Abstract: A medical system (100) provides a setting recommendation (105) for a ventilator. A data interface (110) receives static patient data that includes values of patient parameters that are substantially invariant during a treatment period. A measurement interface (120) receives dynamic patient data that includes values of patient parameters that change during the treatment period. A processing unit (150) determines a new current patient data set based on the currently available patient data immediately after receiving the patient data and initiates, triggered by the determination of the new current patient data set, a comparison between the values of the current patient data set and stored assignment rules from a rule memory. Based on the comparison, a recommended device setting (134) of the ventilator, in view of the current patient data set, is received from a rule memory unit. A recommendation is output based on a comparison with a current device setting.

Abstract: A process coordinates the acoustic alarm signals output by different medical devices (1). A first medical device (1a) outputs, at a time interval before an output of a n acoustic alarm signal, a pre-signal which differs from the acoustic alarm signal with respect to at least one property. A further device receives the pre-signal output by the first medical device (1a) and carries out an analysis of the received pre-signal. As a function of a result of the analysis of the pre-signal, an alarm signal output unit (4) of a second medical device (1b) is driven in such a way that, as a function of the result of the analysis, at least one property of an alarm signal which is currently being output or will be output by the alarm signal output unit (4) is at least temporarily changed and/or a pre-signal is transmitted by the second medical device (1b).

Abstract: A system and process monitor a patient with an evaluation unit (1), a first interface (2) for receiving patient status values from a plurality of medical devices (3) to be available to the evaluation unit (1). The evaluation unit (1) generates a signal with patient-specific information based on the received patient status values and a further setpoint and/or actual value and transmits the signal to a receiver unit (5) via the first and/or a second interface (4). The evaluation unit (1) includes a suggestion module (6) that determines a suggested value which corresponds to a limit value for at least one patient status value based on the patient status values obtained from at least two medical devices (3) and the further setpoint and/or actual value, and to transmit this suggested value to the receiving unit (5) via the first and/or the at least one second interface (2, 4).

Abstract: A device, process and computer program based process provide a suggestion for at least one adapted alarm condition for a user in a medical system. The device includes a processing device configured to generate at least one adapted alarm condition of an alarm concerning at least one parameter triggering the alarm. The alarm condition is provided to offer to the user a possibility of adapting the alarm condition when an alarm frequency exceeds a limit value. The device further includes an interface, which is configured to provide the suggestion for the at least one adapted alarm condition of the alarm. The process includes the generation of at least one adapted alarm condition of an alarm concerning at least one parameter triggering the alarm. This adapted alarm condition is provided to offer the user the possibility of adapting the alarm condition when an alarm frequency exceeds a limit value.

Abstract: A valve module (20) for a ventilation system (100), includes a tube interface (21) for connection to a counter-tube interface (14) of an exhalation end (13) of a ventilation tube element (11) as well as a device interface (22) for connection to a counter-device interface (114) of an exhalation port (113) of a ventilator (110). The device interface has an exhalation valve section (24) providing an exhalation flow (93) of exhaled air (92) with an exhalation pressure (94). The exhaled air from the tube interface (21) flows through a module space (23). A ventilation tube device (10), the ventilator (110) as well as the ventilation system are provided with the valve module. Processes are provided for severing and establishing a connection between the device interface, the ventilation tube device and the counter-device interface of the exhalation port of the ventilator of the ventilation system.

Abstract: A patient management system (100) manages an assignment to a patient, with a plurality of patient identifiers (110, 110?, 110?) and with a central patient monitoring device (120). Each of the patient identifiers has patient-specific information (112) stored thereon and is assigned to one of a plurality of patients. Each patient identifier includes a communication interface (114) configured to wirelessly output the patient-specific information. The central patient monitoring device is configured to detect and to store an assignment between the patient-specific information and the patient identifier based on the output (116) of the communication interface of the patient identifier. The patient monitoring device is configured to receive a forwarded signal (126) assigned to the patient identifier or to the patient-specific information and to process this forwarded signal based on the stored assignment.

