Providence Health & Services - Oregon

Oregon Health & Science University

Tricol Biomedical, Inc.

Hemcon Medical Technologies, Inc.

Hua Xie

Lisa A Buckley

Simon J McCarthy

Kenneth E Perry

Mattie R Jones

Kenneth P Perry

Lisa Lucchesi

Brintha Enestvedt

The present disclosure relates to a gastrointestinal delivery device of a chitosan dressing, where the delivery device is capable of stop bleeding, in particular in connection with TURP procedures. The delivery device may be used in all gastrointestinal bleeding applications and can be used with a biocompatible, foldable, thin profile, chitosan dressing. Various aspects of the device and its uses are provided herein.

Delivery systems for control of bleeding in transurethral prostatectomy

The present disclosure relates to a gastrointestinal delivery device of a dressing, where the delivery device is capable of fitting through a narrow channel before expanding and applying the dressing. The gastrointestinal delivery device may be used in all gastrointestinal bleeding applications and can be used with a biocompatible, foldable, thin profile, chitosan dressing. Various aspects of the device and its uses are provided herein.

Delivery systems for control of gastrointestinal bleeding

The present invention provides an absorbent wound dressing assembly that can be used to stanch, seal, or stabilize a site of tissue injury, tissue trauma, or tissue access. The wound dressing assembly is flexible so that it can be adapted and used to fit in narrow and small wound sites. Generally the wound dressing assembly comprises a flexible carrier material that is impregnated with a non-mammalian material for control of severe bleeding. The preferred non-mammalian material is poly [&#x3b2;-(1&#x2192;4)-2-amino-2-deoxy-D-glucopyranose] more commonly referred to as chitosan.

Wound dressing devices and methods

A bioprosthetic valve graft comprises a valve frame and valve flaps, the latter acting to open or close a valve aperture to directionally control fluid flow through the bioprosthesis. The bioprosthetic valve graft comprises method for suturelessly attaching a biomaterial suturelessly bonded to the A method for securing a biomaterial to a valve frame includes positioning a flexible valve frame defining an open area on a first major surface of a biomaterial sheet having a peripheral edge, wherein positioning serves to approximate the valve frame and the peripheral edge of the biomaterial sheet to form an at least first bonding locus; and suturelessly bonding the biomaterial to the valve frame at the at least first bonding locus. The method avoids the disadvantages associated with conventional sutures and substantially reduces medical complications in implantations.

Method for suturelessly attaching a biomaterial to an implantable bioprosthesis frame

A bioprosthetic stent graft is disclosed, having a stent frame and a biomaterial sheath suturelessly bonded to the stent frame. Sutureless bonding avoids sutures and substantially reducing medical complications in implantation of the stent graft. A device and method for manufacturing the stent graft further is disclosed. A mandrel is employed for shaping the stent graft, and means for irradiating the biomaterial effects sutureless bonding.

Method for manufacturing sutureless bioprosthetic stent

A bioprosthetic valve graft comprises a valve frame and valve flaps, the latter acting to open or close a valve aperture to directionally control fluid flow through the bioprosthesis. The bioprosthetic valve graft comprises a biomaterial suturelessly bonded to the valve frame, avoiding sutures and substantially reducing medical complications in implantations.

Bioprosthesis and method for suturelessly making same

An insertable stent is provided for joining together and facilitating healing of adjacent tissues. Typically, the tissues are mammalian tissues. The insertable stent is made from completely non-toxic, bio- and blood-compatible materials. Each of the tissues employed herein defines an internal cavity. The insertable stent body defines a bore. The bore permits fluid to pass through the insertable stent body. In use, the insertable stent body is introduced into the internal cavities of the tissues. The insertable stent body fits within the confines of, and in contact with, each of the adjacent tissues. Typically, at least a portion of the insertable stent body is fusible to the adjacent tissues for facilitating healing of these tissues.

Growing community of inventors

Portland, OR, United States of America

Hua Xie