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DK3101571T3 - Målesystem til måling af koncentrationen af en analyt med en subkutan analytsensor - Google Patents

Målesystem til måling af koncentrationen af en analyt med en subkutan analytsensor Download PDF

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Publication number
DK3101571T3
DK3101571T3 DK15170388.1T DK15170388T DK3101571T3 DK 3101571 T3 DK3101571 T3 DK 3101571T3 DK 15170388 T DK15170388 T DK 15170388T DK 3101571 T3 DK3101571 T3 DK 3101571T3
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Denmark
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medical
data
application
processor
wireless communication
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DK15170388.1T
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English (en)
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Stefan Riebel
Ralf Schmitz
Kai-Oliver Schwenker
Thomas Eissenloeffel
Carsten Mueglitz
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Hoffmann La Roche
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    • A61B5/0015—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network characterised by features of the telemetry system
    • A61B5/0022—Monitoring a patient using a global network, e.g. telephone networks, internet
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    • A61B5/0015—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network characterised by features of the telemetry system
    • A61B5/002—Monitoring the patient using a local or closed circuit, e.g. in a room or building
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  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
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Claims (13)

1. Medicinalsystem (100, 200, 300) omfattende en styreenhed (102) og et medicinaludstyr (104), - hvor medicinaludstyret er et krops-båret medicinaludstyr, hvor medicinaludstyret omfatter en subkutan del (110), hvor medicinaludstyret strømforsynes af et første batteri (120), hvor medicinaludstyret omfatter et første trådløst kommunikationsmodul (116), hvor medicinaludstyret omfatter en første processor (114) og en første hukommelse (118), hvor den første hukommelse indeholder medicinaludstyr-instruktioner (122) til drift af medicinaludstyret, hvor medicinaludstyret omfatter et overvågningssystem (112), hvor overvågningsystemet omfatter en sensor (110) til at måle en analytkoncentration (124), hvor den subkutane del omfatter mindst en del af en analytsensor; - hvor styreenheden strømforsynes af et andet batteri (130), hvor styreenheden yderligere omfatter et andet trådløst kommunikationsmodul (132) hvor styreenheden omfatter en anden processor (134) og en anden hukommelse (136), hvor den anden hukommelse omfatter en anvendelsesdeling (138) og en persisterende deling (140), hvor anvendelsesfordelingen indeholder en medicinske anvendelse (142) og anvendelsesdata (144), hvor den persisterende deling indeholder arkivdata (146), hvor de arkiverede data omfatter en kopi af mindst en del af anvendelsesdataet; - hvor det første kommunikationsmodul og det andet trådløse kommunikationsmodul er operable til dannelse af en trådløs kommunikationskanal (152) mellem medicinaludstyret og styreenheden; - hvor den medicinske anvendelse i styreenheden er konfigureret til at styre medicinaludstyret ved at sende beskeder til den første processor via den trådløse kommunikationskanal, hvor udførelse af kontrollerinstruktionerne forårsager den anden processor til at styre overvågningssystemet via den trådløse kommunikationskanal, hvor den medicinske anvendelse er konfigureret til at modificere anvendelsesdataet i anvendelsesfordelingen og lagre den del af anvendelsesdataene omfattet i de arkiverede data i den persisterende deling (140); - hvor den medicinske dataregistrering omfatter analytkoncentrationen, hvor udførelsen af medicinaludstyr-instruktionerne forårsager den første processor til at: • optage analytkoncentrationen under anvendelse af overvågning ssyste m et, • generere en medicinsk-dataregistrering mindst delvist under anvendelse af analytkoncentrationen, og • overføre den medicinske dataregistrering til styreenheden under anvendelse af den trådløse kommunikationskanal, hvor anvendelsesdataet omfatter den medicinske dataregistrering; og - hvor den anden hukommelse yderligere indeholder et driftssystem, hvor driftssystemet er operabelt til de-installation af den medicinske anvendelse, hvor de-installationen fjerner anvendelsesdataet og opbevarer de arkiverede data på den persistente fordeling.
