Integrated medication and infusion monitoring system
View Patent ↗A System manages IV pumps so that clinicians automatically receive alerts, decisions, and actions required to maintain a patient IV medication therapy according to a prescribed treatment protocol. An infusion pump monitoring system, includes an acquisition processor for acquiring fluid infusion parameters comprising a patient identifier, infusion fluid identifier and a rate of fluid infusion, for administration of an infusion fluid to a patient at a point of care using an infusion pump. The system also includes a repository of patient medical record information. A fluid infusion monitor uses acquired fluid infusion parameters for automatically searching a patient medical record in the repository for information concerning rate of fluid infusion of a particular infusion fluid and determining if a rate of a previously administered dose of the particular infusion fluid was lower than a rate indicated in the fluid infusion parameters. An interface processor automatically initiates generation of a message indicating a potential adverse reaction to the particular infusion fluid in response to a determination of a lower rate being employed for previously administering the particular infusion fluid.
1. An infusion pump monitoring system, comprising:
an acquisition processor for acquiring fluid infusion parameters comprising a patient identifier, infusion fluid identifier and a rate of fluid infusion to be used for a patient, for administration of an infusion fluid to a patient at a point of care using an infusion pump;
a repository of patient medical record information;
a fluid infusion monitor for using acquired fluid infusion parameters for automatically searching a patient medical record in said repository for information concerning rate of fluid infusion of a particular infusion fluid and determining if a rate of a previously administered dose of said particular infusion fluid was lower than a rate indicated in said fluid infusion parameters; and
an interface processor for automatically initiating generation of a message indicating a potential adverse reaction to said particular infusion fluid in response to a determination of a lower rate being employed for previously administering said particular infusion fluid to said patient, wherein said interface processor initiates generation of a message for communication to an infusion pump to at least one of, (a) reduce rate of fluid infusion and (b) inhibit operation of an infusion pump until a healthcare worker enters a command to acknowledge said message indicating said potential adverse reaction in response to said determination.
2. A system according to claim 1 , wherein said medical record identifies the fluid infusion medication and the infusion rate that resulted in the adverse reaction and the lower infusion rate that resulted in a reaction-free infusion administration and said message prompts a healthcare worker to lower said rate indicated in said fluid infusion parameters.
3. A system according to claim 1 , wherein said message indicating a potential adverse reaction to said particular infusion fluid comprises a displayed alert message to a healthcare worker.
4. A system according to claim 1 , wherein said message indicating a potential adverse reaction to said particular infusion fluid comprises an indication of said lower rate employed for previously administering said particular infusion fluid.
5. A system according to claim 1 , wherein said acquisition processor acquires said fluid infusion parameters from a Bar-code Point of Care system.
6. A system according to claim 1 , wherein said acquisition processor acquires said fluid infusion parameters from an infusion pump.
7. A system according to claim 1 , wherein said interface processor automatically initiates generation of a message indicating a potential adverse reaction to said particular infusion fluid for communication to a pharmacy information system.
8. A method of monitoring a plurality of medical infusion pumps, comprising the steps of:
acquiring fluid infusion parameters comprising a patient identifier, infusion fluid identifier and a rate of fluid infusion to be used for a patient, for administration of an infusion fluid to a patient at a point of care using an infusion pump;
storing in at least one repository, patient medical record information;
using acquired fluid infusion parameters for automatically searching a patient medical record in said repository for information concerning rate of fluid infusion of a particular infusion fluid and determining if a rate of a previously administered dose of said particular infusion fluid was lower than a rate indicated in said fluid infusion parameters;
automatically initiating generation of a message indicating a potential adverse reaction to said particular infusion fluid in response to a determination of a lower rate being employed for previously administering said particular infusion to said patient; and
automatically initiating generation of a message for communication to an infusion pump to at least one of, (a) reduce rate of fluid infusion and (b) inhibit operation of an infusion pump until a healthcare worker enters a command to acknowledge said message indicating said potential adverse reaction in response to said determination.