The present technology is directed to a respiratory pressure therapy system, that includes a plenum chamber pressurisable to a therapeutic pressure above ambient air pressure, a seal-forming structure to form a seal with an entrance to the patient's airways to maintain said therapeutic pressure in the plenum chamber throughout the patient's respiratory cycle in use, a positioning and stabilising structure constructed and arranged to provide an elastic force to hold the seal-forming structure in a therapeutically effective position on the patient's head, a blower configured to generate the flow of air and pressurise the plenum chamber to the therapeutic pressure, the blower having a motor, the blower being connected to the plenum chamber such that the blower is suspended from the patient's head and the axis of rotation of the motor is perpendicular to the patient's sagittal plane, and a power supply configured to provide electrical power to the blower.

A method for communicating with devices may include monitoring brain activity of a subject via an EEG monitoring system coupled to the subject. The method also may include detecting a predefined state of brain activity of the subject. Further, based on the detecting the predefined state, the method may include wirelessly transmitting instructions from the EEG monitoring system to the at least one household device to adjust a setting of the at least one household device.

Methods for treating hydrocephalus using a shunt, the shunt having one or more CSF intake openings in a distal portion, a valve disposed in a proximal portion of the shunt, and a lumen extending between the one or more CSF intake openings and the valve, the method comprises deploying the shunt in a body of a patient so that the distal portion of the shunt is at least partially disposed within a CP angle cistern, a body of the shunt is at least partially disposed within an IPS of the patient, and the proximal portion of the shunt is at least partially disposed within or proximate to a JV of the patient, wherein, after deployment of the shunt, CSF flows from the CP angle cistern to the JV via the shunt lumen at a flow rate in a range of 5 ml per hour to 15 ml per hour.

A handheld device configured to provide tactile stimulation to a head of a human user. The handheld device comprises an outer housing sized and shaped to fit ergonomically and substantially within a hand of the human user. The outer housing defines an internal space and skin facing surface for placement adjacent to or proximate the user's head. A controller is contained within internal space of the outer housing, wherein the controller is configured to generate a signal corresponding to a pattern sequence. A vibration unit is in electronic communication with the controller, the vibration unit being configured to be actuated in response to a signal from the controller so as to generate vibrations that correspond to the pattern sequence.

Methods for treating hydrocephalus using a shunt, the shunt having one or more CSF intake openings in a distal portion, a valve disposed in a proximal portion of the shunt, and a lumen extending between the one or more CSF intake openings and the valve, the method comprises deploying the shunt in a body of a patient so that the distal portion of the shunt is at least partially disposed within a CP angle cistern, a body of the shunt is at least partially disposed within an IPS of the patient, and the proximal portion of the shunt is at least partially disposed within or proximate to a JV of the patient, wherein, after deployment of the shunt, CSF flows from the CP angle cistern to the JV via the shunt lumen at a flow rate in a range of 5 ml per hour to 15 ml per hour.

A pressure support device (4) for providing pressure support therapy to a patient includes a pressure generating system (6,18) structured to generate pressure to provide pressure compensation to the patient via a patient circuit (12,14), one or more sensors (22,27,28) structured to gather data indicative of disordered breathing events of the patient, and a processing unit (24) structured to control the pressure generating system to provide a pressure compensation regimen to the patient; to analyze outputs of the one or more sensors while pressure support therapy is provided to the patient to determine if the pressure compensation regimen provided to the patient is effective to relieve one or more disordered breathing events, and to output an alert if it is determined that the pressure compensation regimen provided to the patient is not effective in relieving the one or more disordered breathing events.

Methods and devices to quickly and accurately apply medication to a paranasal sinus are disclosed. Additionally, the methods and devices prevent the medication applied to a paranasal sinus from flowing down a patient's throat by expanding, using an inflation lumen of a device, an expandable member of the device adjacent to the patient's choana.

A mask system for use between a patient and device to deliver a breathable gas to the patient includes a mouth cushion, a pair of nasal prongs, an elbow, and a headgear assembly. The mouth cushion is structured to sealingly engage around an exterior of a patient's mouth in use, and the pair of nasal prongs are structured to sealingly communicate with nasal passages of a patient's nose in use. The elbow delivers breathable gas to the patient. The headgear assembly maintains the mouth cushion and the nasal prongs in a desired position on the patient's face. The headgear assembly provides a substantially round crown strap that cups the parietal bone and occipital bone of the patient's head in use.

A PAP system is adapted for treatment of respiratory disease or sleep disordered breathing. The PAP system includes headgear, a patient interface and a flow generator. The flow generator includes a blower adapted to provide pressurized breathable gas to a patient through the patient interface. The blower is at least partially vibrationally isolated from the patient's head by at least one foam layer mounted within the flow generator to secure the blower. The at least one foam layer is adapted to reduce the amount of transmitted vibration received by the patient. The flow generator further includes a mounting structure limiting an extent of a compression of the at least one foam layer due to the weight of the blower. The mounting structure includes at least one protrusion extending from an interior surface of the flow generator toward the blower.

A catheter holder assembly for selectively holding a portion of a one or more catheter tubes to a head of a user. Comprising head mount assembly, a one or more catheter holders, the one or more catheter tubes, a catheter. The one or more catheter holders comprise a first catheter holder. The one or more catheter holders are attached to the head mount assembly. Head mount assembly is configured to releaseably attach to the head of the user. The one or more catheter holders releaseably hold the one or more catheter tubes. The one or more catheter tubes each comprise the catheter at a first end being a downstream of the one or more catheter holders and an IV bag at a second end being an upstream of the one or more catheter holders. The catheter is configured to attach to a portion of the user at an insertion point.