A61J15/008

Docking station for an enteral feeding device

A docking station receives an enteral feeding pump or food pod into a cradle with a scales platform. The docking station is calibrated to determine nutritional data consumption and remaining available food on the basis of remaining food weight and nutritional data read from a tag using NFC. The station has a sealing sleeve with a sealing rim to confine any spillages in a manner which does not affect weight of the device on a weighting platform.

APPLIANCE FOR ENTERAL NUTRITION
20170304154 · 2017-10-26 ·

An appliance (1) for enteral nutrition by means of a probe of the type comprising a tubular element of elongated shape and substantially flexible which defines a feeding channel open at the extremities for the introduction of nutritional substances in the stomach of a patient and which comprises at least a first inflatable balloon for detecting the pressure inside the oesophagus of a patient, the tubular element comprising at least a first inlet/outlet mouth for the air in/from the first balloon, the appliance (1) further comprising: at least a pneumatic circuit (3) having pumping means (4) associable at least with the first inlet/outlet mouth for inflating/deflating the first balloon; processing means (8) comprising: detection means which can be connected to the first balloon to detect the patient's oesophageal pressure (p.sub.es); reading means of the pressure of the respiratory tract (p.sub.aw) which can be connected to an external detection device; calculation means operatively connected to the detection means and to the reading means and able to calculate at least the transpulmonary pressure (p.sub.tp); graphic display means (10) operatively connected to the processing means (8) and able to display at least one of the oesophageal pressure (p.sub.es), the pressure of the respiratory tract (p.sub.aw) and the transpulmonary pressure (p.sub.tp).

Detection system for flow control apparatus

A flow control apparatus adapted to receive a feeding set includes a housing capable of receiving at least a portion of the feeding set. A pumping device is supported by the housing and positioned to contact the feeding set when the feeding set is received by the housing so the pumping device acts on the feeding set to produce fluid flow in the feeding set for delivery of fluid to a subject. An ultrasonic sensor is supported by the housing and arranged with respect to the pumping device to produce a sensor signal indicative of a viscosity of the fluid delivered through the feeding set. A control circuit is in communication with the ultrasonic sensor for receiving the sensor signal from the sensor indicative of the viscosity of the fluid and in communication with the pumping device to control operation thereof.

SYSTEMS, DEVICES AND METHODS FOR DETERMINING LARYNGOPHARYNGEAL PRESSURE AND/OR LOWER OESOPHAGEAL SPHINCTER PRESSURE

Embodiments generally relate to a device for monitoring air pressure in the body of a patient. The device comprises a tube comprising a feeding lumen; a sensor lumen positioned parallel to the feeding lumen; at least one sensor positioned in the sensor lumen; and at least one perforation positioned to expose the at least one sensor to an air pressure within the body of a patient when the device is positioned at least partially in the airway of the patient. The at least one sensor is configured to generate data related to the pressure to which the sensor has been exposed.

DEVICES AND METHODS TO MEASURE GASTRIC RESIDUAL VOLUME

Devices and methods to measure gastric residual volume (GRV) are described where at least one additive component (a GRV indicator) may be dispersed in a body lumen such as a stomach. The GRV indicator may changes a physical (chemical, electrical, thermal, mechanical, optical, etc.) characteristic within the stomach by a measureable degree. This degree of change and/or the rate of return to the previous state, may be used to determine the GRV of a patient. The determined GRV can also be used to automatically or semi-automatically control the patient's feeding rate and/or volume and/or frequency to adequately nourish the patient but avoid complications. The physical characteristic(s) may also be used to detect that the feeding catheter or tube is in the correct location (ie stomach vs lung or esophagus.

INSERTION DEVICE POSITIONING GUIDANCE SYSTEM AND METHOD
20220117676 · 2022-04-21 ·

There is provided herein a guidance system for positioning an insertion device comprising: an electromagnetic field generator configured to generate an electromagnetic field covering a treatment area, an insertion device comprising an electromagnetic sensor, the electromagnetic sensor configured to receive signals indicative of the electromagnetic field, and a processing circuitry configured to: load an X-ray, CT, ultrasound or MRI image of the subject's chest, mark a location of a first and a second anatomic landmarks on the subject's torso using a registration sensor and obtaining a subject coordinate system based thereon, identify the location of the first and the second anatomic landmarks on the loaded X-ray, CT, ultrasound or MRI image of the subject's chest; aligning the subject coordinate system with the loaded X-ray, CT, ultrasound or MRI image, and display, on the image, a path of the insertion device insertion with respect to the first and the second anatomic locations; wherein the path is generated according to changes in the strength of the electromagnetic field sensed by the tip sensor's during the insertion of the insertion device.

INTERACTIVE NGT SYSTEM
20210353505 · 2021-11-18 · ·

Disclosed is an NGT system, the system comprises a nasogastric tube having a diameter and length configured to pass through an esophagus such that the lumen of the NGT maintains fluid communication with a portion of the digestive tract, and a digestive tract sensor operatively associated with the NGT, the digestive tract sensor configured to sense from inside the body and transmit signals in response to one or both of conditions relating to nourishment states of the digestive tract, and positioning of the NGT.

System for determining gastric motility and for feeding a patient

A system (100) for artificially feeding a patient, comprising: a pressure sensor (114) fluidly connectable to an inflatable balloon (B) via a first lumen of a balloon catheter (130); a controller (110) operatively connected to the pressure sensor (114) for obtaining the measured pressure values; a food pump (112) fluidly connectable to a second lumen of the balloon catheter having at least one opening (132) for providing food; the controller (110) operatively connected to the food pump (112) for driving the food pump at a configurable flow rate; wherein the controller (110) contains computer executable instructions comprising: first code fragments for performing a first algorithm (1300) for extracting gastric motility information from the measured pressure values, and second code fragments for performing a second algorithm for dynamically adjusting (708) said flow rate based on said extracted gastric motility information.

Hub Component for Vented Connector
20220280766 · 2022-09-08 ·

A hub component for a vented connector including a generally elongate cylindrical body having a first end and a second end. The first end of the hub component includes one or more fingers or clips for engagement with one or more vents of the vented connector. The second end of the hub component can be configured for compatible engagement with a carbon dioxide detector.

INSERTION DEVICE POSITIONING GUIDANCE SYSTEM AND METHOD
20220313367 · 2022-10-06 ·

There is provided herein a guidance system for positioning an insertion device comprising: an electromagnetic field generator configured to generate an electromagnetic field covering a treatment area, an insertion device comprising an electromagnetic sensor, the electromagnetic sensor configured to receive signals indicative of the electromagnetic field, and a processing circuitry configured to: load an X-ray, CT, ultrasound or MRI image of the subject's chest, mark a location of a first and a second anatomic landmarks on the subject's torso using a registration sensor and obtaining a subject coordinate system based thereon, identify the location of the first and the second anatomic landmarks on the loaded X-ray, CT, ultrasound or MRI image of the subject's chest; aligning the subject coordinate system with the loaded X-ray, CT, ultrasound or MRI image, and display, on the image, a path of the insertion device insertion with respect to the first and the second anatomic locations; wherein the path is generated according to changes in the strength of the electromagnetic field sensed by the tip sensor's during the insertion of the insertion device.