Abstract:
A guide conduit for facilitating insertion of flexible instruments into body lumens, the conduit defining a lumen extending from an opening at a proximal end of the conduit to a distal opening at the distal end of the conduit, the conduit comprises an outer layer forming a substantially smooth outer surface and a plastically deformable layer radially within the outer layer, the plastically deformable inner layer constructed to maintain its shape when subjected to a force below a predetermined threshold level and to assume a new shape when subjected to a bending force greater than the threshold level, wherein the threshold level is selected to be greater than a range of forces to which the conduit will be subjected by instruments inserted therethrough.
Abstract:
Endoluminally delivered tissue patches and related systems and methods for delivering the tissue patches for treating lesions of the alimentary tract are disclosed. A tissue patch includes a substrate, a tissue implant attached to the substrate, and a protective liner covering at least a portion of the tissue implant. A method includes providing a tissue patch having a tissue implant attached to a substrate and a protective liner covering at least a portion of the tissue implant. The tissue patch is formed into a contracted state and inserted into a lumen containing the lesion. The tissue patch then is positioned in the vicinity of the lesion. After removing the protective liner to reveal the tissue implant, the tissue implant is placed in the lesion.
Abstract:
A medical device includes a handle and a shaft having a working channel. A biopsy port at the exterior of the handle provides a path for instruments leading to the working channel. A conduit that runs through the handle for supplying fluids is also provided a path to the working channel. As compared between the path from the biopsy port to the working channel and the path from the conduit to the working channel, the path from the biopsy port to the working channel is the more direct path of the two.
Abstract:
Various embodiments of a medical device (e.g., tissue acquisition device) having a separate hemostasis capability and related methods of use are disclosed. The device may include an elongated tubular member having a proximal end and a distal end, a tissue cutting member proximate the distal end of the tubular member, and a hemostatic member proximate the distal end of the tubular member and adjacent the tissue cutting member. At least one of the tissue cutting member and the hemostatic member may be fixedly connected to the tubular member.
Abstract:
A porous weave of bioabsorbable filaments having an open mesh configuration is formed into an oblate shape having dimensions greater than the esophageal opening and gastric outlet of a stomach. The resulting prosthesis is deployed in the stomach and is of a size to be retained in the proximate portion thereof for exerting pressure on the upper fundus. The prosthesis limits the amount of food that may be held within the stomach, and exerts pressure on the fundus to create a sensation of being full, resulting in weight loss.
Abstract:
A stenting system for insertion into the lumen of a body duct or vessel for delivering a therapeutic agent to a treatment site on the duct or vessel. The stenting system includes an a tubular stent member having a lumen there through to allow the passage of material, an outer membrane attached to the stent at least a portion of which is porous to the therapeutic agent to allow the agent to pass to the treatment site, an inner membrane attached to the stent which is nonporous to the therapeutic agent to prevent the agent from entering the lumen of the stent, and a chamber located between the inner and outer membranes for holding the therapeutic agent. The therapeutic agent in the chamber may diffuse through the porous portion of the membrane and be deposited directly on the body site.
Abstract:
A stent deployment device for deploying a stent within a body cavity comprises an endoscope having a protective cap, a flexible stent, a sheath, and a flexible, elongated member. The protective cap is mounted on the distal end of the endoscope providing a protected surface for retaining the stent. The flexible stent is circumferentially compressed over the perimeter of the cap, and the sheath is then releasably wrapped around the stent to hold it in a compressed configuration over the cap. The flexible, elongated member, such as a wire extending through a working channel of the endoscope, is attached to either the sheath directly or to a releasing device for the sheath. After the endoscopic device is inserted in a body cavity, the flexible, elongated member is pulled through the working channel to release the sheath and deploy the stent into a desired body opening in the body cavity. After deployment of the stent, the sheath can be left in the body cavity for subsequent retrieval or retracted through the endoscopic device.
Abstract:
A cryogenic tissue ablation instrument includes an elongate flexible body with a proximal supply port for coupling with a pressurized coolant, a supply lumen in communication with the proximal supply port, and an expandable balloon carried on the elongate body. A dispersion member coupled to the elongate body has an interior lumen in communication with the supply lumen, the dispersion member having one or more coolant dispersion apertures sized and located such that a pressurized flowable coolant will enter the balloon interior in the form of a liquid spray that contacts and provides substantially uniform cooling of the balloon.
Abstract:
Disclosed are implantable or insertable medical devices that provide resistance to microbial growth on and in the environment of the device and resistance to microbial adhesion and biofilm formation on the device. In particular, the invention discloses implantable or insertable medical devices that comprise at least one biocompatible matrix polymer region, an antimicrobial agent for providing resistance to microbial growth and a microbial adhesion/biofilm synthesis inhibitor for inhibiting the attachment of microbes and the synthesis and accumulation of biofilm on the surface of the medical device. Also disclosed are methods of manufacturing such devices under conditions that substantially prevent preferential partitioning of any of said bioactive agents to a surface of the biocompatible matrix polymer and substantially prevent chemical modification of said bioactive agents
Abstract:
The present invention relates to devices and methods for creating and securing a tissue fold during an endoluminal medical procedure. The devices and methods may be used for folding and securing, for example, a fundus wall onto an esophagus wall. An aspect of the invention includes a two-piece tissue clip configured to be installed through an endoluminal device to secure a tissue fold. The clip includes a female member and a male member configured to engage one another to secure the tissue fold. Another aspect of the invention includes a clipping device comprising a tissue clip magazine. The magazine is configured to hold a plurality of tissue clips and install the plurality of tissue clips in a single actuation of the magazine. A method for using the clipping device together with the tissue clips of the present invention to create and secure a fold of tissue during an endoluminal procedure also is disclosed.