CA2437475A1 - Doppler directed suture ligation device and method - Google Patents
Doppler directed suture ligation device and method Download PDFInfo
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- CA2437475A1 CA2437475A1 CA002437475A CA2437475A CA2437475A1 CA 2437475 A1 CA2437475 A1 CA 2437475A1 CA 002437475 A CA002437475 A CA 002437475A CA 2437475 A CA2437475 A CA 2437475A CA 2437475 A1 CA2437475 A1 CA 2437475A1
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- cannula
- extendable member
- distal end
- extendable
- ligation
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/32—Surgical cutting instruments
- A61B17/3205—Excision instruments
- A61B17/32056—Surgical snare instruments
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0469—Suturing instruments for use in minimally invasive surgery, e.g. endoscopic surgery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
- A61B17/12009—Implements for ligaturing other than by clamps or clips, e.g. using a loop with a slip knot
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0482—Needle or suture guides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1477—Needle-like probes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1482—Probes or electrodes therefor having a long rigid shaft for accessing the inner body transcutaneously in minimal invasive surgery, e.g. laparoscopy
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00349—Needle-like instruments having hook or barb-like gripping means, e.g. for grasping suture or tissue
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0469—Suturing instruments for use in minimally invasive surgery, e.g. endoscopic surgery
- A61B2017/0472—Multiple-needled, e.g. double-needled, instruments
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- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06066—Needles, e.g. needle tip configurations
- A61B2017/06104—Needles, e.g. needle tip configurations interconnected at their distal ends, e.g. two hollow needles forming a loop for passing a suture
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- A61B2018/0063—Sealing
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- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/1206—Generators therefor
- A61B2018/1246—Generators therefor characterised by the output polarity
- A61B2018/126—Generators therefor characterised by the output polarity bipolar
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- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
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- A61B2018/1405—Electrodes having a specific shape
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- A61B90/36—Image-producing devices or illumination devices not otherwise provided for
- A61B90/37—Surgical systems with images on a monitor during operation
- A61B2090/378—Surgical systems with images on a monitor during operation using ultrasound
Abstract
A ligation device (100) includes a cannula (104) having first and second extendable members (120, 122) and a Doppler wand (140). The Doppler wand (14 0) permits an anatomical vessel, such as a blood vessel, to be located in close proximity to the distal end of the cannula (104). The extendable members (12 0, 122) are extendable on two opposite sides of the vessel. A length of ligatio n material, such as suture material, extends through the first extendable memb er and is attached to a detachable element (124) mounted to the distal most end of the extendable member. The second extendable member (122) includes a snar e (126). The first extendable member (120) includes curved portions which, whe n the member (120) is extended distally, extend the detachable element (124) into position for the snare (126) so that the snare (126) can grab the loop. Once ensnared, the detachable element (124) is released from the first extendable member (120), which pulls the ligation material around the vessel . The ligation device (100) does not require prior visualization or dissection of the area around the vessel.
Description
-1_ DOPPLER DIRECTED SUTURE LIGATION DEVICE AND METHOD
BACKGROUND OF THE INVENTION
Field of the Invention The present invention relates to ligation devices and methods, and more particularly to devices and methods for accurately locating and ligating an anatomical vessel.
Brief Description of the Related Art The Doppler effect is currently utilized in many fields. For example, Doppler stethoscopes and Doppler wands are currently utilized to generate images of internal anatomical structures in patients, especially in mammalian patients.
Continuous wave doppler sound signals are used to identify blood 'vessels, but do not provide feedback as to the distance of the vessel from the Doppler probe used. Pulsed wave Doppler has been used to identify blood vessels and, in conjunction with two dimensional (2D) imaging systems, identify the distance to a blood vessel and blood flow characteristics. Ultrasound systems with Doppler imaging are also currently used in medical fields, and typically produce gray-scale two-dimensional images. The addition of Doppler processing allows for the evaluation of fluid flow velocities through fluid conduits within the patient, and the relative position of these vessels to other anatomical structures.
Ligation devices have previously been proposed. These prior ligation devices have typically been used in laparascopic procedures, and have typically required that the anatomical feature of interest be dissected or visualized prior to ligation of that feature.
BACKGROUND OF THE INVENTION
Field of the Invention The present invention relates to ligation devices and methods, and more particularly to devices and methods for accurately locating and ligating an anatomical vessel.
Brief Description of the Related Art The Doppler effect is currently utilized in many fields. For example, Doppler stethoscopes and Doppler wands are currently utilized to generate images of internal anatomical structures in patients, especially in mammalian patients.
Continuous wave doppler sound signals are used to identify blood 'vessels, but do not provide feedback as to the distance of the vessel from the Doppler probe used. Pulsed wave Doppler has been used to identify blood vessels and, in conjunction with two dimensional (2D) imaging systems, identify the distance to a blood vessel and blood flow characteristics. Ultrasound systems with Doppler imaging are also currently used in medical fields, and typically produce gray-scale two-dimensional images. The addition of Doppler processing allows for the evaluation of fluid flow velocities through fluid conduits within the patient, and the relative position of these vessels to other anatomical structures.
Ligation devices have previously been proposed. These prior ligation devices have typically been used in laparascopic procedures, and have typically required that the anatomical feature of interest be dissected or visualized prior to ligation of that feature.
SUMMARY OF THE INVENTION
According to a first exemplary embodiment, a ligation device comprises a cannula having a proximal end, a distal end, and at least one lumen extending longitudinally from said proximal end to said distal end, a first extendable member slidably received in said cannula lumen, said first extendable member having a distal end and being movable in said lumen from a retracted position in which said first extendable member distal end is proximal said bannula distal end, and an extended position in which said first extendable member distal end is distal of said cannula distal end, said first extendable member including a detachable element at said first extendable member distal end, a second extendable member slidably received in said cannula lumen, said second extendable member having a distal end and being movable in said lumen from a retracted position in which said second extendable member distal end is proximal said cannula distal end, and an extended position in which said second extendable member distal end is distal of said cannula distal end, said second extendable-member including a snare at said second extendable member distal end, and at least one of said first extendable member and said second extendable member including curved portions which extend laterally across said cannula when said at least one of said first extendable member and said second extendable member is in said extended position.
According to a second exemplary embodiment, a method bf preparing an anatomical vessel for ligation comprises the steps of positioning a cannula adj scent to said vessel, said cannula including a first extendable member, a second extendable member, and a Doppler wand, and a distal end, transmitting ultrasound signals toward said vessel with said Doppler wand, receiving ultrasound signals reflected by said vessel with said Doppler wand, extending said first extendable member on a first side of said vessel, extending said second extendable member on a second side of said vessel opposite said first sizle, and extending a length of ligation material between said first and second extendable members on a side of said vessel opposite said cannula distal end.
According to a third exemplary embodiment, a device useful for guiding a length of ligation material around an anatomical feature comprises a cannula including a hollow interior, a distal end, and a fenestration in the cannula proximal of the distal end, a hollow arias positioned in the cannula at the fenestration, the hollow arm including a rotatable pivot by which the arm is mounted to the cannula, the arm being rotatable from a retracted orientation with the arm positioned inside the cannula and a deployed orientation with a portion of the arm rotated about the pivot and through the fenestration, at least one wire connected to the arm and extending proximally, and wherein when the at least one wire is.pulled proximally, the arm is rotated about the pivot into the deployed orientation.
' Still other objects, features, and attendant advantages of the present invention will become apparent to those skilled in the art from a reading of the following detailed description of embodiments constructed in accordance therewith, taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention of the present application will now be described in more detail with reference to preferred embodiments of the apparatus and method, given only by way of example, and with reference to the accompanying drawings, in which:
Fig. 1 illustrates a top, distal, side perspective view of an exemplary embodiment of a doppler directed ligation device in accordance with the present invention;
Fig. 2 illustrates the ligation device of Fig. 1, with.portions removed;
Fig. 3 illustrates a cross sectional view taken along line 3-3 in Fig. 1;
According to a first exemplary embodiment, a ligation device comprises a cannula having a proximal end, a distal end, and at least one lumen extending longitudinally from said proximal end to said distal end, a first extendable member slidably received in said cannula lumen, said first extendable member having a distal end and being movable in said lumen from a retracted position in which said first extendable member distal end is proximal said bannula distal end, and an extended position in which said first extendable member distal end is distal of said cannula distal end, said first extendable member including a detachable element at said first extendable member distal end, a second extendable member slidably received in said cannula lumen, said second extendable member having a distal end and being movable in said lumen from a retracted position in which said second extendable member distal end is proximal said cannula distal end, and an extended position in which said second extendable member distal end is distal of said cannula distal end, said second extendable-member including a snare at said second extendable member distal end, and at least one of said first extendable member and said second extendable member including curved portions which extend laterally across said cannula when said at least one of said first extendable member and said second extendable member is in said extended position.
According to a second exemplary embodiment, a method bf preparing an anatomical vessel for ligation comprises the steps of positioning a cannula adj scent to said vessel, said cannula including a first extendable member, a second extendable member, and a Doppler wand, and a distal end, transmitting ultrasound signals toward said vessel with said Doppler wand, receiving ultrasound signals reflected by said vessel with said Doppler wand, extending said first extendable member on a first side of said vessel, extending said second extendable member on a second side of said vessel opposite said first sizle, and extending a length of ligation material between said first and second extendable members on a side of said vessel opposite said cannula distal end.
According to a third exemplary embodiment, a device useful for guiding a length of ligation material around an anatomical feature comprises a cannula including a hollow interior, a distal end, and a fenestration in the cannula proximal of the distal end, a hollow arias positioned in the cannula at the fenestration, the hollow arm including a rotatable pivot by which the arm is mounted to the cannula, the arm being rotatable from a retracted orientation with the arm positioned inside the cannula and a deployed orientation with a portion of the arm rotated about the pivot and through the fenestration, at least one wire connected to the arm and extending proximally, and wherein when the at least one wire is.pulled proximally, the arm is rotated about the pivot into the deployed orientation.
' Still other objects, features, and attendant advantages of the present invention will become apparent to those skilled in the art from a reading of the following detailed description of embodiments constructed in accordance therewith, taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention of the present application will now be described in more detail with reference to preferred embodiments of the apparatus and method, given only by way of example, and with reference to the accompanying drawings, in which:
Fig. 1 illustrates a top, distal, side perspective view of an exemplary embodiment of a doppler directed ligation device in accordance with the present invention;
Fig. 2 illustrates the ligation device of Fig. 1, with.portions removed;
Fig. 3 illustrates a cross sectional view taken along line 3-3 in Fig. 1;
Figs. 4-6 illustrate a snare in accordance with the present invention;
Fig. 7 illustrates an enlarged perspective view of the distal end of the embodiment illustrated in Fig. 1;
Figs. 8-10 illustrate a loop in accordance with the present invention;
Figs. 11-13 illustrate portions of the device illustrated in Fig. 1;
Fig. 14 illustrates a portion of the device illustrated in Fig. l;
Fig. 15 illustrates an enlarged view of the portions illustrated in Fig. 14;
Fig. 16 illustrates a cross sectional view taken along line 16-16 in Fig. 1;
Figs. 17-19 illustrate enlarged plan views of further embodiments in accordance with the present invention;
Figs. 20-24 illustrate the device of Fig. 1 used in accordance with an exemplary embodiment of a method of ligating an anatomical feature in a patient;
Fig. 25 illustrates portions of yet another embodiment of the present invention;
Figs. 26A and 26B illustrate portions of further embodiments of the present invention; and Figs. 27-30 illustrate several views of yet another embodiment in accordance with the present invention.
DESCRIPTION OF PREFERRED EMBODIMENTS
Referring to the drawing figures, like reference numerals designate identical or corresponding elements throughout the several figures.
Figure 1 illustrates a top, distal end, side perspective view of an exemplary embodiment of a doppler directed ligation device 100 in accordance with the present invention. Figure 1 illustrates device 100 deployed to enable a practitioner to ligate a fluid vessel 10. While vessel 10 is preferably a uterine artery, other vessels, such as other arteries, veins, fallopian tubes, urinary ducts such as the ureter, and other fluid vessels can be ligated with device 100 within the spirit and scope of the present invention, as will be readily appreciated by one of ordinary skill in the art.
Different from ligation devices which have previously been proposed, as well as their uses, ligation devices and methods in accordance with the present invention do not require dissection of the vessel 10, and does not require actual visualization of the vessel, prior to ligation. The capability enabled by the present invention of advancing a ligation device through tissue beds and/or tissue planes without the need for dissection can provide benefits as described elsewhere herein and as will be readily appreciated by one of ordinary skill in the art.
Ligation device 100 includes a proximal handle 102 and a cannula 104 extending distally from the handle. Handle 102 includes a hollow housing 103 sized and shaped to fit comfortably in the hand of a practitioner. A proximal thumb ring 106 is fixed to the housing 103 opposite cannula 104. A pair of top slots 108, 110 are formed in the top surface 107 of the housing 103, and a pair of side slots 109, 111, are formed in the sidewalls 113, 115. A first actuation ring 112 and a second actuation ring 114 are slidably mounted in housing 103, through the opposite side slots 109, 111 (see also Fig. 2) of the housing. Upstanding tabs 116, 118, extend from the interior of housing 103, through slots 108, 110, respectively, to outside the housing.
The slots 109, 111 limit the range of motion of the rings 112, 114, and the slots 108, 110 function to limit the range of motion of the tabs 116, 118 along longitudinal direction X.
Cannula 104 is fixedly mounted to the distal end of handle 102. Cannula 104 includes a plurality of lumenae extending longitudinally through the cannula, which are best illustrated in Figure 3. Ligation device 100 includes a first extendable element 120 which is longitudinally slidable through cannula 104 between a retracted position (see,.e.g., Fig. 20) in which the first extendable element is housed entirely inside the cannula, and an extended position (see, e.g., Fig. 21) in which the first extendable element extends distally beyond the distal end 150 of the cannula.
Fig. 7 illustrates an enlarged perspective view of the distal end of the embodiment illustrated in Fig. 1;
Figs. 8-10 illustrate a loop in accordance with the present invention;
Figs. 11-13 illustrate portions of the device illustrated in Fig. 1;
Fig. 14 illustrates a portion of the device illustrated in Fig. l;
Fig. 15 illustrates an enlarged view of the portions illustrated in Fig. 14;
Fig. 16 illustrates a cross sectional view taken along line 16-16 in Fig. 1;
Figs. 17-19 illustrate enlarged plan views of further embodiments in accordance with the present invention;
Figs. 20-24 illustrate the device of Fig. 1 used in accordance with an exemplary embodiment of a method of ligating an anatomical feature in a patient;
Fig. 25 illustrates portions of yet another embodiment of the present invention;
Figs. 26A and 26B illustrate portions of further embodiments of the present invention; and Figs. 27-30 illustrate several views of yet another embodiment in accordance with the present invention.
DESCRIPTION OF PREFERRED EMBODIMENTS
Referring to the drawing figures, like reference numerals designate identical or corresponding elements throughout the several figures.
Figure 1 illustrates a top, distal end, side perspective view of an exemplary embodiment of a doppler directed ligation device 100 in accordance with the present invention. Figure 1 illustrates device 100 deployed to enable a practitioner to ligate a fluid vessel 10. While vessel 10 is preferably a uterine artery, other vessels, such as other arteries, veins, fallopian tubes, urinary ducts such as the ureter, and other fluid vessels can be ligated with device 100 within the spirit and scope of the present invention, as will be readily appreciated by one of ordinary skill in the art.
Different from ligation devices which have previously been proposed, as well as their uses, ligation devices and methods in accordance with the present invention do not require dissection of the vessel 10, and does not require actual visualization of the vessel, prior to ligation. The capability enabled by the present invention of advancing a ligation device through tissue beds and/or tissue planes without the need for dissection can provide benefits as described elsewhere herein and as will be readily appreciated by one of ordinary skill in the art.
Ligation device 100 includes a proximal handle 102 and a cannula 104 extending distally from the handle. Handle 102 includes a hollow housing 103 sized and shaped to fit comfortably in the hand of a practitioner. A proximal thumb ring 106 is fixed to the housing 103 opposite cannula 104. A pair of top slots 108, 110 are formed in the top surface 107 of the housing 103, and a pair of side slots 109, 111, are formed in the sidewalls 113, 115. A first actuation ring 112 and a second actuation ring 114 are slidably mounted in housing 103, through the opposite side slots 109, 111 (see also Fig. 2) of the housing. Upstanding tabs 116, 118, extend from the interior of housing 103, through slots 108, 110, respectively, to outside the housing.
The slots 109, 111 limit the range of motion of the rings 112, 114, and the slots 108, 110 function to limit the range of motion of the tabs 116, 118 along longitudinal direction X.
Cannula 104 is fixedly mounted to the distal end of handle 102. Cannula 104 includes a plurality of lumenae extending longitudinally through the cannula, which are best illustrated in Figure 3. Ligation device 100 includes a first extendable element 120 which is longitudinally slidable through cannula 104 between a retracted position (see,.e.g., Fig. 20) in which the first extendable element is housed entirely inside the cannula, and an extended position (see, e.g., Fig. 21) in which the first extendable element extends distally beyond the distal end 150 of the cannula.
Ligation device also includes a second extendable element 122 which, similar to first extendable element 120, is longitudinally slidable through cannula 104 between retracted and extended positions. First and second extendable elements 120, 122 are connected to first and second actuation rings 112, 114, respectively, at the proximal ends of the extendable elements, so that the rings can be used to longitudinally advance and retract the extendable elements in carmula 104.
