Object: Provided is a dysphonia treatment tool in which a front surface piece is bent. Resolution means: A dysphonia treatment tool includes a plurality of clamping sections (1, 1) each including a front surface piece (1a) disposed from a cut end surface of thyroid cartilage incised to a front surface, and a rear surface piece (1b) disposed on a rear surface of the thyroid cartilage, and being fitted respectively to cut ends of the thyroid cartilage that are opposite each other, and a bridging section (2) linking the plurality of clamping sections (1, 1) to each other. The front surface piece (1a) is bent in an intermediation section between a base end and a distal end of the front surface piece (1a).

A prosthetic heart valve system may include a prosthetic heart valve, a tether having a first end configured to connect to the prosthetic heart valve and a second end, and a collapsible and expandable anchor. The anchor includes a center rim configured to couple to the second end of the tether. The anchor further includes a plurality of struts extending radially outward from the center rim forming an inner dome that is concave toward a heart when the anchor is in a resting configuration implanted on an apex of the heart. The anchor further includes a plurality of wings extending radially outward from the struts.

A wearable medical device assembly for therapeutic treatment of a person includes: a wearable medical device configured to be applied over a portion of the person; a first anchor and a second anchor each comprising an adhesive configured to affix the respective anchor to the person's skin; and an attachment system that selectively attaches the wearable medical device to the first anchor and the second anchor, wherein the attachment system permits the wearable medical device to be detached from, and re-attached to, one or both of the anchors while both of the anchors remain affixed to the person's skin

The present invention provides a jig for forming a dysphonia treatment tool, the jig being capable of bending a front piece in a position not through a hole. A jig 20C for forming a dysphonia treatment tool X by deformation, the dysphonia treatment tool X including: a plurality of clamping sections each having a front piece 1a disposed on a front surface of incised thyroid cartilage and a rear piece disposed on a rear surface of the thyroid cartilage, the clamping sections configured to be fit to respective cut ends of the thyroid cartilage facing each other; and a bridging section linking the clamping sections to each other, the front piece having a hole 3 formed therein, the forming jig includes a clip section 22 having a pair of maintaining sections 21a, 21b configured to sandwich the front piece 1a from both surfaces to cover at least a portion of the hole 3.

Artificial heart valves, their manufacture, and methods of use are described. Generally, artificial heart valves can be deployed to replace or supplement defective heart valves in a patient. These artificial heart valves can comprise a frame with an inner skirt and leaflets. These inner skirt and leaflets can be generated from regenerative tissue to allow integration of the tissue with the body of a patient, while the frame can be generated from bioabsorbable material to allow dissolution of the frame over time. This combination of materials may allow for the artificial valve to grow with a patient and avoid costly and potentially dangerous replacement for patients receiving artificial valves.

In some examples, a medical system including a stent configured to be positioned within a ureter of a patient. The stent includes one or more distal petals and/or one or more proximal petals resiliently biased to deploy radially outwards from a stent body. The stent may be configured to position the distal petals in a kidney of a patient and position the proximal petals in a bladder of the patient. The distal petals and/or proximal petals may be configured to resist a migration of the stent within the ureter. The stent may include suture configured to cause the distal petals and/or proximal petals to substantially to collapse for withdrawal of the stent. The medical system may include a sheath to retain the distal petals and/or proximal petals in a collapsed condition during, for example, implantation in the patient.

A method of delivering a prosthetic mitral valve includes delivering a distal anchor from a delivery sheath such that the distal anchor self-expands inside a first heart chamber on a first side of the mitral valve annulus, pulling proximally on the distal anchor such that the distal anchor self-aligns within the mitral valve annulus and the distal anchor rests against tissue of the ventricular heart chamber, and delivering a proximal anchor from the delivery sheath to a second heart chamber on a second side of the mitral valve annulus such that the proximal anchor self-expands and moves towards the distal anchor to rest against tissue of the second heart chamber. The self-expansion of the proximal anchor captures tissue of the mitral valve annulus therebetween.

Methods are described herein for delivering a replacement valve to a native valve location. In one method, ventricular anchors of the replacement valve are released and allowed to reverse orientation while positioned in the atrium of a human heart. After reversing orientation, the ventricular anchors extend in a generally proximal direction. The ventricular anchors can then be advanced through the annulus into the ventricle and then moved back toward the atrium to capture native valve leaflets between the main body and the ventricular anchors of the replacement valve. In one modification, the ventricular anchors are allowed to reverse orientation at a level adjacent the annulus. The implantation methods described herein are preferably performed via a transseptal delivery approach or a transapical delivery approach.

Described is a catheter for being retained inside the body for extended periods, and a catheter mating device that can connect to the catheter to move the catheter inside of the body or remove it from the body. The catheter mating device has a stem with an apparatus at its distal end. The apparatus is moveable between a first position and a second position. When in its first position, the distal end is configured to fit in the proximal end of the catheter. When in its second position, the distal end engages the proximal end of the catheter and connects the catheter mating device to the catheter.

Some embodiments described herein include a heart valve replacement system that may be delivered to a targeted native heart valve site via one or more delivery catheters. In some embodiments, a prosthetic heart valve of the system includes structural features that securely anchor the prosthetic heart valve to the site of the native heart valve. Such structural features can provide robust migration resistance. In particular implementations, the prosthetic heart valves occupy a smaller delivery profile, thereby facilitating a smaller delivery catheter for advancement to the heart.