Defibrillation electrode pad assembly including CPR pad

• US 7,245,974 B2
• Filed: 08/03/2004
• Issued: 07/17/2007
• Est. Priority Date: 09/14/2001
• Status: Expired due to Term

• Current Assignee: Zoll Medical Corporation (Asahi Kasei Corporation)
• Original Assignee: Zoll Medical Corporation (Asahi Kasei Corporation)
• Inventors: Faller, Frederick W., Hamilton, Ward, Dupelle, Michael R., Jones, Deborah T.
• Primary Examiner(s): DROESCH, KRISTEN L
• Application Number:
  US10/911,187
• Publication Number:
  US 20050010274A1
• Time in Patent Office: 1,078 Days
• Field of Search: 607 1- 2, 607 4- 5, 607/115, 607/148, 607/149, 607/152, 600/372, 600/382, 600/386, 600388-393
• US Class Current: 607/142
• CPC Class Codes: A61N 1/046 Specially adapted for shock therapy, e.g. defibrillation
• CPC Class Codes: A61N 1/0492 Patch electrodes A61N1/0412, A61N1/0428 take precedence

Abstract

Electrode assemblies are provided, in which a pair of electrodes is joined by a central member. In some implementations, the electrode assemblies are foldable, and are configured to facilitate correct placement on a patient'"'"'s chest. Some electrode assemblies include a separable electrode, allowing the electrode assembly to be fitted to patients having particularly large chests.

Claims

1. A method of applying a defibrillation electrode assembly to a patient, comprising

removing an electrode pad assembly from a package, the electrode pad assembly comprising

a pair of defibrillation electrodes configured to be attached to a patient'"'"'s chest, to acquire data indicative of the patient'"'"'s heart rhythm and to deliver a defibrillating shock if appropriate;

a central member joining the electrodes; and

an indicia on an exposed surface of the electrode assembly, the indicia including a first portion and a second portion, the indicia being positioned so that alignment of the first portion with a patient'"'"'s nipples and alignment of the second portion with the patient'"'"'s sternum will correctly position the electrodes on the patient'"'"'s chest for effective defibrillation treatment;

applying the electrode pad assembly to the patient by

aligning the first portion of the indicia with the patient'"'"'s nipples, and

aligning the second portion of the indicia with the patient'"'"'s sternum.

2. The method of claim 1 wherein the indicia are located so that when the indicia are aligned with the nipples and sternum the indicia will indicate to a caregiver where the caregiver'"'"'s hands should be placed during the delivery of CPR chest compressions.

3. The method of claim 1 wherein the indicia are disposed on the central member.

4. The method of claim 1 wherein the electrode pad assembly further comprises a CPR pad, mounted on the central member, the indicia being disposed on the CPR pad.

5. The method of claim 4 wherein the CPR pad includes a concave upper surface shaped to facilitate placement of the caregiver'"'"'s hand.

6. The method of claim 4 wherein the CPR pad includes a convex lower surface shaped to conform to the patient'"'"'s sternal notch area.

7. The method of claim 4 wherein the CPR pad includes a sensor constructed to acquire data indicative of the depth of CPR compressions.

8. The method of claim 4 or 7 wherein the CPR pad includes a sensor constructed to acquire data indicative of the rate of CPR compressions.

9. A method of applying a defibrillation electrode assembly to a patient, comprising

removing an electrode pad assembly from a package, the electrode pad assembly comprising

a pair of electrodes configured to be attached to a patient'"'"'s chest, to acquire data indicative of the patient'"'"'s heart rhythm and to deliver a defibrillating shock if appropriate;

and

a central member joining the electrodes;

the electrodes being folded about the central member and the electrode assembly further including labeling indicating how a caregiver should unfold the electrode assembly and apply it to a patient;

applying the electrode pad assembly to the patient by

observing the labeling to determine a procedure for unfolding the electrodes;

following the procedure to unfold the electrodes.

10. An electrode assembly for use with a defibrillator, comprising

an apex electrode and a sternum electrode, the electrodes being configured to be attached to a patient'"'"'s chest, to acquire data indicative of the patient'"'"'s heart rhythm and to deliver a defibrillating shock if appropriate;

and

a central member joining the electrodes;

wherein one of the electrodes is configured to be optionally separated mechanically from the central member but to remain electrically connected to the defibrillator, wherein the electrode assembly is configured so that the optional separation can occur while the apex electrode, central member, and sternum electrode are being applied to the patient'"'"'s chest,

wherein the electrode that has been optionally separated is separably joined to the central member by a separable flexible fastener.

11. The electrode assembly of claim 10 wherein said separable flexible fastener comprises a separable hinge.

12. The electrode assembly of claim 11 wherein said separable hinge includes a locking pin constructed to be removed by a caregiver to separate the hinge.

13. The electrode assembly of claim 10 wherein said separable flexible fastener comprises a hook and loop fastener tape.

14. The electrode assembly of claim 10 wherein the separable flexible fastener includes a tear-away strip.

15. An electrode assembly for use with a defibrillator, comprising

an apex electrode and a sternum electrode, the electrodes being configured to be attached to a patient'"'"'s chest, to acquire data indicative of the patient'"'"'s heart rhythm and to deliver a defibrillating shock if appropriate;

and

a central member joining the electrodes;

wherein one of the electrodes is configured to be optionally separated mechanically from the central member but to remain electrically connected to the defibrillator, wherein the electrode assembly is configured so that the optional separation can occur while the apex electrode, central member, and sternum electrode are being applied to the patient'"'"'s chest,

wherein the electrode that has been optionally separated, after separation from the central member, is joined to the central member only by an electrical connector.

16. The electrode assembly of claim 15 wherein the electrode that has been optionally separated is the apex electrode.

17. The electrode assembly of claim 15 wherein the electrodes have a combined active area of at least 150 cm².

18. The electrode assembly of claim 15 wherein each electrode has an active area of at least 50 cm².

19. The electrode assembly of claim 18 wherein each electrode has an active area of at least 75 cm².

20. The electrode assembly of claim 15 further comprising lead wires configured to electrically connect the electrodes to the defibrillator, wherein prior to use the lead wires are substantially completely enclosed within the electrode assembly.

21. The electrode assembly of claim 15 further comprising a release sheet, mounted on a surface of each electrode to protect the electrodes, the release sheet being configured to be removable when the electrode is positioned adjacent the patient'"'"'s skin.