The first and second extendable elements 120, 122 are positioned laterally opposite each other.in cannula 104, as best illustrated in Fig. 3, so that When they are in their extended positions they can be positioned on opposite sides of an anatomical vessel, such as vessel 10. Furthermore, first and second extendable elements 120, 122 are sized so that they both are extendable farther than a distance Xref from the distal end 150, described in greater detail below, so that a vessel 10 can be bracketed by the.
extendable elements when the vessel is within Xref from the distal end of cannula 104.
First extendable element 120 carries a detachable element at its distal end.
In the embodiment illustrated in Figure 1, the detachable element is a loop 124.
Loop 124 is attached, either directly or indirectly as will be described in greater detail below, to a length of threadlike material, such as suture material, which may optionally further include a leader, which extends proximally through cannula 104.
Second extendable element 122 carries a snare element which is sized and configured to grab, ensnare,'or otherwise become secured with the detachable element of the first extendable element 120 when the first and second extendable elements are in their extended positions (see Figs. 1 and 23). In the embodiment illustrated in Figure 3, the snare element is a hook 126. Loop 1,24 and snare 126 will be described in greater detail below with reference to Figs. 4-13.
Ligation device 100 further includes a doppler ultrasound device ~or wand 140 mounted in the ligation device. In accordance with the present invention, the Doppler ultrasound device can be removably mounted in 'the ligation device, or the components of a doppler ultrasound device can be integrated into the ligation device, e.g. into cannula 104, so as not to be removable. Thus, when the Doppler ultrasound device is removably mounted in ligation device 100, the Doppler ultrasound device can be removed at the termination of a use, removed from the remainder of the ligation device, and the Doppler ultrasound device sterilized and reused.
Alternatively, when the Doppler ultrasound device's components are integrated into the ligation .device 100, the entire ligation device can be disposed of at the conclusion of a use.
Cannula 104 includes a third center lumen 138 (see Figs., 3 and 7) into which a removable doppler wand 140 is removably inserted. According to certain embodiments of the present invention, a distal end 152 of the doppler wand is proximal of the distal end 150 of the cannula. According to other embodiments of the present invention, the distal end 152 of the doppler wand 140 is positioned at the distal end 150 of the cannula. ~ According to other embodiments of the present invention, the distal end 152 of the doppler wand 140 is positioned distal of the distal end 150 of the cannula. Preferably, housing 103 includes portions which receive the proximal portions of doppler wand 140, so that the doppler wand can be removed and reused after ligation device 100 has been used. For example and not by way of limitation, housing 103 can include portions which are hinged together and secured with a snap, lock, or the like, so that the housing can be opened up, a doppler wand 140 inserted into ligation device 100, and the housing portions closed and locked to secure the doppler wand in the ligation device.
Doppler ultrasound wands suitable for use in the present invention are presently commercially available. For example, Koven model ES ~ 100X MiniDop VRP-8 probe (St. Louis, MO) is a continuous wave doppler wand suitable for use as doppler wand 140, and DWL/Neuro Scan Medical Systems' Multi-Dop B~- system _$_ with their 8 MHz handheld probe (Sterling, VA) is a continuous and pulsed wave doppler wand suitable for use as wand 140. Commercially available doppler stethoscopes or wands have an ultrasound dispersion pattern which is generally conical, i.e., the wand "looks" out along a cone-shaped portion of a plane originating at the end of the wand. Thus, vessels with fluid flow in them, such as a blood vessel, which lie anywhere in this conical plane and within the effective range of the wand would be picked up by the wand. Doppler wands presently available are attached to a signal processing and display unit 156, which processes the electrical signals generated by wand 140 to generate displays and/or other data derived from the electrical signals for additional uses. Alternatively, the Doppler system can be gated to identify blood vessels within a predetermined distance range, e.g. from between 0 to 5 cm, more preferably between 0.5 and 3 cm.
Unit 156 includes a display 158 which indicates the distance from the distal tip 152 the source of reflected ultrasound waves is located, e.g., vessel 10. This information is typically calculated utilizing a predetermined function, because the distance is a function of the time it takes for the ultrasound waves to travel to and from the wand. Unit 156 preferably also includes a display or meter 160 of the magnitude of the reflected ultrasound waves's doppler shift, which is the indication of , the velocity of the fluid flowing through vessel 10. Unit 156 also preferably includes a sound source 162 which gives an audible indication of the doppler shift, which can be louder when the Doppler shift is greater or the vessel is optimally positioned.
Tn the ligation device of the present invention, however, such a wide conical "field of view" typically returned by many commercially available doppler wands is not preferable, because the practitioner is concerned with locating the vessel between the extendable elements in order to ligate the vessel. Were the present invention to .
utilize such "wide-view" Doppler wands without narrowing or otherwise affecting their field of view, vessels which are not directly distal of ligation device 100 would be piclced up by the device, and would return doppler shift data for vessels not of interest in the use of the ligation device. Ligation device 100, and specifically cannula 104, is therefore sized so that the distalmost end 152 of doppler wand 140 is spaced proximally from the distal end 150 of the caxmula, for use with "wide-view"
wands to collimate the signal. Some commercially available doppler wands, such as the aforementioned DWL probe, however, produce a sufficiently collimated signal so that further collimation is not necessary.
When utilizing a Doppler probe which does not produce, a sufficiently collimated signal, lumen 138 is preferably coated, formed of a material, or is otherwise provided with a sleeve of a material on the interior surface of which collimates the sound waves emanating from doppler wand 140. By way of example and not of limitation, lumen 138 can be coated or formed of polycarbonate, although other materials are also usable within the spirit and scope of the present invention.
The result of spacing distal end 152 proximally of distal end 150, and optionally further providing a material and/or sleeve which acoustically collimates the ultrasound waves from wand 140, is that ligation device 100 is substantially unidirectional in its doppler field of view in a direction parallel with, and preferably between,. first and second extendable elements 120, 122, and longitude ally distal of distal end 150. Stated differently, legation device 100 is capable of receiving reflected ultrasound waves, originating from doppler wand 140, reflected back from anatomical features directly distal of distal end 150. Thus, because distal end 152 is a fixed and known distance from distal end 150, and X~ef is known, a maximum distance Xm~
is predetermined by the structures of legation device 100 within which a vessel 10 must be in order for the legation device to be capable of legating it. Stated somewhat differently, once it is determined that a vessel is within a predetermined distance of distal end 152, which is indicated by the time lag of the reflected ultrasound waves, legation device 100 can be used to legate that vessel.
According to another embodiment in accordance with the present invention, a doppler wand can be chosen which has a "field of view" which is narrow enough that, when used in the combination of the ligating device 100, additional collimation structures are not necessary. For example, selection of a probe is based on its field of view and its operating frequency, and should also be based on the distance between the target artery and the Doppler probe so that the probe's depth of view is larger than this distance yet not so long as to include other blood vessels. By way of example and not of limitation, a DWL Doppler probe as described above can be used as wand without requiring either a collimating sleeve and without spacing the distal end proximal of distal end 150. In general, Doppler wands suitable for use as Doppler wand 140 are selected with small enough diameter to be insertable in cannula 104, preferably.operate at a frequency which is sufficiently sensitive to blood flow to monitor uterine artery blood flow, have a relatively narrow field of view and limited depth of view so as not to generate a signal from other blood vessels, and can be based on either pulsed or continuous wave Doppler signals.
Figure 3 illustrates a cross-section view of ligation device 100, as seen along line 3-3 in Figure 1, and Figure 7 illustrates an enlarged distal end perspective view of ligation device 100. Cannula 104 preferably has an oval cross sectional profile, so that the cannula can be relatively compact while still meeting the requirement that doppler wand 140 be laterally between extendable elements 120, 122. As illustrated in Figure 3, cannula 104 includes a first lumen 130 which longitudinally and slidingly receives first extendable element 120. Preferably, element 120 itself includes a lumen 142 through which a tubular suture and loop advancing element 134 is longitudinally slidable. Element 120 further optionally is provided with a slot or cutout 170 at its distal end in the wall of the element 120 adjacent to or facing element 122, to assist in guiding or positioning loop advancing element 134 in a desired direction and to assist in preventing rotation of the loop advancing element relative to the element 120.
Suture advancing element 134 at least in part is formed of a superelastic material, less preferably a shape-memory alloy (SMA) material, also less preferably (surgical) stainless steel. NiTi (nitinol) is preferred, although other superelastic, SMA, and biocornpatible materials are within the scope of the present invention.
Forming at least portions of suture advancing element 134 of NiTi allows the suture advancing element to be preformed with a curved distal end, so that the suture advancing element can be easily retracted into first extendable element 120, yet the distal end will accurately position loop 124 to be snared by extendable element 122 when the suture advancing element is advanced out of the first extendable element.
Suture/loop advancing element 134 preferably is a hollow tube and includes structure at the distal end of the element which holds loop 124, the loop in turn being attached to a length of suture material 154 (see also Fig. 24).' A more detailed description of the structures at the distal ends of extendable elements 120,122 is presented below with reference to Figs. 4-13.
Cannula 104 includes a second lumen 132 in which second extendable element 122 is longitudinally slidably received. Second extendable element 122 preferably includes a lumen 144 which longitudinally slidably receives an extendible , hooking or snaring element 136. Cannula 104 also includes a third lumen 138 which removably receives doppler wand 140, so that the doppler wand can be used with the other structures of ligation device 100 and then disassembled, as discussed above.
Optionally, the ligation device 100, including the third lumen 138, can non-removably house the functional components of a Doppler wand, so that the entire ligation device can be conveniently disposed of.
As illustrated in Figure 7, the first and second extendable elements 120, 122 can optionally further be provided with closed, preferably comically or frustoconically shaped tips 121, 123, respectively. The closed tips 121, 123 permit the extendable elements 120, 122 to be more easily advanced through tissue beds and planes.
When provided with the closed tips 121, 123, the extendable elements 120, 122 further include laterally inwardly facing openings 125, 127 so that the elements 134, 136 can pass out of the elements 120, 122, as described elsewhere herein. Further optionally, the distal interiors of one or both of the closed tips can be provided with cam surfaces (not illustrated) to assist in guiding the detachable elements and/or the snaring elements.
Figures 4- .6 illustrate several views of snaring element 136 including hook or snare 126. As detailed in Figure 5, snare 126 includes an enlarged head 160 having an angled slot 1.62. A hook portion 164 is formed distally of slot 162. Slot 162 has a width W~ and extends into head 160 at an angle cc. A shank 166 is attached at the proximal end of head 160, and is, preferably formed integrally therewith from a single piece of material. Alternatively, shank 166 and head 160 can be press-fit, welded, adhesively bonded, or otherwise formed separately and thereafter joined together as will be readily apparent to one of ordinary skill in the art. Width W, is selected to be greater than the width WZ of loop 124 (see Fig. 9), so that the loop can be deflected into slot 162 by hook portion 164 and slide into the slot and be grabbed by snare 126.
Optionally, the proximal portions of head 160 adjacent to the opening to slot 162 can be widened, as indicated in phantom lines in Fig. 5, which can facilitate loop being deflected by hook portion 164 into slot 162.
Figures 8-13 illustrate distal end portions of suture/loop advancing element 134. As illustrated in Figs. 8-10, loop 124 is preferably roughly oval in shape, and is temporarily mounted to the distal end of a tubular curved element 172 (see also Fig.
13). A length of suture material 154 or the like is tied, glued, crimped, or otherwise secured to loop 124, and extends proximally through tube 172. As illustrated in Figs 11-13, suture/loop advancing element 134 includes a straight portion 174 and a curved portion 172, both of which are hollow tubes. Straight portion 174 and curved portion 172 are joined together at a joint 180. Optionally, element 134 can be a monolithic element without such a joint 180, and a straight portion 174 and a curved portion 172 can be formed therein, as will be readily appreciated by one of ordinary skill in the art.
At least curved portion 172 of element 134 is preferably formed of a superelastic material. Alternatively, portion 172 can be formed of a SMA
material.
While the characteristics and use of superelastic materials are readily appreciated by , one of ordinary skill in the art, a brief description as applied to curved portion 172 will aid in an understanding of the present invention. Portion 172 is preferably formed of an superelastic material, e.g., NiTi (nitinol). Portion 172 is given a curvature or bent configuration which, upon heating of the curved portion above a certain temperature for the superelastic material, is 'remembered' by the curved portion. In the embodiment illustrated in Figs. 11-13 curved portion 172 is formed into an arc having a radius R and the distal end 176 being at an angle (3 from a line perpendicular to straight portion 174. Distal end 176, when curved portion 172 is in its curved configuration, is a lateral distance Y from the straight portion 174.
The length of curved portion 172 and the shape, as well as the distance Y, are selected so that when curved portion 172 is in its curved configuration, loop 124 is positioned directed distally of second extendable element 122. In this location, snare 126 can be extended and can hook loop 124, to be pulled from suture/loop advancing element 134. The angular orientation of the lateral direction in which curved portion 172 extends when in its curved configuration can be preset so that loop 124 registers or lines up with snare 126, and slot 170 assists in maintaining this orientation. This present angular orientation can be determined, by way of example and not of limitation, by heating curved portion 172 above its transition temperature and rotating element 134 until loop 124 is directly distal of snare 126, prior to using device 100.
Curved portion 172 and straight portion 174 can both be formed of the same (superelastic) material. Alternatively, only portion 172 is formed of an superelastic material, and straight portion 174 can be formed of another material, e.g., stainless steel, and the two portions 172, 174 can be joined together at joint 180, as by welding, , crimping, swaging, adhesive bonding, or the like. The distalmost end of portion 172 includes a slot 178 in which loop 124 is temporarily held. Slot 178 has a width W3 and a depth D selected so~ that loop 124 can be received therein by a press fit, or loosely received and crimped therein. Loop 124 is not permanently held in slot 178, however, and is mounted in the slot so that the loop can be pulled out of the slot by a preselected force transmitted by snare 126 after the loop has been hooked by the snare (see, e.g., Fig. 3).
Figure 14 illustrates internal portions of ligation device 100. First and second extendable elements 120, 122 are mounted in a block 190 to which rings 112, 114 are also fixedly secured. Thus, as described above, proximal and distal longitudinal movement of rings 112, 114 moves first and second extendable elements 120, 122.
Block 190 includes a pair of slots 192, 194 formed in a top surface thereof in which tabs or pins 116, 118 are slidably received, respectively. Thus, the slots 192, 194 constrain the tabs 116, 118 laterally, while permitting them to move longitudinally over a range limited by the length of the slots.
Figure 15 illustrates a top plan view of distal portions of the view illustrated in Figure 14. As can be seen in Figure 15, the block 190 includes slots 192,,194, described above. According to one embodiment of the present invention, block includes first and second lateral portions 196, 198, which are cylindrical in shape, in which the first and second extendable elements 120, 122 are mounted, respectively.
According to one embodiment of the present invention, lateral portions 196, 198 can be fixedly joined together as a with a web 200, so that movement of one of the rings 112, 114 moves both lateral portions. According to yet another embodiment of the present invention, lateral portions 196 and 198 are not joined together, and are therefore separately and individually longitudinally moveable in housing 103.
Also visible in Figure 15 are mounting blocks 202 and 204 positioned iri block 190. Mounting block 202 fixedly receives the proximal portion of extendable element 134 and lower portions of tab 116, and mounting block 204 fixedly receives the proximal portion of extendable element 136 and tab 118. Block 202 thus joins together extendable element 134 with tab 116, and block 204 thus joins together extendable element 136 with tab 118. Additionally, blocks 202 and 204 constrain tabs 116 and 118 from being pulled up and out from block 190, as their lateral extents are larger than slots 192, 194, respectively.
Figure 16 illustrates a cross-sectional view of proximal portions of ligation device 100. As can be seen in Figure 16, the housing 103 includes an interior chamber or cavity 210 which slidingly receives block 190 and its components.
Block 190 includes an interior chamber or cavity 208 which slidingly receives blocks and 204 (block 204 is not visible in the view of Figure 16), and a proximal opening 206 which communicates interior chamber 208 with interior chamber 210.
Proximal opening 206 also permits blocks 202, 204 to extend into interior chamber 210.
Figure 16 also illustrates suture 154 extending through loop advancing element 134, block 202, interior chamber 208, interior chamber 210, and exiting housing 103 through one of slots 108-111.
Figures 17-19 illustrate further embodiments in accordance with the present invention. In the embodiment illustrated in Figure 17, both a loop advancing element 220 and a snare advancing element 222 are formed of a superelastic, SMA, or stainless steel material, and curve to meet each other. In the embodiment illustrated in Figure 18, snare advancing element 136 is formed of .a superelastic, SMA, or stainless steel material, and loop advancing element 134 is advanced directly longitudinally distally to be snared by the snare 126. In the embodiment illustrated in Figure 19, a first curved tube 230 of a superelastic, SMA, or stainless steel material, and a second curved tube 232 of a superelastic, SMA, or stainless steel material, meet in a manner similar to the embodiment illustrated in Figure 17. The distal ends of tubes 230, 232 mate in a somewhat different fashion, one of the tubes 230, 232 bearing a snare which is a receptacle 234 having a bore 238 having an internal diameter larger than the external, diameter of the other of tubes 230, 232. Thus, when the tubes 230, 232 meet, the distal ends engage. A pushrod or wire 236, to which suture 154 is attached, is positioned in one of the lumens of tubes,230, 232, and is pushed distally down that tube, through receptacle 234, and proximally up the other of tubes 230, 232.
Thus, a suture can be advanced around a blood vessel of interest in a manner similar to the embodiments described above.
