Infusion devices and related methods and systems for preemptive alerting
First Claim
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1. A method of alerting a user, the method comprising:
- periodically obtaining interstitial fluid measurement values for a physiological condition in a body of the user from a sensing arrangement including one or more interstitial sensing elements, the physiological condition being influenced by a fluid delivered by an infusion device; and
in response to each new interstitial fluid measurement value of the interstitial fluid measurement values;
obtaining a current amount of active fluid in the body of the user;
determining an estimated correction bolus amount of the fluid based at least in part on the current amount of active fluid, a target value for the physiological condition, and a current interstitial fluid measurement value for the physiological condition;
determining a trend adjustment factor based on a difference between the current interstitial fluid measurement value and a preceding interstitial fluid measurement value;
adjusting the estimated correction bolus amount by multiplying the estimated correction bolus amount by the trend adjustment factor; and
generating an alert when the estimated correction bolus amount is greater than an alert threshold value.
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Abstract
Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of alerting a user associated with an infusion device delivering fluid to the body of the user involves obtaining a measurement value for a physiological condition being influenced by the fluid, obtaining a current amount of active fluid in the body of the user, determining a homeostasis metric based at least in part on the current amount of active fluid and the measurement value for the physiological condition, and generating an alert based at least in part on the homeostasis metric.
244 Citations
20 Claims
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1. A method of alerting a user, the method comprising:
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periodically obtaining interstitial fluid measurement values for a physiological condition in a body of the user from a sensing arrangement including one or more interstitial sensing elements, the physiological condition being influenced by a fluid delivered by an infusion device; and in response to each new interstitial fluid measurement value of the interstitial fluid measurement values; obtaining a current amount of active fluid in the body of the user; determining an estimated correction bolus amount of the fluid based at least in part on the current amount of active fluid, a target value for the physiological condition, and a current interstitial fluid measurement value for the physiological condition; determining a trend adjustment factor based on a difference between the current interstitial fluid measurement value and a preceding interstitial fluid measurement value; adjusting the estimated correction bolus amount by multiplying the estimated correction bolus amount by the trend adjustment factor; and generating an alert when the estimated correction bolus amount is greater than an alert threshold value. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20)
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Specification