Abstract: An apparatus for monitoring an obstetrics patient during labour is provided. The apparatus receives a contraction signal conveying information related to occurrences of uterine contractions over time and processes his signal to derive a sequence of rates of uterine contractions over time. The apparatus also implements a Graphical User Interface (GUI) presenting a tracing of at least part of the sequence of rates of uterine contractions over time along with a threshold rate of uterine contractions GUI is dynamically adapted over time based on the contraction signal received. The sequence of rates of uterine contractions derived over time is also processed to detect occurrences of anomalous contraction rates and to identify one or more portions of the tracing corresponding to sustained anomalous contraction rate segments during which anomalous contraction rates have persisted for time durations exceeding a pre-determined time duration.

Abstract: A graphical user interface is provided displaying a first viewing window selected from a set of possible viewing windows conveying respective feature measurements related to labor progression. At least one viewing window in the set of possible viewing windows conveys a given feature measurement and a safety limit associated to the given feature measurement. The graphical user interface also displays at least one control allowing a user to select a subset of viewing windows from the set of possible viewing windows, the subset of viewing windows including at least one viewing window other than the first viewing window. The selected subset of viewing windows is displayed simultaneously with the first viewing window. In response to the given feature measurement exceeding the associated safety limit, information is displayed to attract the attention of the user to the viewing window conveying the given feature measurement.

Abstract: A system and apparatus for implementing a user interface for displaying uterine contraction information is provided. The graphical user interface displays first information conveying a rate of uterine contractions, the first information being derived at least in part on the basis of at least a portion of a contraction signal. The graphical user interface also displays, concurrently with the first information, second information conveying a threshold rate of uterine contractions. In specific examples of implementation, the graphical user interface is adapted for selectively causing an alarm event based at least in part on a rate of uterine contractions conveyed by the first information and the threshold rate of uterine contractions.

Abstract: A system and apparatus implementing a graphical user interface module for displaying information conveying a level of risk of delivery with shoulder dystocia associated to an obstetrics patient. The graphical user interface module displays a set of user modifiable information fields for allowing a user to enter a set of patient information data elements associated to the obstetrics patient. The graphical user interface module also displays a control allowing a user to cause the set of information data elements to be transmitted to a processing unit adapted to derive patient risk data at least in part on the basis of the set of information data elements, the patient risk data conveying a level of risk of delivery with shoulder dystocia. The graphical user interface module then displays the patient risk data with reference to risk assessment information.

Abstract: A method and an apparatus for estimating a level of risk of shoulder dystocia with neonatal injury associated to an obstetrics patient are provided. A set of information data elements associated to an obstetrics patient is received including information derived from a maternal weight component, a maternal height component and a fetal weight component. The set of information data elements is processing to derive a ranking data element associated to the obstetrics patient. The ranking data element conveys a level of risk of shoulder dystocia associated to the obstetrics patient. The ranking data element is then released.