Figures 20-24 illustrate several steps of an exemplary method in accordance with the present invention. While Figures 20-24 illustrate, and the following description makes reference to, ligation device 100, methods in accordance with the present invention are not limited to use of ligation device 100, and other apparatus can be utilized in practicing the present methods without departing from the spirit and scope of the present invention.
Figure 20 illustrates the distal end of ligation device 100 after having been positioned proximate a vessel of interest in a patient, e.g., a uterine artery 10. Distal end 150 of cannula 104 is initially positioned away from vessel 10. Distal end 150 is accurately positioned within Xm~ of the vessel by pointing cannula 104 in several directions around where the practitioner believes the vessel is located, monitoring the output of unit 156 for distance and velocity data to determine the relative location of the vessel relative to distal end 150, and repositioning the distal end until the distal end is a distance X from vessel 10 less than Xm~. As described above, reflected ultrasound waves 182, which are preferably collimated, are received by doppler wand 140 (or the functional components thereof, integrated into ligation device 100) and are processed by unit 156 to indicate the relative location of vessel 10. For example, Doppler sound is utilized to fmd the vessel location, and thereafter pulsed wave Doppler is utilized to identify a more precise location and the distance to the artery 10.
Once the practitioner has established that vessel 10 is directly distal of the distal end 150 of cannula 104, first and second actuation rings 112, 114 axe moved distally to move first and second extendable members 120, 122 distally, as illustrated in Fig. 21. Then, as illustrated in Figs. 22 and 23, suture/loop advancing element 134 and snaring element 136 are both distally advanced by pushing tabs 116, 118 distally;
the advancement of elements 134 and 136 can be serial, simultaneous, or combinations thereof. Because suture/loop advancing element 134 is inside a (preferably mammalian) patient while it is advanced, the suture/loop advancing element is heated up iu situ above its SMA transition temperature, and transforms from its straight configuration to its 'remembered' or curved configuration.
Thus, advancement of advancing element 134 out of member 120 is accompanied by element 134 assuming, or having already assumed, its curved configuration.
Element 134 and loop 124 are therefore advanced in a lateral direction and toward element 136 and snare 126.
While the loop 124 is positioned directly distal of snare 126, snaring element 136.is moved distally to advance snare 126 distally. Snare 126, and more particularly head 160, enters loop 124, and is pushed through the loop. Snare 126 is then retracted -25 proximally so that hook portion 164 deflects loop 124 into slot 162; thus causing the .
loop to be grabbed by the snare. In this respect, a widened mouth to slot 162, as suggested by phantom line 168, can facilitate capture of loop 124.
With loop 124 ensnared by snare 126, snaring element 136 is retracted proximally, which pulls on the loop in a proximal direction. As the materials out of which portions 172, 174 are formed are relatively rigid (superelastic, SMA, and stainless steel being preferable), the force applied by snaring element 136 to loop 124 will cause the joint between loop 124 and slot 178 to break or otherwise release the loop from element 134. As will be readily appreciated by one of ordinary skill in the art, the joint between loop 124 and slot 178 is designed as a breakaway element, with the minimum force needed to break the joint selected so that the loop will not . prematurely break free of curved portion 172, yet not so high that a practitioner will not readily be able to generate the required force by pulling proximally on tab 118.
Once loop 124 has been broken free of slot 178, snaring element 136 and second extendable element 122 are further pulled proximally so that the loop is pulled into cannula 104. As described above, suture material 154 extends through curved portion 172 and is secured to loop 124, and is therefore pulled along with the loop.
Thus, suture material 154 is advanced distally past vessel 10 by distal extension of first extendable element 120 and suture/loop advancing element 134, is advanced laterally behind the vessel by curved portion 172 having assumed its curved superelastic configuration, and is advanced proximally by proximal retraction of loop 124 after having been grabbed by snare 126. With the loop of suture material passing around vessel 10, ligation device 100 can be pulled proximally, leaving the loop of suture material around vessel 10, as illustrated in Figure 24. At this point, the practitioner can make whatever form of ligation she chooses, as the loop of suture material has been accurately passed around the vessel 10 of interest.
Figure 25 illustrates yet another embodiment in accordance with the present invention. The embodiment illustrated in Figure 25 is similar to that illustrated in Figure 3, but differs in the cross-sectional profile of the device 250.
Instead of the oval cross-sectional profile illustrated in Figure 3, device 250 includes the coplanar lumenae 130, 132, 138 defined in three adjacent and joined tubes 252, 254, 256.
Figures 26A and 26B illustrate alternative embodiments useful for passing and ensnaring suture material, such as, suture material 154, as devices 260, 280.
The device 260 includes a detachable arrowhead shaped element 262 at the end of suture/loop advancing element 134 to which a length of ligation material is attached as discussed elsewhere herein. A inwardly laterally directed opening 264 is formed in the end of snaring element 136. The opening 264 has an inner dimension selected so that the arrowhead element 262 will pass into the passageway 264 when properly aligned therewith. Once the arrowhead element 262 has passed into the opening 264, the snaring element 136 can be retracted in a manner similar to that described above, causing the arrowhead element 262 to be caught and ensnared in the interior of the snaring element, and thereafter detached from the element 134. The snaring element 136 can optionally further be provided with a second opening 266 .(indicated in phantom) opposite the first opening 264, so that the arrowhead element 262 can be passed entirely through the snaring element to be ensnared.
Further optionally, the element 134 can be electrically insulated on its exterior surface proximal of the detachable arrowhead 262, as indicated by dithering 268, and element 136 can similarly be electrically insulated on its exterior surface proximal of a preselected point 270, as indicated by dithering 272. When provided with this electrical insulation, the arrowhead 262 and the portion 274 of the element 136 distal of the point 270 can be electrically connected to opposite poles of a bipolar RF
electrical energy source (not illustrated) and the arrowhead can be used as an RF
cutter to easily push through tissue beds and tissue planes which lie between it and the opening 264. For example, pxoximal portions of the elements 134, 136 can be electrically connected to an RF energy source to permit the arrowhead 262 to act as an RF.cutter, as will be readily appreciated by one of ordinary skill in the art., Figure 26B illustrates aspects of yet another alternative embodiment in accordance with the present invention, device 280. Device 280 is similar in some respects to device 260. Device 280 includes a detachable ball 282 mounted,at the distal end of element 134. The ball 282, when advanced into opening 284 or through to opening 286, is ensnared by the snaring element 136 in a manner similar to that described elsewhere herein.
Figures 27-30 illustrate several views of yet another embodiment in accordance with the present invention. Turning to Figure 27, an extendible element 300 is illustrated with portions removed to aid in a better understanding of the extendible element. Element 300 can be used instead of any of the above-described extendible elements, e.g., elements 120, 122.
Element 300 includes a longitudinally 'extending cannula or tube 302 having a hollow interior 303. A stationary guide tube 304 is mounted in the cannula 302 and has a distal end 305 which is positioned proximally of the distal end of the tube 302.
The guide tube 304 is provided to guide a pushrod or the like carrying a length of suture material (not illustrated) toward the distal end of the tube 302. A
pair of wire glades 306, 308 are mounted to the top and bottom of the of the guide tube 304 .
.. adj acent to. its distal end, and extend distally out of the distal end 305 of the guide tube. The guides 306, 308 are preferably formed of a flexible material and are flat in cross-section so that when a suture-bearing pushrod~ or the like is advanced out the distal end of the guide tube 304, the pushrod is caused to follow a path between the wire guides 306, 308.
The distal ends of the wire guides 306, 308 are positioned in a hollow arm 310, and are preferably not secured to the hollow arm. The arm 310 is attached to the cannula 302 at a pivot 326. The cannula 302 includes a window, cutout, or fenestration 320 adjacent to the arm 310, and is sized and positioned so that the arm 310 can rotate between a deployed orientation, illustrated in Figures 27 and 2$, and a retracted orientation, illustrated in Figure 29, without hitting or otherwise interfering with the cannula. The arm 310 can have any of a number of cross-sectional configurations, including the somewhat rectilinear shape illustrated in the embodiment of Figures 27-30.
The element 300 also includes two pulling elements with which the orientation of the arm 310 can be controlled. In the embodiment illustrated in Figures 27-30, the pulling elements include a pair of upper pullwires 312, 314, which extend from within proximal portions of the cannula 302 to an attachment region 350 on the arm 310.
The pulling elements also include a pair of lower pullwires 316, 318, which extend from within proximal portions of the cannula 302 to an attachment region 352 on the arm 310. As'the attachment regions 350, 352 are on opposite sides of the arm (top, bottom, respectively), pulling on the pullwire pairs will result in moving the arm to either the deployed orientation or the retracted orientation. More specifically, pulling on the upper pullwire pair 312, 314 causes the arm to rotate clockwise (in the view illustrated in Figure 27), so that the arm extends generally transverse to the cannula 302. Conversely, pulling on the lower pullwire pair 316, 318 causes the arm to rotate counterclockwise (again, in the view illustrated in Figure 27), so that the arm is within the cannula's hollow interior and extends longitudinally.
The element 300 preferably includes one or more structures which facilitates operation of the upper pullwires 312, 314. A port 328 is preferably formed through the cannula wall somewhat proximally of the fenestration 320, and the upper pullwire pair extends through this upper port. Additionally, a groove or trough 330 is optionally formed in the outer surface of the cannula between the port 328 and the fenestration 320. The trough 330 is sized to be deep enough to receive the upper pullwire pair so that when the arm 310 is in the retracted orientation, the pullwires are positioned in the trough and do not extend much or at all beyond the outer diameter of _22_ the cannula. Figures 29 and 30 illustrate the arm 310 in the retracted orientation, and the upper pullwires 312, 314 positioned in the trough 330. Thus, the proximal lip of the port 328 acts as a bearing surface for the upper pullwires 312, 314 as they move longitudinally and the arm 310 pivots about pivot 326.
The element 300 preferably includes structure which permits the lower pullwires to rotate the arm 310. In the embodiment illustrated zn Figures 27-30, a yolk 322 is positioned in the cannula 302 with the lower pullwires 316, 318 extending around the yolk. Figures 28 and 30 better illustrate details of the yolk 322.
The yolk 322 is mounted in the cannula 302 distally of the pivot point 326 and preferably below the pivot point. As will be readily appreciated from Figures 27-30, pulling proximally on pullwires 316, 318 results in the arm 310 rotating down into the cannula 302 through the fenestration 320, and into the retracted orientation.
For ease of positioning the yolk 322 into the element 300, the cannula 302 may optionally include an opening 332 into which the yollc partially extends. The opening 332 can be eliminated.
Also illustrated in Figure 27 is a stationary tube 324 which extends along the bottom of the cannula 302. The stationary tube 324 is provided so that a practitioner can advance other tools through the element 300 without interfering with the operation of the arm 310. By way of example and not of limitation, tools such as an anesthesia needle or the like can be advanced distally through the tube 324 from its proximal end (not illustrated) to its distal end 336 (see Figure 28): The arm 310 also preferably includes a cutout portion 340 on the upper surface of the arm (when.in the retracted position; on the proximal face when in the deployed orientation) through which~the wire guides 306, 308 extend. The cutout 340 is provided so that a pushrod carrying a suture (not illustrated) can follow a path into the arm 310 which is more gently curved than if the cutout is not provided, and therefore the cutout facilitates use of the element 300 to pass a length of suture material around a blood vessel.
Fingers 354, 356 are also optionally provided adjacent to structures in the element 300 on which a suture may snag during deployment, such as attachment portion 350 and the proximal end of the wire guides 306,. 308. The forgers 354, 356 provide a ramp-to deflect the advancing suture away from the structure against which the suture may snag, and therefore facilitate use of the element 300.
Turning now to Figure 28, the element 300 preferably includes a distalinost tapered tip 334 in which the distal port 336 of the tube 324 is formed. The tip 334 optionally includes a blind bore 338 in its interior which facilitates assembly of the tip to the cannula 302. Also illustrated in Figure 28 is the yolk 322 secured to the interior of the cannula 302 with the stationary tube 324 extending over the yollc and for which the yolk is provided with a unique shape.
Figure 29 illustrated the element 300 with the arm 310 in its retracted orientation resulting from the lower pullwires 316, 318 having been pulled proximally. As illustrated in Figure 29, the free distal ends of the wire guides 306, 308 are, when the arm 310 is in the retracted orientation, preferably within the hollow interior of the arm, so that the wire guides do not interfere with the arm passing through the fenestration 320 and into the interior of the cannula 302.
Figure 30 illustrates across-sectional view of the element 300, taken at line 30-30 in Figure 29. Beginning at the top of the figure, the upper pullwires 312, 314 are illustrated in the trough 330. The exemplary cross-sectional shape of the arm 310 (rectilinear) can~be seen as well as the generally rectilinear cross-sectional shape of the guide tube 304. The yolk 322 includes a pair of arms 342, 344, which are secured to the interior of the cannula 302. A IT-shaped curved middle portion 346 extends between the two yolk arms 342, 344, and is sized to receive the tube 324 therethrough. The lower pullwires 316, 318 extend. around the yolk arms 342, 344, and the yolk acts as a bearing surface for the pullwires to pull the arni 310.back into the cannula 302. Also illustrated in Figure 30 is an exemplary tool 348 extending through the tube 324, e.g., an anesthesia needle. Optional opening 332 is also illustrated.
The operation of the embodiment illustrated in Figures 27-30 will now be described with reference to the drawing figures. The element 300 is extended adj acent to a blood vessel of interest, as described above with reference to Figures 1-26. Optionally, anesthesia can be administered using a needle, e.g., needle 348. Once in position, the upper pullwires 312, 314 are pulled proximally, which rotates the arm 310 out of the cannula 302 and into the deployed orientation. Thereafter, a pushrod or the like, carrying a length of suture material 154, is advanced distally through the tube 304, between the wire guides 306, 308, laterally into the interior of the arm 310 and still between the wire guides 306, 308, and out of the arm 310. The suture is then snared by a snaring element such as those previously described, and pulled proximally, thus looping the length of suture material around the blood vessel of interest. The lower pullwires 316, 318 can be pulled proximally to rotate the arm~310 back into the cannula 302 when desired.
While the invention has been described in detail with reference to preferred embodiments thereof, it will be apparent to one skilled in the art that various changes can be made, and equivalents employed, without departing from the scope of the invention.
The first and second extendable elements 120, 122 are positioned laterally opposite each other.in cannula 104, as best illustrated in Fig. 3, so that When they are in their extended positions they can be positioned on opposite sides of an anatomical vessel, such as vessel 10. Furthermore, first and second extendable elements 120, 122 are sized so that they both are extendable farther than a distance Xref from the distal end 150, described in greater detail below, so that a vessel 10 can be bracketed by the.
extendable elements when the vessel is within Xref from the distal end of cannula 104.
First extendable element 120 carries a detachable element at its distal end.
In the embodiment illustrated in Figure 1, the detachable element is a loop 124.
Loop 124 is attached, either directly or indirectly as will be described in greater detail below, to a length of threadlike material, such as suture material, which may optionally further include a leader, which extends proximally through cannula 104.
Second extendable element 122 carries a snare element which is sized and configured to grab, ensnare,'or otherwise become secured with the detachable element of the first extendable element 120 when the first and second extendable elements are in their extended positions (see Figs. 1 and 23). In the embodiment illustrated in Figure 3, the snare element is a hook 126. Loop 1,24 and snare 126 will be described in greater detail below with reference to Figs. 4-13.
Ligation device 100 further includes a doppler ultrasound device ~or wand 140 mounted in the ligation device. In accordance with the present invention, the Doppler ultrasound device can be removably mounted in 'the ligation device, or the components of a doppler ultrasound device can be integrated into the ligation device, e.g. into cannula 104, so as not to be removable. Thus, when the Doppler ultrasound device is removably mounted in ligation device 100, the Doppler ultrasound device can be removed at the termination of a use, removed from the remainder of the ligation device, and the Doppler ultrasound device sterilized and reused.
Alternatively, when the Doppler ultrasound device's components are integrated into the ligation .device 100, the entire ligation device can be disposed of at the conclusion of a use.
Cannula 104 includes a third center lumen 138 (see Figs., 3 and 7) into which a removable doppler wand 140 is removably inserted. According to certain embodiments of the present invention, a distal end 152 of the doppler wand is proximal of the distal end 150 of the cannula. According to other embodiments of the present invention, the distal end 152 of the doppler wand 140 is positioned at the distal end 150 of the cannula. ~ According to other embodiments of the present invention, the distal end 152 of the doppler wand 140 is positioned distal of the distal end 150 of the cannula. Preferably, housing 103 includes portions which receive the proximal portions of doppler wand 140, so that the doppler wand can be removed and reused after ligation device 100 has been used. For example and not by way of limitation, housing 103 can include portions which are hinged together and secured with a snap, lock, or the like, so that the housing can be opened up, a doppler wand 140 inserted into ligation device 100, and the housing portions closed and locked to secure the doppler wand in the ligation device.
Doppler ultrasound wands suitable for use in the present invention are presently commercially available. For example, Koven model ES ~ 100X MiniDop VRP-8 probe (St. Louis, MO) is a continuous wave doppler wand suitable for use as doppler wand 140, and DWL/Neuro Scan Medical Systems' Multi-Dop B~- system _$_ with their 8 MHz handheld probe (Sterling, VA) is a continuous and pulsed wave doppler wand suitable for use as wand 140. Commercially available doppler stethoscopes or wands have an ultrasound dispersion pattern which is generally conical, i.e., the wand "looks" out along a cone-shaped portion of a plane originating at the end of the wand. Thus, vessels with fluid flow in them, such as a blood vessel, which lie anywhere in this conical plane and within the effective range of the wand would be picked up by the wand. Doppler wands presently available are attached to a signal processing and display unit 156, which processes the electrical signals generated by wand 140 to generate displays and/or other data derived from the electrical signals for additional uses. Alternatively, the Doppler system can be gated to identify blood vessels within a predetermined distance range, e.g. from between 0 to 5 cm, more preferably between 0.5 and 3 cm.