Abstract: A patient management system (100) for managing an assignment to a patient, includes a plurality of patient identifiers (110). The patient identifiers are intended for use by a medical staff. Each of the patient identifiers, in which patient-specific information (112) is stored, is assigned to a corresponding one of a plurality of patients. A mobile user carrier device (120) is configured to store a plurality of patient identifiers, so that a number of patient identifiers currently being stored at the mobile user carrier device can be visually recognized. The mobile user carrier device has an energy storage device (122) and a communication interface (124). The mobile user carrier device is configured to read out the respective patient-specific information of the patient identifiers being stored at the mobile user carrier device, at least partially, and to output same wirelessly via the communication interface.

Abstract: A device, process and computer program based process provide a suggestion for at least one adapted alarm condition for a user in a medical system. The device includes a processing device configured to generate at least one adapted alarm condition of an alarm concerning at least one parameter triggering the alarm. The alarm condition is provided to offer to the user a possibility of adapting the alarm condition when an alarm frequency exceeds a limit value. The device further includes an interface, which is configured to provide the suggestion for the at least one adapted alarm condition of the alarm. The process includes the generation of at least one adapted alarm condition of an alarm concerning at least one parameter triggering the alarm. This adapted alarm condition is provided to offer the user the possibility of adapting the alarm condition when an alarm frequency exceeds a limit value.

Abstract: A medical device is provided with an alarm organization. A process for alarm organization of a medical device is also provided. Based on pressure measured values and flow measured values and with a comparison criterion, it is determined whether an elevation of an airway pressure of an anesthesia device or of a ventilator is caused by a coughing event. A visual and/or acoustic output of a warning or alarm is adapted, indicating the elevated airway pressure PAW_High.

Abstract: A process for operating a medical device (10) includes applying a counter-torque, which acts during the rotation of a rotary knob (12) and depends on a current measured value (34). An actuator (20) applies the counter torque. A medical device (10) operates according to the process.

Abstract: A medical device determines operating situations and a method determines operating situations in a medical device. Based on pressure measured values (99) and flow measured values (97), it is determined whether an elevation of an airway pressure (105) in a medical device is due to a cough event (113) or to a plurality of cough events (117), which indicate an accumulation of secretion. An outputting (41, 42, 44) of a warning (44) or alarm (41, 42) is provided indicating the accumulation of secretion.

Abstract: A ventilator (1) determines states with cough attacks and an operating method for a ventilator determines cough attacks. It is determined on the basis of pressure measured values (13, 21, 19) and flow measured values (11, 15, 17) whether consecutive elevations of an airway pressure in a ventilator (1) are due to one cough event or due to a plurality of cough events. A plurality of cough events indicates a state of a cough attack. An output (41, 42, 44) of a warning (44) or alarm (42) is issued indicating the state.

Abstract: A device, a process and a computer program for a medical device, which is arranged in a first room, includes the monitoring (12) of sensor signals of a patient receiving medical care. An alarm situation is detected (14) based on the sensor signals and the provision (16) of an alarm signal when an alarm situation is present. The process (10) further includes waiting (18) for a predefined time period, the outputting (20) of a control signal if no confirmation signal was received for the alarm signal during the predefined time period, and the provision (22) of information on the alarm situation in a second room based on the control signal.

Abstract: A transfer unit (20), for a ventilator (1), is provided for carrying out a ventilation process of a patient. A ventilator (1) for carrying out a ventilation process of a patient, is provided that includes a ventilation unit (10) with a pneumatic unit (16) for carrying out the ventilation process as well as the transfer unit (20) mounted reversibly at the ventilation unit (10). A ventilation system (100) for carrying out a ventilation process of a patient, is provided including a transfer unit (20) and at least two ventilation units (10). A process for changing a ventilator (1) is provided for the ventilation process of a patient, wherein the transfer unit (20) can be mounted in the ventilation system (100) at a first ventilation unit (10) for forming a first ventilator (1) and at a second ventilation unit (10) for forming a second ventilator (1).

