512 results about "Patient ventilated" patented technology

A method and system for managing mechanical ventilation of patients with respiratory disorders is described. The main objective of the system is to generate executable instructions for patient care which take into account a large number of parameters of patient condition and ventilation. Data regarding the state of the patient are stored in a database. Patient data are processed according to a set of protocols which contain rules for patient care decisions arranged in a logical sequence to generate detailed, executable instructions for patient care. Instructions are updated when new data are entered into the database. The data can be acquired in an automated fashion, or the clinician can be instructed to collect and enter new data into the clinical database. Likewise, patient care instructions can be carried out automatically or manually, but it is preferred that instructions are carried out manually as a safety check. The preferred embodiment of the invention includes a computer system, software for processing patient data, and a display device for presenting patient care instructions to the clinician. The system maintains a record of patient data, patient care instructions, whether instructions were followed by the clinical staff, and if not, a reason why.

The present disclosure relates to systems, methods, and devices for controlling delivery of aerosolized formulations to patients in need of treatment, which optimizes aerosol deposition to the respiratory tract of the patient and can be adapted for use in spontaneously breathing patients or in those requiring mechanical ventilation.

In order to select an optimal ventilation mode for mechanically ventilating a patient, from among a number of ventilation modes, a mathematical description of the patient's respiratory system is produced in a computer from measured parameters related to properties of the respiratory system, and in the computer the mathematical descriptions for different modes of ventilation are tested on the mathematical description to obtain simulated results. An operator can selected a mode of ventilation to be analyzed by comparing the simulated results with a therapeutic goal, so that an optimal ventilation mode can be selected. Alternatively, the computer can iteratively test a number of modeled ventilation modes to identify the ventilation mode which comes closest to the therapeutic goal.

Methods, systems and devices are described for providing mechanical ventilation support of a patient using an open airway patient interface. The system includes gas delivery circuit and patient interface configurations to optimize performance and efficiency of the ventilation system. A ventilation system may include a ventilator for supplying ventilation gas. A patient interface may include distal end in communication with a patient airway, a proximal end in communication with ambient air, and an airflow channel between the distal end and the proximal end. A gas delivery circuit may be adapted to attach to the patient interface without occluding the patient interface to allow ambient air to flow from outside the patient interface to the patient airway. The ventilation gas may entrain air from ambient and from the patient airway.

A portable mechanical ventilator having a Roots blower is configured to provide a desired gas flow and pressure to a patient circuit. The mechanical ventilator includes a flow meter operative to measure gas flow produced by the Roots blower and an exhalation control module configured to operate an exhalation valve connected to the patient circuit. A bias valve connected between the Roots blower and the patient circuit is specifically configured to generate a bias pressure relative to the patient circuit pressure at the exhalation control module. The bias valve is further configured to attenuate pulsating gas flow produced by the Roots blower such that gas flowing to the mass flow meter exhibits a substantially constant pressure characteristic. The bias pressure facilitates closing of the exhalation valve at the start of inspiration, regulates positive end expiratory pressure during exhalation, and purges sense lines via a pressure transducer module.

A method for controlling operation of a CPAP apparatus. The apparatus has a blower (2), a patient interface (6), an air delivery conduit (8) for delivering air from the blower (2) to the patient interface (6), a sensor (4p) for determining the pressure in the patient interface (6), and a control mechanism (15) that causes air to be delivered at a desired pressure to the patient interface (6) and that detects transitions between inhalation and exhalation of a respiratory cycle of a patient in order to synchronise the blower output with the patient's efforts. In one form the CPAP apparatus provides pressure in accordance with a bi-level waveform with at least one characterising parameter of the waveform being automatically adjusted in accordance with indications of sleep disordered breathing. The indications of sleep disordered breathing can be one or more of snoring, apnea, hypopnea, and flow limitation.

An out flow resistance switching ventilator and its methodology for providing mechanical ventilation support to the respiratory failure patient are claimed. Based on the continuous out flow impounding ventilation mechanism, the apparatus provides ventilation by switching flow resistance between two different levels at a continuous gas flow system outlet valve controlled by patient's spontaneous breathing or preset mandatory parameters, resulting in airway pressure levels switching, and therefore creating lung volume switching, which is totally different from either volume ventilation or pressure ventilation mechanism utilized in the current conventional ventilators.

