A device for targeted delivery of a substance to an airway may include a conduit and at least two applicators. The conduit may include a proximal end and a bifurcated distal portion having two distal ends. Each applicator may be coupled with one of the distill ends of the conduit and may be configured to direct the substance out of the applicator toward one of two sides of an airway. A method for targeted delivery of a substance to an airway may involve advancing a substance delivery device into the airway, contacting two sides of the airway with at least two applicators of the substance delivery device, such that each applicator contacts the airway near a glossopharyngeal nerve and/or a superior laryngeal nerve on each of the two sides of the airway, and delivering the substance through the applicators to contact the airway along the two sides.

A respiratory device can include an oxygen generator and a ventilator. The oxygen generator can include a first inlet to ambient air, a vacuum or pressure swing oxygen generating system in fluid communication with the first inlet, a first fluid pathway, and a first outlet. The ventilator can include a second inlet to ambient air and a blower in fluid communication with the second inlet to draw ambient air. The ventilator can include a third inlet in fluid communication with the first fluid pathway upstream of the first outlet. The blower can also be in fluid communication with the second inlet to draw at least some of the extracted oxygen. The ventilator can also include a second outlet in fluid communication with the blower to dispense a mixture of the ambient air and the extracted oxygen to the user.

Disclosed are methods and devices for regulating fluid flow to and from a region of a patient's lung, such as to achieve a desired fluid flow dynamic to a lung region during respiration and/or to induce collapse in one or more lung regions. Pursuant to an exemplary procedure, an identified region of the lung is targeted for treatment. The targeted lung region is then bronchially isolated to regulate airflow into and/or out of the targeted lung region through one or more bronchial passageways that feed air to the targeted lung region. An exemplary flow control device is configured to block fluid flow in the inspiratory direction and the expiratory direction at normal breathing pressures and allow fluid flow in the expiratory direction at higher than normal breathing pressures.

A patient interface including a seal-forming structure with a textile membrane that has at least one hole such that the flow of air at a therapeutic pressure is delivered to at least an entrance to the patients nares and/or an entrance to the patients mouth. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in a cavity of a plenum chamber throughout the patients respiratory cycle, in use. The textile membrane includes a first portion that is held in a relaxed state and a second portion that is held in a taut state. The taut state of the second portion is configured to allow the seal-forming structure to include a three-dimensional shape that has multiple curvatures.

Nasal cannulas are described herein. The nasal cannula (110) includes a cannula housing (112), a reservoir (160), a nebulizer channel (154), and a gas channel (120). The cannula housing includes at least one nasal extension (116) extending from the cannula housing, wherein the at least one nasal extension is configured to be disposed within a patient's nares. The reservoir includes a reservoir volume configured to dispense a medicament. The nebulizer channel is in fluid communication with the reservoir volume and the at least one nasal extension. The gas channel is configured to direct a gas flow toward the at least one nasal extension through the nebulizer channel, drawing a portion of the medicament from the reservoir through the nebulizer channel with the gas flow toward the at least one nasal extension.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.

An automatic control system for a manual mechanical ventilation device comprising a servomotor, an actuator and a stepper cylinder adapted to compress the mechanical ventilation device in response to signals sent by a controller. The controller is further connected to at least one flow sensor and one pressure sensor and has a human-machine interface for the insertion of pressure and oxygen flow output values to be received by a patient.

The present invention relates to an intubation system comprising insertion unit to be connected to a bending section of a medical instrument comprising an inner elongated shaft structure being capable of torque transmission around its length axis and an outer elongated shaft structure surrounding the inner elongated shaft structure and having a continuous outer surface, and an orientation controller being attached to the inner elongated shaft, such that when the orientation controller rotates, the bending section turns around itself.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.

An adapter (1) for establishes a flow channel (2) between a breathing gas supply and a patient connection piece. A set (20) and a system (30) for ventilation or respiratory support, each include the adapter (1). The adapter (1) includes a first connection structure (3) configured to connect to the breathing gas supply and a second connection structure (4) configured to connect to a patient connection piece. A bypass channel (5) branches off from the flow channel (2) and is provided with an extraction opening (7) which can be closed at least temporarily by a safety valve (6). The safety valve (6) is configured such that the extraction opening (7) is closed when a ventilation pressure prevailing in the flow channel (2) is lower than a pressure prevailing on a side of the safety valve facing away from the flow channel (2).