Moisture sensors
US-9780554-B2 · Oct 3, 2017 · US
US10716895B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10716895-B2 |
| Application number | US-201615240208-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 18, 2016 |
| Priority date | Jun 3, 2013 |
| Publication date | Jul 21, 2020 |
| Grant date | Jul 21, 2020 |
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Some embodiments of an infusion pump system may be configured to detect when at least one component of the pump system is exposed to a moisture level above a threshold level. In particular embodiments, the infusion pump system can be equipped with a moisture level detection system that can sense when a moisture level above the threshold level has occurred to the pump device, which thereby enables the infusion pump system to initiate one or more patient safety countermeasures.
Opening claim text (preview).
What is claimed is: 1. A medical infusion pump system, comprising: a portable housing defining a space to receive a medicine; a pump drive system to dispense medicine from the portable housing when the medicine is received in the space; control circuitry that electrically communicates with the pump drive system to control dispensation of the medicine from the portable housing when the medicine is received in the space; and hydrophilic foam material positioned in the portable housing and in electrical communication with the control circuitry, the control circuitry being adapted to detect absorption of moisture into the hydrophilic foam material, wherein the portable housing defines one or more liquid weep holes, and wherein the one or more liquid weep holes have a predefined size for passage of liquid through the outer wall the portable housing after a submersion in liquid at a particular threshold depth or greater and for a particular threshold duration of time. 2. The medical infusion pump system of claim 1 , wherein the control circuitry is adapted to provide an indication of a moisture level in the portable housing. 3. The medical infusion pump system of claim 1 , wherein the control circuitry is adapted to determine if a moisture level in the portable housing is greater than or equal to a predetermine non-zero threshold level of moisture. 4. The medical infusion pump system of claim 3 , wherein the control circuitry is configured to initiate an alarm in response to the indication that the moisture level in the portable housing is greater than or equal to the predetermined non-zero threshold level of moisture. 5. The portable infusion pump system of claim 4 , wherein, in response to the indication that the moisture level in the portable housing is greater than or equal to the predetermined non-zero threshold level of moisture, the control circuitry is configured to disable the drive system, activate an audible alarm, and display of one or more messages on a user interface display located on the portable housing. 6. The portable infusion pump system of claim 2 , wherein the indication of the moisture level in the portable housing is based on a change in electrical resistance of the hydrophilic foam material. 7. The medical infusion pump system of claim 1 , wherein the control circuitry is housed in a controller housing that is removably attachable to the portable housing. 8. The medical infusion pump system of claim 1 , wherein the one or more liquid weep holes are positioned adjacent the hydrophilic foam material. 9. A method of controlling a portable infusion pump system, comprising: sensing that a hydrophilic foam material positioned in a portable infusion pump system has a change in an electrical resistance; and in response to the sensing that the change in an electrical resistance exceeds a threshold, disabling a pump drive system housed in the portable infusion pump system, wherein the portable infusion pump system defines one or more liquid weep holes, and wherein the one or more liquid weep holes have a predefined size for passage of liquid through an outer wall a pump housing of the portable infusion pump system after a submersion in liquid at a particular threshold depth or greater and for a particular threshold duration of time. 10. The method of claim 9 , further comprising in response to the sensing that the change in an electrical resistance exceeds a threshold, emitting an audible alarm. 11. The method of claim 10 , further comprising in response to the sensing that the change in an electrical resistance exceeds a threshold, displaying one or more alert messages on a user interface display of the portable infusion pump system. 12. The method of claim 11 , further comprising in response to the sensing that the change in an electrical resistance exceeds a threshold, activating a light source of the portable infusion pump system that is different from the user interface display. 13. The method of claim 9 , wherein the one or more liquid weep holes are positioned adjacent the hydrophilic foam material. 14. A medical infusion pump system, comprising: a portable housing defining a space to receive a medicine; a pump drive system to dispense medicine from the portable housing when the medicine is received in the space; control circuitry that electrically communicates with the pump drive system to control dispensation of the medicine from the portable housing when the medicine is received in the space; hydrophilic foam material positioned in the portable housing and in electrical communication with the control circuitry, the control circuitry being adapted to detect absorption of moisture into the hydrophilic foam material; and a plurality of conductive pads including a first conductive pad, a second conductive pad, and a third conductive pad that are each in electrical communication with the hydrophilic foam material, wherein the control circuitry is adapted to (i) detect, based on detected voltage levels of the first conductive pad and the third conductive pad, absorption of moisture to a first portion of the hydrophilic foam material and (ii) detect, based on detected voltage levels of the second conductive pad and the third conductive pad, absorption of moisture to a second portion of the hydrophilic foam material wherein the first conductive pad and the second conductive pad are connected to one or more voltage sources and the third conductive pad is connected to ground. 15. The medical infusion pump system of claim 14 , wherein the portable housing defines one or more liquid weep holes positioned adjacent the hydrophilic foam material. 16. The medical infusion pump system of claim 15 , wherein the one or more liquid weep holes have a predefined size for passage of liquid through the outer wall the portable housing after a submersion in liquid at a particular threshold depth or greater and for a particular threshold duration of time. 17. The medical infusion pump system of claim 14 , wherein the first conductive pad, the second conductive pad, and the third conductive pad are respectively coupled to a first coupling portion, a second coupling portion, a third coupling portion of the hydrophilic foam material, and wherein the first portion of the hydrophilic foam material is between the first coupling portion and the third coupling portion of the hydrophilic foam material and the second portion of the hydrophilic foam material is between the second coupling portion and the third coupling portion of the hydrophilic foam material.
adapted to be carried by the patient, e.g. portable on the body · CPC title
with means for compensating influence from the environment · CPC title
characterised by a particular materials · CPC title
Monitoring, detecting, signalling or eliminating infusion flow anomalies (low-level float-valves causing cut-off A61M5/40; indicating or recording presence, absence or direction of flow in general G01P13/0066) · CPC title
using feedback of body parameters, e.g. blood-sugar, pressure (measurement of body parameters A61B5/00) · CPC title
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