An endotracheal tube for mechanically ventilating patients is disclosed. The endotracheal tube comprises a distal end for insertion into the patient's airway, past the vocal chords, through the subglottal region, and into the patient's lung; and a proximal end for connection to a mechanical ventilator. The endotracheal tube further comprises a cuff at the distal end of the endotracheal tube to be located in the subglottal region of the patient below the vocal chords, an inflating lumen for inflating the cuff, and a suction lumen having a suction inlet port leading from the outer surface of the endotracheal tube, and to be located in the subglottal region, for evacuating secretions and/or rinsing fluid from the subglottal region during the mechanical ventilation of the patient. The distal end of the endotracheal tube is formed with an outer surface configuration effective to prevent blockage of the suction inlet port by the cuff or by tracheal mucosal tissue of the patient during a negative pressure condition in the suction lumen.

An apparatus for determining a patient's volemic status can make use of a physiological heart-lung interaction during spontaneous breathing or mechanical ventilation. Further, a computer program for determining the patient's volemic status has instructions for carrying out the steps of generating data of a physiological heart-lung interaction during spontaneous breathing or mechanical ventilation, and determining the patient's volemic status when making use of the data of the physiological heart-lung interaction, when run on a computer.

In accordance with the present invention, there is provided a mask for achieving positive pressure mechanical ventilation (inclusive of CPAP, ventilator support, critical care ventilation, emergency applications), and a method for a operating a ventilation system including such mask. The mask of the present invention includes a piloted exhalation valve that is used to achieve the target pressures/flows to the patient. The pilot for the valve may be pneumatic and driven from the gas supply tubing from the ventilator. The pilot may also be a preset pressure derived in the mask, a separate pneumatic line from the ventilator, or an electro-mechanical control. The mask of the present invention may further include a heat and moisture exchanger (HME) which is integrated therein.

Respiratory support and/or controlled mechanical ventilation of a patient are provided. A ventilation apparatus may include a ventilator, a transtracheal prosthesis, and a respiratory relief device. The transtracheal prostheses and ventilation catheter may be arranged such that the patient can breathe freely through the upper airway and/or the tracheal prostheses. Respiratory sensors may measure a breathing rate, lung pressure, airway pressure, or a combination thereof. Pulses of gas may be provided to the patient through the ventilation catheter during inspiration. The pulses may have a first volume while the patient breathes normal and a second volume when the sensors detect a cessation of breathing or reduction in breathing volume. The second volume may be provided at 1-5 times the normal breathing rate, with a volume 25-500% times the first volume, or both.

In accordance with the present invention, there is provided a mask for achieving positive pressure mechanical ventilation (inclusive of CPAP, ventilator support, critical care ventilation, emergency applications), and a method for a operating a ventilation system including such mask. The mask of the present invention includes a piloted exhalation valve that is used to achieve the target pressures/flows to the patient. The pilot for the valve may be pneumatic and driven from the gas supply tubing from the ventilator. The pilot may also be a preset pressure derived in the mask, a separate pneumatic line from the ventilator, or an electro-mechanical control. The mask of the present invention may further include a heat and moisture exchanger (HME) which is integrated therein.

A method of setting inspiratory time, expiratory time, and a subject's breath size in controlled mechanical ventilation comprises: a) setting a subject's expiratory time; b) setting the subject's inspiratory time; and c) setting the subject's breath size, all based on various criteria.

The invention belongs to the field of indoor air purification and relates to a wall-mounted type air purifier based on thermal regeneration and a purification method thereof. The purifier comprises a sealed cabin, a draught fan, an air channel body which is composed of a plurality of air valves, a low efficient filter, efficient reproducible volatile organic compounds (VOCs) absorption module, a formaldehyde absorption module, a heating wire, a VOCs sensor, a temperature sensor, and a programmable logic controller; the sealed cabin of the air purifier comprises an air purification chamber and a heating regeneration chamber; the low efficient filter, the efficient reproducible VOCs absorption module, the formaldehyde absorption module, the draught fan and the VOCs sensor are installed in the air purification chamber of the sealed cabin from bottom to top; the heating wire and the temperature sensor are installed in the heating regeneration chamber from top to bottom; the programmable logic controller is connected with the draught fan, the temperature sensor, the VOCs sensor and circuits of the multiple air valves. The purification method comprises four modes of purifying, thermal regenerating, pollution discharging and fresh air, and further comprises two functions of indoor purification and mechanical ventilation. According to the wall-mounted type air purifier based on thermal regeneration and the purification method thereof, indoor VOCs and indoor formaldehyde can be purified quickly, continuously and effectively, and the service life of the wall-mounted type air purifier is prolonged.

