A tool for use in conjunction with a pressure support system that is structured to provide therapy to a patient to treat a condition of the patient by delivering a flow of breathing gas to the patient. The tool may be implemented on a portable electronic device or a PC and is configured to, among other things, provide customized/personalized education and feedback to the patient based, at least in part, on data that is measured by the pressure support system during the provision of therapy to the patient. The tool utilizes certain patient/therapy metrics, wherein each patient/therapy metric comprises raw data that was measured by the pressure support system and that has been processed (e.g., summarized and/or otherwise manipulated) to form the patient/therapy metric.

A respiratory assistance device 10 includes: a mask 13 having an expiratory hole 13a; an expiratory valve 15 provided in the mask 13, for opening and closing the expiratory hole 13a; and a control unit 17 for performing overall control on the entire device. The mask 13 and the expiratory valve 15 together form an opening and closing device. The expiratory valve 15 is deformable by deformation of a piezo element 15a. The expiratory valve 15 is disposed on an inner surface 13f so that a deformation direction thereof, i.e., a thickness direction thereof, extends along the inner surface 13f of the mask 13 and a side surface 15m slides along the inner surface 13f by the deformation thereof.

Devices, systems, and methods for degassing fluid prior to applying fluid to a treatment site during ablation therapy are provided. In one embodiment, an ablation system can include an elongate body, an ablation element, a heating assembly, and a fluid source. Fluid in the fluid source can be at least partially degassed prior to being provided as part of the system, or, in some embodiments, a degassing apparatus can be provided that can be configured to degas fluid within the system prior to applying the fluid to the treatment site. The degassing apparatus can include one or more gas-permeable and fluid-impermeable tubes disposed therein, which can allow gas to be removed from fluid passing through the apparatus. Other exemplary devices, systems, and methods are also provided.

In an embodiment, the present invention discloses a medical assembly, including a sub-urethral implant, a strap, a dilator, and a suture. The implant includes a first end portion and a second end portion such that the strap is configured to be attached to the first end portion of the implant. The strap is attached to the implant through a weld. The strap is further configured to be coupled to the dilator. The suture can be coupled to the dilator.

An imaging apparatus includes: a light source section (2, 40) including a light source having a wavelength of a plurality of bands; an imaging section (15) configured to convert measurement light source light images of the plurality of bands from the light source section into a plurality of electrical measurement imaging signals, the measurement light source light images being reflected from a surface and an inside of the subject; a calculation section (13, 16, 19) configured to measure a shape of the surface and a shape of the inside in the subject based on the plurality of electrical measurement imaging signals obtained through the conversion in the imaging section; and a composition processing section (19) configured to composition-process the shape of the surface and the shape of the inside measured by the calculation section to create two-dimensional image data or three-dimensional image data about the subject.

A device and a method for calibrating the coordinate system of imaging systems having a tracking system prior or during image data acquisition, e.g. by way of magnetic resonance tomography.

Methods and implants to treat anterior cruciate ligament (ACL) injuries are disclosed. The methods involve advancing the insertion of the patellar tendon to the proximal tibia by means of a partial osteotomy and a wedge-shaped cage (30). The wedge-shaped cage is specifically designed to facilitate transfer of not only compressive loads, but also of shear loads due to pull by the patellar tendon at its insertion to the tibial tuberosity. The cage decreases the angle between the patellar tendon and the common tangent plane formed by the condyles of the femur and the condyles of the tibia (sometimes called tibial plateau) and consequently modifies the internal joint force, restoring stability to the joint even if the ACL is ruptured. The methods and implants are applicable to both human and canine patients.

An embodiment in accordance with the present invention provides a method for non-invasively determining the functional severity of coronary artery stenosis. The method includes gathering patient-specific data related to concentration of a contrast agent within a coronary artery of a patient using a coronary computed tomography angiography scan (CCTA). The patient-specific data is used to calculate a patient-specific transluminal attenuation gradient for the coronary artery of the patient. The patient specific transluminal attenuation gradient is used to determine an estimate of a coronary flow velocity, pressure gradient, loss coefficient, coronary flow reserve, and/or fractional flow reserve for the patient. Coronary flow velocity, pressure gradient, loss coefficient, coronary flow reserve, and fractional flow reserve can then be used to estimate the functional severity of coronary artery stenosis.

A device is described for treating a nasal airway by modifying a property of a nasal tissue of or near a nasal valve of the airway, without using a surgical incision or an implant, to decrease airflow resistance or perceived airflow resistance in the nasal airway. Various embodiments include an elongate shaft, a bipolar radiofrequency delivery member extending from one end of the shaft, and a handle attached to the elongate shaft at an opposite end from the radiofrequency delivery member. The radiofrequency delivery member is sized to be inserted into a nose and configured to at least temporarily deform the nasal tissue and deliver radiofrequency energy. The radiofrequency delivery member includes two rows of protruding electrodes disposed on a tissue contact surface, and the device is configured to deliver radiofrequency energy from one row of electrodes to the other row of electrodes.

Devices and methods for shaping an ablation treatment volume formed in fluid enhanced ablation therapy are provided. The devices and methods disclosed herein utilize the interaction of fluids to create ablation treatment volumes having a variety of shapes. In one embodiment, a method for forming an ablation treatment volume having a desired shape includes delivering therapeutic energy to tissue to form an ablation treatment volume and simultaneously delivering a first fluid and a second fluid to the tissue. The first and second fluids can convect the therapeutic energy in a desired direction such that the ablation treatment volume has a desired shape.