Unit 156 includes a display 158 which indicates the distance from the distal tip 152 the source of reflected ultrasound waves is located, e.g., vessel 10. This information is typically calculated utilizing a predetermined function, because the distance is a function of the time it takes for the ultrasound waves to travel to and from the wand. Unit 156 preferably also includes a display or meter 160 of the magnitude of the reflected ultrasound waves's doppler shift, which is the indication of , the velocity of the fluid flowing through vessel 10. Unit 156 also preferably includes a sound source 162 which gives an audible indication of the doppler shift, which can be louder when the Doppler shift is greater or the vessel is optimally positioned.
Tn the ligation device of the present invention, however, such a wide conical "field of view" typically returned by many commercially available doppler wands is not preferable, because the practitioner is concerned with locating the vessel between the extendable elements in order to ligate the vessel. Were the present invention to .
utilize such "wide-view" Doppler wands without narrowing or otherwise affecting their field of view, vessels which are not directly distal of ligation device 100 would be piclced up by the device, and would return doppler shift data for vessels not of interest in the use of the ligation device. Ligation device 100, and specifically cannula 104, is therefore sized so that the distalmost end 152 of doppler wand 140 is spaced proximally from the distal end 150 of the caxmula, for use with "wide-view"
wands to collimate the signal. Some commercially available doppler wands, such as the aforementioned DWL probe, however, produce a sufficiently collimated signal so that further collimation is not necessary.
When utilizing a Doppler probe which does not produce, a sufficiently collimated signal, lumen 138 is preferably coated, formed of a material, or is otherwise provided with a sleeve of a material on the interior surface of which collimates the sound waves emanating from doppler wand 140. By way of example and not of limitation, lumen 138 can be coated or formed of polycarbonate, although other materials are also usable within the spirit and scope of the present invention.
The result of spacing distal end 152 proximally of distal end 150, and optionally further providing a material and/or sleeve which acoustically collimates the ultrasound waves from wand 140, is that ligation device 100 is substantially unidirectional in its doppler field of view in a direction parallel with, and preferably between,. first and second extendable elements 120, 122, and longitude ally distal of distal end 150. Stated differently, legation device 100 is capable of receiving reflected ultrasound waves, originating from doppler wand 140, reflected back from anatomical features directly distal of distal end 150. Thus, because distal end 152 is a fixed and known distance from distal end 150, and X~ef is known, a maximum distance Xm~
is predetermined by the structures of legation device 100 within which a vessel 10 must be in order for the legation device to be capable of legating it. Stated somewhat differently, once it is determined that a vessel is within a predetermined distance of distal end 152, which is indicated by the time lag of the reflected ultrasound waves, legation device 100 can be used to legate that vessel.
According to another embodiment in accordance with the present invention, a doppler wand can be chosen which has a "field of view" which is narrow enough that, when used in the combination of the ligating device 100, additional collimation structures are not necessary. For example, selection of a probe is based on its field of view and its operating frequency, and should also be based on the distance between the target artery and the Doppler probe so that the probe's depth of view is larger than this distance yet not so long as to include other blood vessels. By way of example and not of limitation, a DWL Doppler probe as described above can be used as wand without requiring either a collimating sleeve and without spacing the distal end proximal of distal end 150. In general, Doppler wands suitable for use as Doppler wand 140 are selected with small enough diameter to be insertable in cannula 104, preferably.operate at a frequency which is sufficiently sensitive to blood flow to monitor uterine artery blood flow, have a relatively narrow field of view and limited depth of view so as not to generate a signal from other blood vessels, and can be based on either pulsed or continuous wave Doppler signals.
Figure 3 illustrates a cross-section view of ligation device 100, as seen along line 3-3 in Figure 1, and Figure 7 illustrates an enlarged distal end perspective view of ligation device 100. Cannula 104 preferably has an oval cross sectional profile, so that the cannula can be relatively compact while still meeting the requirement that doppler wand 140 be laterally between extendable elements 120, 122. As illustrated in Figure 3, cannula 104 includes a first lumen 130 which longitudinally and slidingly receives first extendable element 120. Preferably, element 120 itself includes a lumen 142 through which a tubular suture and loop advancing element 134 is longitudinally slidable. Element 120 further optionally is provided with a slot or cutout 170 at its distal end in the wall of the element 120 adjacent to or facing element 122, to assist in guiding or positioning loop advancing element 134 in a desired direction and to assist in preventing rotation of the loop advancing element relative to the element 120.
Suture advancing element 134 at least in part is formed of a superelastic material, less preferably a shape-memory alloy (SMA) material, also less preferably (surgical) stainless steel. NiTi (nitinol) is preferred, although other superelastic, SMA, and biocornpatible materials are within the scope of the present invention.
Forming at least portions of suture advancing element 134 of NiTi allows the suture advancing element to be preformed with a curved distal end, so that the suture advancing element can be easily retracted into first extendable element 120, yet the distal end will accurately position loop 124 to be snared by extendable element 122 when the suture advancing element is advanced out of the first extendable element.
Suture/loop advancing element 134 preferably is a hollow tube and includes structure at the distal end of the element which holds loop 124, the loop in turn being attached to a length of suture material 154 (see also Fig. 24).' A more detailed description of the structures at the distal ends of extendable elements 120,122 is presented below with reference to Figs. 4-13.
Cannula 104 includes a second lumen 132 in which second extendable element 122 is longitudinally slidably received. Second extendable element 122 preferably includes a lumen 144 which longitudinally slidably receives an extendible , hooking or snaring element 136. Cannula 104 also includes a third lumen 138 which removably receives doppler wand 140, so that the doppler wand can be used with the other structures of ligation device 100 and then disassembled, as discussed above.
Optionally, the ligation device 100, including the third lumen 138, can non-removably house the functional components of a Doppler wand, so that the entire ligation device can be conveniently disposed of.
As illustrated in Figure 7, the first and second extendable elements 120, 122 can optionally further be provided with closed, preferably comically or frustoconically shaped tips 121, 123, respectively. The closed tips 121, 123 permit the extendable elements 120, 122 to be more easily advanced through tissue beds and planes.
When provided with the closed tips 121, 123, the extendable elements 120, 122 further include laterally inwardly facing openings 125, 127 so that the elements 134, 136 can pass out of the elements 120, 122, as described elsewhere herein. Further optionally, the distal interiors of one or both of the closed tips can be provided with cam surfaces (not illustrated) to assist in guiding the detachable elements and/or the snaring elements.
Figures 4- .6 illustrate several views of snaring element 136 including hook or snare 126. As detailed in Figure 5, snare 126 includes an enlarged head 160 having an angled slot 1.62. A hook portion 164 is formed distally of slot 162. Slot 162 has a width W~ and extends into head 160 at an angle cc. A shank 166 is attached at the proximal end of head 160, and is, preferably formed integrally therewith from a single piece of material. Alternatively, shank 166 and head 160 can be press-fit, welded, adhesively bonded, or otherwise formed separately and thereafter joined together as will be readily apparent to one of ordinary skill in the art. Width W, is selected to be greater than the width WZ of loop 124 (see Fig. 9), so that the loop can be deflected into slot 162 by hook portion 164 and slide into the slot and be grabbed by snare 126.
Optionally, the proximal portions of head 160 adjacent to the opening to slot 162 can be widened, as indicated in phantom lines in Fig. 5, which can facilitate loop being deflected by hook portion 164 into slot 162.
Figures 8-13 illustrate distal end portions of suture/loop advancing element 134. As illustrated in Figs. 8-10, loop 124 is preferably roughly oval in shape, and is temporarily mounted to the distal end of a tubular curved element 172 (see also Fig.
13). A length of suture material 154 or the like is tied, glued, crimped, or otherwise secured to loop 124, and extends proximally through tube 172. As illustrated in Figs 11-13, suture/loop advancing element 134 includes a straight portion 174 and a curved portion 172, both of which are hollow tubes. Straight portion 174 and curved portion 172 are joined together at a joint 180. Optionally, element 134 can be a monolithic element without such a joint 180, and a straight portion 174 and a curved portion 172 can be formed therein, as will be readily appreciated by one of ordinary skill in the art.
At least curved portion 172 of element 134 is preferably formed of a superelastic material. Alternatively, portion 172 can be formed of a SMA
material.
While the characteristics and use of superelastic materials are readily appreciated by , one of ordinary skill in the art, a brief description as applied to curved portion 172 will aid in an understanding of the present invention. Portion 172 is preferably formed of an superelastic material, e.g., NiTi (nitinol). Portion 172 is given a curvature or bent configuration which, upon heating of the curved portion above a certain temperature for the superelastic material, is 'remembered' by the curved portion. In the embodiment illustrated in Figs. 11-13 curved portion 172 is formed into an arc having a radius R and the distal end 176 being at an angle (3 from a line perpendicular to straight portion 174. Distal end 176, when curved portion 172 is in its curved configuration, is a lateral distance Y from the straight portion 174.
The length of curved portion 172 and the shape, as well as the distance Y, are selected so that when curved portion 172 is in its curved configuration, loop 124 is positioned directed distally of second extendable element 122. In this location, snare 126 can be extended and can hook loop 124, to be pulled from suture/loop advancing element 134. The angular orientation of the lateral direction in which curved portion 172 extends when in its curved configuration can be preset so that loop 124 registers or lines up with snare 126, and slot 170 assists in maintaining this orientation. This present angular orientation can be determined, by way of example and not of limitation, by heating curved portion 172 above its transition temperature and rotating element 134 until loop 124 is directly distal of snare 126, prior to using device 100.
Curved portion 172 and straight portion 174 can both be formed of the same (superelastic) material. Alternatively, only portion 172 is formed of an superelastic material, and straight portion 174 can be formed of another material, e.g., stainless steel, and the two portions 172, 174 can be joined together at joint 180, as by welding, , crimping, swaging, adhesive bonding, or the like. The distalmost end of portion 172 includes a slot 178 in which loop 124 is temporarily held. Slot 178 has a width W3 and a depth D selected so~ that loop 124 can be received therein by a press fit, or loosely received and crimped therein. Loop 124 is not permanently held in slot 178, however, and is mounted in the slot so that the loop can be pulled out of the slot by a preselected force transmitted by snare 126 after the loop has been hooked by the snare (see, e.g., Fig. 3).
Figure 14 illustrates internal portions of ligation device 100. First and second extendable elements 120, 122 are mounted in a block 190 to which rings 112, 114 are also fixedly secured. Thus, as described above, proximal and distal longitudinal movement of rings 112, 114 moves first and second extendable elements 120, 122.
Block 190 includes a pair of slots 192, 194 formed in a top surface thereof in which tabs or pins 116, 118 are slidably received, respectively. Thus, the slots 192, 194 constrain the tabs 116, 118 laterally, while permitting them to move longitudinally over a range limited by the length of the slots.
Figure 15 illustrates a top plan view of distal portions of the view illustrated in Figure 14. As can be seen in Figure 15, the block 190 includes slots 192,,194, described above. According to one embodiment of the present invention, block includes first and second lateral portions 196, 198, which are cylindrical in shape, in which the first and second extendable elements 120, 122 are mounted, respectively.
According to one embodiment of the present invention, lateral portions 196, 198 can be fixedly joined together as a with a web 200, so that movement of one of the rings 112, 114 moves both lateral portions. According to yet another embodiment of the present invention, lateral portions 196 and 198 are not joined together, and are therefore separately and individually longitudinally moveable in housing 103.
Also visible in Figure 15 are mounting blocks 202 and 204 positioned iri block 190. Mounting block 202 fixedly receives the proximal portion of extendable element 134 and lower portions of tab 116, and mounting block 204 fixedly receives the proximal portion of extendable element 136 and tab 118. Block 202 thus joins together extendable element 134 with tab 116, and block 204 thus joins together extendable element 136 with tab 118. Additionally, blocks 202 and 204 constrain tabs 116 and 118 from being pulled up and out from block 190, as their lateral extents are larger than slots 192, 194, respectively.
Figure 16 illustrates a cross-sectional view of proximal portions of ligation device 100. As can be seen in Figure 16, the housing 103 includes an interior chamber or cavity 210 which slidingly receives block 190 and its components.
Block 190 includes an interior chamber or cavity 208 which slidingly receives blocks and 204 (block 204 is not visible in the view of Figure 16), and a proximal opening 206 which communicates interior chamber 208 with interior chamber 210.
Proximal opening 206 also permits blocks 202, 204 to extend into interior chamber 210.
Figure 16 also illustrates suture 154 extending through loop advancing element 134, block 202, interior chamber 208, interior chamber 210, and exiting housing 103 through one of slots 108-111.
Figures 17-19 illustrate further embodiments in accordance with the present invention. In the embodiment illustrated in Figure 17, both a loop advancing element 220 and a snare advancing element 222 are formed of a superelastic, SMA, or stainless steel material, and curve to meet each other. In the embodiment illustrated in Figure 18, snare advancing element 136 is formed of .a superelastic, SMA, or stainless steel material, and loop advancing element 134 is advanced directly longitudinally distally to be snared by the snare 126. In the embodiment illustrated in Figure 19, a first curved tube 230 of a superelastic, SMA, or stainless steel material, and a second curved tube 232 of a superelastic, SMA, or stainless steel material, meet in a manner similar to the embodiment illustrated in Figure 17. The distal ends of tubes 230, 232 mate in a somewhat different fashion, one of the tubes 230, 232 bearing a snare which is a receptacle 234 having a bore 238 having an internal diameter larger than the external, diameter of the other of tubes 230, 232. Thus, when the tubes 230, 232 meet, the distal ends engage. A pushrod or wire 236, to which suture 154 is attached, is positioned in one of the lumens of tubes,230, 232, and is pushed distally down that tube, through receptacle 234, and proximally up the other of tubes 230, 232.
Thus, a suture can be advanced around a blood vessel of interest in a manner similar to the embodiments described above.
Figures 20-24 illustrate several steps of an exemplary method in accordance with the present invention. While Figures 20-24 illustrate, and the following description makes reference to, ligation device 100, methods in accordance with the present invention are not limited to use of ligation device 100, and other apparatus can be utilized in practicing the present methods without departing from the spirit and scope of the present invention.
Figure 20 illustrates the distal end of ligation device 100 after having been positioned proximate a vessel of interest in a patient, e.g., a uterine artery 10. Distal end 150 of cannula 104 is initially positioned away from vessel 10. Distal end 150 is accurately positioned within Xm~ of the vessel by pointing cannula 104 in several directions around where the practitioner believes the vessel is located, monitoring the output of unit 156 for distance and velocity data to determine the relative location of the vessel relative to distal end 150, and repositioning the distal end until the distal end is a distance X from vessel 10 less than Xm~. As described above, reflected ultrasound waves 182, which are preferably collimated, are received by doppler wand 140 (or the functional components thereof, integrated into ligation device 100) and are processed by unit 156 to indicate the relative location of vessel 10. For example, Doppler sound is utilized to fmd the vessel location, and thereafter pulsed wave Doppler is utilized to identify a more precise location and the distance to the artery 10.
Once the practitioner has established that vessel 10 is directly distal of the distal end 150 of cannula 104, first and second actuation rings 112, 114 axe moved distally to move first and second extendable members 120, 122 distally, as illustrated in Fig. 21. Then, as illustrated in Figs. 22 and 23, suture/loop advancing element 134 and snaring element 136 are both distally advanced by pushing tabs 116, 118 distally;
the advancement of elements 134 and 136 can be serial, simultaneous, or combinations thereof. Because suture/loop advancing element 134 is inside a (preferably mammalian) patient while it is advanced, the suture/loop advancing element is heated up iu situ above its SMA transition temperature, and transforms from its straight configuration to its 'remembered' or curved configuration.
Thus, advancement of advancing element 134 out of member 120 is accompanied by element 134 assuming, or having already assumed, its curved configuration.
Element 134 and loop 124 are therefore advanced in a lateral direction and toward element 136 and snare 126.
While the loop 124 is positioned directly distal of snare 126, snaring element 136.is moved distally to advance snare 126 distally. Snare 126, and more particularly head 160, enters loop 124, and is pushed through the loop. Snare 126 is then retracted -25 proximally so that hook portion 164 deflects loop 124 into slot 162; thus causing the .
loop to be grabbed by the snare. In this respect, a widened mouth to slot 162, as suggested by phantom line 168, can facilitate capture of loop 124.
With loop 124 ensnared by snare 126, snaring element 136 is retracted proximally, which pulls on the loop in a proximal direction. As the materials out of which portions 172, 174 are formed are relatively rigid (superelastic, SMA, and stainless steel being preferable), the force applied by snaring element 136 to loop 124 will cause the joint between loop 124 and slot 178 to break or otherwise release the loop from element 134. As will be readily appreciated by one of ordinary skill in the art, the joint between loop 124 and slot 178 is designed as a breakaway element, with the minimum force needed to break the joint selected so that the loop will not . prematurely break free of curved portion 172, yet not so high that a practitioner will not readily be able to generate the required force by pulling proximally on tab 118.
Once loop 124 has been broken free of slot 178, snaring element 136 and second extendable element 122 are further pulled proximally so that the loop is pulled into cannula 104. As described above, suture material 154 extends through curved portion 172 and is secured to loop 124, and is therefore pulled along with the loop.
