摘要:
The present invention relates to a segmental self-sealing graft for implantation in a patient including a base tubing element, a tubular access element overlying the base tubing, and a strand-like compression element wound over the access element so as to provide radially inward compression, and a method of making same.
摘要:
An apparatus is disclosed including: an optical coherence tomographic system; a spinal needle having a needle tip adapted to penetrate tissue; and an optical delivery system adapted to direct probe light from the optical coherence tomographic system onto tissue located in front of the needle tip, collect test light backscattered from the tissue, and transmit the test light to the optical coherence tomographic system. The optical coherence tomographic system is adapted to provide information indicative of one or more properties of the tissue based on the test light.
摘要:
The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or “prosthetic modules,” may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.
摘要:
The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or "prosthetic modules," may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.
摘要:
The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or "prosthetic modules," may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.
摘要:
A high-strength ligament prosthesis having biological acceptability, flexibility, porosity and resistance to prolonged stress in excess of 100 Kg with little change in modulus, and less than 20% ultimate elongation is provided. These characteristics make the high-strength prosthesis favorable for critical applications, such as knee and ankle repair. The high-strength prosthesis is constructed of a biological compatible yarn having an outer shell with an "H-beam" cross-section and a velour surface to encourage rapid invasion by host tissue and a reinforcing core of the same yarn. The ends of the reinforcing core and outer wall are fitted with end tips to limit displacement of the core within the outer shell and to facilitate positioning of the prosthesis during surgery with minimal effort. An enlarged elongated end tip is particularly well adapted for special surgical procedures, such as arthoscopic procedures.
摘要:
A fatigue testing system provides simultaneous cycle testing for a plurality of prosthetic devices under simulated physiological loading conditions. A plurality of sample holders containing test samples of prosthetic devices is positioned between a distribution chamber and a return fluid chamber to form an integrated test chamber. A reciprocating linear drive motor operates a rolling bellows diaphragm to cyclically pressurize fluid within the test chamber and drive the pressurized fluid through the prosthetic devices being tested. The test chamber defines a return flow conduit in fluid communication with each of the sample holders, the return fluid chamber, and the distribution chamber. Compliance chambers and throttle valves associated with each of the sample holders regulate the pressure gradient and back pressure across the prosthetic devices being tested.
摘要:
The present invention provides controlled expansion endoluminal prostheses and methods for their deployment and expansion. The present stent-grafts generally comprise a radially expansible tubular frame and a plastically expansible liner on the frame. Either the frame or the liner includes a reinforcing element which limits expansion of the stent-graft at a predetermined expanded size. In some embodiments, the reinforcing element restrains the frame, for example, by limiting the circumferential diagonals of perforations on a perforate frame structure. Generally, however, the reinforcing element is included in the liner as circumferentially oriented yarn. A particularly advantageous liner includes composite circumferential yarns having inexpansible fibers wrapped around an expansible fiber, such as a partially oriented yarn, PTFE, or the like.
摘要:
Prostheses are fatigue tested using an apparatus under simulated physiological loading conditions. A fluid housing defines an entrance chamber having fluid outflow ports and an exit chamber having opposing fluid inflow ports and a central flow conduit in communication with the entrance chamber and the exit chamber. A plurality of housing tubes into which prosthesis are deployed may extend between the fluid outflow and inflow ports. Alternatively, tubular prostheses may be connected directly between the inflow and outflow ports. A reciprocating linear drive pump having a flexible diaphragm is provided to cyclically pressurize fluid through a common closed loop within the fluid housing and drive the pressurized fluid through the prosthesis being tested. The test system is capable of rotation independent of the motor drive for accurate diameter measurements of all test samples at elevated frequencies.