A medical system having a ventilator is provided. The medical system includes a memory for storing one or more patient and ventilation parameters. A processor is programmed to organize the one or more patient parameters into at least one of past patient and ventilation parameters, present patient and ventilation parameters, or future patient and ventilation parameters. A viewer displays at least one of the past patient or ventilation parameters, the present patient or ventilation parameters, or the future patient or ventilation parameters. The past patient and ventilation parameters, the present patient and ventilation parameters, and the future patient and ventilation parameters are selectable on the viewer.

An apparatus (1) for non-invasive mechanical ventilation comprises a fan (2) of Bi-level type, or BiPAP, for generating an air flow according to a succession of inspiration steps, or IPAP, and exhalation steps, or EPAP. The flow is conveyed in the aerial ducts of a patient (25) by means of a flexible tube (3) connected to a nasal mask (4). A flexible air reservoir (5) is provided pneumatically connected to the duct (3) and the nasal mask (4) in order to subtract from the inspiration flow a certain air amount before that it reaches the patient (25) at the beginning of an IPAP step. During the exhalation EPAP step, since the air flow pressure decreases automatically, there is the emptying at least partial of the flexible air reservoir (5), whereas the air exhaled by the patient exits through an opening (14) made on the nasal mask (4). This way an air exchange occurs also in the most peripheral patient's aerial ducts and the amount of gaseous exchanges is increased, reducing at the same time the duration of the treatment.

A method and an apparatus for controlling a ventilator to automatically adjust ventilation assistance to an active or passive subject. The method includes determining volume and flow rate of gas to the patient during inspiration on an ongoing basis, and generating control signals in proportion to the volume and flow rate of gas to the patient wherein proportionality factors, and support levels for the elastic and resistive components of pressure are automatically adjusted by the ventilator. The ongoing pressure applied by the ventilator is a sum of elastic and resistive pressures that are automatically controlled by the system. When the patient breathes spontaneously, the support levels are automatically adjusted based on the patient's requirements. If the patient does not breathe spontaneously, the ventilator provides ventilation at an optimal level and rate. The method may be used in weaning or in a management phase of ventilation.

A residential controller is described which is used to manage the mechanical ventilation systems of a home, installed to meet whole-house ventilation requirements, at the same time reducing energy costs. This is achieved in part by shifting the ventilation load of the whole-house system to off peak hours and by taking into account exogenous mechanical ventilation induced by other systems. The controller is linked by wire or wirelessly to other house ventilation systems using any one of a number of communication protocols, sensing the on-off status of such exogenous systems. An operational algorithm preloaded and/or modified at the point of use is used to control the on-off status or fan speed of a whole-house ventilation fan which forms a part of the home ventilation system, the operating status of the whole-house fan in part responsive to the status of other home ventilation systems, and in part based on time of day.

A method of setting expiratory time in controlled mechanical ventilation sets a subject's expiratory time based on when the subject's natural exhalation flow ceases. Another method determines when the subject's natural exhalation flow ceases and sets the subject's expiratory time based on the determination. A device for use in controlled mechanical ventilation comprises a flow rate sensor configured to determine when a subject's natural exhalation flow ceases and bases the subject's expiratory time on the determination.

A method of setting expiratory time in controlled mechanical ventilation sets a subject's expiratory time based on the subject's natural exhalation time. Another method determines the subject's natural exhalation time and sets the subject's expiratory time based on the determination. A device for use in controlled mechanical ventilation comprises a flow rate sensor configured to determine a subject's natural exhalation time and base the subject's expiratory time on the determination.