside of the base of the heart by any known method.
- attachment may be biological, chemical or mechanical.
- Biological attachment may be brought about by the interaction of the device with the surrounding tissues and cells, and can be promoted by providing appropriate enhancers of tissue growth.
- chemical attachment may be provided by supplying a mechanism for chemical attachment of the device, or portions thereof, to the external surface of the heart.
- the rigidity and tightness of the device around the heart may provide for sufficient mechanical attachment due to the forces of the heart against the device without the need for other means of attachment.
- the device further comprises attachment members, such as the eyelets shown therein.
- Specific anchor points or loops made of any biocompatible and implantable material may be attached to the edges or to the center portion or both to facilitate anchoring.
- Suitable materials include, inter alia, polyester, polypropylene or complex polymers.
- Alternative attachment members may comprise suture materials, protrusions that serve as sites for suturing or stapling, as well as other structural members that facilitate attachment to the surface of the heart.
- the size of the device depends on the purpose for which it is being implanted, it is contemplated that the device will be wide enough (measured from the outside of the first or top edge, i.e. the base edge, to the outside of the second or bottom edge, i.e. the apex edge) to provide efficient support to the atrio-ventricular grove.
- the device is between 2 and 5 centimeters wide. In other embodiments, the device may be adapted to provide support over a larger area of the heart.
- the distance between the base and the bottom of the apex of the heart can be expressed as distance "X". Because the focus of the device of the present invention is base stabilization,' it is generally preferred that the width of the device be less than or equal to 1/2 X, and be adapted for placement around the top half of the distance X, i.e. closer to the base than the bottom of the apex.
- Implantation The ECBAS or BASE system may be implanted through a conventional midline total sternotomy, sub maximal sternotomy or partial upper or lower sternotomy.
- the device may be implanted through a thoracotomy incision, or a Video
- the BASE system can also be implanted by a sub-costal incision as in the Sub-Costal Hand- Assisted Cardiac Surgery (SHACS). Additionally, he BASE system may be implanted with sutures onto epicardium or clips, staples, or adhesive material that can secure the device on the heart accurately.
- SHACS Sub-Costal Hand- Assisted Cardiac Surgery
- the device may also be implanted using robotic placement of the device along the posterior aspects of the base of the heart.
- the method of implantation and the adequacy of the external annuloplasty can be dynamically assessed by intra-operative trans-esophageal echocardiography, epicardial echocardiography or trans-thoracic echocardiography.
- the size of the device is assessed based on external circumference measurements of the cardiac base in the fully loaded beating heart state.
- the ECBAS may completely encircle the cardiac base or just partially support the mitral and tricuspid valve portion of the cardiac base. b. BACE with extension
- a limited extension of the ECBAS or a remote patch may be applied to reinforce an area of myocardium that has been reconstructed to exclude an aneurysm or scar.
- the ECBAS has attached close to or within it epicardial steroid eluting pacing wires that can facilitate multi-site ventricular pacing for heart failure.
- the device has fluid filled chambers that may be inflated gradually over time, to gradually reduce the size of the cardiac base. These chambers may also effect passive transfer of energy to facilitate diastolic and systolic support with a closed pericardium e. Smart & dynamic BACE
- the bio-material would have the capability to shrink to a preformed size over a period of time, based on the memory of the material or some other programmable characteristic. This would achieve controlled reduction over a period of time of the base of the heart. f. Cellular BACE
- the bio-material uses available matrix technology, and seeding of appropriate cells to provide dynamic reduction and assistance to the cardiac base.
- Timek TA Dagum P, Lai DT, Liang DH, Daughters GT, Ingels NB, Miller DC : Pathogenesis of mitral regurgitation in tachycardia induced cardiomyopathy (TIC) . Circulation 2000; 102(18) Suppl. 11:420.
- BACE Basal Annuloplasty of the Cardia Externally
- Careful pre-operative screening included radionuclide ventriculography to document left ventricular ejection fraction, a detailed trans-thoracic echocardiogram, a coronary angiogram, and in most cases a stress thallium and/or a Positron Emission Tomographic Scan looking for myocardial viability.
- the functional status of the patients were carefully documented by a heart failure cardiologist and nurse.
- BACE Basal Annuloplasty of the Cardia Externally
- Surgical Technique The circumference of the base of the heart at the level of the atrio-ventricular groove was measured before the patient was connected to cardio-pulmonary bypass (CPB). Based on these measurements, a strip of polyester mesh measuring 2.5 to 3 cm in width was cut to size and fashioned, such that its length would be less than the basal circumference by about 2.5 to 4.5 cms. Once the patient was connected to cardiopulmonary bypass, the coronary artery bypass grafts were performed. Left ventricular reconstruction was performed when indicated. The constructed BACE mesh was anchored posteriorly at the level of the atrio- ventricular groove, on atrial and ventricular sides with combination of 4/0 TicronTM sutures and hernia staples, which were placed about 1.5 to 2 cm apart. The mesh was secured laterally as well.
- the correction can be tailored under trans-esophageal echocardiographic guidance. This avoids intra- cavitary manipulation. In selected cases, this procedure could be performed with heart beating also and without using the heart-lung machine, making it an "off-pump" procedure.
- LVEF left ventricular ejection fraction
- the BACE procedure was performed on cardio-pulmonary bypass with the heart decompressed. The procedure took approximately 15 minutes of extra bypass time and about 5 minutes of extra cross-clamp time.
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003526265A JP4083683B2 (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external heart fixation |
DK02780272T DK1423066T3 (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external cardiac stabilization |
CA2459196A CA2459196C (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external stabilization of the heart |
AU2002343336A AU2002343336C1 (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external heart stabilization |
EP02780272A EP1423066B1 (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external heart stabilization |
DE60227676T DE60227676D1 (en) | 2001-09-07 | 2002-09-06 | METHOD AND DEVICE FOR EXTERNAL HEART STABILIZATION |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31817201P | 2001-09-07 | 2001-09-07 | |
US60/318,172 | 2001-09-07 |
Publications (3)
Publication Number | Publication Date |
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WO2003022131A2 true WO2003022131A2 (en) | 2003-03-20 |
WO2003022131A3 WO2003022131A3 (en) | 2003-08-14 |
WO2003022131A8 WO2003022131A8 (en) | 2004-12-29 |
Family
ID=23236976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2002/028372 WO2003022131A2 (en) | 2001-09-07 | 2002-09-06 | Method and apparatus for external heart stabilization |
Country Status (12)
Country | Link |
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US (9) | US6716158B2 (en) |
EP (1) | EP1423066B1 (en) |
JP (2) | JP4083683B2 (en) |
AT (1) | ATE401042T1 (en) |
AU (1) | AU2002343336C1 (en) |
CA (1) | CA2459196C (en) |
CY (1) | CY1109528T1 (en) |
DE (1) | DE60227676D1 (en) |
DK (1) | DK1423066T3 (en) |
ES (1) | ES2310609T3 (en) |
PT (1) | PT1423066E (en) |
WO (1) | WO2003022131A2 (en) |
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