A medical assistance device capable of improving handling or an operation of a medical device. The medical assistance device is connected to the medical device which is inserted into a biological lumen and is used in a procedure in the biological lumen. The medical assistance device includes a support, a winding unit which is rotatably provided about a support shaft with respect to the support and winds the medical device, and a connection section which is provided in the winding unit and is connected to an end portion of the medical device.

Disclosed herein in is a medical tube comprising a hydrogenated styrenic block copolymer having a formula A-B-A, (A-B-A).sub.nX or (A-B).sub.nX is disclosed, where n is an integer from 2 to 30, and X is residue of a coupling agent. Prior to hydrogenation, each A block is a monoalkenyl arene homopolymer block having a true peak molecular weight of 5 kg/mol to 15 kg/mol. Each B block is a controlled distribution copolymer block having a true peak molecular weight of 30 kg/mol to 200 kg/mol. The hydrogenated styrenic block copolymer has a midblock poly(monoalkenyl arene) content of 35 wt. % to 50 wt. % based on the total weight of the midblock, and physical properties that makes it useful for producing medical tubes having kink resistance.

Disclosed herein in is a medical tube comprising a hydrogenated styrenic block copolymer having a formula A-B-A, (A-B-A).sub.nX or (A-B).sub.nX is disclosed, where n is an integer from 2 to 30, and X is residue of a coupling agent. Prior to hydrogenation, each A block is a monoalkenyl arene homopolymer block having a true peak molecular weight of 5 kg/mol to 15 kg/mol. Each B block is a controlled distribution copolymer block having a true peak molecular weight of 30 kg/mol to 200 kg/mol. The hydrogenated styrenic block copolymer has a midblock poly(monoalkenyl arene) content of 35 wt. % to 50 wt. % based on the total weight of the midblock, and physical properties that makes it useful for producing medical tubes having kink resistance.

A fluid sensing apparatus and a method for detecting pressure and a presence of bubbles within a fluid tube. The fluid sensing apparatus comprises a housing configured to receive a portion of the tube and to house a pressure sensor and an ultrasonic transmitter. The pressure sensor is positioned adjacent the tube and is configured to receive a pressure sensor signal, which correlates to a detected pressure differential within the tube. A controller transmits a drive signal to the ultrasonic transmitter, which emits ultrasonic waves through the portion of the tube and to the pressure sensor. The pressure sensor receives both the ultrasonic waves and the pressure sensor signal, and subsequently transmits an output signal to the controller. In a presence of a pressure differential or a bubble within the tube, the output signal will exhibit a DC shift or a distortion of signal characteristics of the output signal, respectively.

A fluid sensing apparatus and a method for detecting pressure and a presence of bubbles within a fluid tube. The fluid sensing apparatus comprises a housing configured to receive a portion of the tube and to house a pressure sensor and an ultrasonic transmitter. The pressure sensor is positioned adjacent the tube and is configured to receive a pressure sensor signal, which correlates to a detected pressure differential within the tube. A controller transmits a drive signal to the ultrasonic transmitter, which emits ultrasonic waves through the portion of the tube and to the pressure sensor. The pressure sensor receives both the ultrasonic waves and the pressure sensor signal, and subsequently transmits an output signal to the controller. In a presence of a pressure differential or a bubble within the tube, the output signal will exhibit a DC shift or a distortion of signal characteristics of the output signal, respectively.

One variation of a method for video conferencing includes, during a setup period: accessing a test video feed; and generating a face model, representing facial characteristics of a first user depicted in the test video feed, based on features detected in the test video feed. The method also includes, during an operating period: accessing a video feed; representing constellations of facial landmarks, detected in frames in the video feed, in a feed of facial landmark containers; representing sets of facial muscle actions, detected in frames in the video feed, in a feed of facial expression containers; and transforming the feed of facial landmark containers, the feed of facial expression containers, and the face model into a feed of synthetic face images according to the synthetic face generator.

One variation of a method for video conferencing includes, during a setup period: accessing a test video feed; and generating a face model, representing facial characteristics of a first user depicted in the test video feed, based on features detected in the test video feed. The method also includes, during an operating period: accessing a video feed; representing constellations of facial landmarks, detected in frames in the video feed, in a feed of facial landmark containers; representing sets of facial muscle actions, detected in frames in the video feed, in a feed of facial expression containers; and transforming the feed of facial landmark containers, the feed of facial expression containers, and the face model into a feed of synthetic face images according to the synthetic face generator.

Infusion systems and methods for administering an infusion fluid into a patients anatomic space at a variable flow rate without flow control include an administration set having a flexible tube fluidically connected to a needle connector, the needle connector including a receiving end fluidically connected to flexible tube, and an administering end opposite the receiving end and fluidically connected with an infusion needle, and the infusion needle having an inside diameter of about 0.0104 inches to about 0.0135 inches and fluidically connected to the administering end of the flexible tubing to deliver the infusion fluid to the patients anatomic space at variable flow rates dependent upon the saturation of the infusion fluid at the patients injection site.

Described herein is an implantable access port device with a catheter compartment which permits lengthening or shortening the catheter in response to changes in tension of the distal catheter. Implantable access port devices are used extensively in the medical field to facilitate the performance of recurrent therapeutic tasks such as repeated drug delivery, drainage, blood sampling, transfusions, or total parental nutrition. In current access port systems, the catheter is rigidly attached to the access port via a connection ring. As such, the system does not provide any flexibility or ability for catheter length adjustments, which can lead to long-term complications such as dislodgement of catheters, migration of catheters, port separation with extravasation, suture disruption, and mechanical failure of the access port system. These catheter-related complications carry serious risks for the patients. The implantable access port system described herein permits self-adjusting catheter length, thereby reducing catheter-related complications.

A wound irrigation system and method of making and using. The system uses a pored, closed-ended delivery conduit to enhance the consistency and speed with which anti-microbial or related irrigation fluids may be delivered in order to promote cleansing, debridement and biofilm reduction in wounds. The ease of use of the system as a moist wound healing cascade makes it applicable to both in-home and in-facility environments that is not offered through traditional instillation negative pressure systems. In one form, the fluid delivery conduit is used as part of a dual-conduit approach in order to also help promote the removal of drainage, waste, irrigation overflow or other fluid from the wound. Utilization of such a pored, closed-ended delivery conduit in conjunction with a separate drainage conduit infusing helps reduce the frequency of dressing changes as well as the likelihood of microorganism formation and colonization.