Thus, suture material 154 is advanced distally past vessel 10 by distal extension of first extendable element 120 and suture/loop advancing element 134, is advanced laterally behind the vessel by curved portion 172 having assumed its curved superelastic configuration, and is advanced proximally by proximal retraction of loop 124 after having been grabbed by snare 126. With the loop of suture material passing around vessel 10, ligation device 100 can be pulled proximally, leaving the loop of suture material around vessel 10, as illustrated in Figure 24. At this point, the practitioner can make whatever form of ligation she chooses, as the loop of suture material has been accurately passed around the vessel 10 of interest.
Figure 25 illustrates yet another embodiment in accordance with the present invention. The embodiment illustrated in Figure 25 is similar to that illustrated in Figure 3, but differs in the cross-sectional profile of the device 250.
Instead of the oval cross-sectional profile illustrated in Figure 3, device 250 includes the coplanar lumenae 130, 132, 138 defined in three adjacent and joined tubes 252, 254, 256.
Figures 26A and 26B illustrate alternative embodiments useful for passing and ensnaring suture material, such as, suture material 154, as devices 260, 280.
The device 260 includes a detachable arrowhead shaped element 262 at the end of suture/loop advancing element 134 to which a length of ligation material is attached as discussed elsewhere herein. A inwardly laterally directed opening 264 is formed in the end of snaring element 136. The opening 264 has an inner dimension selected so that the arrowhead element 262 will pass into the passageway 264 when properly aligned therewith. Once the arrowhead element 262 has passed into the opening 264, the snaring element 136 can be retracted in a manner similar to that described above, causing the arrowhead element 262 to be caught and ensnared in the interior of the snaring element, and thereafter detached from the element 134. The snaring element 136 can optionally further be provided with a second opening 266 .(indicated in phantom) opposite the first opening 264, so that the arrowhead element 262 can be passed entirely through the snaring element to be ensnared.
Further optionally, the element 134 can be electrically insulated on its exterior surface proximal of the detachable arrowhead 262, as indicated by dithering 268, and element 136 can similarly be electrically insulated on its exterior surface proximal of a preselected point 270, as indicated by dithering 272. When provided with this electrical insulation, the arrowhead 262 and the portion 274 of the element 136 distal of the point 270 can be electrically connected to opposite poles of a bipolar RF
electrical energy source (not illustrated) and the arrowhead can be used as an RF
cutter to easily push through tissue beds and tissue planes which lie between it and the opening 264. For example, pxoximal portions of the elements 134, 136 can be electrically connected to an RF energy source to permit the arrowhead 262 to act as an RF.cutter, as will be readily appreciated by one of ordinary skill in the art., Figure 26B illustrates aspects of yet another alternative embodiment in accordance with the present invention, device 280. Device 280 is similar in some respects to device 260. Device 280 includes a detachable ball 282 mounted,at the distal end of element 134. The ball 282, when advanced into opening 284 or through to opening 286, is ensnared by the snaring element 136 in a manner similar to that described elsewhere herein.
Figures 27-30 illustrate several views of yet another embodiment in accordance with the present invention. Turning to Figure 27, an extendible element 300 is illustrated with portions removed to aid in a better understanding of the extendible element. Element 300 can be used instead of any of the above-described extendible elements, e.g., elements 120, 122.
Element 300 includes a longitudinally 'extending cannula or tube 302 having a hollow interior 303. A stationary guide tube 304 is mounted in the cannula 302 and has a distal end 305 which is positioned proximally of the distal end of the tube 302.
The guide tube 304 is provided to guide a pushrod or the like carrying a length of suture material (not illustrated) toward the distal end of the tube 302. A
pair of wire glades 306, 308 are mounted to the top and bottom of the of the guide tube 304 .
.. adj acent to. its distal end, and extend distally out of the distal end 305 of the guide tube. The guides 306, 308 are preferably formed of a flexible material and are flat in cross-section so that when a suture-bearing pushrod~ or the like is advanced out the distal end of the guide tube 304, the pushrod is caused to follow a path between the wire guides 306, 308.
The distal ends of the wire guides 306, 308 are positioned in a hollow arm 310, and are preferably not secured to the hollow arm. The arm 310 is attached to the cannula 302 at a pivot 326. The cannula 302 includes a window, cutout, or fenestration 320 adjacent to the arm 310, and is sized and positioned so that the arm 310 can rotate between a deployed orientation, illustrated in Figures 27 and 2$, and a retracted orientation, illustrated in Figure 29, without hitting or otherwise interfering with the cannula. The arm 310 can have any of a number of cross-sectional configurations, including the somewhat rectilinear shape illustrated in the embodiment of Figures 27-30.
The element 300 also includes two pulling elements with which the orientation of the arm 310 can be controlled. In the embodiment illustrated in Figures 27-30, the pulling elements include a pair of upper pullwires 312, 314, which extend from within proximal portions of the cannula 302 to an attachment region 350 on the arm 310.
The pulling elements also include a pair of lower pullwires 316, 318, which extend from within proximal portions of the cannula 302 to an attachment region 352 on the arm 310. As'the attachment regions 350, 352 are on opposite sides of the arm (top, bottom, respectively), pulling on the pullwire pairs will result in moving the arm to either the deployed orientation or the retracted orientation. More specifically, pulling on the upper pullwire pair 312, 314 causes the arm to rotate clockwise (in the view illustrated in Figure 27), so that the arm extends generally transverse to the cannula 302. Conversely, pulling on the lower pullwire pair 316, 318 causes the arm to rotate counterclockwise (again, in the view illustrated in Figure 27), so that the arm is within the cannula's hollow interior and extends longitudinally.
The element 300 preferably includes one or more structures which facilitates operation of the upper pullwires 312, 314. A port 328 is preferably formed through the cannula wall somewhat proximally of the fenestration 320, and the upper pullwire pair extends through this upper port. Additionally, a groove or trough 330 is optionally formed in the outer surface of the cannula between the port 328 and the fenestration 320. The trough 330 is sized to be deep enough to receive the upper pullwire pair so that when the arm 310 is in the retracted orientation, the pullwires are positioned in the trough and do not extend much or at all beyond the outer diameter of _22_ the cannula. Figures 29 and 30 illustrate the arm 310 in the retracted orientation, and the upper pullwires 312, 314 positioned in the trough 330. Thus, the proximal lip of the port 328 acts as a bearing surface for the upper pullwires 312, 314 as they move longitudinally and the arm 310 pivots about pivot 326.
The element 300 preferably includes structure which permits the lower pullwires to rotate the arm 310. In the embodiment illustrated zn Figures 27-30, a yolk 322 is positioned in the cannula 302 with the lower pullwires 316, 318 extending around the yolk. Figures 28 and 30 better illustrate details of the yolk 322.
The yolk 322 is mounted in the cannula 302 distally of the pivot point 326 and preferably below the pivot point. As will be readily appreciated from Figures 27-30, pulling proximally on pullwires 316, 318 results in the arm 310 rotating down into the cannula 302 through the fenestration 320, and into the retracted orientation.
For ease of positioning the yolk 322 into the element 300, the cannula 302 may optionally include an opening 332 into which the yollc partially extends. The opening 332 can be eliminated.
Also illustrated in Figure 27 is a stationary tube 324 which extends along the bottom of the cannula 302. The stationary tube 324 is provided so that a practitioner can advance other tools through the element 300 without interfering with the operation of the arm 310. By way of example and not of limitation, tools such as an anesthesia needle or the like can be advanced distally through the tube 324 from its proximal end (not illustrated) to its distal end 336 (see Figure 28): The arm 310 also preferably includes a cutout portion 340 on the upper surface of the arm (when.in the retracted position; on the proximal face when in the deployed orientation) through which~the wire guides 306, 308 extend. The cutout 340 is provided so that a pushrod carrying a suture (not illustrated) can follow a path into the arm 310 which is more gently curved than if the cutout is not provided, and therefore the cutout facilitates use of the element 300 to pass a length of suture material around a blood vessel.
Fingers 354, 356 are also optionally provided adjacent to structures in the element 300 on which a suture may snag during deployment, such as attachment portion 350 and the proximal end of the wire guides 306,. 308. The forgers 354, 356 provide a ramp-to deflect the advancing suture away from the structure against which the suture may snag, and therefore facilitate use of the element 300.
Turning now to Figure 28, the element 300 preferably includes a distalinost tapered tip 334 in which the distal port 336 of the tube 324 is formed. The tip 334 optionally includes a blind bore 338 in its interior which facilitates assembly of the tip to the cannula 302. Also illustrated in Figure 28 is the yolk 322 secured to the interior of the cannula 302 with the stationary tube 324 extending over the yollc and for which the yolk is provided with a unique shape.
Figure 29 illustrated the element 300 with the arm 310 in its retracted orientation resulting from the lower pullwires 316, 318 having been pulled proximally. As illustrated in Figure 29, the free distal ends of the wire guides 306, 308 are, when the arm 310 is in the retracted orientation, preferably within the hollow interior of the arm, so that the wire guides do not interfere with the arm passing through the fenestration 320 and into the interior of the cannula 302.
Figure 30 illustrates across-sectional view of the element 300, taken at line 30-30 in Figure 29. Beginning at the top of the figure, the upper pullwires 312, 314 are illustrated in the trough 330. The exemplary cross-sectional shape of the arm 310 (rectilinear) can~be seen as well as the generally rectilinear cross-sectional shape of the guide tube 304. The yolk 322 includes a pair of arms 342, 344, which are secured to the interior of the cannula 302. A IT-shaped curved middle portion 346 extends between the two yolk arms 342, 344, and is sized to receive the tube 324 therethrough. The lower pullwires 316, 318 extend. around the yolk arms 342, 344, and the yolk acts as a bearing surface for the pullwires to pull the arni 310.back into the cannula 302. Also illustrated in Figure 30 is an exemplary tool 348 extending through the tube 324, e.g., an anesthesia needle. Optional opening 332 is also illustrated.
The operation of the embodiment illustrated in Figures 27-30 will now be described with reference to the drawing figures. The element 300 is extended adj acent to a blood vessel of interest, as described above with reference to Figures 1-26. Optionally, anesthesia can be administered using a needle, e.g., needle 348. Once in position, the upper pullwires 312, 314 are pulled proximally, which rotates the arm 310 out of the cannula 302 and into the deployed orientation. Thereafter, a pushrod or the like, carrying a length of suture material 154, is advanced distally through the tube 304, between the wire guides 306, 308, laterally into the interior of the arm 310 and still between the wire guides 306, 308, and out of the arm 310. The suture is then snared by a snaring element such as those previously described, and pulled proximally, thus looping the length of suture material around the blood vessel of interest. The lower pullwires 316, 318 can be pulled proximally to rotate the arm~310 back into the cannula 302 when desired.
While the invention has been described in detail with reference to preferred embodiments thereof, it will be apparent to one skilled in the art that various changes can be made, and equivalents employed, without departing from the scope of the invention.
Claims (42)
1. A ligation device comprising:
a cannula having a proximal end, a distal end, and at least one lumen extending longitudinally from said proximal end to said distal end;
a first extendable member slidably received in said cannula lumen, said first extendable member having a distal end and being movable in said lumen from a retracted position in which said first extendable member distal end is proximal said cannula distal end, and an extended position in which said first extendable member distal end is distal of said cannula distal end, said first extendable member including a detachable element at said first extendable member distal end;
a second extendable member slidably received in said cannula lumen, said second extendable member having a distal end and being movable in said lumen from a retracted position in which said second extendable member distal end is proximal said cannula distal end, and an extended position in which said second extendable member distal end is distal of said cannula distal end, said second extendable member including a snare at said second extendable member distal end;
and at least one of said first extendable member and said second extendable member including curved portions which extend laterally across said cannula when said at least one of said first extendable member and said second extendable member is in said extended position.
a cannula having a proximal end, a distal end, and at least one lumen extending longitudinally from said proximal end to said distal end;
a first extendable member slidably received in said cannula lumen, said first extendable member having a distal end and being movable in said lumen from a retracted position in which said first extendable member distal end is proximal said cannula distal end, and an extended position in which said first extendable member distal end is distal of said cannula distal end, said first extendable member including a detachable element at said first extendable member distal end;
a second extendable member slidably received in said cannula lumen, said second extendable member having a distal end and being movable in said lumen from a retracted position in which said second extendable member distal end is proximal said cannula distal end, and an extended position in which said second extendable member distal end is distal of said cannula distal end, said second extendable member including a snare at said second extendable member distal end;
and at least one of said first extendable member and said second extendable member including curved portions which extend laterally across said cannula when said at least one of said first extendable member and said second extendable member is in said extended position.
2. A ligation device according to Claim 1, wherein said first extendable member comprises a first hollow tube and a second hollow tube slidably received in said first hollow tube.
3. A ligation device according to Claim 2, further comprising a length of ligation material extending through said second hollow tube and secured to said detachable element.
4. A ligation device according to Claim 1, further comprising a length of ligation material extending through said first extendable member and secured to said detachable element.
5. A ligation device according to Claim 1, further comprising a Doppler wand in said cannula.
6. A ligation device according to Claim 5, wherein said Doppler wand is removably mounted in said device.
7. A ligation device according to Claim 5, wherein said Doppler wand is mounted in said device so as not to be removable.
8. A ligation device according to Claim 5, wherein said Doppler wand, said first extendable member, and said second extendable member are coplanar.
7. A ligation device according to Claim 5, wherein said Doppler wand is mounted in said device so as not to be removable.
8. A ligation device according to Claim 5, wherein said Doppler wand, said first extendable member, and said second extendable member are coplanar.
7. A ligation device according to Claim 5, wherein said Doppler wand has a distal end proximal of said cannula distal end.
8. A ligation device according to Claim 5, wherein said Doppler wand has a distal end distal of said cannula distal end.
9. A ligation device according to Claim 7, wherein said cannula comprises a second lumen, said Doppler wand being positioned in said cannula second lumen.
10. A ligation device according to Claim 1, wherein said detachable element comprises a loop, and wherein said snare comprises a slot sized to receive portions of said loop therein.
11. A ligation device according to Claim 1, wherein said first extendable member curved portions are formed of a superelastic material.
12. A ligation device according to Claim 11, wherein said superelastic material comprises nitinol.
13. A ligation device according to Claim 1, further comprising a handle attached to said cannula proximal end.
14. A ligation device according to Claim 13, wherein said handle comprises:
a housing;
a first actuation member slidably mounted in said housing, said first actuation member attached to said first extendable member; and a second actuation member slidably mounted in said housing, said second actuation member attached to said second extendable member.
a housing;
a first actuation member slidably mounted in said housing, said first actuation member attached to said first extendable member; and a second actuation member slidably mounted in said housing, said second actuation member attached to said second extendable member.
15. A ligation device according to Claim 14, wherein each of said first and second actuation members include first portions extending outside said housing which allow a practitioner to manipulate the first and second actuation members.
16. A ligation device according to Claim 14, wherein said housing comprises two longitudinally extending slots, and each of said first and second actuation members include tabs extending through said slots to limit the range of motion of said first and second actuation members.
17. A ligation device according to Claim 1, wherein the first extendable member comprises a slot at the distal end of said first extendable member, and said loop is releasably mounted in said slot.
18. A ligation device according to Claim 1, further comprising:
a first block, a proximal portion of said first extendable member fixedly mounted to said first block; and a second block, a proximal portion of said second extendable member fixedly mounted to said first block.
a first block, a proximal portion of said first extendable member fixedly mounted to said first block; and a second block, a proximal portion of said second extendable member fixedly mounted to said first block.
19. A ligation device according to Claim 18, wherein said first and second blocks are connected together.
20. A ligation device according to Claim 18, wherein said first and second blocks are both cylindrically shaped.
21. A ligation device according to Claim 18, wherein each of said first and second blocks includes an interior chamber and a slot communicating said interior chamber with the exterior of said block.
22. A ligation device according to Claim 21, wherein said first and second extendable members include proximal portions extending through said slots of said first and second blocks, respectively.
23. A ligation device according to Claim 1, wherein both of said first and second extendable members include curved portions.
24. A ligation device according to Claim 1, wherein said detachable element comprises an arrowhead, and said snare comprises a lateral opening in a distal portion of second extendable member sized and positioned to receive and ensnare said arrowhead in the lateral opening.
25. A ligation device according to Claim 24, wherein said first extendable member and said second extendable member both include exterior surfaces having electrical insulation thereon.
26. A ligation device according to Claim 1, wherein said detachable element comprises a ball, and said snare comprises a lateral opening in a distal portion of second extendable member sized and positioned to receive and ensnare said ball in the lateral opening.
27. A ligation device according to Claim 1, wherein said first extendable member and said second extendable member both include closed distal ends and laterally inwardly directed openings.
28. A ligation device according to Claim 27, wherein said closed distal ends of said first and second extendable members are conically shaped.
29. A method of preparing an anatomical vessel for ligation, comprising the steps of:
positioning a cannula adjacent to said vessel, said cannula including a first extendable member, a second extendable member, a Doppler wand, and a distal end;
transmitting ultrasound signals toward said vessel with said Doppler wand;
receiving ultrasound signals reflected by said vessel with said Doppler wand;
extending said first extendable member on a first side of said vessel;
extending said second extendable member on a second side of said vessel opposite said first side; and extending a length of ligation material between said first and second extendable members on a side of said vessel opposite said cannula distal end.
positioning a cannula adjacent to said vessel, said cannula including a first extendable member, a second extendable member, a Doppler wand, and a distal end;
transmitting ultrasound signals toward said vessel with said Doppler wand;
receiving ultrasound signals reflected by said vessel with said Doppler wand;
extending said first extendable member on a first side of said vessel;
extending said second extendable member on a second side of said vessel opposite said first side; and extending a length of ligation material between said first and second extendable members on a side of said vessel opposite said cannula distal end.
