Abstract: Flexible, low-cost, physically robust optical coupling patches for use in spectrophotometric patient monitoring, and methods of fabrication thereof, are described. The optical coupling patch comprises a flexible base layer having a skin-contacting surface and a first aperture formed therethrough that establishes an optical interface with a skin surface when the base layer is placed against the skin surface. The optical coupling patch further comprises an elastomeric waveguiding member laterally disposed on a surface of the base layer opposite the skin-contacting surface. The optical coupling patch guides optical radiation between a laterally propagating state at a first location laterally distal from the first aperture and a generally vertically propagating state at the first aperture.

Abstract: NAD-dependent ligase is identified as an indicator of micro-organisms in a sample. A method of detecting the presence of an NAD-dependent ligase expressing micro-organism in a sample comprises the steps of: (a) contacting the sample with a nucleic acid molecule which acts as a substrate for NAD-dependent ligase activity in the sample, (b) incubating the thus contacted sample under conditions suitable for NAD-dependent ligase activity; and (c) specifically determining the presence of a ligated nucleic acid molecule resulting from the action of the NAD-dependent ligase on the substrate nucleic acid molecule to indicate the presence of the NAD-dependent ligase expressing micro-organism. The method has a number of applications and kits for carrying out the methods are also provided.

Abstract: The present invention relates to a treating apparatus which can be used with a radiation source and which can particularly be employed in lithotripsy, a shockwave source being provided which generates shockwaves and with which shockwaves can be sent to an object to be treated, and a radiation locating device being also provided which is integrated into the shockwave source. To provide a treating apparatus of this type which despite the use with a radiation source permits a high image quality and accurate focusing of the shockwaves in a way which is as easy as possible, the radiation locating device comprises a radiation receiving unit which is configured as a solid-state detector. The solid-state detector can include both radiation locating units and ultrasonic locating units.

Abstract: Methods, devices, and systems are described herein for applying energy to tissue for ablation of tissue while allowing the tissue to be resorbed within the body. Such methods, devices, and systems control application of energy to maintain a temperature of target tissue above an ablation temperature, being dependent upon the activation time, and below a transformation temperature, also being dependent upon the activation time, where the transformation prevents or hinders resorption of the treated tissue by the body.

Abstract: A system and method for a lithotripter is provided. The system can include a shockwave generator and an ultrasonic transmitting/receiving unit, which are in communication with an evaluating unit. The transmitting/receiving unit can include an ultrasonic transducer that emits ultrasonic pulses and receives ultrasonic waves reflected from a target area of the shockwave generator. The evaluating unit can determine a correlation coefficient of the time correlation between the ultrasonic waves and the ultrasonic pulses and provide a signal related to the coefficient. The method can include emitting ultrasonic pulses from the transducer into a body, receiving the ultrasonic waves reflected from a target object in the body, evaluating the received ultrasonic waves with the evaluating unit to determine the correlation coefficient, and providing a signal related to the correlation coefficient.

Abstract: An interocclusal sports prophylaxis includes a core having an arch shaped occlusal plate with upwardly extending buccal and lingual walls. A labial force dispersal shield and molar framing braces extend downwardly from the plate at incisor and lingual zones of the plate. The occlusal plate is thickened at the molar and incisor zones so that breathing spaces are provided between mandibular occlusal surfaces not registered with the zones and a mandibular face of the plate. A shock absorption dentition encasement is molded over the upper surface of the core and also covers the molar and incisor zones. The prophylaxis is heated in water, seated in the mouth and then biting pressure is applied to embed the maxillary dentition in the encasement and the lower incisor and molar occlusal surfaces in the encasement covering the zones.

Abstract: Non-invasive spectrophotometric monitoring of oxygen saturation levels based on a combination of continuous wave spectrophotometry (CWS) and phase modulation spectrophotometry (PMS) is described. First information representative of absolute oxygen saturation levels in relatively shallow regions of a patient tissue volume are acquired from PMS-based monitoring thereof during a reference interval. Second information representative of non-absolute oxygen saturation levels in relatively deep regions of the tissue volume are acquired from CWS-based monitoring thereof during the reference interval. Based on the first and second information acquired during the reference interval, a mapping is automatically determined between the second information and estimated absolute oxygen saturation metrics for the relatively deep regions.

