Devices, systems, and methods described herein can provide a simulated fluid environment similar to the mother's womb to recreate an ideal or more familiar environment for infants who are born before their ideal due date. In some embodiments, the premature infant amniotic bath incubator can comprise an incubating tank with synthetic or simulated amniotic fluid, a heating element(s), a temperature sensor(s), and/or thermostat(s) for temperature regulation.

A respiratory humidification system includes a humidifier that is capable of electronic communication with one or more other components of the system thereby permitting transfer of data or control signals between the humidifier and other components of the system. In some systems, a flow generator, such as a ventilator, is provided to supply a flow of breathing gas. The humidifier and the flow generator are capable of electronic communication with one another. In some arrangements, an operating mode or parameter of the humidifier to be set or confirmed by the flow generator, either automatically or manually through a user interface of the flow generator. The humidifier can also utilize data provided by the flow generator or other system component, such as an incubator, to set or confirm an operating mode or parameter of the humidifier. In some arrangements, a user interface of the humidifier can display data from another system component, such as a nebulizer or pulse oximeter.

A respiratory humidification system includes a humidifier that is capable of electronic communication with one or more other components of the system thereby permitting transfer of data or control signals between the humidifier and other components of the system. In some systems, a flow generator, such as a ventilator, is provided to supply a flow of breathing gas. The humidifier and the flow generator are capable of electronic communication with one another. In some arrangements, an operating mode or parameter of the humidifier to be set or confirmed by the flow generator, either automatically or manually through a user interface of the flow generator. The humidifier can also utilize data provided by the flow generator or other system component, such as an incubator, to set or confirm an operating mode or parameter of the humidifier. In some arrangements, a user interface of the humidifier can display data from another system component, such as a nebulizer or pulse oximeter.

An infant warming system comprising a platform for supporting an infant, at least two chest electrodes configured to connect to and detect cardiac potentials from a chest of the infant, an ECG monitor configured to receive the cardiac potentials from the at least two chest electrodes and determine a heart rate based on the cardiac potentials, a pulse oximeter device configured to determine an SpO.sub.2 for the infant, and a processor configured to compare the heart rate for the infant to a first heart rate threshold and compare the SpO.sub.2 for the infant to a first SpO.sub.2 threshold. The processor can also adjust a display of the heart rate and the SpO.sub.2 on a display device based on the comparisons and generate a first care instruction via a user interface based on the heart rate, the SpO.sub.2, or a combination thereof.

An infant warming system comprising a platform for supporting an infant, at least two chest electrodes configured to connect to and detect cardiac potentials from a chest of the infant, an ECG monitor configured to receive the cardiac potentials from the at least two chest electrodes and determine a heart rate based on the cardiac potentials, a pulse oximeter device configured to determine an SpO.sub.2 for the infant, and a processor configured to compare the heart rate for the infant to a first heart rate threshold and compare the SpO.sub.2 for the infant to a first SpO.sub.2 threshold. The processor can also adjust a display of the heart rate and the SpO.sub.2 on a display device based on the comparisons and generate a first care instruction via a user interface based on the heart rate, the SpO.sub.2, or a combination thereof.

This disclosure generally relates to systems and methods for detecting, monitoring, and responding to abnormalities in a subject's breathing or heartbeat. One or more sensing devices may collect breathing or heartbeat related data, which may be filtered and converted to a frequency signal. The frequency signal may be monitored for irregularity or stoppage, and a processing module may determine whether the irregularity or stoppage is caused by an actual stoppage or irregularity in breathing or heartbeat. If breathing or heartbeat is determined to have stopped, a corrective action may be performed.

Systems and methods are provided for an infant incubator having features for active noise cancellation, including enclosure designs, positioning systems, and error sensor selection.

Systems and methods are provided for an infant incubator having features for active noise cancellation, including enclosure designs, positioning systems, and error sensor selection.

An infant care station is described herein that can include a wall of the infant care station, wherein the wall comprises a primary latch and at least one secondary latch comprising a hinge with at least one bottom pin and at least one top pin, wherein the infant care station is an incubator, a warmer, or a combination thereof. In some examples, one or more pin acceptors are proximate the hinge, wherein the one or more pin acceptors hold the at least one bottom pin and the at least one top pin of the hinge in a closed position of the wall, and wherein the at least one top pin of the wall is released from the one or more pin acceptors in response to a force applied to the wall.

Various systems and devices are provided for determining a weaning readiness for weaning a patient from a thermoregulated microenvironment. In one example, a method includes receiving a plurality of current patient parameters of a patient housed in a thermoregulated microenvironment, applying a weaning model to the plurality of current patient parameters to generate a weaning index representing a likelihood that the patient will be successfully weaned from the microenvironment if weaned at that time, the weaning model trained to correlate the current patient parameters with the likelihood based on historical data of prior patients and known outcomes for those prior patients, and outputting the weaning index for display on a display device and/or for storage in a medical record of the patient.