A Neonatal CNN (N-CNN) is provided for detecting neonatal pain emotion based upon facial recognition. A cascaded N-CNN is trained using a Neonatal Pain Assessment Database (NPAD) to automatically identify a neonatal patient experience pain in real-time. These results show that the automatic recognition of neonatal pain provided by the embodiments of the present invention is a viable and more efficient alternative to the current standard of pain assessment.

Physiological monitoring systems, apparatuses and methods are disclosed. In an embodiment, a system includes an umbilical cord clamp having a sensor and a base station. The clamp is moveable between an open position and a clamped position in which the sensor contacts the umbilical cord to sense a physiological parameter of a neonate. The base station is operable to transmit an interrogation signal wirelessly to the sensor, and in response to the interrogation signal, receive a response signal wirelessly that is indicative of the sensed physiological parameter.

Generally, a system for soothing a baby during imaging by an imaging device is provided. The system can include: a capsule incubator for positioning the baby within the imaging device, the capsule incubator can include: a bottom portion having an inner surface, a bed positioned on top of the inner surface for positioning the baby thereon, and one or more members coupled to the bottom portion that are positioned in a first position to open the capsule incubator and a second position to close the capsule incubator; a vibrational device including a vibrational element that extends from outside of the capsule incubator into the capsule incubator and is coupled to the bed to cause the bed to vibrate with a predetermined vibrational frequency, thus causing the baby to vibrate with the predetermined vibrational frequency.

A nasal airway pressure monitoring system and method for use with neonatal patients is provided. The nasal airway pressure monitoring system has a nasal catheter, a pressure monitor, and a respiratory circuit supplying a respiratory gas. The nasal catheter is connected at a first end to the pressure monitor via a sample line and the second end of the nasal catheter is positioned in a nares. Upon delivery of gas flow through the patient respiratory circuit, the nasal catheter transmits pressure waveform data from the nasal airway to the pressure monitor. The pressure monitor processes the pressure waveform data. If the mean airway pressure is outside of a pre-set range of maximum and minimum limits, an alarm is triggered.

The invention features soluble FGF decoy polypeptides and fusion polypeptides comprising an FGF decoy polypeptide linked to a heterologous polypeptide, such as an aggrecan binding protein. Both soluble FGF decoy polypeptides and fusion polypeptides can be used to prevent or treat skeletal disorders, such as achondroplasia.

A method of controlling an infant care device includes identifying, via a location tracking system, a device location of the infant care device within a care facility by locating a device location tag on the infant care device, and also identifying any local clinician tags worn by a clinician within a predetermined area around the device location. The local clinician tags are compared to a list of authorized clinician tags to identify whether at least one local authorized clinician tag is within the predetermined area around the infant care device. User input is received at a user interface associated with the infant care device to modify operation of the infant care device. Operation of the infant care device is modified based on the user input only if at least one local authorized clinician tag is within the predetermined area around the infant care device at the time of receiving the user input.

The present invention relates to methods for diagnosing Respiratory Distress Syndrome of newborn.

This disclosure generally relates to systems and methods for detecting, monitoring, and responding to abnormalities in an infant's breathing. One or more sensing devices may collect infant breathing 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 infant breathing. If infant breathing is determined to have stopped, a corrective action may be performed.

A method and system for generating pulse oximetry predictive scores for predicting adverse outcomes in preterm infants.

An infant joint compression device and methods of use including decreasing the length of stay in a neonatal intensive care unit and/or increasing bone density of a premature infant are disclosed. A device can include an elongated, generally cocoon-shaped device pod having a head pod end, a foot pod end and a pod interior extending between the head pod end and the foot pod end; a head opening at the head pod end and communicating with the pod interior; and a pod slit extending from the head opening toward the foot pod end and communicating with the pod interior.