Abstract: A tissue evacuation device may be designed to provide a high-energy fluid (e.g., a heated vapor) to targeted tissue for breaking down the targeted tissue, such as the nucleus of an intervertebral disc. An inner tube positioned within an outer tube, having a nozzle coupled to distal ends of the tubes, having a heating element positioned between the inner and outer tubes, delivers a heated vapor through a port to the nozzle to break down tissue. After the nucleus or other targeted tissue is broken down, the tissue evacuation device may also remove some or all of the broken down tissue.

Abstract: A method for the capture from a sample of micro-organisms having a hydrophobic surface, which method includes contacting the micro-organisms with a capture reagent, which capture reagent has both a hydrophobic character whereby the capture reagent binds the micro-organisms by hydrophobic interaction therewith and a polar character, the capture reagent either being present on a surface and capturing the micro-organisms thereto, or being present in solution, the method then further including capturing the micro-organisms to a surface by binding the capture reagent to the surface by polar interaction between the surface and the capture reagent.

Abstract: The invention relates to a multi-application robotized platform for neurosurgery, comprising: a planning console comprising processing means that can especially receive and process digital images; a positioning robot arm comprising a plurality of arm segments, one of which is terminal and proximal and the other is terminal and distal, said segments being interconnected by articulated elements, the terminal distal arm segment comprising a receiving element arranged in such a way as to receive tools, and the robot arm being guided by the planning console; at least one video image recording means able to record images of the anatomical region to be processed, said means being electrically connectable to the processing means of the planning console, and able to be positioned and fixed to the receiving element of the distal arm segment in a removable manner; tools, instruments and others suitable for being positioned and fixed to the receiving element of the terminal distal arm segment in a removable manner; means

Abstract: Devices and methods for thermally-mediated treatment of blood vessels to elicit an immune response to cause rapid endothelial growth over at least portions of an implant or stent to prevent adverse events such as restenosis.

Abstract: A surgical instrument for thermally-mediated therapies in targeted tissue volumes and for causing thermal effects in polymer tissue-contacting members. In one embodiment, the instrument has a working end with an interior chamber that is supplied with a biocompatible liquid. An energy source causes a liquid-to-vapor phase change within the interior of the instrument. The vapor phase media then is ejected from the working surface of the instrument, and a controlled vapor-to-liquid phase change in an interface with tissue applies thermal energy substantially equal to the heat of vaporization to ablate tissue. The vapor-to-liquid phase transitions, or internal energy releases, can be provided about thin-film flexible structures for engaging body lumens and cavities. An exemplary embodiment can be used for shrinking, sealing, welding or creating lesions in tissue—while causing limited collateral thermal damage and while totally eliminating electrical current flow in the engaged tissue.

Abstract: This invention relates to the working end of a medical instrument that applies energy to tissue. In one embodiment, the instrument has a microfluidic tissue-engaging surface fabricated by soft lithography means together with optional superlattice cooling means that allows for very precise control of energy application, for example in neurosurgery applications. The tissue-engaging surface can eject a high-heat content vapor into the engaged tissue for treating tissue, while the superlattice cooling structure can prevent collateral thermal damage. Also, the superlattice cooling structure can be used to localize heat at a selected depth in tissue and prevent surface ablation. Also, the superlattice cooling structure can be used to prevent tissue sticking to a thermal energy delivery surface. In another embodiment, the tissue-engaging surface can be used in a jaw structure for sealing tissue together with hydrojet means for transecting the tissue.

Abstract: A system for breaking obstructions in body lumens includes a catheter including an elongated carrier, a balloon about the carrier in sealed relation thereto, the balloon being arranged to receive a fluid therein that inflates the balloon, and an arc generator including at least one electrode within the balloon that forms a mechanical shock wave within the balloon. The system further includes a power source that provides electrical energy to the arc generator.