Cardiac Biosensor Devices and Methods

• US 20080033260A1
• Filed: 08/02/2007
• Published: 02/07/2008
• Est. Priority Date: 08/03/2006
• Status: Abandoned Application

• Current Assignee: MicroCHIPS Inc.
• Original Assignee: MicroCHIPS Inc.
• Inventors: Santini, John T., Sheppard, Norman F.
• Application Number:
  US11/833,011
• Publication Number:
  US 20080033260A1
• Time in Patent Office: Days
• US Class Current: 600/301
• CPC Class Codes: A61B 5/0002 Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network A61B5/07 takes precedence; transmission systems for measured values G08C; transmission H04B; transmission of digital information H04L; wireless communication networks H04W
• CPC Class Codes: A61B 5/0215 by means inserted into the body catheters A61M25/00
• CPC Class Codes: A61B 5/026 Measuring blood flow A61B3/1233, A61B3/1241 take precedence
• CPC Class Codes: A61B 5/145 Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissuemeasuring of blood pressure or blood flow A61B5/02; non-radiation detecting or locating of foreign bodies in blood A61B5/06
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14539 for measuring pH
• CPC Class Codes: A61N 1/05 for implantation or insertion into the body, e.g. heart electrode A61N1/06 takes precedence
• CPC Class Codes: A61N 1/36557 controlled by chemical substances in blood

Abstract

Implantable medical devices for cardiac care are provided that include a housing having a power source and control electronics; at least one lead extending from the housing and having one or more discrete reservoirs therein, each reservoir having an opening to an outer surface of the lead; one or more sensors, which monitor or detects an analyte, biomarker, or physical parameter that is associated with cardiac health, located in the reservoirs and in operable communication with said control electronics; and at least one selectively disintegratable reservoir cap sealing each of the reservoir openings, wherein the reservoir cap is operably connected to the power source and control electronics to disintegrate the reservoir cap and expose the sensors in vivo. The sensor may detect an analyte or biomarker selected from potassium ion, sodium ion, lithium ion, magnesium ion, ammonium ion, ionized calcium, lactate, oxygen, carbon dioxide, and creatinine, urea, BUN, and bilirubin.

Claims

1. An implantable medical device comprising:

a housing which includes a power source and control electronics;

at least one lead extending from the housing and having one or more discrete reservoirs therein, each reservoir having at least one opening to an outer surface of the lead;

one or more sensors, which monitor or detects in vivo an analyte, biomarker, or physical parameter that is associated with cardiac health, located in the one or more reservoirs and in operable communication with said control electronics; and

at least one selectively disintegratable reservoir cap sealing each of said at least one opening of said one or more reservoirs,

wherein the at least one reservoir cap is operably connected to the power source and control electronics to selectively disintegrate the reservoir cap and expose the one or more sensors in vivo.

2. The device of claim 1, wherein the one or more sensors comprises a biosensor for the monitoring or detecting of an analyte or a biomarker selected from the group consisting of potassium ion, sodium ion, lithium ion, magnesium ion, ammonium ion, ionized calcium, lactate, oxygen, carbon dioxide, creatinine, urea, BUN, bilirabin, alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase, lactic dehydrogenase, gamma glutamyl transpeptidase, heparin, warfarin, ischemia modified albumin (IMA), myeloperoxidase, matrix metalloproteinase (MMP), pH, and placental growth factor.

3. The device of claim 1, wherein the one or more sensors or sensing components measures an ECG, an EKG, or another intrinsic electrical signal.

4. The device of claim 1, wherein the one or more reservoirs are located on a tip portion of the at least one lead.

5. The device of claim 1, wherein the at least one lead further comprises a secondary sensor located on an external surface of the at least one lead and not in the one or more reservoirs.

6. The device of claim 1, wherein the at least one lead further comprises an electrode for cardiac pacing, defibrillation, or neurostimulation.

7. The device of claim 1, wherein the at least one lead further comprises one or more secondary reservoirs containing at least one drug for controlled release in vivo.

8. The device of claim 7, wherein release of the at least one drug from the one or more secondary reservoirs is passively controlled.

9. The device of claim 7, wherein release of the at least one drug from the one or more secondary reservoirs is actively controlled.

10. The device of claim 1, further comprising at least one secondary lead without a sensor.

11. The device of claim 10, wherein the at least one secondary lead further comprises an electrode for cardiac pacing, defibrillation, or neurostimulation.

12. The device of claim 10, wherein the at least one secondary lead further comprises a plurality of drug reservoirs for controlled release of drug in vivo.

13. The device of claim 1, further comprising a transmitter for communicating an electrical signal from the one or more sensors to a remote receiver.

14. The device of claim 13, wherein the remote receiver is operably coupled to a controller for controlling delivery of a drug.

15. The device of claim 13, wherein the remote receiver is operably coupled to a controller for controlling cardiac pacing, defibrillation, or neurostimulation.

16. The device of claim 1, wherein the control electronics comprise a microprocessor or state machine.

17. A method of monitoring a patient in need of cardiac care comprising:

implanting into a patient a medical device which comprises

a housing which includes a power source and control electronics,

at least one lead extending from the housing and having one or more discrete reservoirs therein, each reservoir having at least one opening to an outer surface of the lead,

one or more sensors, which monitor or detects in vivo an analyte, biomarker, or physical parameter that is associated with cardiac health, located in the one or more reservoirs and in operable communication with said control electronics, and

at least one reservoir cap sealing each of said at least one opening of said one or more reservoirs, wherein the at least one reservoir cap is operably connected to the power source and control electronics;

opening the at least one opening of the at least one reservoir in response to the control electronics and exposing the one or more sensors in vivo; and

using the one or more sensors to monitor or detect an analyte, biomarker, or physical parameter associated with the health of the patient'"'"'s heart.

18. The method of claim 17, wherein the analyte or biomarker is selected from the group consisting of potassium ion, sodium ion, lithium ion, magnesium ion, ammonium ion, ionized calcium, lactate, oxygen, carbon dioxide, creatinine, urea, BUN, bilirubin, alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase, lactic dehydrogenase, gamma glutamyl transpeptidase, heparin, warfarin, ischemia modified albumin (IMA), myeloperoxidase, matrix metalloproteinase (MMP), pH, and placental growth factor.

19. The method of claim 17, wherein the physical parameter comprises a fluid flowrate, pressure, or viscosity.

20. The method of claim 17, wherein the physical parameter comprises an ECG, EKG, or another intrinsic electrical signal.

21. The method of claim 17, wherein the medical device further comprises an electrode for cardiac pacing, defibrillation, or neurostimulation.

22. The method of claim 17, wherein the medical device further comprises a drug for controlled release in vivo.

23. The method of claim 17, wherein the medical device comprises a plurality of discrete microreservoirs and a plurality of corresponding discrete reservoir caps which comprise a metal film and are mechanically and electrically connected to a pair of electrical leads.

24. The method of claim 17, wherein the step of opening the at least one opening of the at least one reservoir by permeabilizing or disintegrating the at least one reservoir cap.