Described is an autoinjector comprising a case, a door hingedly coupled to the case and having an open position and a closed position, a plunger slidably disposed in the case, and at least one drive spring applying a biasing force on the plunger relative to the case, wherein the door is operably coupled to the plunger, and wherein rotation of the door from the closed position to the open position moves the plunger from a distal position in the case to a proximal position in the case and compresses the at least one drive spring.

System and methods for controlling healthcare devices and systems using voice commands are presented. In some aspects a listening device may receive voice command from a person. The voice command may be translated into human readable or machine readable text via a speech-to-text service. A control component may receive the text and send device-specific instructions to a medical device associated with a patient based on the translated voice command. In response to the instructions, the medical device may take an action on a patient. Some examples of actions taken may include setting an alarm limit on a monitor actively monitoring a patient and adjusting the amount of medication delivered by an infusion pump. Because these devices may be controlled using a voice command, in some cases, no physical or manual interaction is needed with the device. As such, multiple devices may be hands-free controlled from any location.

Various control methods can indirectly determine incorrect connections between components in a respiratory therapy system. For example, incorrect connections can occur between a patient interface, a humidifier and/or a gases source. The methods can indirectly detect if reverse flow conditions or other error conditions exist. A reverse flow condition can occur when gases flows in a direction different from an intended direction of flow. The methods can be implemented at the humidifier side, at the gases source side, or both.

Techniques described herein can identify usage information for sensors. In one example, an anesthesia device can include a processor to obtain usage information from a first flow sensor coupled to the anesthesia device. The processor can also determine the usage information exceeds a predetermined limit and generate an alert indicating the first flow sensor is to be replaced.

A therapeutic gas delivery system with at least one gas supply subsystem is disclosed. The at least one gas supply subsystem may include a gas source coupling configured to receive a therapeutic gas source and form a fluid flow connection with the therapeutic gas source, a therapeutic gas delivery system controller, and one or more display(s) configured to be in communication over a communication path with the therapeutic gas delivery system controller. The display may be configured to display a graphical, illustrative, or numerical indicator of one or more flow or system parameters.

A system for confirmation of fluid delivery to a patient at the clinical point of use is provided. The system includes a wearable electronic device. The wearable electronic device has a housing; at least one imaging sensor associated with the housing; a data transmission interface; a data reporting accessory for providing data to the user; a microprocessor for managing the at least one imaging sensor, the data transmission interface, and the data reporting accessory; and a program for acquiring and processing images from the at least one imaging sensor. The system further includes a fluid delivery apparatus; and one or more identification tags attached to or integrally formed with the fluid delivery apparatus. The program processes an image captured by the at least one imaging sensor to identify the one or more identification tags and acquires fluid delivery apparatus information from the one or more identification tags.

A ventilation monitoring system for assisting in proper placement of an endotracheal tube in a subject includes: a capnography sensor configured to be placed in fluid communication with the endotracheal tube and to provide information representative of the subject's breath; and a processor in communication with the capnography sensor. The processor is configured to provide an indication of proper endotracheal tube placement when (1) a first indication of the subject's breath and a positive result of a first auscultation are identified within a first predetermined time period, and (2) a second indication of the subject's breath and a positive result of a second auscultation are identified within a second predetermined time period. The first auscultation includes auscultation of a subject's left lung, right lung, left axillary region, right axillary region, or abdomen. The second auscultation includes auscultation of another region of the subject different from the first auscultation.

Disclosed is an auto-injector for administering a medicament, comprising: a housing; a cartridge receiver configured to receive a cartridge comprising a first stopper; a drive module coupled to move a plunger rod configured to move the first stopper; a resistance sensor configured to provide a resistance signal indicative of resistance against movement of the plunger rod; and a processing unit coupled to the drive module and to the resistance sensor. The processing unit being configured to: control the drive module to move the plunger rod towards the extended plunger rod position; determine present plunger rod position; receive the resistance signal; determine a cartridge parameter based on the resistance signal and the present plunger rod position; and control the drive module to adjust the movement of the plunger rod based on the cartridge parameter.

An inhaler tracker module is secured to an inhaler and has an activation sensor for sensing use of the inhaler. The tracker module includes a memory for storing inhaler use data, and a communications component for wirelessly transmitting the stored inhaler use data. The tracker module is wrapped around the inhaler body and includes a pressure switch located at the top of the canister to detect a user pressing the canister into the body for inhaler use. The tracking module has a standby mode in which it remains until inhaler use or until inhaler use data is stored and it is transmitted. A pairing function is provided.