30. A method according to Claim 29, wherein said first extendable member includes a detachable element to which said ligation material is attached, and further comprising grabbing said detachable element with portions of said second extendable member.
31. A method according to Claim 30,further comprising the steps of:
retracting said second extendable member in a proximal direction; and releasing said detachable element from said first extendable member.
retracting said second extendable member in a proximal direction; and releasing said detachable element from said first extendable member.
32. A device useful for guiding a length of ligation material around an anatomical feature comprising:
a cannula including a hollow interior, a distal end, and a fenestration in the cannula proximal of the distal end;
a hollow arm positioned in the cannula at the fenestration, the hollow arm including a rotatable pivot by which the arm is mounted to the cannula, the arm being rotatable from a retracted orientation with the arm positioned inside the cannula and a deployed orientation with a portion of the arm rotated about the pivot and through the fenestration;
at least one wire connected to the arm and extending proximally;
wherein when the at least one wire is pulled proximally, the arm is rotated about the pivot into the deployed orientation.
a cannula including a hollow interior, a distal end, and a fenestration in the cannula proximal of the distal end;
a hollow arm positioned in the cannula at the fenestration, the hollow arm including a rotatable pivot by which the arm is mounted to the cannula, the arm being rotatable from a retracted orientation with the arm positioned inside the cannula and a deployed orientation with a portion of the arm rotated about the pivot and through the fenestration;
at least one wire connected to the arm and extending proximally;
wherein when the at least one wire is pulled proximally, the arm is rotated about the pivot into the deployed orientation.
33. A device in accordance with Claim 31, wherein said at least one wire comprises:
a first pullwire connected to the arm on a first side of the arm and extending proximally;
a second pullwire connected to the arm on a second side of the arm opposite the first side of the arm and extending proximally; and wherein when the second pullwire is pulled proximally, the arm is rotated about the pivot into the retracted orientation.
a first pullwire connected to the arm on a first side of the arm and extending proximally;
a second pullwire connected to the arm on a second side of the arm opposite the first side of the arm and extending proximally; and wherein when the second pullwire is pulled proximally, the arm is rotated about the pivot into the retracted orientation.
34. A device in accordance with Claim 33, further comprising a yolk mounted in the cannula, the second pullwire passing around the yolk, the yolk acting as a bearing surface for the pullwire.
35. A device in accordance with Claim 34, wherein the yolk comprises:
a pair of arms secured to the cannula; and a curved middle portion extending between the yolk arms.
a pair of arms secured to the cannula; and a curved middle portion extending between the yolk arms.
36. A device in accordance with Claim 34, wherein the yolk is positioned distally of the arm pivot.
37. A device in accordance with Claim 32, wherein the cannula further comprises a wire port proximal of the fenestration and on the same side of the cannula as the fenestration, the at least one wire extending through the wire port.
38. A device in accordance with Claim 37, wherein the cannula further comprises a trough in the exterior of the cannula and extending between the wire port and the fenestration.
39. A device in accordance with Claim 32, further comprising:
a pair of flexible and flat wire guides connected to the cannula and extending distally into the arm.
a pair of flexible and flat wire guides connected to the cannula and extending distally into the arm.
40. A device in accordance with Claim 39, wherein the wire guides have distal ends which are not secured to the arm.
41. A device in accordance with Claim 39, wherein the arm further comprises a cutout portion, the wire guides extending through the cutout portion when the arm is in the deployed orientation.
42. A device in accordance with Claim 39, further comprising a guide tube mounted in the cannula, the wire guides including proximal ends secured to the guide tube, the at least one wire extending between the guide tube and the cannula.
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US09/713,020 | 2000-11-16 | ||
US09/713,020 US6638286B1 (en) | 2000-11-16 | 2000-11-16 | Doppler directed suture ligation device and method |
PCT/US2001/027792 WO2002039905A1 (en) | 2000-11-16 | 2001-11-01 | Doppler directed suture ligation device and method |
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CA2437475A1 true CA2437475A1 (en) | 2002-05-23 |
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CA002437475A Abandoned CA2437475A1 (en) | 2000-11-16 | 2001-11-01 | Doppler directed suture ligation device and method |
CA002431649A Expired - Fee Related CA2431649C (en) | 2000-11-16 | 2001-11-01 | Doppler directed suture ligation device and method |
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CA002431649A Expired - Fee Related CA2431649C (en) | 2000-11-16 | 2001-11-01 | Doppler directed suture ligation device and method |
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Families Citing this family (213)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9149261B2 (en) | 2001-03-09 | 2015-10-06 | Boston Scientific Scimed, Inc. | Systems, methods and devices relating to delivery of medical implants |
US7087064B1 (en) | 2002-10-15 | 2006-08-08 | Advanced Cardiovascular Systems, Inc. | Apparatuses and methods for heart valve repair |
US7335213B1 (en) * | 2002-11-15 | 2008-02-26 | Abbott Cardiovascular Systems Inc. | Apparatus and methods for heart valve repair |
US7485143B2 (en) | 2002-11-15 | 2009-02-03 | Abbott Cardiovascular Systems Inc. | Apparatuses and methods for heart valve repair |
US9149602B2 (en) | 2005-04-22 | 2015-10-06 | Advanced Cardiovascular Systems, Inc. | Dual needle delivery system |
US7404824B1 (en) | 2002-11-15 | 2008-07-29 | Advanced Cardiovascular Systems, Inc. | Valve aptation assist device |
US8187324B2 (en) | 2002-11-15 | 2012-05-29 | Advanced Cardiovascular Systems, Inc. | Telescoping apparatus for delivering and adjusting a medical device in a vessel |
US20060069398A1 (en) * | 2003-02-26 | 2006-03-30 | Yutaka Suzuki | Medical instrument |
US7662099B2 (en) * | 2003-06-30 | 2010-02-16 | Ethicon, Inc. | Method and instrumentation to sense thermal lesion formation by ultrasound imaging |
US7998112B2 (en) | 2003-09-30 | 2011-08-16 | Abbott Cardiovascular Systems Inc. | Deflectable catheter assembly and method of making same |
US7731726B2 (en) * | 2003-12-03 | 2010-06-08 | St. Jude Medical Puerto Rico Llc | Suture based vascular closure apparatus and method incorporating a pre-tied knot |
KR101198495B1 (en) | 2004-03-02 | 2012-11-06 | 코비디엔 아게 | Medical suturing tool |
JP4212494B2 (en) * | 2004-03-02 | 2009-01-21 | 日本シャーウッド株式会社 | Medical suture tool |
JP4669315B2 (en) * | 2005-04-21 | 2011-04-13 | 日本シャーウッド株式会社 | Organ fixture and organ fixture set |
JP2006102255A (en) * | 2004-10-06 | 2006-04-20 | Nippon Sherwood Medical Industries Ltd | Connecting structure of infusion line and connector with the connecting structure |
US9801708B2 (en) | 2004-11-05 | 2017-10-31 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US7909851B2 (en) | 2006-02-03 | 2011-03-22 | Biomet Sports Medicine, Llc | Soft tissue repair device and associated methods |
US7749250B2 (en) | 2006-02-03 | 2010-07-06 | Biomet Sports Medicine, Llc | Soft tissue repair assembly and associated method |
US7658751B2 (en) | 2006-09-29 | 2010-02-09 | Biomet Sports Medicine, Llc | Method for implanting soft tissue |
US8361113B2 (en) | 2006-02-03 | 2013-01-29 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US8118836B2 (en) | 2004-11-05 | 2012-02-21 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US8128658B2 (en) | 2004-11-05 | 2012-03-06 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to bone |
US8298262B2 (en) | 2006-02-03 | 2012-10-30 | Biomet Sports Medicine, Llc | Method for tissue fixation |
US8088130B2 (en) | 2006-02-03 | 2012-01-03 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US9017381B2 (en) | 2007-04-10 | 2015-04-28 | Biomet Sports Medicine, Llc | Adjustable knotless loops |
US8303604B2 (en) | 2004-11-05 | 2012-11-06 | Biomet Sports Medicine, Llc | Soft tissue repair device and method |
US8137382B2 (en) | 2004-11-05 | 2012-03-20 | Biomet Sports Medicine, Llc | Method and apparatus for coupling anatomical features |
US7905904B2 (en) * | 2006-02-03 | 2011-03-15 | Biomet Sports Medicine, Llc | Soft tissue repair device and associated methods |
US7918795B2 (en) | 2005-02-02 | 2011-04-05 | Gynesonics, Inc. | Method and device for uterine fibroid treatment |
US7753935B2 (en) * | 2005-04-29 | 2010-07-13 | Vivasure Medical Limited | Interventional medical closure device |
US20090043295A1 (en) * | 2005-06-06 | 2009-02-12 | Ams Research Corporation | Fibroid Treatment Methods and Devices |
US20060276808A1 (en) * | 2005-06-06 | 2006-12-07 | Arnal Kevin R | Minimally Invasive Methods and Apparatus for Accessing and Ligating Uterine Arteries with Sutures |
AU2006254973A1 (en) | 2005-06-06 | 2006-12-14 | Ams Research Corporation | Devices and methods for ligating uterine arteries |
EP1909703A4 (en) | 2005-08-04 | 2011-01-12 | Bard Inc C R | Pelvic implant systems and methods |
JP4488981B2 (en) * | 2005-08-23 | 2010-06-23 | 日本シャーウッド株式会社 | Extractor and medical suture tool set |
US7588583B2 (en) | 2005-09-14 | 2009-09-15 | Rhaphis Medical, Inc. | Suturing device, system and method |
ES2470338T3 (en) | 2005-11-14 | 2014-06-23 | C.R. Bard, Inc. | Sling anchor system |
JP4614451B2 (en) * | 2005-12-26 | 2011-01-19 | 日本シャーウッド株式会社 | Medical suture tool |
US9357977B2 (en) | 2006-01-12 | 2016-06-07 | Gynesonics, Inc. | Interventional deployment and imaging system |
US11259825B2 (en) | 2006-01-12 | 2022-03-01 | Gynesonics, Inc. | Devices and methods for treatment of tissue |
US7874986B2 (en) | 2006-04-20 | 2011-01-25 | Gynesonics, Inc. | Methods and devices for visualization and ablation of tissue |
US10058342B2 (en) | 2006-01-12 | 2018-08-28 | Gynesonics, Inc. | Devices and methods for treatment of tissue |
US7815571B2 (en) | 2006-04-20 | 2010-10-19 | Gynesonics, Inc. | Rigid delivery systems having inclined ultrasound and needle |
US10517587B2 (en) | 2006-02-03 | 2019-12-31 | Biomet Sports Medicine, Llc | Method and apparatus for forming a self-locking adjustable loop |
US9538998B2 (en) | 2006-02-03 | 2017-01-10 | Biomet Sports Medicine, Llc | Method and apparatus for fracture fixation |
US9408599B2 (en) | 2006-02-03 | 2016-08-09 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US8597327B2 (en) | 2006-02-03 | 2013-12-03 | Biomet Manufacturing, Llc | Method and apparatus for sternal closure |
US8562647B2 (en) | 2006-09-29 | 2013-10-22 | Biomet Sports Medicine, Llc | Method and apparatus for securing soft tissue to bone |
US9078644B2 (en) | 2006-09-29 | 2015-07-14 | Biomet Sports Medicine, Llc | Fracture fixation device |
US8801783B2 (en) | 2006-09-29 | 2014-08-12 | Biomet Sports Medicine, Llc | Prosthetic ligament system for knee joint |
US8968364B2 (en) | 2006-02-03 | 2015-03-03 | Biomet Sports Medicine, Llc | Method and apparatus for fixation of an ACL graft |
US9149267B2 (en) | 2006-02-03 | 2015-10-06 | Biomet Sports Medicine, Llc | Method and apparatus for coupling soft tissue to a bone |
US8562645B2 (en) | 2006-09-29 | 2013-10-22 | Biomet Sports Medicine, Llc | Method and apparatus for forming a self-locking adjustable loop |
US11259792B2 (en) | 2006-02-03 | 2022-03-01 | Biomet Sports Medicine, Llc | Method and apparatus for coupling anatomical features |
US11311287B2 (en) | 2006-02-03 | 2022-04-26 | Biomet Sports Medicine, Llc | Method for tissue fixation |
US8652171B2 (en) | 2006-02-03 | 2014-02-18 | Biomet Sports Medicine, Llc | Method and apparatus for soft tissue fixation |
US8652172B2 (en) | 2006-02-03 | 2014-02-18 | Biomet Sports Medicine, Llc | Flexible anchors for tissue fixation |
US8936621B2 (en) | 2006-02-03 | 2015-01-20 | Biomet Sports Medicine, Llc | Method and apparatus for forming a self-locking adjustable loop |
US20070198035A1 (en) * | 2006-02-17 | 2007-08-23 | Threlkeld Judson E | Method and surgical instrument operable for percutaneous ligation of a vein or vessel |
US10595819B2 (en) | 2006-04-20 | 2020-03-24 | Gynesonics, Inc. | Ablation device with articulated imaging transducer |
US8206300B2 (en) | 2008-08-26 | 2012-06-26 | Gynesonics, Inc. | Ablation device with articulated imaging transducer |
US8876842B2 (en) * | 2006-05-22 | 2014-11-04 | Covidien Lp | Meniscal repair device |
CA2652512C (en) * | 2006-05-22 | 2016-04-05 | Scandius Biomedical, Inc. | Method and apparatus for meniscal repair |
ATE518484T1 (en) * | 2006-05-31 | 2011-08-15 | Covidien Ag | MEDICAL SUTURE INSTRUMENT WITH GRIPPER DEVICE |
US20090093758A1 (en) * | 2006-07-24 | 2009-04-09 | Yossi Gross | Fibroid treatment apparatus and method |
US8480559B2 (en) | 2006-09-13 | 2013-07-09 | C. R. Bard, Inc. | Urethral support system |
US8672969B2 (en) | 2006-09-29 | 2014-03-18 | Biomet Sports Medicine, Llc | Fracture fixation device |
US11259794B2 (en) | 2006-09-29 | 2022-03-01 | Biomet Sports Medicine, Llc | Method for implanting soft tissue |
US9918826B2 (en) | 2006-09-29 | 2018-03-20 | Biomet Sports Medicine, Llc | Scaffold for spring ligament repair |
US8500818B2 (en) | 2006-09-29 | 2013-08-06 | Biomet Manufacturing, Llc | Knee prosthesis assembly with ligament link |
JP4536698B2 (en) * | 2006-10-05 | 2010-09-01 | 日本シャーウッド株式会社 | Medical suture tool |
US20080114382A1 (en) * | 2006-11-03 | 2008-05-15 | Ams Research Corporation | Uterine Artery Ligation Devices and Methods |
US7655004B2 (en) | 2007-02-15 | 2010-02-02 | Ethicon Endo-Surgery, Inc. | Electroporation ablation apparatus, system, and method |
JP4565576B2 (en) | 2007-02-20 | 2010-10-20 | 日本シャーウッド株式会社 | Puncture needle assist tool |
US20080221437A1 (en) * | 2007-03-09 | 2008-09-11 | Agro Mark A | Steerable snare for use in the colon and method for the same |
WO2008113076A2 (en) | 2007-03-15 | 2008-09-18 | Rhaphis Medical, Inc. | Limited access suturing devices, system, and methods |
US8075572B2 (en) * | 2007-04-26 | 2011-12-13 | Ethicon Endo-Surgery, Inc. | Surgical suturing apparatus |
US8100922B2 (en) | 2007-04-27 | 2012-01-24 | Ethicon Endo-Surgery, Inc. | Curved needle suturing tool |
US20090157064A1 (en) * | 2007-05-11 | 2009-06-18 | Hodel Michael R | RFID System and Method Therefor |
US9486286B2 (en) | 2007-05-14 | 2016-11-08 | Boston Scientific Scimed, Inc. | Medical laser user interface |
