A dental appliance is provided. The dental appliance includes a dental form configured to receive a portion of a dental arch of an individual, and an adhesive strip comprising a first side and a second side. The first side of the adhesive strip is attached to a portion of the dental form. The second side of the adhesive strip comprises a mucoadhesive configured to adhere the adhesive strip to a tongue of the individual such that the tongue of the individual can be selectively attached to the dental appliance.

The present disclosure discloses a humidification device, a humidifier and a ventilator, overcoming the deficiency that when the structure of a water tank of a current ventilator causes the water tank to tilt or sway, it is easy for a large amount of water to enter a heating portion. The humidification device comprises a heating portion and a liquid inlet structure adding liquid to the heating portion. The heating portion comprises an accommodating chamber and a transition chamber limiting the amount of liquid in the accommodating chamber, and the liquid inlet structure is communicated with the transition chamber and allows the liquid to enter the transition chamber. According to embodiments of the present disclosure, a large amount of stored water may be prevented from entering the heating portion and thus affecting the heating efficiency when a water tank or a similar humidification device tilts.

Apparatus and method for imaging a patient in an MRI system. This includes a frame, and at least one assembly that includes an earpiece positioner connected to a reference position on the frame, a first lockable joint on the positioner; and an earpiece connected to a patient-proximal end of the positioner by a second joint, wherein the first earpiece is moveably positioned to a selected pitch angle, a selected yaw angle, and a selected one of a plurality of distances relative to the reference position on the frame. The first lockable joint is configured to be tightened to yieldably hold the first earpiece at the selected pitch and yaw angles, and at the selected one of the plurality of distances, relative to the reference position. Optionally a second substantially similar earpiece and assembly are provided. The earpiece(s) optionally include audio transducer(s) and/or RF coil(s).

Apparatus and method for imaging a patient in an MRI system. This includes a frame, and at least one assembly that includes an earpiece positioner connected to a reference position on the frame, a first lockable joint on the positioner; and an earpiece connected to a patient-proximal end of the positioner by a second joint, wherein the first earpiece is moveably positioned to a selected pitch angle, a selected yaw angle, and a selected one of a plurality of distances relative to the reference position on the frame. The first lockable joint is configured to be tightened to yieldably hold the first earpiece at the selected pitch and yaw angles, and at the selected one of the plurality of distances, relative to the reference position. Optionally a second substantially similar earpiece and assembly are provided. The earpiece(s) optionally include audio transducer(s) and/or RF coil(s).

The present invention provides for systems and methods for inhaled CO therapy to prevent, attenuate, or delay processes that accelerate the loss of organ or tissue function, thereby increasing the lifespan of transplanted organs or tissues, or slowing the decline of native organs or tissues, or delaying the need for replacement of diseased native organs with organ transplants. Such biological processes that are prevented, attenuated, or delayed include chronic persistent inflammation, fibrosis, scarring, as well as immunologic or autoimmune attack.

A minimal weight patient interface device that delivers breathing gas to a user includes a cushion assembling including a support cushion assembly and a sealing member is described herein. In one exemplary embodiment, the support cushion assembly includes a wedge that is made of a high density foam received within a wedge receiving portion of the support cushion assembly. In the exemplary embodiment, the cushion assembly is formed by the sealing member fitting over the support cushion assembly. The sealing member, in one embodiment, is made of silicone, for example, having a low durometer value (e.g., between 5-10 Shore 00). Furthermore, in one embodiment, the patient interface device also includes a faceplate that is placed over the cushion assembly and is made of a thermoform, such as a high density foam laminated between two pieces of fabric, such as polyester.

A mechanical ventilator (10) is connected with a ventilated patient (12) to provide ventilation in accordance with ventilator settings of the mechanical ventilator. Physiological values (variables) are acquired for the ventilated patient using physiological sensors (32). A ventilated patient cardiopulmonary (CP) model (40) is fitted to the acquired physiological variables values to generate a fitted ventilated patient CP model by fine-tuning its parameters (50). Updated ventilator settings are determined by adjusting model ventilator settings of the fitted ventilated patient CP model to minimize a cost function (60). The updated ventilator settings may be displayed on a display component (22) as recommended ventilator settings for the ventilated patient, or the ventilator settings of the mechanical ventilator may be automatically changed to the updated ventilator settings so as to automatically control the mechanical ventilator.

A medical ventilator (10) performs a method including: receiving measurements of pressure of air inspired by or expired from a ventilated patient (12) operatively connected with the medical ventilator; receiving measurements of air flow into or out of the ventilated patient operatively connected with the medical ventilator; dividing a breath time interval into a plurality of fitting regions (60); and simultaneously estimating respiratory system's resistance and compliance or elastance, and respiratory muscle pressure in each fitting region by fitting to a time series of pressure and air flow samples in that fitting region. In one approach, the fitting includes parameterizing the respiratory muscle pressure by a continuous differentiable function, such as a polynomial function, over the fitting region. In another approach, the fitting is to an equation of motion of the lungs in each fitting region, while monotonicity constraints and inequalities bounding at least the respiratory muscle pressure P.sub.mus(t) and respiratory system's resistence R and compliance C are applied to the respiratory muscle pressure in each region.

[Problems] To provide a driving method for a metering pump, a driving apparatus for a metering pump, a vaporizer and an anesthesia apparatus which are capable of suppressing a pulsation in the metering pump, and lowering the costs and reducing the sizes of the vaporizer and the anesthesia apparatus.

[Means for solving the Problems] A metering pump 16 is joined to the stepping motor 15, includes an eccentric mechanism converting a revolving motion of the stepping motor 15 into a reciprocating motion of a plunger 16A, and makes a constant liquid delivery by sucking and discharging an anesthetic agent through variations in the cubic volume of a cylinder 16D caused by the reciprocating motion of the plunger 16A. The control section 12: calculates a suction and discharge cycle T of the metering pump 16 on the basis of a set anesthetic-gas concentration and a fresh-gas flow rate; sets a discharge period T2 of the cycle T to be longer than a suction period T1 of the cycle T; and controls the revolution speed of the stepping motor 15 so that the travelling speed of the plunger 16A is kept constant during the discharge period T2.

An oxygen concentrator comprises a product tank that is fluidly coupled to at least one sieve bed, and a product gas accumulator tank that is fluidly coupled to the product tank via a first conduit and to an outlet port via a second conduit, wherein the first conduit and the second conduit are disposed to allow at least a portion of product gas to flow from the product tank to the outlet port.