Abstract: An irrigating intraluminal suction inner cannula system for a tracheostomy tube may be a suction-powered system that may be used for suction alone or a combination of rinse and intraluminal suction for tracheostomy tubes in place of conventional catheter-based intraluminal suction. An inner cannula includes chambers, or regions, and holes that facilitate intraluminal suction and cleaning at multiple locations within the tracheostomy tube. It may be applied/actuated by a patient, healthcare worker, caretaker, or via an electronic system either on-demand or on regular or triggered intervals, in either inpatient/hospital or outpatient/ambulatory care setting.

Abstract: A device (1), for a ventilation system (100), includes an inhalation valve (10) with an inhalation opening (11) for flow (301) of breathing gas (300) into a pressure chamber (110) to provide breathing gas in the pressure chamber for ventilating a patient (200). A closing element (12) is arranged movably, to close the inhalation opening to flow in a closed position (320) and to at least partially release flow in an open position (310). A transmission device (13) is connected via a connection element (14) to the closing element, to hold the closing element in the closed position in a starting position of the transmission device, such that the inhalation valve is normally closed. A control pressure source (130) provides a control pressure (PS) in a control pressure chamber (15) for the transmission device to move the transmission device out of the starting position by the control pressure.

Abstract: A customizable drug delivery system and method utilizing a laser pattern generator (LPG) to define application of a drug delivery payload (DDP) contained within a drug delivery device (DDD) to a drug delivery target (DDT) is disclosed. A computer control device (CCD) supervises the LPG to select a drug payload pathway (DPP) from a drug pathway database (DPD) and writes the selected DPP to the DDD. This pathway patterning process (PPP) modifies the hydrophilic properties of the DDD and enables the DDD to selectively attract and absorb the DDP. The DDD is then injected with the DDP or exposed for drug exposure time (DET) by the CCD and DPD during which the DPP written to the DDD absorbs a controlled amount of DDP. The DDD when subsequently inserted into a drug delivery target (DDT) delivers the DDP to the DDT under controlled delivery rates defined by the DPP and the DET.

Abstract: A treatment force application device preferably for use on biological tissue includes a proximal end having a weight and having a support for a practitioner; a distal end having a treatment interface configured for applying a therapeutic treatment including at least a treatment force; and a connection between the support and the treatment interface. The connection is lockably adjustable by the practitioner to establish a placement of the treatment interface relative to the support. The weight is sufficient to substantially prevent movement of the treatment interface relative to the support when the connection is locked. The support enables movement of the practitioner to provide a practitioner force, and the practitioner force is transferred from the support to the treatment interface through the connection. The support includes at least one flexible brace against which the practitioner can press to provide the practitioner force.

Abstract: The massage machine includes a massage unit for treating a treatment target person, a first drive unit for driving the massage unit in a direction facing a treatment site of at least the treatment target person, and a control unit that controls driving of at least the first drive unit. The massage unit is configured to include a treatment unit in an articulated structure with at least two or more joints, and a second drive unit that drives the treatment unit in the direction facing the treatment target site of the treatment target person. The at least the two or more joints are shifted from each other in a direction intersecting a longitudinal direction of the treatment target site.

Abstract: A suction catheter system is described with a suction extension interfaced with a guide catheter to form a continuous suction lumen extending through a portion of the guide catheter and through the suction extension. The suction extension can be positioned by tracking the suction nozzle through a vessel while moving a proximal portion of the suction extension within the lumen of the guide catheter. The suction extension can comprise a connecting section with a non-circular cross section for interfacing with the inner lumen of an engagement section of the guide catheter. The tubular body of the guide catheter can have a reduced diameter distal section the can be useful to restrain the movement of the suction extension.

Abstract: A percussive massage device includes a motor including a rotor, a push rod operatively connected to the motor and configured to reciprocate in response to activation of the motor, a massage attachment coupled to a distal end of the push rod, a sensor configured to detect a rotor position of the rotor, and a controller configured to receive the rotor position, determine a rotational speed of the motor therefrom, and compare the rotational speed to a predetermined speed, wherein the controller is configured to increase operating power of the motor when the rotational speed is lower than the predetermined speed.

Abstract: A ventilation device includes a mechanical ventilator (10), respiratory sensors (30, 32) configured to acquire measurements of respiratory variables including at least measurements of airway pressure and airway flow, and an electronic processor (14) programmed to perform a ventilation method including: operating the mechanical ventilator to provide mechanical ventilation controlled using measurements acquired by the respiratory sensors; performing a pause maneuver comprising closing at least one of an inhalation valve (38) and an exhalation valve (40) for a pause interval and estimating a respiratory mechanics index from one or more respiratory system parameters estimated from measurements acquired by the respiratory sensors during or after the pause interval; and triggering a pause maneuver in response to detecting a change in the estimated respiratory mechanics index.

Abstract: A method for performing a gastrectomy (stomach reduction surgery).

Abstract: A wearable stimulation device includes a wearable member, a stimulation unit, and a driver. The stimulation unit is secured to the wearable member. The stimulation unit includes an immovable end, a stimulation end, and a power element. The power element is connected between the immovable end and the stimulation end for driving the stimulation end to reciprocate relative to the immovable end. The driver is in signal connection with the power element. The driver is configured to output a vibration signal to the power element for the stimulation end to have a stroke of between 8.8 mm and 10.8 mm, a thrust of between 5.6 N and 7.6 N and a reciprocating frequency of between 180 Hz and 220 Hz, thereby stimulating the deep muscles of the abdomen or waist of a human body without affecting the superficial muscles.