Abstract: A valve module (20) for a ventilation system (100), includes a tube interface (21) for connection to a counter-tube interface (14) of an exhalation end (13) of a ventilation tube element (11) as well as a device interface (22) for connection to a counter-device interface (114) of an exhalation port (113) of a ventilator (110). The device interface has an exhalation valve section (24) providing an exhalation flow (93) of exhaled air (92) with an exhalation pressure (94). The exhaled air from the tube interface (21) flows through a module space (23). A ventilation tube device (10), the ventilator (110) as well as the ventilation system are provided with the valve module. Processes are provided for severing and establishing a connection between the device interface, the ventilation tube device and the counter-device interface of the exhalation port of the ventilator of the ventilation system.

Abstract: A device, a process and a computer program for a medical device, which is arranged in a first room, includes the monitoring (12) of sensor signals of a patient receiving medical care. An alarm situation is detected (14) based on the sensor signals and the provision (16) of an alarm signal when an alarm situation is present. The process (10) further includes waiting (18) for a predefined time period, the outputting (20) of a control signal if no confirmation signal was received for the alarm signal during the predefined time period, and the provision (22) of information on the alarm situation in a second room based on the control signal.

Abstract: A method sends an alarm to persons (P1, P2, P3, P4, P5), who are located in an area of a warning device (1, 2, 3, 4, 5), as a function of request signals (S1, S2) of at least one alarm source (10, 11). Each warning device specifies current countdowns (S1C1, S1C2, S1C3, S1C4, S1C5, S2C1, S2C2, S2C3, S2C4, S2C5) for each alarm source. When a request signal is sent by one of the alarm sources, the corresponding countdowns of all warning devices that receive the request signal are started. The warning device, with a countdown that has come to an end, sends an alarm signal (S1A1, S1A2, S1A3, S1A4, S1A5, S2A1, S2A2, S2A3, S2A4, S2A5). A manual acceptance of the sent alarm signal by a person, who is located in the area of the warning device that sends the alarm signal, ends the started countdowns of the other warning devices.

Abstract: A device (10) for the alarm server (100) includes an interface (12) for communication with one or more alarm sources (200) and with one or more alarm generators (300). A memory (14) stores information relating to alarms. A control module (16) is configured to control the one or more interfaces (12) and the memory (14) and receive an indication relating to an alarm from an alarm source (200) via the one or more interfaces (12) and to store information relating to the alarm in the memory (14) and to receive an alarm request from an alarm generator (300) via the one or more interfaces and to provide information relating to the alarm for the alarm generator (300) upon receipt of the alarm request if information relating to the alarm is stored in the memory (14).

Abstract: A method sends an alarm to persons (P1, P2, P3, P4, P5), who are located in an area of a warning device (1, 2, 3, 4, 5), as a function of request signals (S1, S2) of at least one alarm source (10, 11). Each warning device specifies current countdowns (S1C1, S1C2, S1C3, S1C4, S1C5, S2C1, S2C2, S2C3, S2C4, S2C5) for each alarm source. When a request signal is sent by one of the alarm sources, the corresponding countdowns of all warning devices that receive the request signal are started. The warning device, with a countdown that has come to an end, sends an alarm signal (S1A1, S1A2, S1A3, S1A4, S1A5, S2A1, S2A2, S2A3, S2A4, S2A5). A manual acceptance of the sent alarm signal by a person, who is located in the area of the warning device that sends the alarm signal, ends the started countdowns of the other warning devices.

Abstract: A medical device determines operating situations and a method determines operating situations in a medical device. Based on pressure measured values (99) and flow measured values (97), it is determined whether an elevation of an airway pressure (105) in a medical device is due to a cough event (113) or to a plurality of cough events (117), which indicate an accumulation of secretion. An outputting (41, 42, 44) of a warning (44) or alarm (41, 42) is provided indicating the accumulation of secretion.