2. Medicinalsystem ifølge krav 1, hvor styreenheden yderligere omfatter en dataudvekslingsbrugerflade (150) til udveksling af data med et computersystem, hvor anvendelsesdataet og/eller arkiverede data er tilgængeligt til computersystemet via dataudvekslingsbrugerfladen.
3. Medicinalsystemet ifølge kravene 1 eller 2, hvor medicinaludstyr-instruktionerne omfatter et første sæt linjeparringsinstruktioner (122'), hvor anvendelsesdataet omfatter et andet sæt linjeparringsinstruktioner (124'), hvor det arkiverede data omfatter det andet sæt linjeparringsinstruktioner, hvor udførelse af det første sæt linjeparringsinstruktioner med den første processor og udførelse af det andet sæt linjeparringsinstruktioner med den anden processor forårsager det første kommunikationsmodul til at parre med det andet kommunikationsmodul til at danne den trådløse kommunikationskanal, hvor den medicinske anvendelse er konfigureret til søgning i den persisterende deling efter det andet sæt linjeparringsinstruktioner efter at være blevet re-installeret, hvor den medicinske anvendelse er konfigureret til re-etablering af den trådløse kommunikationskanal, hvis det andet sæt linjeparringsinstruktioner er detekteret.
4. Medicinalsystemet ifølge et hvilket som helst af de foregående krav; hvor anvendelsesdataet omfatter mindst en dataregistrering (306) omfattende en logdataregistrering, medicinsk dataregistrering, og/elleren systemdataregistrering; hvor udførelse af den medicinske anvendelse forårsager den anden processor til at: • generere dataregistreringer; • på hæg te/ved hæfte dataregistreringen til anvendelsesdataet; og • påhægte dataregistreringen til det arkiverede data.
5. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor udførelse af den medicinske anvendelse forårsager den anden processor til at generere en fejlmeddelelse som respons på en styreenhedsfunktionsfejl eller en medicinaludstyrsfunktionsfejl, hvor log-dataregistreringen genereres mindst delvist under anvendelse af fejlmeddelelsen.
6. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor udførelse af den medicinske anvendelse forårsager den anden processor til at generere en system-log-deskription afen hardware-konfiguration af styreenheden og/eller en software-konfiguration af styreenheden, hvor systemdataregistreringen genereres mindst delvist under anvendelse af system-log'en.
7. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor udførelse af den medicinske anvendelse yderligere forårsager den anden processor til at kryptere dataregistreringen med en krypteringsnøgle (212) før påhæftning af dataregistreringen til anvendelsesdataet.
8. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor udførelse af den medicinske anvendelse forårsager den anden processor til at kryptere de arkiverede data.
9. Medicinalsystemet ifølge kravene 7 eller 8, hvor krypteringsnøglen for logdataregistreringen og/eller system-dataregistreringen er en offentlig nøgle (212) af et asymmetrisk nøglepar.
10. Medicinalsystemet ifølge et hvilket som helst af kravene 7 til 9, hvor krypteringsnøglen for den medicinske dataregistrering er en offentlig nøgle af et symmetrisk nøglepar.
11. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor den subkutane del omfatter mindst en del af en glucosesensor, hvor medicinaludstyret omfatter et glucoseovervågningssystem.
12. Medicinalsystemet ifølge et hvilket som helst af de foregående krav, hvor den subkutane del omfatter mindst en kanyle, hvor medicinaludstyret omfatter et pumpesystem.
13. Medicinalsystem ifølge krav 12, hvor pumpesystemet omfatter en hvilken som helst af følgende: en insulinpumpe til at pumpe insulin gennem den mindst ene kanyle, en glucagonpumpe til at pumpe glucagon gennem den mindst ene kanyle, og kombinationer deraf; og hvor udførelse af kontrollerinstruktionerne forårsager den anden processor til at styre pumpesystemet via trådløs kommunikationskanal.
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US10660521B2 (en) 2020-05-26
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