Abstract: A venous air capture chamber for use in dialysis, includes an upwardly extending fluid inlet terminating in first and second fluid inlet ports (102). The first and second fluid inlet ports (102) are opposedly positioned on the fluid inlet at an angle of about 180°. The venous air capture chamber also includes a fluid outlet (104) at the bottom of the chamber body. The venous air capture chamber provides improved fluid dynamics, reducing both stagnant flow and turbulence. The venous air capture chamber also provides for bidirectional flow of fluid through the chamber.

Abstract: A process (10), with a computer program, a device (30) and a ventilation system (40) detect a leak in a patient gas module, which suctions and analyzes a continuous sample gas stream from a ventilated patient (20), in a ventilation system for ventilating a patient (20). The process includes a determination (12) of a first time curve of a carbon dioxide concentration in a breathing gas mixture of the patient (20) and the determination (14) of a second time curve of a concentration of another gas in the breathing gas mixture, which gas is different from carbon dioxide. The process (10) further includes a determination (16) of a statistical similarity indicator between the first time curve and the second time curve and the detection (18) of the leak based on the similarity indicator.

Abstract: The present disclosure pertains to a system and method for facilitating pressure support therapy, mechanical inexsufflation therapy, and suctioning therapy for a subject. The system and method described herein offer a novel combination of mechanical inexsufflation with suctioning from a vacuum system. The invasive nature of current closed suctioning systems poses many potential risks, such as tissue trauma, less optimum secretion clearance at the peripheral airway, and lung decruitment. The system and method described herein provide a non-invasive method of suctioning with a suctioning volume measurement and a monitoring alarm to ensure a baseline lung volume and a positive end expiratory pressure (PEEP) level are maintained. This non-invasive method of suctioning is provided together with mechanical inexsufflation and pressure support therapy.

Abstract: Extracorporeal blood flow circuit devices can be used during medical procedures such as on-pump open-heart surgery. For example, extracorporeal heat exchange and oxygenation devices can be used to facilitate surgical procedures such as coronary artery bypass grafting. In some embodiments, such an oxygenation device can include an integrated air removal structure. In particular embodiments, the air removal structure can comprise one or more porous hollow fibers.

Abstract: A massaging system including a boot assembly, a sock assembly, a hydrotherapy assembly and a remote assembly is disclosed. The boot assembly includes a boot with a reservoir for water that is filled through a valve and sealed with a valve cap. Within the boot is a cavity to suspend a sock of the sock assembly within. Along the perimeter of the cavity are jet nozzles to spray water from the reservoir to the sock to provide hydrotherapy to a foot of a user received within the sock. Openings are also located about the perimeter of the cavity allowing water to be returned to the reservoir for continued use. The hydrotherapy assembly includes a water pump and a water heater that cooperate with the jet nozzles to control the settings thereof. The user is able to control the jet nozzles with a remote to customize the hydrotherapy received.

Abstract: The invention relates to a blood treatment device for carrying out an extracorporeal blood treatment in which blood is guided in a blood guidance device having a main blood line and at least one secondary line, the latter being fluidically connected to the main blood line and the main blood line having a dialyzer and, downstream from the dialyzer, a blood treatment element, wherein the blood treatment device has a control device; and a pump configuration, which is equipped for generating blood flows in the main blood line and also in the at least one secondary line, wherein the control device is designed to operate the pump configuration in such a way that a first blood flow rate in the dialyzer is decoupled from a second blood flow rate in the blood treatment element. Furthermore, the invention relates to a blood guidance device for cooperation with the blood treatment device as well as for a blood treatment system.

Abstract: A massage head for a massage gun and a massage gun containing the same, relates to the technical field of massage devices, and solves the technical problem of the single function of the massage gun. The massage head comprises a massage head cover, a massage member, a cooling and heating component and a conductive quick-connecting component; wherein the massage head cover and the massage member are provided oppositely, the massage head cover and the massage member encircle an accommodating cavity for accommodating the cooling and heating component, and the conductive quick-connecting component is provided at the end of the massage head cover away from the massage member and electrically connected to the cooling and heating component; the massage head is detachably electrically connected to the massage gun body through the conductive quick-connecting component; the massage gun comprises a massage gun body, a grip handle, a reciprocating driving mechanism, a main circuit board, and a massage head.

Abstract: A dialysis system (e.g., a hemodialysis (HD) system) can be designed to operate in alternative environments, such as disaster relief settings or underdeveloped regions. The dialysis system can include a solar panel for generating electricity to power the dialysis machine and an atmospheric water generator for extracting water from ambient air. The extracted water can be used to generate dialysate and saline on-site. One or more of the components of the dialysis machine can be discrete components that are configured to facilitate fast shipping and simple on-site assembly (e.g., at a remote location). In some implementations, the discrete components may be configured to be attached to an existing dialysis system (e.g., a dialysis system designed for operation in a traditional environment) to permit the dialysis system to operate in an alternative environment.

Abstract: A respiratory assistance apparatus includes a conduit connecting a flow generator and an outlet. The conduit includes a venture formation. The apparatus further includes an oxygen inlet in fluid communication or selective fluid communication with an oxygen outlet. The oxygen outlet is directed into the conduit and toward a mouth of the venture formation. The flow generator provides a flow path for air to enter the conduit when the flow generator is not operating.

Abstract: A multimodal wearable band which uses mechanical vibrations to stimulate sensory neurons in the wrist or ankle in order to reduce the severity of tremors, rigidity, involuntary muscle contractions, and bradykinesia caused by neurological movement disorders and to free users from freezing induced by movement disorders. The device uses sensors to provide output used by a processing unit to determine the optimal stimulation pattern for each user and to determine when stimulation is necessary, and then uses one or more vibration motors to accordingly stimulate the user's neurological pathways to lessen the severity of a user's symptoms. The device can also be adapted to integrate with 3rd party devices.