Wearable cardioverter defibrillator with a non-invasive blood pressure monitor
A wearable cardioverter defibrillator (WCD) system comprises a plurality of patient parameter electrodes and a plurality of defibrillator electrodes to contact a patient's skin when the WCD is delivering therapy to the patient, a processor to receive one or more patient parameters from the one or more patient parameter electrodes, an energy storage device to store a charge to provide electrical therapy to the patient via the plurality of defibrillator electrodes, and a non-invasive blood pressure (NIBP) monitor to obtain a blood pressure measurement of the patient and to provide the blood pressure measurement to the processor. The processor is to determine whether to provide electrical therapy to the patient based on the one or more patient parameters during an episode, and to obtain the blood pressure measurement from the NIBP monitor during the episode.
1. A wearable cardioverter defibrillator (WCD) system, comprising:
a support structure configured to be worn by a patient;
a plurality of patient parameter electrodes and a plurality of defibrillator electrodes to contact a patient's skin when the patient is wearing the support structure and the WCD is delivering therapy to the patient;
a processor to receive one or more patient parameters from the one or more patient parameter electrodes;
an energy storage device to store a charge to provide electrical therapy to the patient via the plurality of defibrillator electrodes;
an alert button configured to receive a patient input to abort the electrical therapy; and
a non-invasive blood pressure (NIBP) monitor to obtain a blood pressure measurement of the patient and to provide the blood pressure measurement to the processor;
wherein the processor is to determine whether to provide electrical therapy to the patient based on the one or more patient parameters during an episode, and to obtain the blood pressure measurement from the NIBP monitor during the episode;
wherein the NIBP monitor is disposed in the alert button, and the processor is configured to obtain the blood pressure measurement when the patient contacts the alert button.
2. The WCD system of claim 1 , wherein the processor is to generate an alert when the blood pressure measurement has a value that is below a minimum value or above a maximum value.
3. The WCD system of claim 1 , wherein the processor is to generate a prompt for the patient to obtain a blood pressure measurement.
4. The WCD system of claim 1 , wherein the processor is to use the blood pressure measurement during the episode in combination with the one or more patient parameters to determine whether to provide electrical therapy to the patient.
5. The WCD system of claim 1 , wherein the NIBP monitor is coupled to one or more of the patient parameter electrodes.
6. The WCD system of claim 1 , wherein the NIBP monitor is attachable to an arm, a leg, a wrist, or an ankle of the patient, or at another location on the patient's body.
7. The WCD system of claim 1 , wherein the NIBP monitor is disposed in a smartphone or a wearable device that is capable of transmitting the blood pressure measurement to processor via a wired or a wireless communication link.
8. The WCD system of claim 1 , wherein the NIBP monitor comprises an SpO2 sensor or a temperature sensor, or a combination thereof.
9. A wearable cardioverter defibrillator (WCD) system, comprising:
a support structure configured to be worn by a patient;
a plurality of patient parameter electrodes and a plurality of defibrillator electrodes to contact a patient's skin when the patient is wearing the support structure and the WCD is delivering therapy to the patient;
a processor to receive one or more patient parameters from the one or more patient parameter electrodes, wherein the one or more patient parameters includes electrocardiogram (ECG) data;
an energy storage device to store a charge to provide electrical therapy to the patient via the plurality of defibrillator electrodes;
an alert button configured to receive a patient input to abort the electrical therapy; and
a non-invasive blood pressure (NIBP) monitor to obtain a blood pressure measurement of the patient and to provide the blood pressure measurement to the processor;
wherein the processor is to determine whether to provide electrical therapy to the patient based on the one or more patient parameters and the blood pressure measurement during an episode;
wherein the NIBP monitor is disposed in the alert button, and the processor is configured to obtain the blood pressure measurement when the patient contacts the alert button.
10. The WCD system of claim 9 , wherein the electrical therapy is applied to the patient when the processor determines that the patient has a heart rate above a heart rate threshold and a blood pressure below a blood pressure threshold.
11. The WCD system of claim 10 , wherein the processor is to analyze the ECG data in segments of ECG data and to obtain a blood pressure measurement for each of the segments of ECG data, wherein a determination is made to provide electrical therapy to the patient when a string of a predetermined number of segments indicate a shock decision should be made and ventricular tachycardia (VT) criterion is met and the patient is in a non-perfusing state.
12. The WCD system of claim 11 , wherein a determination is not made to provide electrical therapy to the patient when the VT criterion is met and the patient is perfusing, or when a super ventricular tachycardia (SVT) criterion is met and the patient is non-perfusing.
13. The WCD system of claim 9 , wherein a determination is made to provide electrical therapy to the patient when the processor determines that the patient has a disorganized ventricular rhythm and has a blood pressure reading below a predetermined threshold, or when the ECG data indicates the patient is in the ventricular fibrillation (VF) zone, and wherein time between shocks is increased to allow a heart rhythm to self-terminate when the patient is perfusing.
14. The WCD system of claim 9 , wherein a determination is made to provide electrical therapy to the patient when the patient's heart rate is above a minimum threshold and the patient is non-perfusing, or when the patient's QRS complex width is above a minimum threshold and the patient is non-perfusing, or when a sudden drop in blood pressure occurs coincident with an increased heart rate, an increase in R-wave width, and a disorganized heart rhythm.
15. The WCD system of claim 9 , wherein the NIBP monitor is to obtain a heart rate value independent from the ECG data.