WO2008152617A2 (en) | 2007-06-15 | 2008-12-18 | Zerusa Limited | A closure device |
US8702731B2 (en) | 2007-07-03 | 2014-04-22 | Ceterix Orthopaedics, Inc. | Suturing and repairing tissue using in vivo suture loading |
US8465505B2 (en) | 2011-05-06 | 2013-06-18 | Ceterix Orthopaedics, Inc. | Suture passer devices and methods |
US9211119B2 (en) | 2007-07-03 | 2015-12-15 | Ceterix Orthopaedics, Inc. | Suture passers and methods of passing suture |
US9861354B2 (en) | 2011-05-06 | 2018-01-09 | Ceterix Orthopaedics, Inc. | Meniscus repair |
US8911456B2 (en) | 2007-07-03 | 2014-12-16 | Ceterix Orthopaedics, Inc. | Methods and devices for preventing tissue bridging while suturing |
US8500809B2 (en) | 2011-01-10 | 2013-08-06 | Ceterix Orthopaedics, Inc. | Implant and method for repair of the anterior cruciate ligament |
US9314234B2 (en) | 2007-07-03 | 2016-04-19 | Ceterix Orthopaedics, Inc. | Pre-tied surgical knots for use with suture passers |
US8663253B2 (en) | 2007-07-03 | 2014-03-04 | Ceterix Orthopaedics, Inc. | Methods of meniscus repair |
US10441273B2 (en) | 2007-07-03 | 2019-10-15 | Ceterix Orthopaedics, Inc. | Pre-tied surgical knots for use with suture passers |
MX2010001019A (en) * | 2007-07-26 | 2010-08-10 | Alpha Scient Corp | Surgical suturing device, method and tools used therewith. |
US9226748B2 (en) * | 2007-07-26 | 2016-01-05 | Alpha Scientific Corporation | Surgical suturing device, method and tools used therewith |
US20090043317A1 (en) * | 2007-08-08 | 2009-02-12 | Cavanaugh Brian J | Method and apparatus for delivery of a ligating suture |
WO2009025766A2 (en) * | 2007-08-18 | 2009-02-26 | Spectral Energetics | A noninvasive sensor system and method for detection of internal pathologic conditions |
US20090054915A1 (en) * | 2007-08-23 | 2009-02-26 | Peter Meier | Obstruction of uterine arteries to treat uterine fibroids using mechanical instruments to twist the vessels |
US20090054916A1 (en) * | 2007-08-23 | 2009-02-26 | Peter Meier | Clip-based method for treatment of uterine fibroids by obstruction of the uterine arteries |
US20090062827A1 (en) * | 2007-08-31 | 2009-03-05 | Peter Meier | Vacuum-based method for obstruction of uterine arteries to treat uterine fibroids |
US8262655B2 (en) | 2007-11-21 | 2012-09-11 | Ethicon Endo-Surgery, Inc. | Bipolar forceps |
US8568410B2 (en) | 2007-08-31 | 2013-10-29 | Ethicon Endo-Surgery, Inc. | Electrical ablation surgical instruments |
US8579897B2 (en) | 2007-11-21 | 2013-11-12 | Ethicon Endo-Surgery, Inc. | Bipolar forceps |
US8088072B2 (en) | 2007-10-12 | 2012-01-03 | Gynesonics, Inc. | Methods and systems for controlled deployment of needles in tissue |
US8480657B2 (en) | 2007-10-31 | 2013-07-09 | Ethicon Endo-Surgery, Inc. | Detachable distal overtube section and methods for forming a sealable opening in the wall of an organ |
US20090112059A1 (en) | 2007-10-31 | 2009-04-30 | Nobis Rudolph H | Apparatus and methods for closing a gastrotomy |
WO2009061504A1 (en) | 2007-11-05 | 2009-05-14 | Revolutionary Surgical Device, Llc | Suture passing instrument and method |
US8206280B2 (en) | 2007-11-13 | 2012-06-26 | C. R. Bard, Inc. | Adjustable tissue support member |
US8603112B2 (en) * | 2007-11-30 | 2013-12-10 | Easylap Ltd. | Suturing assembly and method |
AU2009221903B2 (en) * | 2008-03-04 | 2015-07-02 | Cayenne Medical, Inc. | Arthroscopic meniscal repair systems and methods |
US8262680B2 (en) | 2008-03-10 | 2012-09-11 | Ethicon Endo-Surgery, Inc. | Anastomotic device |
US8679003B2 (en) | 2008-05-30 | 2014-03-25 | Ethicon Endo-Surgery, Inc. | Surgical device and endoscope including same |
US8317806B2 (en) | 2008-05-30 | 2012-11-27 | Ethicon Endo-Surgery, Inc. | Endoscopic suturing tension controlling and indication devices |
US8070759B2 (en) | 2008-05-30 | 2011-12-06 | Ethicon Endo-Surgery, Inc. | Surgical fastening device |
US8652150B2 (en) | 2008-05-30 | 2014-02-18 | Ethicon Endo-Surgery, Inc. | Multifunction surgical device |
US8771260B2 (en) | 2008-05-30 | 2014-07-08 | Ethicon Endo-Surgery, Inc. | Actuating and articulating surgical device |
US8114072B2 (en) | 2008-05-30 | 2012-02-14 | Ethicon Endo-Surgery, Inc. | Electrical ablation device |
US8906035B2 (en) | 2008-06-04 | 2014-12-09 | Ethicon Endo-Surgery, Inc. | Endoscopic drop off bag |
US8403926B2 (en) | 2008-06-05 | 2013-03-26 | Ethicon Endo-Surgery, Inc. | Manually articulating devices |
JP5185706B2 (en) * | 2008-06-24 | 2013-04-17 | 日本コヴィディエン株式会社 | Puncture needle assist tool |
US8361112B2 (en) | 2008-06-27 | 2013-01-29 | Ethicon Endo-Surgery, Inc. | Surgical suture arrangement |
US8262563B2 (en) | 2008-07-14 | 2012-09-11 | Ethicon Endo-Surgery, Inc. | Endoscopic translumenal articulatable steerable overtube |
US8888792B2 (en) | 2008-07-14 | 2014-11-18 | Ethicon Endo-Surgery, Inc. | Tissue apposition clip application devices and methods |
US8211125B2 (en) | 2008-08-15 | 2012-07-03 | Ethicon Endo-Surgery, Inc. | Sterile appliance delivery device for endoscopic procedures |
US8529563B2 (en) | 2008-08-25 | 2013-09-10 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices |
US8241204B2 (en) | 2008-08-29 | 2012-08-14 | Ethicon Endo-Surgery, Inc. | Articulating end cap |
US8480689B2 (en) | 2008-09-02 | 2013-07-09 | Ethicon Endo-Surgery, Inc. | Suturing device |
US8409200B2 (en) | 2008-09-03 | 2013-04-02 | Ethicon Endo-Surgery, Inc. | Surgical grasping device |
US8114119B2 (en) | 2008-09-09 | 2012-02-14 | Ethicon Endo-Surgery, Inc. | Surgical grasping device |
US9526502B2 (en) * | 2008-09-10 | 2016-12-27 | Unique Surgical Innovations Llc | Surgical string applicator for anastomosis surgery |
US8337394B2 (en) | 2008-10-01 | 2012-12-25 | Ethicon Endo-Surgery, Inc. | Overtube with expandable tip |
AU2009308484B2 (en) * | 2008-10-21 | 2013-03-07 | Cayenne Medical, Inc. | Meniscal repair systems |
US8394112B2 (en) * | 2008-10-22 | 2013-03-12 | Cayenne Medical, Inc. | Arthroscopic suture passing devices and methods |
US8157834B2 (en) | 2008-11-25 | 2012-04-17 | Ethicon Endo-Surgery, Inc. | Rotational coupling device for surgical instrument with flexible actuators |
US8172772B2 (en) | 2008-12-11 | 2012-05-08 | Ethicon Endo-Surgery, Inc. | Specimen retrieval device |
US8828031B2 (en) | 2009-01-12 | 2014-09-09 | Ethicon Endo-Surgery, Inc. | Apparatus for forming an anastomosis |
US8361066B2 (en) | 2009-01-12 | 2013-01-29 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices |
WO2010083110A1 (en) * | 2009-01-16 | 2010-07-22 | Rhaphis Medical, Inc. | Surgical suturing latch |
US9226772B2 (en) | 2009-01-30 | 2016-01-05 | Ethicon Endo-Surgery, Inc. | Surgical device |
US8037591B2 (en) | 2009-02-02 | 2011-10-18 | Ethicon Endo-Surgery, Inc. | Surgical scissors |
US9445806B2 (en) * | 2009-02-06 | 2016-09-20 | Karl Storz Gmbh & Co. Kg | Suture holder delivery system |
US8262574B2 (en) | 2009-02-27 | 2012-09-11 | Gynesonics, Inc. | Needle and tine deployment mechanism |
US8177796B2 (en) | 2009-03-23 | 2012-05-15 | Linvatec Corporation | Suture passing apparatus and method |
CA2760666A1 (en) * | 2009-05-01 | 2010-11-04 | Cook Medical Technologies Llc | Medical systems, devices and methods for suturing perforations |
US9486208B2 (en) * | 2009-05-01 | 2016-11-08 | Cayenne Medical, Inc. | Meniscal repair systems and methods |
US8545523B2 (en) * | 2009-06-15 | 2013-10-01 | Easylap Ltd. | Tissue repair method and kit |
WO2011006067A1 (en) | 2009-07-09 | 2011-01-13 | Ams Research Corporation | Apparatus and methods of treatment of pathologic proliferative conditions uterine tissue |
DK200970073A (en) * | 2009-07-22 | 2011-01-23 | Coloplast As | Suturing system and assembly |
US8403953B2 (en) * | 2009-07-27 | 2013-03-26 | Fibro Control, Inc. | Balloon with rigid tube for occluding the uterine artery |
US20110098704A1 (en) | 2009-10-28 | 2011-04-28 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices |
US8608652B2 (en) | 2009-11-05 | 2013-12-17 | Ethicon Endo-Surgery, Inc. | Vaginal entry surgical devices, kit, system, and method |
US9011454B2 (en) | 2009-11-09 | 2015-04-21 | Ceterix Orthopaedics, Inc. | Suture passer with radiused upper jaw |
US9848868B2 (en) | 2011-01-10 | 2017-12-26 | Ceterix Orthopaedics, Inc. | Suture methods for forming locking loops stitches |
JP5719374B2 (en) | 2009-11-09 | 2015-05-20 | セテリックス オーソピーディクス インコーポレイテッド | Device, system, and method for repairing a meniscus |
US11744575B2 (en) | 2009-11-09 | 2023-09-05 | Ceterix Orthopaedics, Inc. | Suture passer devices and methods |
US8496574B2 (en) | 2009-12-17 | 2013-07-30 | Ethicon Endo-Surgery, Inc. | Selectively positionable camera for surgical guide tube assembly |
US8353487B2 (en) | 2009-12-17 | 2013-01-15 | Ethicon Endo-Surgery, Inc. | User interface support devices for endoscopic surgical instruments |
US8506564B2 (en) | 2009-12-18 | 2013-08-13 | Ethicon Endo-Surgery, Inc. | Surgical instrument comprising an electrode |
US9028483B2 (en) | 2009-12-18 | 2015-05-12 | Ethicon Endo-Surgery, Inc. | Surgical instrument comprising an electrode |
US11357486B2 (en) | 2009-12-30 | 2022-06-14 | Vivasure Medical Limited | Closure system and uses thereof |
US9005198B2 (en) | 2010-01-29 | 2015-04-14 | Ethicon Endo-Surgery, Inc. | Surgical instrument comprising an electrode |
EP2552325A4 (en) | 2010-03-31 | 2015-05-27 | Siesta Medical Inc | Suture passer systems and methods for tongue or other tissue suspension and compression |
US20110306992A1 (en) | 2010-06-09 | 2011-12-15 | C.R. Bard, Inc. | Instruments for delivering transfascial sutures, transfascial suture assemblies, and methods of transfascial suturing |
US9149271B2 (en) * | 2010-11-22 | 2015-10-06 | The Board Of Trustees Of The Leland Stanford, Jr. University | Device and method for treatment of hemorrhoids |
US9060751B2 (en) | 2010-12-30 | 2015-06-23 | Vivasure Medical Limited | Surgical closure systems and methods |
US9913638B2 (en) | 2011-01-10 | 2018-03-13 | Ceterix Orthopaedics, Inc. | Transosteal anchoring methods for tissue repair |
US10092291B2 (en) | 2011-01-25 | 2018-10-09 | Ethicon Endo-Surgery, Inc. | Surgical instrument with selectively rigidizable features |
US9314620B2 (en) | 2011-02-28 | 2016-04-19 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices and methods |
US9254169B2 (en) | 2011-02-28 | 2016-02-09 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices and methods |
US9233241B2 (en) | 2011-02-28 | 2016-01-12 | Ethicon Endo-Surgery, Inc. | Electrical ablation devices and methods |
US9049987B2 (en) | 2011-03-17 | 2015-06-09 | Ethicon Endo-Surgery, Inc. | Hand held surgical device for manipulating an internal magnet assembly within a patient |
JP5738039B2 (en) * | 2011-03-31 | 2015-06-17 | 日本コヴィディエン株式会社 | Medical suture tool |
CA2838722C (en) | 2011-06-08 | 2019-04-02 | Suturenetics, Inc. | Offset jaw suturing device, system, and methods |
US8992550B2 (en) | 2011-07-20 | 2015-03-31 | Coloplast A/S | Suture system with capsule eyelet providing multiple suture tissue fixation |
US10524778B2 (en) | 2011-09-28 | 2020-01-07 | Ceterix Orthopaedics | Suture passers adapted for use in constrained regions |
US9826972B2 (en) | 2011-10-24 | 2017-11-28 | C.R. Bard, Inc. | Instruments for delivering transfascial sutures, transfascial suture assemblies and methods of transfascial suturing |
US9357991B2 (en) | 2011-11-03 | 2016-06-07 | Biomet Sports Medicine, Llc | Method and apparatus for stitching tendons |
US9039721B2 (en) * | 2011-11-07 | 2015-05-26 | C.R. Bard, Inc. | Instruments for delivering transfascial sutures and methods of transfascial suturing |
US9078648B2 (en) | 2011-11-07 | 2015-07-14 | C.R. Bard, Inc. | Instruments for delivering transfascial sutures and methods of transfascial suturing |
US9924938B2 (en) | 2011-11-07 | 2018-03-27 | C.R. Bard, Inc. | Instruments for delivering transfascial sutures and methods of transfascial suturing |
US9381013B2 (en) | 2011-11-10 | 2016-07-05 | Biomet Sports Medicine, Llc | Method for coupling soft tissue to a bone |
US9357992B2 (en) | 2011-11-10 | 2016-06-07 | Biomet Sports Medicine, Llc | Method for coupling soft tissue to a bone |
US8523808B2 (en) * | 2011-11-18 | 2013-09-03 | Biosense Webster (Israel), Ltd. | Medical device control handle with independent self holding puller wire actuators |
US8535339B2 (en) | 2011-12-18 | 2013-09-17 | Via Surgical Ltd. | Apparatus and method for suturing |
US8986199B2 (en) | 2012-02-17 | 2015-03-24 | Ethicon Endo-Surgery, Inc. | Apparatus and methods for cleaning the lens of an endoscope |
US9737286B2 (en) | 2012-02-29 | 2017-08-22 | Vivasure Medical Limited | Implants and methods for percutaneous perforation closure |
US9427255B2 (en) | 2012-05-14 | 2016-08-30 | Ethicon Endo-Surgery, Inc. | Apparatus for introducing a steerable camera assembly into a patient |
US9888913B2 (en) | 2012-05-31 | 2018-02-13 | Via Surgical Ltd. | Variable depth surgical fixation |
US9078662B2 (en) | 2012-07-03 | 2015-07-14 | Ethicon Endo-Surgery, Inc. | Endoscopic cap electrode and method for using the same |
US9545290B2 (en) | 2012-07-30 | 2017-01-17 | Ethicon Endo-Surgery, Inc. | Needle probe guide |
US10314649B2 (en) | 2012-08-02 | 2019-06-11 | Ethicon Endo-Surgery, Inc. | Flexible expandable electrode and method of intraluminal delivery of pulsed power |
US9572623B2 (en) | 2012-08-02 | 2017-02-21 | Ethicon Endo-Surgery, Inc. | Reusable electrode and disposable sheath |
US9277957B2 (en) | 2012-08-15 | 2016-03-08 | Ethicon Endo-Surgery, Inc. | Electrosurgical devices and methods |
US9463014B2 (en) | 2012-09-07 | 2016-10-11 | Siesta Medical, Inc. | Tether line systems and methods for tongue or other tissue suspension or compression |
US10098527B2 (en) | 2013-02-27 | 2018-10-16 | Ethidcon Endo-Surgery, Inc. | System for performing a minimally invasive surgical procedure |
ES2684316T3 (en) | 2013-03-11 | 2018-10-02 | Via Surgical Ltd. | Quality indicator with surgical spinner |
US9636110B2 (en) | 2013-03-13 | 2017-05-02 | Alpha Scientific Corporation | Structural support incorporating multiple strands |
US9918827B2 (en) | 2013-03-14 | 2018-03-20 | Biomet Sports Medicine, Llc | Scaffold for spring ligament repair |
CA2906862A1 (en) | 2013-03-15 | 2014-09-18 | Alpha Scientific Corporation | Surgical suturing device with transverse engagement |
US9850013B2 (en) | 2013-03-15 | 2017-12-26 | Vivasure Medical Limited | Loading devices and methods for percutaneous perforation closure systems |
US9247935B2 (en) | 2013-09-23 | 2016-02-02 | Ceterix Orthopaedics, Inc. | Arthroscopic knot pusher and suture cutter |
WO2015095133A1 (en) | 2013-12-16 | 2015-06-25 | Ceterix Orthopaedics, Inc. | Automatically reloading suture passer devices having pre-tied knots and methods |
WO2015134763A1 (en) | 2014-03-05 | 2015-09-11 | Siesta Medical, Inc. | Systems and methods for tissue suspension and compression |
EP2929841B1 (en) | 2014-04-08 | 2017-11-15 | Ceterix Orthopaedics, Inc. | Suture passers adapted for use in constrained regions |
WO2016096932A1 (en) | 2014-12-15 | 2016-06-23 | Vivasure Medical Limited | Closure apparatus with flexible sealable member and flexible support member |
