Fluid Delivery Device With Integrated Monitoring Of Physiological Characteristics

• US 20100063438A1
• Filed: 01/12/2006
• Published: 03/11/2010
• Est. Priority Date: 01/17/2005
• Status: Abandoned Application

• Current Assignee: Novo Nordisk A/S
• Original Assignee: Novo Nordisk A/S
• Inventors: Bengtsson, Henrik
• Application Number:
  US11/813,429
• Publication Number:
  US 20100063438A1
• Time in Patent Office: Days
• US Class Current: 604/66
• CPC Class Codes: A61B 2560/0468 Built-in electrodes
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61M 2005/14268 with a reusable and a disposable component
• CPC Class Codes: A61M 2205/332 Force measuring means
• CPC Class Codes: A61M 2230/201 Glucose concentration
• CPC Class Codes: A61M 2230/62 Posture
• CPC Class Codes: A61M 5/14248 of the skin patch type
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00

Abstract

The present application relates to a drug delivery device (100) for delivering liquids to a subject user. More specifically, the drug delivery device provides monitoring facilities of ECG related signals picked up by ECG sensor elements (151) incorporated in or on the housing (101) of the drug delivery device. Additional sensor elements (152) may be included in the drug delivery device to facilitate recording of additional physiological parameters. The drug delivery device may comprise storage capabilities or dedicated signal processing circuitry (120) for analyzing the received signals, and means for providing an output as a response to a detected physiological condition. Other aspects include an optional external device which may provide analyzing circuitry for presenting and displaying of sensor data or identified physiological conditions.

Claims

1. A fluid delivery device (100) for attachment to the skin of a subject user, the delivery device comprising:

a housing,

a reservoir (111) adapted to contain a fluid and comprising, in a situation of use, associated transcutaneous access means (113) communicating, in a situation of use, with the interior of the reservoir (111) and adapted to penetrate the skin of the subject,

expelling means (112) for expelling a fluid out of the reservoir (111) through the transcutaneous access means (113),

first sensor elements (151) disposed on or in said housing and adapted for obtaining electric signals representative of ECG signals of said subject, and

electronic circuitry coupled to said first sensor elements (151) and adapted to measure, monitor, calculate, and/or store data related to said sensed ECG signals.

2. A fluid delivery device as defined in claim 1, wherein said first sensor elements (151) comprises sensors capable of sensing one or more physiological parameters selected from the group consisting of heart rate, heart rate variability (HRV), QT interval, QT dispersion, polarity of T wave, amplitude of the T-wave, T-wave ratio, QRS amplitude, QRS length and respiration rate.

3. A fluid delivery device as defined in claim 1, wherein said first sensor elements (151) are further adapted to sense physiological parameters selected from the group consisting of skin resistance, skin impedance and electromyogram (EMG).

4. A fluid delivery device as defined in claim 1, wherein the delivery device further comprises secondary sensor elements (152) capable of sensing physiological parameters selected from the group consisting of skin temperature, ambient temperature, oxygen saturation, blood pressure, pulse rate, respiration rate, glucose level, CO₂ content of blood, position of patient, movement of body, acoustic sounds produced by the heart and pH.

5. A fluid delivery device as defined in claim 1, wherein the delivery device further comprises communication means for receiving physiological parameters detected and transmitted by an external device (153, 200), the external device comprising sensors capable of sensing parameters selected from the group consisting of skin temperature, ambient temperature, ECG, EEG, mean or peak frequency of the alpha wave, oxygen saturation, blood pressure, lung wetness, glucose level, thoracic impedance, ICV pressure, CO₂ content of blood, position of patient, movement of body, acoustic sounds produced by the heart and pH.

6. A fluid delivery device as defined in claim 1, further comprising means for storing data related to sensor signals obtained by the first sensor elements (151).

7. A fluid delivery device as defined in claim 4, further comprising means for storing data related to sensor signals obtained by the secondary sensor elements (152, 153).

8. A fluid delivery device as defined in claim 1, further comprising processing means (120) for processing said sensed signals to provide data indicative of the presence or onset of a physiological condition of said subject.

9. A fluid delivery device as defined in claim 8, wherein the physiological condition is selected from the group consisting of hypoglycemia, hyperglycemia, level of blood glucose, physical activity level and sleep activity.

10. A fluid delivery device as defined in claim 1, further comprising means for transmitting data related to said sensed signals to an external device (200).

11. A fluid delivery device as defined in claim 1, wherein the first sensor elements (151) are adapted for obtaining native electrical signals not provoked by subcutaneously implanted devices.

12. A fluid delivery device as defined in claim 1, wherein the delivery device (100) is adapted for placement at the abdomen of the subject user.

13. A fluid delivery device as defined in claim 1, wherein the first sensor elements (151) comprises two or more electrodes adapted for contacting the skin of said subject.

14. A fluid delivery device as defined in claim 1, wherein said transcutaneous access means (113) constitutes one of said first sensor elements (151).

15. A fluid delivery device as defined in claim 1, further comprising a mounting surface (104) adapted for application to the skin of the subject, wherein the mounting surface (104) of said fluid delivery device (100) constitutes one of said first sensor elements (151).

16. A fluid delivery device as defined in claim 1, wherein the transcutaneous access means (113) are selected from the group of infusion needles, flexible infusion cannulas, micro-penetrators or electrotransport devices.

17. A fluid delivery device as defined in claim 1, wherein the fluid is selected from the group consisting of insulin and glucagons.

18. A fluid delivery device as defined in claim 8, wherein the delivery device comprises response means (160) for providing a response as a function of an identified presence or onset of a physiological condition of said subject.

19. A fluid delivery device as defined in claim 18, wherein the response means (160) comprises output means (161,163) providing signals selected from the group consisting of audible signals, visual signals, tactile signals, electro-muscle stimulation and vibratory signals.

20. A fluid delivery device as defined in claim 18, wherein the expelling means (112) are controlled by a control signal, and that said control signal is based at least in part on the response taken by the response means (160).

21. A fluid delivery device as defined in claim 1, further comprising a mounting surface (104) adapted for application to the skin of the subject, wherein the mounting surface (104) comprises adhesive means which allows the device to be affixed to the skin of the subject user.

22. A fluid delivery device as defined in claim 1, wherein one or more of the first sensor elements (151) are provided with an electrical conducting adhesive for attachment to the skin of the user.

23. A system including a fluid delivery device (100) as defined in claim 1, and further comprising an external device (200) separate from said fluid delivery device (100), wherein:

said fluid delivery device (100) comprises communication means for communicating with said external device (200),

said external device (200) comprises communication means adapted for communicating with the fluid delivery device (100) such that information related to sensor signals obtained by the delivery device (100) can be transferred to the external device (200).

24. A system as defined in claim 23, wherein said transferred information comprises partial or full representations of sensed ECG signals.

25. A system as defined in claim 23, wherein said transferred information comprises extracted features of sensed ECG signals.

26. A system as defined claim 23, wherein the external device (200) further comprises processing means for processing said transferred information to provide data indicative of the presence or onset of a physiological condition of said subject.

27. A system as defined in claim 26, wherein said external device (200) comprises means for presenting an output as a response to an identified presence or onset of a physiological condition of said subject.

28. A system as defined in claim 26, wherein said external device (200) further comprises means for transferring information related to an identified presence or onset of a physiological condition of said subject to said fluid delivery device (100).