EP3232939B1 (en) | 2014-12-15 | 2020-09-23 | Vivasure Medical Limited | Implantable sealable member with mesh layer |
WO2016170423A1 (en) | 2015-04-23 | 2016-10-27 | Via Surgical Ltd. | Surgical fastener delivery and locking mechanism |
US10226245B2 (en) | 2015-07-21 | 2019-03-12 | Ceterix Orthopaedics, Inc. | Automatically reloading suture passer devices that prevent entanglement |
US10405853B2 (en) | 2015-10-02 | 2019-09-10 | Ceterix Orthpaedics, Inc. | Knot tying accessory |
US10251639B1 (en) * | 2015-11-20 | 2019-04-09 | Ronald Yamada | Meniscus repair system |
WO2017102941A1 (en) | 2015-12-15 | 2017-06-22 | Vivasure Medical Limited | Arteriotomy closure apparatus with slotted shoe for advantageous pressure distribution |
US10300287B2 (en) * | 2016-06-27 | 2019-05-28 | Medtronic, Inc. | Delivery systems for implantable medical devices, and associated tethering assemblies and methods |
JP7237829B2 (en) | 2016-11-11 | 2023-03-13 | ガイネソニックス, インコーポレイテッド | Dynamic interaction of tissue controlled treatment with tissue and/or treatment data and their comparison |
US10934923B2 (en) | 2019-01-09 | 2021-03-02 | Caterpillar Inc. | Heat shield assembly for shielding a wire harness |
US11617573B2 (en) | 2019-09-06 | 2023-04-04 | Boston Scientific Scimed Inc. | Devices and methods for suturing tissue |
US20210322003A1 (en) * | 2020-04-16 | 2021-10-21 | Covidien Lp | Endoscopic stitching device for single hand operation |
Family Cites Families (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3209753A (en) | 1962-05-04 | 1965-10-05 | Donald B Hawkins | Intestinal clamps and the like |
US3411505A (en) | 1965-12-15 | 1968-11-19 | Paul D. Nobis | Device for interrupting arterial flow |
US4428374A (en) | 1978-12-20 | 1984-01-31 | Auburn Robert M | Umbilical cord clamping assembly |
US4292960A (en) | 1979-04-30 | 1981-10-06 | Rca Corporation | Apparatus and method for application of radioactive and microwave energy to the body |
US4509528A (en) | 1981-12-16 | 1985-04-09 | Harvinder Sahota | Hemostat with blood flow sensor |
US4428379A (en) | 1982-01-07 | 1984-01-31 | Technicare Corporation | Passive ultrasound needle probe locator |
US5370675A (en) | 1992-08-12 | 1994-12-06 | Vidamed, Inc. | Medical probe device and method |
US4650466A (en) | 1985-11-01 | 1987-03-17 | Angiobrade Partners | Angioplasty device |
US4991588A (en) * | 1986-07-21 | 1991-02-12 | Pfizer Hospital Products Group, Inc. | Doppler guide wire |
US4757823A (en) | 1987-01-27 | 1988-07-19 | Hofmeister John F | Method and apparatus for measuring uterine blood flow |
US4994069A (en) | 1988-11-02 | 1991-02-19 | Target Therapeutics | Vaso-occlusion coil and method |
US5201314A (en) | 1989-03-09 | 1993-04-13 | Vance Products Incorporated | Echogenic devices, material and method |
US5081997A (en) | 1989-03-09 | 1992-01-21 | Vance Products Incorporated | Echogenic devices, material and method |
US5289831A (en) | 1989-03-09 | 1994-03-01 | Vance Products Incorporated | Surface-treated stent, catheter, cannula, and the like |
US5749879A (en) * | 1989-08-16 | 1998-05-12 | Medtronic, Inc. | Device or apparatus for manipulating matter |
US5108408A (en) | 1990-04-20 | 1992-04-28 | Lally James J | Uterine-ring hysterectomy clamp |
US5037433A (en) * | 1990-05-17 | 1991-08-06 | Wilk Peter J | Endoscopic suturing device and related method and suture |
US5100423A (en) | 1990-08-21 | 1992-03-31 | Medical Engineering & Development Institute, Inc. | Ablation catheter |
US5261409A (en) * | 1991-05-27 | 1993-11-16 | Sulzer Brothers Limited | Puncturing device for blood vessels |
US5226911A (en) | 1991-10-02 | 1993-07-13 | Target Therapeutics | Vasoocclusion coil with attached fibrous element(s) |
US5662680A (en) | 1991-10-18 | 1997-09-02 | Desai; Ashvin H. | Endoscopic surgical instrument |
US5713896A (en) | 1991-11-01 | 1998-02-03 | Medical Scientific, Inc. | Impedance feedback electrosurgical system |
US5704361A (en) * | 1991-11-08 | 1998-01-06 | Mayo Foundation For Medical Education And Research | Volumetric image ultrasound transducer underfluid catheter system |
CA2134071C (en) | 1992-04-23 | 1999-04-27 | Sew Wah Tay | Apparatus and method for sealing vascular punctures |
US5443470A (en) | 1992-05-01 | 1995-08-22 | Vesta Medical, Inc. | Method and apparatus for endometrial ablation |
US5336231A (en) | 1992-05-01 | 1994-08-09 | Adair Edwin Lloyd | Parallel channel fixation, repair and ligation suture device |
NL9201118A (en) | 1992-06-24 | 1994-01-17 | Leuven K U Res & Dev | TOOL KIT FOR LAPAROSCOPIC VAGINAL HYSTERECTOMY. |
US5672153A (en) | 1992-08-12 | 1997-09-30 | Vidamed, Inc. | Medical probe device and method |
AU4926193A (en) | 1992-09-21 | 1994-04-12 | Vitaphore Corporation | Embolization plugs for blood vessels |
CA2102084A1 (en) | 1992-11-09 | 1994-05-10 | Howard C. Topel | Surgical cutting instrument for coring tissue affixed thereto |
US5275166A (en) | 1992-11-16 | 1994-01-04 | Ethicon, Inc. | Method and apparatus for performing ultrasonic assisted surgical procedures |
US5336229A (en) * | 1993-02-09 | 1994-08-09 | Laparomed Corporation | Dual ligating and dividing apparatus |
US5383922A (en) | 1993-03-15 | 1995-01-24 | Medtronic, Inc. | RF lead fixation and implantable lead |
US5542944A (en) | 1993-04-19 | 1996-08-06 | Bhatta; Krishan M. | Surgical device and method |
GB9314640D0 (en) | 1993-07-15 | 1993-08-25 | Salim Aws S M | Tunnellimg catheter |
GB9314641D0 (en) | 1993-07-15 | 1993-08-25 | Salim Aws S M | Tunnelling umbrella |
US5496331A (en) * | 1993-07-28 | 1996-03-05 | Terumo Kabushiki Kaisha | Knot-forming instrument and method of forming knots |
US5858018A (en) | 1993-08-25 | 1999-01-12 | Apollo Camera, Llc | Low profile tool for applying spring action ligation clips |
WO1995019148A1 (en) | 1994-01-18 | 1995-07-20 | Endovascular, Inc. | Apparatus and method for venous ligation |
DE59403873D1 (en) | 1994-03-07 | 1997-10-02 | Maurer Sa Ing A | Device for filtering fluid media |
US5458596A (en) | 1994-05-06 | 1995-10-17 | Dorsal Orthopedic Corporation | Method and apparatus for controlled contraction of soft tissue |
US5707349A (en) | 1994-05-09 | 1998-01-13 | Somnus Medical Technologies, Inc. | Method for treatment of air way obstructions |
US5672172A (en) | 1994-06-23 | 1997-09-30 | Vros Corporation | Surgical instrument with ultrasound pulse generator |
US5549624A (en) | 1994-06-24 | 1996-08-27 | Target Therapeutics, Inc. | Fibered vasooclusion coils |
US5697942A (en) | 1994-07-31 | 1997-12-16 | Palti; Yoram | Internal vascular clamp |
US6032673A (en) | 1994-10-13 | 2000-03-07 | Femrx, Inc. | Methods and devices for tissue removal |
US5702407A (en) * | 1994-11-29 | 1997-12-30 | Olympus Optical Co., Ltd. | Ligating apparatus |
US5588960A (en) | 1994-12-01 | 1996-12-31 | Vidamed, Inc. | Transurethral needle delivery device with cystoscope and method for treatment of urinary incontinence |
US5614204A (en) | 1995-01-23 | 1997-03-25 | The Regents Of The University Of California | Angiographic vascular occlusion agents and a method for hemostatic occlusion |
US6019724A (en) | 1995-02-22 | 2000-02-01 | Gronningsaeter; Aage | Method for ultrasound guidance during clinical procedures |
US5715832A (en) | 1995-02-28 | 1998-02-10 | Boston Scientific Corporation | Deflectable biopsy catheter |
US5665096A (en) * | 1995-03-07 | 1997-09-09 | Yoon; Inbae | Needle driving apparatus and methods of suturing tissue |
US5766135A (en) | 1995-03-08 | 1998-06-16 | Terwilliger; Richard A. | Echogenic needle tip |
US5817022A (en) | 1995-03-28 | 1998-10-06 | Sonometrics Corporation | System for displaying a 2-D ultrasound image within a 3-D viewing environment |
US5899861A (en) | 1995-03-31 | 1999-05-04 | Siemens Medical Systems, Inc. | 3-dimensional volume by aggregating ultrasound fields of view |
US5626607A (en) | 1995-04-03 | 1997-05-06 | Heartport, Inc. | Clamp assembly and method of use |
US5570692A (en) | 1995-05-19 | 1996-11-05 | Hayashi Denki Co. Ltd. | Ultrasonic doppler blood flow detector for hemorrhoid artery ligation |
US5658299A (en) * | 1995-07-20 | 1997-08-19 | Applied Medical Resources | Surgical ligating device and method for using same |
DE19528440C2 (en) | 1995-08-02 | 1998-09-10 | Harald Dr Med Kuebler | Surgical cutting instrument |
US5979453A (en) | 1995-11-09 | 1999-11-09 | Femrx, Inc. | Needle myolysis system for uterine fibriods |
US5716389A (en) | 1995-11-13 | 1998-02-10 | Walinsky; Paul | Cardiac ablation catheter arrangement with movable guidewire |
ATE247429T1 (en) | 1996-02-02 | 2003-09-15 | Transvascular Inc | SYSTEM FOR INTERSTITIAL TRANSVASCULAR SURGICAL PROCEDURES |
EP0921765B1 (en) | 1996-03-05 | 2007-05-02 | Vnus Medical Technologies, Inc. | Vascular catheter-based system for heating tissue |
US5691314A (en) | 1996-03-18 | 1997-11-25 | The Medical College Of Hampton Roads | Adjunctive therapy |
DE19706751A1 (en) | 1996-03-27 | 1997-10-02 | Valleylab Inc | Electrosurgical device for removing tissue in body areas |
US6077257A (en) | 1996-05-06 | 2000-06-20 | Vidacare, Inc. | Ablation of rectal and other internal body structures |
US6066139A (en) | 1996-05-14 | 2000-05-23 | Sherwood Services Ag | Apparatus and method for sterilization and embolization |
US5911691A (en) | 1996-05-21 | 1999-06-15 | Aloka Co., Ltd. | Ultrasound image processing apparatus and method of forming and displaying ultrasound images by the apparatus |
JPH09313487A (en) | 1996-05-29 | 1997-12-09 | Ge Yokogawa Medical Syst Ltd | Method and device for ultrasonic three-dimensional photographing |
US5720743A (en) | 1996-06-07 | 1998-02-24 | Bischof; John C. | Thermally insulating surgical probe |
IL119151A0 (en) | 1996-06-10 | 1996-11-14 | Influence Med Tech Ltd | Surgical suture insertion device and method for treatment of urinary stress incontinence using fixation to bone |
US5776129A (en) | 1996-06-12 | 1998-07-07 | Ethicon Endo-Surgery, Inc. | Endometrial ablation apparatus and method |
US5904651A (en) * | 1996-10-28 | 1999-05-18 | Ep Technologies, Inc. | Systems and methods for visualizing tissue during diagnostic or therapeutic procedures |
ATE279213T1 (en) | 1996-11-06 | 2004-10-15 | Sts Biopolymers Inc | COATING WITH GAS-CONTAINING CAVITIES TO AMPLIFY ULTRASONIC ECHOS |
US6106473A (en) | 1996-11-06 | 2000-08-22 | Sts Biopolymers, Inc. | Echogenic coatings |
US6035238A (en) | 1997-08-13 | 2000-03-07 | Surx, Inc. | Noninvasive devices, methods, and systems for shrinking of tissues |
US5797397A (en) | 1996-11-25 | 1998-08-25 | Hewlett-Packard Company | Ultrasound imaging system and method using intensity highlighting to facilitate tissue differentiation |
US5895386A (en) | 1996-12-20 | 1999-04-20 | Electroscope, Inc. | Bipolar coagulation apparatus and method for arthroscopy |
US5759154A (en) | 1996-12-23 | 1998-06-02 | C. R. Bard, Inc. | Print mask technique for echogenic enhancement of a medical device |
US6045508A (en) | 1997-02-27 | 2000-04-04 | Acuson Corporation | Ultrasonic probe, system and method for two-dimensional imaging or three-dimensional reconstruction |
US5910484A (en) | 1997-05-30 | 1999-06-08 | The General Hospital Corporation | Treatment of ischemic cardiac malfunction |
WO1999000057A1 (en) | 1997-06-27 | 1999-01-07 | Michigan Instruments, Inc. | Non-invasive aortic impingement |
US5895395A (en) * | 1997-07-17 | 1999-04-20 | Yeung; Teresa T. | Partial to full thickness suture device & method for endoscopic surgeries |
US5941889A (en) | 1997-10-14 | 1999-08-24 | Civco Medical Instruments Inc. | Multiple angle disposable needle guide system |
US6015541A (en) | 1997-11-03 | 2000-01-18 | Micro Therapeutics, Inc. | Radioactive embolizing compositions |
US6280441B1 (en) | 1997-12-15 | 2001-08-28 | Sherwood Services Ag | Apparatus and method for RF lesioning |
CN1127752C (en) | 1997-12-16 | 2003-11-12 | 皇家菲利浦电子有限公司 | High-pressure discharge lamp |
CA2323540C (en) | 1998-03-20 | 2004-12-07 | Scimed Life Systems, Inc. | Endoscopic suture systems |
US6261234B1 (en) | 1998-05-07 | 2001-07-17 | Diasonics Ultrasound, Inc. | Method and apparatus for ultrasound imaging with biplane instrument guidance |
AU4574599A (en) * | 1998-06-17 | 2000-01-05 | Inbae Yoon | Suturing instrument with integral imaging device and method for use thereof |
JP3331177B2 (en) * | 1998-07-29 | 2002-10-07 | 旭光学工業株式会社 | Sector scan ultrasound probe |
US5921933A (en) | 1998-08-17 | 1999-07-13 | Medtronic, Inc. | Medical devices with echogenic coatings |
US6425867B1 (en) | 1998-09-18 | 2002-07-30 | University Of Washington | Noise-free real time ultrasonic imaging of a treatment site undergoing high intensity focused ultrasound therapy |
US6013088A (en) | 1998-11-17 | 2000-01-11 | Karavidas; Theocharis | Surgical clamp with removable tips |
US6254601B1 (en) * | 1998-12-08 | 2001-07-03 | Hysterx, Inc. | Methods for occlusion of the uterine arteries |
US6231515B1 (en) | 1999-01-13 | 2001-05-15 | Scimed Life Systems, Inc. | Safety mechanism and method to prevent rotating imaging guide device from exiting a catheter |
EP1072282A1 (en) | 1999-07-19 | 2001-01-31 | EndoArt S.A. | Flow control device |
US6210330B1 (en) | 1999-08-04 | 2001-04-03 | Rontech Medical Ltd. | Apparatus, system and method for real-time endovaginal sonography guidance of intra-uterine, cervical and tubal procedures |
DE20022012U1 (en) | 2000-04-18 | 2001-05-10 | Hofstetter Alfons | Medical clamp |
-
2000
- 2000-11-16 US US09/713,020 patent/US6638286B1/en not_active Expired - Fee Related
-
2001
- 2001-11-01 WO PCT/US2001/027792 patent/WO2002039905A1/en not_active Application Discontinuation
- 2001-11-01 CA CA002437475A patent/CA2437475A1/en not_active Abandoned
- 2001-11-01 EP EP01979242A patent/EP1345534B1/en not_active Expired - Lifetime
- 2001-11-01 AU AU2002224319A patent/AU2002224319A1/en not_active Abandoned
- 2001-11-01 AT AT01979242T patent/ATE510501T1/en not_active IP Right Cessation
- 2001-11-01 EP EP01996335A patent/EP1343417A1/en not_active Withdrawn
- 2001-11-01 JP JP2002542281A patent/JP4094947B2/en not_active Expired - Lifetime
- 2001-11-01 JP JP2002542282A patent/JP2004513702A/en active Pending
- 2001-11-01 CA CA002431649A patent/CA2431649C/en not_active Expired - Fee Related
- 2001-11-01 AU AU2002211227A patent/AU2002211227A1/en not_active Abandoned
- 2001-11-01 ES ES01979242T patent/ES2364627T3/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP4094947B2 (en) | 2008-06-04 |
AU2002211227A1 (en) | 2002-05-27 |
EP1345534A1 (en) | 2003-09-24 |
WO2002039905A9 (en) | 2003-03-27 |
US6638286B1 (en) | 2003-10-28 |
CA2431649A1 (en) | 2002-05-23 |
ATE510501T1 (en) | 2011-06-15 |
EP1343417A1 (en) | 2003-09-17 |
EP1345534B1 (en) | 2011-05-25 |
ES2364627T3 (en) | 2011-09-08 |
AU2002224319A1 (en) | 2002-05-27 |
JP2004513702A (en) | 2004-05-13 |
CA2431649C (en) | 2007-01-02 |
EP1345534A4 (en) | 2008-04-23 |
JP2004520867A (en) | 2004-07-15 |
WO2002039905A1 (en) | 2002-05-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |